WO2005004256A2 - Annular fuel processor and methods - Google Patents

Annular fuel processor and methods Download PDF

Info

Publication number
WO2005004256A2
WO2005004256A2 PCT/US2004/020299 US2004020299W WO2005004256A2 WO 2005004256 A2 WO2005004256 A2 WO 2005004256A2 US 2004020299 W US2004020299 W US 2004020299W WO 2005004256 A2 WO2005004256 A2 WO 2005004256A2
Authority
WO
WIPO (PCT)
Prior art keywords
burner
fuel processor
dewar
reformer
fuel
Prior art date
Application number
PCT/US2004/020299
Other languages
French (fr)
Other versions
WO2005004256A3 (en
Inventor
Ian W. Kaye
Arpad Somogyvari
Qailmus Khan
Original Assignee
Ultracell Corporation
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ultracell Corporation filed Critical Ultracell Corporation
Priority to JP2006517622A priority Critical patent/JP2007524562A/en
Priority to EP04756039A priority patent/EP1644111A4/en
Publication of WO2005004256A2 publication Critical patent/WO2005004256A2/en
Publication of WO2005004256A3 publication Critical patent/WO2005004256A3/en

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
    • B01J8/0285Heating or cooling the reactor
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01BBOILING; BOILING APPARATUS ; EVAPORATION; EVAPORATION APPARATUS
    • B01B1/00Boiling; Boiling apparatus for physical or chemical purposes ; Evaporation in general
    • B01B1/005Evaporation for physical or chemical purposes; Evaporation apparatus therefor, e.g. evaporation of liquids for gas phase reactions
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J12/00Chemical processes in general for reacting gaseous media with gaseous media; Apparatus specially adapted therefor
    • B01J12/007Chemical processes in general for reacting gaseous media with gaseous media; Apparatus specially adapted therefor in the presence of catalytically active bodies, e.g. porous plates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J15/00Chemical processes in general for reacting gaseous media with non-particulate solids, e.g. sheet material; Apparatus specially adapted therefor
    • B01J15/005Chemical processes in general for reacting gaseous media with non-particulate solids, e.g. sheet material; Apparatus specially adapted therefor in the presence of catalytically active bodies, e.g. porous plates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/24Stationary reactors without moving elements inside
    • B01J19/248Reactors comprising multiple separated flow channels
    • B01J19/2485Monolithic reactors
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/24Stationary reactors without moving elements inside
    • B01J19/248Reactors comprising multiple separated flow channels
    • B01J19/249Plate-type reactors
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/24Stationary reactors without moving elements inside
    • B01J19/248Reactors comprising multiple separated flow channels
    • B01J19/2495Net-type reactors
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
    • B01J8/04Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid passing successively through two or more beds
    • B01J8/0496Heating or cooling the reactor
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/32Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
    • C01B3/323Catalytic reaction of gaseous or liquid organic compounds other than hydrocarbons with gasifying agents
    • GPHYSICS
    • G06COMPUTING; CALCULATING OR COUNTING
    • G06FELECTRIC DIGITAL DATA PROCESSING
    • G06F1/00Details not covered by groups G06F3/00 - G06F13/00 and G06F21/00
    • G06F1/26Power supply means, e.g. regulation thereof
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/04Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
    • H01M8/04007Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids related to heat exchange
    • H01M8/04014Heat exchange using gaseous fluids; Heat exchange by combustion of reactants
    • H01M8/04022Heating by combustion
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/06Combination of fuel cells with means for production of reactants or for treatment of residues
    • H01M8/0606Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants
    • H01M8/0612Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants from carbon-containing material
    • H01M8/0618Reforming processes, e.g. autothermal, partial oxidation or steam reforming
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/06Combination of fuel cells with means for production of reactants or for treatment of residues
    • H01M8/0606Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants
    • H01M8/0612Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants from carbon-containing material
    • H01M8/0625Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants from carbon-containing material in a modular combined reactor/fuel cell structure
    • H01M8/0631Reactor construction specially adapted for combination reactor/fuel cell
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008Controlling the process
    • B01J2208/00017Controlling the temperature
    • B01J2208/00106Controlling the temperature by indirect heat exchange
    • B01J2208/00168Controlling the temperature by indirect heat exchange with heat exchange elements outside the bed of solid particles
    • B01J2208/00203Coils
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008Controlling the process
    • B01J2208/00017Controlling the temperature
    • B01J2208/00106Controlling the temperature by indirect heat exchange
    • B01J2208/00168Controlling the temperature by indirect heat exchange with heat exchange elements outside the bed of solid particles
    • B01J2208/00212Plates; Jackets; Cylinders
    • B01J2208/00221Plates; Jackets; Cylinders comprising baffles for guiding the flow of the heat exchange medium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008Controlling the process
    • B01J2208/00017Controlling the temperature
    • B01J2208/00106Controlling the temperature by indirect heat exchange
    • B01J2208/00309Controlling the temperature by indirect heat exchange with two or more reactions in heat exchange with each other, such as an endothermic reaction in heat exchange with an exothermic reaction
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008Controlling the process
    • B01J2208/00017Controlling the temperature
    • B01J2208/00477Controlling the temperature by thermal insulation means
    • B01J2208/00495Controlling the temperature by thermal insulation means using insulating materials or refractories
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008Controlling the process
    • B01J2208/00017Controlling the temperature
    • B01J2208/00504Controlling the temperature by means of a burner
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008Controlling the process
    • B01J2208/00017Controlling the temperature
    • B01J2208/0053Controlling multiple zones along the direction of flow, e.g. pre-heating and after-cooling
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008Controlling the process
    • B01J2208/00654Controlling the process by measures relating to the particulate material
    • B01J2208/00672Particle size selection
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00049Controlling or regulating processes
    • B01J2219/00051Controlling the temperature
    • B01J2219/00157Controlling the temperature by means of a burner
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00049Controlling or regulating processes
    • B01J2219/00051Controlling the temperature
    • B01J2219/00159Controlling the temperature controlling multiple zones along the direction of flow, e.g. pre-heating and after-cooling
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00781Aspects relating to microreactors
    • B01J2219/00783Laminate assemblies, i.e. the reactor comprising a stack of plates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00781Aspects relating to microreactors
    • B01J2219/00788Three-dimensional assemblies, i.e. the reactor comprising a form other than a stack of plates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00781Aspects relating to microreactors
    • B01J2219/00801Means to assemble
    • B01J2219/00804Plurality of plates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00781Aspects relating to microreactors
    • B01J2219/00819Materials of construction
    • B01J2219/00822Metal
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00781Aspects relating to microreactors
    • B01J2219/00819Materials of construction
    • B01J2219/00824Ceramic
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00781Aspects relating to microreactors
    • B01J2219/00819Materials of construction
    • B01J2219/00824Ceramic
    • B01J2219/00828Silicon wafers or plates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00781Aspects relating to microreactors
    • B01J2219/00819Materials of construction
    • B01J2219/00835Comprising catalytically active material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00781Aspects relating to microreactors
    • B01J2219/00851Additional features
    • B01J2219/00858Aspects relating to the size of the reactor
    • B01J2219/0086Dimensions of the flow channels
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00781Aspects relating to microreactors
    • B01J2219/00851Additional features
    • B01J2219/00858Aspects relating to the size of the reactor
    • B01J2219/00862Dimensions of the reaction cavity itself
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00781Aspects relating to microreactors
    • B01J2219/00851Additional features
    • B01J2219/00869Microreactors placed in parallel, on the same or on different supports
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00781Aspects relating to microreactors
    • B01J2219/00851Additional features
    • B01J2219/00871Modular assembly
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00781Aspects relating to microreactors
    • B01J2219/00873Heat exchange
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00781Aspects relating to microreactors
    • B01J2219/00993Design aspects
    • B01J2219/00997Strategical arrangements of multiple microreactor systems
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/19Details relating to the geometry of the reactor
    • B01J2219/192Details relating to the geometry of the reactor polygonal
    • B01J2219/1923Details relating to the geometry of the reactor polygonal square or square-derived
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/19Details relating to the geometry of the reactor
    • B01J2219/194Details relating to the geometry of the reactor round
    • B01J2219/1941Details relating to the geometry of the reactor round circular or disk-shaped
    • B01J2219/1943Details relating to the geometry of the reactor round circular or disk-shaped cylindrical
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/24Stationary reactors without moving elements inside
    • B01J2219/2401Reactors comprising multiple separate flow channels
    • B01J2219/245Plate-type reactors
    • B01J2219/2451Geometry of the reactor
    • B01J2219/2453Plates arranged in parallel
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/24Stationary reactors without moving elements inside
    • B01J2219/2401Reactors comprising multiple separate flow channels
    • B01J2219/245Plate-type reactors
    • B01J2219/2451Geometry of the reactor
    • B01J2219/2456Geometry of the plates
    • B01J2219/2458Flat plates, i.e. plates which are not corrugated or otherwise structured, e.g. plates with cylindrical shape
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/24Stationary reactors without moving elements inside
    • B01J2219/2401Reactors comprising multiple separate flow channels
    • B01J2219/245Plate-type reactors
    • B01J2219/2451Geometry of the reactor
    • B01J2219/2456Geometry of the plates
    • B01J2219/2459Corrugated plates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/24Stationary reactors without moving elements inside
    • B01J2219/2401Reactors comprising multiple separate flow channels
    • B01J2219/245Plate-type reactors
    • B01J2219/2461Heat exchange aspects
    • B01J2219/2462Heat exchange aspects the reactants being in indirect heat exchange with a non reacting heat exchange medium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/24Stationary reactors without moving elements inside
    • B01J2219/2401Reactors comprising multiple separate flow channels
    • B01J2219/245Plate-type reactors
    • B01J2219/2461Heat exchange aspects
    • B01J2219/2465Two reactions in indirect heat exchange with each other
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/24Stationary reactors without moving elements inside
    • B01J2219/2401Reactors comprising multiple separate flow channels
    • B01J2219/245Plate-type reactors
    • B01J2219/2476Construction materials
    • B01J2219/2477Construction materials of the catalysts
    • B01J2219/2479Catalysts coated on the surface of plates or inserts
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/24Stationary reactors without moving elements inside
    • B01J2219/2401Reactors comprising multiple separate flow channels
    • B01J2219/245Plate-type reactors
    • B01J2219/2476Construction materials
    • B01J2219/2477Construction materials of the catalysts
    • B01J2219/2481Catalysts in granular from between plates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/24Stationary reactors without moving elements inside
    • B01J2219/2401Reactors comprising multiple separate flow channels
    • B01J2219/245Plate-type reactors
    • B01J2219/2476Construction materials
    • B01J2219/2483Construction materials of the plates
    • B01J2219/2485Metals or alloys
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/24Stationary reactors without moving elements inside
    • B01J2219/2401Reactors comprising multiple separate flow channels
    • B01J2219/245Plate-type reactors
    • B01J2219/2491Other constructional details
    • B01J2219/2492Assembling means
    • B01J2219/2493Means for assembling plates together, e.g. sealing means, screws, bolts
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/24Stationary reactors without moving elements inside
    • B01J2219/2401Reactors comprising multiple separate flow channels
    • B01J2219/245Plate-type reactors
    • B01J2219/2491Other constructional details
    • B01J2219/2497Size aspects, i.e. concrete sizes are being mentioned in the classified document
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/02Processes for making hydrogen or synthesis gas
    • C01B2203/0205Processes for making hydrogen or synthesis gas containing a reforming step
    • C01B2203/0227Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step
    • C01B2203/0233Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step the reforming step being a steam reforming step
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/02Processes for making hydrogen or synthesis gas
    • C01B2203/0205Processes for making hydrogen or synthesis gas containing a reforming step
    • C01B2203/0227Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step
    • C01B2203/0244Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step the reforming step being an autothermal reforming step, e.g. secondary reforming processes
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/02Processes for making hydrogen or synthesis gas
    • C01B2203/025Processes for making hydrogen or synthesis gas containing a partial oxidation step
    • C01B2203/0261Processes for making hydrogen or synthesis gas containing a partial oxidation step containing a catalytic partial oxidation step [CPO]
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/06Integration with other chemical processes
    • C01B2203/066Integration with other chemical processes with fuel cells
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/08Methods of heating or cooling
    • C01B2203/0805Methods of heating the process for making hydrogen or synthesis gas
    • C01B2203/0811Methods of heating the process for making hydrogen or synthesis gas by combustion of fuel
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/08Methods of heating or cooling
    • C01B2203/0805Methods of heating the process for making hydrogen or synthesis gas
    • C01B2203/0811Methods of heating the process for making hydrogen or synthesis gas by combustion of fuel
    • C01B2203/0816Heating by flames
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/08Methods of heating or cooling
    • C01B2203/0805Methods of heating the process for making hydrogen or synthesis gas
    • C01B2203/0811Methods of heating the process for making hydrogen or synthesis gas by combustion of fuel
    • C01B2203/0822Methods of heating the process for making hydrogen or synthesis gas by combustion of fuel the fuel containing hydrogen
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/08Methods of heating or cooling
    • C01B2203/0805Methods of heating the process for making hydrogen or synthesis gas
    • C01B2203/0811Methods of heating the process for making hydrogen or synthesis gas by combustion of fuel
    • C01B2203/0827Methods of heating the process for making hydrogen or synthesis gas by combustion of fuel at least part of the fuel being a recycle stream
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/08Methods of heating or cooling
    • C01B2203/0805Methods of heating the process for making hydrogen or synthesis gas
    • C01B2203/0838Methods of heating the process for making hydrogen or synthesis gas by heat exchange with exothermic reactions, other than by combustion of fuel
    • C01B2203/0844Methods of heating the process for making hydrogen or synthesis gas by heat exchange with exothermic reactions, other than by combustion of fuel the non-combustive exothermic reaction being another reforming reaction as defined in groups C01B2203/02 - C01B2203/0294
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/12Feeding the process for making hydrogen or synthesis gas
    • C01B2203/1205Composition of the feed
    • C01B2203/1211Organic compounds or organic mixtures used in the process for making hydrogen or synthesis gas
    • C01B2203/1217Alcohols
    • C01B2203/1223Methanol
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/12Feeding the process for making hydrogen or synthesis gas
    • C01B2203/1288Evaporation of one or more of the different feed components
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/14Details of the flowsheet
    • C01B2203/142At least two reforming, decomposition or partial oxidation steps in series
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/80Aspect of integrated processes for the production of hydrogen or synthesis gas not covered by groups C01B2203/02 - C01B2203/1695
    • C01B2203/82Several process steps of C01B2203/02 - C01B2203/08 integrated into a single apparatus
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/10Fuel cells with solid electrolytes
    • H01M2008/1095Fuel cells with polymeric electrolytes
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/50Fuel cells
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/10Process efficiency
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/10Process efficiency
    • Y02P20/129Energy recovery, e.g. by cogeneration, H2recovery or pressure recovery turbines

Definitions

  • the present invention relates to fuel cell technology.
  • the invention relates to fuel processors that generate hydrogen and are suitable for use in portable applications.
  • a fuel cell electrochemically combines hydrogen and oxygen to produce electricity.
  • the ambient air readily supplies oxygen.
  • Hydrogen provision calls for a working supply.
  • Gaseous hydrogen has a low energy density that reduces its practicality as a portable fuel.
  • Liquid hydrogen which has a suitable energy density, must be stored at extremely low temperatures and high pressures, making storing and transporting liquid hydrogen burdensome.
  • a reformed hydrogen supply processes a fuel source to produce hydrogen.
  • the fuel source acts as a hydrogen carrier.
  • hydrocarbon fuel sources include methanol, ethanol, gasoline, propane and natural gas.
  • Liquid hydrocarbon fuel sources offer high energy densities and the ability to be readily stored and transported.
  • a fuel processor reforms the hydrocarbon fuel source and to produce hydrogen. Fuel cell evolution so far has concentrated on large-scale applications such as industrial size generators for electrical power back-up. Consumer electronics devices and other portable electrical power applications currently rely on lithium ion and similar battery technologies. Fuel processors for portable applications such as electronics would be desirable but are not yet commercially available. In addition, techniques that reduce fuel processor size or increase fuel processor efficiency would be highly beneficial.
  • the present invention relates to a fuel processor that produces hydrogen from a fuel source.
  • the fuel processor comprises a reformer and burner.
  • the reformer includes a catalyst that facilitates the production of hydrogen from the fuel source.
  • Voluminous reformer chamber designs are provided that increase the amount of catalyst that can be used in a reformer and increase hydrogen output for a given fuel processor size.
  • the burner provides heat to the reformer.
  • One or more burners may be configured to surround a reformer on multiple sides to increase thermal transfer to the reformer.
  • Dewars are also described that improve thermal management of a fuel processor by reducing heat loss and increasing burner efficiency.
  • a dewar includes one or more dewar chambers that receive inlet process gases or liquids before a reactor receives them. The dewar is arranged such that inlet process gases or liquids passing through the dewar chamber intercepts heat generated in the burner before the heat escapes the fuel processor.
  • Passing inlet process gases or liquids through a dewar chamber in this manner performs three functions: a) active cooling of dissipation of heat generated in burner before is reaches outer portions of the fuel processor, and b) heating of the air before receipt by the burner, and c) absorbing and recycling heat back into the burner increasing burner efficiency.
  • the burner relies on catalytic combustion to produce heat, heat generated in the burner warms cool process gases or liquids in the burner according to the temperature of the process gases or liquids. This steals heat from the reformer, reduces heating efficiency of a burner and typically results in greater consumption of the fuel source.
  • the present invention relates to a fuel processor for producing hydrogen from a fuel source.
  • the fuel processor comprises a reformer configured to receive the fuel source, configured to output hydrogen, and including a catalyst that facilitates the production of hydrogen.
  • the fuel processor also comprises a boiler configured to heat the fuel source before the reformer receives the fuel source.
  • the fuel processor further comprises at least one burner configured to provide heat to the reformer and disposed annularly about the reformer.
  • the fuel processor may also comprise a boiler that heats the burner liquid fuel feed.
  • the present invention relates to a fuel processor for producing hydrogen from a fuel source.
  • the fuel processor comprises a reformer configured to receive the fuel source, configured to output hydrogen, including a catalyst that facilitates the production of hydrogen.
  • the reformer also includes a reformer chamber having a volume greater than about 0.1 cubic centimeters and less than about 50 cubic centimeters and is characterized by a cross sectional width and a cross sectional height that is greater than one-third the cross sectional width.
  • the fuel processor also comprises a boiler configured to heat the fuel source before the reformer receives the fuel source.
  • the fuel processor further comprises at least one burner configured to provide heat to the reformer.
  • the present invention relates to a fuel processor for producing hydrogen from a fuel source.
  • the fuel processor comprises a reformer configured to receive the hydrogen fuel source, configured to output hydrogen, and including a catalyst that facilitates the production of hydrogen.
  • the fuel processor also comprises a burner that is configured to provide heat to the reformer.
  • the fuel processor further comprises a dewar that at least partially contains the reformer and the burner and includes a set of dewar walls that form a dewar chamber that is configured to receive an inlet process gas or liquid before the burner receives the inlet process gas or liquid.
  • the fuel processor additionally comprises a housing including a set of housing walls that at least partially contain the dewar and provide external mechanical protection for the reformer and the burner.
  • the present invention relates to a method for managing heat in a fuel processor.
  • the fuel processor comprises a burner, a reformer and a dewar that at least partially contains the burner.
  • the method comprises generating heat in the burner.
  • the method also comprises passing an inlet process gas or liquid through a dewar chamber.
  • the method further comprises heating the inlet process gas or liquid in the dewar chamber using heat generated in the burner.
  • the present invention relates to a method for generating hydrogen in a fuel processor.
  • the fuel processor comprises a burner, a reformer and a dewar that at least partially contains the burner and reformer.
  • the method comprises generating heat in the burner.
  • the method also comprises passing an inlet process gas or liquid through a dewar chamber.
  • the method further comprises heating the inlet process gas or liquid in the dewar chamber using heat generated in the burner.
  • the method additionally comprises supplying the inlet process gas or liquid to the burner after it has been heated in the dewar chamber.
  • the method also comprises transferring heat generated in the burner to the reformer.
  • the method further comprises reforming a fuel source to produce hydrogen.
  • the present invention relates to a fuel processor for producing hydrogen from a fuel source.
  • the fuel processor comprises a reformer that includes a set of reformer channels disposed in a first substrate.
  • the reformer also includes a reformer catalyst that facilitates the production of hydrogen from the fuel source.
  • the fuel processor further comprises a boiler including a set of channels disposed in a second substrate and configured to heat the fuel source before the reformer receives the fuel source.
  • the fuel processor also comprises a burner configured to provide heat to the reformer and configured to provide heat to the boiler.
  • the fuel processor additionally comprises a dock configured to maintain position of the reformer and boiler within the fuel processor by applying a compliant securing force that passes through a portion of the first substrate and a portion of the second substrate.
  • the present invention relates to a fuel processor for producing hydrogen from a fuel source.
  • the fuel processor comprises a reformer that includes a set of reformer channels disposed in a first substrate.
  • the reformer also includes a reformer catalyst that facilitates the production of hydrogen from the fuel source.
  • the fuel processor further comprises a boiler including a set of channels disposed in a second substrate and configured to heat the fuel source before the reformer receives the fuel source.
  • the fuel processor also comprises a catalytic burner including a catalyst that facilitates the production of heat using the fuel source, configured to provide heat to the first substrate and the second substrate, and including a set of channels disposed in one of the first substrate and the second substrate.
  • the present invention relates to a fuel processor for producing hydrogen from a fuel source.
  • the fuel processor comprises a reformer that includes a set of reformer channels disposed in a first substrate.
  • the reformer also includes a reformer catalyst that facilitates the production of hydrogen from the fuel source.
  • the fuel processor further comprises a burner configured to provide heat to the reformer.
  • the fuel processor also comprises a dewar that contains the reformer and the burner and includes a set of dewar walls that form a dewar chamber configured to receive the fuel source or oxygen before the reformer receives the fuel source or oxygen.
  • FIG. 2A illustrates a cross-sectional side view of a fuel processor used in the fuel cell system of FIG. 1 A in accordance with one embodiment of the present invention.
  • FIG. 2B illustrates a cross-sectional front view of the fuel processor used in the fuel cell system of FIG. 1A taken through a mid-plane of fuel processor.
  • FIG. 3 A illustrates a cross-sectional front view of a monolithic structure employed in the fuel processor of FIG. 2 A in accordance with one embodiment of the present invention.
  • FIG. 3B illustrates a cross-sectional layout of a tubular design for use in a fuel processor in accordance with another embodiment of the present invention.
  • FIG. 3C illustrates a cross-sectional front view of a monolithic structure in a fuel processor that comprises a single burner having an 'O-shape' that completely surrounds a reformer chamber in accordance with one embodiment of the present invention.
  • FIG. 3D illustrates an outside view of an end plate used in the fuel processor of FIG. 2A.
  • FIG. 3E illustrates a fuel processor 15 in accordance with another embodiment of the present invention.
  • FIG. 4A illustrates a side cross-sectional view of the fuel processor of FIG. 2A and movement of air created by a dewar in accordance with one embodiment of the present invention.
  • FIG. 4B illustrates a front cross-sectional view of the fuel processor of FIG. 2A and demonstrates thermal management benefits gained by the dewar.
  • FIG. 4C shows a thermal diagram of the heat path produced by a dewar wall used in the fuel processor of FIG. 2 A.
  • FIG. 4D illustrates a cross sectional view of a fuel processor that increases the convective path that air flows over a dewar wall in accordance with another embodiment of the present invention.
  • FIG. 4E illustrates a dewar in accordance with another embodiment of the present invention.
  • FIGs. 4F and 4G illustrate a cross section of a fuel processor including a monolithic structure and multipass dewar in accordance with another embodiment of the present invention.
  • FIG. 4H illustrates spiral dewar in an unrolled form during initial construction in accordance with another embodiment of the present invention.
  • FIG. 41 and 4J illustrate wash coatings on a wall of a burner in accordance with two embodiments of the present invention.
  • FIG. 5 illustrates a process flow for generating hydrogen in a fuel processor in accordance with one embodiment of the present invention.
  • FIG. 6A illustrates a top view of fuel processor in accordance with one embodiment of the present invention.
  • FIG. 6B illustrates a side cross section of the fuel processor of FIG. 6 A taken through line K-K.
  • FIG. 6C illustrates a side cross section of the fuel processor of FIG. 6 A taken through line L-L.
  • FIG. 6D illustrates a side cross section of the fuel processor of FIG. 6A taken through line A-A.
  • FIG. 6E illustrates a side cross section of the fuel processor of FIG. 6A taken through line M-M.
  • FIG. 6A illustrates a top view of fuel processor in accordance with one embodiment of the present invention.
  • FIG. 6B illustrates a side cross section of the fuel processor of FIG. 6 A taken through line
  • FIG. 6F illustrates a side cross section of the fuel processor of FIG. 6 A taken through line N-N.
  • FIG. 6G illustrates a front cross section of the fuel processor of FIG. 6 A taken through line B-B.
  • FIG. 6H illustrates a front cross section of the fuel processor of FIG. 6 A taken through line C-C.
  • FIG 61 illustrates a front cross section of the fuel processor of FIG. 6A taken through line D-D.
  • FIG. 6J illustrates an expanded view of a portion of the shown in FIG. 6G.
  • FIG. 1 A illustrates a fuel cell system 10 for producing electrical energy in accordance with one embodiment of the present invention.
  • Fuel cell system 10 comprises storage device 16, fuel processor 15 and fuel cell 20.
  • a 'reformed' hydrogen supply processes a fuel source to produce hydrogen.
  • the reformed hydrogen supply comprises a fuel processor 15 and a fuel source storage device 16.
  • Storage device 16 stores fuel source 17, and may include a portable and/or disposable fuel cartridge.
  • a disposable cartridge offers instant recharging to a consumer.
  • the cartridge includes a collapsible bladder within a hard plastic dispenser case.
  • a separate fuel pump typically controls fuel source 17 flow from storage device 16. If system 10 is load following, then a control system meters fuel source 17 to deliver fuel source 17 to processor 15 at a flow rate determined by the required power level output of fuel cell 20.
  • Fuel source 17 acts as a carrier for hydrogen and can be processed to separate hydrogen.
  • Fuel source 17 may include any hydrogen bearing fuel stream, hydrocarbon fuel or other hydrogen fuel source such as ammonia.
  • hydrocarbon fuel sources 17 suitable for use with the present invention include gasoline, Ci to C 4 hydrocarbons, their oxygenated analogues and/or their combinations, for example. Several hydrocarbon and ammonia products may also produce a suitable fuel source 17.
  • Liquid fuel sources 17 offer high energy densities and the ability to be readily stored and shipped.
  • Storage device 16 may contain a fuel mixture.
  • the fuel processor 15 comprises a steam reformer
  • storage device 16 may contain a fuel mixture of a hydrocarbon fuel source and water.
  • Hydrocarbon fuel source/water fuel mixtures are frequently represented as a percentage fuel source in water.
  • fuel source 17 comprises methanol or ethanol concentrations in water in the range of l%-99.9%.
  • Other liquid fuels such as butane, propane, gasoline, military grade "JP8" etc. may also be contained in storage device
  • Fuel processor 15 processes the hydrocarbon fuel source 17 and outputs hydrogen.
  • a hydrocarbon fuel processor 15 heats and processes a hydrocarbon fuel source 17 in the presence of a catalyst to produce hydrogen.
  • Fuel processor 15 comprises a reformer, which is a catalytic device that converts a liquid or gaseous hydrocarbon fuel source 17 into hydrogen and carbon dioxide. As the term is used herein, reforming refers to the process of producing hydrogen from a fuel source.
  • Fuel processor 15 may output either pure hydrogen or a hydrogen bearing gas stream. Fuel processor 15 is described in further detail below.
  • Fuel cell 20 electrochemically converts hydrogen and oxygen to water, generating electricity and heat in the process. Ambient air commonly supplies oxygen for fuel cell 20. A pure or direct oxygen source may also be used for oxygen supply. The water often forms as a vapor, depending on the temperature of fuel cell 20 components. The electrochemical reaction also produces carbon dioxide as a byproduct for many fuel cells.
  • fuel cell 20 is a low volume polymer electrolyte membrane (PEM) fuel cell suitable for use with portable applications such as consumer electronics.
  • a polymer electrolyte membrane fuel cell comprises a membrane electrode assembly 40 that carries out the electrical energy generating electrochemical reaction.
  • the membrane electrode assembly 40 includes a hydrogen catalyst, an oxygen catalyst and an ion conductive membrane that a) selectively conducts protons and b) electrically isolates the hydrogen catalyst from the oxygen catalyst.
  • a hydrogen gas distribution layer contains the hydrogen catalyst and allows the diffusion of hydrogen therethrough.
  • An oxygen gas distribution layer contains the oxygen catalyst and allows the diffusion of oxygen and hydrogen protons therethrough.
  • the ion conductive membrane separates the hydrogen and oxygen gas distribution layers.
  • the anode comprises the hydrogen gas distribution layer and hydrogen catalyst, while the cathode comprises the oxygen gas distribution layer and oxygen catalyst.
  • a PEM fuel cell often includes a fuel cell stack having a set of bi-polar plates.
  • a membrane electrode assembly is disposed between two bi-polar plates.
  • Hydrogen distribution 43 occurs via a channel field on one plate while oxygen distribution 45 occurs via a channel field on a second facing plate.
  • a first channel field distributes hydrogen to the hydrogen gas distribution layer
  • a second channel field distributes oxygen to the oxygen gas distribution layer.
  • the 'term 'bi-polar' refers electrically to a bi-polar plate (whether comprised of one plate or two plates) sandwiched between two membrane electrode assembly layers.
  • the bipolar plate acts as both a negative terminal for one adjacent membrane electrode assembly and a positive terminal for a second adjacent membrane electrode assembly arranged on the opposite face of the bi-polar plate.
  • the anode includes the hydrogen gas distribution layer, hydrogen catalyst and bi-polar plate.
  • the anode acts as the negative electrode for fuel cell 20 and conducts electrons that are freed from hydrogen molecules so that they can be used externally, e.g., to power an external circuit.
  • the bi- polar plates are connected in series to add the potential gained in each layer of the stack.
  • the cathode includes the oxygen gas distribution layer, oxygen catalyst and bi-polar plate.
  • the cathode represents the positive electrode for fuel cell 20 and conducts the electrons back from the external electrical circuit to the oxygen catalyst, where they can recombine with hydrogen ions and oxygen to form water.
  • the hydrogen catalyst separates the hydrogen into protons and electrons.
  • the ion conductive membrane blocks the electrons, and electrically isolates the chemical anode (hydrogen gas distribution layer and hydrogen catalyst) from the chemical cathode.
  • the ion conductive membrane also selectively conducts positively charged ions. Electrically, the anode conducts electrons to a load (electricity is produced) or battery (energy is stored). Meanwhile, protons move through the ion conductive membrane, to combine with oxygen. The protons and used electrons subsequently meet on the cathode side, and combine with oxygen to form water.
  • the oxygen catalyst in the oxygen gas distribution layer facilitates this reaction.
  • One common oxygen catalyst comprises platinum powder very thinly coated onto a carbon paper or cloth. Many designs employ a rough and porous catalyst to increase surface area of the platinum exposed to the hydrogen and oxygen.
  • fuel cell 20 comprises a set of bi-polar plates that each includes channel fields on opposite faces that distribute the hydrogen and oxygen. One channel field distributes hydrogen while a channel field on the opposite face distributes oxygen. Multiple bi-polar plates can be stacked to produce a 'fuel cell stack' in which a membrane electrode assembly is disposed between each pair of adjacent bi-polar plates. Since the electrical generation process in fuel cell 20 is exothermic, fuel cell 20 may implement a thermal management system to dissipate heat from the fuel cell. Fuel cell 20 may also employ a number of humidification plates (HP) to manage moisture levels in the fuel cell.
  • HP humidification plates
  • fuel cell 20 is phosphoric acid fuel cell that employs liquid phosphoric acid for ion exchange.
  • Solid oxide fuel cells employ a hard, non-porous ceramic compound for ion exchange and may be suitable for use with the present invention.
  • Fuel cell 20 generates dc voltage that may be used in a wide variety of applications. For example, electricity generated by fuel cell 20 may be used to power a motor or light. In one embodiment, the present invention provides 'small' fuel cells that are designed to output less than 200 watts of power (net or total). Fuel cells of this size are commonly referred to as 'micro fuel cells' and are well suited for use with portable electronics. In one embodiment, fuel cell 20 is configured to generate from about 1 milliwatt to about 200 watts. In another embodiment, fuel cell 20 generates from about 3 W to about 20 W.
  • Fuel cell 20 may also be a stand-alone fuel cell, which is a single unit that produces power as long as it has an a) oxygen and b) hydrogen or a hydrocarbon fuel supply.
  • a fuel cell 20 that outputs from about 40W to about 100W is well suited to power a laptop computer.
  • FIG. IB illustrates schematic operation for fuel cell system 10 in accordance with a specific embodiment of the present invention. As shown, fuel cell system 10 comprises fuel container 16, hydrogen fuel source 17, fuel processor 15, fuel cell 20, multiple pumps 21 and fans 35, fuel lines and gas lines, and one or more valves 23. While the present invention will now primarily be described with respect to methanol as fuel source 17, it is understood that the present invention may employ another fuel source 17 such as one provided above.
  • Fuel container 16 stores methanol as a hydrogen fuel source 17.
  • An outlet 26 of fuel container 16 provides methanol 17 into hydrogen fuel source line 25.
  • line 25 divides into two lines: a first line 27 that transports methanol 17 to a burner 30 for fuel processor 15 and a second line 29 that transports methanol 17 to reformer 32 in fuel processor 15.
  • Lines 25, 27 and 29 may comprise plastic tubing, for example.
  • Separate pumps 21a and 21b are provided for lines 27 and 29, respectively, to pressurize the lines and transmit the fuel source at independent rates if desired.
  • a model P625 pump as provided by Instech of Plymouth Meeting, PA is suitable to transmit liquid methanol for system 10 is suitable in this embodiment.
  • a flow sensor or valve 23 situated on line 29 between storage device 16 and fuel processor 18 detects and communicates the amount of methanol 17 transfer between storage device 16 and reformer 32.
  • pump 21b regulates methanol 17 provision from storage device 16 to reformer 32.
  • Fan 35a delivers oxygen and air from the ambient room through line 31 to regenerator 36 of fuel processor 15.
  • Fan 35b delivers oxygen and air from the ambient room through line 33 to regenerator 36 of fuel processor 15.
  • a model AD2005DX-K70 fan as provided by Adda USA of California is suitable to transmit oxygen and air for fuel cell system 10.
  • a fan 37 blows cooling air over fuel cell 20 and its heat transfer appendages 46.
  • Fuel processor 15 receives methanol 17 from storage device 16 and outputs hydrogen.
  • Fuel processor 15 comprises burner 30, reformer 32, boiler 34 and dewar 150.
  • Burner 30 includes an inlet that receives methanol 17 from line 27 and a catalyst that generates heat with methanol presence.
  • burner 30 includes an outlet that exhausts heated gases to a line 41, which transmits the heated gases over heat transfer appendages 46 of fuel cell 20 to pre-heat the fuel cell and expedite warm-up time needed when initially turning on fuel cell 20.
  • An outlet of burner 30 may also exhaust heated gases into the ambient room.
  • Boiler 34 includes an inlet that receives methanol 17 from line 29.
  • boiler 34 permits heat produced in burner 30 to heat methanol 17 in boiler 34 before reformer 32 receives the methanol 17.
  • Boiler 34 includes an outlet that provides heated methanol 17 to reformer 32.
  • Reformer 32 includes an inlet that receives heated methanol 17 from boiler 34.
  • a catalyst in reformer 32 reacts with the methanol 17 and produces hydrogen and carbon dioxide. This reaction is slightly endothermic and draws heat from burner 30.
  • a hydrogen outlet of reformer 32 outputs hydrogen to line 39.
  • fuel processor 15 also includes a preferential oxidizer that intercepts reformer 32 hydrogen exhaust and decreases the amount of carbon monoxide in the exhaust.
  • the preferential oxidizer employs oxygen from an air inlet to the preferential oxidizer and a catalyst based on, for example ruthenium or platinum, that is preferential to carbon monoxide over carbon dioxide.
  • Dewar 150 pre-heats a process gas or liquid before the air enters burner 30. Dewar 150 also reduces heat loss from fuel cell 15 by heating the incoming process liquids or gases before the heat escapes fuel processor 15. In one sense, dewar 150 acts as a regenerator that uses waste heat in fuel processor 15 to improve thermal management and thermal efficiency of the fuel processor. Specifically, waste heat from burner 30 may be used to pre-heat incoming air provided to burner 30 to reduce heat transfer to the air in the burner so more heat transfers to reformer 32. Dewar 150 is described in further detail below.
  • Line 39 transports hydrogen from fuel processor 15 to fuel cell 20.
  • Gaseous delivery lines 31, 33 and 39 may comprise polymeric or metallic tubing, for example.
  • a hydrogen flow sensor (not shown) may also be added on line 39 to detect and coimnunicate the amount of hydrogen being delivered to fuel cell 20.
  • fuel processor 15 regulates hydrogen gas provision to fuel cell 20.
  • Fuel cell 20 includes an hydrogen inlet port that receives hydrogen from line
  • An oxygen inlet port of fuel cell 20 receives oxygen from line 33 and delivers it to an oxygen intake manifold for delivery to one or more bi-polar plates and their oxygen distribution channels.
  • An anode exhaust manifold collects gases from the hydrogen distribution channels and delivers them to an anode exhaust port, which outlets the exhaust gases into the ambient room.
  • a cathode exhaust manifold collects gases from the oxygen distribution channels and delivers them to a cathode exhaust port.
  • system 10 may also include other elements such as electronic controls, additional pumps and valves, added system sensors, manifolds, heat exchangers and electrical interconnects useful for carrying out functionality of system 10 that are known to one of skill in the art and omitted herein for sake of brevity.
  • FIG. IC illustrates an embodiment of fuel system 10 that routes unused hydrogen from fuel cell 20 back to burner 30.
  • Burner 30 includes a catalyst that reacts with the unused hydrogen to produce heat. Since hydrogen consumption within fuel cell 20 is often incomplete and the anode exhaust often includes unused hydrogen, re- routing the anode exhaust to burner 30 allows fuel cell system 10 to capitalize on unused hydrogen in fuel cell 20 and increase hydrogen usage and efficiency in system 10.
  • unused hydrogen generally refers to hydrogen output from a fuel cell.
  • Line 51 is configured to transmit unused hydrogen from fuel cell 20 to burner 30 of fuel processor 15.
  • burner 30 includes two inlets: an inlet 55 configured to receive the hydrogen fuel source 17 and an inlet 53 configured to receive the hydrogen from line 51.
  • Anode gas collection channels which distribute hydrogen from fuel processor 15 to each membrane electrode assembly layer, collect and exhaust the unused hydrogen.
  • An inlet fan pressurizes line 39 that delivers the hydrogen from an outlet of fuel processor 15 to an anode inlet of fuel cell 20. The inlet fan also pressurizes the anode gas collection channels for distribution of hydrogen within fuel cell 20.
  • gaseous delivery in line 51 back to fuel processor 15 relies on pressure at the exhaust of the anode gas distribution channels, e.g., in the anode exhaust manifold.
  • an extra fan is added to line 51 to pressurize line 51 and return unused hydrogen back to fuel processor 15.
  • Burner 30 also includes an inlet 59 configured to receive oxygen from an oxygen exhaust included in fuel cell 20. Cathode gas collection channels, which distribute oxygen and air from the ambient room to each membrane electrode assembly layer, collect and exhaust the unused oxygen.
  • Line 61 delivers unused oxygen from an exhaust manifold, which collects oxygen from each cathode gas collection channel, to inlet 59.
  • Burner 30 thus includes two oxygen inlets: inlet 59 and an inlet 57 configured to receive oxygen from the ambient room after delivery though dewar 150. Since oxygen consumption within fuel cell 20 is often incomplete and the cathode exhaust includes unused oxygen, re-routing the cathode exhaust to burner 30 allows fuel cell system 10 to capitalize on unused oxygen in fuel cell 20 and increase oxygen usage and efficiency in system 10.
  • fuel processor 15 is a steam reformer that only needs steam to produce hydrogen.
  • Several types of reformers suitable for use in fuel cell system 10 include steam reformers, auto thermal reformers (ATR) or catalytic partial oxidizers (CPOX). ATR and CPOX reformers mix air with the fuel and steam mix.
  • FIG. 2A illustrates a cross-sectional side view of fuel processor 15 in accordance with one embodiment of the present invention.
  • FIG. 2B illustrates a cross- sectional front view of fuel processor 15 taken through a mid-plane of processor 15 that also shows features of end plate 82.
  • Fuel processor 15 reforms methanol to produce hydrogen.
  • Fuel processor 15 comprises monolithic structure 100, end plates 82 and 84, reformer 32, burner 30, boiler 34, boiler 108, dewar 150 and housing 152.
  • 'monolithic' refers to a single and integrated structure that includes at least portions of multiple components used in fuel processor 15.
  • monolithic structure 100 includes reformer 32, burner 30, boiler 34 and boiler 108.
  • Monolithic structure 100 may also include associated plumbing inlets and outlets for reformer 32, burner 30 and boiler 34.
  • Monolithic structure 100 comprises a common material 141 that constitutes the structure.
  • Common material 141 is included in walls that define the reformer 32, burner 32 and boilers 34 and 108. Specifically, walls 111, 119, 120, 122, 130, 132, 134 and 136 all comprise common material 141.
  • Common material 141 may comprise a metal, such as copper, silicon, stainless steel, inconel and other metal/alloys displaying favorable thermal conducting properties.
  • the monolithic structure 100 and common material 141 simplify manufacture of fuel processor 15. For example, using a metal for common material 141 allows monolithic structure 100 to be formed by extrusion or casting. In some cases, monolithic structure 100 is consistent in cross sectional dimensions between end plates 82 and 84 and solely comprises copper formed in a single extrusion.
  • Common material 141 may also include a ceramic, for example.
  • a ceramic monolithic structure 100 maybe formed by sintering.
  • Housing 152 provides mechanical protection for internal components of fuel processor 15 such as burner 30 and reformer 32. Housing 152 also provides separation from the environment external to processor 15 and includes inlet and outlet ports for gaseous and liquid communication in and out of fuel processor 15.
  • Housing 152 includes a set of housing walls 161 that at least partially contain a dewar 150 and provide external mechanical protection for components in fuel processor 15. Walls 161 may comprises a suitably stiff material such as a metal or a rigid polymer, for example.
  • Dewar 150 improves thermal heat management for fuel processor 15 and will be discussed in further detail with respect to FIG. 4A.
  • monolithic structure 100 and end plates 82 and 84 structurally define reformer 32, burner 30, boiler 34 and boiler 108 and their respective chambers. Monolithic structure 100 and end plates 82 and 84 are shown separate in FIG. 2A for illustrative purposes, while FIG. 4A shows them together.
  • boiler 34 heats methanol before reformer 32 receives the methanol.
  • Boiler 34 receives the methanol via fuel source inlet 81, which couples to the methanol supply line 27 of FIG. IB. Since methanol reforming and hydrogen production via a catalyst 102 in reformer 32 often requires elevated methanol temperatures, fuel processor 15 pre-heats the methanol before receipt by reformer 32 via boiler 34.
  • Boiler 34 is disposed in proximity to burner 30 to receive heat generated in burner 30. The heat transfers via conduction through monolithic structure from burner 30 to boiler 34 and via convection from boiler 34 walls to the methanol passing therethrough.
  • boiler 34 is configured to vaporize liquid methanol. Boiler 34 then passes the gaseous methanol to reformer 32 for gaseous interaction with catalyst 102. Reformer 32 is configured to receive methanol from boiler 34.
  • Walls 111 in monolithic structure 100 see cross section in FIG. 3 A
  • end walls 113 (FIG. 2B) on end plates 82 and 84 define dimensions for a reformer chamber 103.
  • end plate 82 and/or end plate 84 includes also channels 95 (FIG.
  • Reformer 32 includes a catalyst 102 that facilitates the production of hydrogen.
  • Catalyst 102 reacts with methanol 17 and facilitates the production of hydrogen gas and carbon dioxide.
  • catalyst 102 comprises pellets packed to form a porous bed or otherwise suitably filled into the volume of reformer chamber 103.
  • pellet sizes are designed to maximize the amount of surface area exposure to the incoming methanol.
  • Pellet diameters ranging from about 50 microns to about 1.5 millimeters are suitable for many applications.
  • Pellet diameters ranging from about 300 microns to about 1500 microns are suitable for use with reformer chamber 103.
  • Pellet sizes and packing may also be varied to control the pressure drop that occurs through reformer chamber 103.
  • pressure drops from about 0.2 to about 5 psi gauge are suitable between the inlet and outlet of reformer chamber 103.
  • Pellet sizes may be varied relative to the cross sectional size of reformer chamber 103, e.g., as reformer chamber 103 increases in size so may catalyst 102 pellet diameters.
  • the ratio of pellet diameter (d) to cross sectional height 117 (D) may range from about 0.0125 to about 1.
  • a D/d ratio from about 5 to about 20 is also suitable for many applications.
  • a packing density may also characterize packing of catalyst 102 in reformer chamber 103.
  • packing densities from about 0.3 grams/milliliter to about 2 grams/milliliter are suitable. Packing densities from about 0.9 grams/milliliter to about 1.4 grams/milliliter are appropriate for the embodiment shown in FIG. 3 A.
  • One suitable catalyst 102 may include CuZn on alumina pellets when methanol is used as a hydrocarbon fuel source 17.
  • Catalyst 102 pellets are commercially available from a number of vendors known to those of skill in the art.
  • Pellet catalysts may also be disposed within a baffling system disposed in the reformer chamber 103.
  • the baffling system includes a set of walls that guide the fuel source along a nonlinear path. The baffling slows and controls flow of gaseous methanol in chamber 103 to improve interaction between the gaseous methanol and pellet catalyst 102.
  • Catalyst 102 may alternatively comprise catalyst materials listed above coated onto a metal sponge or metal foam.
  • a wash coat of the desired metal catalyst material onto the walls of reformer chamber 103 may also be used for reformer 32.
  • Reformer 32 is configured to output hydrogen and includes an outlet port 87 that communicates hydrogen formed in reformer 32 outside of fuel processor 15.
  • port 87 communicates hydrogen to line 39 for provision to hydrogen distribution 43 in fuel cell 20.
  • Port 87 is disposed on a wall of end plate 82 and includes a hole that passes through the wall (see FIG. 2B).
  • the outlet hole port may be disposed on any suitable wall 111 or 113.
  • Hydrogen production in reformer 32 is slightly endothermic and draws heat from burner 30. Burner 30 generates heat and is configured to provide heat to reformer 32. Burner 30 is disposed annularly about reformer 32, as will be discussed in further detail below.
  • burner 30 comprises two burners (or burner sections) 30a and 30b and their respective burner chambers 105a and 105b that surround reformer 32.
  • Burner 30 includes an inlet that receives methanol 17 from boiler 108 via a channel in one of end plates 82 or 84.
  • the burner inlet opens into burner chamber 105 a.
  • the methanol then travels the length 142 of burner chamber 105 a to channels disposed in end plate 82 that route methanol from burner chamber 105a to burner chamber 105b.
  • the methanol then travels the back through the length 142 of burner chamber 105b to burner exhaust 89.
  • the burner inlet opens into both chambers 105a and 105b.
  • burner 30 employs catalytic combustion to produce heat.
  • a catalyst 104 disposed in each burner chamber 105 helps a burner fuel passed through the chamber generate heat, hi one embodiment, methanol produces heat in burner 30 and catalyst 104 facilitates the methanol production of heat.
  • waste hydrogen from fuel cell 20 produces heat in the presence of catalyst 104.
  • Suitable burner catalysts 104 may include platinum or palladium coated onto a suitable support or alumina pellets for example. Other materials suitable for catalyst 104 include iron, tin oxide, other noble-metal catalysts, reducible oxides, and mixtures thereof.
  • the catalyst 104 is commercially available from a number of vendors known to those of skill in the art as small pellets.
  • the pellets that may be packed into burner chamber 105 to form a porous bed or otherwise suitably filled into the burner chamber volume.
  • Catalyst 104 pellet sizes may be varied relative to the cross sectional size of burner chamber 105.
  • Catalyst 104 may also comprise catalyst materials listed above coated onto a metal sponge or metal foam or wash coated onto the walls of burner chamber 105.
  • a burner outlet port 89 (FIG. 2A) communicates exhaust formed in burner 30 outside of fuel processor 15. Some fuel sources generate additional heat in burner 30, or generate heat more efficiently, with elevated temperatures.
  • Fuel processor 15 includes a boiler 108 that heats methanol before burner 30 receives the fuel source.
  • boiler 108 receives the methanol via fuel source inlet 85.
  • Boiler 108 is disposed in proximity to burner 30 to receive heat generated in burner 30. The heat transfers via conduction through monolithic structure from burner 30 to boiler 108 and via convection from boiler 108 walls to the methanol passing therethrough. Air including oxygen enters fuel processor 15 via air inlet port 91. Burner 30 uses the oxygen for catalytic combustion of methanol. As will be discussed in further detail below with respect to FIGs. 4A and 4B, air first passes along the outside of dewar 150 before passing through apertures in the dewar and along the inside of dewar 150. This heats the air before receipt by air inlet port 93 of burner 30. FIG.
  • Monolithic structure 100 extends from end plate 82 to end plate 84.
  • the cross section of monolithic structure 100 shown in FIG. 3 A extends from one end of structure 100 at end plate 82 to the other end of structure 100 at end plate 84.
  • Monolithic structure 100 includes reformer 32, burner 30, boiler 34 and boiler 108 between end plates 82 and 84.
  • Reformer 32 includes a reformer chamber 103, which is a voluminous space in fuel processor 15 that includes the reforming catalyst 102, opens to the fuel source inlet (from boiler 34 for fuel processor 15), and opens to hydrogen outlet 87.
  • Side walls 111 define a non-planar cross-sectional shape for reformer 32 and its reformer chamber 103. Walls 113 on end plates 82 and 84 close the reformer chamber 103 on either end of the chamber 103 and include the inlet and outlet ports to the chamber 103. Reformer chamber 103 includes a non-planar volume. As the term is used herein, a non-planar reformer chamber 103 refers to a shape in cross section that is substantially non-flat or non-linear. A cross section refers to a planar slice that cuts through the fuel processor or component. For cross sections that include multiple fuel processor components (e.g., both burner 30 and reformer 32), the cross section includes both components. For the vertical and front cross section 121 shown in FIG.
  • Reformer 32 and its reformer chamber 103 may employ a quadrilateral or non-quadrilateral cross-sectional shape.
  • Four sides define a quadrilateral reformer chamber 103 in cross section.
  • Four substantially orthogonal sides define rectangular and square quadrilateral reformers 32.
  • a non-quadrilateral reformer 32 may employ cross-sectional geometries with more or less sides, an elliptical shape (see FIG. 3B), and more complex cross-sectional shapes. As shown in FIG.
  • reformer 32 includes a six-sided cross-sectional 'P-shape' with chamfered comers. One corner section of reformer 32 is removed from monolithic structure 100 to allow for boiler 34 proximity to burner 30. Reformer chamber 103 is characterized by a cross-sectional width 115 and a cross-sectional height 117. A maximum linear distance between inner walls 111 of chamber 103 in a direction spanning a cross section of reformer chamber 103 quantifies cross-sectional width 155. A maximum linear distance between inner walls 111 of chamber 103 orthogonal to the width 115 quantifies cross-sectional height 117. As shown, cross-sectional height 117 is greater than one-third the cross-sectional width 115.
  • reformer chamber 103 includes a length 142 (orthogonal to the width 115 and height 117) that extends from one end of monolithic structure 100 at end plate 82 to the other end of structure 100 at end plate 84.
  • reformer chamber 103 has a length 142 to width 115 ratio less than 20:1.
  • reformer chamber 103 has a length 142 to width 115 ratio less than 10:1.
  • Reformer 32 provides a voluminous reformer chamber 103.
  • This three dimensional configuration for reformer chamber 103 contrasts micro fuel processor designs where the reformer chamber is etched as micro channels onto a planar substrate.
  • the non-planar dimensions of reformer chamber 103 permit greater volumes for reformer 32 and permit more catalyst 102 for a given size of fuel processor 15. This increases the amount of methanol that can be processed and increases hydrogen output for a particular fuel processor 15 size. Reformer 32 thus improves fuel processor's 15 suitability and performance in portable applications where fuel processor size is important or limited. In other words, since the size of inlet and outlet plumbing and ports varies little while increasing the reformer chamber 103 volume, this allows fuel processor 15 to increase hydrogen output and increase power density for portable applications while maintaining size and weight of the associated plumbing relatively constant.
  • reformer chamber 103 comprises a volume greater than about 0.1 cubic centimeters and less than about 50 cubic centimeters. In some embodiments, reformer 32 volumes between about 0.5 cubic centimeters and about 2.5 cubic centimeters are suitable for laptop computer applications.
  • Fuel processor 15 includes at least one burner 30. Each burner 30 includes a burner chamber 105. For a catalytic burner 30, the burner chamber 105 is a voluminous space in fuel processor 15 that includes catalyst 104. For communication or burner reactants and products to and from the burner chamber 105, the burner chamber 105 may directly or indirectly open to a fuel source inlet (from boiler 108 for fuel processor 15), open to an air inlet 93, and open to a burner exhaust 89. The number of burners 30 and burner chambers 105 may vary with design.
  • Monolithic structure 100 of FIG. 3A includes a dual burner 30a and 30b design having two burner chambers 105a and 105b, respectively, forming non-continuous chambers that substantially surround reformer 32 in cross section.
  • Burner 30a comprises side walls 119a (FIG. 3 A) included in monolithic structure 100 and end walls 113 on end plates 82 and 84 (FIG. 2B) that define burner chamber 105 a.
  • burner 30b includes side walls 119b (FIG. 3 A) included in monolithic structure 100 and end walls 113 on end plates 82 and 84 (FIG. 2B) that define burner chamber 105b.
  • Monolithic structure 100 of FIG. 3C includes a single burner 30c with a single burner chamber 105c that fully surrounds reformer 32.
  • Tubular arrangement of FIG. 3B includes over forty burners 204 that fully surround reformer 202.
  • Monolithic structure 452 of FIG. 4F includes a single burner divided into 104 burner chambers that fully surround reformer 32.
  • each burner 30 is configured relative to reformer 32 such that heat generated in a burner 30 transfers to reformer 32.
  • the one or more burners 30 are annularly disposed about reformer 32.
  • annular configuration of at least one burner 30 relative to reformer 32 refers to the burner 30 having, made up of, or formed by, continuous or non- continuous segments or chambers 105 that surround reformer 32. The annular relationship is apparent in cross section.
  • surrounding refers to a burner 30 bordering or neighboring the perimeter of reformer 32 such that heat may travel from a burner 30 to the reformer 32.
  • Burners 30a and 30b may surround reformer 32 about the perimeter of reformer 32 to varying degrees based on design. At the least, one or more burners 30 surround greater than 50 percent of the reformer 32 cross-sectional perimeter. This differentiates fuel processor 15 from planar and plate designs where the burner and reformer are co-planar and of similar dimensions, and by geometric logic, the burner neighbors less than 50 percent of the reformer perimeter. In one embodiment, one or more burners 30 surround greater than 75 percent of the reformer 32 cross-sectional perimeter. Increasing the extent to which burner 30 surrounds reformer 32 perimeter in cross section increases the surface area of reformer 32 that can be used to heat the reformer volume via heat generated in the burner.
  • one or more burners 30 may surround greater than 90 percent of the reformer 32 cross-sectional perimeter.
  • burner 30 surrounds the entire reformer 32 cross-sectional perimeter.
  • monolithic structure 100 may comprise the reverse configuration. That is, reformer 32 may be annularly disposed about burner 30.
  • reformer 32 may comprise one or more continuous or non-continuous segments or chambers 103 that surround burner 30.
  • each burner 30 and its burner chamber 105 has a non- planar cross-sectional shape.
  • a non-planar burner 30 may employ cross-sectional shapes such as quadrilaterals, non-quadrilateral geometries with more or less sides, an elliptical shape (see FIG. 3B for circular/tubular burners 30), or more complex cross- sectional shapes.
  • each burner 30 includes a six-sided cross- sectional 'L' shape (with chamfered comers) that bends 90 degrees about reformer 32.
  • Each burner 30 thus bilaterally borders reformer 32.
  • N-lateral bordering in this sense refers to the number of sides, N, of reformer 32 that a burner 30 (and its burner chamber 105) borders in cross section.
  • burner 30b borders the right and bottom sides of reformer 32, while burner 30a borders the top and left sides of reformer 32.
  • a 'U-shaped' burner 30 may be employed to trilaterally border reformer 32 on three sides. Together, burners 30a and 30b quadrilaterally border reformer 32 on all four orthogonal reformer 32 sides.
  • the reformer 32 used in the configuration of FIG. 3B includes multiple tubular burners that quadrilaterally border reformer 32.
  • FIG. 3C illustrates a cross-sectional front view of monolithic structure 100 that comprises a single burner 30c having an 'O-shape' that completely surrounds reformer chamber 103 in accordance with one embodiment of the present invention.
  • Burner 30c is a continuous chamber about the perimeter of reformer 32 and quadrilaterally borders reformer 32. Heat generated in burner 30 transfers directly and/or indirectly to reformer 32.
  • each burner 30 and reformer 32 share common walls 120 and 122 and heat generated in each burner 30 transfers directly to reformer 32 via conductive heat transfer through common walls 120 and 122.
  • Wall 120 forms a boundary wall for burner 30b and a boundary wall for reformer 32. As shown, one side of wall 120 opens to burner chamber 105b while another portion of the wall opens to reformer chamber 103. Wall 120 thus permits direct conductive heat transfer between burner 30b and reformer 32.
  • wall 122 forms a boundary wall for burner 30a and a boundary wall for reformer 32, opens to burner chamber 105 a, opens to reformer chamber 103, and permits direct conductive heat transfer between burner 30a and reformer 32.
  • Walls 120 and 122 are both non-planar in cross section and border multiple sides of reformer chamber 103 that are neighbored by burners 30b and 30a.
  • Wall 120 thus provides direct conductive heat transfer in multiple orthogonal directions 128 and 129 from burner 30a to reformer 32.
  • Wall 122 similarly provides direct conductive heat transfer in directions opposite to 128 and 129 from burner 30b to reformer 32.
  • Boiler 34 comprises cylindrical walls 143 included in monolithic structure 100 and end walls 113 on end plates 82 and 84 (see FIG.
  • Boiler 34 is disposed in proximity to burners 30a and 30b to receive heat generated in each burner 30.
  • boiler 34 shares a common wall 130 with burner 30a and a common wall 132 with burner 30b. Common walls 130 and 132 permit direct conductive heat transfer from each burner 30 to boiler 34.
  • Boiler 34 is also disposed between burners 30 and reformer 32 to intercept thermal conduction consistently moving from the high temperature and heat generating burners 30 to the endothermic reformer 32.
  • Boiler 108 is configured to receive heat from burner 30 to heat methanol before burner 30 receives the methanol.
  • Boiler 108 also comprises a tubular shape having a circular cross section that extends through monolithic structure 100 from end plate 82 to end plate 84. Boiler 108 is disposed in proximity to burners 30a and 30b to receive heat generated in each burner 30, which is used to heat the methanol. Boiler 108 shares a common wall 134 with burner 30a and a common wall 136 with burner 30b. Common walls 134 and 136 permit direct conductive heat transfer from burners 30a and 30b to boiler 108.
  • FIG. 3D illustrates an outside view of end plate 82 in accordance with one embodiment of the present invention. End plate 82 includes fuel source inlet 81, fuel source fuel source inlet 85, hydrogen outlet port 87 and burner air inlet 93.
  • Fuel source inlet 81 includes a hole or port in end wall 113 of end plate 82 that communicates methanol (usually as a liquid) from an external methanol supply to boiler 34 for heating the methanol before receipt by reformer 32.
  • Methanol fuel source inlet 85 includes a hole or port in end wall 113 of end plate 82 that communicates methanol (usually as a liquid) from an external methanol supply to boiler 108 for heating the methanol before receipt by burner 30.
  • Burner air inlet 93 includes a hole or port in end wall 113 of end plate 82 that communicates air and oxygen from the ambient room after it has been preheated in dewar 150.
  • Hydrogen outlet port 87 communicates gaseous hydrogen from reforming chamber 103 outside fuel processor 15.
  • FIG. 3B illustrates a cross-sectional layout of a tubular design 200 for use in fuel processor 15 in place of monolithic structure 100 in accordance with another embodiment of the present invention.
  • Structure 200 includes a reformer 202, burner 204, boiler 206 and boiler 208.
  • the cross-sectional design 200 shown in FIG. 3B is consistent throughout a cylindrical length between end plates (not shown) that include inlet and outlet ports for supply and exhaust of gases to components of design 200.
  • reformer 202 includes cylindrical walls 203 that define a substantially circular cross section. Reformer 232 thus resembles a hollow cylinder in three dimensions that defines a tubular reformer chamber 210.
  • reformer 202 may include any elliptical shape (a circle represents an ellipse of about equal orthogonal dimensions) suitable for containing the catalyst 102, for methanol flow through reformer chamber 210, for hydrogen production in reformer chamber 210, and for hydrogen flow in reformer chamber 210.
  • reformer chamber 210 is defined by a cross sectional width and a cross sectional height that are substantially equal and thus reformer 202 includes a 1 : 1 cross sectional aspect ratio.
  • Burner 204 comprises a set of cylindrical walls 214 that each defines a tubular burner chamber 212.
  • tubular design 200 includes over forty tubular burner chambers 212 that fully sunound the cross sectional perimeter of reformer 32.
  • Each tubular burner chamber 212 includes a substantially circular cross-section defined by the cylindrical wall 214.
  • Each tubular burner chamber 212 includes catalyst 104 that facilitates heat generation from methanol.
  • Burner 204 may comprise from about two to about two hundred cylindrical walls 214 and tubular burner chambers 212.
  • each cylindrical wall 214 comprises a metal and is extruded to its desired dimensions.
  • cylindrical wall 214 comprises nickel.
  • the nickel wall 214 may be formed by electroplating nickel onto a suitable substrate such as zinc or aluminum that may subsequently etched out to leave the nickel tube.
  • suitable substrate such as zinc or aluminum
  • Other materials that a nickel wall 214 may be formed onto include zinc, tin, lead, wax or plastics.
  • wall 214 may include gold, silver, copper, stainless steel, ceramics and materials that display suitable thermal properties without causing complications with burner catalyst 104. As shown, burner 204 fully annularly sunounds the cross-sectional perimeter of reformer 202.
  • burner 204 comprises three ring-like layers 216, 218 and 220 of tubes 214 disposed circularly about reformer 202 and at three different radii.
  • the tubes 214 in each layer 216, 218 and 220 circumscribe reformer 202.
  • Heat generated in each tubular chamber 212 of burner 30 transfers directly or indirectly to reformer 202 via several paths: a) heat conduction through the tubes 214 in layer 216 to the walls of reformer 202; b) heat conduction through the tubes 214 in outer layers 218 and 220 to tubes 214 in layer 216 and to the walls of reformer 202; and/or c) heat radiation between tubes 214 in outer layers 218 and 220 and tubes 214 and then conduction inward to reformer 202.
  • Boiler 206 is configured to heat methanol before reformer 202 receives the methanol.
  • Boiler 206 receives heat from burner 204 and comprises a cylindrical wall 207 that defines a tubular shape for the boiler.
  • Boiler 206 is disposed in proximity to burner tubes 214 to receive heat generated in each burner chamber 212.
  • boiler 206 is disposed in the second ring-like layer 218 and receives heat from adjacent burner chambers 212 in layers 216, 218 and 220.
  • Burner 204 provides heat to boiler 206 via conduction through the walls of each adjacent tube 214 and through wall 207.
  • Boiler 208 is configured to heat methanol before burner 204 receives the methanol.
  • Boiler 208 receives heat from burner 204 and also comprises a cylindrical wall 209 that defines a tubular shape for the boiler. Similar to boiler 206, boiler 208 is disposed in the second ring-like layer 218 and receives heat from adjacent burner chambers 212 in layers 216, 218 and 220.
  • a monolithic fuel processor 15 comprises multiple segments joined together in the direction of gas flow in reformer chamber 103 and joined at sectional lines 121. Each segment has a common profile as shown in FIG. 3A and may comprise metal or ceramic elements that are bonded or brazed perpendicular to the direction of gas flow.
  • fuel processor 15 may comprise a single long monolithic piece that bounds all of reformer 32, burner 30, boiler 34 and boiler 108 except for areas bound by end pieces 82 and 84.
  • fuel processor 15 comprises multiple pieces joined together in cross section.
  • FIG. 3E illustrates a fuel processor 15 in accordance with another embodiment of the present invention, hi this case, fuel processor 15 comprises three pieces: lower piece 280, middle piece 282 and cap piece 284. Lower piece 280 and middle piece 282 attach to form reformer 32 and two burner chambers 30. Cap piece 284 and middle piece 282 attach to form boilers 34 and 108.
  • Each piece 208, 282 and 284 comprises a common material and may be extruded or cast to suitable dimensions.
  • FIG. 4A illustrates a side cross-sectional view of fuel processor 15 and movement of air created by dewar 150 in accordance with one embodiment of the present invention.
  • FIG. 4B illustrates a front cross-sectional view of fuel processor 15 and demonstrates thermal management benefits gained by dewar 150. While thermal management techniques described herein will now be described as fuel processor components, those skilled in the art will recognize that the present invention encompasses methods of thermal management for general application.
  • a burner 30 in fuel processor 15 generates heat and typically operates at an elevated temperature. Burner 30 operating temperatures greater than 200 degrees Celsius are common. Standards for the manufacture of electronics devices typically dictate a maximum surface temperature for a device.
  • fuel processor 15 comprises a dewar 150 to improve thermal management for fuel processor 15.
  • Dewar 150 at least partially thermally isolates components internal to housing 152 - such as burner 30 - and contains heat within fuel processor 15.
  • Dewar 150 reduces heat loss from fuel processor 15 and helps manage the temperature gradient between burner 30 and outer surface of housing 152. And as will be described below, dewar 150 also pre-heats air before it is received by burner 30.
  • Dewar 150 at least partially contains burner 30 and reformer 32, and includes a set of dewar walls 154 that help form a dewar chamber 156 and a chamber 158. hi some embodiments, dewar 150 fully surrounds burner 30 and reformer 32 in a cross sectional view and at both ends of burner 30 and reformer 32. Less containment by dewar 150 is also suitable to provide thermal benefits described herein.
  • the multipass dewar 300 of FIG. 4E only partially encloses burner 30 and reformer 32 in cross section. In some cases, dewar 150 does not extends fully along the length of monolithic structure 100 and provides less than full containment. As shown in FIG. 4B, dewar 150 annularly surrounds burner 30 in cross section.
  • the set of walls 154 includes side walls 154a and 154c that combine with top and bottom walls 154b and 154d to form the rectangular cross section shown in FIG. 4B; and includes two end walls 154e and 154f that combine with top and bottom walls 154b and 154d to form the rectangular cross section shown in FIG. 4A.
  • End wall 154f includes apertures that permit the passage of inlet and outlet ports 85, 87 and 89 therethough.
  • Dewar chamber 156 is formed within dewar walls 154 and comprises all space within the dewar walls 154 not occupied by monolithic structure 100. As shown in FIG. 4B, dewar chamber 156 sunounds monolithic structure 100. As shown in FIG.
  • chamber 156 comprises ducts between monolithic structure 100 and walls 154 on all four sides of dewar 150.
  • chamber 156 comprises air pockets between end walls of dewar 150 and outside surfaces of end plates 82 and 84 on both ends of monolithic structure 100 (FIG. 4A).
  • Chamber 158 is fomied outside dewar walls 154 between dewar 150 and housing 152.
  • Chamber 158 comprises all space within housing 152 not occupied by dewar 150.
  • housing 152 encloses dewar 150 and the further internal monolithic structure 100.
  • Chamber 158 comprises ducts between walls 154 on all four sides of dewar 150 and housing 152.
  • chamber 158 comprises air pockets 167 between dewar 150 and housing 152 on both ends that prevent contact and conductive heat transfer between dewar 150 and housing 152 (FIG. 4A).
  • Dewar 150 is configured such that a process gas or liquid passing through dewar chamber 156 receives heat generated in burner 30.
  • the process gas or liquid may include any reactant used in fuel processor such as oxygen, air, or fuel source 17, for example.
  • Dewar 150 offers thus two functions for fuel processor 15: a) it permits active cooling of components within fuel processor 15 before the heat reaches an outer portion of the fuel processor, and b) it pre-heats the air going to burner 30. For the former, air moves through fuel processor 15 and across walls 154 of dewar 150 such that the cooler air absorbs heat from the warmer fuel processor 15 components.
  • housing 152 includes an air inlet port 91 or hole that pennits the passage of air from outside housing 152 into air into chamber 158.
  • a fan usually provides the air directly to fuel processor 15 and pressurizes the air coming through port 91.
  • Top and bottom walls 154b and 154d include air inlet ports or holes 172 that allow air to pass from chamber 158 to dewar chamber 156.
  • Air flow through fuel processor 15 then flows: in air inlet port 91, through chamber 158 along the length of the dewar 150, through holes 172 in walls 154b and 154d, through chamber 156 back along the length of the dewar 150 in the opposite direction as in through chamber 158, and into air inlet ports 176 that allow the air to enter burner 30.
  • the air a) moves across the outside surface of dewar walls 154 and absorbs heat convectively from dewar walls 154, and b) moves across the inside surface of housing 152 and absorbs heat convectively from the housing 152 walls (when housing 152 is at a greater temperature than the air),
  • hi chamber 156 the air a) moves across the outside surface of monolithic structure 100 and absorbs heat convectively from the walls of monolithic structure 100, and b) moves across the inside surface of dewar 150 and absorbs heat convectively from dewar walls 154.
  • Dewar 150 is thus configured such that air passing through the dewar receives heat generated in burner 30 via direct convective heat transfer from walls in monolithic structure 100 on the outside of burner 30 to air passing through dewar chamber 156.
  • Dewar 150 is also configured to such that air passing through chamber 156 receives heat indirectly from burner 30. Indirectly in this sense refers to heat generated in burner 30 moving to another structure in fuel processor 15 before receipt by the air.
  • FIG. 4C illustrates a thermal diagram of the heat path produced by a wall 154 of dewar 150. Heat from burner 30 conducts through monolithic structure 100 to a surface of structure 100 that opens into dewar chamber 156.
  • the heat a) conducts into the air passing through dewar chamber 156, thereby heating the air; b) radiates to the inner wall 155 of dewar wall 154, from which the heat convects into the air passing through dewar chamber 156; c) radiates to the inner wall 155 of dewar wall 154, conducts through wall 154 to the outer surface 157 of dewar wall 154, from which the heat convects into the air passing through dewar chamber 158, and d) radiates to the inner wall 155 of dewar wall 154, conducts through wall 154 to the outer surface 157 of dewar wall 154, radiates to a wall of housing 152, from which the heat convects into the air passing through dewar chamber 158.
  • Dewar 150 thus provides two streams of convective heat dissipation and active air-cooling in volumes 156 and 158 that prevent heat generated in burner 30 (or other internal parts of fuel processor 15) from escaping the fuel processor. Reflectance of heat back into chamber 156 decreases the amount of heat lost from fuel processor 150 and increases the heating of air passing through chamber 156.
  • an inside surface of dewar wall 154 may include a radiative layer 160 to decrease radiative heat transfer into wall 154 (see FIG. 4B or 4C). Radiative layer 160 is disposed on an inner surface 155 on one or more of walls 154 to increase radiative heat reflectance of the inner surface 155.
  • the material used in radiative layer 160 has a lower emissivity than the material used in walls 154.
  • Materials suitable for use with walls 154 of dewar 150 include nickel or a ceramic, for example.
  • Radiative layer 160 may comprise gold, platinum, silver, palladium, nickel and the metal may be sputter coated onto the inner surface 155. Radiative layer 160 may also include a low heat conductance. In this case, radiative layer 160 may comprise a ceramic, for example.
  • burner 4A and 4B are well suited to contain heat within housing 152 and manage heat transfer from the fuel processor.
  • burner operates at a temperature greater than about 200 degrees Celsius and the outer side of the housing remains less than about 50 degrees Celsius.
  • volumes 156 and 158 are relatively small and comprise narrow channels and ducts, h some cases, the height of channels in volumes 156 and 158 is less than 5 millimeters and a wall of burner 30 on monolithic structure is no greater than 10 millimeters from a wall of housing 152.
  • the thermal benefits gained by use of dewar 150 also permit the use of higher temperature burning fuels as a fuel source for hydrogen production, such as ethanol and gasoline.
  • the thermal management benefits gained by use of dewar 150 permit reformer 32 to process methanol at temperatures well above 100 degrees Celsius and at temperatures high enough that carbon monoxide production in reformer 32 drops to an amount such that a preferential oxidizer is not needed.
  • dewar 150 offers a second function for fuel processor 15 by pre-heating the air going to a burner. Burner 30 relies on catalytic combustion to produce heat. Oxygen in the air provided to burner 30 is consumed as part of the combustion process. Heat generated in the burner 30 will heat cool incoming air, depending on the temperature of the air. This heat loss to incoming cool air reduces the heating efficiency of burner 30, and typically results in a greater consumption of methanol.
  • the present invention heats the incoming air so less heat generated in the burner passes into the incoming air. ha other words, chambers and air flow formed by dewar 150 allow waste heat from the burner to pre-heat air before reaching the burner, thus acting as a regenerator for fuel cell 15. While fuel processor 15 of FIGs. 4A and 4B shows dewar 150 encapsulating monolithic structure 100, the present invention may also employ other architectures for dewar 150 and relationships between burner 30 or reformer 32 and dewar 150 that cany out one or both of the dewar functions described above. FIG.
  • FIG. 4D illustrates a cross sectional view of a fuel processor 15 that elongates the convective path for cool air flow over a warmer dewar wall 254 in accordance with another embodiment of the present invention.
  • Fuel processor 15 includes a tubular design for the bumer 30 and reformer 32.
  • Dewar 250 routes cool incoming air across an elongated heat transfer path.
  • Dewar 250 includes a spiral wall 254 in cross section that surrounds burner 30 and reformer 32.
  • Spiral wall 254 defines a spiral dewar chamber 256. Cool air enters dewar chamber 256 at a dewar entrance 252.
  • the innermost portion 257 of wall 254 attaches to an outer wall 258 of burner 30. Heat from burner 30 conducts linearly through spiral wall 254.
  • inner portion 257 is the warmest portion of wall 254, while wall 254 at entrance 252 is typically the coolest. Air progressively warmths as it travels through dewar chamber 256. As the air travels inward, temperature of wall 254 rises, as does the amount of heat available for transfer to the air. Depending on the transient temperature of the air, the amount of heat lost from wall 154 may also increase as the air progresses inward.
  • Spiral dewar 250 elongates convection interaction between the incoming cool air and a wall warmed by the burner. Dewar 250 also increases the number of walls and convective layers in a given radial direction from the fuel processor center. As shown in FIG.
  • dewar 250 comprises 4-5 walls and convective layers in a given radial direction, depending on where the number is counted.
  • the number of walls and convective in a radial direction may vary with design, hi one embodiment, spiral dewar 250 is configured with from 1 layer to about 50 walls and convective layers in a given radial direction from the fuel processor center. Three layers to 20 layers are suitable for many applications.
  • a channel width 260 defines the duct space between adjacent walls 254. In one embodiment, channel width 260 ranges from about V millimeters to about 5 millimeters.
  • Spiral dewar 250 may be constructed by electroplating nickel onto a removable layer such as aluminum or zinc. FIG.
  • FIG. 4H illustrates spiral dewar 250 in an unrolled form during initial construction in accordance with another embodiment of the present invention.
  • Initial aluminum or zinc layer 262 is added to control channel width 260 during rolling.
  • the removable layer 262 is subsequently electroplated with the wall 214 choice of material, for example nickel.
  • After which the aluminum or zinc layer is etched out employing an electroforming technique thus leaving a spiral dewar 250.
  • the spiral dewar 250 shown in FIG. 4H also employs an embossed or folded burner structure 264 that wraps around reformer 32.
  • FIGs. 41 and 4J illustrate wash coatings 266 on a wall 268 of burner 30 in accordance with two embodiments of the present invention. For the folded burner structure 264 of FIG.
  • a wash coat 266 including the burner catalyst 104 is applied to both sides of wall 268.
  • a flat wall 270 suitable for use in spiral dewar 250 is shown in FIG. 4J.
  • Flat wall 270 includes channels 272 etched or otherwise disposed along its surface.
  • a wash coat 266 including the burner catalyst 104 is then added over the surface of flat wall 270 and channels 272.
  • Fuel processors 15 such as that shown in FIG. 4D are very well suited to contain internally generated heat.
  • burner 30 operates at a temperature greater than about 350 degrees Celsius and the outer side of the housing remains less than about 75 degrees Celsius. This facilitates the use of higher temperature burning fuel sources within burner 30 such as ethanol and propane, for example. Dewars as shown in FIGs.
  • FIG. 4A and 4D may be considered 'multipass' since the incoming air passes over multiple surfaces for convective heat transfer between the warmer surfaces and cooler air.
  • the embodiment in FIG. 4A illustrates a two-pass system where the air passes through two dewar chambers, while the embodiment in FIG. 4D illustrates an N-pass where N is the number of dewar walls in a given radial direction from the fuel processor center.
  • FIG. 4E illustrates a cross sectional view of a multipass dewar 300 in accordance with another embodiment of the present invention.
  • Dewar 300 comprises four dewar walls 302a-d that connect to a housing wall 304.
  • Dewar 300 partially contains monolithic structure 100.
  • Dewar wall 302a cooperates with housing wall 304 to enclose monolithic structure 100, which includes burner 30.
  • Dewar wall 302b and housing wall 304 enclose dewar wall 302a and burner 30.
  • dewar wall 302c and housing wall 304 enclose dewar wall 302b
  • dewar wall 302d and housing wall 304 enclose dewar wall 302c.
  • Dewar walls 302a-d form four volumes for incoming air to pass over warmer walls and receive heat. Air enters dewar inlet port 310 and flows through dewar chamber 308a and into dewar chamber 308b through port 312 after travelling through substantially the whole chamber 308a. Air then serially passes into and through chambers 308c and 308d before entering burner inlet 314. FIGs.
  • FIG. 4F and 4G illustrate a cross section of a fuel processor 15 including a monolithic structure 452 and multipass dewar 450 in accordance with another embodiment of the present invention.
  • Monolithic structure 452 includes multiple reformer chambers 454 that are disposed in a central portion of structure 452. Multiple burner chambers 456 sunound and quadrilaterally border the reformer chambers 454. Reformer boiler 458 is ananged within the cross section of burner chambers 456, while burner boiler 460 is arranged in external portion of the cross section.
  • Dewar 462 comprises four dewar walls 462a-d. In the cross section shown in FIG. 4F, dewar wall 462a surrounds monolithic structure 452. Dewar wall 462b sunounds and encloses dewar wall 462a.
  • Dewar wall 462c surrounds and encloses dewar wall 462b, while dewar wall 462d surrounds and encloses dewar wall 462c.
  • Dewar walls 462a-d form four dewar volumes for incoming air to pass through and receive heat. As shown in FIG. 4G, air enters dewar inlet port 464 and flows through dewar chamber 468a and into dewar chamber 468b after traveling through substantially the whole chamber 468a along the length of monolithic structure 452. Air then serially passes from chamber 468b to chamber 468c and chamber 468d before entering burner inlet 470.
  • FIGs. 6A-6J illustrate a fuel processor 615 in accordance with another embodiment of the present invention.
  • FIG. 6 A illustrates a top view of fuel processor 615.
  • Fuel processor 615 comprises reformer 632, burner 630, boiler 634, dock 638, shell 675, preferential oxidizer 650 and plates 641, 649 and 653 (FIG. 6J).
  • Fuel processor 615 includes substrates 640, 642 and 644.
  • Each substrate 640, 642 and 644 comprises two substantially planar faces on opposite sides of the substrate.
  • each substrate 640, 642 and 644 comprises silicon and the set of substrates 640, 642 and 644 is refened to as a 'chipset'.
  • Channels are formed into a face of substrates 640, 642 and 644 to form reformer 632, burner 630, boiler 634 and preferential oxidizer 650.
  • a channel refers to a trench formed in the substrate. Each channel guides the movement of a gas or liquid passed therein.
  • Silicon substrates 640, 642 and 644 permit the use of semiconductor fabrication techniques for the construction of fuel processor 615.
  • reformer channels 637, burner channels 631 and/or boiler channels 635 are formed in a silicon substrate using an etch process, such as a DRE etch or a wet etch
  • each substrate 640, 642 and 644 comprises a silicon alloy, silicon carbide, or a metal such as Stainless Steel, Titanium or friconel.
  • the metal facilitates heat transfer between burner 632 and reformer 630 and between burner 632 and boiler 634.
  • MEMs manufacturing techniques such as layering and etching may also be used to fabricate substrates 640, 642 and 644 and channels disposed therein. Refe ing to FIGs. 6B, 6G and 6J, boiler 634 heats methanol before reformer
  • Boiler 634 receives the methanol.
  • Boiler 634 comprises a set of boiler channels 635 disposed in a face 640a of substrate 640.
  • a plate 641 attaches to face 640a and covers the open side of each channel 635.
  • Boiler 634 includes a volume determined by the cumulative size of boiler channels 635 in the set.
  • Boiler 634 is disposed in proximity to burner 630 to receive heat generated in burner 630.
  • boiler channels 635 are disposed on an opposite face 640a of substrate 640 from the face 640b of substrate 640 including burner channels 631 (FIG. 6J). Heat then transfers 1) via conduction through substrate 640 from burner 630 to boiler 634 and 2) via convection from boiler channel 635 walls to the methanol passing therethrough.
  • boiler 634 is configured to vaporize liquid methanol. Gaseous methanol exiting boiler 634 then passes to reformer 632 for gaseous interaction with catalyst 702.
  • Boiler 634 receives methanol via fuel source inlet 681 (FIG. 6B), which couples to the methanol supply line 27 of FIG. IB.
  • Inlet 681 comprises a socket 682 disposed in a wall 728b of dock 638 and configured to receive a tube 27 that transports methanol to fuel processor 615.
  • An inlet manifold 684 transports liquid methanol from socket 682 to substrate 640 and reformer channels 635 in substrate 640.
  • Manifold 684 comprises an aperture or hole that passes through compliant material 710, substrates 640 and 642, and plate 641.
  • Reformer 632 comprises a set of refonner channels 637 disposed in a face 642b of substrate 642. A plate 649 attaches to face 642b and covers the open side of each channel 637. Reformer 632 includes a volume determined by the cumulative volume and size of reformer channels 637 in the set. More specifically, reformer 632 includes a segmented volume that includes contributions from multiple channels 637. hi one embodiment, channels 637 are substantially rectangular in cross section. Channels 637 widths 637b from about 20 to about 400 microns are suitable for many applications.
  • channels 637 include a width 637b of about 100 microns.
  • One or more aspect ratios may also be used to characterize the size of channels 637.
  • a length 637c to width 637b ratio describes the planar area of channels 637 on the face of a substrate.
  • Channels 637 having a length to width ratio from about 10000:1 to about 10:1 are suitable for many applications, hi a specific embodiment, channels 637 include a length to width ratio of about 200:1.
  • a depth 637a to width 637b ratio describes the cross sectional size of channels 637 along their length 637c. Channels 637 including a depth to width ratio from about 2:1 to about 100:1 are suitable for many applications.
  • channels 637 include a depth to width ratio of about 630:1.
  • the set of channels includes at least one channel.
  • the number and size of channels 637 for refonner 632 may vary with a desired hydrogen output for fuel processor 615, e.g., based on the production capacity of the fuel source and reformer catalyst 702.
  • Refonner 632 is configured to receive methanol after it has passed through boiler 634. Reformer 632 receives the methanol via conduit 671, which transports methanol output from channels 635 of boiler 634 to channels 637 of reformer 632 (FIG 2B).
  • conduit 671 communicates methanol from face 640a of substrate 640, traverses through substrates 640 and 642, and opens to channels 637 on face 642b of substrate 642.
  • a catalyst 702 in refomier 632 facilitates the production of hydrogen.
  • Catalyst 702 reacts with methanol 17 and facilitates the production of hydrogen gas and carbon dioxide.
  • catalyst 702 comprises a wash coat disposed over each channel 637.
  • a wash coat of the desired catalyst may be sputtered or sprayed onto the substrate and etched back to maintain a flat surface 642b.
  • the catalyst 702 then forms as thin layer over the walls of each channel 637.
  • One suitable catalyst 702 includes CuZn when methanol is used as a hydrocarbon fuel source.
  • a preferential oxidizer 650 intercepts reformer 632 hydrogen exhaust and decreases the amount of carbon monoxide in the exhaust (FIG 2G).
  • Preferential oxidizer 650 comprises a set of oxidizer channels 651 disposed in a face 644b of substrate 644 (FIG 2J).
  • a plate 653 attaches to face 644b and covers the open side of each oxidizer channel 651.
  • Preferential oxidizer 650 includes a volume determined by the cumulative size of boiler channels 651 in the set.
  • Preferential oxidizer 650 employs oxygen from an air inlet 707 (FIG 2C).
  • Air inlet 707 receives air from the ambient room and comprises a socket 711 and manifold 712.
  • Socket 711 is disposed in a wall 728b of dock 638 and sized to receive a tube that transports air to fuel processor 615. Socket 711 opens to manifold 712, which transports the air to channels 651 in substrate 644. More specifically, manifold 712 traverses through compliant material 710, through plate 640, through substrates 642 and 640, through plate 649, through spacer 730 and through substrate 644 to open to channels 651.
  • a catalyst 714 is wash coated onto the walls of channels 651 and may comprise one or a combination of the following materials: Cu, Zn, Pt, Ru, Rh, an aluminum oxide, a calcium oxide, a silicon oxide, iridium and/or another catalyst that is preferential to carbon monoxide over carbon dioxide.
  • An outlet port 87 communicates hydrogen formed in reformer 632 outside of fuel processor 615 (FIG 2E). In fuel cell system 10 of FIG. IB, port 87 communicates hydrogen to line 39 for hydrogen provision to fuel cell 20.
  • Port 87 is disposed in a wall of dock 638 and includes a socket 701 and manifold 703 that open through wall 728. Socket 701 is sized to receive a metal or plastic tube for line 39 for hydrogen communication from fuel processor 615.
  • An adhesive may fix the tube to an inner wall of socket 701.
  • a metal tube may be brazed to an inner wall of socket 701.
  • fuel processor 615 includes preferential oxidizer 650 as shown
  • manifold 703 transports hydrogen from preferential oxidizer 650, through substrate 644, tlirough spacer 730, through plate 649, through substrates 642 and 640, through plate 640, through compliant material 710 and to socket 701 (FIG. 6B).
  • preferential oxidizer 650 is not used in fuel processor 615 and reformer 632 is configured to directly output hydrogen from fuel processor 615.
  • channels 637 in reformer 632 provide gas to manifold 703 for hydrogen communication from fuel processor 615.
  • manifold 703 transports hydrogen from refomier channels 637 in substrate 642, through substrates 642 and 640, through plate 640, through compliant material 710 and to socket 701. Hydrogen production in reformer 632 is slightly endothermic and draws heat from burner 630. Burner 630 generates heat and is configured to provide heat to refonner 632. Burner 630 comprises two sets of burner channels 631: a first set of channels 631a disposed in a face 642a of substrate 642 and a second set of channels 631b disposed in a face 640b of substrate 640.
  • Substrates 640 and 642 are positioned and attached such that channels 631a and 631b on opposite faces 642a and 640b open to each other.
  • Burner 630 includes a volume determined by the cumulative size of burner channels 631a and channels 631b.
  • Burner 630, boiler 634 and preferential oxidizer 650 each include a volume determined by the cumulative volume and size of channels in their respective channel set(s).
  • Channel dimensions as described above with respect to reformer channels 637 may also be used for channels 635 of boiler 634, channels 631 of burner 630, and channels 651 of preferential oxidizer 650.
  • channel widths, channel length to width ratios and channel depth to width ratios described above for channels 637 are also suitable for channels 635, channels 631 and channels 651.
  • burner 630 employs catalytic combustion to produce heat.
  • a catalyst 704 in burner 630 helps a burner fuel passed tlirough the chamber generate heat,
  • methanol produces heat in burner 630 and catalyst 704 facilitates the methanol production of heat using methanol.
  • Suitable methanol burner catalysts 704 may include platinum, palladium, iron, tin oxide, other noble-metal catalysts and reducible oxides.
  • Other suitable catalyst 704 materials include one or a combination of the following materials: Cu, Zn, Pt, Ru, Rh, an aluminum oxide, a calcium oxide, a silicon oxide, and/or iridium.
  • waste hydrogen from fuel cell 20 produces heat in the presence of catalyst 704.
  • Catalyst 704 is commercially available from a number of vendors known to those of skill in the art.
  • catalyst 704 comprises a wash coat disposed over each channel 631.
  • a wash coat of the desired catalyst 704 may injected into the micro-channels using well known mixing, injection, evaporation and reduction methods.
  • the catalyst 704 then forms as thin, porous and high surface area layer over the walls of each channel 631.
  • Burner 630 includes an inlet 714 that receives methanol 17 (FIG. 6F).
  • Burner inlet 714 comprises a socket 716 disposed in a wall 728b of dock 638 and configured to receive a tube 27 (FIG. IB) that transports methanol to fuel processor 615.
  • a methanol inlet manifold 718 transports methanol from socket 716 to burner channels 631 in substrates 640 and 642. Air including oxygen enters dock 638 via air inlet port 691 (FIG. 6F). Burner 630 uses the oxygen for catalytic combustion of methanol.
  • a burner outlet port 720 (FIG. 6D) communicates exhaust formed in burner 630 outside of fuel processor 615. Burner outlet port 720 comprises a socket 722 disposed in a wall of dock 638 and configured to receive a tube that transports the exhaust away from fuel processor 615.
  • a burner outlet manifold 124 transports the exhaust from channels 631 to socket 716.
  • fuel processor 615 includes a boiler that heats methanol before burner 630 receives the fuel source.
  • the boiler receives the methanol via fuel source inlet 714.
  • the boiler is disposed in proximity to burner 630 to receive heat generated in burner 630.
  • Burner 630 is configured to provide heat to reformer 632 and configured to provide heat to boiler 634. Disposing a set of burner channels 63 la in substrate 642 allows heat generated in each burner channel 631a to transfer via conduction through substrate 642 to reformer 632 and channels 637 of reformer 632. The heat then conducts from substrate 642 in the vicinity of each channel 637 into catalyst 702.
  • the heat may also convect into the channels 637 and heat the methanol.
  • Disposing a set of burner chamiels 63 lb in substrate 640 allows heat generated in each channel 63 lb to transfer via conduction through substrate 640 to boiler 634 and channels 635 of boiler 634.
  • Situating burner 630 and reformer 632 on the same chip and in close proximity to each other allows heat to flow directly from the burner catalyst 704 through a thin separating substrate 642, and into the reformer catalyst 702. Since the heat transfer is conducted from one catalyst structure, through a thin solid into the next catalyst microstructure, fuel processor 615 does need a large heat transfer area to transfer heat from burner 630 to reformer 632. This reduces the overall volume of fuel processor 615.
  • Burner 630 need not include burner channels 631 in both substrate 640 and substrate 642. If only one substrate includes a set of burner channels 631, then heat may conduct from the substrate having the set of burner channels to the other substrate and then to boiler 634 or reformer 632.
  • fuel processor 615 has so far been described with respect to a catalytic burner 632, it is understood that some embodiments of the present invention may employ an electric burner 630 configured to provide heat to the reformer and configured to provide heat to the boiler.
  • the electric burner 630 includes an resistive heating element that produces heat in response to input current.
  • the electric burner 630 may be disposed between substrates 640 and 642 to provide conductive heat transfer to both substrates 640 and 642.
  • Plates 641, 649 and 653 cover and seal the open portion of channels in a substrate that the each plate neighbors. Each plate 641, 649 and 653 also increases mechanical strength of the chipset. Each plate 641, 649 and 653 may attach and bond to a substrate using a suitable adhesive, for example. In a specific embodiment, plates 641, 649 and 653 comprise glass, which has a low thermal conductivity when compared to silicon and reduces overall heat loss from fuel processor 615. Dock 638 maintains position of reformer 632 and boiler 634 within fuel processor 615.
  • Dock comprises screw 726, a set of dock walls 728, spacer 730, compliant material 710, and sockets 684, 711, 722, 701, and 716 for transport of process gases or liquids to and from reformer 632, burner 630 and boiler 634.
  • Dock walls 728 include a securing wall 728a, wall 728b that opposes securing wall 728a and one or more side walls wall 728c that extend between securing wall 728a and wall 728b (FIG. 6C).
  • Securing wall 728a includes a threaded hole for receiving screw 726.
  • a spring may also be used to push the chipset against compliant material 710 and dock 638.
  • Dock walls 728 combine to form an enclosure that partially surround a portion of reformer 632, boiler 634 and burner 630.
  • Dock walls 728 may comprise, for example, mica glass, a ceramic, a glass filled polyester, or a metal such as copper.
  • Dock 638 applies a compliant securing force that passes through a portion of substrate 640 and a portion of substrate 642.
  • Screw 726 threads through securing wall 728a, or the spring compresses, until it applies a compressive force onto plate 653. This compressive force locks substrates 640 and 642 and plates 641, 649 and 653 in place, and prevents them from shifting during handling.
  • Wall 728b geometrically opposes securing wall 728a and provides a resistive force to the compressive force provided by screw 726 as it translates through components in the stack therebetween.
  • a line 732 between where screw 726 meets plate 653 and wall 728b may be used to roughly describe a compressive force path between screw 726 and wall 728b (FIG. 6G).
  • the compressive force generates in the threads of screw 726, transmits through a portion of plate 653 near where plate 653 meets screw 726, transmits through a portion of substrate 644 near line 732, through a portion of spacer 730 near line 732, through a portion of plate 649 near line 732, through a portion of substrate 642 near line 732, through a portion of substrate 640 near line 732, through a portion of plate
  • portions of substrates 640 and 642 affected by the compressive force of screw 726 comprise an end that nears where the compressive force propagates through the substrates, hi one embodiment, substrates 640 and 642 and plates 641, 649 and 653 resemble cantilevered beams held together and in position via a compressive force applied by screw 726 (or spring).
  • Compliant material 710 intercepts the securing force provided by screw 726 and establishes an upper limit for the compliant securing force. As shown in FIG.
  • compliant material 710 is disposed between plate 641 and wall 728b intercepts the securing force between plate 641 and wall 728b.
  • Compliant material 710 includes a material of known and predetennined compliance that sets an upper limit for the compressive force applied by screw 726.
  • material 710 comprises a rigidity or elastic modulus less than the rigidity or elastic modulus of substrates 640 and 642. Compliance in material 710 then allows stresses onto substrates 640 and 642 to transfer onto material 710. This reduces localized stresses on substrates 640 and
  • compliant material 710 reduces translation of mechanical stress between substrates 640 or 642 and a tube attached into a socket in dock 638. Deformation of compliant material 710 may reduce also pressure variations in portions of substrates 640 and 642 near material 710.
  • Compliant material 710 also reduces stresses induced between substrates 640 and 642 and plates 641 and 649 resulting from thermal expansion and contraction of each component, thus resulting in a more robust mechanical structure and increased protection for refonner 632, boiler 634 and burner 630.
  • Materials suitable for use with compliant material 710 include high temperature silicone, Teflon, or any other material with a suitable compliance and ability to handle the elevated temperatures used in fuel processor 615.
  • the compliant material 710 comprises Grafoil as provided by GrafTech International of Wilmington DE.
  • compliant material 710 acts as a gasket that seals the inlet and exit ports between plate 640 and the inside of wall 728b.
  • the gasket In addition to sealing the gas streams, the gasket also thermally isolates the chipset from dock 638 and dewar 150 (see below), thereby reducing the overall heat loss from fuel processor 615.
  • Spacer 730 maintains separation of substrate 642 and substrate 644. This reduces heat transfer from substrate 642 to a cooler substrate 644 and permits more heat to remain in substrate 642 and transfer to reformer 632 (e.g., catalyst 702 or the methanol in channels 637).
  • spacer 730 comprises a rigid and low heat conductance material such as a ceramic.
  • spacer 730 may comprise another layer of compliant material 710 to further control forces in fuel processor 615 and protect substrates 640 and 642 and plates 641 and 649.
  • Dock walls 728 provide mechanical protection for internal components of fuel processor 615 such as substrates 640 and 642, plates 641 and 649, reformer 632, burner 630 and boiler 634.
  • Shell 675 attaches to dock 638 and also provides mechanical protection for internal components of fuel processor 615.
  • Shell 675 includes a set of walls 77 that at least partially contain reformer 632, burner 630 and boiler 634. Walls 77 comprise a suitably stiff material such as a metal, ceramic or a rigid polymer, for example.
  • Shell 675 may attach to dock 638 using an adhesive or via one ore more screws.
  • Shell 675 and dock 638 collectively encapsulate reformer 632, burner 630 and boiler 634.
  • shell 675 and dock 638 may also contribute thermal management benefits for fuel processor 615.
  • fuel processor 615 includes a screw 726 to provide a compressive force
  • screw 726 may be replaced with a spring clip or shim configured to provide a compressive force onto a chipset.
  • Dock 638 also includes inlet and outlet ports for gaseous and liquid communication in and out of fuel processor 615. Via port 681 and socket 682 described above, dock 638 permits transport of methanol to reformer 632 from outside fuel processor 615 though wall 728b.
  • FIG. 5 illustrates a process flow 500 for generating hydrogen in a fuel processor in accordance with one embodiment of the present invention.
  • the fuel processor comprises a burner, a reformer and a dewar that at least partially contains the burner and reformer.
  • dewars described herein are also useful to contain heat in other reformer and burner designs.
  • Many architectures employ a planar reformer disposed on top or below to a planar burner.
  • Process flow 500 begins by generating heat in the burner (502).
  • Catalytic burner architectures may include those described above or a micro-channel design on silicon. Further description of a micro-channel fuel processor suitable for use with the present invention is included in commonly owned co-pending patent application entitled "Planar Micro Fuel Processor” naming Ian Kaye as inventor and filed on the same day as this patent application. This application is incorporated by reference for all purposes.
  • a catalyst in the burner facilitates heat generation in the presence of the heating fuel.
  • the burner may also employ an electric burner that includes an resistive heating element that produces heat in response to input cunent.
  • burner 30 and dewar 150 share a wall and the air passes through the dewar chamber 156 in a direction that at least partially counters a direction that the air passes through burner chamber 105.
  • the air is then heated in the dewar chamber using heat generated in the burner (506). Heat travels from burner 30 to dewar chamber 156 via conductive heat transfer. Heat may also travel from a burner to a dewar chamber via convective and/or radiative heat transfer. Once in the dewar chamber, the air is typically heated via convective heat transfer from a wall of the dewar to the air.
  • the dewar shares a wall with the burner and air in the dewar chamber is heated using heat from the shared wall. Heat from the burner wall may also travel to other walls in the dewar and heat air in the dewar chamber after the heat transfers from the shared wall to another non-shared dewar wall. Heat traveling between the shared wall and non-shared dewar wall transfer by conduction between connected walls or radiation between facing walls.
  • Process flow 500 then supplies the warmed air to the burner after it has been heated in the dewar chamber (508).
  • the fuel processor includes an exit to the dewar chamber and an inlet to the burner - along with any intermittent plumbing - that allow the heated air to pass therebetween. For the fuel processor shown in FIG.
  • space between dewar 150 and burner 30 at the ends of the burner route the air from the dewar to the burner.
  • the air is then used in the burner for catalytic combustion to generate heat.
  • the generated heat is then transfened from the burner to the reformer (510).
  • the heat is then used in reforming a fuel source to produce hydrogen (512).
  • the first three elements (502, 504, and 506) of process flow 500 also form a method of managing heat in a fuel processor, hi this case, heat generated in the burner (502) passes to air in the dewar (504).
  • the dewar 150 at least partially thermally isolates components internal to the fuel processor housing- such as the burner - and contains heat within the fuel processor.
  • the dewar thus reduces heat loss from the fuel processor and helps manage the temperature gradient between the burner and outer surfaces of the housing.
  • the dewar may also contain extended and/or multiple dewar chambers through which the air passes and is heated by heat generated in the burner.
  • FIG. 4A illustrates a second dewar chamber 158 formed between the dewar and a housing for the fuel processor. Air passes first through chamber 158 then into dewar chamber 156.
  • FIG. 4D illustrates a spiral dewar including an extended dewar chamber 408.
  • dewar 250 includes one wall that increasingly provides heat as incoming air nears the burner.
  • FIG. 4E illustrates a dewar 300 including four partially dewar chambers 308 where each dewar chamber heats incoming air in turn as it nears the burner.
  • FIG. 4F illustrates a dewar including four annular and concentric and rectangular dewar chambers 408 that each heat incoming air in turn as it travels to the burner.
  • reformer 32 includes chamfered comers as shown in FIG. 3A
  • the present invention may employ non-chamfered comers in reformer 32.
  • the present invention has been described in terms of a monolithic structure 100 that forms the volumetric reformer 32, the present invention is not limited to volumetric refomiers disposed in monolithic structures. It is therefore intended that the scope of the invention should be determined with reference to the appended claims.

Abstract

A fuel processor (15) that produces hydrogen (39) from a fuel source (29). The fuel processor (15) comprises a reformer (32) and a burner (30). The reformer (32) includes a catalyst for production of the hydrogen (39). Voluminous reformer chambers increase the amount of catalyst used in the reformer (32) and consequently increase hydrogen production for given fuel processor size. The burner (30) provides heat to the reformer (32). One or multiple burners can surround the reformer on multiple sides to increase heat transfer. Dewars (150) can be used to further increase thermal management of the fuel processor (15) and increase burner efficiency. A dewar (150) includes one or more dewar chambers that receive inlet air (31) before the burner (30) receives the air (31). The air (31) is preheated in the dewar (150) chamber using heat generated by the burner (30).

Description

Annular Fuel Processor and Methods
BACKGROUND OF THE INVENTION The present invention relates to fuel cell technology. In particular, the invention relates to fuel processors that generate hydrogen and are suitable for use in portable applications. A fuel cell electrochemically combines hydrogen and oxygen to produce electricity. The ambient air readily supplies oxygen. Hydrogen provision, however, calls for a working supply. Gaseous hydrogen has a low energy density that reduces its practicality as a portable fuel. Liquid hydrogen, which has a suitable energy density, must be stored at extremely low temperatures and high pressures, making storing and transporting liquid hydrogen burdensome. A reformed hydrogen supply processes a fuel source to produce hydrogen. The fuel source acts as a hydrogen carrier. Currently available hydrocarbon fuel sources include methanol, ethanol, gasoline, propane and natural gas. Liquid hydrocarbon fuel sources offer high energy densities and the ability to be readily stored and transported. A fuel processor reforms the hydrocarbon fuel source and to produce hydrogen. Fuel cell evolution so far has concentrated on large-scale applications such as industrial size generators for electrical power back-up. Consumer electronics devices and other portable electrical power applications currently rely on lithium ion and similar battery technologies. Fuel processors for portable applications such as electronics would be desirable but are not yet commercially available. In addition, techniques that reduce fuel processor size or increase fuel processor efficiency would be highly beneficial. SUMMARY OF THE INVENTION The present invention relates to a fuel processor that produces hydrogen from a fuel source. The fuel processor comprises a reformer and burner. The reformer includes a catalyst that facilitates the production of hydrogen from the fuel source. Voluminous reformer chamber designs are provided that increase the amount of catalyst that can be used in a reformer and increase hydrogen output for a given fuel processor size. The burner provides heat to the reformer. One or more burners may be configured to surround a reformer on multiple sides to increase thermal transfer to the reformer. Dewars are also described that improve thermal management of a fuel processor by reducing heat loss and increasing burner efficiency. A dewar includes one or more dewar chambers that receive inlet process gases or liquids before a reactor receives them. The dewar is arranged such that inlet process gases or liquids passing through the dewar chamber intercepts heat generated in the burner before the heat escapes the fuel processor. Passing inlet process gases or liquids through a dewar chamber in this manner performs three functions: a) active cooling of dissipation of heat generated in burner before is reaches outer portions of the fuel processor, and b) heating of the air before receipt by the burner, and c) absorbing and recycling heat back into the burner increasing burner efficiency. When the burner relies on catalytic combustion to produce heat, heat generated in the burner warms cool process gases or liquids in the burner according to the temperature of the process gases or liquids. This steals heat from the reformer, reduces heating efficiency of a burner and typically results in greater consumption of the fuel source. The dewar thus pre-heats the incoming process gases or liquids before burner arrival so the burner passes less heat to the process gases or liquids that would otherwise transfer to the reformer. In one aspect, the present invention relates to a fuel processor for producing hydrogen from a fuel source. The fuel processor comprises a reformer configured to receive the fuel source, configured to output hydrogen, and including a catalyst that facilitates the production of hydrogen. The fuel processor also comprises a boiler configured to heat the fuel source before the reformer receives the fuel source. The fuel processor further comprises at least one burner configured to provide heat to the reformer and disposed annularly about the reformer. The fuel processor may also comprise a boiler that heats the burner liquid fuel feed. In another aspect, the present invention relates to a fuel processor for producing hydrogen from a fuel source. The fuel processor comprises a reformer configured to receive the fuel source, configured to output hydrogen, including a catalyst that facilitates the production of hydrogen. The reformer also includes a reformer chamber having a volume greater than about 0.1 cubic centimeters and less than about 50 cubic centimeters and is characterized by a cross sectional width and a cross sectional height that is greater than one-third the cross sectional width. The fuel processor also comprises a boiler configured to heat the fuel source before the reformer receives the fuel source. The fuel processor further comprises at least one burner configured to provide heat to the reformer. hi yet another aspect, the present invention relates to a fuel processor for producing hydrogen from a fuel source. The fuel processor comprises a reformer configured to receive the hydrogen fuel source, configured to output hydrogen, and including a catalyst that facilitates the production of hydrogen. The fuel processor also comprises a burner that is configured to provide heat to the reformer. The fuel processor further comprises a dewar that at least partially contains the reformer and the burner and includes a set of dewar walls that form a dewar chamber that is configured to receive an inlet process gas or liquid before the burner receives the inlet process gas or liquid. The fuel processor additionally comprises a housing including a set of housing walls that at least partially contain the dewar and provide external mechanical protection for the reformer and the burner. In still another aspect, the present invention relates to a method for managing heat in a fuel processor. The fuel processor comprises a burner, a reformer and a dewar that at least partially contains the burner. The method comprises generating heat in the burner. The method also comprises passing an inlet process gas or liquid through a dewar chamber. The method further comprises heating the inlet process gas or liquid in the dewar chamber using heat generated in the burner. In another aspect, the present invention relates to a method for generating hydrogen in a fuel processor. The fuel processor comprises a burner, a reformer and a dewar that at least partially contains the burner and reformer. The method comprises generating heat in the burner. The method also comprises passing an inlet process gas or liquid through a dewar chamber. The method further comprises heating the inlet process gas or liquid in the dewar chamber using heat generated in the burner. The method additionally comprises supplying the inlet process gas or liquid to the burner after it has been heated in the dewar chamber. The method also comprises transferring heat generated in the burner to the reformer. The method further comprises reforming a fuel source to produce hydrogen. In one aspect, the present invention relates to a fuel processor for producing hydrogen from a fuel source. The fuel processor comprises a reformer that includes a set of reformer channels disposed in a first substrate. The reformer also includes a reformer catalyst that facilitates the production of hydrogen from the fuel source. The fuel processor further comprises a boiler including a set of channels disposed in a second substrate and configured to heat the fuel source before the reformer receives the fuel source. The fuel processor also comprises a burner configured to provide heat to the reformer and configured to provide heat to the boiler. The fuel processor additionally comprises a dock configured to maintain position of the reformer and boiler within the fuel processor by applying a compliant securing force that passes through a portion of the first substrate and a portion of the second substrate. In another aspect, the present invention relates to a fuel processor for producing hydrogen from a fuel source. The fuel processor comprises a reformer that includes a set of reformer channels disposed in a first substrate. The reformer also includes a reformer catalyst that facilitates the production of hydrogen from the fuel source. The fuel processor further comprises a boiler including a set of channels disposed in a second substrate and configured to heat the fuel source before the reformer receives the fuel source. The fuel processor also comprises a catalytic burner including a catalyst that facilitates the production of heat using the fuel source, configured to provide heat to the first substrate and the second substrate, and including a set of channels disposed in one of the first substrate and the second substrate. In yet another aspect, the present invention relates to a fuel processor for producing hydrogen from a fuel source. The fuel processor comprises a reformer that includes a set of reformer channels disposed in a first substrate. The reformer also includes a reformer catalyst that facilitates the production of hydrogen from the fuel source. The fuel processor further comprises a burner configured to provide heat to the reformer. The fuel processor also comprises a dewar that contains the reformer and the burner and includes a set of dewar walls that form a dewar chamber configured to receive the fuel source or oxygen before the reformer receives the fuel source or oxygen. These and other features and advantages of the present invention will be described in the following description of the invention and associated figures. BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 A illustrates a fuel cell system for producing electrical energy in accordance with one embodiment of the present invention. FIG. IB illustrates schematic operation for the fuel cell system of FIG. 1 A in accordance with a specific embodiment of the present invention. FIG. IC illustrates an embodiment of the fuel cell system of FIG. 1A that routes hydrogen from an anode exhaust of the fuel cell back to a burner in the fuel processor. FIG. 2A illustrates a cross-sectional side view of a fuel processor used in the fuel cell system of FIG. 1 A in accordance with one embodiment of the present invention. FIG. 2B illustrates a cross-sectional front view of the fuel processor used in the fuel cell system of FIG. 1A taken through a mid-plane of fuel processor. FIG. 3 A illustrates a cross-sectional front view of a monolithic structure employed in the fuel processor of FIG. 2 A in accordance with one embodiment of the present invention. FIG. 3B illustrates a cross-sectional layout of a tubular design for use in a fuel processor in accordance with another embodiment of the present invention. FIG. 3C illustrates a cross-sectional front view of a monolithic structure in a fuel processor that comprises a single burner having an 'O-shape' that completely surrounds a reformer chamber in accordance with one embodiment of the present invention. FIG. 3D illustrates an outside view of an end plate used in the fuel processor of FIG. 2A. FIG. 3E illustrates a fuel processor 15 in accordance with another embodiment of the present invention. FIG. 4A illustrates a side cross-sectional view of the fuel processor of FIG. 2A and movement of air created by a dewar in accordance with one embodiment of the present invention. FIG. 4B illustrates a front cross-sectional view of the fuel processor of FIG. 2A and demonstrates thermal management benefits gained by the dewar. FIG. 4C shows a thermal diagram of the heat path produced by a dewar wall used in the fuel processor of FIG. 2 A. FIG. 4D illustrates a cross sectional view of a fuel processor that increases the convective path that air flows over a dewar wall in accordance with another embodiment of the present invention. FIG. 4E illustrates a dewar in accordance with another embodiment of the present invention. FIGs. 4F and 4G illustrate a cross section of a fuel processor including a monolithic structure and multipass dewar in accordance with another embodiment of the present invention. FIG. 4H illustrates spiral dewar in an unrolled form during initial construction in accordance with another embodiment of the present invention. FIGs. 41 and 4J illustrate wash coatings on a wall of a burner in accordance with two embodiments of the present invention. FIG. 5 illustrates a process flow for generating hydrogen in a fuel processor in accordance with one embodiment of the present invention. FIG. 6A illustrates a top view of fuel processor in accordance with one embodiment of the present invention. FIG. 6B illustrates a side cross section of the fuel processor of FIG. 6 A taken through line K-K. FIG. 6C illustrates a side cross section of the fuel processor of FIG. 6 A taken through line L-L. FIG. 6D illustrates a side cross section of the fuel processor of FIG. 6A taken through line A-A. FIG. 6E illustrates a side cross section of the fuel processor of FIG. 6A taken through line M-M. FIG. 6F illustrates a side cross section of the fuel processor of FIG. 6 A taken through line N-N. FIG. 6G illustrates a front cross section of the fuel processor of FIG. 6 A taken through line B-B. FIG. 6H illustrates a front cross section of the fuel processor of FIG. 6 A taken through line C-C. FIG 61 illustrates a front cross section of the fuel processor of FIG. 6A taken through line D-D. FIG. 6J illustrates an expanded view of a portion of the shown in FIG. 6G.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention is described in detail with reference to a few preferred embodiments as illustrated in the accompanying drawings. In the following description, numerous specific details are set forth in order to provide a thorough understanding of the present invention. It will be apparent, however, to one skilled in the art, that the present invention may be practiced without some or all of these specific details. In other instances, well known process steps and/or structures have not been described in detail in order to not unnecessarily obscure the present invention. FIG. 1 A illustrates a fuel cell system 10 for producing electrical energy in accordance with one embodiment of the present invention. Fuel cell system 10 comprises storage device 16, fuel processor 15 and fuel cell 20. A 'reformed' hydrogen supply processes a fuel source to produce hydrogen. As shown, the reformed hydrogen supply comprises a fuel processor 15 and a fuel source storage device 16. Storage device 16 stores fuel source 17, and may include a portable and/or disposable fuel cartridge. A disposable cartridge offers instant recharging to a consumer. In one embodiment, the cartridge includes a collapsible bladder within a hard plastic dispenser case. A separate fuel pump typically controls fuel source 17 flow from storage device 16. If system 10 is load following, then a control system meters fuel source 17 to deliver fuel source 17 to processor 15 at a flow rate determined by the required power level output of fuel cell 20. Fuel source 17 acts as a carrier for hydrogen and can be processed to separate hydrogen. Fuel source 17 may include any hydrogen bearing fuel stream, hydrocarbon fuel or other hydrogen fuel source such as ammonia. Currently available hydrocarbon fuel sources 17 suitable for use with the present invention include gasoline, Ci to C4 hydrocarbons, their oxygenated analogues and/or their combinations, for example. Several hydrocarbon and ammonia products may also produce a suitable fuel source 17. Liquid fuel sources 17 offer high energy densities and the ability to be readily stored and shipped. Storage device 16 may contain a fuel mixture. When the fuel processor 15 comprises a steam reformer, storage device 16 may contain a fuel mixture of a hydrocarbon fuel source and water. Hydrocarbon fuel source/water fuel mixtures are frequently represented as a percentage fuel source in water. In one embodiment, fuel source 17 comprises methanol or ethanol concentrations in water in the range of l%-99.9%. Other liquid fuels such as butane, propane, gasoline, military grade "JP8" etc. may also be contained in storage device
16 with concentrations in water from 5-100%. hi a specific embodiment, fuel source
17 comprises 67% methanol by volume. Fuel processor 15 processes the hydrocarbon fuel source 17 and outputs hydrogen. A hydrocarbon fuel processor 15 heats and processes a hydrocarbon fuel source 17 in the presence of a catalyst to produce hydrogen. Fuel processor 15 comprises a reformer, which is a catalytic device that converts a liquid or gaseous hydrocarbon fuel source 17 into hydrogen and carbon dioxide. As the term is used herein, reforming refers to the process of producing hydrogen from a fuel source.
Fuel processor 15 may output either pure hydrogen or a hydrogen bearing gas stream. Fuel processor 15 is described in further detail below. Fuel cell 20 electrochemically converts hydrogen and oxygen to water, generating electricity and heat in the process. Ambient air commonly supplies oxygen for fuel cell 20. A pure or direct oxygen source may also be used for oxygen supply. The water often forms as a vapor, depending on the temperature of fuel cell 20 components. The electrochemical reaction also produces carbon dioxide as a byproduct for many fuel cells. In one embodiment, fuel cell 20 is a low volume polymer electrolyte membrane (PEM) fuel cell suitable for use with portable applications such as consumer electronics. A polymer electrolyte membrane fuel cell comprises a membrane electrode assembly 40 that carries out the electrical energy generating electrochemical reaction. The membrane electrode assembly 40 includes a hydrogen catalyst, an oxygen catalyst and an ion conductive membrane that a) selectively conducts protons and b) electrically isolates the hydrogen catalyst from the oxygen catalyst. A hydrogen gas distribution layer contains the hydrogen catalyst and allows the diffusion of hydrogen therethrough. An oxygen gas distribution layer contains the oxygen catalyst and allows the diffusion of oxygen and hydrogen protons therethrough. The ion conductive membrane separates the hydrogen and oxygen gas distribution layers. In chemical terms, the anode comprises the hydrogen gas distribution layer and hydrogen catalyst, while the cathode comprises the oxygen gas distribution layer and oxygen catalyst. A PEM fuel cell often includes a fuel cell stack having a set of bi-polar plates.
A membrane electrode assembly is disposed between two bi-polar plates. Hydrogen distribution 43 occurs via a channel field on one plate while oxygen distribution 45 occurs via a channel field on a second facing plate. Specifically, a first channel field distributes hydrogen to the hydrogen gas distribution layer, while a second channel field distributes oxygen to the oxygen gas distribution layer. The 'term 'bi-polar' refers electrically to a bi-polar plate (whether comprised of one plate or two plates) sandwiched between two membrane electrode assembly layers. In this case, the bipolar plate acts as both a negative terminal for one adjacent membrane electrode assembly and a positive terminal for a second adjacent membrane electrode assembly arranged on the opposite face of the bi-polar plate. In electrical terms, the anode includes the hydrogen gas distribution layer, hydrogen catalyst and bi-polar plate. The anode acts as the negative electrode for fuel cell 20 and conducts electrons that are freed from hydrogen molecules so that they can be used externally, e.g., to power an external circuit. In a fuel cell stack, the bi- polar plates are connected in series to add the potential gained in each layer of the stack. In electrical terms, the cathode includes the oxygen gas distribution layer, oxygen catalyst and bi-polar plate. The cathode represents the positive electrode for fuel cell 20 and conducts the electrons back from the external electrical circuit to the oxygen catalyst, where they can recombine with hydrogen ions and oxygen to form water. The hydrogen catalyst separates the hydrogen into protons and electrons. The ion conductive membrane blocks the electrons, and electrically isolates the chemical anode (hydrogen gas distribution layer and hydrogen catalyst) from the chemical cathode. The ion conductive membrane also selectively conducts positively charged ions. Electrically, the anode conducts electrons to a load (electricity is produced) or battery (energy is stored). Meanwhile, protons move through the ion conductive membrane, to combine with oxygen. The protons and used electrons subsequently meet on the cathode side, and combine with oxygen to form water. The oxygen catalyst in the oxygen gas distribution layer facilitates this reaction. One common oxygen catalyst comprises platinum powder very thinly coated onto a carbon paper or cloth. Many designs employ a rough and porous catalyst to increase surface area of the platinum exposed to the hydrogen and oxygen. In one embodiment, fuel cell 20 comprises a set of bi-polar plates that each includes channel fields on opposite faces that distribute the hydrogen and oxygen. One channel field distributes hydrogen while a channel field on the opposite face distributes oxygen. Multiple bi-polar plates can be stacked to produce a 'fuel cell stack' in which a membrane electrode assembly is disposed between each pair of adjacent bi-polar plates. Since the electrical generation process in fuel cell 20 is exothermic, fuel cell 20 may implement a thermal management system to dissipate heat from the fuel cell. Fuel cell 20 may also employ a number of humidification plates (HP) to manage moisture levels in the fuel cell. Further description of a fuel cell suitable for use with the present invention is included in commonly owned co- pending patent application entitled "Micro Fuel Cell Architecture" naming Ian Kaye as inventor and filed on the same day as this patent application. This application is incorporated by reference for all purposes. While the present invention will mainly be discussed with respect to PEM fuel cells, it is understood that the present invention may be practiced with other fuel cell architectures. The main difference between fuel cell architectures is the type of ion conductive membrane used. In one embodiment, fuel cell 20 is phosphoric acid fuel cell that employs liquid phosphoric acid for ion exchange. Solid oxide fuel cells employ a hard, non-porous ceramic compound for ion exchange and may be suitable for use with the present invention. Generally, any fuel cell architecture may benefit from fuel processor improvements described herein. Other such fuel cell architectures include direct methanol, alkaline and molten carbonate fuel cells. Fuel cell 20 generates dc voltage that may be used in a wide variety of applications. For example, electricity generated by fuel cell 20 may be used to power a motor or light. In one embodiment, the present invention provides 'small' fuel cells that are designed to output less than 200 watts of power (net or total). Fuel cells of this size are commonly referred to as 'micro fuel cells' and are well suited for use with portable electronics. In one embodiment, fuel cell 20 is configured to generate from about 1 milliwatt to about 200 watts. In another embodiment, fuel cell 20 generates from about 3 W to about 20 W. Fuel cell 20 may also be a stand-alone fuel cell, which is a single unit that produces power as long as it has an a) oxygen and b) hydrogen or a hydrocarbon fuel supply. A fuel cell 20 that outputs from about 40W to about 100W is well suited to power a laptop computer. FIG. IB illustrates schematic operation for fuel cell system 10 in accordance with a specific embodiment of the present invention. As shown, fuel cell system 10 comprises fuel container 16, hydrogen fuel source 17, fuel processor 15, fuel cell 20, multiple pumps 21 and fans 35, fuel lines and gas lines, and one or more valves 23. While the present invention will now primarily be described with respect to methanol as fuel source 17, it is understood that the present invention may employ another fuel source 17 such as one provided above. Fuel container 16 stores methanol as a hydrogen fuel source 17. An outlet 26 of fuel container 16 provides methanol 17 into hydrogen fuel source line 25. As shown, line 25 divides into two lines: a first line 27 that transports methanol 17 to a burner 30 for fuel processor 15 and a second line 29 that transports methanol 17 to reformer 32 in fuel processor 15. Lines 25, 27 and 29 may comprise plastic tubing, for example. Separate pumps 21a and 21b are provided for lines 27 and 29, respectively, to pressurize the lines and transmit the fuel source at independent rates if desired. A model P625 pump as provided by Instech of Plymouth Meeting, PA is suitable to transmit liquid methanol for system 10 is suitable in this embodiment. A flow sensor or valve 23 situated on line 29 between storage device 16 and fuel processor 18 detects and communicates the amount of methanol 17 transfer between storage device 16 and reformer 32. In conjunction with the sensor or valve 23 and suitable control, such as digital control applied by a processor that implements instructions from stored software, pump 21b regulates methanol 17 provision from storage device 16 to reformer 32. Fan 35a delivers oxygen and air from the ambient room through line 31 to regenerator 36 of fuel processor 15. Fan 35b delivers oxygen and air from the ambient room through line 33 to regenerator 36 of fuel processor 15. In this embodiment, a model AD2005DX-K70 fan as provided by Adda USA of California is suitable to transmit oxygen and air for fuel cell system 10. A fan 37 blows cooling air over fuel cell 20 and its heat transfer appendages 46. Fuel processor 15 receives methanol 17 from storage device 16 and outputs hydrogen. Fuel processor 15 comprises burner 30, reformer 32, boiler 34 and dewar 150. Burner 30 includes an inlet that receives methanol 17 from line 27 and a catalyst that generates heat with methanol presence. In one embodiment, burner 30 includes an outlet that exhausts heated gases to a line 41, which transmits the heated gases over heat transfer appendages 46 of fuel cell 20 to pre-heat the fuel cell and expedite warm-up time needed when initially turning on fuel cell 20. An outlet of burner 30 may also exhaust heated gases into the ambient room. Boiler 34 includes an inlet that receives methanol 17 from line 29. The structure of boiler 34 permits heat produced in burner 30 to heat methanol 17 in boiler 34 before reformer 32 receives the methanol 17. Boiler 34 includes an outlet that provides heated methanol 17 to reformer 32. Reformer 32 includes an inlet that receives heated methanol 17 from boiler 34. A catalyst in reformer 32 reacts with the methanol 17 and produces hydrogen and carbon dioxide. This reaction is slightly endothermic and draws heat from burner 30. A hydrogen outlet of reformer 32 outputs hydrogen to line 39. In one embodiment, fuel processor 15 also includes a preferential oxidizer that intercepts reformer 32 hydrogen exhaust and decreases the amount of carbon monoxide in the exhaust. The preferential oxidizer employs oxygen from an air inlet to the preferential oxidizer and a catalyst based on, for example ruthenium or platinum, that is preferential to carbon monoxide over carbon dioxide. Dewar 150 pre-heats a process gas or liquid before the air enters burner 30. Dewar 150 also reduces heat loss from fuel cell 15 by heating the incoming process liquids or gases before the heat escapes fuel processor 15. In one sense, dewar 150 acts as a regenerator that uses waste heat in fuel processor 15 to improve thermal management and thermal efficiency of the fuel processor. Specifically, waste heat from burner 30 may be used to pre-heat incoming air provided to burner 30 to reduce heat transfer to the air in the burner so more heat transfers to reformer 32. Dewar 150 is described in further detail below. Line 39 transports hydrogen from fuel processor 15 to fuel cell 20. Gaseous delivery lines 31, 33 and 39 may comprise polymeric or metallic tubing, for example. A hydrogen flow sensor (not shown) may also be added on line 39 to detect and coimnunicate the amount of hydrogen being delivered to fuel cell 20. In conjunction with the hydrogen flow sensor and suitable control, such as digital control applied by a processor that implements instructions from stored software, fuel processor 15 regulates hydrogen gas provision to fuel cell 20. Fuel cell 20 includes an hydrogen inlet port that receives hydrogen from line
39 and delivers it to a hydrogen intake manifold for delivery to one or more bi-polar plates and their hydrogen distribution channels. An oxygen inlet port of fuel cell 20 receives oxygen from line 33 and delivers it to an oxygen intake manifold for delivery to one or more bi-polar plates and their oxygen distribution channels. An anode exhaust manifold collects gases from the hydrogen distribution channels and delivers them to an anode exhaust port, which outlets the exhaust gases into the ambient room. A cathode exhaust manifold collects gases from the oxygen distribution channels and delivers them to a cathode exhaust port. The schematic operation for fuel cell system 10 shown in FIG. IB is exemplary and other variations on fuel cell system design, such as reactant and byproduct plumbing, are contemplated. In addition to the components shown in shown in FIG. IB, system 10 may also include other elements such as electronic controls, additional pumps and valves, added system sensors, manifolds, heat exchangers and electrical interconnects useful for carrying out functionality of system 10 that are known to one of skill in the art and omitted herein for sake of brevity. FIG. IC illustrates an embodiment of fuel system 10 that routes unused hydrogen from fuel cell 20 back to burner 30. Burner 30 includes a catalyst that reacts with the unused hydrogen to produce heat. Since hydrogen consumption within fuel cell 20 is often incomplete and the anode exhaust often includes unused hydrogen, re- routing the anode exhaust to burner 30 allows fuel cell system 10 to capitalize on unused hydrogen in fuel cell 20 and increase hydrogen usage and efficiency in system 10. As the term is used herein, unused hydrogen generally refers to hydrogen output from a fuel cell. Line 51 is configured to transmit unused hydrogen from fuel cell 20 to burner 30 of fuel processor 15. For FIG. IC, burner 30 includes two inlets: an inlet 55 configured to receive the hydrogen fuel source 17 and an inlet 53 configured to receive the hydrogen from line 51. Anode gas collection channels, which distribute hydrogen from fuel processor 15 to each membrane electrode assembly layer, collect and exhaust the unused hydrogen. An inlet fan pressurizes line 39 that delivers the hydrogen from an outlet of fuel processor 15 to an anode inlet of fuel cell 20. The inlet fan also pressurizes the anode gas collection channels for distribution of hydrogen within fuel cell 20. In one embodiment, gaseous delivery in line 51 back to fuel processor 15 relies on pressure at the exhaust of the anode gas distribution channels, e.g., in the anode exhaust manifold. In another embodiment, an extra fan is added to line 51 to pressurize line 51 and return unused hydrogen back to fuel processor 15. Burner 30 also includes an inlet 59 configured to receive oxygen from an oxygen exhaust included in fuel cell 20. Cathode gas collection channels, which distribute oxygen and air from the ambient room to each membrane electrode assembly layer, collect and exhaust the unused oxygen. Line 61 delivers unused oxygen from an exhaust manifold, which collects oxygen from each cathode gas collection channel, to inlet 59. Burner 30 thus includes two oxygen inlets: inlet 59 and an inlet 57 configured to receive oxygen from the ambient room after delivery though dewar 150. Since oxygen consumption within fuel cell 20 is often incomplete and the cathode exhaust includes unused oxygen, re-routing the cathode exhaust to burner 30 allows fuel cell system 10 to capitalize on unused oxygen in fuel cell 20 and increase oxygen usage and efficiency in system 10. In one embodiment, fuel processor 15 is a steam reformer that only needs steam to produce hydrogen. Several types of reformers suitable for use in fuel cell system 10 include steam reformers, auto thermal reformers (ATR) or catalytic partial oxidizers (CPOX). ATR and CPOX reformers mix air with the fuel and steam mix. ATR and CPOX systems reform fuels such as methanol, diesel, regular unleaded gasoline and other hydrocarbons. In a specific embodiment, storage device 16 provides methanol 17 to fuel processor 15, which reforms the methanol at about 250°C or less and allows fuel cell system 10 use in applications where temperature is to be minimized. FIG. 2A illustrates a cross-sectional side view of fuel processor 15 in accordance with one embodiment of the present invention. FIG. 2B illustrates a cross- sectional front view of fuel processor 15 taken through a mid-plane of processor 15 that also shows features of end plate 82. Fuel processor 15 reforms methanol to produce hydrogen. Fuel processor 15 comprises monolithic structure 100, end plates 82 and 84, reformer 32, burner 30, boiler 34, boiler 108, dewar 150 and housing 152. Although the present invention will now be described with respect to methanol consumption for hydrogen production, it is understood that fuel processors of the present invention may consume another fuel source, as one of skill in the art will appreciate. As the term is used herein, 'monolithic' refers to a single and integrated structure that includes at least portions of multiple components used in fuel processor 15. As shown, monolithic structure 100 includes reformer 32, burner 30, boiler 34 and boiler 108. Monolithic structure 100 may also include associated plumbing inlets and outlets for reformer 32, burner 30 and boiler 34. Monolithic structure 100 comprises a common material 141 that constitutes the structure. Common material 141 is included in walls that define the reformer 32, burner 32 and boilers 34 and 108. Specifically, walls 111, 119, 120, 122, 130, 132, 134 and 136 all comprise common material 141. Common material 141 may comprise a metal, such as copper, silicon, stainless steel, inconel and other metal/alloys displaying favorable thermal conducting properties. The monolithic structure 100 and common material 141 simplify manufacture of fuel processor 15. For example, using a metal for common material 141 allows monolithic structure 100 to be formed by extrusion or casting. In some cases, monolithic structure 100 is consistent in cross sectional dimensions between end plates 82 and 84 and solely comprises copper formed in a single extrusion. Common material 141 may also include a ceramic, for example. A ceramic monolithic structure 100 maybe formed by sintering. Housing 152 provides mechanical protection for internal components of fuel processor 15 such as burner 30 and reformer 32. Housing 152 also provides separation from the environment external to processor 15 and includes inlet and outlet ports for gaseous and liquid communication in and out of fuel processor 15. Housing 152 includes a set of housing walls 161 that at least partially contain a dewar 150 and provide external mechanical protection for components in fuel processor 15. Walls 161 may comprises a suitably stiff material such as a metal or a rigid polymer, for example. Dewar 150 improves thermal heat management for fuel processor 15 and will be discussed in further detail with respect to FIG. 4A. Together, monolithic structure 100 and end plates 82 and 84 structurally define reformer 32, burner 30, boiler 34 and boiler 108 and their respective chambers. Monolithic structure 100 and end plates 82 and 84 are shown separate in FIG. 2A for illustrative purposes, while FIG. 4A shows them together. Referring to FIG. 2B, boiler 34 heats methanol before reformer 32 receives the methanol. Boiler 34 receives the methanol via fuel source inlet 81, which couples to the methanol supply line 27 of FIG. IB. Since methanol reforming and hydrogen production via a catalyst 102 in reformer 32 often requires elevated methanol temperatures, fuel processor 15 pre-heats the methanol before receipt by reformer 32 via boiler 34. Boiler 34 is disposed in proximity to burner 30 to receive heat generated in burner 30. The heat transfers via conduction through monolithic structure from burner 30 to boiler 34 and via convection from boiler 34 walls to the methanol passing therethrough. In one embodiment, boiler 34 is configured to vaporize liquid methanol. Boiler 34 then passes the gaseous methanol to reformer 32 for gaseous interaction with catalyst 102. Reformer 32 is configured to receive methanol from boiler 34. Walls 111 in monolithic structure 100 (see cross section in FIG. 3 A) and end walls 113 (FIG. 2B) on end plates 82 and 84 define dimensions for a reformer chamber 103. In one embodiment, end plate 82 and/or end plate 84 includes also channels 95 (FIG. 2A) that route heated methanol exhausted from boiler 34 into reformer 32. The heated methanol then enters the reformer chamber 103 at one end of monolithic structure 100 and passes to the other end where the reformer exhaust is disposed, hi another embodiment, a hole disposed in a reformer 32 wall receives inlet heated methanol from a line or other supply. The inlet hole or port may be disposed on a suitable wall 111 or 113 of reformer 32. Reformer 32 includes a catalyst 102 that facilitates the production of hydrogen. Catalyst 102 reacts with methanol 17 and facilitates the production of hydrogen gas and carbon dioxide. In one embodiment, catalyst 102 comprises pellets packed to form a porous bed or otherwise suitably filled into the volume of reformer chamber 103. h one embodiment, pellet sizes are designed to maximize the amount of surface area exposure to the incoming methanol. Pellet diameters ranging from about 50 microns to about 1.5 millimeters are suitable for many applications. Pellet diameters ranging from about 300 microns to about 1500 microns are suitable for use with reformer chamber 103. Pellet sizes and packing may also be varied to control the pressure drop that occurs through reformer chamber 103. hi one embodiment, pressure drops from about 0.2 to about 5 psi gauge are suitable between the inlet and outlet of reformer chamber 103. Pellet sizes may be varied relative to the cross sectional size of reformer chamber 103, e.g., as reformer chamber 103 increases in size so may catalyst 102 pellet diameters. In one embodiment, the ratio of pellet diameter (d) to cross sectional height 117 (D) may range from about 0.0125 to about 1. A D/d ratio from about 5 to about 20 is also suitable for many applications. A packing density may also characterize packing of catalyst 102 in reformer chamber 103. For a copper zinc catalyst 102, packing densities from about 0.3 grams/milliliter to about 2 grams/milliliter are suitable. Packing densities from about 0.9 grams/milliliter to about 1.4 grams/milliliter are appropriate for the embodiment shown in FIG. 3 A. One suitable catalyst 102 may include CuZn on alumina pellets when methanol is used as a hydrocarbon fuel source 17. Other materials suitable for catalyst 102 may be based on nickel, platinum, palladium, or other precious metal catalysts either alone or in combination, for example. Catalyst 102 pellets are commercially available from a number of vendors known to those of skill in the art. Pellet catalysts may also be disposed within a baffling system disposed in the reformer chamber 103. The baffling system includes a set of walls that guide the fuel source along a nonlinear path. The baffling slows and controls flow of gaseous methanol in chamber 103 to improve interaction between the gaseous methanol and pellet catalyst 102. Catalyst 102 may alternatively comprise catalyst materials listed above coated onto a metal sponge or metal foam. A wash coat of the desired metal catalyst material onto the walls of reformer chamber 103 may also be used for reformer 32. Reformer 32 is configured to output hydrogen and includes an outlet port 87 that communicates hydrogen formed in reformer 32 outside of fuel processor 15. In fuel cell system 10, port 87 communicates hydrogen to line 39 for provision to hydrogen distribution 43 in fuel cell 20. Port 87 is disposed on a wall of end plate 82 and includes a hole that passes through the wall (see FIG. 2B). The outlet hole port may be disposed on any suitable wall 111 or 113. Hydrogen production in reformer 32 is slightly endothermic and draws heat from burner 30. Burner 30 generates heat and is configured to provide heat to reformer 32. Burner 30 is disposed annularly about reformer 32, as will be discussed in further detail below. As shown in FIG. 2B, burner 30 comprises two burners (or burner sections) 30a and 30b and their respective burner chambers 105a and 105b that surround reformer 32. Burner 30 includes an inlet that receives methanol 17 from boiler 108 via a channel in one of end plates 82 or 84. In one embodiment, the burner inlet opens into burner chamber 105 a. The methanol then travels the length 142 of burner chamber 105 a to channels disposed in end plate 82 that route methanol from burner chamber 105a to burner chamber 105b. The methanol then travels the back through the length 142 of burner chamber 105b to burner exhaust 89. hi another embodiment, the burner inlet opens into both chambers 105a and 105b. The methanol then travels the length 142 of both chambers 105a and 105b to burner exhaust 89. In one embodiment, burner 30 employs catalytic combustion to produce heat. A catalyst 104 disposed in each burner chamber 105 helps a burner fuel passed through the chamber generate heat, hi one embodiment, methanol produces heat in burner 30 and catalyst 104 facilitates the methanol production of heat. In another embodiment, waste hydrogen from fuel cell 20 produces heat in the presence of catalyst 104. Suitable burner catalysts 104 may include platinum or palladium coated onto a suitable support or alumina pellets for example. Other materials suitable for catalyst 104 include iron, tin oxide, other noble-metal catalysts, reducible oxides, and mixtures thereof. The catalyst 104 is commercially available from a number of vendors known to those of skill in the art as small pellets. The pellets that may be packed into burner chamber 105 to form a porous bed or otherwise suitably filled into the burner chamber volume. Catalyst 104 pellet sizes may be varied relative to the cross sectional size of burner chamber 105. Catalyst 104 may also comprise catalyst materials listed above coated onto a metal sponge or metal foam or wash coated onto the walls of burner chamber 105. A burner outlet port 89 (FIG. 2A) communicates exhaust formed in burner 30 outside of fuel processor 15. Some fuel sources generate additional heat in burner 30, or generate heat more efficiently, with elevated temperatures. Fuel processor 15 includes a boiler 108 that heats methanol before burner 30 receives the fuel source. In this case, boiler 108 receives the methanol via fuel source inlet 85. Boiler 108 is disposed in proximity to burner 30 to receive heat generated in burner 30. The heat transfers via conduction through monolithic structure from burner 30 to boiler 108 and via convection from boiler 108 walls to the methanol passing therethrough. Air including oxygen enters fuel processor 15 via air inlet port 91. Burner 30 uses the oxygen for catalytic combustion of methanol. As will be discussed in further detail below with respect to FIGs. 4A and 4B, air first passes along the outside of dewar 150 before passing through apertures in the dewar and along the inside of dewar 150. This heats the air before receipt by air inlet port 93 of burner 30. FIG. 3 A illustrates a cross-sectional front view of monolithic structure 100 as taken through a mid-plane 121 in accordance with one embodiment of the present invention. Monolithic structure 100 extends from end plate 82 to end plate 84. The cross section of monolithic structure 100 shown in FIG. 3 A extends from one end of structure 100 at end plate 82 to the other end of structure 100 at end plate 84. Monolithic structure 100 includes reformer 32, burner 30, boiler 34 and boiler 108 between end plates 82 and 84. Reformer 32 includes a reformer chamber 103, which is a voluminous space in fuel processor 15 that includes the reforming catalyst 102, opens to the fuel source inlet (from boiler 34 for fuel processor 15), and opens to hydrogen outlet 87. Side walls 111 define a non-planar cross-sectional shape for reformer 32 and its reformer chamber 103. Walls 113 on end plates 82 and 84 close the reformer chamber 103 on either end of the chamber 103 and include the inlet and outlet ports to the chamber 103. Reformer chamber 103 includes a non-planar volume. As the term is used herein, a non-planar reformer chamber 103 refers to a shape in cross section that is substantially non-flat or non-linear. A cross section refers to a planar slice that cuts through the fuel processor or component. For cross sections that include multiple fuel processor components (e.g., both burner 30 and reformer 32), the cross section includes both components. For the vertical and front cross section 121 shown in FIG. 3 A, the cross section dimensions shown are consistent for monolithic structure 100 from end plate 82 to end plate 84, and are consistent at each cross section 121 (FIG. 2A). Reformer 32 and its reformer chamber 103 may employ a quadrilateral or non-quadrilateral cross-sectional shape. Four sides define a quadrilateral reformer chamber 103 in cross section. Four substantially orthogonal sides define rectangular and square quadrilateral reformers 32. A non-quadrilateral reformer 32 may employ cross-sectional geometries with more or less sides, an elliptical shape (see FIG. 3B), and more complex cross-sectional shapes. As shown in FIG. 3A, reformer 32 includes a six-sided cross-sectional 'P-shape' with chamfered comers. One corner section of reformer 32 is removed from monolithic structure 100 to allow for boiler 34 proximity to burner 30. Reformer chamber 103 is characterized by a cross-sectional width 115 and a cross-sectional height 117. A maximum linear distance between inner walls 111 of chamber 103 in a direction spanning a cross section of reformer chamber 103 quantifies cross-sectional width 155. A maximum linear distance between inner walls 111 of chamber 103 orthogonal to the width 115 quantifies cross-sectional height 117. As shown, cross-sectional height 117 is greater than one-third the cross-sectional width 115. This height/width relationship increases the volume of reformer chamber 103 for a given fuel processor 15. In one embodiment, cross-sectional height 117 is greater than one-half cross-sectional width 115. In another embodiment, cross- sectional height 117 is greater than the cross-sectional width 115. Referring back to FIG. 2 A, reformer chamber 103 includes a length 142 (orthogonal to the width 115 and height 117) that extends from one end of monolithic structure 100 at end plate 82 to the other end of structure 100 at end plate 84. hi one embodiment, reformer chamber 103 has a length 142 to width 115 ratio less than 20:1. hi a less elongated design, reformer chamber 103 has a length 142 to width 115 ratio less than 10:1. Reformer 32 provides a voluminous reformer chamber 103. This three dimensional configuration for reformer chamber 103 contrasts micro fuel processor designs where the reformer chamber is etched as micro channels onto a planar substrate. The non-planar dimensions of reformer chamber 103 permit greater volumes for reformer 32 and permit more catalyst 102 for a given size of fuel processor 15. This increases the amount of methanol that can be processed and increases hydrogen output for a particular fuel processor 15 size. Reformer 32 thus improves fuel processor's 15 suitability and performance in portable applications where fuel processor size is important or limited. In other words, since the size of inlet and outlet plumbing and ports varies little while increasing the reformer chamber 103 volume, this allows fuel processor 15 to increase hydrogen output and increase power density for portable applications while maintaining size and weight of the associated plumbing relatively constant. In one embodiment, reformer chamber 103 comprises a volume greater than about 0.1 cubic centimeters and less than about 50 cubic centimeters. In some embodiments, reformer 32 volumes between about 0.5 cubic centimeters and about 2.5 cubic centimeters are suitable for laptop computer applications. Fuel processor 15 includes at least one burner 30. Each burner 30 includes a burner chamber 105. For a catalytic burner 30, the burner chamber 105 is a voluminous space in fuel processor 15 that includes catalyst 104. For communication or burner reactants and products to and from the burner chamber 105, the burner chamber 105 may directly or indirectly open to a fuel source inlet (from boiler 108 for fuel processor 15), open to an air inlet 93, and open to a burner exhaust 89. The number of burners 30 and burner chambers 105 may vary with design.
Monolithic structure 100 of FIG. 3A includes a dual burner 30a and 30b design having two burner chambers 105a and 105b, respectively, forming non-continuous chambers that substantially surround reformer 32 in cross section. Burner 30a comprises side walls 119a (FIG. 3 A) included in monolithic structure 100 and end walls 113 on end plates 82 and 84 (FIG. 2B) that define burner chamber 105 a. Similarly, burner 30b includes side walls 119b (FIG. 3 A) included in monolithic structure 100 and end walls 113 on end plates 82 and 84 (FIG. 2B) that define burner chamber 105b. Monolithic structure 100 of FIG. 3C includes a single burner 30c with a single burner chamber 105c that fully surrounds reformer 32. Tubular arrangement of FIG. 3B includes over forty burners 204 that fully surround reformer 202.
Monolithic structure 452 of FIG. 4F includes a single burner divided into 104 burner chambers that fully surround reformer 32. Referring to FIG. 2B, each burner 30 is configured relative to reformer 32 such that heat generated in a burner 30 transfers to reformer 32. In one embodiment, the one or more burners 30 are annularly disposed about reformer 32. As the term is used herein, annular configuration of at least one burner 30 relative to reformer 32 refers to the burner 30 having, made up of, or formed by, continuous or non- continuous segments or chambers 105 that surround reformer 32. The annular relationship is apparent in cross section. For burner and reformer arrangements, surrounding refers to a burner 30 bordering or neighboring the perimeter of reformer 32 such that heat may travel from a burner 30 to the reformer 32. Burners 30a and 30b may surround reformer 32 about the perimeter of reformer 32 to varying degrees based on design. At the least, one or more burners 30 surround greater than 50 percent of the reformer 32 cross-sectional perimeter. This differentiates fuel processor 15 from planar and plate designs where the burner and reformer are co-planar and of similar dimensions, and by geometric logic, the burner neighbors less than 50 percent of the reformer perimeter. In one embodiment, one or more burners 30 surround greater than 75 percent of the reformer 32 cross-sectional perimeter. Increasing the extent to which burner 30 surrounds reformer 32 perimeter in cross section increases the surface area of reformer 32 that can be used to heat the reformer volume via heat generated in the burner. For some fuel processor 15 designs, one or more burners 30 may surround greater than 90 percent of the reformer 32 cross-sectional perimeter. For the embodiment shown in FIG. 3B, burner 30 surrounds the entire reformer 32 cross-sectional perimeter. Although the present invention will now be described with respect to burner 30 annularly disposed about refoπner 32, it is understood that monolithic structure 100 may comprise the reverse configuration. That is, reformer 32 may be annularly disposed about burner 30. In this case, reformer 32 may comprise one or more continuous or non-continuous segments or chambers 103 that surround burner 30. hi one embodiment, each burner 30 and its burner chamber 105 has a non- planar cross-sectional shape. A non-planar burner 30 may employ cross-sectional shapes such as quadrilaterals, non-quadrilateral geometries with more or less sides, an elliptical shape (see FIG. 3B for circular/tubular burners 30), or more complex cross- sectional shapes. As shown in FIG. 3A, each burner 30 includes a six-sided cross- sectional 'L' shape (with chamfered comers) that bends 90 degrees about reformer 32. Each burner 30 thus bilaterally borders reformer 32. N-lateral bordering in this sense refers to the number of sides, N, of reformer 32 that a burner 30 (and its burner chamber 105) borders in cross section. Thus, burner 30b borders the right and bottom sides of reformer 32, while burner 30a borders the top and left sides of reformer 32. A 'U-shaped' burner 30 may be employed to trilaterally border reformer 32 on three sides. Together, burners 30a and 30b quadrilaterally border reformer 32 on all four orthogonal reformer 32 sides. The reformer 32 used in the configuration of FIG. 3B includes multiple tubular burners that quadrilaterally border reformer 32. FIG. 3C illustrates a cross-sectional front view of monolithic structure 100 that comprises a single burner 30c having an 'O-shape' that completely surrounds reformer chamber 103 in accordance with one embodiment of the present invention. Burner 30c is a continuous chamber about the perimeter of reformer 32 and quadrilaterally borders reformer 32. Heat generated in burner 30 transfers directly and/or indirectly to reformer 32. For the monolithic structure 100 of FIG. 3A, each burner 30 and reformer 32 share common walls 120 and 122 and heat generated in each burner 30 transfers directly to reformer 32 via conductive heat transfer through common walls 120 and 122. Wall 120 forms a boundary wall for burner 30b and a boundary wall for reformer 32. As shown, one side of wall 120 opens to burner chamber 105b while another portion of the wall opens to reformer chamber 103. Wall 120 thus permits direct conductive heat transfer between burner 30b and reformer 32. Similarly, wall 122 forms a boundary wall for burner 30a and a boundary wall for reformer 32, opens to burner chamber 105 a, opens to reformer chamber 103, and permits direct conductive heat transfer between burner 30a and reformer 32. Walls 120 and 122 are both non-planar in cross section and border multiple sides of reformer chamber 103 that are neighbored by burners 30b and 30a. Wall 120 thus provides direct conductive heat transfer in multiple orthogonal directions 128 and 129 from burner 30a to reformer 32. Wall 122 similarly provides direct conductive heat transfer in directions opposite to 128 and 129 from burner 30b to reformer 32. Boiler 34 comprises cylindrical walls 143 included in monolithic structure 100 and end walls 113 on end plates 82 and 84 (see FIG. 2B) that define boiler chamber 147. Circular walls 143 in cross section form a cylindrical shape for boiler 34 that extends from routing end 82 to routing end 84. Boiler 34 is disposed in proximity to burners 30a and 30b to receive heat generated in each burner 30. For monolithic structure 100, boiler 34 shares a common wall 130 with burner 30a and a common wall 132 with burner 30b. Common walls 130 and 132 permit direct conductive heat transfer from each burner 30 to boiler 34. Boiler 34 is also disposed between burners 30 and reformer 32 to intercept thermal conduction consistently moving from the high temperature and heat generating burners 30 to the endothermic reformer 32. Boiler 108 is configured to receive heat from burner 30 to heat methanol before burner 30 receives the methanol. Boiler 108 also comprises a tubular shape having a circular cross section that extends through monolithic structure 100 from end plate 82 to end plate 84. Boiler 108 is disposed in proximity to burners 30a and 30b to receive heat generated in each burner 30, which is used to heat the methanol. Boiler 108 shares a common wall 134 with burner 30a and a common wall 136 with burner 30b. Common walls 134 and 136 permit direct conductive heat transfer from burners 30a and 30b to boiler 108. FIG. 3D illustrates an outside view of end plate 82 in accordance with one embodiment of the present invention. End plate 82 includes fuel source inlet 81, fuel source fuel source inlet 85, hydrogen outlet port 87 and burner air inlet 93. Fuel source inlet 81 includes a hole or port in end wall 113 of end plate 82 that communicates methanol (usually as a liquid) from an external methanol supply to boiler 34 for heating the methanol before receipt by reformer 32. Methanol fuel source inlet 85 includes a hole or port in end wall 113 of end plate 82 that communicates methanol (usually as a liquid) from an external methanol supply to boiler 108 for heating the methanol before receipt by burner 30. Burner air inlet 93 includes a hole or port in end wall 113 of end plate 82 that communicates air and oxygen from the ambient room after it has been preheated in dewar 150. Hydrogen outlet port 87 communicates gaseous hydrogen from reforming chamber 103 outside fuel processor 15. Bolt holes 153 are disposed in wings 145 of monolithic structure 100. Bolt holes 153 permit the passage of bolts therethrough and allow securing of structure 100 and end plates 82 and 84. FIG. 3B illustrates a cross-sectional layout of a tubular design 200 for use in fuel processor 15 in place of monolithic structure 100 in accordance with another embodiment of the present invention. Structure 200 includes a reformer 202, burner 204, boiler 206 and boiler 208. The cross-sectional design 200 shown in FIG. 3B is consistent throughout a cylindrical length between end plates (not shown) that include inlet and outlet ports for supply and exhaust of gases to components of design 200. The circular shape of reformer 202, burner chambers 212, boiler 206 and boiler 208 thus extends for the entire cylindrical length between the end plates. The end plates may also be responsible for routing gases between individual tubes, such as between tubular burners 234. Reformer 202 includes cylindrical walls 203 that define a substantially circular cross section. Reformer 232 thus resembles a hollow cylinder in three dimensions that defines a tubular reformer chamber 210. hi general, reformer 202 may include any elliptical shape (a circle represents an ellipse of about equal orthogonal dimensions) suitable for containing the catalyst 102, for methanol flow through reformer chamber 210, for hydrogen production in reformer chamber 210, and for hydrogen flow in reformer chamber 210. As shown, reformer chamber 210 is defined by a cross sectional width and a cross sectional height that are substantially equal and thus reformer 202 includes a 1 : 1 cross sectional aspect ratio. Burner 204 comprises a set of cylindrical walls 214 that each defines a tubular burner chamber 212. As shown, tubular design 200 includes over forty tubular burner chambers 212 that fully sunound the cross sectional perimeter of reformer 32. Each tubular burner chamber 212 includes a substantially circular cross-section defined by the cylindrical wall 214. Each tubular burner chamber 212 includes catalyst 104 that facilitates heat generation from methanol. Burner 204 may comprise from about two to about two hundred cylindrical walls 214 and tubular burner chambers 212. Some designs may include from about ten to about sixty tubular burner chambers 212. In one embodiment, each cylindrical wall 214 comprises a metal and is extruded to its desired dimensions. In a specific embodiment, cylindrical wall 214 comprises nickel. The nickel wall 214 may be formed by electroplating nickel onto a suitable substrate such as zinc or aluminum that may subsequently etched out to leave the nickel tube. Other materials that a nickel wall 214 may be formed onto include zinc, tin, lead, wax or plastics. In addition to nickel, wall 214 may include gold, silver, copper, stainless steel, ceramics and materials that display suitable thermal properties without causing complications with burner catalyst 104. As shown, burner 204 fully annularly sunounds the cross-sectional perimeter of reformer 202. In this case, burner 204 comprises three ring-like layers 216, 218 and 220 of tubes 214 disposed circularly about reformer 202 and at three different radii. The tubes 214 in each layer 216, 218 and 220 circumscribe reformer 202. Heat generated in each tubular chamber 212 of burner 30 transfers directly or indirectly to reformer 202 via several paths: a) heat conduction through the tubes 214 in layer 216 to the walls of reformer 202; b) heat conduction through the tubes 214 in outer layers 218 and 220 to tubes 214 in layer 216 and to the walls of reformer 202; and/or c) heat radiation between tubes 214 in outer layers 218 and 220 and tubes 214 and then conduction inward to reformer 202. Boiler 206 is configured to heat methanol before reformer 202 receives the methanol. Boiler 206 receives heat from burner 204 and comprises a cylindrical wall 207 that defines a tubular shape for the boiler. Boiler 206 is disposed in proximity to burner tubes 214 to receive heat generated in each burner chamber 212. Specifically, boiler 206 is disposed in the second ring-like layer 218 and receives heat from adjacent burner chambers 212 in layers 216, 218 and 220. Burner 204 provides heat to boiler 206 via conduction through the walls of each adjacent tube 214 and through wall 207. Boiler 208 is configured to heat methanol before burner 204 receives the methanol. Boiler 208 receives heat from burner 204 and also comprises a cylindrical wall 209 that defines a tubular shape for the boiler. Similar to boiler 206, boiler 208 is disposed in the second ring-like layer 218 and receives heat from adjacent burner chambers 212 in layers 216, 218 and 220. In one embodiment, a monolithic fuel processor 15 comprises multiple segments joined together in the direction of gas flow in reformer chamber 103 and joined at sectional lines 121. Each segment has a common profile as shown in FIG. 3A and may comprise metal or ceramic elements that are bonded or brazed perpendicular to the direction of gas flow. Alternatively, fuel processor 15 may comprise a single long monolithic piece that bounds all of reformer 32, burner 30, boiler 34 and boiler 108 except for areas bound by end pieces 82 and 84. i another embodiment, fuel processor 15 comprises multiple pieces joined together in cross section. FIG. 3E illustrates a fuel processor 15 in accordance with another embodiment of the present invention, hi this case, fuel processor 15 comprises three pieces: lower piece 280, middle piece 282 and cap piece 284. Lower piece 280 and middle piece 282 attach to form reformer 32 and two burner chambers 30. Cap piece 284 and middle piece 282 attach to form boilers 34 and 108. Each piece 208, 282 and 284 comprises a common material and may be extruded or cast to suitable dimensions. Attachment between the pieces may comprise chemical bonding, for example. FIG. 4A illustrates a side cross-sectional view of fuel processor 15 and movement of air created by dewar 150 in accordance with one embodiment of the present invention. FIG. 4B illustrates a front cross-sectional view of fuel processor 15 and demonstrates thermal management benefits gained by dewar 150. While thermal management techniques described herein will now be described as fuel processor components, those skilled in the art will recognize that the present invention encompasses methods of thermal management for general application. A burner 30 in fuel processor 15 generates heat and typically operates at an elevated temperature. Burner 30 operating temperatures greater than 200 degrees Celsius are common. Standards for the manufacture of electronics devices typically dictate a maximum surface temperature for a device. Electronics devices such as laptop computers often include cooling, such as a fan or cooling pipe, to manage and dissipate internal heat. A fuel processor internal to an electronics device that loses heat into the device calls upon the device's cooling system to handle the lost heat. In one embodiment, fuel processor 15 comprises a dewar 150 to improve thermal management for fuel processor 15. Dewar 150 at least partially thermally isolates components internal to housing 152 - such as burner 30 - and contains heat within fuel processor 15. Dewar 150 reduces heat loss from fuel processor 15 and helps manage the temperature gradient between burner 30 and outer surface of housing 152. And as will be described below, dewar 150 also pre-heats air before it is received by burner 30. Dewar 150 at least partially contains burner 30 and reformer 32, and includes a set of dewar walls 154 that help form a dewar chamber 156 and a chamber 158. hi some embodiments, dewar 150 fully surrounds burner 30 and reformer 32 in a cross sectional view and at both ends of burner 30 and reformer 32. Less containment by dewar 150 is also suitable to provide thermal benefits described herein. The multipass dewar 300 of FIG. 4E only partially encloses burner 30 and reformer 32 in cross section. In some cases, dewar 150 does not extends fully along the length of monolithic structure 100 and provides less than full containment. As shown in FIG. 4B, dewar 150 annularly surrounds burner 30 in cross section. The set of walls 154 includes side walls 154a and 154c that combine with top and bottom walls 154b and 154d to form the rectangular cross section shown in FIG. 4B; and includes two end walls 154e and 154f that combine with top and bottom walls 154b and 154d to form the rectangular cross section shown in FIG. 4A. End wall 154f includes apertures that permit the passage of inlet and outlet ports 85, 87 and 89 therethough. Dewar chamber 156 is formed within dewar walls 154 and comprises all space within the dewar walls 154 not occupied by monolithic structure 100. As shown in FIG. 4B, dewar chamber 156 sunounds monolithic structure 100. As shown in FIG. 4B, chamber 156 comprises ducts between monolithic structure 100 and walls 154 on all four sides of dewar 150. In addition, chamber 156 comprises air pockets between end walls of dewar 150 and outside surfaces of end plates 82 and 84 on both ends of monolithic structure 100 (FIG. 4A). Chamber 158 is fomied outside dewar walls 154 between dewar 150 and housing 152. Chamber 158 comprises all space within housing 152 not occupied by dewar 150. As shown in FIG. 4B, housing 152 encloses dewar 150 and the further internal monolithic structure 100. Chamber 158 comprises ducts between walls 154 on all four sides of dewar 150 and housing 152. In addition, chamber 158 comprises air pockets 167 between dewar 150 and housing 152 on both ends that prevent contact and conductive heat transfer between dewar 150 and housing 152 (FIG. 4A). Dewar 150 is configured such that a process gas or liquid passing through dewar chamber 156 receives heat generated in burner 30. The process gas or liquid may include any reactant used in fuel processor such as oxygen, air, or fuel source 17, for example. Dewar 150 offers thus two functions for fuel processor 15: a) it permits active cooling of components within fuel processor 15 before the heat reaches an outer portion of the fuel processor, and b) it pre-heats the air going to burner 30. For the former, air moves through fuel processor 15 and across walls 154 of dewar 150 such that the cooler air absorbs heat from the warmer fuel processor 15 components. As shown in FIG. 4 A, housing 152 includes an air inlet port 91 or hole that pennits the passage of air from outside housing 152 into air into chamber 158. A fan usually provides the air directly to fuel processor 15 and pressurizes the air coming through port 91. Top and bottom walls 154b and 154d include air inlet ports or holes 172 that allow air to pass from chamber 158 to dewar chamber 156. Air flow through fuel processor 15 then flows: in air inlet port 91, through chamber 158 along the length of the dewar 150, through holes 172 in walls 154b and 154d, through chamber 156 back along the length of the dewar 150 in the opposite direction as in through chamber 158, and into air inlet ports 176 that allow the air to enter burner 30. In chamber 158, the air a) moves across the outside surface of dewar walls 154 and absorbs heat convectively from dewar walls 154, and b) moves across the inside surface of housing 152 and absorbs heat convectively from the housing 152 walls (when housing 152 is at a greater temperature than the air), hi chamber 156, the air a) moves across the outside surface of monolithic structure 100 and absorbs heat convectively from the walls of monolithic structure 100, and b) moves across the inside surface of dewar 150 and absorbs heat convectively from dewar walls 154. Dewar 150 is thus configured such that air passing through the dewar receives heat generated in burner 30 via direct convective heat transfer from walls in monolithic structure 100 on the outside of burner 30 to air passing through dewar chamber 156. Dewar 150 is also configured to such that air passing through chamber 156 receives heat indirectly from burner 30. Indirectly in this sense refers to heat generated in burner 30 moving to another structure in fuel processor 15 before receipt by the air. FIG. 4C illustrates a thermal diagram of the heat path produced by a wall 154 of dewar 150. Heat from burner 30 conducts through monolithic structure 100 to a surface of structure 100 that opens into dewar chamber 156. From here, the heat a) conducts into the air passing through dewar chamber 156, thereby heating the air; b) radiates to the inner wall 155 of dewar wall 154, from which the heat convects into the air passing through dewar chamber 156; c) radiates to the inner wall 155 of dewar wall 154, conducts through wall 154 to the outer surface 157 of dewar wall 154, from which the heat convects into the air passing through dewar chamber 158, and d) radiates to the inner wall 155 of dewar wall 154, conducts through wall 154 to the outer surface 157 of dewar wall 154, radiates to a wall of housing 152, from which the heat convects into the air passing through dewar chamber 158. Dewar 150 thus provides two streams of convective heat dissipation and active air-cooling in volumes 156 and 158 that prevent heat generated in burner 30 (or other internal parts of fuel processor 15) from escaping the fuel processor. Reflectance of heat back into chamber 156 decreases the amount of heat lost from fuel processor 150 and increases the heating of air passing through chamber 156. To further improve the radiative reflectance back into chamber 156, an inside surface of dewar wall 154 may include a radiative layer 160 to decrease radiative heat transfer into wall 154 (see FIG. 4B or 4C). Radiative layer 160 is disposed on an inner surface 155 on one or more of walls 154 to increase radiative heat reflectance of the inner surface 155. Generally, the material used in radiative layer 160 has a lower emissivity than the material used in walls 154. Materials suitable for use with walls 154 of dewar 150 include nickel or a ceramic, for example. Radiative layer 160 may comprise gold, platinum, silver, palladium, nickel and the metal may be sputter coated onto the inner surface 155. Radiative layer 160 may also include a low heat conductance. In this case, radiative layer 160 may comprise a ceramic, for example. When dewar 150 fully encapsulates monolithic structure 100, the dewar then bounds heat loss from the structure and decreases the amount of heat passing out of dewar 150 and housing 152. Fuel processors 15 such as that shown in FIGs. 4A and 4B are well suited to contain heat within housing 152 and manage heat transfer from the fuel processor. In one embodiment, burner operates at a temperature greater than about 200 degrees Celsius and the outer side of the housing remains less than about 50 degrees Celsius. In embodiments for portable applications where fuel processor 15 occupies a small volume, volumes 156 and 158 are relatively small and comprise narrow channels and ducts, h some cases, the height of channels in volumes 156 and 158 is less than 5 millimeters and a wall of burner 30 on monolithic structure is no greater than 10 millimeters from a wall of housing 152. The thermal benefits gained by use of dewar 150 also permit the use of higher temperature burning fuels as a fuel source for hydrogen production, such as ethanol and gasoline. In one embodiment, the thermal management benefits gained by use of dewar 150 permit reformer 32 to process methanol at temperatures well above 100 degrees Celsius and at temperatures high enough that carbon monoxide production in reformer 32 drops to an amount such that a preferential oxidizer is not needed. As mentioned above, dewar 150 offers a second function for fuel processor 15 by pre-heating the air going to a burner. Burner 30 relies on catalytic combustion to produce heat. Oxygen in the air provided to burner 30 is consumed as part of the combustion process. Heat generated in the burner 30 will heat cool incoming air, depending on the temperature of the air. This heat loss to incoming cool air reduces the heating efficiency of burner 30, and typically results in a greater consumption of methanol. To increase the heating efficiency of burner 30, the present invention heats the incoming air so less heat generated in the burner passes into the incoming air. ha other words, chambers and air flow formed by dewar 150 allow waste heat from the burner to pre-heat air before reaching the burner, thus acting as a regenerator for fuel cell 15. While fuel processor 15 of FIGs. 4A and 4B shows dewar 150 encapsulating monolithic structure 100, the present invention may also employ other architectures for dewar 150 and relationships between burner 30 or reformer 32 and dewar 150 that cany out one or both of the dewar functions described above. FIG. 4D illustrates a cross sectional view of a fuel processor 15 that elongates the convective path for cool air flow over a warmer dewar wall 254 in accordance with another embodiment of the present invention. Fuel processor 15 includes a tubular design for the bumer 30 and reformer 32. Dewar 250 routes cool incoming air across an elongated heat transfer path. Dewar 250 includes a spiral wall 254 in cross section that surrounds burner 30 and reformer 32. Spiral wall 254 defines a spiral dewar chamber 256. Cool air enters dewar chamber 256 at a dewar entrance 252. The innermost portion 257 of wall 254 attaches to an outer wall 258 of burner 30. Heat from burner 30 conducts linearly through spiral wall 254. Thus, inner portion 257 is the warmest portion of wall 254, while wall 254 at entrance 252 is typically the coolest. Air progressively wanns as it travels through dewar chamber 256. As the air travels inward, temperature of wall 254 rises, as does the amount of heat available for transfer to the air. Depending on the transient temperature of the air, the amount of heat lost from wall 154 may also increase as the air progresses inward. Spiral dewar 250 elongates convection interaction between the incoming cool air and a wall warmed by the burner. Dewar 250 also increases the number of walls and convective layers in a given radial direction from the fuel processor center. As shown in FIG. 4D, dewar 250 comprises 4-5 walls and convective layers in a given radial direction, depending on where the number is counted. The number of walls and convective in a radial direction may vary with design, hi one embodiment, spiral dewar 250 is configured with from 1 layer to about 50 walls and convective layers in a given radial direction from the fuel processor center. Three layers to 20 layers are suitable for many applications. A channel width 260 defines the duct space between adjacent walls 254. In one embodiment, channel width 260 ranges from about V millimeters to about 5 millimeters. Spiral dewar 250 may be constructed by electroplating nickel onto a removable layer such as aluminum or zinc. FIG. 4H illustrates spiral dewar 250 in an unrolled form during initial construction in accordance with another embodiment of the present invention. Initial aluminum or zinc layer 262 is added to control channel width 260 during rolling. The removable layer 262 is subsequently electroplated with the wall 214 choice of material, for example nickel. After which the aluminum or zinc layer is etched out employing an electroforming technique thus leaving a spiral dewar 250. The spiral dewar 250 shown in FIG. 4H also employs an embossed or folded burner structure 264 that wraps around reformer 32. FIGs. 41 and 4J illustrate wash coatings 266 on a wall 268 of burner 30 in accordance with two embodiments of the present invention. For the folded burner structure 264 of FIG. 41, a wash coat 266 including the burner catalyst 104 is applied to both sides of wall 268. A flat wall 270 suitable for use in spiral dewar 250 is shown in FIG. 4J. Flat wall 270 includes channels 272 etched or otherwise disposed along its surface. A wash coat 266 including the burner catalyst 104 is then added over the surface of flat wall 270 and channels 272. Fuel processors 15 such as that shown in FIG. 4D are very well suited to contain internally generated heat. In one embodiment, burner 30 operates at a temperature greater than about 350 degrees Celsius and the outer side of the housing remains less than about 75 degrees Celsius. This facilitates the use of higher temperature burning fuel sources within burner 30 such as ethanol and propane, for example. Dewars as shown in FIGs. 4A and 4D may be considered 'multipass' since the incoming air passes over multiple surfaces for convective heat transfer between the warmer surfaces and cooler air. The embodiment in FIG. 4A illustrates a two-pass system where the air passes through two dewar chambers, while the embodiment in FIG. 4D illustrates an N-pass where N is the number of dewar walls in a given radial direction from the fuel processor center. FIG. 4E illustrates a cross sectional view of a multipass dewar 300 in accordance with another embodiment of the present invention. Dewar 300 comprises four dewar walls 302a-d that connect to a housing wall 304. Dewar 300 partially contains monolithic structure 100. Dewar wall 302a cooperates with housing wall 304 to enclose monolithic structure 100, which includes burner 30. Dewar wall 302b and housing wall 304 enclose dewar wall 302a and burner 30. Similarly, dewar wall 302c and housing wall 304 enclose dewar wall 302b, while dewar wall 302d and housing wall 304 enclose dewar wall 302c. Dewar walls 302a-d form four volumes for incoming air to pass over warmer walls and receive heat. Air enters dewar inlet port 310 and flows through dewar chamber 308a and into dewar chamber 308b through port 312 after travelling through substantially the whole chamber 308a. Air then serially passes into and through chambers 308c and 308d before entering burner inlet 314. FIGs. 4F and 4G illustrate a cross section of a fuel processor 15 including a monolithic structure 452 and multipass dewar 450 in accordance with another embodiment of the present invention. Monolithic structure 452 includes multiple reformer chambers 454 that are disposed in a central portion of structure 452. Multiple burner chambers 456 sunound and quadrilaterally border the reformer chambers 454. Reformer boiler 458 is ananged within the cross section of burner chambers 456, while burner boiler 460 is arranged in external portion of the cross section. Dewar 462 comprises four dewar walls 462a-d. In the cross section shown in FIG. 4F, dewar wall 462a surrounds monolithic structure 452. Dewar wall 462b sunounds and encloses dewar wall 462a. Dewar wall 462c surrounds and encloses dewar wall 462b, while dewar wall 462d surrounds and encloses dewar wall 462c. Dewar walls 462a-d form four dewar volumes for incoming air to pass through and receive heat. As shown in FIG. 4G, air enters dewar inlet port 464 and flows through dewar chamber 468a and into dewar chamber 468b after traveling through substantially the whole chamber 468a along the length of monolithic structure 452. Air then serially passes from chamber 468b to chamber 468c and chamber 468d before entering burner inlet 470. FIGs. 6A-6J illustrate a fuel processor 615 in accordance with another embodiment of the present invention. FIG. 6 A illustrates a top view of fuel processor 615. FIGs. 6B-6F illustrate side cross sections of fuel processor 615 taken at various profiles. FIGs. 6G-6J illustrate front cross sections of fuel processor 615 taken at various profiles. FIG. 6J illustrates an expanded side cross section view of a portion of fuel processor 615 shown in FIG. 6G. Fuel processor 615 comprises reformer 632, burner 630, boiler 634, dock 638, shell 675, preferential oxidizer 650 and plates 641, 649 and 653 (FIG. 6J). Although the present invention will now be described with respect to methanol consumption for hydrogen production, it is understood that fuel processors of the present invention may consume another fuel source, as one of skill in the art will appreciate. Fuel processor 615 includes substrates 640, 642 and 644. Each substrate 640, 642 and 644 comprises two substantially planar faces on opposite sides of the substrate. In one embodiment, each substrate 640, 642 and 644 comprises silicon and the set of substrates 640, 642 and 644 is refened to as a 'chipset'. Channels are formed into a face of substrates 640, 642 and 644 to form reformer 632, burner 630, boiler 634 and preferential oxidizer 650. A channel refers to a trench formed in the substrate. Each channel guides the movement of a gas or liquid passed therein. Silicon substrates 640, 642 and 644 permit the use of semiconductor fabrication techniques for the construction of fuel processor 615. hi a specific embodiment, reformer channels 637, burner channels 631 and/or boiler channels 635 are formed in a silicon substrate using an etch process, such as a DRE etch or a wet etch, hi another embodiment, each substrate 640, 642 and 644 comprises a silicon alloy, silicon carbide, or a metal such as Stainless Steel, Titanium or friconel. The metal facilitates heat transfer between burner 632 and reformer 630 and between burner 632 and boiler 634. MEMs manufacturing techniques such as layering and etching may also be used to fabricate substrates 640, 642 and 644 and channels disposed therein. Refe ing to FIGs. 6B, 6G and 6J, boiler 634 heats methanol before reformer
632 receives the methanol. Boiler 634 comprises a set of boiler channels 635 disposed in a face 640a of substrate 640. A plate 641 attaches to face 640a and covers the open side of each channel 635. Boiler 634 includes a volume determined by the cumulative size of boiler channels 635 in the set. Boiler 634 is disposed in proximity to burner 630 to receive heat generated in burner 630. In the embodiment shown, boiler channels 635 are disposed on an opposite face 640a of substrate 640 from the face 640b of substrate 640 including burner channels 631 (FIG. 6J). Heat then transfers 1) via conduction through substrate 640 from burner 630 to boiler 634 and 2) via convection from boiler channel 635 walls to the methanol passing therethrough. In one embodiment, boiler 634 is configured to vaporize liquid methanol. Gaseous methanol exiting boiler 634 then passes to reformer 632 for gaseous interaction with catalyst 702. Boiler 634 receives methanol via fuel source inlet 681 (FIG. 6B), which couples to the methanol supply line 27 of FIG. IB. Inlet 681 comprises a socket 682 disposed in a wall 728b of dock 638 and configured to receive a tube 27 that transports methanol to fuel processor 615. An inlet manifold 684 transports liquid methanol from socket 682 to substrate 640 and reformer channels 635 in substrate 640. Manifold 684 comprises an aperture or hole that passes through compliant material 710, substrates 640 and 642, and plate 641. Compression of material 710, substrates 640 and 642, and plate 641 by screw 726 seals manifold 684 between the components. Reformer 632 comprises a set of refonner channels 637 disposed in a face 642b of substrate 642. A plate 649 attaches to face 642b and covers the open side of each channel 637. Reformer 632 includes a volume determined by the cumulative volume and size of reformer channels 637 in the set. More specifically, reformer 632 includes a segmented volume that includes contributions from multiple channels 637. hi one embodiment, channels 637 are substantially rectangular in cross section. Channels 637 widths 637b from about 20 to about 400 microns are suitable for many applications. In a specific embodiment, channels 637 include a width 637b of about 100 microns. One or more aspect ratios may also be used to characterize the size of channels 637. A length 637c to width 637b ratio describes the planar area of channels 637 on the face of a substrate. Channels 637 having a length to width ratio from about 10000:1 to about 10:1 are suitable for many applications, hi a specific embodiment, channels 637 include a length to width ratio of about 200:1. A depth 637a to width 637b ratio describes the cross sectional size of channels 637 along their length 637c. Channels 637 including a depth to width ratio from about 2:1 to about 100:1 are suitable for many applications. In a specific embodiment, channels 637 include a depth to width ratio of about 630:1. The set of channels includes at least one channel. The number and size of channels 637 for refonner 632 may vary with a desired hydrogen output for fuel processor 615, e.g., based on the production capacity of the fuel source and reformer catalyst 702. Refonner 632 is configured to receive methanol after it has passed through boiler 634. Reformer 632 receives the methanol via conduit 671, which transports methanol output from channels 635 of boiler 634 to channels 637 of reformer 632 (FIG 2B). More specifically, conduit 671 communicates methanol from face 640a of substrate 640, traverses through substrates 640 and 642, and opens to channels 637 on face 642b of substrate 642. A catalyst 702 in refomier 632 facilitates the production of hydrogen. Catalyst 702 reacts with methanol 17 and facilitates the production of hydrogen gas and carbon dioxide. In one embodiment, catalyst 702 comprises a wash coat disposed over each channel 637. A wash coat of the desired catalyst may be sputtered or sprayed onto the substrate and etched back to maintain a flat surface 642b. The catalyst 702 then forms as thin layer over the walls of each channel 637. One suitable catalyst 702 includes CuZn when methanol is used as a hydrocarbon fuel source. Other materials suitable for catalyst 702 include platinum, palladium, a platinum/ palladium mix, and other precious metal catalysts for example. A combination of the following materials may also be used in catalyst 702: Cu, Zn, Pt, Ru, Rh, aluminum Oxides, calcium oxides, silicon oxides, and/or iridium. A preferential oxidizer 650 intercepts reformer 632 hydrogen exhaust and decreases the amount of carbon monoxide in the exhaust (FIG 2G). Preferential oxidizer 650 comprises a set of oxidizer channels 651 disposed in a face 644b of substrate 644 (FIG 2J). A plate 653 attaches to face 644b and covers the open side of each oxidizer channel 651. Preferential oxidizer 650 includes a volume determined by the cumulative size of boiler channels 651 in the set. Preferential oxidizer 650 employs oxygen from an air inlet 707 (FIG 2C). Air inlet 707 receives air from the ambient room and comprises a socket 711 and manifold 712. Socket 711 is disposed in a wall 728b of dock 638 and sized to receive a tube that transports air to fuel processor 615. Socket 711 opens to manifold 712, which transports the air to channels 651 in substrate 644. More specifically, manifold 712 traverses through compliant material 710, through plate 640, through substrates 642 and 640, through plate 649, through spacer 730 and through substrate 644 to open to channels 651. A catalyst 714 is wash coated onto the walls of channels 651 and may comprise one or a combination of the following materials: Cu, Zn, Pt, Ru, Rh, an aluminum oxide, a calcium oxide, a silicon oxide, iridium and/or another catalyst that is preferential to carbon monoxide over carbon dioxide. An outlet port 87 communicates hydrogen formed in reformer 632 outside of fuel processor 615 (FIG 2E). In fuel cell system 10 of FIG. IB, port 87 communicates hydrogen to line 39 for hydrogen provision to fuel cell 20. Port 87 is disposed in a wall of dock 638 and includes a socket 701 and manifold 703 that open through wall 728. Socket 701 is sized to receive a metal or plastic tube for line 39 for hydrogen communication from fuel processor 615. An adhesive may fix the tube to an inner wall of socket 701. Alternatively, a metal tube may be brazed to an inner wall of socket 701. When fuel processor 615 includes preferential oxidizer 650 as shown, manifold 703 transports hydrogen from preferential oxidizer 650, through substrate 644, tlirough spacer 730, through plate 649, through substrates 642 and 640, through plate 640, through compliant material 710 and to socket 701 (FIG. 6B). hi another embodiment, preferential oxidizer 650 is not used in fuel processor 615 and reformer 632 is configured to directly output hydrogen from fuel processor 615. hi this case, channels 637 in reformer 632 provide gas to manifold 703 for hydrogen communication from fuel processor 615. When fuel processor 615 does not include a preferential oxidizer, manifold 703 transports hydrogen from refomier channels 637 in substrate 642, through substrates 642 and 640, through plate 640, through compliant material 710 and to socket 701. Hydrogen production in reformer 632 is slightly endothermic and draws heat from burner 630. Burner 630 generates heat and is configured to provide heat to refonner 632. Burner 630 comprises two sets of burner channels 631: a first set of channels 631a disposed in a face 642a of substrate 642 and a second set of channels 631b disposed in a face 640b of substrate 640. Substrates 640 and 642 are positioned and attached such that channels 631a and 631b on opposite faces 642a and 640b open to each other. Burner 630 includes a volume determined by the cumulative size of burner channels 631a and channels 631b. Burner 630, boiler 634 and preferential oxidizer 650 each include a volume determined by the cumulative volume and size of channels in their respective channel set(s). Channel dimensions as described above with respect to reformer channels 637 may also be used for channels 635 of boiler 634, channels 631 of burner 630, and channels 651 of preferential oxidizer 650. Thus, channel widths, channel length to width ratios and channel depth to width ratios described above for channels 637 are also suitable for channels 635, channels 631 and channels 651. In one embodiment, burner 630 employs catalytic combustion to produce heat. A catalyst 704 in burner 630 helps a burner fuel passed tlirough the chamber generate heat, hi one embodiment, methanol produces heat in burner 630 and catalyst 704 facilitates the methanol production of heat using methanol. Suitable methanol burner catalysts 704 may include platinum, palladium, iron, tin oxide, other noble-metal catalysts and reducible oxides. Other suitable catalyst 704 materials include one or a combination of the following materials: Cu, Zn, Pt, Ru, Rh, an aluminum oxide, a calcium oxide, a silicon oxide, and/or iridium. hi another embodiment, waste hydrogen from fuel cell 20 produces heat in the presence of catalyst 704. Catalyst 704 is commercially available from a number of vendors known to those of skill in the art. In one embodiment, catalyst 704 comprises a wash coat disposed over each channel 631. A wash coat of the desired catalyst 704 may injected into the micro-channels using well known mixing, injection, evaporation and reduction methods. The catalyst 704 then forms as thin, porous and high surface area layer over the walls of each channel 631. Burner 630 includes an inlet 714 that receives methanol 17 (FIG. 6F). Burner inlet 714 comprises a socket 716 disposed in a wall 728b of dock 638 and configured to receive a tube 27 (FIG. IB) that transports methanol to fuel processor 615. A methanol inlet manifold 718 transports methanol from socket 716 to burner channels 631 in substrates 640 and 642. Air including oxygen enters dock 638 via air inlet port 691 (FIG. 6F). Burner 630 uses the oxygen for catalytic combustion of methanol. A burner outlet port 720 (FIG. 6D) communicates exhaust formed in burner 630 outside of fuel processor 615. Burner outlet port 720 comprises a socket 722 disposed in a wall of dock 638 and configured to receive a tube that transports the exhaust away from fuel processor 615. A burner outlet manifold 124 transports the exhaust from channels 631 to socket 716. Some fuel sources generate additional heat in burner 630, or generate heat more efficiently, with elevated temperatures, hi one embodiment, fuel processor 615 includes a boiler that heats methanol before burner 630 receives the fuel source. In this case, the boiler receives the methanol via fuel source inlet 714. The boiler is disposed in proximity to burner 630 to receive heat generated in burner 630. Burner 630 is configured to provide heat to reformer 632 and configured to provide heat to boiler 634. Disposing a set of burner channels 63 la in substrate 642 allows heat generated in each burner channel 631a to transfer via conduction through substrate 642 to reformer 632 and channels 637 of reformer 632. The heat then conducts from substrate 642 in the vicinity of each channel 637 into catalyst 702. The heat may also convect into the channels 637 and heat the methanol. Disposing a set of burner chamiels 63 lb in substrate 640 allows heat generated in each channel 63 lb to transfer via conduction through substrate 640 to boiler 634 and channels 635 of boiler 634. Situating burner 630 and reformer 632 on the same chip and in close proximity to each other allows heat to flow directly from the burner catalyst 704 through a thin separating substrate 642, and into the reformer catalyst 702. Since the heat transfer is conducted from one catalyst structure, through a thin solid into the next catalyst microstructure, fuel processor 615 does need a large heat transfer area to transfer heat from burner 630 to reformer 632. This reduces the overall volume of fuel processor 615. Burner 630 need not include burner channels 631 in both substrate 640 and substrate 642. If only one substrate includes a set of burner channels 631, then heat may conduct from the substrate having the set of burner channels to the other substrate and then to boiler 634 or reformer 632. Although fuel processor 615 has so far been described with respect to a catalytic burner 632, it is understood that some embodiments of the present invention may employ an electric burner 630 configured to provide heat to the reformer and configured to provide heat to the boiler. The electric burner 630 includes an resistive heating element that produces heat in response to input current. The electric burner 630 may be disposed between substrates 640 and 642 to provide conductive heat transfer to both substrates 640 and 642. Plates 641, 649 and 653 cover and seal the open portion of channels in a substrate that the each plate neighbors. Each plate 641, 649 and 653 also increases mechanical strength of the chipset. Each plate 641, 649 and 653 may attach and bond to a substrate using a suitable adhesive, for example. In a specific embodiment, plates 641, 649 and 653 comprise glass, which has a low thermal conductivity when compared to silicon and reduces overall heat loss from fuel processor 615. Dock 638 maintains position of reformer 632 and boiler 634 within fuel processor 615. Dock comprises screw 726, a set of dock walls 728, spacer 730, compliant material 710, and sockets 684, 711, 722, 701, and 716 for transport of process gases or liquids to and from reformer 632, burner 630 and boiler 634. Dock walls 728 include a securing wall 728a, wall 728b that opposes securing wall 728a and one or more side walls wall 728c that extend between securing wall 728a and wall 728b (FIG. 6C). Securing wall 728a includes a threaded hole for receiving screw 726. In place of screw 726, a spring may also be used to push the chipset against compliant material 710 and dock 638. Dock walls 728 combine to form an enclosure that partially surround a portion of reformer 632, boiler 634 and burner 630. Dock walls 728 may comprise, for example, mica glass, a ceramic, a glass filled polyester, or a metal such as copper. Dock 638 applies a compliant securing force that passes through a portion of substrate 640 and a portion of substrate 642. Screw 726 threads through securing wall 728a, or the spring compresses, until it applies a compressive force onto plate 653. This compressive force locks substrates 640 and 642 and plates 641, 649 and 653 in place, and prevents them from shifting during handling. Wall 728b geometrically opposes securing wall 728a and provides a resistive force to the compressive force provided by screw 726 as it translates through components in the stack therebetween. A line 732 between where screw 726 meets plate 653 and wall 728b may be used to roughly describe a compressive force path between screw 726 and wall 728b (FIG. 6G). The compressive force generates in the threads of screw 726, transmits through a portion of plate 653 near where plate 653 meets screw 726, transmits through a portion of substrate 644 near line 732, through a portion of spacer 730 near line 732, through a portion of plate 649 near line 732, through a portion of substrate 642 near line 732, through a portion of substrate 640 near line 732, through a portion of plate
641 near line 732, through a portion of compliant material 710 near line 732, and to wall 728b. In this case, portions of substrates 640 and 642 affected by the compressive force of screw 726 comprise an end that nears where the compressive force propagates through the substrates, hi one embodiment, substrates 640 and 642 and plates 641, 649 and 653 resemble cantilevered beams held together and in position via a compressive force applied by screw 726 (or spring). Compliant material 710 intercepts the securing force provided by screw 726 and establishes an upper limit for the compliant securing force. As shown in FIG. 6D, compliant material 710 is disposed between plate 641 and wall 728b intercepts the securing force between plate 641 and wall 728b. Compliant material 710 includes a material of known and predetennined compliance that sets an upper limit for the compressive force applied by screw 726. In one embodiment, material 710 comprises a rigidity or elastic modulus less than the rigidity or elastic modulus of substrates 640 and 642. Compliance in material 710 then allows stresses onto substrates 640 and 642 to transfer onto material 710. This reduces localized stresses on substrates 640 and
642 and sets an upper limit for stresses on substrates 640 and 642. When substrates 640 and 642 comprise a brittle material such as silicon, material 710 prevents functional compromise of fuel processor 615 by increasing mechanical buffering and protection of substrates 640 and 642 to external stresses. By providing a mechanical buffer for forces onto substrates 640 and 642 and plates 641 and 649, compliant material 710 reduces translation of mechanical stress between substrates 640 or 642 and a tube attached into a socket in dock 638. Deformation of compliant material 710 may reduce also pressure variations in portions of substrates 640 and 642 near material 710. Compliant material 710 also reduces stresses induced between substrates 640 and 642 and plates 641 and 649 resulting from thermal expansion and contraction of each component, thus resulting in a more robust mechanical structure and increased protection for refonner 632, boiler 634 and burner 630. Materials suitable for use with compliant material 710 include high temperature silicone, Teflon, or any other material with a suitable compliance and ability to handle the elevated temperatures used in fuel processor 615. In a specific embodiment, the compliant material 710 comprises Grafoil as provided by GrafTech International of Wilmington DE. In one embodiment, compliant material 710 acts as a gasket that seals the inlet and exit ports between plate 640 and the inside of wall 728b. In addition to sealing the gas streams, the gasket also thermally isolates the chipset from dock 638 and dewar 150 (see below), thereby reducing the overall heat loss from fuel processor 615. Spacer 730 maintains separation of substrate 642 and substrate 644. This reduces heat transfer from substrate 642 to a cooler substrate 644 and permits more heat to remain in substrate 642 and transfer to reformer 632 (e.g., catalyst 702 or the methanol in channels 637). In one embodiment, spacer 730 comprises a rigid and low heat conductance material such as a ceramic. Alternatively, spacer 730 may comprise another layer of compliant material 710 to further control forces in fuel processor 615 and protect substrates 640 and 642 and plates 641 and 649. Dock walls 728 provide mechanical protection for internal components of fuel processor 615 such as substrates 640 and 642, plates 641 and 649, reformer 632, burner 630 and boiler 634. Shell 675 attaches to dock 638 and also provides mechanical protection for internal components of fuel processor 615. Shell 675 includes a set of walls 77 that at least partially contain reformer 632, burner 630 and boiler 634. Walls 77 comprise a suitably stiff material such as a metal, ceramic or a rigid polymer, for example. Shell 675 may attach to dock 638 using an adhesive or via one ore more screws. Shell 675 and dock 638 collectively encapsulate reformer 632, burner 630 and boiler 634. As described with respect to dewar 150, shell 675 and dock 638 may also contribute thermal management benefits for fuel processor 615. Although fuel processor 615 includes a screw 726 to provide a compressive force, it is contemplated that other mechanical means may be used to apply a force to maintain position of the reformer and boiler within the fuel processor. For example, screw 726 may be replaced with a spring clip or shim configured to provide a compressive force onto a chipset. Dock 638 also includes inlet and outlet ports for gaseous and liquid communication in and out of fuel processor 615. Via port 681 and socket 682 described above, dock 638 permits transport of methanol to reformer 632 from outside fuel processor 615 though wall 728b. Similarly, via port 87 and socket 701 described above, dock 638 permits transport of hydrogen from reformer to outside the fuel processor though a wall included in the dock. Dock 638 thus also provides gaseous and liquid interconnection for components held by dock 638. FIG. 5 illustrates a process flow 500 for generating hydrogen in a fuel processor in accordance with one embodiment of the present invention. The fuel processor comprises a burner, a reformer and a dewar that at least partially contains the burner and reformer. Although the present invention has so far discussed dewars with respect to annular reformer and burner designs described herein, it is also anticipated that dewars described herein are also useful to contain heat in other reformer and burner designs. Many architectures employ a planar reformer disposed on top or below to a planar burner. Micro-channel designs fabricated in silicon commonly employ such stacked planar architectures and would benefit from dewars described herein. Process flow 500 begins by generating heat in the burner (502). Catalytic burner architectures may include those described above or a micro-channel design on silicon. Further description of a micro-channel fuel processor suitable for use with the present invention is included in commonly owned co-pending patent application entitled "Planar Micro Fuel Processor" naming Ian Kaye as inventor and filed on the same day as this patent application. This application is incorporated by reference for all purposes. A catalyst in the burner facilitates heat generation in the presence of the heating fuel. The burner may also employ an electric burner that includes an resistive heating element that produces heat in response to input cunent. Air enters a port for the dewar and passes tlirough a dewar chamber (504). For the dewar of FIG. 4A, burner 30 and dewar 150 share a wall and the air passes through the dewar chamber 156 in a direction that at least partially counters a direction that the air passes through burner chamber 105. The air is then heated in the dewar chamber using heat generated in the burner (506). Heat travels from burner 30 to dewar chamber 156 via conductive heat transfer. Heat may also travel from a burner to a dewar chamber via convective and/or radiative heat transfer. Once in the dewar chamber, the air is typically heated via convective heat transfer from a wall of the dewar to the air. hi one embodiment, the dewar shares a wall with the burner and air in the dewar chamber is heated using heat from the shared wall. Heat from the burner wall may also travel to other walls in the dewar and heat air in the dewar chamber after the heat transfers from the shared wall to another non-shared dewar wall. Heat traveling between the shared wall and non-shared dewar wall transfer by conduction between connected walls or radiation between facing walls. Process flow 500 then supplies the warmed air to the burner after it has been heated in the dewar chamber (508). Typically, the fuel processor includes an exit to the dewar chamber and an inlet to the burner - along with any intermittent plumbing - that allow the heated air to pass therebetween. For the fuel processor shown in FIG. 2A, space between dewar 150 and burner 30 at the ends of the burner route the air from the dewar to the burner. The air is then used in the burner for catalytic combustion to generate heat. The generated heat is then transfened from the burner to the reformer (510). In the reformer, the heat is then used in reforming a fuel source to produce hydrogen (512). The first three elements (502, 504, and 506) of process flow 500 also form a method of managing heat in a fuel processor, hi this case, heat generated in the burner (502) passes to air in the dewar (504). The dewar 150 at least partially thermally isolates components internal to the fuel processor housing- such as the burner - and contains heat within the fuel processor. The dewar thus reduces heat loss from the fuel processor and helps manage the temperature gradient between the burner and outer surfaces of the housing. The dewar may also contain extended and/or multiple dewar chambers through which the air passes and is heated by heat generated in the burner. FIG. 4A illustrates a second dewar chamber 158 formed between the dewar and a housing for the fuel processor. Air passes first through chamber 158 then into dewar chamber 156. FIG. 4D illustrates a spiral dewar including an extended dewar chamber 408. hi this case, dewar 250 includes one wall that increasingly provides heat as incoming air nears the burner. FIG. 4E illustrates a dewar 300 including four partially dewar chambers 308 where each dewar chamber heats incoming air in turn as it nears the burner. FIG. 4F illustrates a dewar including four annular and concentric and rectangular dewar chambers 408 that each heat incoming air in turn as it travels to the burner. While this invention has been described in terms of several preferred embodiments, there are alterations, permutations, and equivalents that fall within the scope of this invention which have been omitted for brevity's sake. For example, although reformer 32 includes chamfered comers as shown in FIG. 3A, the present invention may employ non-chamfered comers in reformer 32. In addition, although the present invention has been described in terms of a monolithic structure 100 that forms the volumetric reformer 32, the present invention is not limited to volumetric refomiers disposed in monolithic structures. It is therefore intended that the scope of the invention should be determined with reference to the appended claims.

Claims

What is claimed is:
1. A fuel processor for producing hydrogen from a fuel source, the fuel processor comprising: a reformer configured to receive the fuel source, configured to output hydrogen, and including a catalyst that facilitates the production of hydrogen; a boiler configured to heat the fuel source before the reformer receives the fuel source; and at least one burner configured to provide heat to the reformer and disposed annularly about the refonner.
2. The fuel processor of claim 1 wherein the at least one burner sunounds greater than 50 percent of the refomier cross-sectional perimeter.
3. The fuel processor of claim 2 wherein the at least one burner surrounds greater than 75 percent of the reformer cross-sectional perimeter.
4. The fuel processor of claim 3 wherein the at least one burner surrounds greater than 90 percent of the reformer cross-sectional perimeter.
5. The fuel processor of claim 1 wherein the at least one burner bilaterally neighbors the reformer.
6. The fuel processor of claim 5 wherein the at least one burner trilaterally neighbors the reformer.
7. The fuel processor of claim 6 wherein the at least one burner quadrilaterally neighbors the reformer.
8. The fuel processor of claim 1 wherein the at least one burner includes a first burner chamber having a non-planar cross-sectional shape.
9. The fuel processor of claim 1 wherein the at least one burner includes a first burner chamber having a non-quadrilateral cross-sectional shape.
10. The fuel processor of claim 9 wherein the at least one burner further includes a second burner chamber including a non-quadrilateral cross-sectional shape.
11. The fuel processor of claim 10 wherein the first burner chamber and the second burner chamber collectively quadrilaterally neighbor the reformer.
12. The fuel processor of claim 1 further comprising a dewar that contains the refomier, contains the at least one burner and includes a set of dewar walls that form a dewar chamber that is configured to receive the fuel source or oxygen before the at least one burner receives the fuel source or oxygen.
13. The fuel processor of claim 12 wherein the dewar includes a radiative layer disposed on an inner wall of the set of dewar walls that improves radiative heat reflectance of the inner wall.
14. The fuel processor of claim 12 wherein the dewar is configured such that air passing tlirough the dewar chamber receives heat generated in the at least one burner.
15. The fuel processor of claim 1 wherein the dewar annularly surrounds the at least one burner in cross section.
16. The fuel processor of claim 1 wherein the dewar includes a second dewar chamber.
17. The fuel processor of claim 17 wherein the second boiler is configured to receive heat from the at least one burner.
18. The fuel processor of claim 1 wherein the fuel processor includes a monolithic structure having a common material included in walls that define the reformer, the at least one burner and the boiler.
19. The fuel processor of claim 18 wherein the common material comprises a metal.
20. The fuel processor of claim 19 wherein the monolithic structure is formed in a single extrusion or casting.
21. The fuel processor of claim 1 wherein the fuel processor comprises a non- planar wall that is shared by the reformer and the at least one burner and permits conductive thermal communication between the at least one burner and the reformer in orthogonal directions.
22. The fuel processor of claim 21 wherein the boiler is configured to receive heat from the at least one burner.
23. The fuel processor of claim 22 further comprising a second boiler that is configured to heat the fuel source before the at least one burner receives the fuel source.
24. A fuel processor for producing hydrogen from a fuel source, the fuel processor comprising: a reformer configured to receive the fuel source, configured to output hydrogen, including a catalyst that facilitates the production of hydrogen, and including a reformer chamber having a volume greater than about 0.1 cubic centimeters and less than about 50 cubic centimeters, and the reformer chamber is characterized by a cross sectional width and a cross sectional height that is greater than one-third the cross sectional width; a boiler configured to heat the fuel source before the reformer receives the fuel source; and at least one burner configured to provide heat to the reformer.
25. The fuel processor of claim 24 wherein the reformer chamber is substantially non-quadrilateral in cross section.
26. The fuel processor of claim 24 wherein the reformer chamber includes a substantially elliptical cross section.
27. The fuel processor of claim 26 wherein the reformer chamber includes a substantially circular cross section.
28. The fuel processor of claim 24 wherein the reformer chamber comprises a volume between about 0.5 cubic centimeters and about 2.5 cubic centimeters.
29. The fuel processor of claim 24 wherein the cross sectional height is greater than one-half the cross sectional width.
30. The fuel processor of claim 24 wherein the cross sectional height is greater than the cross sectional width.
31. The fuel processor of claim 24 wherein the at least one burner includes a first burner chamber having a non-quadrilateral cross-sectional shape.
32. The fuel processor of claim 31 wherein the at least one burner bilaterally neighbors the reformer.
33. The fuel processor of claim 31 wherein the at least one burner further includes a second burner chamber including a non-quadrilateral cross-sectional shape.
34. The fuel processor of claim 33 wherein the first burner chamber and the second burner chamber collectively quadrilaterally neighbor the reformer.
35. The fuel processor of claim 1 wherein the at least one burner suπounds greater than 50 percent of the reformer perimeter.
36. The fuel processor of claim 35 wherein the at least one burner surrounds greater than 90 percent of the reformer perimeter.
38. The fuel processor of claim 24 wherein the boiler is configured to receive heat from the at least one burner.
39. The fuel processor of claim 24 wherein the fuel processor includes a monolithic stracture having a common material included in walls that define the reformer, the burner and the boiler.
40. The fuel processor of claim 39 wherein the common material comprises a metal.
41. The fuel processor of claim 40 wherein the monolithic structure is formed in a single extrusion.
42. The fuel processor of claim 24 wherein the catalyst comprises pellets.
43. The fuel processor of claim 42 wherein the pellets have a diameter ranging from about 300 microns to about 1500 microns.
44. A fuel processor for producing hydrogen from a fuel source, the fuel processor comprising: a reformer configured to receive the hydrogen fuel source, configured to output hydrogen and including a catalyst that facilitates the production of hydrogen; a burner configured to provide heat to the reformer; a dewar that at least partially contains the reformer and the burner and includes a set of dewar walls that form a dewar chamber, the chamber configured to receive a process gas or liquid before the bumer receives the process gas or liquid; and a housing including a set of housing walls that at least partially contain the dewar and provide external mechanical protection for the reformer and the burner.
45. The fuel processor of claim 44 wherein the dewar is configured such that the process gas or liquid passing through the dewar chamber receives heat generated in the burner.
46. The fuel processor of claim 45 wherein the dewar is configured such that the process gas or liquid passing tlirough the dewar chamber receives heat directly from a wall of the burner.
47. The fuel processor of claim 45 wherein the dewar is configured such that the process gas or liquid passing through the dewar chamber receives heat indirectly from the burner.
48. The fuel processor of claim 44 wherein the dewar includes a radiative layer disposed on an inner surface of the set of dewar walls that improves radiative heat reflectance of the inner surface.
49. The fuel processor of claim 44 wherein the burner operates at a temperature greater than about 200 degrees Celsius and the outer side of the housing remains less than about 50 degrees Celsius.
50. The fuel processor of claim 49 wherein a wall of the burner is no greater than 10 millimeters from a wall of the housing.
51. The fuel processor of claim 44 wherein the dewar includes a second dewar chamber.
52. The fuel processor of claim 51 wherein the second dewar chamber comprises space formed between the dewar and the housing.
53. The fuel processor of claim 53 wherein the process gas or liquid passes through the second dewar chamber before entering the first dewar chamber.
54. The fuel processor of claim 44 wherein the dewar comprises a spiral configuration in cross section.
55. The fuel processor of claim 44 wherein the dewar annularly surrounds the burner in cross section.
56. The fuel processor of claim 55 wherein the burner comprises a catalyst wash coated on a wall of the burner.
57. The fuel processor of claim 56 wherein the dewar comprises a spiral wall that spirals in a cross section around the burner.
58. The fuel processor of claim 57 wherein the dewar includes a portion of the spiral wall and the burner share comprises a second portion of the spiral wall including the wash coat.
59. A method for generating hydrogen in a fuel processor, the fuel processor comprising a burner, a reformer and a dewar that at least partially contains the burner and reformer, the method comprising: generating heat in the burner; passing process gas or liquid through a dewar chamber; heating the process gas or liquid in the dewar chamber using heat generated in the burner; supplying the process gas or liquid to the burner after it has been heated in the dewar chamber; transferring heat generated in the burner to the reformer; and reforming a fuel source to produce hydrogen.
60. The method of claim 59 wherein the process gas or liquid passes through the dewar chamber in a direction that at least partially counters a direction that the process gas or liquid passes tlirough the burner chamber.
61. The method of claim 59 wherein the dewar chamber comprises space formed between a wall of the bumer and a set of walls for the dewar.
62. The method of claim 59 wherein the fuel processor comprises a housing that contains the dewar.
63. The method of claim 62 wherein the housing and the dewar create a second dewar chamber that receives the process gas or liquid before the dewar chamber receives the process gas or liquid .
64. The method of claim 63 further comprising heating the process gas or liquid in the second dewar chamber using heat generated in the burner.
65. The method of claim 59 wherein the process gas or liquid in the dewar chamber is heated using heat from a wall shared by the burner and the dewar.
66. The method of claim 65 wherein heating the process gas or liquid comprises convective heat transfer between the shared wall and the process gas or liquid in the dewar chamber.
67. The method of claim 59 wherein the process gas or liquid in the dewar chamber is heated using heat from a wall of the dewar after the heat transfers from the burner to the dewar wall.
68. The method of claim 67 wherein the heat transfers from to dewar wall via conductive heat transfer from a wall shared by the dewar and the burner.
69. The method of claim 68 wherein the heat transfers to the dewar wall via radiative heat transfer from a wall shared by the dewar and the burner.
70. The method of claim 69 wherein the dewar includes a radiative layer disposed on the inner wall that improves radiative heat reflectance of the inner wall.
71. The method of claim 59 wherein the dewar comprises a wall that spirals in a cross section around the burner.
72. A method for managing heat in a fuel processor, the fuel processor comprising a burner, a reformer and a dewar that at least partially contains the burner, the method comprising: generating heat in the burner; passing a process gas or liquid through a dewar chamber; and heating the process gas or liquid in the dewar chamber using heat generated in the burner.
73. The method of claim 72 wherein the process gas or liquid passes through the dewar chamber in a direction that at least partially counters a direction that the process gas or liquid passes through the burner chamber.
74. The method of claim 72 wherein the dewar chamber comprises space formed between a wall of the burner and a set of walls for the dewar.
75. The method of claim 72 wherein the fuel processor comprises a housing that contains the dewar.
76. The method of claim 75 wherein the housing and the dewar create a second dewar chamber that receives the process gas or liquid before the dewar chamber receives the process gas or liquid.
77. The method of claim 76 further comprising heating the process gas or liquid in the second dewar chamber using heat generated in the burner.
78. The method of claim 76 wherein the burner operates at a temperature greater than about 200 degrees Celsius and an outer side of the housing remains less than about 50 degrees Celsius during heat generation in the burner.
79. The method of claim 72 wherein the process gas or liquid in the dewar chamber is heated using heat from a wall shared by the burner and the dewar.
80. The method of claim 78 wherein heating the process gas or liquid comprises convective heat transfer between the shared wall and the process gas or liquid in the dewar chamber.
81. The method of claim 72 wherein the dewar comprises a wall that spirals in a cross section around the burner.
82. The method of claim 72 wherein the burner comprises a catalyst wash coated on a wall of the burner.
83. The method of claim 82 wherein the dewar comprises a spiral wall that spirals in a cross section around the burner. 84. The method of claim 83 wherein the dewar includes a portion of the spiral wall and the burner share comprises a second portion of the spiral wall including the wash coat.
85. A fuel processor for producing hydrogen from a fuel source, the fuel processor comprising: a refonner including a set of reformer channels disposed in a first substrate and including a reformer catalyst that facilitates the production of hydrogen from the fuel source; a boiler including a set of channels disposed in a second substrate and configured to heat the fuel source before the refonner receives the fuel source; a burner configured to provide heat to the reformer and configured to provide heat to the boiler; and a dock configured to maintain position of the reformer and boiler within the fuel processor by applying a compliant securing force that passes through a portion of the first substrate and a portion of the second substrate.
86. The fuel processor of claim 85 further comprising a compliant material that intercepts the securing force and establishes an upper limit for the compliant securing force.
87. The fuel processor of claim 85 wherein the dock comprises a screw that threads through a threaded hole in a first wall of the dock.
88. The fuel processor of claim 87 further comprising a compliant material disposed between a dock wall that opposes the first wall, wherein the compliant material intercepts a securing force provided by the screw and establishes an upper limit for the compliant securing force.
89. The fuel processor of claim 88 wherein the compliant material reduces pressure variation in the portion of the first substrate.
90. The fuel processor of claim 85 wherein the dock is configured to permit transport of hydrogen from the reformer to outside the fuel processor though a wall included in the dock.
91. The fuel processor of claim 85 wherein the dock is configured to permit transport of the fuel source to the reformer from outside the fuel processor though a wall included in the dock.
92. The fuel processor of claim 91 wherein the dock comprises a socket that opens to a manifold that transports a gas or fluid between socket and the reformer.
93. The fuel processor of claim 92 wherein the socket is configured to receive a tube that transports the fuel source to the fuel processor.
94. The fuel processor of claim 93 wherein the dock is configured to reduce translation of mechanical stress between the tube and the first substrate.
95. The fuel processor of claim 85 further comprising a plate disposed adjacent to the first substrate and configured to cover the reformer channels.
96. The fuel processor of claim 85 further comprising a shell attached to the dock, wherein the dock and shell collectively encapsulate the reformer, boiler and burner.
97. The fuel processor of claim 85 wherein the first substrate comprises silicon, silicon alloy, or a metal.
98. The fuel processor of claim 853 wherein the reformer channels are formed in the silicon or metal using an etch process.
99. The fuel processor of claim 85 wherein the reformer catalyst comprises a wash coat disposed over the reformer channels.
100. The fuel processor of claim 85 wherein the reformer channels comprise a width between about 20 microns and about 400 microns.
101. The fuel processor of claim 85 wherein the reformer channels comprise a depth to width ratio from about 2:1 to about 100:1.
102. The fuel processor of claim 85 wherein the burner is a catalytic burner including a catalyst that facilitates the production of heat using the fuel source.
103. A fuel processor for producing hydrogen from a fuel source, the fuel processor comprising: a reformer including a set of reformer channels disposed in a first substrate and including a reformer catalyst that facilitates the production of hydrogen from the fuel source; a boiler including a set of channels disposed in a second substrate and configured to heat the fuel source before the reformer receives the fuel source; and a catalytic burner including a catalyst that facilitates the production of heat using the fuel source, configured to provide heat to the first substrate and the second substrate, and including a set of channels disposed in one of the first substrate and the second substrate.
104. The fuel processor of claim 103 wherein the burner catalyst comprises a wash coat disposed over the burner channels.
105. The fuel processor of claim 103 wherein the first substrate comprises silicon, silicon alloy, or a metal.
106. The fuel processor of claim 105 wherein the burner channels are formed in the silicon, silicon alloy, or a metal using an etch process.
107. The fuel processor of claim 103 wherein the burner channels comprise a width between about 20 microns and about 400 microns.
108. The fuel processor of claim 103 wherein the reformer burner comprises a wash coat disposed over the burner channels.
109. The fuel processor of claim 103 wherein the burner channels comprise a depth to width ratio from about 2:1 to about 100:1.
110. The fuel processor of claim 103 further comprising a second set of burner channels disposed in the other of the first substrate and the second substrate.
111. The fuel processor of claim 110 wherein the first substrate and the second substrate are ananged in contact with each other and channels in the first set of burner channels open to channels in the second set of burner channels.
112. A fuel processor for producing hydrogen from a fuel source, the fuel processor comprising: a reformer including a set of reformer channels disposed in a first substrate and including a reformer catalyst that facilitates the production of hydrogen from the fuel source; a burner configured to provide heat to the reformer; and a dewar that contains the reformer and the burner and includes a set of dewar walls that form a dewar chamber configured to receive the fuel source or oxygen before the reformer receives the fuel source or oxygen. 113. The fuel processor of claim 112 wherein the dewar includes a radiative layer disposed on an inner wall of the set of dewar walls that improves radiative heat reflectance of the inner wall.
114. The fuel processor of claim 112 wherein the dewar is configured such that air passing through the dewar chamber receives heat generated in the burner.
115. The fuel processor of claim 112 wherein the dewar includes a second dewar chamber.
116. The fuel processor of claim 112 wherein air passes through the second dewar chamber before entering the first dewar chamber.
117. The fuel processor of claim 112 wherein the burner is a catalytic burner including a catalyst that facilitates the production of heat using the fuel source.
118. The fuel processor of claim 117 wherein the catalytic burner comprises a set of burner channels and the burner catalyst comprises a wash coat disposed over the burner channels.
119. The fuel processor of claim 112 wherein the reformer channels comprise a width between about 20 microns and about 400 microns.
120. The fuel processor of claim 112 wherein the first substrate comprises silicon or a metal.
121. The fuel processor of claim 120 wherein the reformer channels are formed in the silicon, silicon alloy, or a metal using an etch process.
PCT/US2004/020299 2003-06-27 2004-06-25 Annular fuel processor and methods WO2005004256A2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP2006517622A JP2007524562A (en) 2003-06-27 2004-06-25 Annular fuel processing apparatus and method
EP04756039A EP1644111A4 (en) 2003-06-27 2004-06-25 Annular fuel processor and methods

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US48299603P 2003-06-27 2003-06-27
US48341603P 2003-06-27 2003-06-27
US60/483,416 2003-06-27
US60/482,996 2003-06-27

Publications (2)

Publication Number Publication Date
WO2005004256A2 true WO2005004256A2 (en) 2005-01-13
WO2005004256A3 WO2005004256A3 (en) 2005-08-25

Family

ID=33567669

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2004/020299 WO2005004256A2 (en) 2003-06-27 2004-06-25 Annular fuel processor and methods

Country Status (4)

Country Link
US (7) US7604673B2 (en)
EP (1) EP1644111A4 (en)
JP (1) JP2007524562A (en)
WO (1) WO2005004256A2 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1767268A1 (en) * 2005-09-27 2007-03-28 FUJIFILM Corporation Fluidic device
JP2008536796A (en) * 2005-04-18 2008-09-11 インテリジェント エナジー インコーポレイテッド Compact device for pure hydrogen generation
EP1977822A2 (en) * 2007-03-29 2008-10-08 Samsung SDI Co., Ltd. Reaction vessel and reaction device
FR2937655A1 (en) * 2008-10-29 2010-04-30 Renault Sas METHODS OF DEPOSITING A SOIL / GEL CATALYST BY SUSPENSION OR CHEMICAL VAPOR DEPOSITION ON A MICROSTRUCTURE REACTOR
US8172913B2 (en) 2002-04-23 2012-05-08 Vencill Thomas R Array of planar membrane modules for producing hydrogen
WO2014171263A1 (en) * 2013-04-18 2014-10-23 Honda Motor Co., Ltd. Fuel cell module
GB2616339A (en) * 2022-01-26 2023-09-06 Caterpillar Inc Cryogenic containment system

Families Citing this family (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7922781B2 (en) 2001-03-02 2011-04-12 Chellappa Anand S Hydrogen generation apparatus and method for using same
US7867300B2 (en) * 2001-03-02 2011-01-11 Intelligent Energy, Inc. Ammonia-based hydrogen generation apparatus and method for using same
WO2002071451A2 (en) 2001-03-02 2002-09-12 Mesosystems Technology, Inc. Ammonia-based hydrogen generation apparatus and method for using same
ES2386624T3 (en) * 2001-04-23 2012-08-23 Intelligent Energy, Inc. Hydrogen generation apparatus and method for using it
US7666539B2 (en) 2003-06-27 2010-02-23 Ultracell Corporation Heat efficient portable fuel cell systems
JP2007524562A (en) * 2003-06-27 2007-08-30 ウルトラセル コーポレイション Annular fuel processing apparatus and method
US8821832B2 (en) 2003-06-27 2014-09-02 UltraCell, L.L.C. Fuel processor for use with portable fuel cells
US8318368B2 (en) * 2003-06-27 2012-11-27 UltraCell, L.L.C. Portable systems for engine block
US20060127711A1 (en) * 2004-06-25 2006-06-15 Ultracell Corporation, A California Corporation Systems and methods for fuel cartridge distribution
US20060156627A1 (en) * 2003-06-27 2006-07-20 Ultracell Corporation Fuel processor for use with portable fuel cells
US20050186455A1 (en) * 2003-06-27 2005-08-25 Ultracell Corporation, A California Corporation Micro fuel cell system start up and shut down systems and methods
EP1641671B1 (en) * 2003-06-27 2015-06-24 Portaclave LLP Portable fuel cartridge for fuel cells
WO2005087360A1 (en) * 2004-03-09 2005-09-22 Intelligent Energy, Inc. Modular reformer with enhanced heat recuperation
US7648792B2 (en) * 2004-06-25 2010-01-19 Ultracell Corporation Disposable component on a fuel cartridge and for use with a portable fuel cell system
US7968250B2 (en) * 2004-06-25 2011-06-28 Ultracell Corporation Fuel cartridge connectivity
US20060030481A1 (en) * 2004-08-04 2006-02-09 Labarge William J Exhaust treatment device and methods of making the same
US20060105211A1 (en) * 2004-11-16 2006-05-18 Bos Myles L Fuel cell system
US7678479B2 (en) * 2004-11-29 2010-03-16 Angstrom Power Incorporated Hydrogen fuel delivery systems
KR100649738B1 (en) * 2005-10-17 2006-11-27 삼성전기주식회사 Air-supplying device for fuel cell
DE102005062926A1 (en) * 2005-12-29 2007-07-05 Süd-Chemie AG Catalyst production, for catalytic combustion of hydrocarbon, preferably methane, comprises providing hexa-aluminate and grinding hexa-aluminate
US7951500B2 (en) * 2006-05-25 2011-05-31 Siemens Energy, Inc. Anode gas stack start-up heater and purge gas generator
US20080187797A1 (en) * 2006-07-10 2008-08-07 Protonex Technology Corporation Fuel processor for fuel cell systems
US7575611B2 (en) * 2006-08-09 2009-08-18 Ultracell Corporation Fuel processor for use in a fuel cell system
US20080171255A1 (en) * 2006-08-09 2008-07-17 Ultracell Corporation Fuel cell for use in a portable fuel cell system
US20080213638A1 (en) * 2006-08-09 2008-09-04 Ultracell Corporation Engine block for use in a fuel cell system
KR100818259B1 (en) 2006-10-20 2008-03-31 삼성에스디아이 주식회사 Hydrogen fuel reforming apparatus
US8206025B2 (en) 2007-08-07 2012-06-26 International Business Machines Corporation Microfluid mixer, methods of use and methods of manufacture thereof
US20100047634A1 (en) * 2008-01-09 2010-02-25 Ultracell Corporation Portable reformed fuel cell systems with water recovery
US8129059B2 (en) * 2008-02-22 2012-03-06 UltraCell, L.L.C. Low pressure drop fuel processor for use with portable fuel cells
US20100055518A1 (en) * 2008-08-26 2010-03-04 Idatech, Llc Hydrogen-producing assemblies, fuel cell systems including the same, methods of producing hydrogen gas, and methods of powering an energy-consuming device
US9017436B2 (en) 2008-08-26 2015-04-28 Dcns Fuel processing systems with thermally integrated componentry
US20100090642A1 (en) * 2008-10-10 2010-04-15 Ultracell Corporation Power adaptor for portable fuel cell system
EP2206551B1 (en) * 2008-12-23 2019-08-07 Corning Incorporated Microchannel reactors
TWI465393B (en) * 2009-09-14 2014-12-21 Green Hydrotec Inc Hydrogen generator and the application of the same
US20110097678A1 (en) * 2009-10-05 2011-04-28 Patch Keith D Method of heating and heating apparatus
US8252251B2 (en) * 2010-03-30 2012-08-28 General Electric Company Fluid cooled reformer and method for cooling a reformer
US20110268651A1 (en) * 2010-05-03 2011-11-03 Air Products And Chemicals, Inc. Method and apparatus for storing and delivering hydrogen
KR101223236B1 (en) 2010-11-17 2013-01-17 한국에너지기술연구원 Flameless Steam Reformer
TWI422485B (en) * 2010-12-31 2014-01-11 Tong Hsing Electronic Ind Ltd A ceramic plate with reflective film and method of manufacturing the same
JP5675490B2 (en) 2011-05-13 2015-02-25 本田技研工業株式会社 Fuel cell module
JP5653834B2 (en) 2011-05-13 2015-01-14 本田技研工業株式会社 Fuel cell system
JP5697577B2 (en) 2011-10-19 2015-04-08 本田技研工業株式会社 Fuel cell module
JP5697575B2 (en) 2011-10-19 2015-04-08 本田技研工業株式会社 Fuel cell module
US9102535B2 (en) 2011-12-27 2015-08-11 Korea Institute Of Energy Research Flameless steam reformer
JP6178979B2 (en) * 2013-06-28 2017-08-16 パナソニックIpマネジメント株式会社 Fuel processor
DE102014006367A1 (en) * 2014-05-05 2015-11-05 Gkn Sinter Metals Engineering Gmbh Hydrogen storage and a method of manufacture
DK178850B1 (en) * 2016-01-15 2017-03-27 Serenergy As Extrusion used for Production of a Reformer in a Fuel Cell System
US11380557B2 (en) * 2017-06-05 2022-07-05 Applied Materials, Inc. Apparatus and method for gas delivery in semiconductor process chambers
US11305232B2 (en) 2019-06-03 2022-04-19 Ultracell Llc Filtration systems and methods
CN112260920B (en) * 2020-12-21 2021-04-30 武汉格罗夫氢能汽车有限公司 Network topology structure of hydrogen fuel cell system

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3119671A (en) * 1960-09-28 1964-01-28 Chemical Coustruction Corp Upright fluid heating furnace with heat recovery system
US3541729A (en) * 1968-05-09 1970-11-24 Gen Electric Compact reactor-boiler combination
US3595628A (en) * 1968-11-26 1971-07-27 Chemical Construction Corp Apparatus for reforming hydrocarbons
US4522894A (en) * 1982-09-30 1985-06-11 Engelhard Corporation Fuel cell electric power production

Family Cites Families (130)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3578952A (en) 1969-06-05 1971-05-18 Escoa Fintube Corp Tubular electrical heating element with a segmented helical fin
US4335023A (en) 1980-01-24 1982-06-15 Engelhard Corporation Monolithic catalyst member and support therefor
JPS62210047A (en) * 1986-03-10 1987-09-16 Toyo Eng Corp Apparatus for reaction
US4909808A (en) 1987-10-14 1990-03-20 The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration Steam reformer with catalytic combustor
US5081095A (en) 1990-09-10 1992-01-14 General Motors Corporation Method of making a support containing an alumina-ceria washcoat for a noble metal catalyst
DE4035293C1 (en) 1990-11-07 1992-01-02 Metallgesellschaft Ag, 6000 Frankfurt, De
US5209906A (en) 1991-05-10 1993-05-11 Her Majesty The Queen In Right Of Canada, As Represented By The Minister Of National Defence Modular isothermal reactor
US5534328A (en) 1993-12-02 1996-07-09 E. I. Du Pont De Nemours And Company Integrated chemical processing apparatus and processes for the preparation thereof
JPH06310166A (en) 1993-04-28 1994-11-04 Sanyo Electric Co Ltd Portable fuel cell type power supply
US5601938A (en) 1994-01-21 1997-02-11 Regents Of The University Of California Carbon aerogel electrodes for direct energy conversion
US5611214A (en) 1994-07-29 1997-03-18 Battelle Memorial Institute Microcomponent sheet architecture
US5811062A (en) 1994-07-29 1998-09-22 Battelle Memorial Institute Microcomponent chemical process sheet architecture
US5525436A (en) 1994-11-01 1996-06-11 Case Western Reserve University Proton conducting polymers used as membranes
US5641585A (en) 1995-03-21 1997-06-24 Lockheed Idaho Technologies Company Miniature ceramic fuel cell
US5676911A (en) 1995-12-14 1997-10-14 Her Majesty The Queen In Right Of Canada, As Represented By The Minister Of National Defence Of Her Majesty's Canadian Government Radial flow fuel processor
US5733347A (en) 1995-12-27 1998-03-31 International Fuel Cells Corp. Compact fuel gas reformer assemblage
US5716727A (en) 1996-04-01 1998-02-10 Case Western Reserve University Proton conducting polymers prepared by direct acid casting
US5858314A (en) * 1996-04-12 1999-01-12 Ztek Corporation Thermally enhanced compact reformer
US6783741B2 (en) 1996-10-30 2004-08-31 Idatech, Llc Fuel processing system
US6537352B2 (en) * 1996-10-30 2003-03-25 Idatech, Llc Hydrogen purification membranes, components and fuel processing systems containing the same
US5789093A (en) 1996-12-10 1998-08-04 Texas Instruments Incorporated Low profile fuel cell
DE19721630C1 (en) 1997-05-23 1999-02-11 Fraunhofer Ges Forschung Device for reforming hydrocarbons containing starting materials
US5961932A (en) 1997-06-20 1999-10-05 Eastman Kodak Company Reaction chamber for an integrated micro-ceramic chemical plant
US6200536B1 (en) 1997-06-26 2001-03-13 Battelle Memorial Institute Active microchannel heat exchanger
JPH11106204A (en) * 1997-10-01 1999-04-20 Sanyo Electric Co Ltd Hydrogen production apparatus and hydrogen production process
US5961930A (en) 1997-10-15 1999-10-05 Eastman Kodak Company Integrated micro-ceramic chemical plant with insertable reaction chambers and micro-filters
US6232005B1 (en) 1997-11-20 2001-05-15 General Motors Corporation Fuel cell system combustor
US6077620A (en) 1997-11-26 2000-06-20 General Motors Corporation Fuel cell system with combustor-heated reformer
AU747878B2 (en) 1998-04-09 2002-05-30 California Institute Of Technology Electronic techniques for analyte detection
DE19825102C2 (en) 1998-06-05 2001-09-27 Xcellsis Gmbh Process for the production of a compact catalytic reactor
US6080501A (en) 1998-06-29 2000-06-27 Motorola, Inc. Fuel cell with integral fuel storage
US6238815B1 (en) 1998-07-29 2001-05-29 General Motors Corporation Thermally integrated staged methanol reformer and method
DE19841993B4 (en) 1998-09-04 2005-02-17 P21 - Power For The 21St Century Gmbh Microstructure reactor
US6245214B1 (en) 1998-09-18 2001-06-12 Alliedsignal Inc. Electro-catalytic oxidation (ECO) device to remove CO from reformate for fuel cell application
JP2002531246A (en) 1998-12-02 2002-09-24 マサチューセッツ・インスティチュート・オブ・テクノロジー Integrated palladium-based micromembrane for hydrogen separation and hydrogenation / dehydrogenation reactions
US6638654B2 (en) 1999-02-01 2003-10-28 The Regents Of The University Of California MEMS-based thin-film fuel cells
US6268077B1 (en) 1999-03-01 2001-07-31 Motorola, Inc. Portable fuel cell power supply
JP3625770B2 (en) 1999-04-20 2005-03-02 東京瓦斯株式会社 Single tube cylindrical reformer and its operating method
US6280864B1 (en) * 1999-06-18 2001-08-28 Uop Llc Control system for providing hydrogen for use with fuel cells
US6193501B1 (en) 1999-07-06 2001-02-27 The Board Of Trustees Of The University Of Illinois Microcombustor having submillimeter critical dimensions
US6423434B1 (en) 1999-08-09 2002-07-23 Motorola, Inc. Method and apparatus for managing fuel cell performance
US6312846B1 (en) 1999-11-24 2001-11-06 Integrated Fuel Cell Technologies, Inc. Fuel cell and power chip technology
US6361892B1 (en) 1999-12-06 2002-03-26 Technology Management, Inc. Electrochemical apparatus with reactant micro-channels
GB9930695D0 (en) * 1999-12-24 2000-02-16 Unilever Plc Composition and method for bleaching a substrate
JP4736298B2 (en) * 1999-12-28 2011-07-27 ダイキン工業株式会社 Partial oxidation reformer
JP2003533956A (en) 2000-01-07 2003-11-11 ユニバーシティ・オブ・サザン・カリフォルニア Micro-combustors and thermoelectric micro-generators based on combustion
WO2001051194A1 (en) 2000-01-11 2001-07-19 Accentus Plc Catalytic reactor
US6537506B1 (en) 2000-02-03 2003-03-25 Cellular Process Chemistry, Inc. Miniaturized reaction apparatus
US7056477B1 (en) * 2000-02-03 2006-06-06 Cellular Process Chemistry, Inc. Modular chemical production system incorporating a microreactor
US6415860B1 (en) 2000-02-09 2002-07-09 Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College Crossflow micro heat exchanger
US6406808B1 (en) 2000-04-10 2002-06-18 Motorola, Inc. Method and apparatus for thermal management of fuel cell systems
DE10018485A1 (en) 2000-04-14 2001-10-18 Schmitz Werke Awning cloth and process for its manufacture
US6835488B2 (en) 2000-05-08 2004-12-28 Honda Giken Kogyo Kabushiki Kaisha Fuel cell with patterned electrolyte/electrode interface
US6409939B1 (en) 2000-05-31 2002-06-25 Uop Llc Method for producing a hydrogen-rich fuel stream
HK1037472A2 (en) * 2000-06-28 2002-01-18 Yu Fu Bao Kitchen Equipment Sh Environmental friendly water bladder for steaming tank
US6465119B1 (en) 2000-07-18 2002-10-15 Motorola, Inc. Fuel cell array apparatus and method of fabrication
JP2004513472A (en) 2000-07-19 2004-04-30 ザ ジョンズ ホプキンズ ユニバーシティ Scalable, all-polymer fuel cell
US6569553B1 (en) 2000-08-28 2003-05-27 Motorola, Inc. Fuel processor with integrated fuel cell utilizing ceramic technology
KR20020024525A (en) * 2000-09-25 2002-03-30 요트 루나우 Method for operating a fuel cell battery
US20020061277A1 (en) 2000-09-25 2002-05-23 Engelhard Corporation Non-pyrophoric water-gas shift reaction catalysts
US6645655B1 (en) 2000-11-21 2003-11-11 Mti Microfuel Cells Inc. Passively pumped liquid feed fuel cell system
US20030121906A1 (en) 2000-11-29 2003-07-03 Abbott Richard C. Resistive heaters and uses thereof
US6660423B2 (en) 2000-12-15 2003-12-09 Motorola, Inc. Direct methanol fuel cell including a water management system and method of fabrication
US6916565B2 (en) 2000-12-21 2005-07-12 Casio Computer Co., Ltd. Power supply system, fuel pack constituting the system, and device driven by power generator and power supply system
US6824905B2 (en) 2001-01-15 2004-11-30 Casio Computer Co., Ltd. Power supply system and device driven by power supply system
AU2002226693B8 (en) 2001-01-24 2010-03-25 Casio Computer Co., Ltd. Power supply system, fuel pack constituting the system, and device driven by power generator and power supply system
US6460733B2 (en) 2001-02-20 2002-10-08 Mti Microfuel Cells, Inc. Multiple-walled fuel container and delivery system
JP4479117B2 (en) 2001-03-15 2010-06-09 アイシン精機株式会社 Fuel reformer
US6479920B1 (en) 2001-04-09 2002-11-12 Wisconsin Alumni Research Foundation Direct charge radioisotope activation and power generation
US6677070B2 (en) 2001-04-19 2004-01-13 Hewlett-Packard Development Company, L.P. Hybrid thin film/thick film solid oxide fuel cell and method of manufacturing the same
US6727479B2 (en) 2001-04-23 2004-04-27 Stmicroelectronics S.R.L. Integrated device based upon semiconductor technology, in particular chemical microreactor
KR100423544B1 (en) * 2001-04-23 2004-03-18 주식회사 경동도시가스 Compact steam reformer
DE10122247B4 (en) * 2001-05-08 2004-06-24 Robert Bosch Gmbh Method for phase detection in an internal combustion engine
US6794071B2 (en) 2001-06-14 2004-09-21 Mti Microfuel Cells Inc. Apparatus and method for rapidly increasing power output from a direct oxidation fuel cell
US6673130B2 (en) 2001-06-15 2004-01-06 The Regents Of The University Of California Method of fabrication of electrodes and electrolytes
US20020192537A1 (en) 2001-06-15 2002-12-19 Xiaoming Ren Metallic layer component for use in a direct oxidation fuel cell
US6652987B2 (en) 2001-07-06 2003-11-25 United Technologies Corporation Reflective coatings to reduce radiation heat transfer
JP2003089504A (en) * 2001-07-09 2003-03-28 Mitsubishi Heavy Ind Ltd Apparatus for reforming fuel
US6753036B2 (en) 2001-07-16 2004-06-22 The Regents Of The University Of California Method for fabrication of electrodes
JP4400012B2 (en) 2001-08-01 2010-01-20 カシオ計算機株式会社 Evaporator, reformer, and fuel cell system
US6939632B2 (en) 2001-08-06 2005-09-06 Massachusetts Institute Of Technology Thermally efficient micromachined device
US6696195B2 (en) 2001-08-09 2004-02-24 Motorola, Inc. Direct methanol fuel cell including a water recovery and recirculation system and method of fabrication
JP5131629B2 (en) 2001-08-13 2013-01-30 日産自動車株式会社 Method for producing solid oxide fuel cell
JP2003089502A (en) * 2001-09-12 2003-03-28 Suzuki Motor Corp Methanol reformer
US6666928B2 (en) * 2001-09-13 2003-12-23 Micell Technologies, Inc. Methods and apparatus for holding a substrate in a pressure chamber
US6821666B2 (en) 2001-09-28 2004-11-23 The Regents Of The Univerosity Of California Method of forming a package for mems-based fuel cell
NO321805B1 (en) 2001-10-19 2006-07-03 Norsk Hydro As Method and apparatus for passing two gases in and out of the channels of a multi-channel monolithic unit.
US6936364B2 (en) 2001-10-24 2005-08-30 Modine Manufacturing Company Method and apparatus for vaporizing fuel for a reformer fuel cell system
US7077643B2 (en) 2001-11-07 2006-07-18 Battelle Memorial Institute Microcombustors, microreformers, and methods for combusting and for reforming fluids
US6960235B2 (en) 2001-12-05 2005-11-01 The Regents Of The University Of California Chemical microreactor and method thereof
JP3750597B2 (en) 2001-12-18 2006-03-01 日産自動車株式会社 Catalytic combustor
US7074511B2 (en) 2002-01-08 2006-07-11 The Gillette Company Fuel container and delivery apparatus for a liquid feed fuel cell system
TW592830B (en) 2002-03-29 2004-06-21 Casio Computer Co Ltd Chemical reaction apparatus and power supply system
JP4314776B2 (en) 2002-03-29 2009-08-19 カシオ計算機株式会社 Small chemical reactor and fuel cell system
JP2003290653A (en) 2002-03-29 2003-10-14 Casio Comput Co Ltd Fine reaction part constitution body and manufacture method therefor
JP3891131B2 (en) 2002-03-29 2007-03-14 カシオ計算機株式会社 Chemical reaction apparatus and power supply system
US7169367B2 (en) 2002-04-05 2007-01-30 Casio Computer Co., Ltd. Chemical reaction apparatus and power supply system
US20030194363A1 (en) 2002-04-12 2003-10-16 Koripella Chowdary Ramesh Chemical reactor and fuel processor utilizing ceramic technology
US6911193B2 (en) * 2002-04-19 2005-06-28 Conocophillips Company Integration of mixed catalysts to maximize syngas production
US6921603B2 (en) 2002-04-24 2005-07-26 The Regents Of The University Of California Microfluidic fuel cell systems with embedded materials and structures and method thereof
US7115148B2 (en) 2002-05-14 2006-10-03 Her Majesty The Queen In Right Of Canada, As Respresented By The Minister Of Defence Of Her Majesty's Canadian Government Compact methanol steam reformer with integrated hydrogen separation
JP2003340273A (en) 2002-05-30 2003-12-02 Casio Comput Co Ltd Chemical reaction apparatus, fuel cell system and manufacturing method therefor
JP3748434B2 (en) 2002-06-12 2006-02-22 株式会社東芝 Direct methanol fuel cell system and fuel cartridge
US6913998B2 (en) 2002-07-01 2005-07-05 The Regents Of The University Of California Vapor-deposited porous films for energy conversion
JP4366904B2 (en) 2002-07-29 2009-11-18 カシオ計算機株式会社 Small chemical reactor
JP3979219B2 (en) 2002-08-07 2007-09-19 カシオ計算機株式会社 Small chemical reactor
US7014835B2 (en) 2002-08-15 2006-03-21 Velocys, Inc. Multi-stream microchannel device
JP3941632B2 (en) 2002-08-29 2007-07-04 カシオ計算機株式会社 Reformer, reformer manufacturing method and power generation system
EP1413547A1 (en) 2002-09-26 2004-04-28 Haldor Topsoe A/S Process for the production of synthesis gas
US6960403B2 (en) 2002-09-30 2005-11-01 The Regents Of The University Of California Bonded polyimide fuel cell package and method thereof
KR100533298B1 (en) 2002-09-30 2005-12-05 가부시끼가이샤 도시바 Fuel cell system
US7341609B2 (en) 2002-10-03 2008-03-11 Genesis Fueltech, Inc. Reforming and hydrogen purification system
JP4423847B2 (en) 2002-10-25 2010-03-03 カシオ計算機株式会社 Small chemical reactor
JP4110948B2 (en) 2002-11-28 2008-07-02 カシオ計算機株式会社 Small chemical reactor and fuel cell system
US7122261B2 (en) 2003-02-21 2006-10-17 The Regents Of The University Of California Metal hydride fuel storage and method thereof
US6932958B2 (en) * 2003-03-26 2005-08-23 Gas Technology Institute Simplified three-stage fuel processor
JP4227062B2 (en) * 2003-03-31 2009-02-18 株式会社東芝 FUEL CELL SYSTEM, FUEL CELL SYSTEM FUEL AND FUEL CELL SYSTEM CLOSED CONTAINER
US20040228211A1 (en) 2003-05-13 2004-11-18 Koripella Chowdary R. Internal micromixer
US7666539B2 (en) 2003-06-27 2010-02-23 Ultracell Corporation Heat efficient portable fuel cell systems
US20050186455A1 (en) 2003-06-27 2005-08-25 Ultracell Corporation, A California Corporation Micro fuel cell system start up and shut down systems and methods
JP2007524562A (en) 2003-06-27 2007-08-30 ウルトラセル コーポレイション Annular fuel processing apparatus and method
EP1644997A4 (en) 2003-06-27 2011-03-16 Ultracell Corp Micro fuel cell architecture
JP4592265B2 (en) * 2003-07-11 2010-12-01 大阪瓦斯株式会社 Fuel cell system
US7517603B2 (en) 2003-09-23 2009-04-14 Lilliputian Systems, Inc. Stressed thin-film membrane islands
US20050155889A1 (en) * 2004-01-20 2005-07-21 Lown John M. Modular and stackable tray assembly
JP4273022B2 (en) * 2004-03-08 2009-06-03 本田技研工業株式会社 Starting method at power failure in fuel gas production power generation system
JP4440676B2 (en) * 2004-03-10 2010-03-24 株式会社日立製作所 Fuel cell power generation hot water supply system
JP4009285B2 (en) 2004-11-24 2007-11-14 アイシン精機株式会社 Reformer
US7807313B2 (en) 2004-12-21 2010-10-05 Ultracell Corporation Compact fuel cell package
US7575611B2 (en) 2006-08-09 2009-08-18 Ultracell Corporation Fuel processor for use in a fuel cell system

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3119671A (en) * 1960-09-28 1964-01-28 Chemical Coustruction Corp Upright fluid heating furnace with heat recovery system
US3541729A (en) * 1968-05-09 1970-11-24 Gen Electric Compact reactor-boiler combination
US3595628A (en) * 1968-11-26 1971-07-27 Chemical Construction Corp Apparatus for reforming hydrocarbons
US4522894A (en) * 1982-09-30 1985-06-11 Engelhard Corporation Fuel cell electric power production

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP1644111A2 *

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8172913B2 (en) 2002-04-23 2012-05-08 Vencill Thomas R Array of planar membrane modules for producing hydrogen
JP2011168488A (en) * 2005-04-18 2011-09-01 Intelligent Energy Inc Compact device for generating pure hydrogen
JP2008536796A (en) * 2005-04-18 2008-09-11 インテリジェント エナジー インコーポレイテッド Compact device for pure hydrogen generation
JP4890538B2 (en) * 2005-04-18 2012-03-07 インテリジェント エナジー インコーポレイテッド Compact device for pure hydrogen generation
EP1767268A1 (en) * 2005-09-27 2007-03-28 FUJIFILM Corporation Fluidic device
EP1977822A3 (en) * 2007-03-29 2008-12-24 Samsung SDI Co., Ltd. Reaction vessel and reaction device
US7842260B2 (en) 2007-03-29 2010-11-30 Samsung Sdi Co. Ltd. Reaction vessel and reaction device
EP1977822A2 (en) * 2007-03-29 2008-10-08 Samsung SDI Co., Ltd. Reaction vessel and reaction device
WO2010049655A1 (en) * 2008-10-29 2010-05-06 Commissariat A L'energie Atomique Methods for depositing a catalyst by a sol/gel process, by suspension or by chemical vapour deposition on a microstructured reactor
FR2937655A1 (en) * 2008-10-29 2010-04-30 Renault Sas METHODS OF DEPOSITING A SOIL / GEL CATALYST BY SUSPENSION OR CHEMICAL VAPOR DEPOSITION ON A MICROSTRUCTURE REACTOR
WO2014171263A1 (en) * 2013-04-18 2014-10-23 Honda Motor Co., Ltd. Fuel cell module
GB2616339A (en) * 2022-01-26 2023-09-06 Caterpillar Inc Cryogenic containment system
US11814286B2 (en) 2022-01-26 2023-11-14 Caterpillar Inc. Backup power system with controller

Also Published As

Publication number Publication date
EP1644111A4 (en) 2011-02-09
US7604673B2 (en) 2009-10-20
US7807129B2 (en) 2010-10-05
US7807130B2 (en) 2010-10-05
EP1644111A2 (en) 2006-04-12
US20050011125A1 (en) 2005-01-20
WO2005004256A3 (en) 2005-08-25
US20080008646A1 (en) 2008-01-10
US20050005521A1 (en) 2005-01-13
US20050022448A1 (en) 2005-02-03
US20070294941A1 (en) 2007-12-27
US7462208B2 (en) 2008-12-09
US20090071072A1 (en) 2009-03-19
US7276096B2 (en) 2007-10-02
JP2007524562A (en) 2007-08-30
US20110020197A1 (en) 2011-01-27

Similar Documents

Publication Publication Date Title
US7604673B2 (en) Annular fuel processor and methods
US7807313B2 (en) Compact fuel cell package
US7943263B2 (en) Heat efficient portable fuel cell systems
US7575611B2 (en) Fuel processor for use in a fuel cell system
US7935452B2 (en) Micro fuel cell architecture
US7947407B2 (en) Fuel cell apparatus having a small package size
US20050014040A1 (en) Fuel preheat in fuel cells and portable electronics
US20060156627A1 (en) Fuel processor for use with portable fuel cells
US20080171255A1 (en) Fuel cell for use in a portable fuel cell system
US20060029848A1 (en) Method and system for controlling fluid delivery in a fuel cell
JP5109252B2 (en) Fuel cell
US20090084524A1 (en) Evaporator and vapor production method
WO2006069173A2 (en) Heat efficient portable fuel cell systems
WO2006069057A2 (en) Fuel processor for use with portable fuel cells
US8821832B2 (en) Fuel processor for use with portable fuel cells
CN101447579A (en) Circular fuel processor and method thereof
WO2024045228A1 (en) Heat pipe bipolar plate for fuel cell, and fuel cell stack

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200480024619.0

Country of ref document: CN

AK Designated states

Kind code of ref document: A2

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): BW GH GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 2006517622

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: 16/KOLNP/2006

Country of ref document: IN

WWE Wipo information: entry into national phase

Ref document number: 2004756039

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: 2004756039

Country of ref document: EP