CA1166825A - Two pass endothermic generator - Google Patents

Two pass endothermic generator

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Publication number
CA1166825A
CA1166825A CA000387378A CA387378A CA1166825A CA 1166825 A CA1166825 A CA 1166825A CA 000387378 A CA000387378 A CA 000387378A CA 387378 A CA387378 A CA 387378A CA 1166825 A CA1166825 A CA 1166825A
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CA
Canada
Prior art keywords
conduit
gas
generator
reaction
heating means
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
CA000387378A
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French (fr)
Inventor
Edward W. Grobel
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Individual
Original Assignee
Individual
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Publication of CA1166825A publication Critical patent/CA1166825A/en
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Classifications

    • 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
    • C01B3/34Production 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 by reaction of hydrocarbons with gasifying agents
    • C01B3/36Production 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 by reaction of hydrocarbons with gasifying agents using oxygen or mixtures containing oxygen as gasifying agents
    • C01B3/363Production 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 by reaction of hydrocarbons with gasifying agents using oxygen or mixtures containing oxygen as gasifying agents characterised by the burner used
    • 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
    • B01J19/14Production of inert gas mixtures; Use of inert gases in general
    • 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
    • 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
    • B01J8/06Chemical 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 in tube reactors; the solid particles being arranged in tubes
    • B01J8/067Heating 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
    • C01B3/34Production 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 by reaction of hydrocarbons with gasifying agents
    • C01B3/36Production 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 by reaction of hydrocarbons with gasifying agents using oxygen or mixtures containing oxygen as gasifying agents
    • 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
    • B01J2208/00026Controlling or regulating the heat exchange system
    • B01J2208/00035Controlling or regulating the heat exchange system involving measured parameters
    • B01J2208/00088Flow rate measurement
    • 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
    • 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
    • B01J2208/00389Controlling the temperature using electric heating or cooling elements
    • B01J2208/00415Controlling the temperature using electric heating or cooling elements electric resistance heaters

Abstract

ABSTRACT OF THE DISCLOSURE

A furnace or generator for reacting a hydrocarbon gas which undergoes a reaction having an exothermic phase followed by an endothermic phase, is disclosed.
The generator consists of concentric inner and outer tubes having a reacting gas inlet at the top of the inner tube and a reacted gas outlet near the top of the outer tube. The inner tube has holes adjacent its bottom for communicating the bottom of the inner tube with the annular space between the inner tube and the outer tube. The bottom portion of the generator forms a reactor portion while the top portion forms a recuperator portion. A gas air mixture entering near the top of the inner tube is heated in the recuperator portion by the reacted gas in the annular passage. Additional heating means may be provided.

/ty

Description

. ~` .~ !
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2 0 2-011-0 TITl;E OF THE INVENTION:

IWO PASS ENDOTEIER~qIC GENERATOR

BACKGROUND OF THE INVENTI ON~

Field of the Invention:

The present invention relates to furnaces for reacting a gas capa~le of an exothermic reaction phase followed ~y an endothermic reaction phase.
More particularly, the present invention relates to . a furnace for producing a protective atmosphere .of 40~ N2, 40% II2, and 20% CO (nominally), as well as a method for the operation thereofJ

Description of the Prior Art:
_ Numerolls industrial operations require a pro-tective or shielding atmosphere such as a 40% N2, 40% H2, and 20% CO (nominally) atmosphere. These industrial appIications include the hardening of medium and high carbon steels, the annealing and ,.

.

- 11 B~825 normalizing of carbon steels, carburizing carboni-triding, copper and silver brazing and sintering.
It has been known that a protective atmosphere containing a nominally 40~ N2, 40~ H2, and 20~ CO
(with residual CO2, H2O and CH~) could be produced b~ the cracking of a hydrocarbon gas over a catalyst bed at high temperature. The hydrocarbon gas could include such gases as natural gas, propane, butane, or MFG (manufactured gas). Further, furnaces or generators have been known for carrying out such a cr~cking process. One such furnace is the HYEN
endothermic generator manufactured by the Lindberg Company of Chicago, Illinois.
BFt:l:FF DESCi~IPTION OF TEI;E~ D~WINt~S
In the description which follows -reference will be made to the accompanv;ng drawings~ wherein:
FICURE 1 is a cross sectional view vf a ~rior art endothermic generator wi~h an elong~ted tubular metallic housing;
FIGURE 2 is a cross sectional view of the endothermic generator depicting an outer and inner elongated tubular housin~ forming an annular space between the tubes and embodying the present invention.

~. ~ ~

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- 2a ~

The HYEN endothermic generator is illustrated in Figure 1. It consists of an elongated tubular metallic housing 2 having a length of from approxi-mately 45 to approximately 69 inches and a diameter of approximately 8 inches. The tube has a closed bottom 4 including a reaction gas inlet 6 and insula-- tion layer 8. The top of the tube is also closed except for reacted gas outlet 10. A xeacted gas * Trade Mark ~ 166~

--3~

passage 12 adjacent the top of the tube includes insulation 14.
Screen 16 is supported by the insulation 8 and prevents the catalyst from plugging the gas inlet 6. Over the screen is placed material having good heat transfer characteristics, such as alundum chips 18, while the remainder of the tube is filled with catalyst material. The catalyst material is in the form of porous 1/2" to 1" cubes or spheres impre-gnated with nickel oxide.
The furnace is normally located within an insul-ating jacket ~not shown). Heat may be supplied to the furnace ~y either surrounding the f~rnace with electric resistance coils (not shown)or by supplying hot combustion gases to the interior o~ the insulat-ing ~acket.
~ n use, a reaction gas, such as natural gas, is mixed with air in a carburetor and the mixture enters the furnace at the bottom inlet pipe 6. The catalytic cxacking of the hydrocarbon gas in the mixture is a two phase reaction; the reaction has a first exother-mic phase followed by a subse~uent endothermic phase.

6~

As the reaction gas mixture enters into the alundum chip ~ed, it is heated ~y the heat source until the gas mixture reaches minimum temperature for exother-mic combustion to commence (approximately 1170F).
The heat liberated during the exothermic phase is absorbed by the gas mixture raising its temperature into the endothermic range which commences at appro-ximately 1750F. During the endothermic phase, heat from the heat source is required to maintain the reaction gas temperature a~ove 175~F. until the cracking process is completed.
The insulation 14 in the reacted gas passage pre-vents premature cooling of the reacted gas and the reacted gas product exits at 10 at a tèmperature of approximately 1700.
For example, a mixture of one part natural gas to 2.44 parts air was preheated to 200F, intro-duced into the HYEN generator and reacted at a rate of 1513 cubic feet per hour (CFH~. Heating power was supplied to the generator at the rate of 17.77 kilowatts per hour (I~WjHR). The reacted gas exited the generator at 17G0F~ with a dew point of 28~8F., a methane content of 0.46%, a carbon dioxide content .:

~ ~ &~ 5 ~5--of 0.65~, a carbon monoxide content of approximately 20%, a hydrogen content of approximately 40%, and a nitrogen content of 40%.
,.~
However, the HYEN endothermic generator des-? B 5 cri~ed a~ove has several shortcomings:. First, it falls to provide a uniformity of gas heating during the reaction process. When the gas first enters the bottom of the catalyst bed 20 this area has been h.eated ~y a com~ination of heat supplied by the h.eat source and exothermic reaction taking place in the alundum chip bed. As the reaction gas travels up through th.e catalyst ~ed, all additional heat needed to continue the endothermic reaction must be supplied ~y the heat source.
Since this reaction is initially exothermic, heat is created and driven into the center portion of the 8" diameter furnace retort forcing complete exothermic reaction throughout the first approxi-mately 12" height of the alundum chip bed and the lower portion of the catalyst bed within the retort.

1 ~ ~6~?,5 Factually, this area is not entirely exothermic as the dissociation of ~2 (water vapor) and CO2 ~carbon dioxide) are endothermic and also occur in this area simultaneously.
Further, because of the relatively large 8"
diameter of the generator retort 2 and the insulat-ing quality of the catalyst bed therein, there is insufficient heat penetration into the center por-tion of the catalyst bed.
Therefore, a "cold spot" is formed in the center o~ the generator retort where the temperature is below the desired reaction range, and the gas moving through this cold spot is deprived of heat during the final portion of the travel through the generator retort. As a result, in order to provide sufficient heat so that all of the gas i5 reacted, it is necessary to raise the heat source temperature gas to approximately 200 to 300F higher than the minimum cracking temperature in order to assure that all reacting gas within the generator is above 1750F., the minimum cracking temperature. The ~ 1 6~C.~25 reacted gas entering the insulated area 14 thus ranges in temperature from approximately 1750F. to 1800F. and exits the retort at approximately 1700F.
If a proper reaction does not take place due to insufficient heating to the central core of the catalyst ~ed, the residual methane ~CH~) content can drop out as carbon soot by the reaction CH4 -~C~2 H2.
Further, excesslve sooting can take place down-stream of the reacted gas outlet 10 if cooling is too slow to "freeze" the reverse reaction (2 CO-~C~CO2), thereby producing carbon if the temperature drops too slo~ly through the range of 1250 to 900F.
Further, it is necessary to provide the reaction gas with a head temperature of 200~. to 300F. to assure that a proper reaction takes place which also requires excessive amounts of energy at the furnace heat source.
Further, the need for a 200-300F. head tempera-ture requires the need for a higher grade of alloy retort and electric heating element material and ;6~25 furnace refractory insulation resulting in excess-- ive material costs.
Further, since the reacted gas leaving the furnace at approximately 1700F. temperature enters immediately into a heat exchanger, following the furnace, in order to cool the gas to a useful pro-cessing temperature (approximately 150CF.), all the -heat within the reacted gas on leaving the catalyst bed, and removed by the heat exchanger ~ ~ T
1700nF, ~-~ 150F.~, is thereby being wasted.
Finally, because of the high tem erature involv-ed, more expensive construction material must be used and the life of the material is shortened, SUMMARY -OF THE INVENTION

It is therefore an object of the present inven-tion to provide a generator or furnace for produc-iny a protective atmosphere gas of 40% N2, 40% H , 20% CO (nominally) which requires less heating energy than t~at o the prior art.
It i5 a further object of the present inventlon 2 $

to provide a furnace or generator for a protective atmosphere gas wherein the reacted gas exiting the generator is substantially lower than 1700 ~. by releasing some of its energy to preheat the incoming unreacted gas~
It is a further object of the present invention to provide a furnace or generator for a protective .
atmosphere gas which utilizes the heat from the exothermic portion of the reaction to eliminate the "cold area'1 in the center of the retort catalyst bed, thereby achieving a more uniformly reacted gRS at a lower furnace heat source temperature.
It is a further object of the present invention to produce a two pass furnace or generator for producing a protective atmosphere gas which can also be converted from the prior art generator by a simple retrofit.
Accordingly, here disclosed is a two pass generator constructed of a pair of concentric tubes. The reaction gas can be introduced at ;

~ 3 ~6Pj2 5 --~.o--the top of the inner one of the concen~ric tubes and flows through the tube towards the catalyst bed at the bottom of the tube. After passing through vent holes at the bottom of the inner tube, the reaction gas passes through additional catalyst material and completes the reaction prccess. The hot reacted gases then pass through the space between the inner and outer tubes before exiting the furnace adjacent the top thereof. The reaction - 10 gas init~ally entering the inner tube is therefore preheated by the already reacted gas ~hich is pass-ing upwardly through the space between the tubes on the other side of the inner tube. Therefore, the excessive heat contained in the exiting gas can be transferred to the entering gas for raislng its temperature prior to the exothermic phase of the reaction. As the preheated entry gas passes into the alundum chip bed within the inner tube, it is ~urther heated by the heat from the exothermic phase prior to entering the catalys~ bed in the lower portion of the inner tube, co~m2ncing the ', . , '-''.

6 ~3 2 ~

endothermic phase prior to entering the area between the inner and outer retort tubes where the heat required for the endothermic reactions is supplied to the retort ~y the furnace heat source.
Further J because of the higher reacted gas tempera-ture achieved in the inner tube prior to exiting into the area between the inner tube and outer retort wall and the smaller cross section of the catalyst bed in this "doughnut" shaped area a more uniform and penetrating heat from the furnace heat source reduces the temperature gradient in the outer catalyst bed area thereby xeducing the "head" temp-erature of the furnace heat source while maintaining a uniform temperature for the endothermic reaction.
The reacted gas is finally passed back through the upper recuperator portion in the passage between the inner and outer tubes and exits the generatox.
Because it is not necessary to avoid a "cold spot"
as in the prior art, the maximum temperature within the generator or furnace can be kept down to approxi-mately 1800. Further, because the recuperator ~ ~1 6~ 5 permits the recovery of a portion of the heat, the exit temperature is approximately 1300 F., thereby requiring a ~ T from 1300 to 150 F. in the downstream heat exchanger which facilitates a much more rapid chilling through the reverse reaction range of 1250 F. to 900 F.
while recuperating the heat in the ~ T from 1700 F.
to 1300 ~. within the retort.

I ~ ~ 6 ~

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

A generator embodying the present invention is shown in Figure 2. The generator consists of an outer tube 102 which may be identical to the outer tube 2 of the prior art. The outer tube is held within an insulation jacket 130 and is supported within the jaeket at flanges 132. An inner tube 134 lies concentrically within the outer tube 102, thereby defining an elongated "doughnut"
or annular space between the tubes. The annular space, as well as the space within the inner tube, are divided into a recuperator portion 136 adjacent the top o~ the generator, and a reactor portion 138 in the lower section of the generator. The reactor portion preferably constitutes 2/3 of the length of the generator.
A reaction gas inlet is formed as an inlet pipe 140 extending conoentrically into the inner pipe from the top thereof. A reacted gas outlet 142 extends transversely from the annular space to the 8 ~ $

outside of the generator adjacent the top thereof.
The inner and outer tubes are preferably formed of a heat resistant metallic alloy.
The bottom, top and side walls of the generator are lined with insulating material, as is the top plug 146. Further, the annular space in the recup-erator portion is also lined with insulating material to thereby leave a relatively narrow annular space 148 between the wa~l of the inner tube and the insulating material on the inner wall of the outer tube at the recuperator portion.
Both the lower portion of the inner tube and the annular space within the reactor portion are filled with a bed o~ catalyst material 150, The catal~st material may be of any type which will promote an endothermic reaction of the introduced gases, but preferably consists of porous brick impregnated with NiN2 and fired to form NiO. The brick is preferably in the form of stacked ll/16 inch cubes, but other sizes or shapes are possible.

~9~

Vent holes 152 in the walls of the inner tube adjacent the bottom thereof, permit the passage of reacting gas from the catalyst bed within the inner tube to the catalyst bed within the annular space.
The precise number and diameter of the holes depends upon the flow rate of gas through the generator and should be selected so that the back pressure within the inner tu~e is not excessive. A bed of alundum ch~ps 153 is positioned above the catalyst 150 within the inner tube.
Heat can be provided to the space 154 between the insulating jacket and the outer tube by either gas com~ustion (not shown) or electric resistance heaters 156.
15In use, a hydrocarbon gas suc'n as natural gas~
propane, butane, or ~FG. gas is mixed with air and is introduced into the reaction gas inlet pipe 140 As the reaction gas passes downwardly through the recuperator portion of the inner tube, it absorbs heat from the wall of the inner tube 134 which has ~ 1 ~6~,~S

been heated by the reacted gas passing upwardly through the annular passage 148. secause of the relatively small diameter (3 inches~ of the inner tube, the surface friction effects of the inner tube are relatively large which causes turbulence within the pipe and mixing of the gas within the pipe so that the te~perature across-the diameter of the inner pipe is relatively uniform. Further, because of the relatively small diameter of the inner pipe, heat need only penetrate approximately an inch and a half in order to heat the gas within the pipe to combustion temperature. ~hen the pre-heated gas reaches the top of the alundum chip bed 153 ~ithin the inner pipe, its temperature is raised even further by the heat generated from the exothermal reaction occurring within this - area. Again, ~ecause of the relatively small dia-meter of the inner tube, heating along the length of the exothermic area of this tube is relatively uniform and tle minimum =emperature at any po~nt .

~; ~
- -1 1 t~6~325 in the tube is not substantially under the minimum temperature needed for the endothermic reaction in the annular space outside this tube~
As the reaction continues, the reacted gas passes through the vent holes lS2 and into the annular space between the tu:es. The reaction moves from the exothermal phase to the endothermal phase at approximately the same time that the gas passes through the vent holes.
As the reacting gas passes upward through the annular space between the tubes, the endothermal reaction absoxbs the heat necessary for this reac-tion which is provided by the external;heat source, through the metallic walls of the outer tube. The reacted gas then passes upward through passaye 148 and transfers additional heat to the incoming gas within the inner tube in the recuperator portion.
The insulation within the recuperator portion pre-vents the heat from the reacted gas from being transferred outside of the generator.
The cooled, reac~ed gas exits the generator ' ' ': , ' :.
.
;;

~ ~ ~6~ 5 at outlet pipe 142 at a temperature of about 1300-1400F. The outlet has has, therefore, been rapidly cooled to just above the reverse reaction temperature range (900-1250F.), thus making the freezing reaction in the heat exchanger an easier task thereby limiting the production of soot in the reverse reaction range when using only an air heat exchanger.
Because of the relatively even heating across the annular doughnut shaped endothermic reaction area, the maximum temperature within the generator can be held at close to the 1750F. temperature necessary for the reaction to take place; that is, around 1800F. Because the maximum temperature is thus about 150F. less than that required in the prior art, less expensive construction material may be used and the input of outside heat can be decreased. Further, the lower reacted gas outlet temperature, in addition to reducing the soot output of the generator, eliminates the need for an I ,~ 6 ~; ~3 2 r~

expensive water cooled heat exchanger between the generator and an air cooled heat exchanger.

EX~`1PLE 1 A mixture of one part natural gas to 2.42 parts air was introduced into the generator of the present invention. A heating power of 11.87 kilowatts per hour ~as used to raise the gas to a control tempera-ture of 1800F. The output gas had a volume of 1514 cubic feet per hour, a methane content of 0~44%, a dew point of 20F., a carbon dioxide content of 0724%, a nitrogen content of 40%, a hyarogen content of 39%,~and a carbon monoxide content of 20~.

Natural gas and air at a ratio of one part gas to 2.47 parts air ~as introduced into the generator of the present invention and a heating power of 11.87 kilowatts per hour was introduce~ to raise the control temperature of 1800Fo The output vol-ume of 1506 cubic feet per hour had a methane content of 0.32%, a dew point of 30.8F. and a :
-, , 1 1 66~2~

carbon dioxide percentage of 0-33% + ~2' H2 and CO.
It can therefore be seen that, due to the lower control temperature and the use of a recuperator, that the generator of the present invention uti-lizes signi~icantly less energy than that of theprior art. Further, even if the temperature is raised to 1950F., as in the prior art, there is still an energ~ savings as illustrated by the Example below.

EXAMæLE 3 Natural gas and air were mixed at a ratio of 1 to 2.41 and introduced into the generator of the present i`nvention. A heating power of 16.41 kilo-watts per hour was used to raise the control tem-perature to 1950F. The output gas had a volumeof 1517 cu~ic feet per hour, a methane content of 0.5%, a dew point of 22F. and a carbon dioxide content of 0.57%. A heating power of 1.36 kilo-watts per hour was, therefore, saved even using a 1950F. control temperature.

8 ~ 5 The pr;or art HYEN generator can be easily retrofit to produce the generator of the present invention. It is merely necessary to remove the top and bottom plugs and catalyst from the prior art generator. The outer shell and insulation jacket need not be modified, except for the positioning of the gas outlet pipe 142. The inner tube 134 and catalyst ~ed may then be easily introduced for a relatively simple retrofit.
Obviously, numerous modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be under-stood that within the scope of the appended claims, the invention may be practiced otherwise than as specficially described herein.

~`Q~`e~ J~

Claims (11)

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows;
1. An apparatus for carrying out a reaction having an initial exothermic phase and a subsequent endothermic phase, said apparatus comprising:
a first conduit having a top and bottom, an upper recupterator portion, a lower reactor portion, a reaction production outlet means in said recuperator portion;
a second conduit within said first conduit, said second conduit being coaxial with said first conduit and having a diameter less than that of said first conduit by an amount sufficient to create an annular space between said conduits, said second conduit extending from adjacent said top off said first conduit through at least a portion of said lower reactor portion, said second conduit having reaction gas inlet means and means in said reactor portion for communicating the interior of said second conduit with said annular space;
a catalyst bed in at least a portion of said reactor portion and heating means surrounding only the reactor portion of said first conduit.
2. The apparatus of claim 1 wherein said catalyst bed fills that portion of said inner conduit and that portion of said annular space which lie in said reactor portion.
3. The apparatus of claim 1 or 2 wherein said reactor portion comprises the lower portions of said first and second conduits.
4. The apparatus of claim 1 or 2 wherein said catalyst bed comprises cubes composed of porous brick impregnated with NiN2 fired to form NiO.
5. The apparatus of claim 1 wherein said means for communicating comprises a plurality of vent holes in said second conduit.
6. The apparatus of claim 1 wherein said conduits comprise metallic alloy tubes.
7. The apparatus of claim 1 or 6 including heating means adjacent said reactor portion.
8. The apparatus of claim 1 wherein said heating means comprise electric resistant heating means.
9. The apparatus of claim 1 wherein said heating means comprise gas heating means.
10. The apparatus of claim 1 wherein said reaction gas inlet means comprises a third conduit in said conduit and coaxial therewith.
11. The apparatus of claim 1 including insulation between said first conduit and said annular space, said insulation extending only through said recuperator portion and on the bottom of said first conduit.
CA000387378A 1980-10-07 1981-10-06 Two pass endothermic generator Expired CA1166825A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US06/194,895 US4355003A (en) 1980-10-07 1980-10-07 Two pass endothermic generator
US194,895 1980-10-07

Publications (1)

Publication Number Publication Date
CA1166825A true CA1166825A (en) 1984-05-08

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Family Applications (1)

Application Number Title Priority Date Filing Date
CA000387378A Expired CA1166825A (en) 1980-10-07 1981-10-06 Two pass endothermic generator

Country Status (5)

Country Link
US (1) US4355003A (en)
JP (1) JPS5794342A (en)
CA (1) CA1166825A (en)
GB (1) GB2084894B (en)
MX (1) MX7318E (en)

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DE3402713A1 (en) * 1984-01-26 1985-08-08 Linde Ag, 6200 Wiesbaden METHOD AND REACTOR FOR CARRYING OUT AN ENDOTHERMAL REACTION
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GB2084894A (en) 1982-04-21
MX7318E (en) 1988-05-16
JPS5794342A (en) 1982-06-11
GB2084894B (en) 1984-10-24
US4355003A (en) 1982-10-19
JPH0123173B2 (en) 1989-05-01

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