CA2361809A1 - Purification of natural gas by cryogenic separation - Google Patents
Purification of natural gas by cryogenic separation Download PDFInfo
- Publication number
- CA2361809A1 CA2361809A1 CA002361809A CA2361809A CA2361809A1 CA 2361809 A1 CA2361809 A1 CA 2361809A1 CA 002361809 A CA002361809 A CA 002361809A CA 2361809 A CA2361809 A CA 2361809A CA 2361809 A1 CA2361809 A1 CA 2361809A1
- Authority
- CA
- Canada
- Prior art keywords
- heat exchanger
- refrigerant
- regenerating
- active
- mixture
- 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.)
- Abandoned
Links
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 title description 112
- 238000000926 separation method Methods 0.000 title description 29
- 238000000746 purification Methods 0.000 title description 12
- 239000003345 natural gas Substances 0.000 title description 8
- 239000003507 refrigerant Substances 0.000 claims abstract description 94
- 239000007789 gas Substances 0.000 claims abstract description 57
- 230000001172 regenerating effect Effects 0.000 claims abstract description 35
- 239000000203 mixture Substances 0.000 claims abstract description 27
- 230000008014 freezing Effects 0.000 claims abstract description 10
- 238000007710 freezing Methods 0.000 claims abstract description 10
- 238000001816 cooling Methods 0.000 claims description 14
- 238000007599 discharging Methods 0.000 claims 3
- 239000007787 solid Substances 0.000 abstract description 30
- 238000000859 sublimation Methods 0.000 abstract description 9
- 230000008022 sublimation Effects 0.000 abstract description 9
- BALXUFOVQVENIU-KXNXZCPBSA-N pseudoephedrine hydrochloride Chemical compound [H+].[Cl-].CN[C@@H](C)[C@@H](O)C1=CC=CC=C1 BALXUFOVQVENIU-KXNXZCPBSA-N 0.000 abstract 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 72
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 54
- 239000001569 carbon dioxide Substances 0.000 description 27
- 238000000034 method Methods 0.000 description 22
- 239000000047 product Substances 0.000 description 21
- 238000004821 distillation Methods 0.000 description 18
- 230000008569 process Effects 0.000 description 16
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 10
- 239000000654 additive Substances 0.000 description 10
- 239000003949 liquefied natural gas Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 238000013459 approach Methods 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 8
- 238000012545 processing Methods 0.000 description 7
- 239000012071 phase Substances 0.000 description 6
- 239000012535 impurity Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 5
- 239000001294 propane Substances 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 239000001273 butane Substances 0.000 description 4
- 230000001351 cycling effect Effects 0.000 description 4
- 230000003247 decreasing effect Effects 0.000 description 4
- 239000012528 membrane Substances 0.000 description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 238000005057 refrigeration Methods 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 238000001179 sorption measurement Methods 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000003190 augmentative effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- 239000011368 organic material Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000001473 noxious effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 238000005381 potential energy Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000002910 solid waste Substances 0.000 description 1
- 230000026676 system process Effects 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J3/00—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
- F25J3/06—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation
- F25J3/0605—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation characterised by the feed stream
- F25J3/061—Natural gas or substitute natural gas
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/002—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by condensation
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/0002—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the fluid to be liquefied
- F25J1/0022—Hydrocarbons, e.g. natural gas
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/003—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the kind of cold generation within the liquefaction unit for compensating heat leaks and liquid production
- F25J1/0032—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the kind of cold generation within the liquefaction unit for compensating heat leaks and liquid production using the feed stream itself or separated fractions from it, i.e. "internal refrigeration"
- F25J1/004—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the kind of cold generation within the liquefaction unit for compensating heat leaks and liquid production using the feed stream itself or separated fractions from it, i.e. "internal refrigeration" by flash gas recovery
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/003—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the kind of cold generation within the liquefaction unit for compensating heat leaks and liquid production
- F25J1/0032—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the kind of cold generation within the liquefaction unit for compensating heat leaks and liquid production using the feed stream itself or separated fractions from it, i.e. "internal refrigeration"
- F25J1/0042—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the kind of cold generation within the liquefaction unit for compensating heat leaks and liquid production using the feed stream itself or separated fractions from it, i.e. "internal refrigeration" by liquid expansion with extraction of work
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/003—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the kind of cold generation within the liquefaction unit for compensating heat leaks and liquid production
- F25J1/0047—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the kind of cold generation within the liquefaction unit for compensating heat leaks and liquid production using an "external" refrigerant stream in a closed vapor compression cycle
- F25J1/0052—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures characterised by the kind of cold generation within the liquefaction unit for compensating heat leaks and liquid production using an "external" refrigerant stream in a closed vapor compression cycle by vaporising a liquid refrigerant stream
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J1/00—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures
- F25J1/02—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process
- F25J1/0211—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process using a multi-component refrigerant [MCR] fluid in a closed vapor compression cycle
- F25J1/0212—Processes or apparatus for liquefying or solidifying gases or gaseous mixtures requiring the use of refrigeration, e.g. of helium or hydrogen ; Details and kind of the refrigeration system used; Integration with other units or processes; Controlling aspects of the process using a multi-component refrigerant [MCR] fluid in a closed vapor compression cycle as a single flow MCR cycle
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J3/00—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
- F25J3/06—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation
- F25J3/063—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation characterised by the separated product stream
- F25J3/0635—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation characterised by the separated product stream separation of CnHm with 1 carbon atom or more
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J3/00—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
- F25J3/06—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation
- F25J3/063—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation characterised by the separated product stream
- F25J3/067—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation characterised by the separated product stream separation of carbon dioxide
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2205/00—Processes or apparatus using other separation and/or other processing means
- F25J2205/20—Processes or apparatus using other separation and/or other processing means using solidification of components
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2210/00—Processes characterised by the type or other details of the feed stream
- F25J2210/66—Landfill or fermentation off-gas, e.g. "Bio-gas"
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2215/00—Processes characterised by the type or other details of the product stream
- F25J2215/04—Recovery of liquid products
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2220/00—Processes or apparatus involving steps for the removal of impurities
- F25J2220/60—Separating impurities from natural gas, e.g. mercury, cyclic hydrocarbons
- F25J2220/66—Separating acid gases, e.g. CO2, SO2, H2S or RSH
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2230/00—Processes or apparatus involving steps for increasing the pressure of gaseous process streams
- F25J2230/30—Compression of the feed stream
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2270/00—Refrigeration techniques used
- F25J2270/02—Internal refrigeration with liquid vaporising loop
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2270/00—Refrigeration techniques used
- F25J2270/12—External refrigeration with liquid vaporising loop
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2270/00—Refrigeration techniques used
- F25J2270/66—Closed external refrigeration cycle with multi component refrigerant [MCR], e.g. mixture of hydrocarbons
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2280/00—Control of the process or apparatus
- F25J2280/30—Control of a discontinuous or intermittent ("batch") process
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
- F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
- F25J2290/00—Other details not covered by groups F25J2200/00 - F25J2280/00
- F25J2290/44—Particular materials used, e.g. copper, steel or alloys thereof or surface treatments used, e.g. enhanced surface
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- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02C—CAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
- Y02C20/00—Capture or disposal of greenhouse gases
- Y02C20/40—Capture or disposal of greenhouse gases of CO2
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- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S62/00—Refrigeration
- Y10S62/902—Apparatus
- Y10S62/909—Regeneration
Abstract
An apparatus (2, 20, 200) for separating CO2 from a mixture of gases include s CO2 and a second gas, the apparatus (2, 20, 200) includes an active heat exchanger (216) and a regenerating heat exchanger (221). The active heat exchanger (216) includes a heat exchange surface in contact with the mixture of gases. The mixture of gases is present in the active heat exchanger (216) at a predetermined pressure which is chosen such that CO2 freezes on the hea t exchange surface when the surface is cooled by a refrigerant having a temperature below that at which CO2 freezes at the predetermined pressure. T he regenerating heat exchanger (221) includes a heat exchange surface in contac t with the refrigerant and also in contact with a layer of frozen CO2. The refrigerant enters the regenerating heat exchanger (221) at a temperature above that at which the CO2 in the frozen layer of CO2 sublimates. The sublimation of the solid CO2 cools the refrigerant prior to the refrigerant being expanded through an expansion valve (215), which reduces the temperatu re of the refrigerant to a point below the freezing point of CO2 at the predetermined pressure. The refrigerant is re-compressed by a compressor (60 , 160, 218) after leaving the active heat exchanger (216). In the preferred embodiment of the present invention, the gaseous CO2 released by the regenerating heat exchanger (221) is used to precool the incoming gas mixtur e. A second precooling heat exchanger (167) precools the compressed refrigerant by providing thermal contact with the refrigerant leaving the active heat exchanger (216).
Description
-PURIFICATION OF NATURAL GAS BY CRYOGENIC SEPARATION-Field of the Invention The present invention relates to the process of purification of methane gas sources, and more particularly, to the cryogenic purification of methane gas sources having a high carbon dioxide concentration.
Background of the Invention Low grade methane gas sources such as that arising from the decay of organic materials have been recognized as potential energy sources for at least 50 years. Such gas sources include gas from landfill sites and anaerobic digesters that produce "biogas"
comprised primarily of methane and carbon dioxide. Numerous other trace impurities as well as oxygen and nitrogen may also be present in the biogas in varying amounts.
Biogas escaping from landfill sites possesses both environmental and safety hazards.
Further, both methane and carbon dioxide components in the biogas are potentially valuable products if properly purified. Hence, it would be advantageous to capture the energy value of the biogas while eliminating the environmental and safety hazards. In spite of the desirability of utilizing biogas from landfills and digesters, such methane gas sources have been underutilized because of problems effectively purifying the gas, namely, removing the trace amounts of noxious substances, and then effectively separating the carbon dioxide component from the methane component. About one third to one half of the biogas stream generated by anaerobic decay of organic material is carbon dioxide. Hence, the volumetric energy content of the unpurified biogas stream is substantially less than that of pipeline natural gas.
Accordingly, unpurified biogas cannot be introduced into gas pipelines or easily utilized in conventional equipment without processing the gas mixture to remove the carbon dioxide and other impurities.
Numerous systems for purifying biogas sources have been suggested. Separation systems based on membranes, pressure swing adsorption, temperature swing adsorption, chemical absorption, and cryogenic processes have all been reported. Each of these systems has the potential of successfully purifying biogas at sites where large volumes of biogas are available for processing or where final methane purities below 95% are acceptable.
Background of the Invention Low grade methane gas sources such as that arising from the decay of organic materials have been recognized as potential energy sources for at least 50 years. Such gas sources include gas from landfill sites and anaerobic digesters that produce "biogas"
comprised primarily of methane and carbon dioxide. Numerous other trace impurities as well as oxygen and nitrogen may also be present in the biogas in varying amounts.
Biogas escaping from landfill sites possesses both environmental and safety hazards.
Further, both methane and carbon dioxide components in the biogas are potentially valuable products if properly purified. Hence, it would be advantageous to capture the energy value of the biogas while eliminating the environmental and safety hazards. In spite of the desirability of utilizing biogas from landfills and digesters, such methane gas sources have been underutilized because of problems effectively purifying the gas, namely, removing the trace amounts of noxious substances, and then effectively separating the carbon dioxide component from the methane component. About one third to one half of the biogas stream generated by anaerobic decay of organic material is carbon dioxide. Hence, the volumetric energy content of the unpurified biogas stream is substantially less than that of pipeline natural gas.
Accordingly, unpurified biogas cannot be introduced into gas pipelines or easily utilized in conventional equipment without processing the gas mixture to remove the carbon dioxide and other impurities.
Numerous systems for purifying biogas sources have been suggested. Separation systems based on membranes, pressure swing adsorption, temperature swing adsorption, chemical absorption, and cryogenic processes have all been reported. Each of these systems has the potential of successfully purifying biogas at sites where large volumes of biogas are available for processing or where final methane purities below 95% are acceptable.
However, none of these is economically viable for biogas sources smaller than one to two million standard cubic feet per day. For biogas sources producing less than this volume per day or where high purities are required, the capital investment, the operating costs, and or system complexity limit practical or economic use of existing systems.
The harsh, corrosive, continuous operating environments present at landfill sites limit the effectiveness of systems requiring maintenance, supervision, or chemical additives.
Complex systems generally have higher capital and maintenance costs.
In principle, biogas can be cryogenically separated into its components using distillation techniques. Unfortunately, distillation techniques are more difficult for biogas mixtures of carbon dioxide and methane because of several unique features of the phases present in equilibrium mixtures. Cryogenic separations may be broadly divided into continuous and non-continuous (batch) approaches. Continuous cryogenic systems utilize a region or zone where carbon dioxide and methane are continuously separated from one another through the phase differences between components. For example, to obtain a purity of >98 % methane at a constant pressure below 700 psia, the solid C02 that readily forms must be separated from the mixture feed stream. Operation below the critical point of the mixture is required to maintain distinct phases and allow phase separation.
The range of temperature and pressure values available for such conventional cryogenic distillation is quite limited.
Numerous cryogenic processes for separating carbon dioxide and methane are taught in the prior art. For example, A.S. Holmes, et al. (U.S. Patent 4,462,814) teach a process and apparatus for avoiding a solid carbon dioxide phase in a distillation process.
Commonly termed the Ryan-Holmes process, alkane additives such as propane or butane are used to avoid solid COZ formation during liquid distillation-based separation. The butane or propane is separated from the COZ after co-distillation from the CH4 and is re-circulated into the distillation tower. Heavy hydrocarbons (C3+) are added to the feedstream to allow operation with decreased pressures and elevated temperatures without solid C02 formation. The addition of n-butane to the feedstream allows the distillation of the mixture to occur well within the liquid-vapor phase, eliminating solid COz formation in the distillation column. In addition, the critical pressure of the mixture is raised to create a greater range of acceptable operating pressures.
The harsh, corrosive, continuous operating environments present at landfill sites limit the effectiveness of systems requiring maintenance, supervision, or chemical additives.
Complex systems generally have higher capital and maintenance costs.
In principle, biogas can be cryogenically separated into its components using distillation techniques. Unfortunately, distillation techniques are more difficult for biogas mixtures of carbon dioxide and methane because of several unique features of the phases present in equilibrium mixtures. Cryogenic separations may be broadly divided into continuous and non-continuous (batch) approaches. Continuous cryogenic systems utilize a region or zone where carbon dioxide and methane are continuously separated from one another through the phase differences between components. For example, to obtain a purity of >98 % methane at a constant pressure below 700 psia, the solid C02 that readily forms must be separated from the mixture feed stream. Operation below the critical point of the mixture is required to maintain distinct phases and allow phase separation.
The range of temperature and pressure values available for such conventional cryogenic distillation is quite limited.
Numerous cryogenic processes for separating carbon dioxide and methane are taught in the prior art. For example, A.S. Holmes, et al. (U.S. Patent 4,462,814) teach a process and apparatus for avoiding a solid carbon dioxide phase in a distillation process.
Commonly termed the Ryan-Holmes process, alkane additives such as propane or butane are used to avoid solid COZ formation during liquid distillation-based separation. The butane or propane is separated from the COZ after co-distillation from the CH4 and is re-circulated into the distillation tower. Heavy hydrocarbons (C3+) are added to the feedstream to allow operation with decreased pressures and elevated temperatures without solid C02 formation. The addition of n-butane to the feedstream allows the distillation of the mixture to occur well within the liquid-vapor phase, eliminating solid COz formation in the distillation column. In addition, the critical pressure of the mixture is raised to create a greater range of acceptable operating pressures.
The Ryan-Holmes Process, however, has two significant limitations for biogas purification. First, the system complexity leads to high capital costs and the inability to scale to smaller feedstreams. As pointed out above, such costs are problematic in landfill recovery systems. Second, this process requires a supply of propane or heavier alkanes that are generally not present at landfill sites.
More recently Potts, Jr., et al., (U.S. Patent Number 5,120,338) teach a method for separating a multi-component feedstream using distillation and a controlled freeze zone. This approach differs from the Ryan-Holmes process in that solid carbon dioxide is allowed to form in a controlled manner. This solid is melted and incorporated into the liquid portion of a liquid phase. A third gas phase is enriched in the most volatile component, methane, allowing its separation. By carefully controlling the conditions of solid formation, and gas-liquid distillation, the components may be separated into three streams.
Essentially, this system allowed the desired product purity to be reached without avoiding the formation of solid carbon dioxide or the use of additives. The primary limitations of this process pertain to its scalability. The complexity and capital costs of the system require a biogas source larger than two million cubic feet per day to be economically viable. This approach is too complex and has too high of capital costs to be viable at smaller gas sources.
Several techniques are also taught that employ some cooling in conjunction with a second type of separation mechanism. For instance, Sweeney, et al. (U.S.
Patent #5,570,582), Soffer, et al. (U.S. Patent #5,649,996), and Ojo, et al. (U.S.
Patent #5,531,808) teach processes by which the operation of adsorption systems is augmented by operation at sub-ambient or cryogenic temperatures. Lokhandwala (U.S. Patent # 5,647,227) teaches a process and apparatus by which a mixture of methane, nitrogen, and at least one other component (carbon dioxide) are separated. This processes employs a cryogenic separation augmented by a membrane. Such systems do not rely on solid phase formation or distillation to affect the separation. These hybrid systems also have costs and complexities which limit their use to landfill sites having biogas streams greater than approximately two million cubic feet per day.
In U.S. Patent #5,642,630, Abdelmalek, et al. disclose a solid waste landfill gas treatment and separation process that claims production of a high quality liquefied natural gas stream, liquefied carbon dioxide stream, and a compressed natural gas stream.
The patent teaches the use of a four-stage compressor to generate pressures up to 1800 Asia, as well as three flash drums, the use of chemical additives, and multiple recirculation loops to obtain the desired products. The complexity of this system and related capital costs limit its usefulness at small landfill sites.
In U.S. Patent #4,681,612 O'Brien, et al. disclose a cryogenic separation system that produces a fuel-grade methane product stream and the option of a carbon dioxide product stream. This approach relies on a cryogenic distillation column in which the methane is the more volatile, and thus the overhead product is enriched in methane. The methane is further separated from the overhead product with the use of a selective membrane. The bottom product primarily contains the carbon dioxide with impurities that may be further purified in a separate purification column and used as a product stream if desired. This approach suffers from two problems. First, because the system is a hybrid, using both a distillation column and a membrane, complexity and capital costs are increased. Second, high purity carbon dioxide and methane are not readily produced without subsequent processing and additional capital expenditures. Without the ability to produce high purity products, the applicability of this approach is limited.
Several techniques using chemical additives to separate carbon dioxide and methane in landfill gas and other gas streams have also been reported. Methanol is often used as a chemical additive (Apffel, U.S. Patent #4,675,035). The addition of methanol to the gas mixture during the distillation decreases the temperature and pressure range at which solid carbon dioxide will form. This allows the distillation of the methane to proceed more completely, thereby providing higher purity products. Methanol can be separated from the carbon dioxide and recycled once the distillation process is complete. "Cold Methanol"
separations as they are commonly called have offered one of the best methods to separate biogas to date. These systems, however, do not scale well to smaller biogas sources because of the system complexity, capital costs, and operating costs associated with the combined absorption and distillation processing equipment.
A second system employing chemical additives is taught by Abdelmalek (U.S.
Patent #5,642,630). This approach is one that uses chemical absorption to aid in the separation. As previously mentioned, systems requiring chemical additives and absorption increase operating costs due to the costs of the additive as well as capital costs and complexity to separate and recirculate the additives. Such systems are not economically feasible for biogas sources producing less than approximately two million standard cubic feet per day.
Broadly, it is the object of the present invention to provide an improved separation system process and apparatus for separating a gas stream containing, at a minimum, both carbon dioxide and methane, into high purity methane and high purity carbon dioxide product streams.
It is a yet further object of the present invention to provide a separation system that uses the formation of solid carbon dioxide to affect a highly effective separation.
It is a further object of the present invention to provide a separation system that has lower capital cost than prior art systems.
It is a still further object of the present invention to provide a separation system that is less complex than prior art systems. It is a yet further object of the present invention to provide a separation system that has lower operating costs than prior art systems.
These and other objects of the present invention will become apparent to those skilled in the art from the following detailed description of the invention and the accompanying drawings.
Summary of the Invention The present invention is an apparatus for separating COZ from a mixture of gases that includes C02 and a second gas, the apparatus includes an active heat exchanger and a regenerating heat exchanger. The active heat exchanger includes a heat exchange surface in contact with the mixture of gases. The mixture of gases is present in the active heat exchanger at a predetermined pressure which is chosen such that C02 freezes on the heat exchange surface when the surface is cooled by a refrigerant having a temperature below that at which C02 freezes at the predetermined pressure. The regenerating heat exchanger includes a heat exchange surface in contact with the refrigerant and also in contact with a layer of frozen C02. The refrigerant enters the regenerating heat exchanger at a temperature above that at which the C02 in the frozen layer of COZ sublimates. The sublimation of the solid C02 cools the refrigerant prior to the refrigerant being expanded through an expansion valve, which reduces the temperature of the refrigerant to a point below the freezing point of C02 at the predetermined pressure. The refrigerant is re-compressed by a compressor after leaving the active heat exchanger. In the preferred embodiment of the present invention, the gaseous C02 released by the regenerating heat exchanger is used to precool the incoming gas mixture. A second precooling heat exchanger precook the compressed refrigerant by providing thermal contact with the refrigerant leaving the active heat exchanger. In the preferred embodiment of the present invention, first and second heat exchangers are utilized to provide the active and regenerating heat exchanger. The choice of which heat exchanger is the active heat exchanger at any time is made by a valve system which routes the gas mixture and refrigerant streams to and from the active heat exchanger and regenerating heat exchangers.
Brief Description of the Drawings Figure 1 is a schematic drawing of a portion of a biogas purification system according to the present invention.
Figure 2 is a schematic drawing of the preferred embodiment of a biogas purification system according to the present invention producing LNG.
Figure 3 is a schematic drawing of the present invention producing high purity pressurized methane gas at slightly sub-ambient temperatures.
Detailed Description of the Invention The present invention provides improvements over the art by utilizing a single stage process to separate the C02 and CH4 into high purity product streams without the need for further polishing to enhance the purity of the products. Furthermore, the methane product stream can be liquefied to form a high value product in the same stage in which the separation of carbon dioxide and methane takes place. The incorporation of this processing into a single cryogenic step results in a system that offers lower capital costs, lower operating costs, and reduced complexity. This novel, less expensive approach will allow the exploitation of a large number of smaller landfills that have been uneconomical with prior art, and will offer superior gas processing capabilities at larger landfills that could be or are being currently exploited with existing technology.
The manner in which the present invention obtains its advantages may be more easily understood with reference to Figure l, which is a schematic drawing of a simplified version of a COZ purification system 200 according to the present invention for separating C02 from methane in a biogas feedstream. To simplify the following discussion, only the system configuration relative to one half of the cycle is shown.
Biogas purification systems according to the present invention utilize two heat exchangers, shown at 216 and 221, and a compressor for compressing a refrigerant used to cool the biogas to the point at which the C02 separates out as a solid. The heat exchanger in which the COZ is separated from the methane will be referred to as the "active heat exchanger" in the following discussion. The other heat exchanger will be referred to as the "regenerating heat exchanger" for reasons that will become clear from the following discussion. In the configuration shown in Figure 1, heat exchanger 221 is the regenerating heat exchanger and heat exchanger 16 is the active heat exchanger.
In the simplified version of the system shown in Figure 1, the biogas is cooled in heat exchanger 216 by a refrigerant that is expanded through expansion valve 215.
The COZ is precipitated out of the biogas and forms a coating on the heat exchange surface as shown at 214.
The refrigerant leaving heat exchanger 216 is compressed by compressor 218 and pre-cooled in heat exchanger 221 prior to expansion through valve 215. Heat exchanger 221 was previously the active heat exchanger and is now the regenerating heat exchanger. Heat exchanger 221 has a coating of solid C02 on the heat exchange surface as shown at 222. The sublimation of this coating provides the source of cooling for the refrigerant passing through heat exchanger 221. Hence, the work performed in solidifying the C02 when the COZ was precipitated from the biogas during the period 'in which heat exchanger 221 was the active heat exchanger is re-captured as useful work during the period in which heat exchanger 221 is regenerating.
If the biogas contains significant quantities of water, gases other than methane and C02, or other organic compounds that are unacceptable in the final methane stream, the incoming biogas may be processed through a carbon and/or zeolite separator or other device to remove these components. Such separation systems are known in the art, and hence, will not be discussed in detail here.
As noted above, the system shown in Figure 1 only illustrates one half of the separation cycle. During the second half of the cycle, the roles of heat exchangers 216 and 221 are reversed. That is, heat exchanger 221 becomes the regenerating heat exchanger and heat exchanger 216 becomes the active heat exchanger. The roles must be reversed as soon as the solid COZ in the regenerating heat exchanger is exhausted. However, the heat exchangers can be exchanged as soon as the regenerating heat exchanger has recovered its heat transfer efficiency Refer now to Figure 2, which is a schematic drawing of one embodiment of a C02 purification system 2 according to the present invention for separating a mixed feedstream into pure C02 and CH4 product streams. The feedstream 5 containing, at a minimum, C02 and CH4, enters the separation system coldbox 7, which includes a precooling/recuperative heat exchanger 10. The feedstream is assumed to be free of any significant organic or inorganic trace impurities. The feedstream enters at a pressure of approximately 200 psig.
Pretreatment systems for removing the impurities normally found in landfill gas are known to those skilled in the art, and hence, will not be discussed in detail here. The reader is directed to "Landfill Gas: Resource Evaluation and Development", GRI Report 85/0259, Chicago, IL, August 1985 for a more complete discussion. The feedstream typically contains approximately45-60 % methane, 35-50 % carbon dioxide, and 1-5 % nitrogen and oxygen as it enters the present invention. Coldbox 7 is used to thermally isolate the separation apparatus from ambient temperatures. Precooling recuperative heat exchanger 10 acts to cool the inlet stream 5 such that the maximum thermal energy is recovered from the sublimating C02 as discussed below. The temperatures in heat exchanger 10 are maintained such that no solid COZ forms in heat exchanger 10.
After exiting heat exchanger 10, the cooled feed stream enters a switching valve 15, which directs the feedstream to the currently active heat exchanger surface.
In the current example, switching valve 15 directs the precooled feedstream into the left heat exchange surface module 20 that contains the externally-cooled heat exchange surface 25, which is currently acting to solidify the COZ out of the process stream.
A temperature gradient is established in module 20 by the cold refrigerant fluid passing therethrough, the feedstream inlet end of the module being warmer than the outlet end. For example, the cold end of the module may be near 150 ° K and the warmer end near 195° K. The feedstream continues to cool and become enriched in CH4 as solid COZ is deposited on heat exchange surface 25. In the embodiment shown in Figure 2, the temperature at the outlet end of module 20 is cold enough to liquefy the pure methane component of the feedstream at 200 psig. The LNG product stream 30 exits module 20 and flows to valve 35, which directs the LNG out of the coldbox via pipe 40.
If the final product is compressed natural gas (CNG), the LNG can be compressed in a cryogenic pump and vaporized recuperatively with the incoming process stream to form high purity compressed natural gas (CNG). The vaporization of the LNG can be used to precool the incoming feedstream or the refrigerant thereby substantially recovering the energy used to liquefy the natural gas. In heat exchanger 10, feedstream 5 was precooled by stream 12, which is a high purity C02 gaseous stream at or near 15 psig. This stream is produced in a second heat exchange module 45 that is identical to, and alternatively cycled with, module 20. As shown in Figure 2, module 45 has previously been used as the active heat exchanger and a layer 51 of C02 has accumulated on its heat exchange surface 50. The pressure on the solid C02 side of module 45 is decreased to approximately atmospheric pressure. At this pressure COZ sublimes at a temperature of approximately 195° K.
Accordingly, module 45 can be used to cool the refrigerant stream to approximately this temperature.
The refrigerant fluid in the refrigerator loop provides the source of thermal energy to warm the heat exchange surface in the regenerating module and cause the sublimation to rapidly proceed. The temperature gradient of the heat exchanger surface in module 45 varies from 195° K at the colder end and near 220° K at the warmer end. The sublimation energy is recovered by transferring the energy to the refrigerant fluid tf~at passes through module 45 prior to its entry into expansion valve 75. Valve 35 is closed at the lower end of module 45 which forces the gaseous C02 generated by the sublimation to leave module 45 and travel through switching valve 15. The pure, cold C02 gas acts to precool inlet feed stream 5 in heat exchanger 10 5 thereby recovering the sensible heat in the COZ gas. This additional recovery system substantially increases the efficiency of the system. The purified COZ stream exits heat exchanger 10 and cold box 7 at slightly sub-ambient temperatures and atmospheric pressure.
Cooling for the cryogenic separation unit is provided by a refrigerant loop.
In this 10 embodiment, refrigerant 55 enters compressor 60 with an inlet pressure of about 50 psig and leaves at an outlet pressure of 300 psig. The refrigerant exits compressor 60 above ambient temperature and is cooled by after-cooler 65 to a temperature approximately equal to ambient temperature. The refrigerant then enters coldbox 7 and recuperative heat exchanger 67. Heat exchanger 67 cools the refrigerant prior to it entering switching valve 70. In the preferred embodiment, heat exchanger 67 is a brazed plate-fin heat exchanger or a coiled fin-tube heat exchanger. Switching valve 70 directs the refrigerant to the appropriate module for precooling prior to expansion through valve 75 which cools the refrigerant to the operating temperature of the active heat exchange surface. In the configuration shown in Figure 2, the high pressure refrigerant is directed to module 45 where it is further pre-cooled by the heat of sublimation of the solid COZ as it travels through the non-biogas containing side of heat transfer surface 50. Because the equilibrium sublimation temperature of C02 at a given pressure is known and constant, highly predictable and consistent pre-cooling is possible regardless of the amount of solid COZ present per stage in the regeneration so long as some solid remains. After pre-cooling in the regenerating module, the refrigerant is isenthalpically expanded from about 300 psig to a pressure of about 50 psig through expansion valve 75 to further cool the refrigerant to a temperature slightly below the desired cold temperature of the cold end of the actively freezing module 20. The cold refrigerant at near 150° K then enters the non-biogas containing side of heat exchange surface 25 in module 20 and is warmed as it cools surface 25 and effects the freezing of the COZ. The warmer refrigerant then enters heat exchanger 67 and is further warmed as it pre-cools the higher-pressure refrigerant stream.
The refrigerant is heated to slightly sub-ambient temperatures prior to exiting the coldbox 7 and entering compressor 60 to complete the refrigerant cycle.
While the preferred embodiment utilizes an expansion valve to cool the refrigerant prior to entering the heat exchanger in which the C02 is solidified, other gas expander devices or other refrigeration processes can also be utilized without departing from the teachings of the present invention. For example, a turbine expander could be used instead of a valve to expand and cool the refrigerant.
It should be recognized that the controls, make-up gas composition, phase separators, refrigerant filters, drive motors, and other common components of the gas-cycle refrigerator have been omitted from Figure 2 to simplify the drawing. These components and elements of the refrigerator are conventional in the art.
It should also be noted that the specific cooling system employed for the present invention is not critical to the successful operation of the separation system. While a low pressure mixed refrigerant system is used in the preferred embodiment, other recuperative refrigerators will also work. For instance, the recuperative refrigeration system can be based on isentropic turbo-expander cycles such as the Claude or Brayton cycles using nitrogen, argon, or pure methane gas as their refrigerants. Other expansion cycles such as Linde, high-pressure mixed refrigerant, or cascade cycles may also be utilized. The preferred refrigeration system utilizes a compressor having an output of about 300 psig and an expansion valve arrangement that expands the refrigerant from this pressure to about 50 psig.
Such compressors are available from Carrier or Copeland Corporations. Such a refrigerator is preferred because it is reasonably efficient, inexpensive to build, and highly reliable. As noted above, both capital investment and reliability are important issues in any field operating commercial system. The refrigerant utilized in the preferred embodiment of the present invention is a mixture of butane, propane, ethane, methane, and argon at molar percentages of 23, 8, 23, 34, and 12, respectively. However, other refrigerant mixtures that avoid the use of butane and propane may be utilized.
When heat exchange surface 25 accumulates sufficient solid COZ to become limited either by insufficient heat transfer or increased pressure drop caused by solid C02 clogging the conduits of heat exchange surface 20, the other module 45 should be free of solid C02.
At this point switching value 15 acts to switch the streams, and value 35 acts to allow stream to flow from module 45. Similarly, switching valve 60 alters the refrigerant loop such that module 20 acts to precool the refrigerant flow. It should be noted that expansion valve 75 is shown as a reversing valve to simplify the drawing. In practice, such a valve is constructed from a valve system that redirects the flow through a single expansion valve.
These valuing changes effectively switch module 20 from the actively freezing module to the regenerating module where C02 will sublimate. The converse is true for module 45. The refrigerant flow is reversed such that the pre-expansion cooling unit becomes module 20 and the C02 freezing unit becomes module 45.
In the preferred embodiment of the present invention, the valves are sequenced to allow a brief period when the feedstream is not allowed to enter the active heat exchanger module until the desired temperature gradients are re-established in modules 20 and 45 by the flowing refrigerant stream. This brief interruption in the flow is approximately 5 % of the total period of one cycle of operation that may be several minutes in duration. During this time, inlet valve 98 is closed to prevent the feedstream from entering the system.
The present invention can be configured to produce a pure methane gas stream at slightly sub-ambient temperatures instead of liquid methane. This variation of the present invention may be more easily understood with reference to Figure 3 which is a schematic drawing of a simplified version of a gas processing system 20 according to the present invention for separating a biogas feedstream into pure C02 and CH4 product streams. The feedstream 105 is essentially as described above with reference to Figure 2.
Coldbox 107 is used to thermally isolate the separation apparatus from ambient temperatures. The precooling recuperative heat exchanger 110 cools the inlet stream 105 by recovering energy from the sublimating C02 stream 112, and purified methane stream 195 as discussed below. In the preferred embodiment, heat exchanger 110 is a three pass heat exchanger. Temperatures are maintained in the heat exchanger 110 such that no solid C02 forms in heat exchanger 110.
After exiting heat exchanger 110 the cooled feedstream enters a switching valve 115, which acts to direct the feedstream to the active heat exchanger for purification and selects the output of the currently regenerating heat exchanger as a cooling source.
Switching valve 115 directs precooled stream 105 into heat exchange surface module 120 which contains heat exchange surface 125 on which the C02 is removed from the feedstream.
Heat exchangers 120 and 145 operate essentially as described above with respect to heat exchangers 20 and 45 shown in Figure 2.
In the current embodiment the methane component of the stream leaves the active heat exchanger as a liquid under a pressure of approximately 200 psig. The methane product stream 130 exits module 120 and flows to valve 135, which directs the methane stream to heat exchanger 137. The LNG is vaporized in heat exchanger 137 by transferring heat from the high pressure refrigerant. Stream 140 leaves heat exchanger 137 and enters recuperative/precooling heat exchanger 110 where it is utilized to precool the incoming biogas feedstream as it warms to near ambient temperatures prior to exiting the cold box as stream 195. Care must be taken to ensure that stream 140 is warmed sufficiently in heat exchanger 137 so that no solids will form in heat exchanger 110.
In heat exchanger 110, biogas feedstream 105 was precooled by stream 112, which is a high purity C02 gaseous stream at near 15 psig. This stream is produced in a second heat exchange surface module 145 in a manner analogous to that described above with reference to the embodiment of the present invention shown in Figure 2.
Cooling for the cryogenic separation unit is provided with a gas-cycle refrigerant loop analogous to that described above with reference to Figure 2. In this embodiment, the refrigerant 155 enters compressor 160 with an inlet pressure of about 50 psig and outlet pressure of 300 psig. The refrigerant exits compressor 160 above ambient temperature and is cooled by after-cooler 165 approximately to ambient. The refrigerant then enters coldbox 107 and recuperative heat exchanger 167. Heat exchanger 167 cools the refrigerant prior to it entering switching valve 170. Switching valve 170 directs the refrigerant to the regenerating module for pre-cooling. After pre-cooling in the regenerating module, the refrigerant is directed by switching valve 180 to precooling heat exchanger 137 where it is further cooled by the cold methane stream 130. Following the third precooling stage in heat exchanger 137, the refrigerant is isenthalpically expanded from approximately 300 psig to a pressure of approximately 50 psig through expansion valve 175. This expansion cools the refrigerant to a temperature slightly below the desired cold temperature of the cold end of the actively freezing module 120. The refrigerant is then directed to the active heat exchanger switching valve 180. The cold refrigerant at near 150° K then enters the non-biogas containing side of heat exchange surface 125 in module 120 and is warmed as it cools surface 125 by freezing the C02. The warmer refrigerant then enters heat exchanger 167 and is further warmed as it pre-cools the higher-pressure refrigerant stream. The refrigerant is heated to slightly sub-ambient temperatures prior to exiting the coldbox 107 and entering compressor 160 to complete the refrigerant cycle. Heat exchanger 137 is important to the operation of the gas separation system because it decreases the temperature spanned by the expansion valve and enables methane stream 140 to be warmed to a temperature than will not cause solid formation in heat exchanger 110.
The refrigeration system utilized in this embodiment of the present invention is essentially the same as that described above with reference to the embodiment shown in Figure 2. Accordingly, it will not be discussed further here.
The switching of the active and regenerating heat exchangers in this embodiment of the present invention is essentially the same as described above with reference to the embodiment shown in Figure 2. When the active heat exchanger accumulates sufficient solid C02 to significantly degrade its performance, it is switched with the regenerated heat exchanger.
It is important to note that the cooling provided by the sublimation of the C02 occurs at pressures lower than that required to begin liquefying and freezing the C02 from the biogas stream at higher pressure. This allows the temperature spanned by the expansion of the refrigerant to be greatly decreased and the temperature cycling of the thermal mass in the modules 20/120 and 45/145 is greatly reduced. Thus, the operational pressure of the subliming module is critical to an efficient design. This temperature can be decreased or increased somewhat depending on the pressure maintained in the sublimating module. The outlet pressure of the LNG should be close to that of the pressure in the LNG
storage tanks.
Colder LNG is considered more valuable. Further, the residual C02 present in the LNG is a function of pressure and temperature. Care must be taken to ensure that C02 can not solidify downstream from the heat exchange module. Consistent temperature gradients, inlet end temperatures, and outlet end temperatures should be maintained in heat exchangers 10/110 and 67/167. Further, care should be taken to insure that the flow through these heat exchangers does not reverse during cycling. Likewise, the flow through expansion valve 75/175 should not change direction or fluctuate significantly during cycling.
The exit gas temperature for the refrigerant leaving the regenerating heat exchange surface module should remain constant as long as solid COZ is present. Hence, an increase in this temperature is an indication that regenerating is complete and that cycling should be reversed.
Accordingly, this temperature is monitored in the preferred embodiment of the present invention and used to initiate the exchange of the active and regenerating heat exchangers.
To provide adequate separation of the COZ, heat exchanger 20/120 in Figures 2 and 3 must be run at a pressure near 200 psig and with a coldest temperature below about 150° K.
These conditions assure that the gas exiting heat exchanger 20/120 has no more than 0.02 C02. Alternatively, it may be desirable to produce a methane gas product that has higher 10 C02 levels. If the coldest temperature in the active heat exchanger is raised from about 150°
K, the purified output methane stream will remain as a gas and have a correspondingly higher concentration of COZ upon leaving the active heat exchanger. The concentration of the C02 is directly controllable by adjusting the coldest temperature in the active heat exchanger. The adjustment of this temperature provides a means for controlling the quality of the output gas 15 and provides the present invention with the ability to produce pipeline quality natural gas from biogas where the allowable concentration is C02 is usually less than 2 vol. %.
Although the preferred embodiment is intended for use with biogas, other gas streams containing carbon dioxide and methane can be similarly purified with the present invention.
For example, the present invention may be utilized to purify wellhead gas containing large amounts of carbon dioxide.
Various modifications to the present invention will become apparent to those skilled in the art from the foregoing description and accompanying drawings.
Accordingly, the present invention is to be limited solely by the scope of the following claims.
More recently Potts, Jr., et al., (U.S. Patent Number 5,120,338) teach a method for separating a multi-component feedstream using distillation and a controlled freeze zone. This approach differs from the Ryan-Holmes process in that solid carbon dioxide is allowed to form in a controlled manner. This solid is melted and incorporated into the liquid portion of a liquid phase. A third gas phase is enriched in the most volatile component, methane, allowing its separation. By carefully controlling the conditions of solid formation, and gas-liquid distillation, the components may be separated into three streams.
Essentially, this system allowed the desired product purity to be reached without avoiding the formation of solid carbon dioxide or the use of additives. The primary limitations of this process pertain to its scalability. The complexity and capital costs of the system require a biogas source larger than two million cubic feet per day to be economically viable. This approach is too complex and has too high of capital costs to be viable at smaller gas sources.
Several techniques are also taught that employ some cooling in conjunction with a second type of separation mechanism. For instance, Sweeney, et al. (U.S.
Patent #5,570,582), Soffer, et al. (U.S. Patent #5,649,996), and Ojo, et al. (U.S.
Patent #5,531,808) teach processes by which the operation of adsorption systems is augmented by operation at sub-ambient or cryogenic temperatures. Lokhandwala (U.S. Patent # 5,647,227) teaches a process and apparatus by which a mixture of methane, nitrogen, and at least one other component (carbon dioxide) are separated. This processes employs a cryogenic separation augmented by a membrane. Such systems do not rely on solid phase formation or distillation to affect the separation. These hybrid systems also have costs and complexities which limit their use to landfill sites having biogas streams greater than approximately two million cubic feet per day.
In U.S. Patent #5,642,630, Abdelmalek, et al. disclose a solid waste landfill gas treatment and separation process that claims production of a high quality liquefied natural gas stream, liquefied carbon dioxide stream, and a compressed natural gas stream.
The patent teaches the use of a four-stage compressor to generate pressures up to 1800 Asia, as well as three flash drums, the use of chemical additives, and multiple recirculation loops to obtain the desired products. The complexity of this system and related capital costs limit its usefulness at small landfill sites.
In U.S. Patent #4,681,612 O'Brien, et al. disclose a cryogenic separation system that produces a fuel-grade methane product stream and the option of a carbon dioxide product stream. This approach relies on a cryogenic distillation column in which the methane is the more volatile, and thus the overhead product is enriched in methane. The methane is further separated from the overhead product with the use of a selective membrane. The bottom product primarily contains the carbon dioxide with impurities that may be further purified in a separate purification column and used as a product stream if desired. This approach suffers from two problems. First, because the system is a hybrid, using both a distillation column and a membrane, complexity and capital costs are increased. Second, high purity carbon dioxide and methane are not readily produced without subsequent processing and additional capital expenditures. Without the ability to produce high purity products, the applicability of this approach is limited.
Several techniques using chemical additives to separate carbon dioxide and methane in landfill gas and other gas streams have also been reported. Methanol is often used as a chemical additive (Apffel, U.S. Patent #4,675,035). The addition of methanol to the gas mixture during the distillation decreases the temperature and pressure range at which solid carbon dioxide will form. This allows the distillation of the methane to proceed more completely, thereby providing higher purity products. Methanol can be separated from the carbon dioxide and recycled once the distillation process is complete. "Cold Methanol"
separations as they are commonly called have offered one of the best methods to separate biogas to date. These systems, however, do not scale well to smaller biogas sources because of the system complexity, capital costs, and operating costs associated with the combined absorption and distillation processing equipment.
A second system employing chemical additives is taught by Abdelmalek (U.S.
Patent #5,642,630). This approach is one that uses chemical absorption to aid in the separation. As previously mentioned, systems requiring chemical additives and absorption increase operating costs due to the costs of the additive as well as capital costs and complexity to separate and recirculate the additives. Such systems are not economically feasible for biogas sources producing less than approximately two million standard cubic feet per day.
Broadly, it is the object of the present invention to provide an improved separation system process and apparatus for separating a gas stream containing, at a minimum, both carbon dioxide and methane, into high purity methane and high purity carbon dioxide product streams.
It is a yet further object of the present invention to provide a separation system that uses the formation of solid carbon dioxide to affect a highly effective separation.
It is a further object of the present invention to provide a separation system that has lower capital cost than prior art systems.
It is a still further object of the present invention to provide a separation system that is less complex than prior art systems. It is a yet further object of the present invention to provide a separation system that has lower operating costs than prior art systems.
These and other objects of the present invention will become apparent to those skilled in the art from the following detailed description of the invention and the accompanying drawings.
Summary of the Invention The present invention is an apparatus for separating COZ from a mixture of gases that includes C02 and a second gas, the apparatus includes an active heat exchanger and a regenerating heat exchanger. The active heat exchanger includes a heat exchange surface in contact with the mixture of gases. The mixture of gases is present in the active heat exchanger at a predetermined pressure which is chosen such that C02 freezes on the heat exchange surface when the surface is cooled by a refrigerant having a temperature below that at which C02 freezes at the predetermined pressure. The regenerating heat exchanger includes a heat exchange surface in contact with the refrigerant and also in contact with a layer of frozen C02. The refrigerant enters the regenerating heat exchanger at a temperature above that at which the C02 in the frozen layer of COZ sublimates. The sublimation of the solid C02 cools the refrigerant prior to the refrigerant being expanded through an expansion valve, which reduces the temperature of the refrigerant to a point below the freezing point of C02 at the predetermined pressure. The refrigerant is re-compressed by a compressor after leaving the active heat exchanger. In the preferred embodiment of the present invention, the gaseous C02 released by the regenerating heat exchanger is used to precool the incoming gas mixture. A second precooling heat exchanger precook the compressed refrigerant by providing thermal contact with the refrigerant leaving the active heat exchanger. In the preferred embodiment of the present invention, first and second heat exchangers are utilized to provide the active and regenerating heat exchanger. The choice of which heat exchanger is the active heat exchanger at any time is made by a valve system which routes the gas mixture and refrigerant streams to and from the active heat exchanger and regenerating heat exchangers.
Brief Description of the Drawings Figure 1 is a schematic drawing of a portion of a biogas purification system according to the present invention.
Figure 2 is a schematic drawing of the preferred embodiment of a biogas purification system according to the present invention producing LNG.
Figure 3 is a schematic drawing of the present invention producing high purity pressurized methane gas at slightly sub-ambient temperatures.
Detailed Description of the Invention The present invention provides improvements over the art by utilizing a single stage process to separate the C02 and CH4 into high purity product streams without the need for further polishing to enhance the purity of the products. Furthermore, the methane product stream can be liquefied to form a high value product in the same stage in which the separation of carbon dioxide and methane takes place. The incorporation of this processing into a single cryogenic step results in a system that offers lower capital costs, lower operating costs, and reduced complexity. This novel, less expensive approach will allow the exploitation of a large number of smaller landfills that have been uneconomical with prior art, and will offer superior gas processing capabilities at larger landfills that could be or are being currently exploited with existing technology.
The manner in which the present invention obtains its advantages may be more easily understood with reference to Figure l, which is a schematic drawing of a simplified version of a COZ purification system 200 according to the present invention for separating C02 from methane in a biogas feedstream. To simplify the following discussion, only the system configuration relative to one half of the cycle is shown.
Biogas purification systems according to the present invention utilize two heat exchangers, shown at 216 and 221, and a compressor for compressing a refrigerant used to cool the biogas to the point at which the C02 separates out as a solid. The heat exchanger in which the COZ is separated from the methane will be referred to as the "active heat exchanger" in the following discussion. The other heat exchanger will be referred to as the "regenerating heat exchanger" for reasons that will become clear from the following discussion. In the configuration shown in Figure 1, heat exchanger 221 is the regenerating heat exchanger and heat exchanger 16 is the active heat exchanger.
In the simplified version of the system shown in Figure 1, the biogas is cooled in heat exchanger 216 by a refrigerant that is expanded through expansion valve 215.
The COZ is precipitated out of the biogas and forms a coating on the heat exchange surface as shown at 214.
The refrigerant leaving heat exchanger 216 is compressed by compressor 218 and pre-cooled in heat exchanger 221 prior to expansion through valve 215. Heat exchanger 221 was previously the active heat exchanger and is now the regenerating heat exchanger. Heat exchanger 221 has a coating of solid C02 on the heat exchange surface as shown at 222. The sublimation of this coating provides the source of cooling for the refrigerant passing through heat exchanger 221. Hence, the work performed in solidifying the C02 when the COZ was precipitated from the biogas during the period 'in which heat exchanger 221 was the active heat exchanger is re-captured as useful work during the period in which heat exchanger 221 is regenerating.
If the biogas contains significant quantities of water, gases other than methane and C02, or other organic compounds that are unacceptable in the final methane stream, the incoming biogas may be processed through a carbon and/or zeolite separator or other device to remove these components. Such separation systems are known in the art, and hence, will not be discussed in detail here.
As noted above, the system shown in Figure 1 only illustrates one half of the separation cycle. During the second half of the cycle, the roles of heat exchangers 216 and 221 are reversed. That is, heat exchanger 221 becomes the regenerating heat exchanger and heat exchanger 216 becomes the active heat exchanger. The roles must be reversed as soon as the solid COZ in the regenerating heat exchanger is exhausted. However, the heat exchangers can be exchanged as soon as the regenerating heat exchanger has recovered its heat transfer efficiency Refer now to Figure 2, which is a schematic drawing of one embodiment of a C02 purification system 2 according to the present invention for separating a mixed feedstream into pure C02 and CH4 product streams. The feedstream 5 containing, at a minimum, C02 and CH4, enters the separation system coldbox 7, which includes a precooling/recuperative heat exchanger 10. The feedstream is assumed to be free of any significant organic or inorganic trace impurities. The feedstream enters at a pressure of approximately 200 psig.
Pretreatment systems for removing the impurities normally found in landfill gas are known to those skilled in the art, and hence, will not be discussed in detail here. The reader is directed to "Landfill Gas: Resource Evaluation and Development", GRI Report 85/0259, Chicago, IL, August 1985 for a more complete discussion. The feedstream typically contains approximately45-60 % methane, 35-50 % carbon dioxide, and 1-5 % nitrogen and oxygen as it enters the present invention. Coldbox 7 is used to thermally isolate the separation apparatus from ambient temperatures. Precooling recuperative heat exchanger 10 acts to cool the inlet stream 5 such that the maximum thermal energy is recovered from the sublimating C02 as discussed below. The temperatures in heat exchanger 10 are maintained such that no solid COZ forms in heat exchanger 10.
After exiting heat exchanger 10, the cooled feed stream enters a switching valve 15, which directs the feedstream to the currently active heat exchanger surface.
In the current example, switching valve 15 directs the precooled feedstream into the left heat exchange surface module 20 that contains the externally-cooled heat exchange surface 25, which is currently acting to solidify the COZ out of the process stream.
A temperature gradient is established in module 20 by the cold refrigerant fluid passing therethrough, the feedstream inlet end of the module being warmer than the outlet end. For example, the cold end of the module may be near 150 ° K and the warmer end near 195° K. The feedstream continues to cool and become enriched in CH4 as solid COZ is deposited on heat exchange surface 25. In the embodiment shown in Figure 2, the temperature at the outlet end of module 20 is cold enough to liquefy the pure methane component of the feedstream at 200 psig. The LNG product stream 30 exits module 20 and flows to valve 35, which directs the LNG out of the coldbox via pipe 40.
If the final product is compressed natural gas (CNG), the LNG can be compressed in a cryogenic pump and vaporized recuperatively with the incoming process stream to form high purity compressed natural gas (CNG). The vaporization of the LNG can be used to precool the incoming feedstream or the refrigerant thereby substantially recovering the energy used to liquefy the natural gas. In heat exchanger 10, feedstream 5 was precooled by stream 12, which is a high purity C02 gaseous stream at or near 15 psig. This stream is produced in a second heat exchange module 45 that is identical to, and alternatively cycled with, module 20. As shown in Figure 2, module 45 has previously been used as the active heat exchanger and a layer 51 of C02 has accumulated on its heat exchange surface 50. The pressure on the solid C02 side of module 45 is decreased to approximately atmospheric pressure. At this pressure COZ sublimes at a temperature of approximately 195° K.
Accordingly, module 45 can be used to cool the refrigerant stream to approximately this temperature.
The refrigerant fluid in the refrigerator loop provides the source of thermal energy to warm the heat exchange surface in the regenerating module and cause the sublimation to rapidly proceed. The temperature gradient of the heat exchanger surface in module 45 varies from 195° K at the colder end and near 220° K at the warmer end. The sublimation energy is recovered by transferring the energy to the refrigerant fluid tf~at passes through module 45 prior to its entry into expansion valve 75. Valve 35 is closed at the lower end of module 45 which forces the gaseous C02 generated by the sublimation to leave module 45 and travel through switching valve 15. The pure, cold C02 gas acts to precool inlet feed stream 5 in heat exchanger 10 5 thereby recovering the sensible heat in the COZ gas. This additional recovery system substantially increases the efficiency of the system. The purified COZ stream exits heat exchanger 10 and cold box 7 at slightly sub-ambient temperatures and atmospheric pressure.
Cooling for the cryogenic separation unit is provided by a refrigerant loop.
In this 10 embodiment, refrigerant 55 enters compressor 60 with an inlet pressure of about 50 psig and leaves at an outlet pressure of 300 psig. The refrigerant exits compressor 60 above ambient temperature and is cooled by after-cooler 65 to a temperature approximately equal to ambient temperature. The refrigerant then enters coldbox 7 and recuperative heat exchanger 67. Heat exchanger 67 cools the refrigerant prior to it entering switching valve 70. In the preferred embodiment, heat exchanger 67 is a brazed plate-fin heat exchanger or a coiled fin-tube heat exchanger. Switching valve 70 directs the refrigerant to the appropriate module for precooling prior to expansion through valve 75 which cools the refrigerant to the operating temperature of the active heat exchange surface. In the configuration shown in Figure 2, the high pressure refrigerant is directed to module 45 where it is further pre-cooled by the heat of sublimation of the solid COZ as it travels through the non-biogas containing side of heat transfer surface 50. Because the equilibrium sublimation temperature of C02 at a given pressure is known and constant, highly predictable and consistent pre-cooling is possible regardless of the amount of solid COZ present per stage in the regeneration so long as some solid remains. After pre-cooling in the regenerating module, the refrigerant is isenthalpically expanded from about 300 psig to a pressure of about 50 psig through expansion valve 75 to further cool the refrigerant to a temperature slightly below the desired cold temperature of the cold end of the actively freezing module 20. The cold refrigerant at near 150° K then enters the non-biogas containing side of heat exchange surface 25 in module 20 and is warmed as it cools surface 25 and effects the freezing of the COZ. The warmer refrigerant then enters heat exchanger 67 and is further warmed as it pre-cools the higher-pressure refrigerant stream.
The refrigerant is heated to slightly sub-ambient temperatures prior to exiting the coldbox 7 and entering compressor 60 to complete the refrigerant cycle.
While the preferred embodiment utilizes an expansion valve to cool the refrigerant prior to entering the heat exchanger in which the C02 is solidified, other gas expander devices or other refrigeration processes can also be utilized without departing from the teachings of the present invention. For example, a turbine expander could be used instead of a valve to expand and cool the refrigerant.
It should be recognized that the controls, make-up gas composition, phase separators, refrigerant filters, drive motors, and other common components of the gas-cycle refrigerator have been omitted from Figure 2 to simplify the drawing. These components and elements of the refrigerator are conventional in the art.
It should also be noted that the specific cooling system employed for the present invention is not critical to the successful operation of the separation system. While a low pressure mixed refrigerant system is used in the preferred embodiment, other recuperative refrigerators will also work. For instance, the recuperative refrigeration system can be based on isentropic turbo-expander cycles such as the Claude or Brayton cycles using nitrogen, argon, or pure methane gas as their refrigerants. Other expansion cycles such as Linde, high-pressure mixed refrigerant, or cascade cycles may also be utilized. The preferred refrigeration system utilizes a compressor having an output of about 300 psig and an expansion valve arrangement that expands the refrigerant from this pressure to about 50 psig.
Such compressors are available from Carrier or Copeland Corporations. Such a refrigerator is preferred because it is reasonably efficient, inexpensive to build, and highly reliable. As noted above, both capital investment and reliability are important issues in any field operating commercial system. The refrigerant utilized in the preferred embodiment of the present invention is a mixture of butane, propane, ethane, methane, and argon at molar percentages of 23, 8, 23, 34, and 12, respectively. However, other refrigerant mixtures that avoid the use of butane and propane may be utilized.
When heat exchange surface 25 accumulates sufficient solid COZ to become limited either by insufficient heat transfer or increased pressure drop caused by solid C02 clogging the conduits of heat exchange surface 20, the other module 45 should be free of solid C02.
At this point switching value 15 acts to switch the streams, and value 35 acts to allow stream to flow from module 45. Similarly, switching valve 60 alters the refrigerant loop such that module 20 acts to precool the refrigerant flow. It should be noted that expansion valve 75 is shown as a reversing valve to simplify the drawing. In practice, such a valve is constructed from a valve system that redirects the flow through a single expansion valve.
These valuing changes effectively switch module 20 from the actively freezing module to the regenerating module where C02 will sublimate. The converse is true for module 45. The refrigerant flow is reversed such that the pre-expansion cooling unit becomes module 20 and the C02 freezing unit becomes module 45.
In the preferred embodiment of the present invention, the valves are sequenced to allow a brief period when the feedstream is not allowed to enter the active heat exchanger module until the desired temperature gradients are re-established in modules 20 and 45 by the flowing refrigerant stream. This brief interruption in the flow is approximately 5 % of the total period of one cycle of operation that may be several minutes in duration. During this time, inlet valve 98 is closed to prevent the feedstream from entering the system.
The present invention can be configured to produce a pure methane gas stream at slightly sub-ambient temperatures instead of liquid methane. This variation of the present invention may be more easily understood with reference to Figure 3 which is a schematic drawing of a simplified version of a gas processing system 20 according to the present invention for separating a biogas feedstream into pure C02 and CH4 product streams. The feedstream 105 is essentially as described above with reference to Figure 2.
Coldbox 107 is used to thermally isolate the separation apparatus from ambient temperatures. The precooling recuperative heat exchanger 110 cools the inlet stream 105 by recovering energy from the sublimating C02 stream 112, and purified methane stream 195 as discussed below. In the preferred embodiment, heat exchanger 110 is a three pass heat exchanger. Temperatures are maintained in the heat exchanger 110 such that no solid C02 forms in heat exchanger 110.
After exiting heat exchanger 110 the cooled feedstream enters a switching valve 115, which acts to direct the feedstream to the active heat exchanger for purification and selects the output of the currently regenerating heat exchanger as a cooling source.
Switching valve 115 directs precooled stream 105 into heat exchange surface module 120 which contains heat exchange surface 125 on which the C02 is removed from the feedstream.
Heat exchangers 120 and 145 operate essentially as described above with respect to heat exchangers 20 and 45 shown in Figure 2.
In the current embodiment the methane component of the stream leaves the active heat exchanger as a liquid under a pressure of approximately 200 psig. The methane product stream 130 exits module 120 and flows to valve 135, which directs the methane stream to heat exchanger 137. The LNG is vaporized in heat exchanger 137 by transferring heat from the high pressure refrigerant. Stream 140 leaves heat exchanger 137 and enters recuperative/precooling heat exchanger 110 where it is utilized to precool the incoming biogas feedstream as it warms to near ambient temperatures prior to exiting the cold box as stream 195. Care must be taken to ensure that stream 140 is warmed sufficiently in heat exchanger 137 so that no solids will form in heat exchanger 110.
In heat exchanger 110, biogas feedstream 105 was precooled by stream 112, which is a high purity C02 gaseous stream at near 15 psig. This stream is produced in a second heat exchange surface module 145 in a manner analogous to that described above with reference to the embodiment of the present invention shown in Figure 2.
Cooling for the cryogenic separation unit is provided with a gas-cycle refrigerant loop analogous to that described above with reference to Figure 2. In this embodiment, the refrigerant 155 enters compressor 160 with an inlet pressure of about 50 psig and outlet pressure of 300 psig. The refrigerant exits compressor 160 above ambient temperature and is cooled by after-cooler 165 approximately to ambient. The refrigerant then enters coldbox 107 and recuperative heat exchanger 167. Heat exchanger 167 cools the refrigerant prior to it entering switching valve 170. Switching valve 170 directs the refrigerant to the regenerating module for pre-cooling. After pre-cooling in the regenerating module, the refrigerant is directed by switching valve 180 to precooling heat exchanger 137 where it is further cooled by the cold methane stream 130. Following the third precooling stage in heat exchanger 137, the refrigerant is isenthalpically expanded from approximately 300 psig to a pressure of approximately 50 psig through expansion valve 175. This expansion cools the refrigerant to a temperature slightly below the desired cold temperature of the cold end of the actively freezing module 120. The refrigerant is then directed to the active heat exchanger switching valve 180. The cold refrigerant at near 150° K then enters the non-biogas containing side of heat exchange surface 125 in module 120 and is warmed as it cools surface 125 by freezing the C02. The warmer refrigerant then enters heat exchanger 167 and is further warmed as it pre-cools the higher-pressure refrigerant stream. The refrigerant is heated to slightly sub-ambient temperatures prior to exiting the coldbox 107 and entering compressor 160 to complete the refrigerant cycle. Heat exchanger 137 is important to the operation of the gas separation system because it decreases the temperature spanned by the expansion valve and enables methane stream 140 to be warmed to a temperature than will not cause solid formation in heat exchanger 110.
The refrigeration system utilized in this embodiment of the present invention is essentially the same as that described above with reference to the embodiment shown in Figure 2. Accordingly, it will not be discussed further here.
The switching of the active and regenerating heat exchangers in this embodiment of the present invention is essentially the same as described above with reference to the embodiment shown in Figure 2. When the active heat exchanger accumulates sufficient solid C02 to significantly degrade its performance, it is switched with the regenerated heat exchanger.
It is important to note that the cooling provided by the sublimation of the C02 occurs at pressures lower than that required to begin liquefying and freezing the C02 from the biogas stream at higher pressure. This allows the temperature spanned by the expansion of the refrigerant to be greatly decreased and the temperature cycling of the thermal mass in the modules 20/120 and 45/145 is greatly reduced. Thus, the operational pressure of the subliming module is critical to an efficient design. This temperature can be decreased or increased somewhat depending on the pressure maintained in the sublimating module. The outlet pressure of the LNG should be close to that of the pressure in the LNG
storage tanks.
Colder LNG is considered more valuable. Further, the residual C02 present in the LNG is a function of pressure and temperature. Care must be taken to ensure that C02 can not solidify downstream from the heat exchange module. Consistent temperature gradients, inlet end temperatures, and outlet end temperatures should be maintained in heat exchangers 10/110 and 67/167. Further, care should be taken to insure that the flow through these heat exchangers does not reverse during cycling. Likewise, the flow through expansion valve 75/175 should not change direction or fluctuate significantly during cycling.
The exit gas temperature for the refrigerant leaving the regenerating heat exchange surface module should remain constant as long as solid COZ is present. Hence, an increase in this temperature is an indication that regenerating is complete and that cycling should be reversed.
Accordingly, this temperature is monitored in the preferred embodiment of the present invention and used to initiate the exchange of the active and regenerating heat exchangers.
To provide adequate separation of the COZ, heat exchanger 20/120 in Figures 2 and 3 must be run at a pressure near 200 psig and with a coldest temperature below about 150° K.
These conditions assure that the gas exiting heat exchanger 20/120 has no more than 0.02 C02. Alternatively, it may be desirable to produce a methane gas product that has higher 10 C02 levels. If the coldest temperature in the active heat exchanger is raised from about 150°
K, the purified output methane stream will remain as a gas and have a correspondingly higher concentration of COZ upon leaving the active heat exchanger. The concentration of the C02 is directly controllable by adjusting the coldest temperature in the active heat exchanger. The adjustment of this temperature provides a means for controlling the quality of the output gas 15 and provides the present invention with the ability to produce pipeline quality natural gas from biogas where the allowable concentration is C02 is usually less than 2 vol. %.
Although the preferred embodiment is intended for use with biogas, other gas streams containing carbon dioxide and methane can be similarly purified with the present invention.
For example, the present invention may be utilized to purify wellhead gas containing large amounts of carbon dioxide.
Various modifications to the present invention will become apparent to those skilled in the art from the foregoing description and accompanying drawings.
Accordingly, the present invention is to be limited solely by the scope of the following claims.
Claims (5)
1. An apparatus[2, 20, 200] for separating CO2 from a mixture of gases comprising CO2 and a second gas, said apparatus[2, 20, 200] comprising:
an active heat exchanger[216] for freezing said CO2 in said mixture, said active heat exchanger[216] comprising a heat exchange surface in contact with said mixture of gases, said mixture of gases being present at a predetermined pressure, said heat exchange surface being cooled by a refrigerant having a temperature below that at which CO2 freezes at said predetermined pressure;
a regenerating heat exchanger[221] for pre-cooling said refrigerant, said regenerating heat exchanger[221] comprising a heat exchange surface in contact with said refrigerant and also in contact with a layer of frozen CO2, said refrigerant entering said regenerating heat exchanger[221] at a temperature above that at which said CO2 in said frozen layer of CO2 sublimates;
an expansion valve[215] for expanding said refrigerant after said refrigerant has been pre-cooled in said regenerating heat exchanger[221] and prior to said refrigerant entering said active heat exchanger[216]; and a compressor[60, 160, 218] for compressing said refrigerant after said refrigerant has left said active heat exchanger[216], said compressor[60, 160, 218] having an input port for receiving said refrigerant after said refrigerant has left said active heat exchanger[216] and an output port for discharging said compressed refrigerant.
an active heat exchanger[216] for freezing said CO2 in said mixture, said active heat exchanger[216] comprising a heat exchange surface in contact with said mixture of gases, said mixture of gases being present at a predetermined pressure, said heat exchange surface being cooled by a refrigerant having a temperature below that at which CO2 freezes at said predetermined pressure;
a regenerating heat exchanger[221] for pre-cooling said refrigerant, said regenerating heat exchanger[221] comprising a heat exchange surface in contact with said refrigerant and also in contact with a layer of frozen CO2, said refrigerant entering said regenerating heat exchanger[221] at a temperature above that at which said CO2 in said frozen layer of CO2 sublimates;
an expansion valve[215] for expanding said refrigerant after said refrigerant has been pre-cooled in said regenerating heat exchanger[221] and prior to said refrigerant entering said active heat exchanger[216]; and a compressor[60, 160, 218] for compressing said refrigerant after said refrigerant has left said active heat exchanger[216], said compressor[60, 160, 218] having an input port for receiving said refrigerant after said refrigerant has left said active heat exchanger[216] and an output port for discharging said compressed refrigerant.
2. The apparatus[2, 20, 200] of Claim 1 wherein said apparatus[2, 20, 200]
comprises first and second heat exchangers[20, 25, 120, 145], at any given time, one of said heat exchangers[20, 25, 120, 145] is said active heat exchanger[216] and the other of said heat exchangers[20, 25, 120, 145] is said regenerating heat exchanger[221], said apparatus[2, 20, 200] further comprising a valve system[15, 75, 115, 170, 180] for selecting which of said first and second heat exchangers is said active heat exchanger[216].
comprises first and second heat exchangers[20, 25, 120, 145], at any given time, one of said heat exchangers[20, 25, 120, 145] is said active heat exchanger[216] and the other of said heat exchangers[20, 25, 120, 145] is said regenerating heat exchanger[221], said apparatus[2, 20, 200] further comprising a valve system[15, 75, 115, 170, 180] for selecting which of said first and second heat exchangers is said active heat exchanger[216].
3. The apparatus[2, 20, 200] of Claim 2 wherein each of said heat exchangers comprises:
a heat exchange coil[50] having an input end for receiving refrigerant and an output end for discharging refrigerant, said heat exchange coil[50] having an outer surface that is in thermal contact with refrigerant passing through said heat exchange coil[50];
and a chamber for bringing a gas in contact with said outer surface of said heat exchange coil[50], said chamber having an input port and an output port for receiving and discharging a gas to be cooled by contact with said outer surface of said heat exchange coil[50], and wherein said valve system[15, 75, 115, 170, 180] comprises a first valve system[70, 170] for connecting said output port of said compressor[60, 160, 218] to said input end of said heat exchange coil in said regenerating heat exchanger[221]
and for connecting said output end of said heat exchange coil in said active heat exchanger[216] to said input port of said compressor[60, 160, 218]; and a second valve system[15, 115] for routing said mixture of gases to said input port of said active heat exchanger[216].
a heat exchange coil[50] having an input end for receiving refrigerant and an output end for discharging refrigerant, said heat exchange coil[50] having an outer surface that is in thermal contact with refrigerant passing through said heat exchange coil[50];
and a chamber for bringing a gas in contact with said outer surface of said heat exchange coil[50], said chamber having an input port and an output port for receiving and discharging a gas to be cooled by contact with said outer surface of said heat exchange coil[50], and wherein said valve system[15, 75, 115, 170, 180] comprises a first valve system[70, 170] for connecting said output port of said compressor[60, 160, 218] to said input end of said heat exchange coil in said regenerating heat exchanger[221]
and for connecting said output end of said heat exchange coil in said active heat exchanger[216] to said input port of said compressor[60, 160, 218]; and a second valve system[15, 115] for routing said mixture of gases to said input port of said active heat exchanger[216].
4. The apparatus[2, 20, 200] of Claim 1 further comprising an input gas precooling heat exchanger[110] for precooling said mixture of gases by bringing said mixture of gases into thermal contact with CO2 leaving said regenerating heat exchanger[221].
5. The apparatus[2, 20, 200] of Claim 1 further comprising a refrigerant precooling heat exchanger[167] for cooling said compressed refrigerant by bringing said compressed refrigerant into thermal contact with said refrigerant leaving said active heat exchanger[216]
prior to said compressed refrigerant entering said regenerating heat exchanger[221].
prior to said compressed refrigerant entering said regenerating heat exchanger[221].
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US09/245,570 US6082133A (en) | 1999-02-05 | 1999-02-05 | Apparatus and method for purifying natural gas via cryogenic separation |
US09/245,570 | 1999-02-05 | ||
PCT/US2000/001857 WO2000046559A1 (en) | 1999-02-05 | 2000-01-26 | Purification of natural gas by cryogenic separation |
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CA002361809A Abandoned CA2361809A1 (en) | 1999-02-05 | 2000-01-26 | Purification of natural gas by cryogenic separation |
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EP (1) | EP1153252A4 (en) |
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WO (1) | WO2000046559A1 (en) |
Cited By (2)
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1999
- 1999-02-05 US US09/245,570 patent/US6082133A/en not_active Expired - Lifetime
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2000
- 2000-01-26 EP EP00904562A patent/EP1153252A4/en not_active Withdrawn
- 2000-01-26 KR KR1020017009836A patent/KR20010101983A/en not_active Application Discontinuation
- 2000-01-26 CN CN00804607A patent/CN1342256A/en active Pending
- 2000-01-26 CA CA002361809A patent/CA2361809A1/en not_active Abandoned
- 2000-01-26 AU AU26299/00A patent/AU2629900A/en not_active Abandoned
- 2000-01-26 WO PCT/US2000/001857 patent/WO2000046559A1/en not_active Application Discontinuation
- 2000-01-26 MX MXPA01007954A patent/MXPA01007954A/en not_active Application Discontinuation
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
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US8329458B2 (en) | 2001-07-13 | 2012-12-11 | Co2 Solutions Inc. | Carbonic anhydrase bioreactor and process for CO2 containing gas effluent treatment |
US8329460B2 (en) | 2001-07-13 | 2012-12-11 | CO2 Solutions, Inc. | Carbonic anhydrase bioreactor and process |
US8329459B2 (en) | 2001-07-13 | 2012-12-11 | Co2 Solutions Inc. | Carbonic anhydrase system and process for CO2 containing gas effluent treatment |
US8066965B2 (en) | 2002-09-27 | 2011-11-29 | Co2 Solution Inc. | Process for recycling carbon dioxide emissions from power plants into carbonated species |
US8277769B2 (en) | 2002-09-27 | 2012-10-02 | Co2 Solutions Inc. | Process for treating carbon dioxide containing gas |
US8435479B2 (en) | 2002-09-27 | 2013-05-07 | Co2 Solutions Inc. | Process for treating carbon dioxide containing gas |
Also Published As
Publication number | Publication date |
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US6082133A (en) | 2000-07-04 |
KR20010101983A (en) | 2001-11-15 |
WO2000046559A1 (en) | 2000-08-10 |
CN1342256A (en) | 2002-03-27 |
AU2629900A (en) | 2000-08-25 |
EP1153252A4 (en) | 2003-05-21 |
MXPA01007954A (en) | 2003-07-14 |
EP1153252A1 (en) | 2001-11-14 |
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