Process and system for thermochemical conversion of biomass
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
C07C-001/00
C10L-003/00
B01J-008/00
출원번호
US-0718533
(2010-03-05)
등록번호
US-8541637
(2013-09-24)
발명자
/ 주소
Babicki, Matthew L.
Sellars, Brian G.
Keefer, Bowie G.
Ng, Edson
출원인 / 주소
G4 Insights Inc.
대리인 / 주소
Klarquist Sparkman, LLP
인용정보
피인용 횟수 :
13인용 특허 :
65
초록▼
A system and method for converting biomass into fluid hydrocarbon products to minimize the use of fossil fuels, provide energy and chemical feedstock security, and sustainable and/or carbon neutral electric power, are disclosed. For example, fast pyrolysis can be performed on biomass to produce pyga
A system and method for converting biomass into fluid hydrocarbon products to minimize the use of fossil fuels, provide energy and chemical feedstock security, and sustainable and/or carbon neutral electric power, are disclosed. For example, fast pyrolysis can be performed on biomass to produce pygas and char using a maximum processing temperature of about 650° C. The pygas is provided to an independent reactor without the addition of an oxidizing agent for catalytically converting the pygas to hydrocarbons using a maximum processing temperature of about 650° C. A system comprising fast pyrolysis means producing a pygas and char, independent catalytic conversion means downstream of the fast pyrolysis for converting the pygas to hydrocarbons, and a hydrogen source, external to the system and/or produced by a steam reformer by steam reformation of at least a portion of the hydrocarbons, coupled to catalytic conversion means, also are described.
대표청구항▼
1. A method for producing hydrocarbon from biomass, comprising: performing fast pyrolysis on biomass to produce pygas and char using a maximum processing temperature of about 650° C.; andproviding the pygas and hydrogen to an independent reactor without the addition of an oxidizing agent for catalyt
1. A method for producing hydrocarbon from biomass, comprising: performing fast pyrolysis on biomass to produce pygas and char using a maximum processing temperature of about 650° C.; andproviding the pygas and hydrogen to an independent reactor without the addition of an oxidizing agent for catalytically converting the pygas to hydrocarbons using a maximum processing temperature of about 650° C., where both performing fast pyrolysis and catalytically converting the pygas to hydrocarbon minimizes tar production to less than about 1% of biomass processed relative to amount of tar produced from that biomass. 2. The method according to claim 1 where at least a portion of the hydrogen is added from an external source. 3. The method according to claim 1 where at least a portion of the hydrogen is produced by steam reformation of at least a portion of the hydrocarbons. 4. The method according to claim 3 where the steam produced while catalytically converting the pygas to hydrocarbons is used for the steam reformation. 5. The method according to claim 1 where performing fast pyrolysis comprises producing a char product and where char contact time with the pygas is less than about 5 seconds. 6. The method according to claim 1 where performing fast pyrolysis comprises using a sweep gas comprising hydrogen. 7. The method according to claim 1 where catalytically converting the pygas to hydrocarbons comprises using a stoichiometric ratio of hydrogen over biomass of over 0.5. 8. The method according to claim 1 where catalytically converting the pygas to hydrocarbons comprises using a total atomic hydrogen-to-carbon ratio of gas in the reactor of over 4. 9. The method according to claim 1 where catalytically converting the pygas to hydrocarbons comprises using a catalyst, and the catalyst contact time with the pygas is less than 60 minutes. 10. The method according to claim 1 where performing fast pyrolysis and catalytically converting the pygas to hydrocarbons comprises using a hydrogen partial pressure of from about 0.5 bar to about 100 bar. 11. The method according to claim 1 comprising using a system comprising a biomass pyrolyzer, an independent catalytic converter downstream of the pyrolyzer, and a product purifier downstream of the catalytic converter. 12. The method according to claim 11 where the system further comprises a mineral oil heat exchanger and/or a condenser cooler and/or a pressure swing adsorber downstream of the catalytic converter. 13. The method according to claim 1 where performing fast pyrolysis and catalytically converting the pygas to hydrocarbons comprises using a process pressure between 2 bara to 100 bara. 14. The method according to claim 1 where catalytically converting the pygas to hydrocarbons comprises using an independent reactor and optionally one or more of a guard bed, a single catalyst, multiple catalysts, catalysts incorporating selective hydrocarbon forming catalyst and a support active for cracking oxygenated hydrocarbons, an operation temperature less than about 650° C., a depolymerization section, a hydrodeoxidation section, a moving bed, fixed beds with valving, a catalyst decoker, and any and all combinations thereof. 15. The method according to claim 14 where catalytically converting the pygas to hydrocarbons comprises using a methane-forming catalyst. 16. The method according to claim 15 where the catalyst is nickel on alumina. 17. The method according to claim 14 where the catalyst is a light hydrocarbon forming catalyst. 18. The method according to claim 1 where performing fast pyrolysis and catalytically converting the pygas to hydrocarbons comprises using one or more of an operating pressure of less than 100 bara, an operating temperature of between 400° C. and 650° C., a sweep gas, a moving bed, an auger transport mechanism, a char contact time less than 5 seconds, a stoichiometric ratio of hydrogen over biomass of over 0.5, a hydrogen partial pressure of from about 0.5 bar to about 100 bar, heating media, catalyst cooling, multiple heating vessels operating in staggered phase, gas-solid separators operating above 350° C., and any and all combinations thereof. 19. The method according to claim 1 where performing fast pyrolysis comprises using heating media. 20. The method according to claim 19 where the heating media has a heat capacity greater than 0.3 cal/cm3/K, a weight ratio of heating media to biomass of at least 5:1, a temperature drop following contacting biomass of less than 100° C., and any and all combinations thereof. 21. The method according to claim 19 where the heating media comprises steel or magnetite. 22. The method according to claim 1 where the method comprises fast pyrolysis, independent catalytic conversion and hydrogen recycle. 23. The method according to claim 1 further comprising using char from the pyrolysis process to heat a hydrogen generating reformer. 24. The method according to claim 1 where the method comprises using a product purifier export-to-feed hydrocarbon ratio for controlling hydrogen stoichiometric ratio in the conversion reactor. 25. A method for producing hydrocarbon from biomass that minimizes tar production to less than about 1% of biomass processed relative to amount of tar produced by that biomass, the method comprising: performing fast pyrolysis on biomass to produce pygas and char using a maximum processing temperature of about 650° C. and a sweep gas comprising hydrogen;providing the pygas to an independent reactor without addition of an oxidant for catalytically converting the pygas to hydrocarbons using a maximum processing temperature of about 650° C.;whereby catalytically converting the pygas to hydrocarbons comprises using a stoichiometric ratio of hydrogen over biomass of over 0.5, and a hydrogen partial pressure of from about 0.5 bar to about 100 bar. 26. The method according to claim 25 further comprising adding hydrogen to the independent reactor. 27. The method according to claim 26 where at least a portion of the hydrogen is added from a source external to the system. 28. The method according to claim 26 where at least a portion of the hydrogen is produced by steam reformation of at least a portion of the hydrocarbons where the steam is produced during production of the pygas. 29. A system for producing hydrocarbons from biomass that minimizes tar production to less than about 1% based on mass of biomass processed and amount of tar produced, the system comprising: fast pyrolysis means operating at a process temperature of less than 650° C. for producing a pygas and char;independent catalytic conversion means downstream of the fast pyrolysis means operating at a process temperature of less than 650° C. for converting the pygas to hydrocarbons; anda hydrogen source for adding hydrogen to the independent catalytic conversion means. 30. The system according to claim 29 where the hydrogen is produced by a steam reformer by steam reformation of at least a portion of the hydrocarbons. 31. The system according to claim 29 where the fast pyrolysis means includes a hydrogen sweep gas. 32. The system according to claim 29 where the fast pyrolysis means and catalytic conversion means operate at one or more of a stoichiometric ratio of hydrogen over biomass of over 0.5, a total atomic hydrogen-to-carbon ratio of gas in the reactor of over 4, and a hydrogen partial pressure between 0.5 bar to 100 bar in both the fast pyrolysis means and the catalytic conversion means. 33. The system according to claim 29 further comprising tar minimization means downstream of the catalytic conversion means. 34. The system according to claim 33 where the tar minimization means comprises a mineral oil heat exchanger operating with a high boiling fraction of a paraffinic hydrocarbon mixture and an oil separator. 35. The system according to claim 29 operating at a pressure between 2 bara to 100 bara. 36. The system according to claim 29 where the independent catalytic conversion means optionally includes one or more of a guard bed, a single catalyst, multiple catalysts, catalysts incorporating selective hydrocarbon forming catalyst and a support active for cracking oxygenated hydrocarbons, a depolymerization section, a hydrodeoxidation section, a moving bed, fixed beds with valving, catalyst decoker, and any and all combinations thereof. 37. The system according to claim 36 where the catalyst is a methane-forming catalyst. 38. The system according to claim 36 where the catalyst is a light hydrocarbon forming catalyst. 39. The system according to claim 26 where fast pyrolysis means operates at or includes one or more of an operating pressure of less than 100 bara, an operating temperature of between 400° C. and 650° C., a sweep gas, a moving bed, an auger transport mechanism, a char contact time less than 5 seconds, a hydrogen partial pressure between 0.5 bar to 100 bar, heating media, a heated media contact temperature of less than 650° C., and any and all combinations thereof. 40. The system according to claim 29 where the fast pyrolysis means includes heating media, heating media having a heat capacity greater than 0.3 cal/cm3/K, a weight ratio of heating media to biomass is at least 5:1, and any and all combinations thereof. 41. The system according to claim 40 where the heating media is steel or magnetite. 42. The system according to claim 40 where the heating media is magnetic magnetite particles and the magnetic properties are used in a char separator. 43. The system according to claim 40 where the heating media is magnetic magnetite particles and a steam iron process is utilized to generate hydrogen in a pyrolysis section. 44. The system according to claim 29 where at least a portion of the hydrocarbons is exported as a renewable, sustainable and/or carbon neutral fuel and/or feedstock. 45. The system according to claim 44 where exported hydrocarbons are used for producing renewable, sustainable and/or carbon neutral electric power. 46. A system for producing hydrocarbons from biomass that minimizes tar production to less than about 1% based on mass of biomass processed and amount of tar produced, the system comprising: a biomass fast pyrolyzer operating at a process temperature of less than 650° C. and using a sweep gas comprising hydrogen for producing a pygas and char, the pyrolyzer including heating media;an independent catalytic converter downstream of the fast pyrolyzer operating at a process temperature of less than 650° C. and without addition of an oxidant for converting the pygas to hydrocarbons;a hydrogen source;whereby catalytically converting the pygas to hydrocarbons comprises using a stoichiometric ratio of hydrogen over biomass of over 0.5, and a hydrogen partial pressure of from about 0.5 bar to about 100 bar. 47. A system operating at a pressure between 2 bara to 100 bara for producing hydrocarbons from biomass that minimizes tar production to less than about 1% based on mass of biomass processed and amount of tar produced, the system comprising: a biomass fast pyrolyzer operating at a process temperature of less than 650° C. and using a sweep gas comprising hydrogen for producing a pygas and char;an independent catalytic converter downstream of the fast pyrolyzer operating at a process temperature of less than 650° C. for converting the pygas to hydrocarbons;a steam reformer fluidly coupled to the catalytic converter for producing hydrogen from at least a portion of the hydrocarbons; andwhereby performing fast pyrolysis and catalytically converting the pygas to hydrocarbon comprise using a stoichiometric ratio of hydrogen over biomass of over 0.5, and a hydrogen partial pressure of from about 0.5 bar to about 100 bar. 48. A system operating at a pressure between 2 bara to 100 bara for producing hydrocarbons from biomass that minimizes tar production to less than about 1% based on mass of biomass processed and amount of tar produced, the system comprising: a biomass fast pyrolyzer operating at a process temperature of less than 650° C. and using a hydrogen containing sweep gas for producing a pygas and char;an independent catalytic converter downstream of the fast pyrolyzer for converting the pygas to hydrocarbons;a product purifier downstream of the catalytic converter for withdrawing a portion of the hydrocarbons for export;a steam reformer fluidly coupled to the product purifier for producing hydrogen from at least a portion of the hydrocarbons; andwhereby performing catalytically converting the pygas to hydrocarbon comprise using a stoichiometric ratio of hydrogen over biomass of over 0.5, and a hydrogen partial pressure of from about 0.5 bar to about 100 bar. 49. The system according to claim 48 whereby performing product purification comprises recycling excess hydrogen back to the fast pyrolyzer and catalytic converter. 50. A process for hydrogenating a material in a conversion reactor, comprising: hydrogenating a first portion of the material in a conversion reactor to produce a hydrogenated product;separating a portion of the hydrogenated product in a separator downstream of the conversion reactor to provide a separated hydrogenated product portion; andrecycling residual hydrogen and remaining hydrogenated material back to the conversion reactor, where the separated hydrogenated product portion is selected to control a hydrogen-to-material ratio in the conversion reactor.
연구과제 타임라인
LOADING...
LOADING...
LOADING...
LOADING...
LOADING...
이 특허에 인용된 특허 (65)
Kumar Ravi (Allentown PA) Naheiri Tarik (Bath PA) Watson Charles F. (Orefield PA), Adsorption process with mixed repressurization and purge/equalization.
Lasley, Andrew J.; Fattic, Gerald Thomas; Rajashekara, Kaushik, Apparatus and method for steam engine and thermionic emission based power generation system.
Sanger Robert J. ; Towler Gavin P. ; Doshi Kishore J. ; Vanden Bussche Kurt M. ; Senetar John J., Apparatus for providing a pure hydrogen stream for use with fuel cells.
Gaffney Thomas Richard ; Golden Timothy Christopher ; Mayorga Steven Gerard ; Brzozowski Jeffrey Richard ; Taylor Fred William, Carbon dioxide pressure swing adsorption process using modified alumina adsorbents.
Cortright, Randy D.; Dumesic, James A., Method for producing bio-fuel that integrates heat from carbon-carbon bond-forming reactions to drive biomass gasification reactions.
Dandekar Hemant W. (Chicago IL) Funk Gregory A. (Carol Stream IL) Swift John D. (Hindhead NY GB2) Maurer Richard T. (Nanuet NY), PSA process with reaction for reversible reactions.
Diebold James P. (Lakewood CO) Scahill John W. (Evergreen CO) Chum Helena L. (Arvada CO) Evans Robert J. (Lakewood CO) Rejai Bahman (Lakewood CO) Bain Richard L. (Golden CO) Overend Ralph P. (Lakewoo, Process to convert biomass and refuse derived fuel to ethers and/or alcohols.
Spilker, Kerry K.; Vogel, Roger; Stevens, James F.; Ricci, Peter C., Selective, integrated processing of bio-derived ester species to yield low molecular weight hydrocarbons and hydrogen for the production of biofuels.
Spilker, Kerry K.; Vogel, Roger; Stevens, James F.; Ricci, Peter C., Selective, integrated processing of bio-derived ester species to yield low molecular weight hydrocarbons and hydrogen for the production of biofuels.
Wilkinson David P. (Vancouver CAX) Voss Henry H. (West Vancouver CAX) Watkins David S. (Coquitlam CAX) Prater Keith B. (Vancouver CAX), Solid polymer fuel cell systems incorporating water removal at the anode.
Watson Charles F. (Orefield PA) Whitley Roger D. (Allentown PA) Agrawal Rakesh (Emmaus PA) Kumar Ravi (Allentown PA), Vacuum swing adsorption process with mixed repressurization and provide product depressurization.
Weaver, Samuel C.; Hensley, Daniel L.; Weaver, Samuel P.; Weaver, Daniel C., Methods, systems, and devices for continuous liquid fuel production from biomass.
Weaver, Samuel C.; Hensley, Daniel L.; Weaver, Samuel P.; Weaver, Daniel C.; Smith, Lee S., Methods, systems, and devices for liquid hydrocarbon fuel production, hydrocarbon chemical production, and aerosol capture.
Weaver, Samuel C.; Hensley, Daniel L.; Weaver, Samuel P.; Weaver, Daniel C.; Smith, Lee S., Systems, and devices for liquid hydrocarbon fuel production, hydrocarbon chemical production, and aerosol capture.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.