Use of metal supported copper catalysts for reforming alcohols
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
H01M-008/04
C07C-045/51
출원번호
UP-0687541
(2003-10-16)
등록번호
US-7682724
(2010-04-21)
발명자
/ 주소
Morgenstern, David A.
출원인 / 주소
Monsanto Technology LLC
대리인 / 주소
Senniger Powers LLP
인용정보
피인용 횟수 :
2인용 특허 :
35
초록▼
This invention is directed to a process for reforming an alcohol. The process comprises contacting an alcohol with a reforming catalyst comprising copper at the surface of a metal supporting structure, preferably a metal sponge supporting structure comprising nickel. In a certain preferred embodimen
This invention is directed to a process for reforming an alcohol. The process comprises contacting an alcohol with a reforming catalyst comprising copper at the surface of a metal supporting structure, preferably a metal sponge supporting structure comprising nickel. In a certain preferred embodiment, hydrogen produced by the reforming process is used as a fuel source for a hydrogen fuel cell to generate electric power, particularly for driving a vehicle.
대표청구항▼
What is claimed is: 1. A process for reforming an alcohol, the process comprising: contacting a feed gas mixture comprising an alcohol with a reforming catalyst to produce a reforming product mixture comprising hydrogen, the reforming catalyst comprising a metal sponge supporting structure and a co
What is claimed is: 1. A process for reforming an alcohol, the process comprising: contacting a feed gas mixture comprising an alcohol with a reforming catalyst to produce a reforming product mixture comprising hydrogen, the reforming catalyst comprising a metal sponge supporting structure and a copper coating at least partially covering the surface of the metal sponge supporting structure, wherein the metal sponge supporting structure is prepared by a process comprising leaching aluminum from an alloy comprising aluminum and a base metal. 2. A process as set forth in claim 1, wherein the feed gas mixture comprises a primary alcohol selected from the group consisting of methanol, ethanol and mixtures thereof. 3. A process as set forth in claim 2, wherein the process further comprises introducing hydrogen from the reforming product mixture and oxygen into a fuel cell to produce electric power. 4. A process as set forth in claim 1, wherein the reforming catalyst has a surface area of from about 10 m2/g to about 100 m2/g as measured by the Brunauer-Emmett-Teller method. 5. A process as set forth in claim 4, wherein the reforming catalyst has a surface area of from about 25 m2/g to about 100 m2/g as measured by the Brunauer-Emmett-Teller method. 6. A process as set forth in claim 5, wherein the reforming catalyst has a surface area of from about 30 m2/g to about 80 m2/g as measured by the Brunauer-Emmett-Teller method. 7. A process as set forth in claim 1, wherein the reforming catalyst comprises at least about 10% by weight copper. 8. A process as set forth in claim 1, wherein the reforming catalyst comprises from about 10% to about 90% by weight copper. 9. A process as set forth in claim 1, wherein the metal sponge supporting structure of the reforming catalyst has a surface area of at least about 10 m2/g as measured by the Brunauer-Emmett-Teller method. 10. A process as set forth in claim 9, wherein the metal sponge supporting structure of the reforming catalyst has a surface area of at least about 50 m2/g as measured by the Brunauer-Emmett-Teller method. 11. A process as set forth in claim 10, wherein the metal sponge supporting structure of the reforming catalyst has a surface area of at least about 70 m2/g as measured by the Brunauer-Emmett-Teller method. 12. A process as set forth in claim 9, wherein the metal sponge supporting structure comprises nickel. 13. A process as set forth in claim 12, wherein the metal sponge supporting structure comprises at least about 50% by weight nickel. 14. A process as set forth in claim 13, wherein the metal sponge supporting structure comprises at least about 85% by weight nickel. 15. A process as set forth in claim 12, wherein the reforming catalyst comprises from about 10% to about 80% by weight copper. 16. A process as set forth in claim 15, wherein the reforming catalyst comprises from about 20% to about 45% by weight copper. 17. A process as set forth in claim 12, wherein the reforming catalyst comprises from about 5 to about 100 μmol/g of nickel at the surface of said catalyst. 18. A process as set forth in claim 17, wherein the reforming catalyst comprises from about 10 to about 80 μmol/g of nickel at the surface of said catalyst. 19. A process as set forth in claim 18, wherein the reforming catalyst comprises from about 15 to about 75 μmol/g of nickel at the surface of said catalyst. 20. A process as set forth in claim 12, wherein the feed gas mixture comprises a primary alcohol selected from the group consisting of methanol, ethanol and mixtures thereof. 21. A process as set forth in claim 20, wherein the feed gas mixture comprises ethanol. 22. A process as set forth in claim 21 wherein the reforming product mixture comprises methane. 23. A process as set forth in claim 22 comprising feeding methane obtained in the reforming product mixture to an internal combustion engine. 24. A process as set forth in claim 22 comprising feeding hydrogen obtained in the reforming product mixture to an internal combustion engine. 25. A process as set forth in claim 12, wherein the process further comprises introducing hydrogen from the reforming product mixture and oxygen into a fuel cell to produce electric power. 26. A process as set forth in claim 1, wherein said feed gas mixture is contacted with said reforming catalyst at a temperature below about 400° C. 27. A process as set forth in claim 1, wherein said feed gas mixture is contacted with said reforming catalyst at a temperature of from about 200° C. to about 375° C. 28. A process as set forth in claim 27, wherein said feed gas mixture is contacted with said reforming catalyst at a temperature of from about 250° C. to about 325° C. 29. A process as set forth in claim 1, wherein the reforming catalyst is incorporated onto the surface of a pellet or a monolith substrate. 30. A process as set forth in claim 29, wherein the reforming catalyst comprises a nickel sponge supporting structure. 31. A process as set forth in claim 1 wherein preparation of the reforming catalyst comprises depositing copper onto the metal sponge supporting structure. 32. A process as set forth in claim 31 wherein copper is deposited by a method comprising electrochemical displacement reaction between a metal of the metal sponge supporting structure and copper ions. 33. A process as set forth in claim 31 wherein copper is deposited by a method comprising electroless plating of copper metal on the metal sponge supporting structure. 34. A process as set forth in claim 1 wherein the base metal comprises copper and/or a non-copper metal selected from the group consisting of nickel, cobalt, zinc, silver, palladium, gold, tin, iron and mixtures thereof. 35. A process as set forth in claim 34 wherein the base metal comprises copper and/or a non-copper metal selected from the group consisting of nickel, cobalt and mixtures thereof. 36. A process as set forth in claim 35, wherein the base metal comprises nickel. 37. A process for reforming ethanol, the process comprising contacting a feed gas mixture comprising ethanol with a reforming catalyst at a temperature below about 400° C. to produce a reforming product mixture comprising hydrogen, said reforming catalyst comprising copper on the surface of a metal supporting structure. 38. A process as set forth in claim 37, wherein said feed gas mixture is contacted with said reforming catalyst at a temperature of from about 250° C. to about 300° C. 39. A process as set forth in claim 37, wherein the reforming catalyst has a thermal conductivity at 300K of at least about 50 W/m·K. 40. A process as set forth in claim 39, wherein the reforming catalyst has a thermal conductivity at 300K of at least about 70 W/m·K. 41. A process as set forth in claim 40, wherein the reforming catalyst has a thermal conductivity at 300K of at least about 90 W/m·K. 42. A process as set forth in claim 37, wherein the process further comprises introducing hydrogen from the reforming product mixture and oxygen into a fuel cell to produce electric power. 43. A process as set forth in claim 37, wherein the reforming catalyst has a surface area of from about 10 m2/g to about 100 m2/g as measured by the Brunauer-Emmett-Teller method. 44. A process as set forth in claim 43, wherein the reforming catalyst has a surface area of from about 25 m2/g to about 100 m2/g as measured by the Brunauer-Emmett-Teller method. 45. A process as set forth in claim 44, wherein the reforming catalyst has a surface area of from about 30 m2/g to about 80 m2/g as measured by the Brunauer-Emmett-Teller method. 46. A process as set forth in claim 37, wherein the reforming catalyst comprises at least about 10% by weight copper. 47. A process as set forth in claim 46, wherein the reforming catalyst comprises from about 10% to about 90% by weight copper. 48. A process as set forth in claim 37, wherein the metal supporting structure comprises a metal sponge. 49. A process as set forth in claim 48 wherein the metal sponge supporting structure is prepared by a process comprising leaching aluminum from an alloy comprising aluminum and a base metal. 50. A process as set forth in claim 49 wherein the base metal comprises copper and/or a non-copper metal selected from the group consisting of nickel, cobalt, zinc, silver, palladium, gold, tin, iron and mixtures thereof. 51. A process as set forth in claim 50 wherein the base metal comprises copper and/or a non-copper metal selected from the group consisting of nickel, cobalt and mixtures thereof. 52. A process as set forth in claim 51 wherein the base metal comprises nickel. 53. A process as set forth in claim 48 wherein the reforming catalyst comprises a copper coating at least partially covering the surface of the metal sponge supporting structure. 54. A process as set forth in claim 53 wherein preparation of the reforming catalyst comprises depositing copper onto the metal sponge supporting structure. 55. A process as set forth in claim 54 wherein copper is deposited by a method comprising electrochemical displacement reaction between a metal of the metal sponge supporting structure and copper ions. 56. A process as set forth in claim 54 wherein copper is deposited by a method comprising electroless plating of copper metal on the metal sponge supporting structure. 57. A process as set forth in claim 48, wherein the metal sponge supporting structure of the reforming catalyst has a surface area of at least about 10 m2/g as measured by the Brunauer-Emmett-Teller method. 58. A process as set forth in claim 57, wherein the metal sponge supporting structure of the reforming catalyst has a surface area of at least about 50 m2/g as measured by the Brunauer-Emmett-Teller method. 59. A process as set forth in claim 58, wherein the metal sponge supporting structure of the reforming catalyst has a surface area of at least about 70 m2/g as measured by the Brunauer-Emmett-Teller method. 60. A process as set forth in claim 48, wherein the metal sponge supporting structure comprises nickel. 61. A process as set forth in claim 60, wherein the metal sponge supporting structure comprises at least about 50% by weight nickel. 62. A process as set forth in claim 61, wherein the metal sponge supporting structure comprises at least about 85% by weight nickel. 63. A process as set forth in claim 60, wherein the reforming catalyst comprises from about 10% to about 80% by weight copper. 64. A process as set forth in claim 63, wherein the reforming catalyst comprises from about 20% to about 45% by weight copper. 65. A process as set forth in claim 60, wherein the reforming catalyst comprises from about 5 to about 100 μmol/g of nickel at the surface of said catalyst. 66. A process as set forth in claim 65, wherein the reforming catalyst comprises from about 10 to about 80 μmol/g of nickel at the surface of said catalyst. 67. A process as set forth in claim 66, wherein the reforming catalyst comprises from about 15 to about 75 μmol/g of nickel at the surface of said catalyst. 68. A process as set forth in claim 60, wherein the process further comprises introducing hydrogen from the reforming product mixture and oxygen into a fuel cell to produce electric power. 69. A process as set forth in claim 37, wherein the reforming catalyst is incorporated onto the surface of a pellet or a monolith substrate. 70. A process as set forth in claim 69, wherein the reforming catalyst comprises a nickel sponge supporting structure. 71. A process as set forth in claim 37 wherein the reforming product mixture comprises methane. 72. A process as set forth in claim 71 comprising feeding methane obtained in the reforming product mixture to an internal combustion engine. 73. A process as set forth in claim 71 comprising feeding hydrogen obtained in the reforming product mixture to an internal combustion engine.
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이 특허에 인용된 특허 (35)
Morgenstern, David A.; Arhancet, Juan P.; Berk, Howard C.; Moench, Jr., William L.; Peterson, James C., Catalyst for dehydrogenating primary alcohols to make carboxylic acid salts.
Schuetz Peter (Linsengericht DEX) Burmeister Roland (Geiselbach DEX) Despeyroux Bertrand (Fourgueux FRX) Moesinger Hans (Rodenbach DEX) Krause Helmfried (Rodenbach DEX) Deller Klaus (Hainburg DEX), Catalyst precursor for an activated raney metal fixed-bed catalyst, an activated raney metal fixed-bed catalyst and a pr.
Brannan James R. (Painesville OH) Malkin Irving (University Heights OH), Electrolysis cathodes bearing a melt-sprayed and leached nickel or cobalt coating.
David A. Morgenstern ; Juan P. Arhancet ; Howard C. Berk ; William L. Moench, Jr. ; James C. Peterson, Process and catalyst for dehydrogenating primary alcohols to make carboxylic acid salts.
Anderson, Kenneth B.; Carrado-Gregar, Kathleen; Marshall, Christopher L.; Segal, Scott R., Process for in-situ production of hydrogen (H2) by alcohol decomposition for emission reduction from internal combustion engines.
Patrick Bachinger DE; Berthold Keppeler DE; Oskar Lamla DE; Bernd Schoenrock DE; Martin Schuessler DE; Dagmar Waidelich DE, Process for manufacturing a catalyst body for generating hydrogen and a catalyst body for generating hydrogen.
Ebner Jerry R. (St. Peters MO) Franczyk Thaddeus S. (Maryland Heights MO), Process for preparing carboxylic acid salts and methods for making such catalysts and catalysts useful in such process.
Becker Hans-Joachim (Leverkusen DEX) Schmidt Walter (late of Leverkusen DEX by Hildegard Schmidt ; heiress), Reduction of aromatic nitro compounds with Raney nickel catalyst.
Autenrieth Rainer,DEX ; Heil Dietmar,DEX ; Weger Wolfgang,DEX ; Benz Uwe,DEX, Reforming reactor, particularly for the water vapor reforming of methanol.
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