Introduction of mesoporosity in low Si/Al zeolites
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
B01J-029/08
C01B-039/02
출원번호
US-0911558
(2013-06-06)
등록번호
US-9295980
(2016-03-29)
발명자
/ 주소
Garcia-Martinez, Javier
Johnson, Marvin M.
Valla, Ioulia
출원인 / 주소
Rive Technology, Inc.
대리인 / 주소
Hovey Williams LLP
인용정보
피인용 횟수 :
1인용 특허 :
156
초록
Compositions and methods for preparing mesoporous materials from low Si/Al ratio zeolites. Such compositions can be prepared by acid wash and/or isomorphic substitution pretreatment of low Si/Al ratio zeolites prior to introduction of mesoporosity.
대표청구항▼
1. A method of forming a material comprising at least one mesoporous zeolite, said method comprising the steps of: (a) acid washing a non-mesoporous initial zeolite with an acidic medium thereby forming an acid-washed zeolite, wherein said initial zeolite has a total silicon-to-aluminum (Si/Al) rati
1. A method of forming a material comprising at least one mesoporous zeolite, said method comprising the steps of: (a) acid washing a non-mesoporous initial zeolite with an acidic medium thereby forming an acid-washed zeolite, wherein said initial zeolite has a total silicon-to-aluminum (Si/Al) ratio of less than 30, wherein said acid washing of step (a) removes aluminum atoms from said initial zeolite such that said acid-washed zeolite has a higher Si/Al ratio than said initial zeolite, wherein said acidic medium does not comprise hydrofluoric acid; and(b) subsequent to step (a), contacting said acid-washed zeolite with a mesopore-forming medium different than said acidic medium thereby forming at least one mesopore within said acid-washed zeolite and providing said mesoporous zeolite. 2. The method of claim 1, wherein said initial zeolite has a Si/Al of less than 10. 3. The method of claim 1, wherein said acidic medium comprises at least one acid selected from the group consisting of chlorhidric acid, sulphuric acid, nitric acid, acetic acid, sulfonic acid, oxalic acid, ethylenediaminetetraacetic acid (EDTA), citric acid, and combinations thereof. 4. The method of claim 1, wherein said acid-washed zeolite has at least 1 percent fewer Si—O—Al bonds than said initial zeolite. 5. The method of claim 1, wherein said acid-washed zeolite has a greater number of Si—OH and/or Al—OH terminal groups than said initial zeolite. 6. The method of claim 1, wherein the total pore volume of said mesoporous zeolite is greater than the total pore volume of said acid-washed zeolite. 7. The method of claim 1, wherein said mesoporous zeolite has an increased mesoporosity and a decreased microporosity relative to said acid-washed zeolite. 8. The method of claim 1, wherein said initial zeolite has a total 20 to 80 Å diameter mesopore volume of less than 0.05 cc/g, wherein said mesoporous zeolite has a total 20 to 80 Å diameter mesopore volume of at least 0.1 cc/g. 9. The method of claim 8, wherein the total 1 to 20 Å diameter micropore volume of said mesoporous zeolite is less than the total 1 to 20 Å diameter micropore volume of said acid-washed zeolite. 10. The method of claim 9, wherein said initial zeolite has a total 1 to 20 Å diameter micropore volume of at least 0.3 cc/g. 11. The method of claim 1, wherein said initial zeolite has an average unit cell size of at least 24.40 Å and said acid-washed zeolite has an average unit cell size of at least 24.35 Å. 12. The method of claim 1, wherein said mesoporous zeolite is a mesostructured zeolite, a one-phase hybrid single crystal having long-range crystallinity. 13. The method of claim 1, wherein said acid washing is performed at a temperature of not more than 100° C., wherein said acid washing is performed for a time period of not more than 12 hours. 14. The method of claim 1, wherein said acidic medium comprises an acid that is present in an amount in the range of from about 1 to about 10 milliequivalents per gram of initial zeolite. 15. The method of claim 1, wherein said acidic medium comprises a chelating agent. 16. The method of claim 15, wherein said chelating agent is selected from the group consisting of oxalic acid, citric acid, and ethylenediaminetetraacetic acid (EDTA). 17. The method of claim 1, wherein said acidic medium is in liquid form during said acid-washing. 18. The method of claim 1, wherein said mesopore-forming medium is basic. 19. The method of claim 18, wherein said mesopore-forming medium comprises at least one surfactant. 20. The method of claim 1, further comprising, prior to said contacting of step (b), drying said acid-washed zeolite at a drying temperature greater than 20° C. for a drying time greater than 1 hour. 21. The method of claim 1, further comprising realuminating said mesoporous zeolite to thereby lower the Si/Al ratio of said mesoporous zeolite. 22. The method of claim 1, further comprising blending said mesoporous zeolite with a binder, a matrix, and/or an additive to thereby form a blended material, further comprising shaping said blended material into a catalyst composition. 23. The method of claim 1, wherein said material is a catalyst composition. 24. The method of claim 23, wherein said catalyst composition is a cracking catalyst. 25. The method of claim 24, wherein said cracking catalyst is a fluid catalytic cracking (FCC) catalyst. 26. A method of forming a material comprising at least one mesoporous zeolite, said method comprising the steps of: (a) contacting an initial zeolite with an acidic medium to thereby form an acid-treated zeolite, wherein said initial zeolite has a total silicon-to-aluminum (Si/Al) ratio of less than 15, wherein said acidic medium does not comprise hydrofluoric acid; and(b) subsequent to step (a), forming at least one mesopore within said non-mesoporous acid-treated zeolite thereby forming a mesoporous zeolite. 27. The method of claim 26, wherein said acidic medium comprises at least one acid selected from the group consisting of chlorhidric acid, sulphuric acid, nitric acid, acetic acid, sulfonic acid, oxalic acid, ethylenediaminetetraacetic acid (EDTA), citric acid, and combinations thereof. 28. The method of claim 26, wherein said acidic medium comprises an acid that is present in an amount in the range of from about 1 to about 10 milliequivalents per gram of initial zeolite. 29. The method of claim 26, wherein said acidic medium comprises a chelating agent. 30. The method of claim 26, wherein said contacting of step (a) is carried out at a temperature of not more than 100° C. and for a time period of not more than 12 hours. 31. The method of claim 26, wherein said contacting of step (a) removes aluminum atoms from said initial zeolite. 32. The method of claim 21, wherein said acid-treated zeolite has a higher Si/Al ratio than said initial zeolite. 33. The method of claim 26, wherein said initial zeolite has a total silicon-to-aluminum ratio (Si/Al) of less than 10. 34. The method of claim 26, wherein said mesoporous zeolite has an increased mesoporosity and a decreased microporosity relative to said acid-treated zeolite. 35. The method of claim 26, wherein said initial zeolite has a total 20 to 80 Å diameter mesopore volume of less than 0.05 cc/g, wherein said mesoporous zeolite has a total 20 to 80 Å diameter mesopore volume of at least 0.1 cc/g. 36. The method of claim 26, wherein said initial zeolite has an average unit cell size of at least 24.40 Å and said acid-treated zeolite has an average unit cell size of at least 24.35 Å. 37. The method of claim 26, wherein said acid-treated zeolite has at least 1 percent fewer Si—O—Al bonds than said initial zeolite. 38. The method of claim 26, wherein said acid-treated zeolite has a greater number of Si—OH and/or Al—OH terminal groups than said initial zeolite. 39. The method of claim 26, wherein said forming of step (b) comprises contacting said acid-treated zeolite with a medium comprising at least one base. 40. The method of claim 39, wherein said medium further comprises at least one surfactant. 41. The method of claim 26, wherein said acidic medium is in liquid form during said contacting. 42. A method of forming a mesoporous zeolite, said method comprising: (a) contacting an initial zeolite an with an acidic medium to thereby form an acid-treated zeolite, wherein said initial zeolite has a total silicon-to-aluminum (Si/Al) ratio of less than 10, wherein said contacting of step (a) removes aluminum atoms from said initial zeolite such that said acid-treated zeolite has a higher Si/Al ratio than said initial zeolite, wherein said acidic medium does not comprise hydrofluoric acid; and(b) subsequent to step (a), contacting said acid-treated zeolite with a basic medium to thereby provide a base-treated zeolite having have an increased volume of 20 to 80 Å diameter mesopores relative to said acid-treated zeolite, wherein said base-treated zeolite has a total 20 to 80 Å diameter mesopore volume of at least 0.1 cc/g. 43. The method of claim 42, wherein said initial zeolite has a total 20 to 80 Å diameter mesopore volume of less than 0.05 cc/g. 44. The method of claim 42, wherein the total 1 to 20 Å diameter micropore volume of said base-treated is less than the total 1 to 20 Å diameter micropore volume of said acid-treated zeolite. 45. The method of claim 44, wherein said initial zeolite has a total 1 to 20 Å diameter micropore volume of at least 0.3 cc/g. 46. The method of claim 43, wherein said initial zeolite has an average unit cell size of at least 24.40 Å and said acid-treated zeolite has an average unit cell size of at least 24.35 Å. 47. The method of claim 42, wherein said acidic medium comprises an acid that is present in an amount in the range of from about 1 to about 10 milliequivalents per gram of initial zeolite. 48. The method of claim 42, wherein said acidic medium comprises at least one acid selected from the group consisting of chlorhidric acid, sulphuric acid, nitric acid, acetic acid, sulfonic acid, oxalic acid, ethylenediaminetetraacetic acid (EDTA), citric acid, and combinations thereof. 49. The method of claim 42, wherein said acidic medium comprises a chelating agent. 50. The method of claim 42, wherein said initial zeolite has an extra-framework aluminum content of 25% to 100%. 51. The method of claim 42, wherein said acid-treated zeolite has at least 1 percent fewer Si—O—Al bonds than said initial zeolite. 52. The method of claim 42, wherein said acid-treated zeolite has a greater number of Si—OH and/or Al—OH terminal groups than said initial zeolite. 53. The method of claim 42, wherein said basic medium comprises a pore forming agent. 54. The method of claim 53, wherein said pore forming agent comprises a surfactant. 55. The method of claim 42, wherein said acidic medium is in liquid form during said contacting of step (a). 56. A method of forming a mesoporous zeolite material, said method comprising: (a) providing an initial zeolite material;(b) contacting said initial zeolite material with an acid solution to provide an acid-treated zeolite material, wherein said acid solution comprises at least one chelating agent, wherein said acid solution does not comprise hydrofluoric acid; and(c) further treating said acid-treated zeolite material under conditions sufficient to form at least one mesopore within the acid-treated zeolite material to thereby provide a mesoporous zeolite material. 57. The method of claim 56, wherein said chelating agent is an acid. 58. The method of claim 56, wherein said acid solution comprises at least one ammonium salt of a weak acid. 59. The method of claim 56, wherein said acid solution comprises at least one mineral acid. 60. The method of claim 59, wherein said acid solution comprises at least one organic acid. 61. The method of claim 56, wherein said acid solution comprises sulfuric acid. 62. The method of claim 56, wherein said acid solution comprises an acid that is present in an amount in the range of from about 1.5 to about 4 milliequivalents per gram of initial zeolite material. 63. The method of claim 56, wherein said initial zeolite material is a fully crystalline material having a total 20 to 80 Å diameter mesopore volume of less than 0.05 cc/g and a total 1 to 20 Å diameter micropore volume of at least 0.3 cc/g. 64. The method of claim 56, wherein said further treating of step (c) comprises contacting at least a portion of said acid-treated zeolite material with a basic medium. 65. The method of claim 64, wherein said further treating of step (c) comprises contacting at least a portion of said acid-treated zeolite material with a pore forming agent. 66. The method of claim 56, wherein said mesoporous zeolite material is a fully crystalline zeolite material comprising a plurality of mesopore surfaces that define a plurality of mesopores within the zeolite crystalline structure. 67. The method of claim 56, wherein said mesoporous zeolite material is a one-phase hybrid mesostructured crystalline zeolite material. 68. The method of claim 56, wherein said mesoporous zeolite material has a total 1 to 20 Å diameter micropore volume of less than 1.0 cc/g and a total 20 to 80 Å diameter mesopore volume of at least 0.05 cc/g. 69. The method of claim 56, wherein the mesoporous zeolite material has an average unit cell size of at least 24.30 Å. 70. The method of claim 56, further comprising subsequent to said further treating of step (c), chemically modifying at least a portion of said mesoporous zeolite material to provide a chemically-modified mesoporous zeolite material.
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