IP Library Granted Patent US 7,528,289
Granted Patent B1
US 7,528,289 · App. 08/155,266 · Granted May 5, 2009

Isoparaffin-olefin alkylation

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Quick Facts
Patent No.
US 7,528,289
App. No.
08/155,266
Granted
May 5, 2009
Kind
B1
Abstract

A novel alkylation catalyst is described which is used in processes for alkylating olefin hydrocarbons with isoparaffin hydrocarbons to produce high octane alkylate products suitable for use as a blending component of gasoline motor fuel. The novel catalyst comprises a mixture of a hydrogen halide and a sulfone. The novel alkylation catalyst is utilized in a novel process for alkylating olefin hydrocarbons with isoparaffin hydrocarbons.

Claims (60)

1. A method of improving the quality of an alkylate product produced by an alkylation process including contacting a hydrocarbon mixture containing olefins and isoparaffins with a catalyst containing hydrogen fluoride to thereby produce said alkylate product, the method comprising the step of:

incorporating a sulfone into said catalyst in an amount such that the octane of said alkylate product is higher than said alkylate product produced when said catalyst contains no sulfone.

2. A method as recited in claim 1 wherein said amount of said sulfone incorporated into said catalyst is such that the weight ratio of hydrogen fluoride to sulfone in said catalyst is at least about 1:1.

3. A method as recited in claim 2 wherein said amount of said sulfone incorporated into said catalyst is such that the sulfone present in said catalyst is less than 30 weight percent.

4. A method as recited in claim 3 wherein said amount of said sulfone incorporated into said catalyst is such that the sulfone present in said catalyst is in the range of from 10 to 25 weight percent.

5. A method as recited in claim 4 wherein said sulfone is sulfolane.

6. A method of improving the quality of an alkylate product produced by an alkylation process including contacting a hydrocarbon mixture containing olefins and isoparaffins with a catalyst containing hydrogen fluoride to thereby produce said alkylate product, the method comprising the step of:

incorporating a sulfone into said catalyst in an amount such that the ratio of trimethylpentane to dimethylhexane in said alkylate product is higher than said alkylate product produced when said catalyst contains no sulfone.

7. A method as recited in claim 6 wherein said amount of said sulfone incorporated into said catalyst is such that the weight ratio of hydrogen fluoride to sulfone in said catalyst is at least about 1:1.

8. A method as recited in claim 7 wherein said amount of said sulfone incorporated into said catalyst is such that the sulfone present in said catalyst is less than 30 weight percent.

9. A method as recited in claim 8 wherein said amount of said sulfone incorporated into said catalyst is such that the sulfone present in said catalyst is in the range of from 10 to 25 weight percent.

10. A method as recited in claim 9 wherein said sulfone is sulfolane.

11. An improved alkylation process including contacting a hydrocarbon mixture containing olefins and isoparaffins with a catalyst containing hydrogen fluoride to thereby produce an alkylate product, wherein the improvement comprises:

incorporating a sulfone into said catalyst in an amount such that the sulfone present in said catalyst is less than 50 weight percent, whereby said alkylate product contains more highly branched hydrocarbons than when said catalyst contains no sulfone.

12. An alkylation process as recited in claim 11 wherein said amount of sulfone incorporated into said catalyst is such that the weight ratio of hydrogen fluoride to sulfone in said catalyst is at least about 1:1.

13. An alkylation process as recited in claim 12 wherein said amount of sulfone incorporated into said catalyst is such that the sulfone present in said catalyst is less than 30 weight percent.

14. A method as recited in claim 13 wherein said amount of sulfone incorporated into said catalyst is such that the sulfone present in said catalyst is in the range of from 10 to 25 weight percent.

15. A method as recited in claim 14 wherein said sulfone is sulfolane.

16. A method as recited in claim 1 wherein said amount of said sulfone incorporated into said catalyst is such that the sulfone present in said catalyst is less than 50 weight percent.

17. A method as recited in claim 16 wherein said sulfone is sulfolane.

18. A process comprising contacting under suitable alkylation reaction conditions a hydrocarbon mixture comprising olefins and paraffins with a catalyst composition comprising the components of a hydrogen halide, and a sulfone, wherein the sulfone component is present in said catalyst composition in an amount less than about 50 weight percent of the total weight of said composition, wherein the weight ratio of hydrogen halide to sulfone is at least about 1:1, and wherein said sulfone component is sulfolane.

19. A process as recited in claim 18 wherein said hydrogen halide component is hydrogen fluoride.

20. A process as recited in claim 19 wherein said sulfone component is present in said catalyst composition in an amount in the range of from about 2.5 to about 50 weight percent of the total weight of said composition.

21. A process as recited in claim 19 wherein said sulfone component is present in said composition in an amount in the range of from about 5 to about 35 weight percent of the total weight of said composition.

22. A process as recited in claim 21 wherein said sulfone component is present in said composition in an amount in the range of from about 10 to about 25 weight percent of the total weight of said composition.

23. A process as recited in claim 18 wherein the alkylation reaction temperature is in the range of from about 0° F. to about 150° F. and the alkylation reaction pressure is in the range of from about ambient pressure to about 15 atmospheres.

24. A process as recited in claim 18 wherein the molar ratio of paraffin to olefin in said hydrocarbon mixture is in the range of from about 2 to 1 to about 25 to 1.

25. A process as recited in claim 18 wherein said olefins are mono-olefins having from 2 to 12 carbon atoms, and wherein said paraffins are isoparaffins having from 4 to 8 carbon atoms.

26. A process comprising:

introducing a hydrocarbon mixture comprising olefins and paraffins into a reactor zone; and

contacting said hydrocarbon mixture within said reactor zone, at alkylation reaction conditions, with a catalyst mixture formed from a hydrogen halide and a sulfone, wherein the sulfone is present in said catalyst mixture in an amount less than about 50 weight percent of the total weight of said catalyst mixture, wherein the weight ratio of hydrogen halide to sulfone is at least about 1:1, and wherein said sulfone component is sulfolane.

27. A process as recited in claim 26 wherein said hydrogen halide component is hydrogen fluoride.

28. A process as recited in claim 27 wherein said sulfone component is present in said catalyst composition in an amount in the range of from about 2.5 to about 50 weight percent of the total weight of said composition.

29. A process as recited in claim 27 wherein said sulfone component is present in said composition in an amount in the range of from about 5 to about 35 weight percent of the total weight of said composition.

30. A process as recited in claim 29 wherein said sulfone component is present in said composition in an amount in the range of from about 10 to about 25 weight percent of the total weight of said composition.

31. A process as recited in claim 26 wherein the alkylation reaction temperature is in the range of from about 0° F. to about 150° F. and the alkylation reaction pressure is in the range of from about ambient pressure to about 15 atmospheres.

32. A process as recited in claim 26 wherein the molar ratio of paraffin to olefin in said hydrocarbon mixture is in the range of from about 2 to 1 to about 25 to 1.

33. A process as recited in claim 26 wherein said olefins are mono-olefins having from 2 to 12 carbon atoms, and wherein said paraffins are isoparaffins having from 4 to 8 carbon atoms.

34. In an alkylation process of the type wherein a hydrocarbon mixture including olefins and isoparaffins is contacted with a hydrogen fluoride catalyst, the improvement comprising:

utilizing sulfolane with said hydrogen fluoride catalyst in an amount less than about 50 weight percent of the total weight of said hydrogen fluoride catalyst and sulfolane and in such an amount wherein the weight ratio of hydrogen fluoride in said hydrogen fluoride catalyst to sulfolane is at least 1:1.

35. A process comprising contacting under suitable alkylation reaction conditions a hydrocarbon mixture comprising olefins and paraffins with a catalyst composition consisting essentially of the components of a hydrogen halide, and a sulfone, wherein said sulfone is present in said catalyst composition in an amount less than about 50 weight percent of the total weight of said catalyst composition, wherein the weight ratio of said hydrogen halide to said sulfone is at least about 1:1, and wherein said sulfone is sulfolane.

36. A process as recited in claim 35 wherein said hydrogen halide is hydrogen fluoride.

37. A process as recited in claim 36 wherein said sulfone is present in said catalyst composition in an amount in the range of from about 2.5 to about 50 weight percent of the total weight of said catalyst composition.

38. A process as recited in claim 36 wherein said sulfone is present in said catalyst composition in an amount in the range of from about 5 to about 35 weight percent of the total weight of said catalyst composition.

39. A process as recited in claim 36 wherein said sulfone is present in said catalyst composition in an amount in the range of from about 10 to about 25 weight percent of the total weight of said catalyst composition.

40. A process as recited in claim 39 wherein the alkylation reaction temperature is in the range of from about 0° F. to about 150° F. and the alkylation reaction pressure is in the range of from about ambient pressure to about 15 atmospheres.

41. A process as recited in claim 40 wherein the molar ratio of paraffin to olefin in said hydrocarbon mixture is in the range of from about 2 to 1 to about 25 to 1.

42. A process as recited in claim 41 wherein said olefins are mono-olefins having from 2 to 12 carbon atoms, and wherein said paraffins are isoparaffins having from 4 to 8 carbon atoms.

43. A process as recited in claim 19 wherein said sulfone component is present in said catalyst composition in an amount which is less than about 35 weight percent of the total weight of said composition.

44. A process as recited in claim 19 wherein the sulfone component is present in said catalyst composition in an amount that is less than about 30 weight percent of the total weight of said composition.

45. A process as recited in claim 19 wherein said sulfone component is present in said catalyst composition in an amount that is less than about 25 weight percent of the total weight of said composition.

46. A process as recited in claim 27 wherein said sulfone component is present in said catalyst composition in an amount which is less than about 35 weight percent of the total weight of said composition.

47. A process as recited in claim 27 wherein the sulfone component is present in said catalyst composition in an amount that is less than about 30 weight percent of the total weight of said composition.

48. A process as recited in claim 27 wherein said sulfone component is present in said catalyst composition in an amount that is less than about 25 weight percent of the total weight of said composition.

49. A process as recited in claim 34 wherein said sulfolane is present in said catalyst composition in an amount which is less than about 35 weight percent of the total weight of said composition.

50. A process as recited in claim 34 wherein the sulfolane is present in said catalyst composition in an amount that is less than about 30 weight percent of the total weight of said composition.

51. A process as recited in claim 34 wherein said sulfolane is present in said catalyst composition in an amount that is less than about 25 weight percent of the total weight of said composition.

52. A process as recited in claim 37 wherein said sulfone component is present in said catalyst composition in an amount which is less than about 35 weight percent of the total weight of said composition.

53. A process as recited in claim 37 wherein the sulfone component is present in said catalyst composition in an amount that is less than about 30 weight percent of the total weight of said composition.

54. A process as recited in claim 37 wherein said sulfone component is present in said catalyst composition in an amount that is less than about 25 weight percent of the total weight of said composition.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 5, 2008
From: CONOCOPHILLIPS COMPANY
To: UOP LLC
Reel/Frame 020462/0060 →