Systems and processes for conversion of ethylene feedstocks to hydrocarbon fuels

1. A process, comprising:

a) passing a feedstock comprising ethylene to a gas purification zone to remove water, providing a purified feedstock;

b) passing the purified feedstock to a first oligomerization stage to oligomerize the ethylene in the purified feedstock by contacting the ethylene with a catalyst comprising a metal deposited on a support at a temperature from about 40° C. to 220° C. to form a first oligomerization product, wherein the first oligomerization product comprises a majority concentration of mixed olefins with a carbon number from about C4 to about C8; and

c) passing the first oligomerization product to a second oligomerization stage to oligomerize the mixed olefins by contacting the mixed olefins with a solid acid catalyst at a temperature from greater than 150° C. to about 450° C. to form a second oligomerization product, wherein the second oligomerization product contains mixed linear olefins and branched olefins with a carbon number from about C8 to about C23 in a yield of greater than or equal to 20% useful as fuels and fuel blend stocks.

2. The process of claim 1 , wherein the ethylene-containing feedstock is derived from ethanol.

3. The process of claim 1 , wherein the ethylene-containing feedstock is derived from methanol.

4. The process of claim 1 , wherein the second oligomerization product further comprises aromatic compounds at a concentration of less than or equal to about 4% by weight.

5. The process of claim 1 , wherein the second oligomerization product further comprises aromatic compounds at a concentration from about 4% to about 20% by weight.

6. The process of claim 1 , further comprising fractionating the second oligomerization product to obtain a distillate-range olefin fraction containing distillate-range olefins with a carbon number greater than or equal to C8, and a light fraction containing olefins with a carbon number less than C8.

7. The process of claim 6 , wherein the distillate-range olefin fraction is hydrotreated to yield a mixture of linear and branched paraffins a majority boiling from about 120° C. to about 300° C.

8. The process of claim 6 , wherein the distillate-range olefin fraction includes open chain linear and branched hydrocarbons with a carbon number from about C8 to about C16.

9. The process of claim 8 , wherein the about C8 to about C16 fraction is hydrotreated to form a mixture boiling from about 120° C. to about 300° C.

10. The process of claim 1 , further comprising fractionating the second oligomerization product to obtain a distillate-range olefin fraction containing distillate-range olefins with a carbon number greater than or equal to C11, and a light fraction containing olefins with a carbon number less than C11.

11. The process of claim 10 , wherein the distillate-range olefin fraction is hydrotreated to yield a mixture of linear and branched paraffins a majority boiling from about 160° C. to about 390° C.

12. The process of claim 10 , wherein the distillate-range olefin fraction includes open chain linear and branched hydrocarbons with a carbon number from about C11 to about C23.

13. The process of claim 12 , wherein the about C11 to about C23 fraction is hydrotreated to form linear and branched paraffins which boil in the range from about 160° C. to about 390° C.

14. The process of claim 1 , further comprising fractionating the second oligomerization product to obtain a distillate-range olefin fraction containing distillate-range olefins boiling higher than about 120° C., and a light fraction boiling below about 120° C.

15. The process of claim 14 , wherein the distillate-range olefin fraction is hydrotreated to yield open-chain linear and branched paraffins.

16. The process of claim 14 , further including hydrotreating the light fraction to form open-chain linear and branched paraffins that boil in the gasoline fuel range.

17. The process of claim 14 , wherein the light fraction is recycled to the second oligomerization stage.

18. The process of claim 1 , further comprising fractionating the second oligomerization product to obtain a distillate-range olefin fraction containing distillate-range olefins boiling higher than about 160° C., and a light fraction boiling below about 160° C.

19. The process of claim 18 , wherein the distillate-range olefin fraction is hydrotreated to yield open-chain linear and branched paraffins.

20. The process of claim 18 , further comprising hydrotreating the light fraction to form open-chain linear and branched paraffins that boil in the gasoline fuel range.

21. The process of claim 18 , wherein the light fraction is recycled to the second oligomerization stage.

22. The process of claim 1 , further comprising hydrotreating the second oligomerization product to obtain a hydrotreated product comprising open-chain linear and branched paraffins.

23. The process of claim 22 , wherein the hydrotreated product is fractionated to obtain a light fraction comprising paraffins boiling below 120° C. and a distillate paraffin fraction boiling above 120° C.

24. The process of claim 23 , wherein the distillate paraffin fraction boils in the range from about 120° C. to 300° C.

25. The process of claim 23 , wherein the distillate paraffin fraction comprises open chain linear and branched paraffins with a carbon number from about C8 to about C16.

26. The process of claim 23 , wherein the light fraction boils in the gasoline fuel range.

27. The process of claim 22 , wherein the hydrotreated product is fractionated to obtain a light fraction comprising paraffins boiling below 160° C. and a distillate paraffin fraction boiling above 160° C.

28. The process of claim 27 , wherein the distillate paraffin fraction boils in the range from about 160° C. to 390° C.

29. The process of claim 27 , wherein the light fraction boils in the gasoline fuel range.

30. The process of claim 27 , wherein the distillate paraffin fraction comprises open chain linear and branched paraffins with a carbon number from about C11 to about C23.

31. The process of claim 1 , wherein the catalyst comprises nickel (Ni) on a silica-aluminate support with a nickel concentration of from about 0.2% to about 5% by weight.

32. The process of claim 1 , wherein the support is a Y zeolite, a Beta zeolite, an HZSM-5 zeolite, a Mordenite zeolite, a Ferrierite zeolite, an Al-MCM-41 zeolite, an MCM-48 zeolite, an MCM-22 zeolite, an SAPO-34 zeolite, a Chabazite zeolite, a Group I metal-exchanged zeolite, a Group II metal-exchanged zeolite, and/or any combination thereof.

33. The process of claim 31 , wherein the silica-aluminate support is a Grace 3111 amorphous silicoaluminate support, a Grace 3113 amorphous silicoaluminate support, a Grace 3115 amorphous silicoaluminate support, a Grace 3125 amorphous silicoaluminate support, a Grace X501 amorphous silicoaluminate support, a Group I metal-exchanged amorphous silicoaluminate support, a Group II metal-exchanged amorphous silicoaluminate support, and/or any combination thereof.

34. The process of claim 1 , wherein the solid acid catalyst is a Y zeolite, a Beta zeolite, an HZSM-5 zeolite, a Mordenite zeolite, a Ferrierite zeolite, an AI-MCM-41 zeolite, an MCM-48 zeolite, an MCM-22 zeolite, an SAPO-34 zeolite, a Chabazite zeolite, a hydrogen-exchanged zeolite, an acid form cation exchange resin, and/or any combination thereof.

35. The process of claim 1 , wherein the solid acid catalyst is a Grace 3111 amorphous silicoaluminate catalyst, a Grace 3113 amorphous silicoaluminate catalyst, a Grace 3125 amorphous silicoaluminate catalyst, a Grace X501 amorphous silicoaluminate catalyst, Amberlyst 70, and/or any combination thereof.

36. A process, comprising:

a) passing a feedstock comprising ethylene to a first oligomerization stage to oligomerize the ethylene in the feedstock by contacting the ethylene with a catalyst comprising a metal deposited on a support at a temperature from about 40° C. to 220° C. to form a first oligomerization product, wherein the first oligomerization product comprises a majority concentration of mixed olefins with a carbon number from about C4 to about C8; and

b) passing the first oligomerization product to a second oligomerization stage to oligomerize the mixed olefins by contacting the mixed olefins with a solid acid catalyst at a temperature from greater than 200° C. to about 350° C. to form a second oligomerization product comprising mixed linear olefins and branched olefins with a carbon number from about C8 to about C23 in a yield of greater than or equal to 20%;

c) hydrotreating either (i) the second oligomerization product of step (b) or (ii) a distillate-range olefin fraction comprising linear and branched olefins from step (d)(2) to yield a hydrotreated product comprising a mixture of linear and branched paraffins boiling in the range from about 120° C. to about 300° C.; and

d) fractionating either (1) the hydrotreated product of step (c)(i) to yield a distillate-range fraction comprising linear and branched paraffins a majority boiling from about 120° C. to about 300° C. and a light fraction comprising linear and branched paraffins boiling below 120° C. or (2) the second oligomerization product of step (b) to yield a distillate-range olefin fraction comprising mixed linear and branched olefins having a carbon number greater than or equal to C8 and a light fraction containing mixed linear and branched olefins with a carbon number less than C8; and wherein steps (c) and (d) are performed in any order.

37. A process, comprising:

a) passing a feedstock comprising ethylene to a first oligomerization stage to oligomerize the ethylene in the feedstock by contacting the ethylene with a catalyst comprising a metal deposited on a support at a temperature from about 40° C. to 220° C. to form a first oligomerization product, wherein the first oligomerization product comprises a majority concentration of mixed olefins with a carbon number from about C4 to about C8; and

b) passing the first oligomerization product to a second oligomerization stage to oligomerize the mixed olefins by contacting the mixed olefins with a solid acid catalyst at a temperature from greater than 200° C. to about 350° C. to form a second oligomerization product comprising mixed linear olefins and branched olefins with a carbon number from about C8 to about C23 in a yield of greater than or equal to 20%;

c) hydrotreating either (i) the second oligomerization product of step (b) or (ii) a distillate-range olefin fraction comprising linear and branched olefins from step (d)(2) to yield a hydrotreated product comprising a mixture of linear and branched paraffins boiling in the range from about 160° C. to about 390° C.; and

d) fractionating either (1) the hydrotreated product of step (c)(i) to yield a distillate-range fraction comprising linear and branched paraffins a majority boiling from about 160° C. to about 390° C. and a light fraction comprising linear and branched paraffins boiling below 160° C. or (2) the second oligomerization product of step (b) to yield a distillate-range fraction olefin comprising mixed linear and branched olefins having a carbon number greater than or equal to C11 and a light fraction containing mixed linear and branched olefins with a carbon number less than C11, and wherein steps (c) and (d) are performed in any order.

38. A process, comprising:

passing a feedstock comprising ethylene to a first oligomerization stage to oligomerize the ethylene in the feedstock by contacting the ethylene with a catalyst comprising a metal deposited on a support at a temperature from about 40° C. to 220° C. to form a first oligomerization product, wherein the first oligomerization product comprises a majority concentration of mixed olefins with a carbon number from about C4 to about C8; and

passing the first oligomerization product to a second oligomerization stage to oligomerize the mixed olefins by contacting the mixed olefins with a solid acid catalyst at a temperature from greater than 200° C. to about 350° C. to form a second oligomerization product comprising mixed linear olefins and branched olefins with a carbon number from about C8 to about C23;

performing a hydrotreating step; and

performing a fractionating step.

39. The process of claim 38 , wherein the second oligomerization product further comprises aromatic compounds at a concentration of less than or equal to about 4% by weight.

40. The process of claim 38 , wherein the second oligomerization further comprises aromatic compounds at a concentration from about 4% to about 20% by weight.

41. The process of claim 38 , wherein the catalyst comprises nickel (Ni) on a silica-aluminate support with a nickel concentration of from about 0.2% to about 5% by weight.

42. The process of claim 38 , wherein the solid acid catalyst is a Y zeolite, a Beta zeolite, an HZSM-5 zeolite, a Mordenite zeolite, a Ferrierite zeolite, an AI-MCM-41 zeolite, an MCM-48 zeolite, an MCM-22 zeolite, an SAPO-34 zeolite, a Chabazite zeolite, a hydrogen-exchanged zeolite, an acid form cation exchange resin, and/or any combination thereof.

43. The process of claim 38 , wherein the hydrotreating step comprises hydrotreating the second oligomerization product to produce a hydrotreated product comprising a mixture of linear and branched paraffins and wherein the hydrotreating step is performed before the fractionating step.

44. The process of claim 43 , wherein the fractionating step comprises fractionating the hydrotreated product to produce a distillate-range fraction and a light fraction.

45. The process of claim 44 , where in the distillate-range fraction comprises linear and branched paraffins boiling from about 120° C. to about 300° C. and the light fraction comprises paraffins boiling below 120° C.

46. The process of claim 44 , wherein the distillate-range fraction comprises paraffins boiling from about 160° C. to about 390° C. and the light fraction comprises paraffins boiling below 160° C.

47. The process of claim 38 , wherein the fractionating step comprises fractionating the second oligomerization product to produce a distillate-range olefin fraction containing distillate-range olefins with a carbon number greater than or equal to C8, and a light fraction containing olefins with a carbon number less than C8 and wherein the fractionating step is performed before hydrotreating step.

48. The process of claim 47 , wherein the hydrotreating step comprises hydrotreating the distillate-range olefins to yield open-chain linear and branched paraffins boiling in the range from about 120° C. to about 300° C.

49. The process of claim 38 , wherein the fractionating step comprises fractionating the second oligomerization product to obtain a distillate-range olefin fraction containing distillate-range olefins with a carbon number greater than or equal to C11 and a light fraction containing olefins with a carbon number less than C11, and wherein the fractionating step is performed before hydrotreating step.

50. The process of claim 49 , wherein the hydrotreating step comprises hydrotreating the distillate-range olefins to yield open-chain linear and branched paraffins boiling in the range from about 160° C. to about 390° C.

51. A process, comprising:

passing a feedstock comprising ethylene to a first oligomerization stage to oligomerize the ethylene in the feedstock by contacting the ethylene with a catalyst comprising a metal deposited on a support at a temperature from about 40° C. to 220° C. to form a first oligomerization product, wherein the first oligomerization product comprises a majority concentration of mixed olefins with a carbon number from about C4 to about C8; and

passing the first oligomerization product to a second oligomerization stage to oligomerize the mixed olefins by contacting the mixed olefins with a solid acid catalyst at a temperature from greater than 200° C. to about 350° C. to form a second oligomerization product, wherein the second oligomerization product contains mixed linear olefins and branched olefins with a carbon number from about C8 to about C23 in a yield of greater than or equal to 20% useful as fuels and fuel blend stocks.