IP Library Granted Patent US 10,005,974
Granted Patent B2
US 10,005,974 · App. 15/681,154 · Granted Jun 26, 2018

Systems and processes for conversion of ethylene feedstocks to hydrocarbon fuels

Inventors: Michael A. Lilga (Richland, WA); Richard T. Hallen (Richland, WA); Karl O. Albrecht (Richland, WA); Alan R. Cooper (Kennewick, WA); John G. Frye (Richland, WA); Karthikeyan Kallupalayam Ramasamy (West Richland, WA)
Assignee: Battelle Memorial Institute
C10L1/04C07C2/12C07C2/24C07C2/66C07C5/03C10G3/00C10G29/205C10G45/00C10G50/00C10G69/123C10G69/126C07C2521/04C07C2521/12C07C2523/42C07C2523/755C07C2529/06C07C2529/40C07C2529/70C07C2529/76C10G2300/1081C10G2300/1092C10G2300/1096C10L2200/0469C10L2270/02C10L2270/04C10L2290/24C10L2290/543Y02P30/42
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Quick Facts
Patent No.
US 10,005,974
App. No.
15/681,154
Granted
Jun 26, 2018
Kind
B2
Abstract

Systems, processes, and catalysts are disclosed for obtaining fuels and fuel blends containing selected ratios of open-chain and closed-chain fuel-range hydrocarbons suitable for production of alternate fuels including gasolines, jet fuels, and diesel fuels. Fuel-range hydrocarbons may be derived from ethylene-containing feedstocks and ethanol-containing feedstocks.

Claims (61)

1. A process for providing a fuel blend, comprising:

(i) combining together a first hydrocarbon product, a second hydrocarbon product, and a two-step oligomerization product to obtain the fuel blend; or

(ii) combining together the first hydrocarbon product and the two-step oligomerization product to obtain the fuel blend; wherein:

the first hydrocarbon product is derived from an ethanol-containing feed, the first hydrocarbon product containing hydrocarbons with a carbon number from about C2 to about C12 and comprising a majority concentration of mixed cycloparaffin hydrocarbons and mixed closed chain aromatic hydrocarbons;

the second hydrocarbon product comprises alkylated aromatic hydrocarbons; and

the two-step oligomerization product comprises mixed linear and branched olefins with a carbon number from about C8 to about C23 in a yield of greater than or equal to 20% and wherein the two-step oligomerization product is derived from an ethylene-containing feed via a two-step oligomerization process, which comprises (i) passing the ethylene-containing feed over a catalyst comprising a metal deposited on a support at a temperature ranging from about 40° C. to 220° C. to form a first oligomerization product and (ii) passing the first oligomerization product over a solid acid catalyst at a temperature ranging from greater than 150° C. to about 450° C. to form the two-step oligomerization product.

2. The process of claim 1 , wherein the two-step oligomerization process further comprises

passing the ethylene-containing feed to a gas purification zone to remove water; and

wherein the first oligomerization product comprises a majority concentration of mixed olefins with a carbon number from about C4 to about C8.

3. The process of claim 1 , further including mixing the first oligomerization product with the first hydrocarbon product to make a feed, and alkylating the feed over an alkylation catalyst to form the second hydrocarbon product comprising alkylated aromatic hydrocarbons.

4. The process of claim 3 , wherein the second hydrocarbon product contains more hydrocarbons with carbon numbers greater than C8 than the feed.

5. The process of claim 3 , wherein the second hydrocarbon product contains more hydrocarbons with carbon numbers greater than C10 than the feed.

6. The process of claim 1 , further including hydrotreating the fuel blend to yield a majority of fuel range hydrocarbons boiling in the range of temperatures from about 120° C. to about 390° C.

7. The process of claim 1 , further including hydrotreating each of the first hydrocarbon product, the second hydrocarbon product, and the two-step oligomerization product or the first hydrocarbon product and the two-step oligomerization product prior to combining together (i) the first hydrocarbon product, the second hydrocarbon product, and the two-step oligomerization product or (ii) the first hydrocarbon product and the two-step oligomerization product to yield a majority of fuel range hydrocarbons boiling in the range of temperatures from about 120° C. to about 390° C.

8. The process of claim 1 , further including fractionating the two-step oligomerization product at a selected fractionation temperature to obtain individual fractions, including a fraction containing distillate range olefins boiling at or higher than the fractionation temperature and a light fraction boiling at or below the fractionation temperature.

9. The process of claim 8 , wherein the fractionation temperature is selected in the range from about 100° C. to about 140° C.

10. The process of claim 8 , wherein the fractionation temperature is selected in the range from about 140° C. to about 180° C.

11. The process of claim 8 , further including hydrogenating the distillate-range olefins to form a mixture of open-chain hydrocarbons including linear and branched open chain paraffins.

12. The process of claim 11 , wherein a majority of open-chain hydrocarbons in the mixture are in the jet fuel range.

13. The process of claim 11 , wherein a majority of open-chain hydrocarbons in the mixture are in the diesel fuel range.

14. The process of claim 8 , further including mixing the light fraction with the first hydrocarbon product containing aromatic hydrocarbons to make a feed, and alkylating the feed over an alkylation catalyst to form the second hydrocarbon product comprising alkylated aromatic hydrocarbons.

15. The process of claim 14 , wherein the second hydrocarbon product contains more hydrocarbons with carbon numbers greater than C8 than the feed.

16. The process of claim 14 , wherein the second hydrocarbon product contains more hydrocarbons with carbon numbers greater than C10 than the feed.

17. The process of claim 1 , further including mixing ethylene or an ethylene containing feed with a portion of the first hydrocarbon product containing aromatic hydrocarbons to make a feed, and alkylating the feed over an alkylation catalyst to form the second hydrocarbon product comprising alkylated aromatic hydrocarbons.

18. The process of claim 17 , wherein the second hydrocarbon product contains more hydrocarbons with carbon numbers greater than C8 than the feed.

19. The process of claim 17 , wherein the second hydrocarbon product contains more hydrocarbons with carbon numbers greater than C10 than the feed.

20. The process of claim 1 , wherein the first hydrocarbon product containing aromatic hydrocarbons and the second hydrocarbon product containing alkylated aromatic hydrocarbons are combined to make a feed and hydrogenating the feed to obtain a mixture of closed-chain hydrocarbons including closed-chain aromatics and closed-chain paraffins.

21. The process of claim 20 , wherein hydrogenating includes converting between greater than 0% to about 33% of the closed-chain aromatics to closed-chain paraffins.

22. The process of claim 20 , wherein hydrogenating includes converting from about 33% to about 66% of the closed-chain aromatics to closed-chain paraffins.

23. The process of claim 20 , wherein hydrogenating includes converting from about 66% to about 100% of the closed-chain aromatics to closed-chain paraffins.

24. The process of claim 20 , comprising (i) fractionating the two-step oligomerization product at a fractionation temperature to provide a fraction of the two-step oligomerization product containing distillate-range olefins boiling at or higher than the fractionation temperature; (ii) hydrogenating the fraction of the two-step oligomerization product containing distillate-range olefins boiling at or higher than the fractionation temperature to provide a mixture comprising open chain hydrocarbons; and (iii) combining the mixture containing open chain hydrocarbons with the mixture containing closed-chain hydrocarbons to provide the fuel blend.

25. The process of claim 24 , further including fractionating the fuel blend to obtain individual fractions, including a fraction containing distillate range hydrocarbons boiling in the range of temperatures from about 120° C. to about 300° C., a light fraction boiling below a temperature of about 120° C., and a heavy fraction boiling above a temperature of about 300° C.

26. The process of claim 25 , wherein the distillate range hydrocarbons are in the jet fuel range.

27. The process of claim 25 , wherein the light fraction contains hydrocarbons in the gasoline fuel range.

28. The process of claim 24 , further including fractionating the fuel blend to obtain individual fractions, including a fraction containing distillate range hydrocarbons boiling in the range of temperatures from about 160° C. to about 390° C., a light fraction boiling below a temperature of about 160° C., and a heavy fraction boiling above a temperature of about 390° C.

29. The process of claim 28 , wherein the distillate range hydrocarbons are in the diesel fuel range.

30. The process of claim 28 , wherein the light fraction contains hydrocarbons in the gasoline fuel range.

31. The process of claim 1 , comprising (i) fractionating the two-step oligomerization product at a fractionation temperature to provide a fraction of the two-step oligomerization product containing distillate-range olefins boiling at or higher than the fractionation temperature and (ii) combining the fraction of the two-step oligomerization product containing distillate-range olefins boiling at or higher than the fractionation temperature with the first hydrocarbon product containing aromatic hydrocarbons and the second hydrocarbon product containing alkylated aromatic hydrocarbons to provide the fuel blend.

32. The process of claim 31 , wherein the fuel blend includes up to 33% distillate range olefins.

33. The process of claim 31 , wherein the fuel blend includes up to 66% distillate range olefins.

34. The process of claim 31 , wherein the fuel blend includes up to 100% distillate range olefins.

35. The process of claim 31 , further including hydrogenating the fuel blend to obtain a hydrogenated blend comprising a mixture of closed-chain aromatics, closed-chain paraffins, open-chain paraffins, and open-chain iso paraffins.

36. The process of claim 35 , wherein hydrogenating includes converting between greater than 0% to about 33% of the closed-chain aromatics to closed-chain paraffins.

37. The process of claim 35 , wherein hydrogenating includes converting from about 33% to about 66% of the closed-chain aromatics to closed-chain paraffins.

38. The process of claim 35 , wherein hydrogenating includes converting from about 66% to about 100% of the closed-chain aromatics to closed-chain paraffins.

39. The process of claim 35 , further including fractionating the fuel blend to obtain individual fractions, including a fraction containing distillate range hydrocarbons boiling in the range of temperatures from about 120° C. to about 300° C., a light fraction boiling below a temperature of about 120° C., and a heavy fraction boiling above a temperature of about 300° C.

40. The process of claim 39 , wherein the distillate range hydrocarbons are in the jet fuel range.

41. The process of claim 39 , wherein the light fraction contains hydrocarbons in the gasoline fuel range.

42. The process of claim 35 , further including fractionating the hydrogenated blend to obtain individual fractions, including a fraction containing distillate range hydrocarbons boiling in the range of temperatures from about 160° C. to about 390° C., a light fraction boiling below a temperature of about 160° C., and a heavy fraction boiling above a temperature of about 390° C.

43. The process of claim 42 , wherein the distillate range hydrocarbons are in the diesel fuel range.

44. The process of claim 42 , wherein the light fraction contains hydrocarbons in the gasoline fuel range.

45. A process for conversion of feedstocks to distillate range hydrocarbons for fuels containing any desired ratio of open-chain and closed-chain hydrocarbons, the process comprising:

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

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

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%;

converting ethanol in an ethanol-containing feedstock over an acid catalyst to form a first conversion product containing hydrocarbons with a carbon number from about C2 to about C12 and comprising a majority concentration of closed-chain mixed aromatic hydrocarbons and cycloparaffin hydrocarbons;

alkylating the first conversion product to produce a second conversion product comprising a selected quantity of alkylated aromatic hydrocarbons therein; and

combining selected portions of the first conversion product, the second conversion product, and/or the second oligomerization product together to form a blend containing open-chain and closed-chain hydrocarbons that when hydrotreated yields a majority of fuel range hydrocarbons boiling in the range of temperatures from about 120° C. to about 390° C.

46. The process of claim 1 , wherein the first hydrocarbon product is produced by contacting a feedstock comprising ethanol with an acid catalyst thereby converting the ethanol to a first hydrocarbon product comprising hydrocarbons with a carbon number between about C2 and about C12 and comprising a majority concentration of aromatic hydrocarbons and cycloparaffin hydrocarbons.

47. The process of claim 46 , wherein the feedstock is contacted with the acid catalyst at a temperature of about 280° C. to about 500° C.

48. The process of claim 1 , wherein the second hydrocarbon product is produced by alkylating the first hydrocarbon product.

Assignments (2)
CONFIRMATORY LICENSE Recorded Oct 5, 2018
From: BATTELLE MEMORIAL INSTITUTE
To: UNITED STATES DEPARTMENT OF ENERGY
Reel/Frame 047080/0429 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 24, 2018
From: LILGA, MICHAEL A.; HALLEN, RICHARD T.; ALBRECHT, KARL O.; COOPER, ALAN R.; FRYE, JOHN G.; RAMASAMY, KARTHIKEYAN KALLUPALAYAM
To: BATTELLE MEMORIAL INSTITUTE
Reel/Frame 044716/0254 →
Continuity (2)
Continuation 14528185 · Oct 30, 2014
Related Publication 20170369804A1 · Dec 28, 2017
Cited By (1)
US 12,617,677