IP Library Granted Patent US 9,771,533
Granted Patent B2
US 9,771,533 · App. 14/528,185 · Granted Sep 26, 2017

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 (Richland, 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 9,771,533
App. No.
14/528,185
Granted
Sep 26, 2017
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 (60)

1. A process for converting feedstocks to distillate-range hydrocarbon fuels, comprising:

oligomerizing an ethylene-containing feed over a first catalyst at a temperature selected from about 40° C. to about 220° C. to form a water-free first oligomerization product in a first reaction stage, wherein the water-free first oligomerization product contains a majority concentration of mixed olefins with a carbon number from about C4 to about C8;

oligomerizing the mixed olefins in the water-free first oligomerization product over a second catalyst at a temperature from about 150° C. to about 350° C. to form a two-step oligomerization product at a yield greater than or equal to about 20% containing mixed open-chain linear and branched olefins with a carbon number from about C8 to about C23; and

combining together selected portions of (a) the two-step oligomerization product and a first hydrocarbon product or (b) the two-step oligomerization product, the first hydrocarbon products, and a second hydrocarbon product to form a blend comprising any selected ratio of open-chain and closed-chain hydrocarbons;

wherein the first hydrocarbon product is derived from an ethanol-containing feed and comprises a majority concentration of mixed cycloparaffin hydrocarbons and mixed closed-chain aromatic hydrocarbons with a carbon number between about C3 to about C12; and the second hydrocarbon product comprises a selected quantity of alkylated aromatic hydrocarbons.

2. The process of claim 1 , further including mixing the water-free 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.

3. The process of claim 2 , wherein the second hydrocarbon product contains more hydrocarbons with carbon numbers greater than C8 than the feed.

4. The process of claim 2 , wherein the second hydrocarbon product contains more hydrocarbons with carbon numbers greater than C10 than the feed.

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

6. The process of claim 1 , further including hydrotreating each of the first hydrocarbon product, the second hydrocarbon product, and/or the two-step oligomerization product prior to combining the selected portions together 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 optionally fractionating the two-step oligomerization product at a selected fractionation temperature to obtain individual fractions, 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.

8. The process of claim 7 , wherein the fractionation temperature is selected in the range from about 100° C. to about 140° C.

9. The process of claim 7 , wherein the fractionation temperature is selected in the range from about 140° C. to about 180° C.

10. The process of claim 7 , further including hydrogenating the distillate-range olefins to form a mixture of open-chain hydrocarbons including linear and branched open-chain paraffins.

11. The process of claim 10 , wherein a majority of open-chain hydrocarbons in the mixture are in the jet fuel range.

12. The process of claim 10 , wherein a majority of open-chain hydrocarbons in the mixture are in the diesel fuel range.

13. The process of claim 7 , 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.

14. The process of claim 13 , wherein the second hydrocarbon product contains more hydrocarbons with carbon numbers greater than C8 than the feed.

15. The process of claim 13 , wherein the second hydrocarbon product contains more hydrocarbons with carbon numbers greater than C10 than the feed.

16. The process of claim 1 , further including mixing ethylene or an ethylene-containing feed 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.

17. The process of claim 16 , wherein the second hydrocarbon product contains more hydrocarbons with carbon numbers greater than C8 than the feed.

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

19. The process of claim 1 , further including combining selected ratios of the first hydrocarbon product containing aromatic hydrocarbons and the second hydrocarbon product containing alkylated aromatic hydrocarbons to make a feed and hydrogenating the feed to obtain a mixture of closed-chain hydrocarbons including closed-chain aromatics and closed-chain paraffins.

20. The process of claim 19 , wherein the hydrogenation includes converting from 0% to about 33% of the closed-chain aromatics to closed-chain paraffins.

21. The process of claim 19 , wherein the hydrogenation includes converting from about 33% to about 66% of the closed-chain aromatics to closed-chain paraffins.

22. The process of claim 19 , wherein the hydrogenation includes converting from about 66% to about 100% of the closed-chain aromatics to closed-chain paraffins.

23. The process of claim 19 , further including combining a selected ratio of the mixture containing closed-chain hydrocarbons and a mixture containing open-chain hydrocarbons including linear and branched open-chain paraffins to make a fuel blend, wherein the mixture containing open-chain hydrocarbons is obtained from a fraction derived from fractionation of the two-step oligomerization product containing distillate-range olefins boiling at or higher than the fractionation temperature that is further hydrogenated.

24. The process of claim 23 , further including fractionating the fuel blend to obtain individual fractions, 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.

25. The process of claim 24 , wherein the distillate-range hydrocarbons are in the jet fuel range.

26. The process of claim 24 , wherein the light fraction contains hydrocarbons in the gasoline fuel range.

27. The process of claim 23 , further including fractionating the fuel blend to obtain individual fractions, 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.

28. The process of claim 27 , wherein the distillate-range hydrocarbons are in the diesel fuel range.

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

30. The process of claim 1 , further including combining a selected ratio of the first hydrocarbon product containing aromatic hydrocarbons, the second hydrocarbon product containing alkylated aromatic hydrocarbons and a fraction containing distillate-range olefins to make a fuel blend, wherein the fraction containing distillate-range olefins is obtained from fractionation of the two-step oligomerization product containing distillate-range olefins boiling at or higher than the fractionation temperature.

31. The process of claim 30 , wherein the fuel blend includes up to 33% distillate-range olefins.

32. The process of claim 30 , wherein the fuel blend includes up to 66% distillate-range olefins.

33. The process of claim 30 , wherein the fuel blend includes up to 100% distillate-range olefins.

34. The process of claim 30 , 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.

35. The process of claim 34 , wherein the hydrogenation includes converting from 0% to about 33% of the closed-chain aromatics to closed-chain paraffins.

36. The process of claim 34 , wherein the hydrogenation includes converting from about 33% to about 66% of the closed-chain aromatics to closed-chain paraffins.

37. The process of claim 34 , wherein the hydrogenation includes converting from about 66% to about 100% of the closed-chain aromatics to closed-chain paraffins.

38. The process of claim 34 , further including fractionating the fuel blend to obtain individual fractions, 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.

39. The process of claim 38 , wherein the distillate-range hydrocarbons are in the jet fuel range.

40. The process of claim 38 , wherein the light fraction contains hydrocarbons in the gasoline fuel range.

41. The process of claim 34 , further including fractionating the hydrogenated blend to obtain individual fractions, 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.

42. The process of claim 41 , wherein the distillate-range hydrocarbons are in the diesel fuel range.

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

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

oligomerizing ethylene in an ethylene-containing feedstock over a first catalyst at a temperature selected between about 40° C. and about 220° C. to form a water-free first oligomerization product containing a majority concentration of mixed olefins with a carbon number between about C4 and about C8;

oligomerizing the mixed olefins in the water-free first oligomerization product over a second catalyst at a temperature between about 150° C. and about 350° C. to form a second oligomerization product containing mixed open-chain linear and branched olefins with a carbon number between about C8 and about C23 at a yield greater than or equal to about 20%;

optionally fractionating the second oligomerization product to obtain individual fractions, 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;

converting ethanol in an ethanol-containing feedstock over an acid catalyst to form a first conversion product containing a majority concentration of closed-chain mixed aromatic hydrocarbons and cycloparaffin hydrocarbons with a carbon number between about C3 and about C12;

optionally 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 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.

45. A process for conversion of feedstocks to distillate-range hydrocarbon fuels, comprising combining together selected portions of (a) a two-step oligomerization product and a first hydrocarbon product or (b) the two-step oligomerization product, the first hydrocarbon product, and a second hydrocarbon product to form a blend comprising any selected ratio of open-chain and closed-chain hydrocarbons, wherein:

the first hydrocarbon product is produced by converting ethanol from an ethanol-containing feed into the first hydrocarbon product, which comprises a majority concentration of mixed cycloparaffin hydrocarbons and mixed closed-chain aromatic hydrocarbons with a carbon number between about C3 to about C12;

the second hydrocarbon product comprises a selected quantity of alkylated aromatic hydrocarbons;

the two-step oligomerization product is formed by

oligomerizing an ethylene-containing feed over a first catalyst at a temperature selected from about 40° C. to about 220° C. to form a water-free first oligomerization product in a first reaction stage, wherein the water-free first oligomerization product contains a majority concentration of mixed olefins with a carbon number from about C4 to about C8; and

oligomerizing the mixed olefins in the water-free first oligomerization product over a second catalyst at a temperature from about 150° C. to about 350° C. to form the two-step oligomerization product at a yield greater than or equal to about 20% containing mixed open-chain linear and branched olefins with a carbon number from about C8 to about C23.

Assignments (3)
CONFIRMATORY LICENSE Recorded Oct 3, 2018
From: BATTELLE MEMORIAL INSTITUTE
To: UNITED STATES DEPARTMENT OF ENERGY
Reel/Frame 047053/0060 →
CONFIRMATORY LICENSE Recorded Jan 6, 2015
From: BATTELLE MEMORIAL INSTITUTE, PACIFIC NORTHWEST DIVISION
To: U.S. DEPARTMENT OF ENERGY
Reel/Frame 034642/0728 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 11, 2014
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 034479/0240 →
Continuity (1)
Related Publication 20160194572A1 · Jul 7, 2016