Conversion of alcohols to distillate fuels

Patent metadata

Field	Value
Publication number	US-9914672-B2
Application number	US-201314052972-A
Country	US
Kind code	B2
Filing date	Oct 14, 2013
Priority date	Oct 19, 2012
Publication date	Mar 13, 2018
Grant date	Mar 13, 2018

Abstract

A process for the production of jet and other heavy fuels from alcohols and mixture of alcohols is disclosed. The process may include contacting in a reaction zone at least one C2 to C11 alcohol with a solid catalyst having activity for the simultaneous dehydration of the alcohols to form olefins, isomerization of the olefins to form internal olefins, and oligomerization of the olefins produced in situ via the dehydration reaction to form an effluent comprising mono-olefinic hydrocarbons. Preferably, the alcohol feed is a mixture of alcohols, such as C2 to C7 alcohols or C4 and C6 alcohols, enabling the production of a mixture of branched hydrocarbons that may be used directly as a jet fuel without blending.

First claim

What is claimed:

1. A process for the production of distillate fuel range hydrocarbons, the process comprising:
contacting in a reaction zone a mixture of two or more C2 to C11 alcohols, including at least one secondary alcohol, with a solid acid catalyst, at conditions where the solid acid catalyst has activity for the simultaneous:
i. dehydration of the alcohols to form olefins and water;
ii. isomerization of the resulting olefins to form internal olefins; and
iii. oligomerization of the olefins produced in situ;

to form an effluent comprising mono-olefinic hydrocarbon oligomers including the distillate fuel range hydrocarbons;
wherein the mixture of two or more C2 to C11 alcohols includes one or more C7 to C11 alcohols.

2. The process of claim 1 , further comprising separating the mono-olefinic hydrocarbon oligomers from water, any unreacted alcohols, and any unreacted olefins.

3. The process of claim 2 , further comprising recycling at least one of the unreacted alcohols and the unreacted olefins to the reaction zone.

4. The process of claim 1 , further comprising hydrogenating the mono-olefinic hydrocarbon oligomers to produce a paraffinic hydrocarbon product.

5. The process of claim 4 , further comprising fractionating the paraffinic hydrocarbon product into one or more hydrocarbon fractions useful as a fuel or a fuel blendstock.

6. The process of claim 5 , wherein the one or more hydrocarbon fractions are suitable for use as a fuel grade product, without blending with petroleum-derived fuels.

7. The process of claim 1 , wherein the C2 to C11 alcohols are provided from a biomass fermentation or a biomass gasification to syngas followed by a modified Fischer-Tropsch synthesis.

8. The process of claim 1 , wherein the at least one secondary alcohol comprises at least one of 2-butanol, 2-pentanol, 2-hexanol, and combinations thereof.

9. The process of claim 1 , wherein the mixture of two or more C2 to C11 alcohol comprises either a mixture of C4 and C6 alcohols or a mixture of C2 to C7 alcohols.

10. The process of claim 1 , further comprising fractionating the mono-olefinic hydrocarbon oligomers to produce one or more fractions comprising C10 or C12 and lighter olefins and one or more fractions comprising C11+ or C13+ olefins, respectively.

11. The process of claim 10 , further comprising recycling at least a portion of the one or more fractions comprising C10 or C12 and lighter olefins to the reaction zone for reaction with in situ produced olefins and oligomers.

12. The process of claim 1 , wherein the solid acid catalyst is a beta zeolite-containing catalyst.

13. A process for the production of distillate fuel range hydrocarbons, the process comprising:
reacting an alcohol feedstock in a first reaction zone and a second reaction zone, the first reaction zone comprising a first catalyst bed containing an acid catalyst and operated at conditions where the acid catalyst has activity for the simultaneous dehydration of alcohols to olefins, isomerization of the olefins to form internal olefins, and oligomerization of the olefins produced in situ to form a mono-olefinic hydrocarbon product, and the second reaction zone comprising a second catalyst bed containing a catalyst having activity for the hydrogenation of the mono-olefinic hydrocarbon product to form an effluent comprising paraffinic hydrocarbons, including the distillate fuel range hydrocarbons;
wherein the alcohol feedstock comprises a mixture of two or more C2 to C11 alcohols, and wherein one or more of the C2 to C11 alcohols are C7 to C11 alcohols.

14. The process of claim 13 , wherein the acid catalyst is a beta zeolite-containing catalyst.

15. The process of claim 13 , further comprising separating the paraffinic hydrocarbons from unreacted alcohols.

16. The process of claim 13 , further comprising fractionating the paraffinic hydrocarbons into one or more hydrocarbon fractions useful as a fuel or a fuel blendstock.

17. The process of claim 13 , wherein the first and second reaction zones are contained in the same reaction vessel.

18. The process of claim 13 , further comprising separating water and unreacted alcohols from the molo-olefinic hydrocarbon product intermediate the first reaction zone and the second reaction zone.

19. A process for the production of distillate fuel range hydrocarbons, the process comprising:
contacting in a reaction zone a mixture comprising a C4 alcohol and one or more C7 to C11 alcohols with a solid acid catalyst at operating conditions where the solid acid catalyst has activity for the simultaneous:
i. dehydration of the alcohol to form olefins and water;
ii. isomerization of the resulting olefins to form internal olefins; and
iii. oligomerization of the olefins produced in situ;

to form an effluent comprising mono-olefinic hydrocarbon oligomers including the distillate fuel range hydrocarbons.

20. The process of claim 19 , further comprising separating the mono-olefinic hydrocarbon oligomers from water, any unreacted alcohols, and any unreacted olefins.

21. The process of claim 20 , further comprising recycling at least a portion of the unreacted alcohols to the contacting.

22. The process of claim 20 , further comprising recycling at least a portion of the unreacted olefins to the reaction zone.

23. The process of claim 19 , further comprising fractionating the mono-olefinic hydrocarbon oligomers to produce one or more fractions comprising C12 and lighter olefins and one or more fractions comprising C13+ olefins.

24. The process of claim 23 , further comprising recycling at least a portion of the C12 and lighter olefins fraction(s) to the reaction zone for continued reaction with in situ produced olefins and oligomers.

25. The process of claim 19 , further comprising fractionating the mono-olefinic hydrocarbons oligomers to produce a fraction including C8 and lighter olefinic oligomers, a fraction including C9 to C12 olefinic oligomers, and a fraction including C13+ oligomers.

26. The process of claim 25 , further comprising recycling at least a portion of the fraction including C8 and lighter olefinic oligomers to the reaction zone.

27. The process of claim 25 , further comprising recycling at least a portion of the fraction including C9 to C12 olefinic oligomers to the reaction zone.

28. The process of claim 19 , wherein the C4 alcohol comprises at least one of n-butanol, isobutanol, and 2-butanol.

Assignees

• Lummus Technology Inc

Inventors

• Greene Marvin I
• Song Ruozhi
• Judzis Jr Arvids

Classifications

• C07C5/13

  with simultaneous isomerisation · CPC title

• C07C2/06

  of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond · CPC title

• C10G3/49

  containing crystalline aluminosilicates, e.g. molecular sieves · CPC title

• C10G50/00

  Production of liquid hydrocarbon mixtures from lower carbon number hydrocarbons, e.g. by oligomerisation · CPC title

• C10L1/08

  for compression ignition · CPC title