Production of renewable diesel and propylene

Patent metadata

Field	Value
Publication number	US-9617479-B2
Application number	US-201414573081-A
Country	US
Kind code	B2
Filing date	Dec 17, 2014
Priority date	Jan 30, 2014
Publication date	Apr 11, 2017
Grant date	Apr 11, 2017

Abstract

Feeds containing triglycerides are processed to produce a diesel fuel product and propylene. The diesel product and propylene are generated by deoxygenating the triglyceride-containing feed using processing conditions that enhance preservation of olefins that are present in the triglycerides. The triglyceride-containing feed is processed in the presence of a catalyst containing a Group VI metal and a Group VIII non-noble metal and in the presence of CO.

First claim

What is claimed is:

1. A method for processing a biocomponent feedstock, comprising:
exposing a feedstock, the feedstock comprising at least 40 wt % of a biocomponent feed containing triglycerides, to a first catalyst in the presence of hydrogen and at least 300 vppm of CO under first effective deoxygenation conditions for forming an at least partially deoxygenated effluent, the first catalyst comprising a Group VI metal and a Group VIII non-noble metal, the at least partially deoxygenated effluent having an oxygen content that is at least 40% less than an oxygen content of the feedstock;
separating the at least partially deoxygenated effluent to form a gas phase effluent comprising propylene and a liquid phase effluent; and
separating at least a portion of the propylene from the gas phase effluent.

2. The method of claim 1 , wherein the propylene separated from the gas phase effluent comprises at least about 0.25 wt % of propylene relative to the weight of the biocomponent feed.

3. The method of claim 1 , wherein a relative weight ratio of propylene to propane in the gas phase effluent is at least about 0.25.

4. The method of claim 1 , wherein the biocomponent feed comprises at least 40 wt % of triglycerides.

5. The method of claim 1 , wherein the liquid phase effluent comprises at least about 10 wt % olefins.

6. The method of claim 1 , wherein the liquid phase effluent has an olefin to paraffin ratio of at least about 0.03.

7. The method of claim 1 , wherein the at least one Group VI metal is tungsten or molybdenum and the at least one Group VIII non-noble metal is nickel or cobalt.

8. The method of claim 7 , wherein the first catalyst comprises cobalt and molybdenum.

9. The method of claim 1 , wherein the feedstock is exposed to the first catalyst in the presence of at least about 500 vppm of carbon monoxide, about 5000 vppm or less of carbon monoxide, or a combination thereof.

10. The method of claim 1 , further comprising recycling at least a portion of the gas phase effluent as a hydrogen-containing and CO-containing input for said exposing of the feedstock.

11. The method of claim 10 , wherein at least a portion of CO 2 , H 2 O, H 2 S, or a combination thereof is removed from the at least a portion of the gas phase effluent prior to recycling as a hydrogen-containing and CO-containing input for said exposing of the feedstock.

12. The method of claim 1 , further comprising exposing the liquid effluent to a second catalyst in the presence of hydrogen and at least 300 vppm of carbon monoxide under second effective deoxygenation conditions for forming an effluent having an oxygen content of 300 wppm or less, the second catalyst comprising a Group VI metal and a Group VIII non-noble metal.

13. The method of claim 12 , wherein the first catalyst is different from the second catalyst, the first effective deoxygenation conditions are different from the second deoxygenation conditions, or a combination thereof.

14. The method of claim 12 , further comprising separating the effluent having an oxygen content of 300 wppm or less to form at least a second gas phase effluent comprising propylene, wherein separating at least a portion of the propylene from the gas phase effluent further comprises separating at least a portion of the propylene from the second gas phase effluent.

15. The method of claim 1 , wherein the first effective deoxygenation conditions include a temperature from about 250° C. to about 350° C., an LHSV from about 0.2 hr −1 to about 10 hr −1 , and a hydrogen partial pressure of about 200 psig (1.4 MPag) to about 600 psig (4.1 MPag).

16. The method of claim 1 , further comprising fractionating the liquid phase effluent to form at least a diesel product fraction, and exposing at least one of the liquid phase effluent or the diesel product to a dewaxing catalyst under effective dewaxing conditions.

17. The method of claim 1 , further comprising at least one of:
hydrotreating the liquid phase effluent under effective hydrotreating conditions.

18. The method of claim 1 , further comprising:
hydrotreating the product effluent under effective hydrotreating conditions; and
exposing the hydrotreated product effluent to a dewaxing catalyst under effective dewaxing conditions,
wherein the hydrotreated product effluent is dewaxed prior to the fractionation of the hydrotreated product effluent.

19. The method of claim 1 , wherein the feedstock comprises from about 15 wt % to about 40 wt % triglycerides, and the effective deoxygenation conditions include a temperature from about 500° F. (293° C.) to about 600° F. (316° C.), an LHSV from about 0.2 h −1 to about 10 hr −1 , and a hydrogen partial pressure of about 300 psig (2.1 MPag) to about 500 psig (3.4 MPag).

20. The method of claim 1 , wherein the at least partially deoxygenated effluent has an oxygen content of about 0.5 wt % or less.

Assignees

• Fingland Bradley R
• Gatt Joseph Emmanuel
• Exxonmobil Res & Eng Co

Inventors

• Fingland Bradley R
• Gatt Joseph Emmanuel

Classifications

• Y02P30/20

  using bio-feedstock · CPC title

• B01J23/85

  Chromium, molybdenum or tungsten · CPC title

• C10L2270/026

  for diesel engines, e.g. automobiles, stationary, marine · CPC title

• C10L1/08

  for compression ignition · CPC title

• C10G2300/1014

  of vegetal origin · CPC title