IP Library Granted Patent US 8,679,805
Granted Patent B2
US 8,679,805 · App. 13/635,584 · Granted Mar 25, 2014

Preparation method of transportation fuel or lubricating base oil using biomass

Inventors: Young Min Chung (Daejeon, KR); Ok Youn Kim (Daejeon, KR); Hee Jung Jeon (Daejeon, KR); Young Seek Yoon (Gwangju, KR); Seong Ho Lee (Seoul, KR); Hee Soo Kim (Daejeon, KR); Seung Hoon Oh (Seoul, KR); Yoon Jae Yim (Chungcheongnam-do, KR)
Assignee: SK Innovation Co., Ltd.
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Quick Facts
Patent No.
US 8,679,805
App. No.
13/635,584
Granted
Mar 25, 2014
Kind
B2
Abstract

The present invention relates to a method of economically preparing paraffin compounds corresponding to gasoline fuel or lubricating base oil using volatile fatty acids (VFAs) derived from biomass.

Claims (33)

1. A method of preparing paraffins for transportation fuel or lubricating base oil using biomass, the method comprising the steps of:

A) preparing C2-C7 volatile fatty acids or their salts by fermentation of biomass;

B) producing a mixture of C3-C13 ketones from the volatile fatty acids or their salts of step A); and

C) converting the ketone mixture of step B) into paraffins in the presence of a hydrogenation catalyst

wherein step C) comprises the steps of

i) subjecting the ketone mixture to aldol condensation to prepare hydroxyketones having an increased carbon chain length;

ii) dehydrating the hydroxyketones to form enones;

iii) saturating the enones with hydrogen to form ketones; and

iv) converting the formed ketones into paraffins by hydrodeoxygenation,

and

wherein step C) is carried out in a single reactor.

2. The method of claim 1 , wherein the method further comprises, between steps ii) and iii), the steps of:

iii-a) reacting the enones with a ketone to form hydroxyenones having an increased carbon chain length; and

iii-b) dehydrating the hydroxyenones.

3. The method of claim 1 , wherein the method further comprises, between steps ii) and iii), the steps of:

iii-c) saturating the enones with hydrogen;

iii-d) subjecting the ketone mixture to aldol condensation to prepare hydroxyketones having an increased carbon chain length;

iii-e) dehydrating the hydroxyketones to form enones having an increased carbon chain length; and

iii-f) saturating the enones of step iii-e) with hydrogen.

4. The method of claim 1 , wherein the paraffins are C6-C60 branched paraffins.

5. The method of claim 1 , wherein hydrogen which is used in one or more of steps B) to C) is produced in step A).

6. The method of claim 1 , wherein the catalyst that is used in step C) has one or more of aldol condensation, hydrogenation and hydrodeoxygenation functions.

7. The method of claim 6 , wherein the catalyst is a catalyst system obtained by physical mixing or molding using a binder.

8. The method of claim 6 , wherein the catalyst is a catalyst system having a double bed structure of different catalysts.

9. The method of claim 6 , wherein the catalyst has the aldol condensation function and comprises an acid or base functionality.

10. The method of claim 9 , wherein the catalyst having the aldol condensation function is selected from the group consisting of CeZrOx, CuZrOx, hydrotalcite, niobium oxide, alumina, silica, silica-alumina, zirconia, titania, or mixed oxides thereof, and molecular sieves including zeolite.

11. The method of claim 6 , wherein the catalyst having the hydrogenation function is a metal component selected from the group consisting of Group VIII metals, Group VI metals, and mixtures thereof, which have a hydrogenation function.

12. The method of claim 11 , wherein the metal component is selected from the group consisting of Pd, Pt, Rh, Ru, Ni, Cu, V, Fe, Co, Mo, W, NiMo, CoMo, NiW, or CoW.

13. The method of claim 6 , wherein the catalyst having the hydrodeoxygenation function comprises both hydrogenation and deoxygenation functions.

14. The method of claim 13 , wherein the catalyst having the hydrodeoxygenation is prepared by loading the metal component having the hydrogenation function on a material comprising an acid or base functionality.

15. The method of claim 6 , wherein step C) is carried out at a temperature of 80 to 500° C. at a hydrogen pressure of 1-200 bar.

16. The method of claim 1 , wherein weight hourly space velocity in the single reactor is adjusted to 0 to 5/hr.

17. The method of claim 16 , wherein the weight hourly space velocity is adjusted to 0 to 2/hr.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 17, 2012
From: CHUNG, YOUNG MIN; KIM, OK YOUN; JEON, HEE JUNG; YOON, YOUNG SEEK; LEE, SEONG HO; KIM, HEE SON; OH, SEUNG HOON; YIM, YOON JAE
To: SK INNOVATION CO., LTD.
Reel/Frame 028971/0470 →
Priority Claims (2)
KR 10-2010-0024794 · Mar 19, 2010 · national
KR 10-2010-0069983 · Jul 20, 2010 · national
Continuity (1)
Related Publication 20130017590A1 · Jan 17, 2013