IP Library Granted Patent US 9,862,906
Granted Patent B2
US 9,862,906 · App. 14/112,238 · Granted Jan 9, 2018

Base oils and methods for making the same

Inventors: Nicholas Ohler (Emeryville, CA); Karl Fisher (Emeryville, CA); Shakeel Tirmizi (Emeryville, CA)
Assignee: AMYRIS, INC.
C10M105/02C07C5/03C07C5/05C10L1/04C10M105/04C10M107/14C07C2521/04C07C2523/44C07C2523/75C10M2203/003C10M2203/022C10M2203/024C10M2203/0206C10M2205/083Y02P20/582
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Quick Facts
Patent No.
US 9,862,906
App. No.
14/112,238
Granted
Jan 9, 2018
Kind
B2
Abstract

Provided herein are isoparaffins derived from hydrocarbon terpenes such as myrcene, ocimene and farnesene, and methods for making the same. In certain variations, the isoparaffins have utility as lubricant base stocks.

Claims (48)

1. A method for making a base oil, the method comprising:

coupling a hydrocarbon terpene feedstock obtained from a renewable carbon source with one or more non-terpene olefin co-monomers in the presence of a catalyst to form one or more branched alkenes comprising one or more hydrocarbon terpene:olefin adducts;

hydrogenating the branched alkenes to form one or more isoparaffins; and

making a base oil from at least a portion of the isoparaffins, wherein the base oil has at least 25% renewable carbon content.

2. The method of claim 1 , wherein the one or more non-terpene olefin co-monomers comprise one or more alpha-olefins.

3. The method of claim 1 , wherein the one or more non-terpene olefin co-monomers are a linear alkene or a branched alkene containing at most two branches.

4. The method of claim 1 , adapted for making a base oil with a kinematic viscosity at 100° C. of about 2-3 cSt, about 4-5 cSt, about 6-8 cSt, or about 9-10 cSt.

5. The method of claim 1 , adapted for making a base oil with a viscosity index of at least about 120, about 130, or about 140.

6. The method of claim 1 , comprising one of the following:

selecting the one or more non-terpene olefin co-monomers and/or a coupling mechanism to modulate a degree of branching in the base oil;

tuning coupling conditions to form predominantly 1:1 hydrocarbon terpene:olefin adducts;

tuning coupling conditions to form a mixture of 1:1 hydrocarbon terpene:olefin adducts and 1:2 hydrocarbon terpene:olefin adducts;

distilling the isoparaffins to form one or more distillation cuts, and making the base oil from at least one of the distillation cuts;

adding a pour point depressant to the at least a portion of the isoparaffins to make the base oil; and

adding a viscosity modifier to the at least a portion of the isoparaffins to make the base oil.

7. The method of claim 2 , comprising increasing a carbon chain length of the one or more alpha-olefins to increase a viscosity index of the base oil.

8. The method of claim 2 , wherein the hydrocarbon terpene feedstock comprises a conjugated diene moiety, and the coupling comprises a hydrovinylation reaction between the conjugated diene moiety and the alpha-olefin.

9. The method of claim 8 , wherein the catalyst comprises a Co(I) catalyst.

10. The method of claim 1 , wherein the hydrocarbon terpene feedstock comprises a partially hydrogenated terpene, and the catalyst comprises a cationic initiator.

11. The method of claim 10 , wherein the cationic initiator comprises a protic acid preferrably sulfuric acid.

12. The method of claim 10 , wherein the catalyst comprises a Lewis acid, a first co-catalyst and a second co-catalyst.

13. The method of claim 12 , wherein the Lewis acid comprises BF 3 , the first co-catalyst comprises an alcohol having the formula R 1 OH, and the second co-catalyst comprises an ester having the formula R 2 CO 2 R 1 , with R 1 being a C 1 -C 10 linear or branched alkyl group and R 2 being a C 1 -C 4 linear or branched alkyl group; preferably the first co-catalyst comprises n-butanol; or the first co-catalyst comprises n-butanol and the second co-catalyst comprises n-butyl acetate.

14. The method of claim 13 , capable of forming isoparaffins in which branching originates predominantly from the hydrocarbon terpene feedstock, or branching comprises predominantly methyl groups.

15. The method of claim 1 , wherein the hydrocarbon terpene feedstock comprises β-farnesene.

16. The method of claim 1 , wherein the hydrocarbon terpene feedstock comprises partially hydrogenated hydrocarbon terpene, preferably partially hydrogenated β-farnesene.

17. The method of claim 2 , wherein the one or more alpha-olefins are selected from the group consisting of 1-hexene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicosene, and any combination of two or more thereof.

18. The method of claim 2 , wherein the hydrocarbon terpene feedstock comprises β-farnesene or partially hydrogenated β-farnesene; and the one or more alpha-olefins are selected from the group consisting of 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, and any combination of two or more thereof, preferably selected from the group consisting of 1-tetradecene, 1-hexadecene, or a mixture of 1-tetradecene and 1-hexadecene, more preferably a mixture of 1-tetradecene and 1-hexadecene.

19. The method of claim 1 , comprising distilling the isoparaffins to form one or more distillation cuts, and making the base oil from at least one of the distillation cuts; wherein a first lighter distillation cut of the isoparaffins is used to make a first base oil and a second heavier distillation cut of the isoparaffins is to make a second base oil.

20. A base oil comprising hydrocarbon terpene feedstock:non-terpene olefin adducts, hydrogenated, wherein the hydrocarbon terpene feedstock is obtained from a renewable carbon source, and wherein the base oil has at least 25% renewable carbon content.

21. The base oil of claim 20 , comprising 1:1 hydrocarbon terpene feedstock:non-terpene olefin adducts, hydrogenated; 1:2 hydrocarbon terpene feedstock:non-terpene olefin adducts, hydrogenated; or 2:1 hydrocarbon terpene feedstock:non-terpene olefin adducts, hydrogenated.

22. The base oil of claim 20 , having a viscosity index of at least about 120, about 130, or about 140.

23. The base oil of claim 20 , having a kinematic viscosity at 100° C. of about 4 cSt, about 5 cSt, or about 3 cSt and a viscosity index of about 120 or higher.

24. The base oil of claim 20 , comprising β-farnesene:alpha-olefin adducts or partially hydrogenated β-farnesene:alpha-olefin adducts, hydrogenated.

25. The base oil of claim 24 , comprising

β-farnesene:1-decene adducts or partially hydrogenated β-farnesene:1-decene adducts, hydrogenated;

β-farnesene:1-dodecene adducts or partially hydrogenated β-farnesene:1-dodecene adducts, hydrogenated;

β-farnesene:1-tetracene adducts or partially hydrogenated β-farnesene:1-tetracene adducts, hydrogenated; β-farnesene:1-hexadecene adducts or partially hydrogenated β-farnesene:1-hexadecene adducts, hydrogenated;

β-farnesene:1-octadecene adducts or partially hydrogenated β-farnesene:1-octadecene adducts, hydrogenated;

β-farnesene:1-tetradecene adducts, hydrogenated and β-farnesene:1-hexadecene adducts, hydrogenated; or

partially hydrogenated β-farnesene:1-tetradecene adducts and partially hydrogenated β-farnesene:1-hexadecene adducts, hydrogenated.

26. The base oil of claim 20 , comprising a pour point depressant and/or a viscosity modifier.

27. The base oil of claim 20 , wherein the hydrocarbon terpene feedstock comprises a partially hydrogenated hydrocarbon terpene.

28. The base oil of claim 27 , wherein the hydrocarbon terpene feedstock comprises partially hydrogenated β-farnesene.

29. The base oil of claim 28 , wherein the non-terpene olefin comprises 1-tetradecene, 1-hexadecene, or a mixture of 1-tetradecene and 1-hexadecene.

30. The base oil of claim 20 , comprising at least about 85% 1:1 hydrocarbon terpene feedstock:non-terpene olefin adducts; or at least about 70% trimeric hydrocarbon terpene feedstock:non-terpene olefin adducts.

31. The base oil of claim 20 , having at least about 50% renewable carbon content; or about 100% renewable carbon content.

32. A lubricant composition comprising the base oil of claim 20 and one or more additives selected from the group consisting of antioxidants, viscosity modifiers, pour point depressants, foam inhibitors, detergents, dispersants, dyes, markers, rust inhibitors or other corrosion inhibiors, emulsifiers, de-emulsifiers, flame retardants, antiwear agents, friction modifiers, thermal stability improvers, and multifunctional additives.

33. The lubricant composition of claim 32 , formulated for use in two cycle engines; as a transmission fluid; as a hydraulic fluid; in compressors; in turbines; in an automotive engine oil; or as a marine grade lubricant.

Assignments (12)
SECURITY INTEREST Recorded May 24, 2024
From: AMYRIS, INC.
To: EUAGORE, LLC
Reel/Frame 067528/0467 →
SECURITY INTEREST Recorded Aug 17, 2023
From: AMYRIS, INC.; AMYRIS CLEAN BEAUTY, INC.; AMYRIS FUELS, LLC; AB TECHNOLOGIES LLC; APRINNOVA, LLC; AMYRIS-OLINKA, LLC; ONDA BEAUTY INC.; UPLAND 1 LLC; AMYRIS ECO-FAB LLC; CLEAN BEAUTY 4U HOLDINGS, LLC; AMYRIS CLEAN BEAUTY LATAM LTDA; INTERFACES INDUSTRIA E COMERCIA DE COSMETICOS LTDA; AMYRIS BIOTECHNOLOGIA DO BRASIL LTDA; AMYRIS EUROPE TRADING B.V. (NETHERLANDS); AMYRIS BIO PRODCUTS PORTUGAL, UNIPESSOAL, LDA; BEAUTY LABS INTERNATIONAL LIMITED; AMYRIS UK TRADING LIMITED
To: EUAGORE, LLC
Reel/Frame 064619/0778 →
SECURITY INTEREST Recorded Aug 3, 2023
From: AMYRIS CLEAN BEAUTY, INC.; AMYRIS FUELS, LLC; AB TECHNOLOGIES LLC; AMYRIS, INC.
To: MUIRISC, LLC
Reel/Frame 064492/0518 →
RELEASE OF SECURITY INTEREST Recorded Feb 14, 2023
From: NAXYRIS S.A.
To: AMYRIS, INC.
Reel/Frame 062760/0753 →
RELEASE OF SECURITY INTEREST Recorded Feb 14, 2023
From: SCHOTTENFELD OPPORTUNITIES FUND II, L.P.
To: AMYRIS, INC.
Reel/Frame 062760/0818 →
SECURITY INTEREST Recorded Oct 18, 2022
From: AMYRIS, INC.
To: FORIS VENTURES, LLC
Reel/Frame 061703/0499 →
GRANT OF PATENT SECURITY INTEREST Recorded Nov 20, 2019
From: AMYRIS, INC.
To: SCHOTTENFELD OPPORTUNITIES FUND II, L.P.
Reel/Frame 051072/0310 →
RELEASE OF SECURITY INTEREST Recorded Aug 28, 2019
From: STEGODON CORPORATION
To: AMYRIS, INC.
Reel/Frame 050206/0606 →
SECURITY INTEREST Recorded Aug 16, 2019
From: AMYRIS, INC.
To: NAXYRIS S.A.
Reel/Frame 050081/0106 →
SECURITY INTEREST Recorded Jun 16, 2016
From: HERCULES CAPITAL INC.
To: STEGODON CORPORATION
Reel/Frame 039048/0251 →
SECURITY INTEREST Recorded Jun 3, 2016
From: AMYRIS, INC.
To: HERCULES TECHNOLOGY GROWTH CAPITAL, INC.
Reel/Frame 038878/0381 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 31, 2014
From: OHLER, NICHOLAS; FISHER, KARL; TIRMIZI, SHAKEEL
To: AMYRIS, INC.
Reel/Frame 032566/0045 →
Continuity (7)
Provisional Application 61475217 · Apr 13, 2011
Provisional Application 61475221 · Apr 13, 2011
Provisional Application 61482122 · May 3, 2011
Provisional Application 61493316 · Jun 3, 2011
Provisional Application 61502252 · Jun 28, 2011
Provisional Application 61524143 · Aug 16, 2011
Related Publication 20140221258A1 · Aug 7, 2014