IP Library Granted Patent US 8,633,143
Granted Patent B2
US 8,633,143 · App. 13/754,775 · Granted Jan 21, 2014

Compositions comprising estolide compounds and methods of making and using the same

Inventors: Travis Thompson (Anaheim, CA); Jakob Bredsguard (Irvine, CA); Jeremy Forest (Irvine, CA)
Assignee: Biosynthetic Technologies, LLC
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,633,143
App. No.
13/754,775
Granted
Jan 21, 2014
Kind
B2
Abstract

Provided herein are compositions comprising at least one estolide compound of formula: in which n is an integer equal to or greater than 0; m is an integer equal to or greater than 1; R 1 , independently for each occurrence, is selected from optionally substituted alkyl that is saturated or unsaturated, and branched or unbranched; R 2 is selected from hydrogen and optionally substituted alkyl that is saturated or unsaturated, and branched or unbranched; and R 3 and R 4 , independently for each occurrence, are selected from optionally substituted alkyl that is saturated or unsaturated, and branched or unbranched. Also provided are uses of the compositions described herein.

Claims (45)

1. A composition comprising:

at least one metal sulfonate;

at least one additive comprising a styrene copolymer or a styrene interpolymer;

at least one antioxidant; and

at least one estolide compound selected from compounds of Formula I:

wherein

x is, independently for each occurrence, an integer selected from 0 to 20;

y is, independently for each occurrence, an integer selected from 0 to 20;

n is an integer greater than or equal to 0;

R 1 is an optionally substituted alkyl that is saturated or unsaturated, and branched or unbranched; and

R 2 is an unsubstituted alkyl that is saturated or unsaturated, and branched or unbranched,

wherein each fatty acid chain residue of said at least one estolide compound is unsubstituted.

2. The composition according to claim 1 , wherein

x is, independently for each occurrence, an integer selected from 1 to 10;

y is, independently for each occurrence, an integer selected from 1 to 10;

n is an integer selected from 0 to 8;

R 1 is an optionally substituted C 1 to C 22 alkyl that is saturated or unsaturated, and branched or unbranched; and

R 2 is an unsubstituted C 1 to C 22 alkyl that is saturated or unsaturated, and branched or unbranched,

wherein each fatty acid chain residue is unsubstituted.

3. The composition according to claim 2 , wherein

x+y is, independently for each chain, an integer selected from 13 to 15; and

n is an integer selected from 0 to 6.

4. The composition according to claim 3 , wherein x is, independently for each occurrence, an integer selected from 7 and 8.

5. The composition according to claim 3 , wherein y is, independently for each occurrence, an integer selected from 7 and 8.

6. The composition according to claim 1 , wherein R 2 is an unsubstituted C 1 to C 20 alkyl that is saturated or unsaturated and branched or unbranched.

7. The composition according to claim 6 , wherein R 2 is selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decanyl, undecanyl, dodecanyl, tridecanyl, tetradecanyl, pentadecanyl, hexadecanyl, heptadecanyl, octadecanyl, nonadecanyl, and icosanyl, which are saturated or unsaturated and branched or unbranched.

8. The composition according to claim 6 , wherein R 2 is an unsubstituted C 6 to C 12 alkyl that is saturated and branched.

9. The composition according to claim 1 , wherein R 1 is an unsubstituted alkyl that is saturated or unsaturated, and branched or unbranched.

10. The composition according to claim 9 , wherein R 1 is an unsubstituted C 1 to C 20 alkyl that is saturated or unsaturated, and branched or unbranched.

11. The composition according to claim 10 , wherein R 1 is selected from methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decanyl, undecanyl, dodecanyl, tridecanyl, tetradecanyl, pentadecanyl, hexadecanyl, heptadecanyl, octadecanyl, nonadecanyl, and icosanyl, which are saturated or unsaturated and branched or unbranched.

12. The composition according to claim 10 , wherein R 1 is an unsubstituted C 7 to C 17 alkyl that is unbranched and saturated or unsaturated.

13. The composition according to claim 12 , wherein R 1 is saturated.

14. The composition according to claim 1 , wherein said composition has an EN selected from an integer or fraction of an integer that is equal to or less than 2, wherein EN is the average number of estolide linkages in compounds according to Formula I.

15. The composition according to claim 14 , wherein said at least one estolide compound has a kinematic viscosity equal to or less than 55 cSt when measured at 40° C.

16. The composition according to claim 15 , wherein said at least one estolide compound has a pour point equal to or lower than −25° C.

17. The composition according to claim 1 , wherein said at least one metal sulfonate is selected from one or more of a calcium sulfonate or a magnesium sulfonate.

18. The composition according to claim 1 , wherein the at least antioxidant is selected from one or more of an amine antioxidant, a phenolic antioxidant, or an organometallic antioxidant.

19. The composition according to claim 1 , further comprising at least one extreme pressure agent.

20. The composition according to claim 19 , wherein the at least one extreme pressure agent is a phosphorous extreme pressure agent.

21. The composition according to claim 1 , wherein said composition further comprises at least one of a separation preventer, a stability enhancer, a surfactant, a biocide, a corrosion inhibitor, an abrasion inhibitor, a viscosity index improver, a pour point depressant, a dispersant, or an antifoaming agent.

22. The composition according to claim 1 , wherein said composition comprises an engine lubricant, a hydraulic fluid, a crankcase oil, or a gearbox oil.

23. The composition according to claim 1 , wherein the at least one additive comprises a copolymer prepared from styrene and at least one butadiene.

24. The composition according to claim 1 , wherein the at least one additive comprises an interpolymer prepared from styrene and at least one acrylic ester.

25. The composition according to claim 20 , wherein the phosphorous extreme pressure agent comprises a zinc salt of a phosphorous compound.

26. The composition according to claim 20 , wherein the phosphorous extreme pressure agent is prepared by process that includes reacting a phosphorous compound with zinc oxide.

Assignments (8)
ASSIGNMENT OF SECURITY INTEREST Recorded Mar 23, 2018
From: BP TECHNOLOGY VENTURES INC.
To: BIOSYN HOLDINGS, LLC
Reel/Frame 045688/0600 →
ASSIGNMENT OF SECURITY INTEREST Recorded Mar 23, 2018
From: EVONIK CORPORATION
To: BIOSYN HOLDINGS, LLC
Reel/Frame 045860/0547 →
ASSIGNMENT OF SECURITY INTEREST Recorded Mar 23, 2018
From: EVONIK OIL ADDITIVES USA, INC.
To: BIOSYN HOLDINGS, LLC
Reel/Frame 045684/0293 →
RELEASE OF SECURITY INTEREST Recorded Feb 13, 2018
From: SILICON VALLEY BANK
To: BIOSYNTHETIC TECHNOLOGIES, LLC
Reel/Frame 044916/0936 →
SECURITY INTEREST Recorded Jan 30, 2018
From: BIOSYNTHETIC TECHNOLOGIES, LLC
To: BP TECHNOLOGY VENTURES INC.
Reel/Frame 045196/0587 →
SECURITY INTEREST Recorded Mar 18, 2016
From: BIOSYNTHETIC TECHNOLOGIES, LLC
To: EVONIK OIL ADDITIVES USA, INC.
Reel/Frame 038146/0859 →
SECURITY INTEREST Recorded Nov 30, 2015
From: BIOSYNTHETIC TECHNOLOGIES, LLC
To: EVONIK CORPORATION
Reel/Frame 037162/0364 →
SECURITY INTEREST Recorded Dec 20, 2014
From: BIOSYNTHETIC TECHNOLOGIES, LLC
To: SILICON VALLEY BANK
Reel/Frame 034562/0322 →
Continuity (6)
Continuation 13587120 · Aug 16, 2012
Continuation 13531923 · Jun 25, 2012
Continuation 13404903 · Feb 24, 2012
Provisional Application 61498499 · Jun 17, 2011
Provisional Application 61569046 · Dec 9, 2011
Related Publication 20130172223A1 · Jul 4, 2013