IP Library Granted Patent US 9,076,588
Granted Patent B2
US 9,076,588 · App. 13/936,015 · Granted Jul 7, 2015

Dielectric fluids comprising estolide compounds and methods of making and using the same

Inventors: Travis Thompson (Anaheim, CA); Jakob Bredsguard (Lake Forest, CA); Jeremy Forest (Newport Beach, CA)
Assignee: Biosynthetic Technologies, LLC
H01F41/00Y10T29/4902C10M105/42C10M2203/10C10M2205/028C10M2207/023C10M2207/026C10M2207/08C10M2207/2805C10M2207/281C10M2207/289C10M2207/301C10M2207/40C10M2209/103C10M2215/064C10N2220/00C10N2220/022C10N2230/02C10N2230/60C10N2230/64C10N2240/201H01F27/12H01B3/22
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Quick Facts
Patent No.
US 9,076,588
App. No.
13/936,015
Granted
Jul 7, 2015
Kind
B2
Abstract

Provided herein are dielectric fluids 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 herein are uses of dielectric fluids and electrical devices such as transformers that comprise a dielectric fluid comprising at least one estolide compound.

Claims (42)

1. A method of retrofilling a transformer having a first dielectric fluid, said method comprising:

removing at least a portion of the first dielectric fluid from the transformer; and

replacing the at least a portion of the first dielectric fluid with a quantity of a second dielectric fluid,

wherein said second dielectric fluid comprises an estolide base oil, and said second dielectric fluid exhibits an EN selected from an integer or fraction of an integer that is equal to or less than 1.5, wherein the EN is the average number of estolide linkages in compounds according to Formula I, and wherein said estolide base oil comprises at least one compound 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 equal to or greater than 0;

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

R 2 is selected from hydrogen and optionally substituted alkyl that is saturated or unsaturated, and branched or unbranched,

wherein each fatty acid chain residue of said at least one compound is independently optionally substituted.

2. The method according to claim 1 , wherein

x is, independently for each occurrence, an integer selected from 0 to 14;

y is, independently for each occurrence, an integer selected from 0 to 14;

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 optionally substituted 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 method 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 method according to claim 2 , wherein x is, independently for each occurrence, an integer selected from 7 and 8.

5. The method according to claim 4 , wherein y is, independently for each occurrence, an integer selected from 7 and 8.

6. The method according to claim 3 , wherein x+y is 15 for at least one chain.

7. The method according to claim 4 , wherein R 2 is an unsubstituted C 1 to C 18 alkyl that is saturated, and branched or unbranched.

8. The method according to claim 7 , wherein R 2 is branched.

9. The method according to claim 3 , 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.

10. The method according to claim 8 , wherein R 2 is a branched C 6 to C 12 alkyl.

11. The method according to claim 4 , wherein R 1 is an unsubstituted C 1 to C 18 alkyl that is saturated, and branched or unbranched.

12. The method according to claim 3 , 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.

13. The method according to claim 7 , wherein R 1 is an unsubstituted C 7 to C 17 alkyl that is saturated, and branched or unbranched.

14. The method according to claim 13 , wherein R 1 is unbranched.

15. The method according to claim 1 , wherein the second dielectric fluid has a kinematic viscosity equal to or less than 45 cSt when measured at 40° C.

16. The method according to claim 15 , wherein the second dielectric fluid has a pour point equal to or lower than −25° C.

17. The method according to claim 1 , wherein second dielectric fluid further comprises at least one additive selected from one or more of an antioxidant, an antimicrobial agent, a cold flow modifier, a pour point modifier, a metal chelating agent, or a metal deactivator.

18. The method according to claim 1 , wherein the second dielectric fluid has a fire point of greater than or equal to 300° C.

19. The method according to claim 1 , wherein the second dielectric fluid has a flash point of greater than or equal to 275° C.

20. The method according to claim 1 , wherein the second dielectric fluid has a total acid number equal to or less than 0.1 mg KOH/g.

21. The method according to claim 17 , wherein the at least one additive comprises an antioxidant selected from one or more of BHT, BHA, TBHQ, DBPC, THBP, an alkylated diphenylamine, vitamin E, or ascorbyl palmitate.

22. The method according to claim 1 , wherein the transformer comprises a housing and a core/coil assembly, wherein the core/coil assembly is positioned in the housing and wherein the second dielectric fluid surrounds at least a portion of the core/coil assembly.

23. The method according to claim 1 , wherein the second dielectric fluid further comprises at least one additive selected from one or more of a polyalphaolefin, a synthetic ester, a polyalkylene glycol, a mineral oil, a vegetable oil, an animal-based oil, a monoglyceride, a diglyceride, a triglyceride, or a fatty-acid ester.

24. The method according to claim 4 , wherein y is 0 for each occurrence.

Assignments (6)
ASSIGNMENT OF SECURITY INTEREST Recorded Mar 23, 2018
From: EVONIK OIL ADDITIVES USA, INC.
To: BIOSYN HOLDINGS, LLC
Reel/Frame 045684/0293 →
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 →
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 →
Continuity (5)
Continuation 13552878 · Jul 19, 2012
Continuation 13407402 · Feb 28, 2012
Provisional Application 61548613 · Oct 18, 2011
Provisional Application 61498499 · Jun 17, 2011
Related Publication 20130340246A1 · Dec 26, 2013