IP Library Granted Patent US 9,624,454
Granted Patent B2
US 9,624,454 · App. 14/852,301 · Granted Apr 18, 2017

Reclamation of estolide base oils from compositions comprising immiscible components

Inventor: Jeremy Forest (Honolulu, HI)
Assignee: Biosynthetic Technologies, LLC
C11B13/00B01D17/045C10M175/005C11B3/00
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Quick Facts
Patent No.
US 9,624,454
App. No.
14/852,301
Granted
Apr 18, 2017
Kind
B2
Abstract

Methods and systems for processing a composition comprising an estolide base oil and an immiscible component. In certain embodiments, the process comprises separating an estolide base oil from immiscible components such as water. In certain embodiments, the method comprises one or more of gravity separating, coalescing, and accumulating.

Claims (35)

1. A method comprising:

providing a first composition comprising an estolide base oil, at least one additional component, and at least one immiscible component;

separating the at least one immiscible component from the first composition to provide a second composition comprising the at least one additional component and the estolide base oil; and

removing the at least one additional component from the second composition.

2. The method according to claim 1 , wherein the at least one immiscible component comprises water.

3. The method according to claim 2 , wherein the composition comprises an emulsion.

4. The method according to claim 1 , wherein the separating comprises at least one of gravity separating, coalescing, or accumulating.

5. The method according to claim 1 , wherein the separating comprises the use of at least one coalescer.

6. The method according to claim 5 , wherein the at least one coalescer comprises one or more corrugated plates.

7. The method according to claim 5 , wherein the at least one coalescer comprises an oleophilic material.

8. The method according to claim 7 , wherein the oleophilic material comprises a polymer.

9. The method according to claim 8 , wherein the oleophilic material comprises a polyolefin.

10. The method according to claim 1 , wherein the separating comprises the use of an accumulator.

11. The method according claim 1 , wherein the separating comprises the use of filtration.

12. The method according to claim 1 , wherein the separating comprises the use of adsorption/absorption.

13. The method according to any one claim 1 , wherein the first composition comprises marine bilge water.

14. The method according to claim 1 , wherein the at least one additional component comprises a hydrocarbon.

15. The method according to claim 1 , wherein the removing comprises at least one of distilling or solvent extracting.

16. The method according to claim 1 , wherein the second composition is reused or recycled.

17. The method according to claim 14 , wherein the at least one additional component is selected from one or more of a Group I base oil, a Group II base oil, or a Group III base oil.

18. The method according to claim 1 , wherein the estolide base oil comprises at least one compound selected from 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 selected from hydrogen and optionally substituted alkyl that is saturated or unsaturated, and branched or unbranched; and

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

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

19. The method according to claim 18 , 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 50;

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.

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 (2)
Provisional Application 62055627 · Sep 25, 2014
Related Publication 20160090547A1 · Mar 31, 2016