IP Library Granted Patent US 7,638,116
Granted Patent B2
US 7,638,116 · App. 11/978,041 · Granted Dec 29, 2009

Polyglycerol dimer polyester resins

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Quick Facts
Patent No.
US 7,638,116
App. No.
11/978,041
Granted
Dec 29, 2009
Kind
B2
Abstract

The present invention relates to a series of novel polyesters that are prepared by crosslinking polyglycerol and dimer acid. The nature of the water loving polyglycerol group as well as the fact that a C-36 fatty diacid is used in preparation of the products results in unique products.

Claims (33)

1. A polyester made by esterification reaction consisting of the reaction of:

(a) dimer acid conforming to the following structure:

or hydrogenated dimer acid conforming to the following structure:

or mixtures thereof;

with

(b) a polyglycerol conforming to the following structure;

HO—(CH 2 CH(OH)CH 2 O) n H

n is an integer ranging from 3 to 20.

2. The polyester of claim 1 wherein the mole ratio of hydroxyl groups on the polyglycerol to carboxyl groups on the dimer acid ranges from 2:1 to 4:1.

3. The polyester of claim 2 wherein said esterification reaction is conducted at a temperature of between 120° C. and 200° C. for five to 10 hours.

4. The polyester of claim 2 wherein said dimer acid source is dimer acid.

5. The polyester of claim 2 wherein said dimer acid source is hydrogenated dimer acid.

6. The polyester of claim 1 wherein the mole ratio of hydroxyl groups on the polyglycerol to carboxyl groups on the dimer acid is 2:1.

7. The polyester of claim 1 wherein the mole ratio of hydroxyl groups on the polyglycerol to carboxyl groups on the dimer acid is 3:1.

8. The polyester of claim 1 wherein the mole ratio of hydroxyl groups on the polyglycerol to carboxyl groups on the dimer acid is 4:1.

9. A process for conditioning hair skin and fiber which comprises contacting the hair skin of fiber with an effective conditioning concentration of a polyester made by the reaction consisting of the reaction of:

(a) dimer acid conforming to the following structure:

or hydrogenated dimer acid conforming to the following structure:

or mixtures thereof;

with

(b) a polyglycerol conforming to the following structure;

HO—(CH 2 CH(OH)CH 2 O) n H

n is an integer ranging from 3 to 20.

10. The process of claim 9 wherein the mole ratio of hydroxyl groups on the polyglycerol to carboxyl groups on the dimer acid ranges from 2:1 to 4:1.

11. The process of claim 10 wherein said esterification reaction is conducted at a temperature of between 120° C. and 200° C. for five to 10 hours.

12. The process of claim 10 wherein said dimer acid source is dimer acid.

13. The process of claim 10 wherein said dimer acid source is hydrogenated dimer acid.

14. The process of claim 9 wherein the mole ratio of hydroxyl groups on the polyglycerol to carboxyl groups on the dimer acid is 2:1.

15. The process of claim 9 wherein the mole ratio of hydroxyl groups on the polyglycerol to carboxyl groups on the dimer acid is 3:1.

16. The process of claim 9 wherein the mole ratio of hydroxyl groups on the polyglycerol to carboxyl groups on the dimer acid is 4:1.

17. The process of claim 10 wherein said effective conditioning concentration ranges between 0.1 and 10% by weight.

18. The process of claim 10 wherein said dimer acid source is dimer acid.

19. The process of claim 10 wherein said dimer acid source is hydrogenated dimer acid.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 28, 2011
From: ZENITECH, LLC
To: T C U.S.A. INC.
Reel/Frame 026986/0518 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 8, 2010
From: LAVAY, CARTER
To: ZENITECH LLC
Reel/Frame 024640/0850 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 1, 2010
From: O'LENICK JR., ANTHONY J.
To: ZENITECH LLC
Reel/Frame 024640/0210 →