IP Library Granted Patent US 39,617
Granted Patent E1
US 39,617 · App. 10/655,988 · Granted May 8, 2007

Butadiene polymers having terminal functional groups

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Quick Facts
Patent No.
US 39,617
App. No.
10/655,988
Granted
May 8, 2007
Kind
E1
Abstract

Hydrogenated butadiene polymers having terminal functional groups have minimum viscosity at any molecular weight when the 1,2-addition is between 30% and 70% Hydrogenated butadiene polymers having about two terminal hydroxyl groups per molecule have surprisingly lower viscosities at 30% to 70% 1,2-addition than similar polymers having either higher or lower amounts of 1,2-addition. The polymers are useful in making coatings, sealants, binders, and block copolymers with polyesters, polyamides, and polycarbonates.

Claims (26)

1. A polymer composition, produced by the steps of:

reacting one or more compounds with the terminal functional groups on a polymer, and said polymer consists essentially of:

polymerized 1,3-butadiene having a peak molecular weight between 500 and 20,000, 1,2-addition between 30% and 70%, and hydrogenation of at least 90% of the unsaturation;

a ratio of viscosity ( in poise at room temperature ) to peak molecular weight raised to the 3 . 4 power of at most 2 . 0 times 10 −9 ; and

one about two or more terminal functional groups per molecule.

2. The polymer composition of claim 1 6 , wherein the terminal functional groups of the polymer are selected from a the group consisting of hydroxyl, carboxyl, phenol, epoxy, and amine groups.

3. The polymer of claim 2 , wherein the polymer has a ratio of viscosity (poise at room temperature) to peak molecular weight raised to the 3.4 power of at most 2.0×10 −9 .

4. The polymer composition of claim 3 6 , wherein the polymerized 1 , 3 -butadiene has a peak molecular weight between 1,000 and 10,000.

5. The polymer composition of claim 4 , wherein the polymerized 1 , 3 -butadiene is at least 95% hydrogenated.

6. The polymer composition of claim 5 1 , wherein the ratio of viscosity to peak molecular weight raised to the 3.4 power of the polymer is less than 1.0 × times 10 −9 .

7. The polymer composition of claim 6 , wherein the terminal functional groups of the polymer consist of about two hydroxyl groups per molecule.

8. The polymer composition of claim 1 , wherein the peak molecular weight of the polymer is between 1000 and 10000.

9. The polymer composition of claim 8 6 , wherein the 1,2-addition of the polymerized 1 , 3 -butadiene is between 40% and 60%.

10. The polymer composition of claim 1 , wherein the polymerized 1,3-butadiene has about two hydroxyl groups per molecule.

11. The polymeric polymer composition of claim 10 , wherein the polymerized 1,3-butadiene is reacted with compounds that form a coating.

12. The polymeric polymer composition of claim 10 , wherein the polymerized 1,3-butadiene is reacted with compounds that form a block selected from the group consisting of polyesters, polyamides, and polycarbonates.

13. The polymer composition of claim 8 wherein the polymer has a peak molecular weight of about 10 , 000 .

14. The polymer composition of claim 8 wherein the polymer has a peak molecular weight of about 5 , 000 .

15. The polymer composition of claim 8 wherein the polymer has a peak molecular weight of about 3 , 000 .

16. The polymer composition of claim 8 wherein the polymer has a peak molecular weight of about 2 , 000 .

17. The polymer composition of claim 4 wherein the polymer has a peak molecular weight of about 10 , 000 .

18. The polymer composition of claim 4 wherein the polymer has a peak molecular weight of about 5 , 000 .

19. The polymer composition of claim 4 wherein the polymer has a peak molecular weight of about 3 , 000 .

20. The polymer composition of claim 4 wherein the polymer has a peak molecular weight of about 2 , 000 .

21. The polymer composition of claim 1 wherein the polymerized 1 , 3 - butadiene has 1 . 7 terminal functional groups per molecule.

22. The polymer composition of claim 1 wherein the polymerized 1 , 3 - butadiene has 1 . 9 terminal functional groups per molecule.

Assignments (5)
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT PATENT NUMBER 7720798 AND REPLACE WITH PATENT NUMBER 7220798 PREVIOUSLY RECORDED ON REEL 025845 FRAME 0795. ASSIGNOR(S) HEREBY CONFIRMS THE RELEASE BY SECURED PARTY. Recorded Dec 16, 2015
From: USB AG, STAMFORD BRANCH
To: KRATON POLYMERS U.S. LLC
Reel/Frame 037312/0070 →
RELEASE OF SECURITY INTEREST Recorded Mar 28, 2013
From: BANK OF AMERICA, N.A.
To: KRATON POLYMERS U.S. LLC
Reel/Frame 030108/0288 →
NOTICE OF GRANT OF SECURITY INTEREST IN PATENTS Recorded Mar 4, 2011
From: KRATON POLYMERS U.S. LLC
To: BANK OF AMERICA N.A., AS COLLATERAL AGENT
Reel/Frame 025899/0176 →
RELEASE OF SECURITY INTEREST Recorded Feb 24, 2011
From: UBS AG, STAMFORD BRANCH
To: KRATON POLYMERS U.S. LLC
Reel/Frame 025845/0795 →
SECURITY INTEREST Recorded Jan 2, 2004
From: KRATON POLYMERS U.S. LLC
To: UBS AG, STAMFORD BRANCH
Reel/Frame 014242/0281 →