IP Library Granted Patent US 7,851,558
Granted Patent B2
US 7,851,558 · App. 12/091,346 · Granted Dec 14, 2010

Brominated butadiene/vinyl aromatic copolymers, blends of such copolymers with a vinyl aromatic polymer and polymeric foams formed from such blends

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Quick Facts
Patent No.
US 7,851,558
App. No.
12/091,346
Granted
Dec 14, 2010
Kind
B2
Abstract

A thermally stable brominated butadiene copolymer, such as brominated styrene/butadiene block copolymer, brominated random styrene/butadiene copolymer or brominated styrene/butadiene graft copolymer, preparation of the brominated butadiene copolymers, use of the brominated butadiene copolymers as a flame retardant additive and polymeric compositions, both foamed and non-foamed, that incorporate a flame-retarding amount of brominated butadiene copolymer.

Claims (27)

1. A thermally stable brominated copolymer, the copolymer having polymerized therein a butadiene moiety and a vinyl aromatic monomer moiety, the copolymer having, prior to bromination, a vinyl aromatic monomer content of from 5 to 90 percent by weight, based upon copolymer weight, a 1,2-butadiene isomer content of greater than 0 percent by weight, based upon butadiene moiety weight, and a weight average molecular weight of at least 1000, the brominated copolymer having an unbrominated, non-aromatic double bond content of less than or equal to 15 percent, based upon non-aromatic double bond content of the copolymer prior to bromination as determined by H 1 NMR spectroscopy and a five percent weight loss temperature, as determined by thermogravimetric analysis (TGA) of at least 200 degrees centigrade.

2. The brominated copolymer of claim 1 , wherein the copolymer is selected from the group consisting of block copolymers, random copolymers and graft copolymers.

3. The brominated copolymer of claim 1 , wherein the molecular weight of the copolymer prior to bromination is less than 200,000.

4. The brominated copolymer of claim 1 , wherein the molecular weight of the copolymer prior to bromination is within a range of from 2,000 to 100,000.

5. The brominated copolymer of claim 1 , wherein the molecular weight of the copolymer prior to bromination is within a range of from 50,000 to 100,000.

6. The brominated copolymer of claim 1 , wherein the vinyl aromatic monomer is selected from the group consisting of styrene, alpha-methylstyrene, halogenated styrenes, alkoxylated styrenes, nitrated styrenes, alkylated styrenes, and mixtures thereof.

7. The brominated copolymer of claim 6 , wherein the vinyl aromatic monomer is at least one of styrene, alpha-methylstyrene, 2-bromostyrene, 4-bromostyrene, 2-methoxystyrene, 4-methoxystyrene, 2-methylstyrene, 4-methylstyrene, 2,4-dimethylstyrene, 2-nitrostyrene and 4-nitrostyrene.

8. The brominated copolymer of claim 1 , wherein the copolymer is a block copolymer selected from triblock copolymers and diblock copolymers.

9. The brominated copolymer of claim 1 , wherein the 1,2-butadiene isomer content of the copolymer prior to bromination is greater than 10 percent by weight, based upon butadiene moiety weight.

10. The brominated copolymer of claim 9 , wherein the 1,2-butadiene isomer content of the copolymer prior to bromination is greater than 50 percent by weight, based upon butadiene moiety weight.

11. The brominated copolymer of claim 9 , wherein the 1,2-butadiene isomer content of the copolymer prior to bromination is greater than 70 percent by weight, based upon butadiene moiety weight.

12. The brominated copolymer of claim 9 , wherein the 1,2-butadiene isomer content of the copolymer prior to bromination is greater than 90 percent by weight, based upon butadiene moiety weight.

13. The brominated copolymer of claim 1 , wherein the 5% weight loss temperature is at least 205 degrees centigrade.

14. The brominated copolymer of claim 13 , wherein the 5% weight loss temperature is at least 215 degrees centigrade.

15. The brominated copolymer of claim 13 , wherein the 5% weight loss temperature is at least 225 degrees centigrade.

16. A polymer blend, the blend comprising a vinyl aromatic polymer and a flame-retarding amount of the brominated copolymer of claim 1 .

17. The polymer blend of claim 16 , wherein the vinyl aromatic polymer is at least one polymer selected from the group consisting of polystyrene, ethylene/styrene interpolymers, ethylene/propylene/styrene interpolymers, poly(alpha-methylstyrene), styrene/acrylonitrile copolymers, styrene/acrylic acid and esters, styrene/methacrylic acid and esters, and polymers having polymerized therein at least one moiety selected from styrene, 2-bromostyrene, 4-bromostyrene, 2-methoxystyrene, 4-methoxystyrene, 2-nitrostyrene, 4-nitrostyrene, 2-methylstyrene, 4-methylstyrene, and 2,4-dimethylstyrene.

18. The polymer blend of claim 16 , wherein the flame retarding amount is an amount sufficient to provide the blend with a bromine content within a range of from 0.1 percent by weight to 25 percent by weight, based upon blend weight.

19. The polymer blend of claim 16 , further comprising at least one additive selected from the group consisting of flame retardant additives, flame retardant adjuvants, thermal stabilizers, ultraviolet light stabilizers, nucleating agents, antioxidants, foaming agents, acid scavengers and coloring agents.

20. The polymer blend of claim 16 , which is cellular.

21. The cellular polymer blend of claim 20 , which is an extruded polymer foam or an expanded polymer bead foam.

22. A process of preparing the brominated copolymer of claim 1 , the process comprising:

a. providing a homogeneous reaction solution of a copolymer, a brominating agent and a solvent, the copolymer having polymerized therein a butadiene moiety and a vinyl aromatic monomer moiety, the copolymer having a vinyl aromatic monomer content of from 5 to 90 percent by weight, based upon copolymer weight, a 1,2-butadiene isomer content of greater than 0 percent by weight, based upon butadiene moiety weight, and a weight average molecular weight of at least 1000;

b. maintaining the reaction solution under reaction conditions for a period of time sufficient to brominate at least 85 percent of non-aromatic double bonds contained in the copolymer, based upon non-aromatic double bond content of the copolymer prior to bromination as determined by H 1 NMR spectroscopy.

23. The process of claim 22 , wherein the brominating agent comprises pyridinium tribromide.

24. The process of claim 22 , wherein the solvent is selected from tetrahydrofuran or a blend of carbon tetrachloride and an alcohol.

25. The process of claim 24 , wherein the solvent is a blend of carbon tetrachloride and an alcohol and the brominating agent is elemental bromine.

Assignments (8)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 10, 2024
From: DOW GLOBAL TECHNOLOGIES LLC
To: THE DOW CHEMICAL COMPANY
Reel/Frame 069923/0030 →
CHANGE OF LEGAL ENTITY Recorded Sep 10, 2024
From: DDP SPECIALTY ELECTRONIC MATERIALS US, INC
To: DDP SPECIALTY ELECTRONIC MATERIALS US, LLC
Reel/Frame 068907/0881 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 10, 2024
From: THE DOW CHEMICAL COMPANY
To: DDP SPECIALTY ELECTRONIC MATERIALS US, INC
Reel/Frame 068922/0001 →
CHANGE OF NAME Recorded Jan 9, 2012
From: DOW GLOBAL TECHNOLOGIES INC.
To: DOW GLOBAL TECHNOLOGIES LLC
Reel/Frame 027501/0614 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 8, 2010
From: BEULICH, INKEN
To: DCOMCO, INC.
Reel/Frame 025112/0219 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 8, 2010
From: DCOMCO, INC.
To: THE DOW CHEMICAL COMPANY
Reel/Frame 025112/0248 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 8, 2010
From: KING, BRUCE A.; STOBBY, WILLIAM G.; MURRAY, DANIEL J.; WORKU, ANTENEH Z.; TINETTI, SHEILA M.; HAHN, STEPHEN F.; DRUMRIGHT, RAY E.
To: DOW GLOBAL TECHNOLOGIES INC.
Reel/Frame 025112/0318 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 8, 2010
From: THE DOW CHEMICAL COMPANY
To: DOW GLOBAL TECHNOLOGIES INC.
Reel/Frame 025112/0325 →