IP Library Granted Patent US 7,662,876
Granted Patent B2
US 7,662,876 · App. 10/583,206 · Granted Feb 16, 2010

Arylalkylsilyls used as flame retardant additives

Assignee: Supresta LLC
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Quick Facts
Patent No.
US 7,662,876
App. No.
10/583,206
Granted
Feb 16, 2010
Kind
B2
Abstract

Flame retarded resin compositions comprise at least one resin selected from the group consisting of polycarbonate, polyester and mixtures thereof, and a flame retarding effective amount of at least one nonhalogenated arylalkylsilyl flame retardant, the flame retarded resin composition being substantially free of haloorganic flame retardant and phosphate flame retardant.

Claims (34)

1. A flame retarded resin composition comprising at least one resin selected from the group consisting of polycarbonate, polyester and mixtures thereof, and a flame retarding effective amount of at least one nonhalogenated arylalkylsilyl flame retardant represented by the formula

wherein R 1 , R 3 , R 5 and R 6 each independently is aryl or substituted aryl; R 2 and R 4 each independently is a lower alkyl; X is a bridging group derived from a diol possessing an arylene moiety; and, n has a value of up to about 20; the flame retardant resin composition being substantially free of haloorganic flame retardant and phosphate flame retardant.

2. The flame retarded resin composition of claim 1 wherein the polycarbonate resin is an aromatic polycarbonate and the polyester resin is an aromatic polyester.

3. The flame retarded resin composition of claim 1 further comprising at least one other molding grade thermoplastic resin.

4. The flame retarded resin composition of claim 3 wherein the other molding grade thermoplastic resin is selected from the group consisting of polystyrene, acrylonitrile-butadiene-styrene, high impact polystyrene, polyamides, polyethylene, polypropylene, polysulfone, polyvinyl acetate, ethylene-vinyl acetate copolymers, poly(methyl methacrylate), polyethylene oxide, cellulose acetate, cellulose nitrate and mixtures thereof.

5. The flame retarded resin composition of claim 2 further comprising at least one other molding grade thermoplastic resin.

6. The flame retarded resin composition of claim 5 wherein the other molding grade thermoplastic resin is selected from the group consisting of polystyrene, acrylonitrile-butadiene-styrene, high impact polystyrene, polyamides, polyethylene, polypropylene, polysulfone, polyvinyl acetate, ethylene-vinyl acetate copolymers, poly(methyl methacrylate), polyethylene oxide, cellulose acetate, cellulose nitrate and mixtures thereof.

7. The flame retarded resin composition of claim 1 wherein the polycarbonate resin is present at a level of from about 70 to about 100 weight %.

8. The flame retarded resin composition of claim 1 wherein the polyester resin is present at a level of from about 70 to about 100 weight %.

9. The flame retarded resin composition of claim 1 wherein the polycarbonate resin is present at a level of from about 50 to about 100 weight %.

10. The flame retarded resin composition of claim 1 wherein the polyester resin is present at a level of from about 50 to about 100 weight %.

11. The flame retarded resin composition of claim 3 wherein the other thermoplastic resin is present at a level up to about 50 weight %.

12. The flame retarded resin composition of claim 3 wherein the other thermoplastic resin is present at a level of up to about 30 weight %.

13. The flame retarded composition of claim 1 wherein R 1 , R 3 , R 5 and R 6 each independently is aryl or substituted aryl of from 6 to about 22 carbon atoms, R 2 and R 4 each independently is a lower alkyl of from 1 to about 4 carbon atoms, and n has a value of up to 5.

14. The flame retarded composition of claim 1 wherein R 2 and R 4 each is a methyl group.

15. The flame retarded composition of claim 1 wherein bridging group x is represented by one of the following structures:

16. The flame retarded composition of claim 1 wherein n is 1 or 2.

17. The flame retarded composition of claim 1 wherein the arylalkysilyl flame retardant is present at a level of from 1 to about 30 weight %.

18. The flame retarded composition of claim 2 wherein R 1 , R 3 , R 5 and R 6 each independently is aryl or substituted aryl of from 6 to about 22 carbon atoms, R 2 and R 4 each independently is a lower alkyl of from 1 to about 4 carbon atoms, and n has a value of up to 5.

19. The flame retarded composition of claim 2 wherein R 2 and R 4 each is a methyl group.

20. The flame retarded composition of claim 2 wherein bridging group x is represented by one of the following structures:

21. The flame retarded composition of claim 2 wherein n is 1 or 2.

22. The flame retarded composition of claim 2 wherein the arylalkysilyl flame retardant is present at a level of from 1 to about 30 weight %.

23. The flame retarded composition of claim 3 wherein R 1 , R 3 , R 5 and R 6 each independently is aryl or substituted aryl of from 6 to about 22 carbon atoms, R 2 and R 4 each independently is a lower alkyl of from 1 to about 4 carbon atoms, and n has a value of up to 5.

24. The flame retarded composition of claim 3 wherein R 2 and R 4 each is a methyl group.

25. The flame retarded composition of claim 3 wherein bridging group X is represented by one of the following structures:

26. The flame retarded composition of claim 3 wherein n is 1 or 2.

27. The flame retarded composition of claim 3 wherein the arylalkysilyl flame retardant is present at a level of from 1 to about 30 weight %.

28. The flame retarded composition of claim 5 wherein R 1 , R 3 , R 5 and R 6 each independently is aryl or substituted aryl of from 6 to about 22 carbon atoms, R 2 and R 4 each independently is a lower alkyl of from 1 to about 4 carbon atoms, and n has a value of up to 5.

29. The flame retarded composition of claim 5 wherein R 2 and R 4 each is a methyl group.

30. The flame retarded composition of claim 5 wherein bridging group x is represented by one of the following structures:

31. The flame retarded composition of claim 5 wherein n is 1 or 2.

32. The flame retarded composition of claim 5 wherein the arylalkysilyl flame retardant is present at a level of from 1 to about 30 weight %.

33. A method for making arylalkylsilyl flame retardant of claim 1 having a high weight ratio of dimer to oligomer which comprises reacting a molar excess of an alkyltrichlorosilane with a diphenol to obtain a diphenyl bis(dichloroalkylsilane), removing unreacted alkyltrichlorosilane by distillation, reacting the diphenyl bis(dichloroalkylsilane) from which unreacted aklyltrichlorosilane has been removed with a molar excess of the same or different phenol to provide arylalkylsilyl flame retardant and removing unreacted phenol from the arylalkysilyl flame retardant by distillation.

Assignments (1)
MERGER Recorded Jun 28, 2010
From: SUPRESTA LLC; ICL SUPRESTA INC.
To: ICL-IP AMERICA INC.
Reel/Frame 024599/0313 →
Continuity (2)
Provisional Application 6053093200 · Dec 19, 2003
Related Publication 20070272903A1 · Nov 29, 2007