Brominated flame retardant
View Patent ↗A process for preparing a polybromoaryl ether, comprising adding to a solvent for the polybromoaryl ether a mixture of (1) at least one compound of the structure HO—Ar—X 1 , X 2 , X 3 , X 4 , X 5 , wherein Ar is an aryl group and X 1 , X 2 , X 3 , X 4 , and X 5 are independently selected from hydrogen and bromine, provided that at least one of X 1 , X 2 , X 3 , X 4 , and X 5 is bromine, (2) at least one alkali or alkaline metal hydroxide, and (3) at least one polymerization initiator, wherein the solvent for the polybromoaryl ether is a non-solvent for alkali metal bromides.
1. A polybromoaryl ether prepared by a process comprising:
(A) adding to a solvent for the polybromoaryl ether a mixture of:
(1) at least one compound of the structure
HO—Ar—X 1 X 2 X 3 X 4 X 5 (1)
wherein Ar is an aryl group and X 1 , X 2 , X 3 , X 4 and X 5 are independently selected from the group consisting of hydrogen and bromine, provided that at least one of X 1 , X 2 , X 3 , X 4 and X 5 is bromine,
(2) at least one alkali or alkaline metal hydroxide, and
(3) at least one polymerization initiator, wherein said solvent for the polybromoaryl ether is a non-solvent for alkali or alkaline metal bromides;
(B) mixing the materials prepared in (A) to polymerize compound (I) and form the polybromoaryl ether and at least one alkali or alkaline metal bromide by-product;
(C) quenching the polymerization of compound (I);
(D) filtering insoluble alkali or alkaline metal bromide by-product from the soluble polybromoaryl ether; and
(E) mixing said soluble polybromoaryl ether with a non-solvent to form a polybromoaryl ether precipitate having less than 200 ppm alkali or alkaline metal bromide.
2. The polybromoaryl ether of claim 1 , wherein said solvent is tetrahydrofuran.
3. The polybromoaryl ether of claim 1 , wherein:
said solvent is from about 100 wt % to 600 wt % tetrahydrofuran as based on compound (I);
said alkali metal hydroxide is from about 100 mol % to 120 mol % sodium hydroxide as based on compound (I); and
said polymerization initiator is from about 0.1 mol % to 30 mol % benzoyl peroxide as based on compound (I).
4. The polybromoaryl ether of claim 1 , wherein from 30.0 mol % to 0.5 mol % of benzoyl peroxide is reacted to result in said polybromoaryl ether precipitate having a molecular weight ranging from 4,000 to 62,000 Daltons.
5. The polybromoaryl ether of claim 1 , wherein from 3.0 mol % to 1.0 mol % of benzoyl peroxide is reacted to result in said polybromoaryl ether precipitate having a molecular weight ranging from 15,000 to 40,000 Daltons.
6. The polybromoaryl ether of claim 1 , wherein from 0 ppm to 200 ppm alkali or alkaline metal bromide remains in said polybromoaryl ether precipitate.
7. The polybromoaryl ether of claim 1 , wherein from 0 ppm to 50 ppm alkali or alkaline metal bromide remains in said polybromoaryl ether precipitate.
8. The polybromoaryl ether of claim 1 , wherein said polybromoaryl ether precipitate has an APHA color range from 1 to 300.
9. The polybromoaryl ether of claim 1 , wherein said polybromoaryl ether precipitate has a mass loss rate value in percent/minute in the first 20 minutes of a 33000 isothermal TGA experiment of 0.01 percent/minute to 0.20 percent/minute.
10. The polybromoaryl ether of claim 1 , wherein said polybromoaryl ether precipitate has a mass loss rate value in percent/minute in the first 20 minutes of a 330° C. isothermal TGA experiment of 0.01 percent/minute to 0.10 percent/minute.
11. A composition comprising a mixture of:
(A) a polymeric resin selected from the group consisting of polyamides, polyesters, polycarbonates, polyurethanes, polyolefins, polystyrenes, epoxies and mixtures thereof, and
(B) a polybromoaryl ether prepared by a process comprising:
(1) adding to a solvent for the polybromoaryl ether a mixture of:
(a) at least one compound of the structure
HO—Ar—X 1 X 2 X 3 X 4 X 5 (I)
wherein Ar is an aryl group and X 1 , X 2 , X 3 , X 4 and X 5 are independently selected from the group consisting of hydrogen and bromine, provided that at least one of X 1 , X 2 , X 3 , X 4 and X 5 is bromine,
(b) at least one alkali or alkaline metal hydroxide, and
(c) at least one polymerization initiator, wherein said solvent for the polybromoaryl ether is a non-solvent for alkali or alkaline metal bromides;
(2) mixing the materials prepared in (1) to polymerize compound (I) and form the polybromoaryl ether and at least one alkali or alkaline metal bromide by-product;
(3) quenching the polymerization of compound (I); and then
(4) the filtering insoluble alkali or alkaline metal bromide by-product from the soluble polybromoaryl ether; and
(5) mixing said soluble polybromoaryl ether with a non-solvent to form a polybromoaryl ether precipitate having less than 200 ppm alkali or alkaline metal bromide.
12. The composition of claim 11 , wherein said solvent is tetrahydrofuran.
13. The composition of claim 11 , wherein:
said solvent is from about 100 wt % to 600 wt % tetrahydrofuran as based on compound (I);
said alkali metal hydroxide is from about 100 mol % to 120 mol % sodium hydroxide as based on compound (I); and
said polymerization initiator is from about 0.1 mol % to 30 mol % benzoyl peroxide as based on compound (I).
14. The composition of claim 11 , wherein from 30.0 mol % to 0.5 mol % of benzoyl peroxide is reacted to result in said polybromoaryl ether precipitate having a molecular weight ranging from 4,000 to 62,000 Daltons.
15. The composition of claim 11 , wherein from 3.0 mol % to 1.0 mol % of benzoyl peroxide is reacted to result in said polybromoaryl ether precipitate having a molecular weight ranging from 15,000 to 40,000 Daltons.
16. The composition of claim 11 , further comprising:
about 20 wt % to 90 wt % polyamide resin;
about 0 wt % to 60 wt % inorganic reinforcing agent or filler;
about 5 wt % to 30 wt % polybromoaryl ether precipitate;
about 0 wt % to 15 wt % synergist;
about 0 wt % to 5 wt % mold release; and
about 0 wt % to 5 wt % drip suppressant.
17. The composition of claim 16 , wherein said synergist is selected from the group consisting of sodium antimonate, antimony oxide, zinc borate, zinc stannate, and combinations thereof.
18. The composition of claim 16 , wherein said polyamide resin is a 6T/66 copolymer.
19. The composition of claim 18 , wherein the blister resistance of said composition is from 260 to 280° C.
20. The composition of claim 18 , wherein said composition has a mass loss rate value in percent/minute in the first 20 minutes of a 330° C. isothermal TGA experiment of 0.01 percent/minute to 0.10 percent/minute.
21. The composition of claim 16 , wherein said polyamide resin is PA 4,6.
22. The composition of claim 21 , wherein said composition has a mass loss rate value in percent/minute in the first 20 minutes of a 300° C. isothermal TGA experiment of 0.01 percent/minute to 0.15 percent/minute.
23. The composition of claim 16 , wherein said polyamide resin is PA 6,6.
24. The composition of claim 23 , wherein said composition has a mass loss rate value in percent/minute in the first 20 minutes of a 280° C. isothermal TGA experiment of 0.01 percent/minute to 0.12 percent/minute.
25. The composition of claim 11 , wherein from 0 ppm to 200 ppm alkali or alkaline metal bromide remains in said polybromoaryl ether precipitate.
26. The composition of claim 11 , wherein less than 500 ppm tribromophenol remains in said polybromoaryl ether precipitate.
27. The polybromoaryl ether of claim 1 , wherein less than 500 ppm tribromophenol remains in said polybromoaryl ether precipitate.
28. A composition comprising a mixture of:
(A) a polymeric resin selected from the group consisting of polyamides, polyesters, polycarbonates, polyurethanes, polyolefins, polystyrenes, epoxies and mixtures thereof, and
(B) a polybromoaryl ether precipitate of the formula (II):
wherein R is hydrogen, alkali or alkaline earth metals and X represents the degree of bromination, having less than 200 ppm alkali or alkaline metal bromide and less than 500 ppm tribromophenol remaining in said polybromoaryl ether as precipitated.