IP Library Granted Patent US 7,408,016
Granted Patent B2
US 7,408,016 · App. 11/263,132 · Granted Aug 5, 2008

Methods for producing and purifying 2-hydrocarbyl-3,3-bis(4-hydroxyaryl)phthalimidine monomers and polycarbonates derived therefrom

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Quick Facts
Patent No.
US 7,408,016
App. No.
11/263,132
Granted
Aug 5, 2008
Kind
B2
Abstract

A composition comprising a polycarbonate, wherein the polycarbonate has a weight average molecular weight of greater than 15,000, comprises more than 15 mole percent structural units derived from a 2-aryl-3,3-bis(4-hydroxyaryl)phthalimide: wherein R 1 is selected from the group consisting of aryl groups having 6 to 25 carbon atoms and aralkyl groups having 7 to 25 carbon atoms, and R 2 is selected from the group consisting of a hydrogen, a hydrocarbyl group, and a halogen; and further wherein the polycarbonate has a yellowness index of less than 10 as measured on a 3 millimeter thick plaque in accordance with ASTM D1925 is disclosed.

Claims (33)

1. A composition comprising a polycarbonate, wherein the polycarbonate has a weight average molecular weight of greater than 15,000, comprises more than 15 mole percent structural units derived from a 2-aryl-3,3-bis(4-hydroxyaryl)phthalimide:

wherein R 1 is selected from the group consisting of aryl groups having 6 to 25 carbon atoms and aralkyl groups having 7 to 25 carbon atoms, and R 2 is selected from the group consisting of a hydrogen, a hydrocarbyl group, and a halogen; and the remainder of the structural units derived from 2,2-bis(4-hydroxyphenyl)propane (bisphenol A);

and further wherein the polycarbonate has a yellowness index of less than 10 as measured on a 3 millimeter thick plaque in accordance with ASTM D1925.

2. The composition of claim 1 , wherein the composition further comprises a second thermoplastic polymer selected from the group consisting of a vinyl polymer, a rubber-modified graft copolymer, an acrylic polymer, polyacrylonitrile, a polystyrene, a polyolefin, a polyester, a polyurethane, a polyamide, a polysulfone, a polyimide, a polyetherimide, a polyphenylene ether, a polyphenylene sulfide, a polyether ketone, a polyether ether ketone, an ABS resin, an ASA resin, a polyethersulfone, a polyphenylsulfone, a poly(alkenylaromatic) polymer, a polybutadiene, polyacetal, a polycarbonate, a polyphenylene ether, an ethylene-vinyl acetate copolymer, a polyvinyl acetate, a liquid crystal polymer, an ethylene-tetrafluoroethylene copolymer, an aromatic polyester, a polyvinyl fluoride, a polyvinylidene fluoride, a polyvinylidene chloride, tetrafluoroethylene, a polycarbonate-polyorganosiloxane block copolymer, and a copolymer comprising: (i) an aromatic ester, (ii) an estercarbonate, and a (iii) carbonate repeat units mixtures.

3. The composition according to claim 1 , wherein the polycarbonate has more than 20 mole percent structural units derived from a 2-aryl-3,3-bis(4-hydroxyaryl)phthalimide.

4. The composition according to claim 1 , wherein the polycarbonate has more than 40 mole percent structural units derived from a 2-aryl-3,3 -bis(4-hydroxyaryl)phthalimide and a yellowness index of less than 6 as measured on a 3 millimeter thick plaque in accordance with ASTM D1925.

5. The composition according to claim 4 wherein the polycarbonate has a weight average molecular weight of greater than 20,000.

6. An article comprising the composition of claim 1 .

7. The article of claim 6 , wherein the article is selected from the group consisting of automotive bumpers, other automotive exterior components, automobile mirror housings, automobile wheel covers, automobile instrument panels and trim, automobile glove boxes, automobile door hardware and other interior trim, automobile exterior lights, automobile parts within the engine compartment, plumbing equipment, valves and pumps, air conditioning heating and cooling parts, furnace and heat pump parts, computer parts, electronics parts, projector parts, electronic display parts, copier parts, scanner parts, electronic printer toner cartridges, hair driers, irons, coffee makers, toasters, washing machines, microwaves, ovens, power tools, electric components, lighting parts, dental instruments, medical instruments, cookware, medical instrument trays, animal cages, fibers, laser welded medical devices and fiber optics.

8. The article of claim 6 , wherein the article is selected from the group consisting of food packaging, vials requiring bacteria or plant growth, membranes and membranes bonded to stainless steel.

9. The composition according to claim 1 further comprising a UV stabilizer.

10. The composition according to claim 1 wherein the UV stabilizer is a 2-(2′-Hydroxyphenyl)-benzotriazole.

11. The composition according to claim 10 wherein the 2-(2′-Hydroxyphenyl)-benzotriazole is 2-(2H-benzotriazole-2-yl)-4,6-bis(1-methyl-1-phenylethyl)phenol.

12. An article comprising the composition of claim 10 .

13. The article of claim 12 wherein the article is a selected from the group consisting of a lighting part, a lens and a display device.

14. A composition comprising a polycarbonate and a UV stabilizer selected from the group consisting of 2-(2′-Hydroxyphenyl)-benzotriazoles, wherein the polycarbonate has a weight average molecular weight of greater than 15,000, comprises more than 15 mole percent structural units derived from a 2-aryl-3,3-bis(4-hydroxyaryl)phthalimide:

wherein R 1 is selected from the group consisting of aryl groups having 6 to 25 carbon atoms and aralkyl groups having 7 to 25 carbon atoms, and R 2 is selected from the group consisting of a hydrogen, a hydrocarbyl group, and a halogen; and the remainder of the structural units derived from at least one other aromatic dihydroxy compound having the formula:

wherein each G 1 is an independently aromatic group; E is selected from the group consisting of an alkylene group, an alkylidene group, a cycloaliphatic group, a sulfur-containing linkage group, a phosphorus-containing linkage group, an ether linkage group, a carbonyl group, a tertiary nitrogen group, and a silicon-containing linkage group; R 3 is a hydrogen or a monovalent hydrocarbon group each; Y 1 is independently selected from the groups consisting of a monovalent hydrocarbyl group, an alkenyl group, an allyl group, a halogen, an oxy group and a nitro group; each m is independently a whole number from zero through the number of positions on each respective G 1 available for substitution; p is a whole number from zero through the number of positions on E available for substitution; t is a natural number greater than or equal to one; s is either zero or one; and u is a whole number; and further wherein the polycarbonate has a yellowness index of less than 10 as measured on a 3 millimeter thick plaque in accordance with ASTM D1925.

15. The composition of claim 14 , wherein the UV stabilizer is 2-(2H-benzotriazole-2-yl)-4,6-bis(1-methyl-1-phenylethyl)phenol.

16. The composition according to claim 14 , wherein the polycarbonate has more than 40 mole percent structural units derived from a 2-aryl-3,3 -bis(4-hydroxyaryl)phthalimide and a yellowness index of less than 6 as measured on a 3 millimeter thick plaque in accordance with ASTM D1925.

17. The composition according to claim 16 , wherein the polycarbonate has a weight average molecular weight of greater than 20,000.

18. An article comprising the composition of claim 14 .

19. A lighting part comprising a composition comprising a polycarbonate and a UV stabilizer selected from the group consisting of 2-(2′-Hydroxyphenyl)-benzotriazoles, wherein the polycarbonate has a weight average molecular weight of greater than 15,000, comprises more than 15 mole percent structural units of the following formula derived from a 2-aryl-3,3 -bis(4-hydroxyaryl)phthalimide:

wherein R 1 is selected from the group consisting of aryl groups having 6 to 25 carbon atoms and aralkyl groups having 7 to 25 carbon atoms, and R 2 is selected from the group consisting of a hydrogen, a hydrocarbyl group, and a halogen; and the remainder of the structural units derived from 2,2-bis(4-hydroxyphenyl)propane (bisphenol A); and further wherein the polycarbonate has a yellowness index of less than 10 as measured on a 3 millimeter thick plaque in accordance with ASTM D1925.

20. The lighting part of claim 19 , wherein the UV stabilizer is 2-(2H-benzotriazole-2-yl)-4,6-bis(1-methyl-1-phenylethyl)phenol.

21. The composition of claim 1 , wherein R 1 is phenyl and R 2 is hydrogen.

22. The composition of claim 14 , wherein R 1 is phenyl and R 2 is hydrogen.

23. The composition of claim 19 , wherein R 1 is phenyl and R 2 is hydrogen.

24. The composition of claim 14 , wherein the other aromatic dihydroxy compound is 2,2-bis(4-hydroxyphenyl)propane (bisphenol A).

25. The composition of claim 14 , wherein the other aromatic dihydroxy compound is 2,2-bis(4-hydroxyphenyl)propane (bisphenol A) and wherein the 2-(2′-Hydroxyphenyl)-benzotriazole is 2(2H-benzotriazol-2-yl)-4,6-bis(1-methyl1-phenylethyl)phenol.

26. A composition comprising a polycarbonate and a UV stabilizer selected from the group consisting of 2-(2′-Hydroxyphenyl)-benzotriazoles, wherein the polycarbonate has a weight average molecular weight of greater than 15,000, comprises more than 15 mole percent structural units derived from a 2-phenyl-3,3-bis(4-hydroxyphenyl) phthalimidine having the formula:

and the remainder of the structural units derived from 2,2-bis(4-hydroxyphenyl)propane (bisphenol A);

and further wherein the polycarbonate has a yellowness index of less than 10 as measured on a 3 millimeter thick plaque in accordance with ASTM D1925.

Assignments (7)
CORRECTIVE ASSIGNMENT TO CORRECT THE REMOVE THE APPLICATION NUMBER 15039474 PREVIOUSLY RECORDED AT REEL: 054528 FRAME: 0467. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Mar 23, 2021
From: SABIC GLOBAL TECHNOLOGIES B.V.
To: SHPP GLOBAL TECHNOLOGIES B.V.
Reel/Frame 057453/0680 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 26, 2020
From: SABIC GLOBAL TECHNOLOGIES B.V.
To: SHPP GLOBAL TECHNOLOGIES B.V.
Reel/Frame 054528/0467 →
CHANGE OF NAME Recorded Jun 6, 2016
From: SABIC INNOVATIVE PLASTICS IP B.V.
To: SABIC GLOBAL TECHNOLOGIES B.V.
Reel/Frame 038883/0795 →
RELEASE OF SECURITY INTEREST Recorded Mar 17, 2014
From: CITIBANK, N.A.
To: SABIC INNOVATIVE PLASTICS IP B.V.
Reel/Frame 032459/0798 →
SECURITY AGREEMENT Recorded Aug 18, 2008
From: SABIC INNOVATIVE PLASTICS IP B.V.
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 021423/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 1, 2008
From: GENERAL ELECTRIC COMPANY
To: SABIC INNOVATIVE PLASTICS IP B.V.
Reel/Frame 020985/0551 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 6, 2005
From: CHATTERJEE, GAUTAM; DHANABALAN, ANANTHARAMAN; RAI, VINOD KUMAR; SHANMUGAM, SURESH; SRINIVASAN, VEERARAGHAVAN; GLASGOW, KATHERINE
To: GENERAL ELECTRIC COMPANY
Reel/Frame 017091/0261 →