IP Library Granted Patent US 7,834,125
Granted Patent B2
US 7,834,125 · App. 12/338,229 · Granted Nov 16, 2010

Polycarbonates, compositions made therefrom, methods of manufacture thereof, and articles therefrom

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Quick Facts
Patent No.
US 7,834,125
App. No.
12/338,229
Granted
Nov 16, 2010
Kind
B2
Abstract

A melt polymerized polycarbonate comprising repeat units in the polycarbonate derived from the melt polymerization of monomers (II) and/or (III), monomer (IV), and optionally monomer (VIII), wherein monomers (II) and (III) are diaryl dihydroxy compounds, monomer (IV) is a sterically hindered dihydroxy compound, and monomer (VIII) is a non-sterically hindered dihydroxy diaryl compound; wherein the mole ratio of repeat units in the polycarbonate derived from monomers [(II)+(III)]:(IV):(VIII) is 15-70:1-85:0-50, the sum of the mole percent of repeat units in the polycarbonate derived from monomers [(II)+(III)]+(IV) is greater than or equal to 50 mole %, and the sum of the mole percent of units in the polycarbonate derived from monomers [(II)+(III)]+(IV)+(VIII) is 100 mole %; and wherein the polycarbonate has an L* value that is at least 1 L* unit value higher than the same polycarbonate in which monomer (IV) is replaced by bisphenol A.

Claims (71)

1. A melt polymerized polycarbonate comprising repeat units derived from the melt polymerization of monomers (II), (IV), and optionally (VIII), or from the melt polymerization of monomers (III), (IV), and optionally (VIII), or from the melt polymerization of monomers (II), (III), (IV), and optionally (VIII), wherein

monomer (II) is a first dihydroxy compound of structure (II):

wherein n is 0 to 4, and each R f1 is independently a halogen, a C 1-12 hydrocarbyl group, or a C 1-12 halogen substituted hydrocarbyl group;

monomer (III) is a second dihydroxy compound not the same as monomer (II) and of structure (III):

wherein m is 1 to 4, and R f2 is independently a halogen, a C 1-12 hydrocarbyl group, or a C 1-12 halogen substituted hydrocarbyl group;

monomer (IV) is a third dihydroxy compound of structure (IV):

wherein R a and R b are each independently a halogen or C 1-12 hydrocarbyl group that is meta to the hydroxy group on the same aromatic ring; R c and R d are each independently a halogen or a C 1 -C 12 hydrocarbyl group that is ortho to the hydroxy group on the same aromatic ring; p and q are each independently 0 to 2; v and w are each independently 1 or 2; and X a is a single bond or a C 1-18 organic bridging group connecting the two hydroxy-substituted aromatic groups; and

monomer (VIII) is a fourth dihydroxy compound of structure (VIII):

wherein R a and R b are each independently a halogen or C 1-12 hydrocarbyl group that is meta to the hydroxy group on the same aromatic ring; p and q are each independently integers of 0 to 2; and X a is a single bond or a C 1-18 organic group connecting the two hydroxy-substituted aromatic group;

wherein

the mole ratio of repeat units in the polycarbonate derived from monomers [(II)+(III)]:(IV):(VIII) is 15-70:1-85:0-50,

the sum of the mole percent of repeat units in the polycarbonate derived from monomers [(II)+(III)]+(IV) is greater than or equal to 50 mole %, and

the sum of the mole percent of units in the polycarbonate derived from monomers [(II)+(III)]+(IV)+(VIII) is 100 mole %; and

wherein the polycarbonate has an L* value that is at least 1 L* unit value higher than the same polycarbonate in which monomer (IV) is replaced by bisphenol A.

2. The polycarbonate of claim 1 , wherein a pelletized sample of the melt polymerized polycarbonate, without compounding, exhibits a CIE Lab L* value of greater than or equal to 77.

3. The polycarbonate of claim 1 , wherein after compounding with a phosphorus-containing compound, the compounded polycarbonate exhibits a CIE Lab L* value of greater than or equal to 79.

4. The polycarbonate of claim 3 , wherein the phosphorus-containing compound is a phosphorous-containing acid or the corresponding hydrolytically unstable anhydride or ester.

5. The polycarbonate of claim 3 , wherein an injection molded sample subject to abusive molding at a residence time of 720 seconds and a barrel temperature of 340° C., has lower CIE Lab a* value than the same sample that has not been compounded.

6. The polycarbonate of claim 1 wherein, in monomer (IV), p and q are each 0, R c and R d are each independently a halogen or a C 1-4 alkyl group, and X a is a C 1-9 alkylidene or cycloalkylidene group.

7. The polycarbonate of claim 1 , wherein the monomer (IV) is a bisphenol cyclohexylidene of structure (V):

wherein R c1 and R d1 are each independently C 1-12 alkyl, R c2 and R d2 are each independently hydrogen or C 1-12 alkyl, Rg is C 1-12 alkyl or halogen, and t is 0 to 10.

8. The polycarbonate of claim 1 , wherein the monomer (IV) is of structure (VII):

wherein R c and R d are each independently a halogen or C 1-10 alkyl group that is ortho to the hydroxy group on the same aromatic ring; v and w are each independently integers of 1 to 2; and the bridging group X b is a single bond or a C 1-9 alkylidene of formula —C(R j )(R k )— wherein R j and R k are each independently hydrogen, C 1-4 alkyl, or C 1-4 perfluoroalkyl.

9. The polycarbonate of claim 1 wherein the mole ratio of repeat units in the polycarbonate derived from monomers [(II)+(III)]:(IV):(VIII) is 30-70:1-70:0-50.

10. The polycarbonate of claim 1 wherein the mole ratio of repeat units in the polycarbonate derived from monomers [(II)+(III)]:(IV):(VIII) is 15-70:30-85:0, and the mole % of repeat units in the polycarbonate derived from one of monomers (II) and (III) can be 0.

11. The polycarbonate of claim 1 wherein the mole ratio of repeat units in the polycarbonate derived from monomer [(II)+(III)]:(IV):(VIII) is 45-70:30-55:0, and the mole % of repeat units in the polycarbonate derived from one of monomers (II) and (III) can be 0.

12. The polycarbonate of claim 1 , wherein monomer (II) is hydroquinone, monomer (III) is methyl hydroquinone, and monomer (IV) is dimethyl bisphenol cyclohexane.

13. The polycarbonate of claim 1 , wherein monomer (II) is hydroquinone, monomer (III) is methyl hydroquinone, and monomer (IV) is an ortho-alkyl substituted bisphenol A, wherein the alkyl group has from 1 to 12 carbon atoms.

14. The polycarbonate of claim 1 , wherein monomer (II) is hydroquinone, monomer (III) is methyl hydroquinone, and monomer (IV) is an ortho-t-butyl substituted bisphenol A, wherein the alkyl group has from 1 to 12 carbon atoms.

15. The polycarbonate of claim 1 wherein the polycarbonate further comprises a repeat unit that is derived from the fourth dihydroxy compound of formula (VIII).

16. The polycarbonate of claim 14 wherein the mole ratio of repeat units in the polycarbonate derived from monomers [(II)+(III)]:(IV):(VIII) is 30-70:1-69:1-50, and the mole % of repeat units in the polycarbonate derived from one of monomers (II) and (III) can be 0.

17. The polycarbonate of claim 2 , wherein monomer (II) is hydroquinone, monomer (III) is methyl hydroquinone, monomer (IV) is dimethyl bisphenol cyclohexane, and monomer (VIII) is bisphenol A.

18. A process for the manufacture of the melt polymerized polycarbonate of claim 1 , comprising

melt polymerizing a monomer composition comprising monomers (II), (IV), and optionally (VIII), or comprising monomers (III), (IV), and optionally (VIII), or comprising monomers (II), (III), (IV), and optionally (VIII) with an activated carbonate, in the presence of a transesterification catalyst to form the melt polymerized polycarbonate.

19. The method of claim 18 , wherein the monomer composition further comprises monomer (VIII), wherein R a and R b are each independently a C 1-3 alkyl group that is meta to the hydroxy group on the same aromatic ring; p and q are each independently integers of 0 to 1; and X a is X a is a C 1-18 alkyl group connecting the two hydroxy-substituted aromatic group.

20. A process for the manufacture of the compounded, melt polymerized polycarbonate of claim 3 , comprising

melt polymerizing a monomer composition comprising monomers (II), (IV), and optionally (VIII), or comprising monomers (III), (IV), and optionally (VIII), or comprising monomers (II), (III), (IV), and optionally (VIII) with an activated carbonate, in the presence of a transesterification catalyst to form the melt polymerized polycarbonate; and

compounding the melt-polymerized polycarbonate with a phosphorus-containing compound to form the compounded, melt polymerized polycarbonate.

21. The method of claim 20 , wherein the monomer composition further comprises monomer (VIII), wherein R a and R b are each independently a C 1-3 alkyl group that is meta to the hydroxy group on the same aromatic ring; p and q are each independently integers of 0 to 1; and X a is X a is a C 1-18 alkyl group connecting the two hydroxy-substituted aromatic group.

22. An article comprising the polycarbonate of claim 1 .

23. An article comprising the polycarbonate of claim 3 .

24. A melt polymerized polycarbonate comprising repeat units derived from the melt polymerization of monomers (II), (IV), and optionally (VIII), or from the melt polymerization of monomers (III), (IV), and optionally (VIII), or from the melt polymerization of monomers (II), (III), (IV), and optionally (VIII), wherein

monomer (II) is a first dihydroxy compound of structure (II):

wherein n is 0 to 4, and each R f1 is independently a halogen, a C 1-12 hydrocarbyl group, or a C 1-12 halogen substituted hydrocarbyl group;

monomer (III) is a second dihydroxy compound not the same as monomer (II) and of structure (III):

wherein m is 1 to 4, and R f2 is independently a halogen, a C 1-12 hydrocarbyl group, or a C 1-12 halogen substituted hydrocarbyl group;

monomer (IV) is a bisphenol cyclohexylidene of structure (V):

wherein R c1 and R d1 are each independently C 1-12 alkyl, R c2 and R d2 are each independently hydrogen or C 1-12 alkyl, Rg is C 1-12 alkyl or halogen, and t is 0 to 10; and

monomer (VIII) is a fourth dihydroxy compound of structure (VIII):

wherein R a and R b are each independently a halogen or C 1-12 hydrocarbyl group that is meta to the hydroxy group on the same aromatic ring; p and q are each independently integers of 0 to 2; and X a is a single bond or a C 1-18 organic group connecting the two hydroxy-substituted aromatic group;

wherein

the mole ratio of repeat units in the polycarbonate derived from monomers [(II)+(III)]:(IV):(VIII) is 15-70:1-85:0-50,

the sum of the mole percent of repeat units in the polycarbonate derived from monomers [(II)+(III)]+(IV) is greater than or equal to 50 mole %, and

the sum of the mole percent of units in the polycarbonate derived from monomers [(II)+(III)]+(IV)+(VIII) is 100 mole %; and

wherein the polycarbonate has an L* value that is at least 1 L* unit value higher than the same polycarbonate in which monomer (IV) is replaced by bisphenol A.

25. The polycarbonate of claim 24 , wherein after compounding with a phosphorus-containing acid or the corresponding hydrolytically unstable anhydride or ester, the compounded polycarbonate exhibits a CIE Lab L* value of greater than or equal to 79.

26. A melt polymerized polycarbonate comprising repeat units derived from the melt polymerization of monomers (II), (IV), and (VIII), or from the melt polymerization of monomers (III), (IV), and (VIII), or from the melt polymerization of monomers (II), (III), (IV), and (VIII), wherein

monomer (II) is a first dihydroxy compound of structure (II):

wherein n is 0 to 4, and each R f1 is independently a halogen, a C 1-12 hydrocarbyl group, or a C 1-12 halogen substituted hydrocarbyl group;

monomer (III) is a second dihydroxy compound not the same as monomer (II) and of structure (III):

wherein m is 1 to 4, and R f2 is independently a halogen, a C 1-12 hydrocarbyl group, or a C 1-12 halogen substituted hydrocarbyl group;

monomer (IV) is a third dihydroxy compound of structure (IV):

wherein R a and R b are each independently a halogen or C 1-12 hydrocarbyl group that is meta to the hydroxy group on the same aromatic ring; R c and R d are each independently a halogen or a C 1 -C 12 hydrocarbyl group that is ortho to the hydroxy group on the same aromatic ring; p and q are each independently 0 to 2; v and w are each independently 1 or 2; and X a is a single bond or a C 1-18 organic bridging group connecting the two hydroxy-substituted aromatic groups; and

monomer (VIII) is a fourth dihydroxy compound of structure (VIII):

wherein R a and R b are each independently a halogen or C 1-12 hydrocarbyl group that is meta to the hydroxy group on the same aromatic ring; p and q are each independently integers of 0 to 2; and X a is a single bond or a C 1-18 organic group connecting the two hydroxy-substituted aromatic group;

wherein

the mole ratio of repeat units in the polycarbonate derived from monomers [(II)+(III)]:(IV):(VIII) is 15-70:1-85:0-50,

the sum of the mole percent of repeat units in the polycarbonate derived from monomers [(II)+(III)]+(IV) is greater than or equal to 50 mole %, and

the sum of the mole percent of units in the polycarbonate derived from monomers [(II)+(III)]+(IV)+(VIII) is 100 mole %; and

wherein the polycarbonate has an L* value that is at least 1 L* unit value higher than the same polycarbonate in which monomer (IV) is replaced by bisphenol A.

27. The polycarbonate of claim 26 , wherein after compounding with a phosphorus-containing acid or the corresponding hydrolytically unstable anhydride or ester, the compounded polycarbonate exhibits a CIE Lab L* value of greater than or equal to 79.

Assignments (9)
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 038883/0816 →
CHANGE OF NAME Recorded Jun 6, 2016
From: SABIC INNOVATIVE PLASTICS IP B.V.
To: SABIC GLOBAL TECHNOLOGIES B.V.
Reel/Frame 038883/0830 →
RELEASE OF SECURITY INTEREST Recorded Mar 17, 2014
From: CITIBANK, N.A.
To: SABIC INNOVATIVE PLASTICS IP B.V.
Reel/Frame 032459/0798 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNMENT TO CORRECT THE NAME OF ASSIGNOR JAN-PLEUN LENS, PREVIOUSLY RECORDED ON REEL 022457 FRAME 0538. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNOR(S) HEREBY CONFIRM THE ASSIGNMENT. Recorded Aug 28, 2009
From: BRACK, HANS-PETER; KARLIK, DENNIS; LENS, JAN-PLEUN; WILLEMSE, DENNIS JAMES PATRICK MARIA; BERNDSEN, JOSEF GERARDUS
To: SABIC INNOVATIVE PLASTICS IP B.V.
Reel/Frame 023155/0752 →
SECURITY AGREEMENT Recorded Jun 18, 2009
From: SABIC INNOVATIVE PLASTICS IP B.V.
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 022843/0918 →
CORRECTIVE ASSIGNMENT TO CORRECT THE THE NAME OF THE THIRD INVENTOR ON THE ASSIGNMENT COVER SHEET AND NOTICE OF RECORDATION - DENNIS JAMES PATRICK MARIA WILLEMSE PREVIOUSLY RECORDED ON REEL 022375 FRAME 0491. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Mar 26, 2009
From: BRACK, HANS-PETER; KARLIK, DENNIS; LENS, JAN-PLEUNS; WILLEMSE, DENNIS JAMES PATRICK MARIA; BERNDSEN, JOSEF GERARDUS
To: SABIC INNOVATIVE PLASTICS IP B.V.
Reel/Frame 022457/0538 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 11, 2009
From: BRACK, HANS-PETER; KARLIK, DENNIS; LENS, JAN-PLEUN; WILLEMSE, DENNIS JAMES PARTRICK MARIA; BERNDSEN, JOSEF GERARDUS
To: SABIC INNOVATIVE PLASTICS IP B.V.
Reel/Frame 022375/0491 →