IP Library Granted Patent US 9,315,666
Granted Patent B2
US 9,315,666 · App. 13/913,906 · Granted Apr 19, 2016

Compositions and articles of manufacture containing branched polycarbonate

Inventors: Jean-Francois Morizur (Evansville, IN); Thomas L. Evans (Mount Vernon, IN)
Assignee: SABIC GLOBAL TECHNOLOGIES B.V.
C08L69/00C08G64/14C08K5/0066C08K5/42C08K5/549
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Quick Facts
Patent No.
US 9,315,666
App. No.
13/913,906
Granted
Apr 19, 2016
Kind
B2
Abstract

A polycarbonate containing composition comprising a peak melt viscosity of at least 8,000 poise when measured using a parallel plate melt rheology test at a heating rate of 10° C./min at a temperature of between about 350° C. to about 450° C., and wherein a molded article of the composition has a UL 94 VO rating at a thickness of 1.0 mm, 1.5 mm, 2.0 mm, or between 1.0 mm and 2.0 mm is disclosed.

Claims (55)

1. A composition comprising:

a first polycarbonate, wherein the first polycarbonate comprises

a repeating structural unit of the following formula

wherein at least 60 percent of the total number of R 1 groups contain aromatic groups and the balance thereof are aliphatic or alicyclic groups;

wherein the first polycarbonate was formed in the presence of an end-capping agent and the end-capping agent is not cyanophenol;

wherein the first polycarbonate has a branching level of at least about 2%;

wherein the polycarbonate has a weight average molecular weight of 20,000 g/mole to 54,843 g/mole as measured by gel permeation chromatography using polycarbonate standards; and

wherein the first polycarbonate is prepared by

selecting the branching level, the weight average molecular weight, and the end-capping agent such that the first polycarbonate has a calculated peak melt viscosity of at least 25,000 poise as calculated by a peak melt viscosity equation as follows:

calculated peak melt viscosity=−57135.91+36961.39*BL+14001.13*MW 1/3 −46944.24*pKa−322.51*BL*MW 1/3 −2669.19*BL*pKa+215.83*MW 1/3 *pKa+1125.63*BL 2 −200.11*MW 2/3 +2231.15*pKa 2 ,

wherein BL is determined by dividing a number of moles of branching agent by a total moles of bisphenol from which the first polycarbonate is derived, MW is the weight average molecular weight, and the pKa is the pKa of the end capping agent; and

wherein a molded article of the first polycarbonate has a UL94 V0 rating at a thickness of 1.0 mm;

a flame retardant; and

a second polycarbonate derived from at least bisphenol-A, wherein the second polycarbonate is different from the first polycarbonate;

wherein a molded article of the composition has a UL94 V0 rating at a thickness of 1.5 mm.

2. The composition of claim 1 , wherein the first polycarbonate has a weight average molecular weight of between about 20,000 g/mole to about 40,000 g/mole as measured by gel permeation chromatography using polycarbonate standards.

3. The composition of claim 1 , wherein the end-capping agent has a pKa between about 8.3 and about 11.

4. The composition of claim 1 , wherein the end-capping agent is at least one of the following: phenol and phenol containing one or more substitutions with at least one of the following: an aliphatic group, an olefinic group, an aromatic group, a halogen, an ester group, and an ether group.

5. The composition of claim 4 , wherein the end-capping agent is at least one of the following: phenol, p-t-butylphenol, and p-cumylphenol.

6. The composition of claim 1 , wherein the first polycarbonate of said composition has a branching level of at least about 3%.

7. The composition of claim 1 , wherein the flame retardant is at least one of the following: alkali metal salts of perfluorinated C 1-16 alkyl sulfonates; potassium perfluorobutane sulfonate; potassium perfluoroctane sulfonate; tetraethylammonium perfluorohexane sulfonate; and potassium diphenylsulfone sulfonate.

8. The composition of claim 1 , wherein the composition has a haze value of less than 1.5% at 3.2 mm thickness by ASTM D1003.

9. The composition of claim 1 , wherein the first polycarbonate is derived from bisphenol-A.

10. The composition of claim 1 , wherein the first polycarbonate at least one of the following: a homopolycarbonate derived from a bisphenol; a copolycarbonate derived from more than one bisphenol; and a copolymer derived from one or more bisphenols and containing one or more aliphatic ester units or aromatic ester units or siloxane units.

11. The composition of claim 1 , wherein the second polycarbonate comprises homopolymer derived from bisphenol A.

12. The composition of claim 1 , wherein the second polycarbonate is a polycarbonate copolymer, wherein the polycarbonate copolymer is at least one of the following: polycarbonate-polysiloxane copolymers, and polyester-polycarbonates.

13. The composition of claim 12 , wherein the second polycarbonate comprises copolycarbonate-polyester-polysiloxane terpolymer.

14. The composition of claim 11 , wherein the first polycarbonate has a branching level of at least about 3%.

15. An article comprising the composition of claim 1 .

16. A method of making a composition, comprising:

preparing a first polycarbonate by

selecting a branching level, a desired weight average molecular weight, and an end-capping agent such that the first polycarbonate has a calculated peak melt viscosity of at least 25,000 poise as calculated by a peak melt viscosity equation as follows:

calculated peak melt viscosity=−57135.91+36961.39*BL+14001.13*MW 1/3 −46944.24*pKa−322.51*BL*MW 1/3 −2669.19*BL*pKa+215.83*MW 1/3 *pKa+1125.63*BL 2 −200.11*MW 2/3 +2231.15*pKa 2 ,

wherein BL is determined by dividing a number of moles of branching agent by a total moles of bisphenol from which the first polycarbonate is derived, the MW is the weight-averaged molecular weight of the first polycarbonate and is 20,000 g/mole to 54,843 g/mole as determined by gel permeation chromatography using polycarbonate standards, and the pKa is the pKa of the end capping agent; and

reacting bisphenol, end-capping agent, branching agent, and a carbonate precursor wherein the first polycarbonate has a repeating structural unit of the following formula

wherein at least 60 percent of the total number of R 1 groups contain aromatic groups and the balance thereof are aliphatic or alicyclic groups;

wherein the end-capping agent is not cyanophenol;

wherein the pKa of the end-capping agent is from about 8.3 to about 11; and

wherein a molded article of the first polycarbonate has a UL94 V0 rating at a thickness of 1.0 mm; and

blending with the first polycarbonate a flame retardant and a second polycarbonate derived from at least bisphenol-A different than the first polycarbonate;

wherein a molded article of the composition has a UL94 V0 rating at a thickness of 1.5 mm.

17. The method of claim 16 , wherein the second polycarbonate is a homopolycarbonate derived from bisphenol-A.

18. A method of making an article of manufacture, comprising:

preparing a first polycarbonate by

selecting a branching level, BL, a desired weight average molecular weight, and an end-capping agent such that the first polycarbonate has a calculated peak melt viscosity of at least 25,000 poise is calculated by a peak melt viscosity equation as follows:

calculated peak melt viscosity=−57135.91+36961.39*BL+14001.13*MW 1/3 −46944.24*pKa−322.51*BL*MW 1/3 −2669.19*BL*pKa+215.83*MW 1/3 *pKa+1125.63*BL 2 −200.11*MW 213 +2231.15*pKa 2 ,

wherein BL is determined by dividing a number of moles of branching agent by a total moles of bisphenol from which the first polycarbonate is derived, the MW is the weight-averaged molecular weight of the first polycarbonate and is 20,000 g/mole to 54,843 g/mole as determined by gel permeation chromatography using polycarbonate standards, and the pKa is the pKa of the end capping agent;

reacting the bisphenol, the end-capping agent, the branching agent, and a carbonate precursor, wherein the first polycarbonate comprises a repeating structural unit of the following formula

wherein at least 60 percent of the total number of R 1 groups contain aromatic groups and the balance thereof are aliphatic or alicyclic groups;

wherein the end-capping agent that is not cyanophenol;

wherein an article made from the first polycarbonate has a UL94 V0 rating at a thickness of 1.0 mm;

blending with the first polycarbonate, a flame retardant, and a second polycarbonate derived from at least bisphenol-A different than the first polycarbonate to form the composition; and

forming the composition into the article;

wherein an article made from the composition has a UL94 V0 rating at a thickness of 1.5 mm.

19. The method of claim 18 , wherein the second polycarbonate comprises a bisphenol A homopolymer.

Assignments (5)
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 →
CORRECTIVE ASSIGNMENT TO CORRECT THE 12/116841, 12/123274, 12/345155, 13/177651, 13/234682, 13/259855, 13/355684, 13/904372, 13/956615, 14/146802, 62/011336 PREVIOUSLY RECORDED ON REEL 033591 FRAME 0673. ASSIGNOR(S) HEREBY CONFIRMS THE CHANGE OF NAME. Recorded Aug 29, 2014
From: SABIC INNOVATIVE PLASTICS IP B.V.
To: SABIC GLOBAL TECHNOLOGIES B.V.
Reel/Frame 033663/0427 →
CORRECTIVE ASSIGNMENT TO CORRECT REMOVE 10 APPL. NUMBERS PREVIOUSLY RECORDED AT REEL: 033591 FRAME: 0673. ASSIGNOR(S) HEREBY CONFIRMS THE CHANGE OF NAME. Recorded Aug 28, 2014
From: SABIC INNOVATIVE PLASTICS IP B.V.
To: SABIC GLOBAL TECHNOLOGIES B.V.
Reel/Frame 033649/0529 →
CHANGE OF NAME Recorded Aug 22, 2014
From: SABIC INNOVATIVE PLASTICS IP B.V.
To: SABIC GLOBAL TECHNOLOGIES B.V.
Reel/Frame 033591/0673 →
Continuity (2)
Continuation 12945866 · Nov 14, 2010
Related Publication 20130274392A1 · Oct 17, 2013