IP Library Granted Patent US 9,234,096
Granted Patent B2
US 9,234,096 · App. 13/020,617 · Granted Jan 12, 2016

Color and heat stable polycarbonate compositions and methods of making

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Quick Facts
Patent No.
US 9,234,096
App. No.
13/020,617
Granted
Jan 12, 2016
Kind
B2
Abstract

Provided herein are branched polycarbonate resin compositions The compositions include a first heat stabilizer, a second heat stabilizer, a branched polycarbonate, a cyclic siloxane, and a flame retardant salt. The compositions withstand discoloration and increased melt viscosity when exposed to elevated temperatures. These compositions are useful in the manufacture of various shaped, formed and/or molded articles.

Claims (34)

1. A polycarbonate resin composition comprising

47-50 wt % of a first branched polycarbonate that is a bisphenol-A polycarbonate resin having a carbonate end-capping group derived from p-hydroxybenzonitrile (HBN) and branching derived from tris-(hydroxyphenyl)ethane (THPE) as a branching agent;

22-28 wt % of a second branched polycarbonate that is a bisphenol-A polycarbonate resin having branching derived from tris-(hydroxyphenyl)ethane (THPE) as a branching agent;

21-31 wt % of a high flow polycarbonate that is a bisphenol-A polycarbonate homopolymer having a melt volume flow rate (MVR) of between 21.9 and 31.8 cm 3 /10 min, and a low flow polycarbonate that is a bisphenol-A polycarbonate homopolymer having a melt volume flow rate (MVR) of between 5 and 7 cm 3 /10 min;

0.014-0.016 wt % of a first heat stabilizer that is tris(2,4-di-t-butylphenyl)phosphite;

0.016-0.017 wt % of a second heat stabilizer that is bis(2,4-dicumylphenyl)pentaerythritol diphosphite;

a cyclic siloxane;

a flame retardant salt; and

0.047-0.05 wt % of a hindered phenol heat stabilizer.

2. The resin composition of claim 1 , wherein the cyclic siloxane is at least one of the following: octaphenylcyclotetrasiloxane, hexamethylcyclotrisiloxane, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, dodecmethylcyclohexasiloxane, trimethyltriphenylcyclotrisiloxane, and/or tetramethyltetraphenylcyclotetrasiloxane.

3. The resin composition of claim 1 , wherein the cyclic siloxane is octaphenylcyclotetrasiloxane.

4. The resin composition of claim 1 , comprising 0.05-0.1 wt % of the cyclic siloxane.

5. The resin composition of claim 1 , wherein the flame retardant salt is at least one of the following: alkali metal salt of perfluorinated C 1 -C 16 alkyl sufonates; potassium perfluorobutane sulfonate; potassium perfluoroctane sulfonate; tetraethylammonium perfluorohexane sulfonate; sodium toluene sulfonate; sodium diphenylsulfone sulfonate; and potassium diphenylsulfone sulfonate.

6. The resin composition of claim 1 , wherein the flame retardant salt is potassium perfluorobutane sulfonate.

7. The resin composition of claim 1 , comprising 0.05-0.1 wt % of the flame retardant salt.

8. The resin composition of claim 1 , wherein the cyclic siloxane is octaphenylcyclotetrasiloxane that is present in the composition at 0.05-0.1 wt %, and the flame retardant salt is potassium perfluorobutane sulfonate that is present in the composition at 0.05-0.1 wt %.

9. The resin composition of claim 1 , wherein the hindered phenol heat stabilizer is octadecyl-3(3,5-ditertbutyl-4-hydroxyphenyl)propionate.

10. The resin composition of claim 1 , further comprising a release agent.

11. The resin composition of claim 1 , further comprising a UV additive.

12. The resin composition of claim 1 , further comprising a linear siloxane having the formula:

wherein R 23 is a C 1 -C 18 alkyl group, R 24 is a phenyl, and x 1 and y 1 sum to 1.

13. The resin composition of claim 1 , wherein the resin composition has a viscosity of at least 500 Poise at 300° C.

14. The resin composition of claim 1 , wherein the resin composition has a viscosity build of no greater than 20% after 30 minutes at 300° C.

15. The resin composition of claim 1 , wherein the resin composition has a viscosity build of no greater than 15% after 30 minutes at 300° C.

16. The resin composition of claim 1 , wherein the resin composition has a viscosity build of no greater than 10% after 30 minutes at 300° C.

17. The resin composition of claim 1 , wherein a 3.2 mm thick article formed from the composition has a yellowing index (Yi) of less than 3.

18. The polycarbonate resin composition of claim 1 , wherein a 3.2 mm thick article formed from the composition has a yellowing index (Yi) of less than 2.5.

19. A polycarbonate resin composition, selected from the group consisting of (a)-(c):

(a) a polycarbonate resin composition comprising: 47 wt % of first branched polycarbonate that is a bisphenol-A polycarbonate resin having a carbonate end-capping group derived from p-hydroxybenzonitrile (HBN) and branching derived from tris-(hydroxyphenyl)ethane (THPE) as a branching agent; 22 wt % of a second branched polycarbonate that is a bisphenol-A polycarbonate resin having branching derived from tris-(hydroxyphenyl)ethane (THPE) as a branching agent; 29 wt % of a high flow polycarbonate that is a bisphenol-A polycarbonate homopolymer having a melt volume flow rate (MVR) of between 21.9 and 31.8 cm 3 /10 min; 2 wt % of a low flow polycarbonate that is a bisphenol-A polycarbonate homopolymer having a melt volume flow rate (MVR) of between 5 and 7 cm 3 /10 min; 0.014 wt % of a first heat stabilizer that is tris(2,4-di-t-butylphenyl)phosphite; 0.017 wt % of a second heat stabilizer that is bis(2,4-dicumylphenyl)pentaerythritol diphosphite; 0.1 wt % of a cyclic siloxane; 0.08 wt % of a flame retardant salt; and 0.05 wt % of a hindered phenol heat stabilizer;

(b) a polycarbonate resin composition comprising: 50 wt % of first branched polycarbonate that is a bisphenol-A polycarbonate resin having a carbonate end-capping group derived from p-hydroxybenzonitrile (HBN) and branching derived from tris-(hydroxyphenyl)ethane (THPE) as a branching agent; 28 wt % of a second branched polycarbonate that is a bisphenol-A polycarbonate resin having branching derived from tris-(hydroxyphenyl)ethane (THPE) as a branching agent; 2 wt % of a high flow polycarbonate that is a bisphenol-A polycarbonate homopolymer having a melt volume flow rate (MVR) of between 21.9 and 31.8 cm 3 /10 min; 19 wt % of a low flow polycarbonate that is a bisphenol-A polycarbonate homopolymer having a melt volume flow rate (MVR) of between 5 and 7 cm 3 /10 min; 0.014 wt % of a first heat stabilizer that is tris(2,4-di-t-butylphenyl)phosphite; 0.017 wt % of a second heat stabilizer that is bis(2,4-dicumylphenyl)pentaerythritol diphosphite; 0.1 wt % of a cyclic siloxane; 0.08 wt % of a flame retardant salt; and 0.05 wt % of a hindered phenol heat stabilizer; and

(c) a polycarbonate resin composition comprising: 50 wt % of first branched polycarbonate that is a bisphenol-A polycarbonate resin having a carbonate end-capping group derived from p-hydroxybenzonitrile (HBN) and branching derived from tris-(hydroxyphenyl)ethane (THPE) as a branching agent; 28 wt % of a second branched polycarbonate that is a bisphenol-A polycarbonate resin having branching derived from tris-(hydroxyphenyl)ethane (THPE) as a branching agent; 2 wt % of a high flow polycarbonate that is a bisphenol-A polycarbonate homopolymer having a melt volume flow rate (MVR) of between 21.9 and 31.8 cm 3 /10 min; 19 wt % of a low flow polycarbonate that is a bisphenol-A polycarbonate homopolymer having a melt volume flow rate (MVR) of between 5 and 7 cm 3 /10 min; 0.016 wt % of a first heat stabilizer that is tris(2,4-di-t-butylphenyl)phosphite; 0.016 wt % of a second heat stabilizer that is bis(2,4-dicumylphenyl)pentaerythritol diphosphite; 0.1 wt % of a cyclic siloxane; 0.08 wt % of a flame retardant salt; and 0.047 wt % of a hindered phenol heat stabilizer.

20. The polycarbonate composition of claim 19 , further comprising 0.4 wt % of a linear siloxane additive.

21. The polycarbonate composition of claim 19 , further comprising 0.27 wt % of a UV additive.

22. The polycarbonate composition of claim 19 , further comprising 0.27 wt % of a release agent.

Assignments (6)
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 17, 2011
From: MORIZUR, JEAN FRANCOIS; NIU, YAMING; EVANS, THOMAS
To: SABIC INNOVATIVE PLASTICS IP B.V.
Reel/Frame 025973/0374 →