IP Library Granted Patent US 10,526,483
Granted Patent B2
US 10,526,483 · App. 16/095,557 · Granted Jan 7, 2020

Poly(ester-carbonate) copolymers, articles formed therefrom, and methods of manufacture

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Quick Facts
Patent No.
US 10,526,483
App. No.
16/095,557
Granted
Jan 7, 2020
Kind
B2
Abstract

A poly(ester-carbonate) copolymer comprises carbonate units of the formula (I); and ester units of the formula (II) wherein: T is a C 2-20 alkylene, a C 6-20 cycloalkylene, or a C 6-20 arylene; and R1 and J are each independently a bisphenol A divalent group and a phthalimidine divalent group, provided that the phthalimidine divalent group is present in an amount of 40 to 50 mol % based on the total moles of the bisphenol A divalent groups and the C 1/2 divalent group, and the ester units are present in an amount of 40 to 60 mol % based on the sum of the moles of the carbonate units and the ester units; and wherein the poly(ester-carbonate) copolymer has a weight average molecular weight of 18,000 to 24,000 Daltons; and the composition has a Tg of 210 to 235° C. and a melt viscosity of less than 1050 Pa-s at 644 sec −1 and 350° C.

Claims (58)

1. A poly(ester-carbonate) copolymer, comprising

carbonate units of the formula

 and

ester units of the formula

wherein:

T is a C 2-20 alkylene, a C 6-20 cycloalkylene, or a C 6-20 arylene; and

R 1 and J are each independently

(a) a bisphenol A divalent group of the formula

 and

(b) a phthalimidine divalent group of the formula

wherein

R a and R b are each independently a C 1-12 alkyl, C 2-12 alkenyl, C 3-8 cycloalkyl, or C 1-12 alkoxy,

each R 3 is independently a C 1-6 alkyl,

R 4 is hydrogen, C 1-6 alkyl, or phenyl optionally substituted with 1 to 5 C 1-6 alkyl groups, preferably wherein R 4 is hydrogen, methyl, or phenyl,

p, q, and j are each independently 0 to 4,

provided that

the phthalimidine group (b) is present in an amount of 40 mol % to 50 mol % based on the total moles of the bisphenol A divalent groups (a) and the phthalimidine groups (b);

the ester units are present in an amount of 40 mol % to 60 mol % based on the sum of the moles of the carbonate units and the ester units;

the copolymer comprises phthalimidine-carbonate-phthalimidine linkages in an amount of greater than 15 mol % and less than 50 mol % based on the total moles of the carbonate linkages as determined by carbon 13 nuclear magnetic resonance spectroscopy; and

wherein

the poly(ester-carbonate) copolymer has a weight average molecular weight of 18,000 Daltons to 24,000 Daltons, as measured by gel permeation chromatography, using a crosslinked styrene-divinylbenzene column and calibrated to bisphenol A homopolycarbonate references, the poly(ester-carbonate) copolymer has a shift in melt viscosity of less than 25% at 350° C. over 30 min under a nitrogen atmosphere as measured in a small amplitude oscillatory time sweep rheology at a fixed angular frequency of 10 radians/sec; and a yellowness index of less than 18 determined in accordance with ASTM D1925; and

a molded sample of the composition has

a glass transition temperature of 210° C. to 235° C. as determined by differential scanning calorimetry (DSC) as per ASTM D3418 with a 20° C./min heating rate;

a melt viscosity of less than 1050 Pa·s at 644 sec-1 and 350° C., determined according to ISO11443.

2. The poly(ester-carbonate) copolymer of claim 1 , wherein

R 1 and J are each independently the bisphenol A divalent group or the phthalimidine divalent group; and

at least a portion of the J groups are the phthalimidine divalent group.

3. The poly(ester-carbonate) copolymer of claim 1 , wherein the poly(ester-carbonate) copolymer comprises phthalimidine divalent groups (b) and the mol % of the phthalimidine divalent groups (Mol % PPP), the mol % of the ester units (Mol % Ester), and the weight average molecular weight of the poly(ester-carbonate) copolymer (Mw) are selected according to the following formula:

Tg= 127.1+(0.94375×Mol % PPP )+(0.3875×Mol % Ester)+(0.00164968× Mw ).

4. The poly(ester-carbonate) copolymer of claim 1 , wherein the copolymer comprises phthalimidine-carbonate-phthalimidine linkages in an amount of greater than 15 mol % and less than 40 mol % based on the total moles of the carbonate linkages as determined by carbon 13 nuclear magnetic resonance spectroscopy.

5. The poly(ester-carbonate) copolymer of claim 1 , wherein greater than 20 mol % and less than 35 mol % of the J groups are the phthalimidine group based on the total moles of the J groups.

6. The poly(ester-carbonate) copolymer of claim 1 , having one or more of the following properties:

a glass transition temperature of 220° C. to 235° C. as determined by differential scanning calorimetry (DSC) as per ASTM D3418 with a 20° C./min heating rate;

a Vicat B120 of 220 to 225° C., measured according to ISO 306; or

a melt viscosity of less than 1000 Pa·s at 644 sec −1 and 350° C., determined according to ISO11443.

7. The poly(ester-carbonate) copolymer of claim 1 , wherein R 1 and J consist of the bisphenol A divalent group (a) or the phthalimidine group (b).

8. The poly(ester-carbonate) copolymer of claim 1 , wherein T is a C 6-20 divalent aromatic group.

9. The poly(ester-carbonate) copolymer of claim 1 , wherein T is a divalent isophthaloyl group, a divalent terephthaloyl group, or a combination thereof.

10. The poly(ester-carbonate) copolymer of claim 1 , wherein p, q, and j are zero, and R 4 is hydrogen, methyl, or phenyl.

11. A thermoplastic composition comprising the poly(ester-carbonate) copolymer of claim 1 .

12. The thermoplastic composition of claim 11 further comprising a polycarbonate homopolymer, a second poly(ester-carbonate) different from the poly(ester-carbonate) copolymer, a copolycarbonate, or a combination comprising at least one of the foregoing.

13. The thermoplastic composition of claim 11 , wherein the composition has a haze of less than 15% and a transmission greater than 75%, each measured in accordance with ASTM D1003 using the color space CIE1931 (Illuminant C and a 2° observer) at a 3.2 mm thickness.

14. The poly(ester-carbonate) copolymer of claim 1 , wherein a metalized sample of the poly(ester-carbonate) copolymer has a defect onset temperature that is within 10 degrees Celsius of the heat deflection temperature of the poly(ester-carbonate) copolymer measured flat on a 80×10×4 mm bar with a 64 mm span at 0.45 MPa according to ISO 75/Bf.

15. The poly(ester-carbonate) copolymer of claim 1 , wherein a metalized sample of the poly(ester-carbonate) copolymer has a defect onset temperature of 200 to 220° C.

16. The poly(ester-carbonate) copolymer of claim 1 , wherein the poly(ester-carbonate) copolymer at a given temperature has a melt viscosity of less than 1050 Pa·s at 644 sec −1 and a shift in melt viscosity of less than 25% at the given temperature over 30 min under a nitrogen atmosphere as measured in a small amplitude oscillatory time sweep rheology at a fixed angular frequency of 10 radians/sec.

17. The poly(ester-carbonate) copolymer of claim 1 , wherein the copolymer has a melt flow rate of 10 to 30 cm 3 /10 minutes measured at 330° C. under a load of 2.16 kg in accordance with ASTM D1238-04.

18. An article comprising the copolymer of claim 1 , wherein the article is a molded article, a thermoformed article, an extruded film, an extruded sheet, one or more layers of a multi-layer article, a substrate for a coated article, or a substrate for a metallized article.

19. The article of claim 18 , wherein the article is a metallized article comprising the copolymer of claim 1 , wherein the defect onset temperature of the metallized article is within 10° C. of the heat deflection temperature of the copolymer measured flat on a 80×10×4 mm bar with a 64 mm span at 0.45 MPa according to ISO 75/Bf.

20. The article of claim 19 , comprising

a substrate comprising the copolymer of claim 1 ; and

a metal layer disposed on at least one side of the substrate.

21. A method for the manufacture of the poly(ester-carbonate) copolymer of claim 1 , the method comprising:

providing a slurry comprising water, a water-immiscible organic solvent, a phase transfer catalyst, and bisphenol A;

concurrently but separately adding to the slurry (1) an aromatic dicarboxylic halide of the formula

and

(2) a solution comprising aqueous NaOH or aqueous KOH and a dihydroxy compound of the formula

to provide a polyester oligomer; and

reacting the polyester oligomer with a carbonate source to provide the poly(ester-carbonate).

Assignments (3)
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 22, 2018
From: FARRELL, TONY; SYBERT, PAUL DEAN; MAHOOD, JAMES ALAN
To: SABIC GLOBAL TECHNOLOGIES B.V.
Reel/Frame 047262/0582 →