Compatibilized compositions, articles formed therefrom, and methods of manufacture thereof

US10005902B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10005902-B2
Application numberUS-201515110477-A
CountryUS
Kind codeB2
Filing dateJan 12, 2015
Priority dateJan 10, 2014
Publication dateJun 26, 2018
Grant dateJun 26, 2018

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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Abstract

Official abstract text for this publication.

A thermoplastic composition comprises, based on the total weight of the thermoplastic composition, 10 to 45 wt. % of a poly(etherimide); 35 to 90 wt. % of a poly(carbonate-siloxane); 0.5 to 20 wt. % of compatibilizer polycarbonate component comprising a poly(carbonate-arylate ester); up to 15 wt. % of an ultraviolet light stabilizer; and 0 to 30 wt. % of TiO2; wherein a sample of the composition has a notched Izod impact energy of at least 200 J/m at 23° C. measured in accordance to ASTM D256; and an at least 50% higher notched Izod impact energy value compared to the composition without the compatibilizer component measured in accordance to ASTM D256.

First claim

Opening claim text (preview).

What is claimed is: 1. A thermoplastic composition comprising, based on the total weight of the thermoplastic composition, 10 to 45 wt. % of a poly(etherimide); 35 to 90 wt. % of a poly(carbonate-siloxane); 0.5 to 20 wt. % of compatibilizer polycarbonate component comprising a poly(carbonate-arylate ester); up to 15 wt. % of an ultraviolet light stabilizer; and 0 to 30 wt. % of TiO 2 ; wherein a sample of the composition has a notched Izod impact energy of at least 200 J/m at 23° C. measured in accordance to ASTM D256; and an at least 50% higher notched Izod impact energy value compared to the composition without the compatibilizer component measured in accordance to ASTM D256. 2. The composition of claim 1 , wherein the poly(etherimide) comprises units of the formula wherein R is a C 2-20 hydrocarbon group, and Z is an aromatic C 6-24 monocyclic or polycyclic group optionally substituted with 1 to 6 C 1-8 alkyl groups, 1 to 8 halogen atoms, or a combination thereof, wherein the divalent bonds of the —O—Z—O— group are in the 3,3′, 3,4′, 4,3′, or the 4,4′ positions. 3. The composition of claim 2 , wherein R is a divalent radical of the formula wherein Q is —O—, —S—, —C(O)—, —SO 2 —, —SO—, or —C y H 2y — and a halogenated derivative thereof wherein y is an integer from 1 to 5, and Z is a divalent group of the formula wherein Q 1 is —O—, —S—, —C(O)—, —SO 2 —, —SO—, or —C y H 2y — wherein y is an integer from 1 to 5. 4. The composition of claim 1 , further comprising 0.5 to 10 wt. % of a poly(etherimide-siloxane) copolymer. 5. The composition of claim 1 , wherein the poly(carbonate-siloxane) comprises first repeating units and second repeating units, wherein the first repeating units are bisphenol carbonate units of the formula wherein R a and R b are each independently C 1-12 alkyl, C 1-12 alkenyl, C 3-8 cycloalkyl, or C 1-12 alkoxy, p and q are each independently 0 to 4, and X a is a single bond, —O—, —S—, —S(O)—, —S(O) 2 —, —C(O)—, a C 1-11 alkylidene of formula —C(R c )(R d ) wherein R c and R d are each independently hydrogen or C 1-10 alkyl, or a group of the formula C(═R e )— wherein R e is a divalent C 1-10 hydrocarbon group; and the second repeating units are polysiloxane units of the formula wherein R is each independently a C 1-13 monovalent hydrocarbon group, and E has an average value of 2 to 200. 6. The composition of claim 5 , wherein the siloxane units are of the formula or a combination comprising at least one of the foregoing, wherein E has an average value of 2 to 200, wherein the poly(carbonate-siloxane) comprises 0.5 to 55 wt. % of siloxane units based on the total weight of the poly(carbonate-siloxane). 7. The composition of claim 1 , wherein the poly(carbonate-arylate ester) comprises bisphenol A carbonate units and arylate ester units of the formula wherein R a and R b are each independently C 1-12 alkyl, C 1-12 alkenyl, C 3-8 cycloalkyl, or C 1-12 alkoxy, p and q are each independently 0 to 4, and X a is a single bond, —O—, —S—, —S(O)—, —S(O) 2 —, —C(O)—, a C 1-11 alkylidene of the formula C(R c )(R d )— wherein R c and R d are each independently hydrogen or C 1-10 alkyl, or a group of the formula —C(═R e )— wherein R e is a divalent C 1-10 hydrocarbon group. 8. The composition of claim 7 , wherein the poly(carbonate-arylate ester) is a poly(bisphenol A carbonate)-co-(bisphenol phthalate ester) comprising 55 to 65 wt. % of the ester units, wherein the ester units have a molar ratio of isophthalate to terephthalate of 45:55 to 55:45 or the poly(carbonate-arylate ester) is a poly(bisphenol A carbonate)-co-(bisphenol phthalate ester) comprising 75 to 85 wt. % of the ester units, wherein the ester units have a molar ratio of isophthalate to terephthalate of 98:2 to 88:12. 9. The composition of claim 1 , wherein the poly(carbonate-arylate ester) comprises bisphenol A carbonate units, arylate ester units of the formula optionally, monoaryl carbonate units of the formula and optionally, bisphenol ester units of the formula wherein, in the foregoing formulas R h is each independently a C 1-10 hydrocarbon group, n is 0 to 4, R a and R b are each independently a C 1-12 alkyl, p and q are each independently integers of 0 to 4, and X a is a single bond, —O—, —S—, —S(O)—, —S(O) 2 —, —C(O)—, or a C 1-13 alkylidene of formula —C(R c )(R d )— wherein R c and R d are each independently hydrogen or C 1-12 alkyl, or a group of the formula —C(═R e )— wherein R e is a divalent C 1-12 hydrocarbon group. 10. The composition of claim 9 , wherein the poly(carbonate-arylate ester) comprises 70 to 90 mol % of bisphenol A carbonate units, 10 to 30 mol % of isophthalic acid-terephthalic acid-resorcinol ester units, and optionally, 1 to 60 mol % resorcinol carbonate units, isophthalic acid-terephthalic acid-bisphenol A ester units, or a combination thereof. 11. The composition of claim 9 , wherein the poly(carbonate-arylate ester) comprises 1 to 20 mol % of bisphenol A carbonate units, 60 to 99 mol % of isophthalic acid-terephthalic acid-resorcinol ester units, and optionally, 1 to 20 mol % resorcinol carbonate units, isophthalic acid-terephthalic acid-bisphenol A ester units, or a combination thereof. 12. The composition of claim 1 , wherein the poly(carbonate-arylate ester) is a poly(carbonate-monoaryl arylate ester) further comprising siloxane groups comprising repeating carbonate units of the formula wherein R a and R b are each independently are each independently C 1-12 alkyl, p and q are each independently integers of 0 to 4, and X a is a single bond, —O—, —S—, —S(O)—, —S(O) 2 —, —C(O)—, or a C 1-18 organic group; and arylate ester units of the formula wherein R h is each independently a halogen or C 1-10 hydrocarbon group, and n is 0 to 4; and siloxane units of the formula wherein each R is independently a C 1-13 monovalent hydrocarbon group, and E has an average value of 2 to 500. 13. The composition of claim 12 , wherein in the poly(carbonate-monoaryl arylate ester), the carbonate units are bisphenol A carbonate units; the arylate ester units are isophthalic acid-terephthalic acid-re

Assignees

Inventors

Classifications

  • Titanium dioxide · CPC title

  • Stabilised against heat, light or radiation or oxydation · CPC title

  • Thermoplastic elastomer · CPC title

  • Characterised by the use of polycarbonates; Derivatives of polycarbonates · CPC title

  • Manufacture of articles or shaped materials containing macromolecular substances (manufacture of semi-permeable membranes B01D67/00 - B01D71/00) · CPC title

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What does patent US10005902B2 cover?
A thermoplastic composition comprises, based on the total weight of the thermoplastic composition, 10 to 45 wt. % of a poly(etherimide); 35 to 90 wt. % of a poly(carbonate-siloxane); 0.5 to 20 wt. % of compatibilizer polycarbonate component comprising a poly(carbonate-arylate ester); up to 15 wt. % of an ultraviolet light stabilizer; and 0 to 30 wt. % of TiO2; wherein a sample of the compositio…
Who is the assignee on this patent?
Sabic Global Technologies Bv
What technology area does this patent fall under?
Primary CPC classification C08L69/00. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jun 26 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).