Flame retardant polycarbonate compositions

Claim 2

A flame-retardant copolyester-carbonate composition containing, in admixture: (i) at least one halogen-free and sulfur-containing aromatic copolyester-carbonate resin derived from (a) at least one halogen-free and sulfur-free non-polycyclic dihydric phenol, (b) from about 4 to about 25 mole percent of at least one halogen-free thiodiphenol, based on the total amount of said halogen-free and sulfur-free non-polycyclic dihydric phenol and said halogen-free thiodiphenol employed, (c) at least one difunctional carboxylic acid or a reactive derivative thereof, and (d) a carbonate precursor; and (ii) an amount of at least one organic metal salt of sulfonic acid selected from alkali and alkaline earth metal salts of sulfonic acids which in combination with said thiodiphenol is effective to render said composition flame retardant.

Claim 3

The composition of claim 1 wherein said halogen-free and sulfur-containing aromatic copolyester-carbonate resin is derived from: (i) at least one halogen-free and sufur-free dihydric phenol; (ii) at least one halogen-free thiodiphenol; (iii) at least one difunctional carboxylic acid or a reactive derivative thereof; and (iv) a carbonate precursor.

Claim 4

The composition of claim 2 which contains an amount of said thiodiphenol and an amount of said alkali and alkaline earth metal salt of sulfonic acid which in combination are effective to render said composition flame retardant.

Claim 5

The composition of claim 1 which contains from about 0.001 to about 0.5 part by weight of said alkali or alkaline earth metal salt of sulfonic acid per hundred parts by weight of said halogen-free and sulfur-containing aromatic copolyester-carbonate resin.

Claim 6

The composition of claim 4 which contains from about 4 to about 25 mole percent of said halogen-free thiodiphenol.

Claim 7

The composition of claim 1 wherein said alkali and alkaline earth metal salt of sulfonic acid is selected from: alkali and alkaline earth metal salts of substituted and unsubstituted sulfonic acids of aromatic sulfides; alkali and alkaline earth metal salts of halocycloaliphatic aromatic sulfonic acids; alkali and alkaline earth metal salts of sulfonic acids of heterocyclic compounds; alkali and alkaline earth metal salts of substituted and unsubstituted sulfonic acids of aromatic ketones; alkali and alkaline earth metal salts of monomeric and polymeric aromatic sulfonic acids; alkali and alkaline earth metal salts of monomeric and polymeric substituted aromatic sulfonic acids; alkali and alkaline earth metal salts of monomeric and polymeric aromatic amide sulfonic acids; alkali and alkaline earth metal salts of sulfonic acids of aromatic ethers; alkali and alkaline earth metal salts of perfluoroalkyl sulfonic acids; alkali and alkaline earth metal salts of monomeric and polymeric sulfonic acids of aromatic carboxylic acids; and alkali and alkaline earth metal salts of monomeric and polymeric phenol esters of sulfonic acids.

Claim 8

The composition of claim 1 wherein said halogen-free and sulfur-free non-polycyclic dihydric phenol is represented by the general formula ##STR15## wherein: R is independently selected from monovalent hydrocarbon radicals selected from alkyl radicals, aryl radicals, aralkyl radicals, and alkaryl radicals; R' is independently selected from monovalent hydrocarbon radicals selected from alkyl radicals, aryl radicals, aralkyl radicals, and alkaryl radicals; E is selected from non-cyclo divalent hydrocarbon radicals selected from alkylene radicals and alkylidene radicals, mon-cyclic divalent hydrocarbon radicals selected from cycloalkylene radicals and cycloalkylidene radicals, the --O-- radical, and the ##STR16## radical; n and n' are independently selected from whole numbers having a value of from 0 to 4 inclusive; and p is either zero or one.

Claim 9

The composition of claim 7 wherein said monovalent hydrocarbon radicals are selected from alkyl radicals, aryl radicals, aralkyl radicals, and alkaryl radicals.

Claim 10

The composition of claim 7 wherein said monovalent hydrocarbon radicals are selected from alkyl radicals.

Claim 11

The composition of claim 7 wherein said non-cyclic divalent hydrocarbon radicals are selected from alkylene and alkylidene radicals.

Claim 12

The composition of claim 7 wherein said mono-cyclic divalent hydrocarbon radicals are selected from cycloalkylene and cycloalkylidene radicals.

Claim 13

The composition of claim 7 wherein E is selected from alkylene, alkylidene, cycloalkylene, and cycloalkylidene radicals.

Claim 14

The composition of claim 12 wherein said monovalent hydrocarbon radical is selected from alkyl radicals.

Claim 15

The composition of claim 13 wherein p is one.

Claim 16

The composition of claim 7 wherein said dihydric phenol is bisphenol-A.

Claim 17

The composition of claim 1 wherein said halogen-free thiodiphenol is represented by the general formula ##STR17## wherein: R 2 is independently selected from monovalent hydrocarbon radicals selected from alkyl radicals, aryl radicals, aralkyl radicals, and alkaryl radicals; R 3 is independently selected from monovalent hydrocarbon radicals selected from alkyl radicals, aryl radicals, aralkyl radicals, and alkaryl radicals; and c and c' are independently selected from whole numbers having a value of from 0 to 4 inclusive.

Claim 18

The composition of claim 16 wherein said monovalent hydrocarbon radicals are selected from alkyl, aryl, aralkyl, and alkaryl radicals.

Claim 19

The composition of claim 16 wherein said monovalent hydrocarbon radicals are selected from alkyl radicals.

Claim 20

The composition of claim 18 wherein said thiodiphenol is selected from 3,3',5,5'-tetraalkyl-4,4'-thiodiphenols.

Claim 21

The composition of claim 16 wherein said thiodiphenol is 4,4'-thiodiphenol.

Claim 22

The composition of claim 1 wherein said difunctional carboxylic acid is selected from terephthalic acid, isophthalic acid, and mixtures thereof.

Claim 23

The composition of claim 1 wherein said reactive derivatives of said difunctional carboxylic acids are selected from terephthaloyl dichloride, isophthaloyl dichloride, and mixtures thereof.

Claim 24

The composition of claim 3 which further contains at least one halogen-free and sulfur-free aromatic copolyester-carbonate resin.

Claim 25

The composition of claim 4 wherein said halogen-free and sulfur-free aromatic copolyester-carbonate resin is derived form: (i) at least one halogen-free and sulfur-free dihydric phenol; (ii) at least one difunctional carboxylic acid or a reactive derivative thereof; and (iii) a carbonate precursor.

Claim 26

A flame-retardant copolyester-carbonate composition containing, in admixture: (i) at least one halogen-free and sulfur-free aromatic copolyester-carbonate resin derived from (a) at least one halogen-free and sulfur-free non-polycyclic dihydric phenol, (b) at least one difunctional carboxylic acid or a reactive derivative thereof, and (c) a carbonate precursor; (ii) at least one halogen-free and sulfur-containing aromatic copolyester-carbonate resin derived from (a) at least one halogen-free and sulfur-free non-polycyclic dihydric phenol, (b) from about 4 to about 25 mole percent of at least one halogen-free thiodiphenol, based on the total amount of the halogen-free and sulfur-free non-polycyclic dihydric phenol and the halogen-free thiodiphenol employed, (c) at least one difunctional carboxylic acid or a reactive derivative thereof, and (d) a carbonate precursor; and (iii) an amount of at least one organic metal salt of sulfonic acid selected from the alkali and alkaline earth metal salts of sulfonic acids which in combination with said halogen-free thiodiphenol is effective to render said composition flame retardant.

Claim 27

A flame-retardant copolyester-carbonate composition containing, in admixture: (i) at least one halogen-free and sulfur-free aromatic copolyester-carbonate resin derived from (a) at least one halogen-free and sulfur-free non-polycyclic dihydric phenol, (b) at least one difunctional carboxylic acid or a reactive derivative thereof, and (c) a carbonate precursor; (ii) at least one halogen-free and sulfur-containing aromatic copolyester-carbonate resin derived from (a) at least one halogen-free and sulfur-free non-polycyclic dihydric phenol, (b) from about 4 to about 25 mole percent of at least one halogen-free thiodiphenol, based on the total amount of the halogen-free and sulfur-free non-polycyclic dihydric phenol and the halogen-free thiodiphenol employed, (c) at least one difunctional carboxylic acid or a reactive derivative thereof, and (d) a carbonate precursor; and (iii) an amount of at least one organic metal salt of sulfonic acid selected from the alkali and alkaline earth metal salts of sulfonic acids which in combination with said halogen-free thiodiphenol is effective to render said composition flame retardant.

Claim 28

The composition of claim 25 which contains from about 0.001 to about 0.5 part by weight of said salt per hundred parts by weight of the total amount of said halogen-free and sulfur-free aromatic copolyester-carbonate resin and said halogen-free and sulfur-containing aromatic copolyester-carbonate resin present.

Claim 29

The composition of claim 25 which is non-opaque.