C08G64/10

Brominated cross-linkable polycarbonate compositions

Polymeric compositions having improved flame retardance properties are disclosed. The compositions comprise a cross-linkable polycarbonate resin having a photoactive group derived from a benzophenone, a bromine source, and optionally a non-brominated and non-chlorinated flame retardant. The composition contains a minimum amount of bromine. Articles formed from the compositions have robust flame retardance properties and enhanced chemical resistance.

Post polymerization modification in flow

Techniques regarding post polymerization modifications to polycarbonate polymers via a flow reactor are provided. For example, one or more embodiments described herein can comprise a cyclic carbonate monomer that can be employed to facilitate polymerization of one or more polycarbonate platforms susceptible to post polymerization modification. For instance, one or more embodiments can regard a cyclic carbonate molecular backbone covalently bonded to an aryl halide functional group via in accordance with a chemical structure selected from the group consisting of: ##STR00001##
In the chemical structures, R.sub.1 can be selected from the group consisting of a hydrogen atom and a functional group comprising a first alkyl group; L can represent a linkage group, comprising: a second alkyl group and an end group having at least one member selected from the group consisting of an oxygen atom and a nitrogen atom; and A can represent the aryl halide functional group.

Post polymerization modification in flow

Techniques regarding post polymerization modifications to polycarbonate polymers via a flow reactor are provided. For example, one or more embodiments described herein can comprise a cyclic carbonate monomer that can be employed to facilitate polymerization of one or more polycarbonate platforms susceptible to post polymerization modification. For instance, one or more embodiments can regard a cyclic carbonate molecular backbone covalently bonded to an aryl halide functional group via in accordance with a chemical structure selected from the group consisting of: ##STR00001##
In the chemical structures, R.sub.1 can be selected from the group consisting of a hydrogen atom and a functional group comprising a first alkyl group; L can represent a linkage group, comprising: a second alkyl group and an end group having at least one member selected from the group consisting of an oxygen atom and a nitrogen atom; and A can represent the aryl halide functional group.

BROMINATED CROSS-LINKABLE POLYCARBONATE COMPOSITIONS
20170129996 · 2017-05-11 ·

Polymeric compositions having improved flame retardance properties are disclosed. The compositions comprise a cross-linkable polycarbonate resin having a photoactive group derived from a benzophenone, a bromine source, and optionally a non-brominated and non-chlorinated flame retardant. The composition contains a minimum amount of bromine. Articles formed from the compositions have robust flame retardance properties and enhanced chemical resistance.

BROMINATED CROSS-LINKABLE POLYCARBONATE COMPOSITIONS
20170129996 · 2017-05-11 ·

Polymeric compositions having improved flame retardance properties are disclosed. The compositions comprise a cross-linkable polycarbonate resin having a photoactive group derived from a benzophenone, a bromine source, and optionally a non-brominated and non-chlorinated flame retardant. The composition contains a minimum amount of bromine. Articles formed from the compositions have robust flame retardance properties and enhanced chemical resistance.

Polycarbonate copolymer, coating liquid using same, molded body, and electrophotographic photosensitive body

A polycarbonate copolymer includes: a repeating unit represented by a formula (1) below; and a repeating unit represented by a formula (2) below, in which the repeating unit represented by the formula (1) is formed from a bischloroformate oligomer having an average number of monomer units n represented by a formula (100) below in a range from 0.1 to 1.3. In the formulae (100) and (1), Ar.sup.1 represents a group represented by a formula (3) below. In the formula (2), Ar.sup.2 represents a divalent aromatic group. In the formula (3) below, X.sub.1 represents a single bond or an oxygen atom. R.sub.11 each independently represents a methyl group or an ethyl group. ##STR00001##

Polycarbonate copolymer, coating liquid using same, molded body, and electrophotographic photosensitive body

A polycarbonate copolymer includes: a repeating unit represented by a formula (1) below; and a repeating unit represented by a formula (2) below, in which the repeating unit represented by the formula (1) is formed from a bischloroformate oligomer having an average number of monomer units n represented by a formula (100) below in a range from 0.1 to 1.3. In the formulae (100) and (1), Ar.sup.1 represents a group represented by a formula (3) below. In the formula (2), Ar.sup.2 represents a divalent aromatic group. In the formula (3) below, X.sub.1 represents a single bond or an oxygen atom. R.sub.11 each independently represents a methyl group or an ethyl group. ##STR00001##

Method for the manufacture of polycarbonate

The present invention relates to a method for the manufacture of a (co)polycarbonate comprising reacting tetrabromo bisphenol A and optionally one or more bisphenol comonomer(s) with phosgene wherein the tetrabromo bisphenol A contains an amount of tetrabromo bisphenol A dimer of at most 3.0 wt. % based on the weight of the tetrabromo bisphenol A, determined after heat treating the tetrabromo bisphenol A at a temperature of 260 C. for a period of 15 minutes.

Method for the manufacture of polycarbonate

The present invention relates to a method for the manufacture of a (co)polycarbonate comprising reacting tetrabromo bisphenol A and optionally one or more bisphenol comonomer(s) with phosgene wherein the tetrabromo bisphenol A contains an amount of tetrabromo bisphenol A dimer of at most 3.0 wt. % based on the weight of the tetrabromo bisphenol A, determined after heat treating the tetrabromo bisphenol A at a temperature of 260 C. for a period of 15 minutes.