A flame retardant composition comprising: a poly(carbonate-bisphenol phthalate ester); an organophosphorous compound wherein the organophosphorous compound is present in an amount effective to provide 0.5-0.9 wt % of added phosphorous, based on the total weight of the composition; and a poly(carbonate-monoarylate phthalate ester), wherein the composition has a bromine or chlorine content of less than or equal to 100 parts per million by weight, less than or equal to 75 parts per million by weight, or less than or equal to 50 parts per million by weight, based on the total parts by weight of the composition; and wherein a molded sample of the flame retardant composition has a UL 94 rating of V0 at a thickness of 0.6 millimeter, and a transmission of at least 70% according to ASTM D 1003 at a thickness of 1.0 millimeter.

In various aspects, the disclosure relates to polycarbonate compositions exhibiting improved impact strength, both multi axial and notched Izod, as well as thin-walled flame resistance while free or substantially free of bromine or chlorine flame retardant additives. The polycarbonate compositions may comprise non-bonding glass fiber, butyl tosylate, and/or a phosphorous based stabilizer.

In various aspects, the disclosure relates to polycarbonate compositions exhibiting improved impact strength, both multi axial and notched Izod, as well as thin-walled flame resistance while free or substantially free of bromine or chlorine flame retardant additives. The polycarbonate compositions may comprise non-bonding glass fiber, butyl tosylate, and/or a phosphorous based stabilizer.

The present disclosure discloses polyester composites and their preparation methods, and belongs to the technical field of polymer processing and modification. The polyester composites of the present disclosure comprise 65 to 90 parts of polyester, 5 to 35 parts of an elastomer, 0.05 to 3 parts of a chain extender and 0.01 to 5 parts of a functional additive. The polyester composites of the present disclosure not only have ultra-high toughness, but also can maintain high tensile strength, have excellent hydrolysis resistance, can be matched with an antibacterial agent or an antistatic agent to have good antibacterial or antistatic additional functions, can be widely applied to the fields of fibers and fabrics, plastic structural parts, plastic packages or automobile interior parts, and have a wide prospect.

The present disclosure discloses polyester composites and their preparation methods, and belongs to the technical field of polymer processing and modification. The polyester composites of the present disclosure comprise 65 to 90 parts of polyester, 5 to 35 parts of an elastomer, 0.05 to 3 parts of a chain extender and 0.01 to 5 parts of a functional additive. The polyester composites of the present disclosure not only have ultra-high toughness, but also can maintain high tensile strength, have excellent hydrolysis resistance, can be matched with an antibacterial agent or an antistatic agent to have good antibacterial or antistatic additional functions, can be widely applied to the fields of fibers and fabrics, plastic structural parts, plastic packages or automobile interior parts, and have a wide prospect.

Disclosed is a composite from about 50 wt. % to about 90 wt. % of a thermoplastic resin, wherein the thermoplastic resin comprises a polycarbonate polysiloxane copolymer; and from about 10 wt. % to about 50 wt. % of a carbon-based filler. The composite exhibits a dielectric constant ε′ of between 5 and 20 and a dissipation loss ε″ of between 0.1 and 6, measured at frequencies between about 10 and 120 GHz.

Disclosed is a composite from about 50 wt. % to about 90 wt. % of a thermoplastic resin, wherein the thermoplastic resin comprises a polycarbonate polysiloxane copolymer; and from about 10 wt. % to about 50 wt. % of a carbon-based filler. The composite exhibits a dielectric constant ε′ of between 5 and 20 and a dissipation loss ε″ of between 0.1 and 6, measured at frequencies between about 10 and 120 GHz.

A thermoplastic polymer composition (I) comprising: (A) block copolymer A comprising A1: 60 to 95 wt.-% vinyl aromatic monomer, and A2: 5 to 40 wt.-% conjugated diene; (B) a stabilizer combination consisting of: B1: 200 to 2500 ppm 2,6-di-tert-butyl-4-(4,6-bis(octylthio)-1,3,5-triazin-2-ylamino) phenol, B2: 500 to 2500 ppm 2-[1-(2-hydroxy-3,5-di-tert-pentylphenyl)ethyl]-4,6-di-tert-pentylphenyl acrylate and/or 2-tert-butyl-6-(3-tert-butyl-2-hydroxy-5-methylbenzyl)-4-methylphenyl acrylate, and B3: 500 to 2000 ppm tris(2,4-di-tert.-butylphenyl)phosphite; (C) 0 to 5000 ppm stabilizers different from (B1), (B2) and (B3); (D) optionally additives and/or processing aids other than (B) and (C), (E) optionally thermoplastic polymer TP other than block copolymer A, a process for its preparation, and its use for the preparation of shrink films is described.

A thermoplastic polymer composition (I) comprising: (A) block copolymer A comprising A1: 60 to 95 wt.-% vinyl aromatic monomer, and A2: 5 to 40 wt.-% conjugated diene; (B) a stabilizer combination consisting of: B1: 200 to 2500 ppm 2,6-di-tert-butyl-4-(4,6-bis(octylthio)-1,3,5-triazin-2-ylamino) phenol, B2: 500 to 2500 ppm 2-[1-(2-hydroxy-3,5-di-tert-pentylphenyl)ethyl]-4,6-di-tert-pentylphenyl acrylate and/or 2-tert-butyl-6-(3-tert-butyl-2-hydroxy-5-methylbenzyl)-4-methylphenyl acrylate, and B3: 500 to 2000 ppm tris(2,4-di-tert.-butylphenyl)phosphite; (C) 0 to 5000 ppm stabilizers different from (B1), (B2) and (B3); (D) optionally additives and/or processing aids other than (B) and (C), (E) optionally thermoplastic polymer TP other than block copolymer A, a process for its preparation, and its use for the preparation of shrink films is described.

A thermoplastic polymer composition (I) comprising: (A) block copolymer A comprising A1: 60 to 95 wt.-% vinyl aromatic monomer, and A2: 5 to 40 wt.-% conjugated diene; (B) a stabilizer combination consisting of: B1: 200 to 2500 ppm 2,6-di-tert-butyl-4-(4,6-bis(octylthio)-1,3,5-triazin-2-ylamino) phenol, B2: 500 to 2500 ppm 2-[1-(2-hydroxy-3,5-di-tert-pentylphenyl)ethyl]-4,6-di-tert-pentylphenyl acrylate and/or 2-tert-butyl-6-(3-tert-butyl-2-hydroxy-5-methylbenzyl)-4-methylphenyl acrylate, and B3: 500 to 2000 ppm tris(2,4-di-tert.-butylphenyl)phosphite; (C) 0 to 5000 ppm stabilizers different from (B1), (B2) and (B3); (D) optionally additives and/or processing aids other than (B) and (C), (E) optionally thermoplastic polymer TP other than block copolymer A, a process for its preparation, and its use for the preparation of shrink films is described.