Abstract: A composition includes specific amounts of a poly(phenylene ether), a rubber-modified polystyrene, a flame retardant containing an organophosphate ester, and a mold release agent containing a high viscosity polydiorganosiloxane. The composition excludes polyolefin waxes. The high viscosity polydiorganosiloxane can be provided in the form of a room temperature solid masterbatch, thereby facilitating compounding of the composition. The composition is useful for injection molding, and particularly useful for injection molding battery holders for cell phone tower back-up power systems.

Abstract: A composition includes specific amounts of a poly(phenylene ether), a rubber-modified polystyrene, a flame retardant containing an organophosphate ester, and a mold release agent containing a high viscosity polydiorganosiloxane. The composition excludes polyolefin waxes. The high viscosity polydiorganosiloxane can be provided in the form of a room temperature solid masterbatch, thereby facilitating compounding of the composition. The composition is useful for injection molding, and particularly useful for injection molding battery holders for cell phone tower back-up power systems.

Abstract: This invention generally relates to transparent compositions containing a blend of poly(phenylene ether) and styrenic polymer, methods for their manufacture, and food packaging films and containers derived therefrom.

Abstract: This invention generally relates to transparent compositions containing a blend of poly(phenylene ether) and styrenic polymer, methods for their manufacture, and food packaging films and containers derived therefrom.

Abstract: The present invention is directed to a process for preparing halogen-free melt-filtered polymer compositions, compositions prepared by the process, as well as articles derived therefrom. The process comprises filtering the melted composition through a filter to remove particulate impurities that are 0.5 mm2 in size or larger. The composition comprises: (a) 60 to 90 percent by weight of a poly(phenylene ether); (b) 3 to 23 percent by weight of a styrenic polymer; (c) 5-11 percent by weight of a halogen-free flame retardant comprising at least one organic phosphate flame retardant, wherein the composition has: (i) a melt viscosity of 620 Pa·s or less as measured according at 280° C. and 1500 s?1; and (ii) a heat deflection temperature that is 135° C. or more as measured according to ASTM D648 on 6.4 mm thick bars at 1.82 MPa.

Abstract: A composition includes specific amounts of a poly(phenylene ether), a rubber-modified polystyrene, an organophosphate ester, and polymerized acrylonitrile residue. When combusted in air, the composition yields a specific amount of ash. The composition can be prepared using a post-consumer recycled rubber-modified polystyrene that contains as impurities acrylonitrile copolymer and a metal oxide pigment that survives combustion of the composition. The composition is useful for molding large, flat parts, such as back panels for flat screen televisions.

Abstract: A molding composition is disclosed which contains specific amounts of poly(arylene ether), styrenic polymer, hydrogenated block copolymer, flame retardant, and polytetrafluoroethylene. The molding composition performs well on a battery of tests, including heat resistance, impact strength, melt flow, and flame retardancy, and is particularly useful for producing photovoltaic junction boxes and connectors.

Abstract: The present invention is directed to a process for preparing halogen-free melt-filtered polymer compositions, compositions prepared by the process, as well as articles derived therefrom. The process comprises filtering the melted composition through a filter to remove particulate impurities that are 0.5 mm2 in size or larger. The composition comprises: (a) 60 to 90 percent by weight of a poly(phenylene ether); (b) 3 to 23 percent by weight of a styrenic polymer; (c) 5-11 percent by weight of a halogen-free flame retardant comprising at least one organic phosphate flame retardant, wherein the composition has: (i) a melt viscosity of 620 Pa·s or less as measured according at 280° C. and 1500 s?1; and (ii) a heat deflection temperature that is 135° C. or more as measured according to ASTM D648 on 6.4 mm thick bars at 1.82 MPa.

Abstract: A composition includes specific amounts of poly(phenylene ether), polymerized styrene residue, and polymerized acrylonitrile residue. The composition can be prepared using a recycled homopolystyrene that includes an acrylonitrile copolymer as an impurity. The composition largely preserves the desirable properties of a corresponding composition prepared from virgin resins without requiring chemical compatibilization of the poly(phenylene ether) and the acrylonitrile copolymer.

Abstract: A molding composition is disclosed which contains specific amounts of poly(arylene ether), styrenic polymer, hydrogenated block copolymer, flame retardant, and polytetrafluoroethylene. The molding composition performs well on a battery of tests, including heat resistance, impact strength, melt flow, and flame retardancy, and is particularly useful for producing photovoltaic junction boxes and connectors.

Abstract: Inorganic/organic hybrid polymers containing silsesquioxane cages are robust and exhibit desirable physical properties such as strength, hardness, and optical transparency at infrared and ultraviolet wavelengths. The polymers are prepared by polymerizing functionalized polyhedral silsesquioxane monomers such as polyhedral silsesquioxanes bearing two complementarily reactive functional groups bonded to cage silicon atoms by means of spacer moieties. The spacer moieties allow for steric mobility and more complete cure than polyhedral silsesquioxanes bearing reactive functional groups bound directly to cage silicon atoms.

Abstract: Inorganic/organic hybrid polymers containing silsesquioxane cages are robust and exhibit desirable physical properties such as strength, hardness, and optical transparency at infrared and ultraviolet wavelengths. The polymers are prepared by polymerizing functionalized polyhedral silsesquioxane monomers such as polyhedral silsesquioxanes bearing two complementarily reactive functional groups bonded to cage silicon atoms by means of spacer moieties. The spacer moieties allow for steric mobility and more complete cure than polyhedral silsesquioxanes bearing reactive functional groups bound directly to cage silicon atoms.

Abstract: Polyhedral silsesquioxane anions are economically prepared by reaction of a silica source derived from combusted organic material with a quaternary ammonium hydroxide compound. Reaction of the resulting anions with chlorosilanes may be effected in near stoichiometric fashion in organic solvent containing reactive quantities of organic acids such as formic acid. The functional groups on the resulting functionalized silsesquioxanes may be substituted for other functional groups by reaction with di- or polysiloxanes in the presence of a synthetic ion exchange resin.

Abstract: Inorganic/organic hybrid polymers containing silsesquioxane cages are robust and exhibit desirable physical properties such as strength, hardness, and optical transparency at infrared and ultraviolet wavelengths. The polymers are prepared by polymerizing functionalized polyhedral silsesquioxane monomers such as polyhedral silsesquioxanes bearing two complementarily reactive functional groups bonded to cage silicon atoms by means of spacer moieties. The spacer moieties allow for steric mobility and more complete cure than polyhedral silsesquioxanes bearing reactive functional groups bound directly to cage silicon atoms.

Abstract: Polyhedral silsesquioxane anions are economically prepared by reaction of a silica source derived from combusted organic material with a quaternary ammonium hydroxide compound. Reaction of the resulting anions with chlorosilanes may be effected in near stoichiometric fashion in organic solvent containing reactive quantities of organic acids such as formic acid. The functional groups on the resulting functionalized silsesquioxanes may be substituted for other functional groups by reaction with di- or polysiloxanes in the presence of a synthetic ion exchange resin.