A sole assembly for an article of footwear has a first portion having a lower ground engaging surface, an upper surface, and a recess formed in the upper surface. A second portion is seated in the recess in the first portion and has an upper surface. The second portion is formed from a first foam material prepared by a reaction product of a composition having about 10 to about 100 phr of a hydrogenated copolymer and about 10 to about 90 phr of a copolymer of ethlylene and an alpha olefin, the alpha olefin having up to 20 carbon atoms. The first foam material has a hardness of 25 to 45 Asker C and a density of less than 0.18 g/cm3.

The present invention relates to a polymer-graphene composite, in which a polymer has been introduced onto the surface of graphene while maintaining the structural features and mechanical properties of the graphene, thereby realizing an excellent dispersibility in an organic solvent, a method for preparing the same, and a polymer-graphene composite composition using the same.

The present invention relates to a separator for a secondary battery and a lithium secondary battery including the separator, the separator including: a porous substrate and a heat-resistant layer disposed on at least one surface of the porous substrate, wherein the heat-resistant layer includes an acrylic heat-resistant binder, an adhering binder, and a filler, the acrylic heat-resistant binder including a structural unit derived from (meth)acrylate or (meth)acrylic acid, a cyano group-containing structural unit, and a sulfonate group-containing structural unit, the adhering binder includes a structural unit including a structural unit including hydroxyl group, a structural unit including an acetate group, and a structural unit including an alkali metal.

Porous polymeric materials having a very high content of thermally conductive and/or electrically conductive fillers. Process for the preparation of the porous composite material including at least one binder-forming polymeric phase and one or more fillers, this process including the stages of hot mixing, by the molten route, the polymeric phase, the fillers and a sacrificial polymeric phase, so as to obtain a mixture, of shaping the mixture and of removing the sacrificial polymeric phase.

The present invention relates to self-supported elastomeric film made from a composition comprising polymer latex particles bearing ethylenically unsaturated groups pending from the polymeric backbone of the latex particles wherein the ethylenic unsaturation is separated from the polymeric backbone by at least 3 chemical bonds, to an article comprising the self-supported elastomeric film and to a method for making a self-supported elastomeric film from a composition comprising said polymer latex particles.

The present invention relates to a thermoplastic resin composition, a method of preparing the same, and an injection-molded article including the same. More particularly, the present invention relates to a thermoplastic resin composition having superior vibration welding properties along with ABS-based resin-specific impact resistance, heat resistance, and the like due to inclusion of an ABS-based graft copolymer including a conjugated diene-based rubber polymer having an average particle diameter of 0.25 to 0.35 μm; a rubber-modified graft copolymer including a diene-based rubber polymer having an average particle diameter of 0.6 to 10 μm and prepared by continuous bulk polymerization; and a matrix resin, and an injection-molded article including the thermoplastic resin composition.

Methods of making self-expended lignofoams are provided. In embodiments, such a method comprises exposing a self-expanding lignofoam composition comprising raw lignin and a thermoplastic polymer to an elevated temperature for a period of time to soften the composition, desorb water from the raw lignin or induce at least some hydroxyl groups of the raw lignin to undergo dehydration reactions to generate water or both, vaporize the water, and generate pores throughout the softened composition. The method further comprises cooling the porous, softened composition to room temperature to provide the self-expanded lignofoam. The self-expanding lignofoam composition is free of an added plasticizer, an added lubricant, an added foaming agent, and an added blowing agent, and the thermoplastic polymer is not a starch, not a polyurethane, and not a polysiloxane. The resulting self-expanded lignofoams are also provided.

A fire resistant syntactic foam material, the material comprising the reaction product of a reaction mixture including a resole cold curing phenolic resin and incorporating a plurality of hollow spheres, the reaction mixture also including a solution of a partial phosphate ester, a low viscosity phosphate plasticiser, a reinforcing filler and a particulate filler.

The present invention aims to provide a masterbatch for foam molding which can be suitably used in molding involving high shear force or molding requiring low molding temperature and which can provide a foam molded article having a high expansion ratio and good appearance quality. The present invention also aims to provide a foam molded article formed from the masterbatch for foam molding. Provided is a masterbatch for foam molding, containing: a base resin; and a thermally expandable microcapsule, the masterbatch having a true specific gravity of 0.80 g/cm.sup.3 or more and a Mooney viscosity ML 1+4 (100 C.) of 20 to 90, the base resin containing an EPDM resin, the masterbatch containing the thermally expandable microcapsule in an amount of 40 to 300 parts by weight relative to 100 parts by weight of the base resin.

A sole assembly for an article of footwear has a first portion having a lower ground engaging surface, an upper surface, and a recess formed in the upper surface. A second portion is seated in the recess in the first portion and has an upper surface. The second portion is formed from a first foam material prepared by a reaction product of a composition having about 10 to about 100 phr of a hydrogenated copolymer and about 10 to about 90 phr of a copolymer of ethlylene and an alpha olefin, the alpha olefin having up to 20 carbon atoms. The first foam material has a hardness of 25 to 45 Asker C and a density of less than 0.18 g/cm3.