A polyphenylene ether resin composition includes a modified polyphenylene ether copolymer, a high-molecular-weight compound, and a crosslinking agent for the modified polyphenylene ether copolymer. The modified polyphenylene ether copolymer includes a substituent having a carbon-carbon unsaturated double bond at a molecular chain end of the modified polyphenylene ether copolymer. The high-molecular-weight compound has a glass transition temperature (Tg) measured by differential scanning calorimetry of 20° C. or lower and has a number-average molecular weight Mn ranging from 1000 to 10000, inclusive. The crosslinking agent includes at least two carbon-carbon unsaturated double bonds per molecule, and includes at least one of dicyclopentadiene acrylate and dicyclopentadiene methacrylate. In a cured state of the polyphenylene ether resin composition, the modified polyphenylene ether copolymer is phase separated from the high-molecular-weight compound.

A process of manufacturing a free-flowing solid encapsulated drag reducing additive comprises: forming a solid drag reducing additive from one or more C.sub.5-20 olefin monomers; dispersing the solid drag reducing additive in a liquid medium to form a dispersion, the liquid medium comprising an encapsulant and a non-solvent; grinding the solid drag reducing additive in the liquid medium under non-cryogenic grinding conditions to form an encapsulated drag reducing additive in a particulate form; and removing the non-solvent by a drying technique including spray drying, flash drying, or rotating disc drying to form the free-flowing solid encapsulated drag reducing additive.

A film is described comprising a first film layer having a Tg ranging from 30° C. to 60° C. The first film layer comprises a (meth)acrylic polymer and polyvinyl acetal polymer composition. The film further comprises a second layer proximate the first film layer. The second layer is different than the first film layer. The second may be a cured (meth)acrylic polymer film or coating; a backing such as thermoplastic polymer, woven or nonwoven fabrics, metal foils, paper, foams; or a coverfilm such as a fluoropolymer.

An absorbent article containing a polyolefin film is provided. The polyolefin film is formed by a thermoplastic composition containing a continuous phase that includes a polyolefin matrix polymer and nanoinclusion additive is provided. The nanoinclusion additive is dispersed within the continuous phase as discrete nano-scale phase domains. When drawn, the nano-scale phase domains are able to interact with the matrix in a unique manner to create a network of nanopores.

The present invention provides a laminated film for molded decoration including a transparent polymer substrate, a hard coat layer having a thickness of 2 to 10 μm, and a protective layer having a thickness of 50 to 200 nm laminated in that order, in which the hard coat layer is a cured layer of a hard coating composition, the protective layer is a cured layer of a coating composition for forming a protective layer, the laminated film for molded decoration has an extension rate within a range of 15 to 80%, and after a scratch test involving 200 reciprocations under a load of 2 N per 4 cm.sup.2 of a surface of the laminated film for molded decoration, the laminated film for molded decoration has no scratches and no deterioration in visibility due to change in appearance.

The invention relates to a non-cross-linked copolymer foam with polyamide blocks and polyether blocks, wherein: the polyamide blocks of the copolymer have an average molar mass of from 200 to 1,500 g/mol; the polyether blocks of the copolymer have an average molar mass of from 800 to 2,500 g/mol; and the weight ratio of the polyamide blocks to the polyether blocks of the copolymer is from 0.1 to 0.9. The invention also relates to a method for manufacturing said foam and items manufactured from said foam.

A barrier film including a substrate; a base polymer layer adjacent to the substrate; an oxide layer adjacent to the base polymer layer; a adhesion-modifying layer adjacent to the oxide layer; and a top coat polymer layer adjacent to the adhesion-modifying layer. An optional inorganic layer can be applied over the top coat polymer layer. The inclusion of a adhesion-modifying layer provides for enhanced resistance to moisture and improved peel strength adhesion of the top coat polymer layer to the underlying barrier stack layers.

A film is described comprising a (meth)acrylic polymer and a polyvinyl acetal (e.g. butyral) resin. In some embodiments, the film has a glass transition temperature (i.e. Tg) ranging from 30 C. to 60 C. In some embodiments, the film has a gel content of at least 20% or greater. In some embodiments, the film has an elongation at break of at least 175%. The film typically comprises photoinitiator as a result of the method by which the film was made. The film may be a monolithic film or a layer of a multilayer film.

The present invention relates to a polymeric composition comprising an impact modifier and a mineral filler and its process of preparation and its use. In particular, the present invention relates to a polymeric composition comprising an impact modifier and a mineral filler and its use for thermoplastic polymers. More particularly the present invention relates to the process of preparation of polymeric composition comprising an impact modifier and a mineral filler and its use for the impact modification of thermoplastic polymers.

The present invention relates to a waterborne dispersion comprising (A) amphiphilic block copolymer obtained with a controlled radical polymerization process and comprising at least blocks [A] and [B], whereby block [A] comprises ethylenically unsaturated monomer(s) bearing water-soluble and/or water-dispersible functional groups (monomer(s) (i)), and block [B] comprises ethylenically unsaturated monomer(s) different from monomer(s) (i) (monomer(s) (ii)); and (B) polymer P comprising ethylenically unsaturated monomer(s) different from (i) (monomer(s) (ii)), characterized in that the amount of block copolymer is higher than 1 and lower than 30 wt. %, based on the total weight of monomers used to prepare the block copolymer and polymer P; the acid value of the composition consisting of block copolymer and polymer P is higher than 1 and at most 35 mg KOH per g of the block copolymer-polymer P composition; the block copolymer has a calculated glass transition temperature of higher than 10 C. and lower than 250 C.; and polymer P comprises at least 20 wt. % (relative to the total monomer composition to prepare the polymer P) of a polymer fraction with calculated glass transition temperature higher than 10 C. and lower than 100 C.