A method for forming an isoporous graded film comprising multiblock copolymers and isoporous graded films. The films have a surface layer and a bulk layer. The surface layer can have at least 1×10.sup.14 pores/m.sup.2 and a pore size distribution (d.sub.max/d.sub.min)) of less than 3. The bulk layer has an asymmetric structure. The films can be used in filtration applications.

A block-copolymer pellet having 100 parts by weight of a pellet-shaped article of a block copolymer (A) and 0.01 to 5 parts by weight of a hydrocarbon-based dusting agent (B) is provided, wherein the block copolymer (A) has at least one aromatic vinyl polymer block and at least one conjugated diene polymer block, the hydrocarbon-based dusting agent (B) has a BET specific surface area of 0.50 to 3.00 m.sup.2/g, a volume average particle size of 2.0 to 20 μm, a bulk density of 0.10 to 0.34 g/cm.sup.3, and a melting point of 75° C. or higher, and the block-copolymer pellet has a Shore A hardness of 10 to 80, and a BET specific surface area of 0.001 to 0.05 m.sup.2/g measured by a Kr adsorption method.

A main object of the present invention is to provide a block copolymer composition which has good elasticity, while having excellent stress relaxation properties. The object is achieved by providing a block copolymer composition obtained by a modification treatment, the block copolymer composition comprising a block copolymer B formed by introducing a functional group capable of forming a non-covalent bond into a block copolymer A including at least one aromatic vinyl polymer block and at least one conjugated diene polymer block.

A main object of the present invention is to provide a block copolymer composition which has good elasticity, while having excellent stress relaxation properties. The object is achieved by providing a block copolymer composition obtained by a modification treatment, the block copolymer composition comprising a block copolymer B formed by introducing a functional group capable of forming a non-covalent bond into a block copolymer A including at least one aromatic vinyl polymer block and at least one conjugated diene polymer block.

A latex of an acid-modified conjugated diene polymer including the acid-modified conjugated diene polymer obtained by modifying a conjugated diene polymer with an acid group-containing compound, in which a content of a structural unit derived from the acid group-containing compound is 0.2 to 0.7 parts by weight with respect to 100 parts by weight of the acid-modified conjugated diene polymer; a content of a water-soluble polymer in the latex is 2 parts by weight or less with respect to 100 parts by weight of the acid-modified conjugated diene polymer; when a solids content of the latex is adjusted to 60 wt %, a viscosity at 25° C. is 800 mPa.Math.s or less; and when the solids content of the latex is adjusted to 50 wt %, the viscosity at 25° C. is 300 mPa.Math.s or less.

A porous membrane includes a triblock copolymer of the formula ABC. B is a hydrogenated vinyl aromatic block present in a range from 30 to 90 weight percent, based on the total weight of the copolymer and has a T.sub.g of ≥110° C. C is a rubbery block present in a range from 10 to 70 weight percent, based on the total weight of the copolymer and has a T.sub.g≤25° C. A is substantially incompatible with both the B and C blocks and is derived from ring-opening polymerization. B+C is present in a range from 70 to 95 weight percent, based on the total weight of the copolymer.

A binder composition for a non-aqueous secondary battery contains water-soluble macromolecules, water, and a particulate polymer formed of a polymer that includes a block region formed of an aromatic vinyl monomer unit. Surface acid content A of the particulate polymer is 0.05 mmol/g or more, acid content B in an aqueous phase of the binder composition per 1 g of the particulate polymer is not less than 0.03 mmol/g and not more than 0.80 mmol/g, and a ratio (A/B) of the surface acid content A of the particulate polymer and the acid content B in the aqueous phase of the binder composition is not less than 0.5 and not more than 5.0.

A display device that includes a display element including a light source, and a surface film disposed so as to overlap with the display element and including a thermoplastic elastomer composition, the thermoplastic elastomer composition satisfying conditions (1) and (2) below, and the surface film satisfying conditions (3) and (4) below: (1) The melt flow rate (ASTM D1238, 230° C., 2.16 kg load; MFR) is not less than 30 g/10 min. (2) The type A hardness (momentary value) measured by a method in accordance with JIS K6253 is 60 to 90. (3) The thickness is not less than 300 μm and not more than 2 mm. (4) The total light transmittance measured by a method in accordance with JIS K7361 is 3 to 60%.

A display device that includes a display element including a light source, and a surface film disposed so as to overlap with the display element and including a thermoplastic elastomer composition, the thermoplastic elastomer composition satisfying conditions (1) and (2) below, and the surface film satisfying conditions (3) and (4) below: (1) The melt flow rate (ASTM D1238, 230° C., 2.16 kg load; MFR) is not less than 30 g/10 min. (2) The type A hardness (momentary value) measured by a method in accordance with JIS K6253 is 60 to 90. (3) The thickness is not less than 300 μm and not more than 2 mm. (4) The total light transmittance measured by a method in accordance with JIS K7361 is 3 to 60%.

A thermoplastic resin composition includes a resin component (A) in an amount of 97 to 80 parts by mass; and a hitting sound reducing material (B) in an amount of 3 to 20 parts by mass. The hitting sound reducing material (B) is a hydrogenated copolymer derived from hydrogenation of a copolymer formed of a block portion (I) primarily including structural units derived from an aromatic vinyl-based compound, and a random portion (II) primarily including structural units derived from an aromatic vinyl-based compound and derived from butadiene. The structural units derived from an aromatic vinyl-based compound in the block portion (I) and derived from an aromatic vinyl-based compound in the random portion (II) are present in a total content of 55 to 80 mass % relative to a 100 total mass % of the copolymer, and the hydrogenated copolymer has a primary dispersion peak of tan δ at 0° C. or greater.