Abstract: A container body which comprises a base and a side wall extending from the base, wherein said container body includes a polyester and a polymer YY. wherein said polymer YY is selected from the group comprising cyclic block copolymers (CBC) and cyclic olefin polymers (COP).

Abstract: A container body which comprises a base and a side wall extending from the base, wherein said container body includes a polyester and a polymer YY. wherein said polymer YY is selected from the group comprising cyclic block copolymers (CBC) and cyclic olefin polymers (COP).

A bend sensor comprising a sensor section in which a polymer electrolyte film is sandwiched between a pair of electrode films, wherein each of the electrode films contains: a block copolymer (Z) having a polymer block (S) composed of a structural unit derived from an aromatic vinyl compound, and containing an ion-conducting group, and an amorphous polymer block (T) composed of a structural unit derived from an unsaturated aliphatic hydrocarbon; and a conducting particle; which block copolymer (Z) forms a lamellar structure, which bend sensor therefore allows generation of enhanced voltage between the electrode films when deformation of the sensor occurs as it follows movement of an object, is provided.

A bend sensor comprising a sensor section in which a polymer electrolyte film is sandwiched between a pair of electrode films, wherein each of the electrode films contains: a block copolymer (Z) having a polymer block (S) composed of a structural unit derived from an aromatic vinyl compound, and containing an ion-conducting group, and an amorphous polymer block (T) composed of a structural unit derived from an unsaturated aliphatic hydrocarbon; and a conducting particle; which block copolymer (Z) forms a lamellar structure, which bend sensor therefore allows generation of enhanced voltage between the electrode films when deformation of the sensor occurs as it follows movement of an object, is provided.

Some embodiments of the present disclosure relate to a method comprising mixing at least one compatibilizer precursor with at least one polymer, so as to result in a polymer concentrate and mixing the polymer concentrate with asphalt, so as to result in a polymer modified asphalt (“PMA”). Some embodiments of the present disclosure relate to formulations comprising a compatibilizer precursor, a polymer concentrate, PMA, or any combination thereof.

Some embodiments of the present disclosure relate to a method comprising mixing at least one compatibilizer precursor with at least one polymer, so as to result in a polymer concentrate and mixing the polymer concentrate with asphalt, so as to result in a polymer modified asphalt (“PMA”). Some embodiments of the present disclosure relate to formulations comprising a compatibilizer precursor, a polymer concentrate, PMA, or any combination thereof.

A thermoplastic elastomer composition including an acrylic block copolymer (I) and a hydrogenated block copolymer (II). The content of the acrylic block copolymer (I) is 70 to 300 parts by mass with respect to 100 parts by mass of the hydrogenated block copolymer (II); the hydrogenated block copolymer (II) is a hydrogenated product of a block copolymer (P) including a polymer block (A1) containing structural units derived from an aromatic vinyl compound, and a polymer block (B1) containing 1 to 100 mass % of structural units (b1) derived from farnesene and 99 to 0 mass % of structural units (b2) derived from a conjugated diene other than farnesene, the mass ratio [(A1)/(B1)] of the polymer block (A1) to the polymer block (B1) being 1/99 to 70/30; and the hydrogenation ratio of carbon-carbon double bonds in the polymer block (B1) is 50 to 100 mol %.

A thermoplastic elastomer composition including an acrylic block copolymer (I) and a hydrogenated block copolymer (II). The content of the acrylic block copolymer (I) is 70 to 300 parts by mass with respect to 100 parts by mass of the hydrogenated block copolymer (II); the hydrogenated block copolymer (II) is a hydrogenated product of a block copolymer (P) including a polymer block (A1) containing structural units derived from an aromatic vinyl compound, and a polymer block (B1) containing 1 to 100 mass % of structural units (b1) derived from farnesene and 99 to 0 mass % of structural units (b2) derived from a conjugated diene other than farnesene, the mass ratio [(A1)/(B1)] of the polymer block (A1) to the polymer block (B1) being 1/99 to 70/30; and the hydrogenation ratio of carbon-carbon double bonds in the polymer block (B1) is 50 to 100 mol %.

Embodiments of the present disclosure are directed to thermoplastic elastomer blends comprising at least one non-hydrogenated styrene isoprene block copolymer (SIS) having a Weight Average Molecular Weight (Mw) greater than or equal to 50,000 g/mol and a Tan Delta Peak Temperature greater than or equal to 15° C. and less than or equal to 25° C. at least one of: at least one hydrogenated SIS having an Mw greater than or equal to 75,000 g/mol and a Tan Delta Peak Temperature less than or equal to 20° C.; and a styrene-ethylene/butylene-styrene block copolymer (SEBS) having a Mw greater than or equal to 75,000 g/mol and a Tan Delta Peak Temperature less than or equal to 20° C.; and a tackifier having a softening point greater than or equal to 80° C.

Embodiments of the present disclosure are directed to thermoplastic elastomer blends comprising at least one non-hydrogenated styrene isoprene block copolymer (SIS) having a Weight Average Molecular Weight (Mw) greater than or equal to 50,000 g/mol and a Tan Delta Peak Temperature greater than or equal to 15° C. and less than or equal to 25° C. at least one of: at least one hydrogenated SIS having an Mw greater than or equal to 75,000 g/mol and a Tan Delta Peak Temperature less than or equal to 20° C.; and a styrene-ethylene/butylene-styrene block copolymer (SEBS) having a Mw greater than or equal to 75,000 g/mol and a Tan Delta Peak Temperature less than or equal to 20° C.; and a tackifier having a softening point greater than or equal to 80° C.