Polyolefin composition comprising high density polyethylene, polyolefin elastomer and polypropylene, wherein the polypropylene is selected from homopolymer PP or impact PP and wherein the amount of high density polyethylene is more than 40% by weight of the total amount of high density polyethylene, polyolefin elastomer and impact or homopolymer polypropylene and wherein the total amount of high density polyethylene, polyolefin elastomer and polypropylene is 100% by weight and wherein the high density polyethylene has a density in the range from 940 to 960 kg/m3.

Provided are a heterophasic propylene polymerization material and an olefin polymer having a small high-boiling-point component amount index (FOG). The heterophasic propylene polymerization material satisfies the following formula (3): (X2×Y2)/Z2≤7.0 (3) wherein X2 represents a cold xylene soluble component amount (mass %) of the heterophasic propylene polymerization material; Y2 represents a percentage (%) of a component having a molecular weight of 104.0 or less in terms of polystyrene and contained in a cold xylene soluble component of the heterophasic propylene polymerization material based on all components of the cold xylene soluble component of the heterophasic propylene polymerization material as measured by gel permeation chromatography; and Z2 represents a content (mass %) of a propylene-based copolymer contained in the heterophasic propylene polymerization material and containing a propylene-derived monomer unit and a monomer unit derived from at least one compound selected from the group consisting of ethylene and C4-12 α-olefins.

Polymerization-induced phase separation enables fine control over thermoset network morphologies, yielding heterogeneous structures with domain sizes tunable over 1-100 nm. However, the controlled chain-growth polymerization techniques exclusively employed to regulate morphology at these length scales are unsuitable for most thermoset materials typically formed through step-growth mechanisms. By employing binary mixtures in place of the classic constituents of phase-separating thermosets—resin, curing agent, and secondary polymer—facile tunability over morphology can be achieved through a single compositional parameter. Indeed, this method yields morphologies spanning nano-scale to macro-scale, controlled by the relative reactivities and thermodynamic compatibility of the network components. Due to the connection between chain dynamics and microstructure in these materials, the tunable morphology enables exquisite control over glass transition and other physical and mechanical properties.

A pipe-wrapping material or compound, comprising a thermoplastic blend, wherein the thermoplastic blend includes at least one isobutylene-isoprene copolymer; at least one multi-arm polymer based on ethylene/propylene; at least one ethylene copolymer; and at least one polybutene polymer; at least one filler; at least paraffinic oil; and at least one biocide, wherein the at least one biocide is formulated to be effective against anaerobic bacteria, and wherein the anaerobic bacteria include sulfate-reducing bacteria.

An ultra-light graphene-rubber foam particle for soles is prepared from, by weight, 60-65 parts of natural rubber, 8-12 parts of isoprene rubber, 8-12 parts of butadiene rubber, 6-8 parts of styrene butadiene rubber, 0.8-1.0 parts of modified graphene, 0.08-0.12 parts of poly(N-vinylacetamide), 0.8-1.0 parts of silicone oil, 3.0-3.5 parts of inorganic nano-particles, 1.2-1.5 parts of activated zinc oxide, 0.8-1.0 parts of zinc stearate, 1.0-1.2 parts of stearic acid, 0.8-1.0 parts of cross-linking agents, 2.0-3.0 parts of flow promotors, and 1.5-1.8 parts of foaming agents. According to the invention, the modified graphene is uniformly dispersed into the rubber materials, so that the ultra-light graphene-rubber foam particle has good thermal stability, wear resistance and tensile strength, the permanent compressive-deformation performance and thermal contraction resistance are improved, and the weight is reduced by over 50%.

A thermoplastic resin composition of the present invention comprises: a polycarbonate resin; a rubber-modified vinyl-based graft copolymer; a large particle size rubbery polymer having an average particle size of about 400 to about 1,500 nm; an aromatic vinyl-based copolymer resin; a phosphorus-based flame retardant; talc; wollastonite; a maleic anhydride grafted rubbery polymer; and a black pigment. The thermoplastic resin composition is superior in terms of adhesion to metal, strength, flame retardancy, fluidity, and appearance.

A thermoplastic resin composition includes 100 parts by weight of a base resin including 5 to 40% by weight of a vinyl cyanide compound-conjugated diene rubber-aromatic vinyl compound graft copolymer (a) containing conjugated diene rubber having a particle diameter of 0.05 μm to 0.2 μm, 5 to 40% by weight of a vinyl cyanide compound-conjugated diene rubber-aromatic vinyl compound graft copolymer (b) containing conjugated diene rubber having a particle diameter of greater than 0.2 μm and less than or equal to 0.5 μm, and 50 to 80% by weight of an aromatic vinyl compound-vinyl cyanide compound copolymer (c); and more than 0.01 parts by weight and less than 2 parts by weight of a compound having a kinematic viscosity (25° C.) greater than 5 cSt and less than 200 cSt. The resin composition has excellent plating characteristics.

The present disclosure provides a curable resin composition including a thermoset resin, an aliphatic polyketone as a toughener and a hardener. The curable resin composition may be combined with reinforcing fibers and then cured to form a fiber-reinforced composite article having a high glass transition temperature, excellent mechanical properties and low moisture absorption. The fiber-reinforced composite article may be used in various applications, such as in transport applications including aerospace, aeronautical, nautical and land vehicles.

The present invention relates to a moulding compound containing: A) at least one polymer selected from the group consisting of polycarbonate and polyester carbonate; B) a polymer containing B1) at least one rubber-modified vinyl(co)polymer containing B1.1) 80 to 95 wt. %, based on B1, of at least one vinyl monomer and B1.2) 5 to 20 wt. %, based on B1, of one or more rubber-elastic polybutadiene-containing graft foundations, wherein B1 contains polybutadiene-containing rubber particles, which are grafted with the vinyl monomers B1.1 and contain inclusions of vinyl(co)polymer consisting of the vinyl monomers B1.1, and a vinyl(co)polymer matrix which consists of the vinyl monomers B1.1 and is not bonded to these rubber particles and not enclosed in rubber particles, and optionally B2) further rubber particles, grafted with vinyl monomers, from B2.1) 5 to 75 wt. %, based on B.2, of at least one vinyl monomer grafted onto B2.2) 25 to 95 wt. %, based on B2, of one or more rubber-elastic graft foundations, wherein the weight ratio of the components B1 to B2 is at least 5:1; C) a master batch, which is solid at room temperature, containing C1) one or more copolymers containing structural units derived from an olefin and structural units derived from a polar comonomer; C2) a vulcanised silicone elastomer. The invention also relates to a method for preparing the moulding compound, to the use of the moulding compound for producing moulded bodies, and to the moulded bodies themselves.

A resin composition for a sealant, comprising an ethylene/polar monomer copolymer (A), an adhesion-imparting resin (B) and a 4-methyl-1-pentene/α-olefin copolymer (C), a content of the 4-methyl-1-pentene/α-olefin copolymer (C) being from 1% by mass to 20% by mass with respect to a total mass of the resin composition for a sealant.