The present disclosure provides a process. The process includes (i) crosslinking pellets composed of a silane-grafted ethylene/α-olefin multi-block copolymer (Si-g-OBC) to a gel content from 10% to 80% to form crosslinked Si-g-OBC pellets; and (ii) foaming the crosslinked Si-g-OBC pellets to form crosslinked Si-g-OBC foam beads having a gel content from 10% to 80%.

A thermoplastic olefinic elastomer expanded bead, which is an expanded bead including a thermoplastic olefinic elastomer as a main component, wherein the expanded bead has an average particle diameter of 0.5 to 5 mm, the expanded bead has a heat of fusion of 60 to 80 J/g, and a difference [Tm−Tc] between a melting point (Tm) and a crystallization temperature (Tc) of the expanded bead is 20° C. or lower.

A film is provided with void spaces having a porous structure with less cracks and a high proportion of void space as well as having strength. The film with void spaces includes one kind or two or more kinds of structural units that form a structure with minute void spaces, wherein the structural units are chemically bonded through catalysis. For example, the abrasion resistance measured with BEMCOT® is in the range from 60% to 100%, and the folding endurance measured by the MIT test is 100 times or more. The film with void spaces can be produced by forming the precursor of the silicone porous body using sol containing pulverized products of a gelled silicon compound and then chemically bonding the pulverized products contained in the precursor of the silicone porous body. The chemical bond among the pulverized products is preferably a chemical crosslinking bond among the pulverized products.

A crosslinked olefin-based thermoplastic elastomer expanded bead including a base polymer having an olefin-based thermoplastic elastomer and a brominated bisphenol-based flame retardant having a chemical structure represented by formula (1). A difference Tm.sub.TPO-T.sub.FR is −5° C. to 40° C., where Tm.sub.TPO is a melting point of the olefin-based thermoplastic elastomer and T.sub.FR is the lower of a glass transition temperature T.sub.gFR and a melting point Tm.sub.FR of the brominated bisphenol-based flame retardant. A xylene insoluble content is 5 mass % to 80 mass %. R.sup.1 and R.sup.3 in the formula (1) are monovalent substituents, R.sup.2 is a divalent substituent, and n is an integer from 1 to 6:

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A method of fabrication of a porous polymer aerogel amine material includes preparing a solution comprising at least a solvent, amine monomers having protecting groups, one or more crosslinkers, and one or more radical initiators, heating the solution to promote polymerization and to produce a polymerized material, performing solvent exchange with the polymerized material, causing a deprotection reaction in the polymerized material to remove the protecting groups to produce a deprotected material, soaking and rinsing the deprotected material to remove excess reagents and any byproducts of the deprotection reaction, and drying the deprotecting material to produce the amine sorbent. A system to separate CO.sub.2 from other gases has a polymer porous aerogel sorbent having greater than 5 wt % of amine containing vinyl monomers integrated into a polymer backbone, and the amine containing vinyl monomers may have a molecular weight of less than 100 g/mol.

A polyolefin resin foam sheet includes a resin mixture as a base resin, the resin mixture including 0% by mass or more and 30% by mass or less of polyethylene resin, 30% by mass or more and 80% by mass or less of polypropylene resin, and 20% by mass or more and 40% by mass or less of a polyolefin elastomer, the polyolefin resin foam sheet fulfilling a range of −35% or more and 0% or less for dimensional changes in machine and transverse directions under heating for 10 minutes at a temperature 20° C. higher than a maximum melting point that is a highest melting peak in a differential scanning calorimetry.

The present disclosure relates to a preparation method of a super absorbent polymer. More specifically, it relates to a preparation method of a super absorbent polymer with improved permeability and anti-caking efficiency while having a high absorption rate by adding an additive having a specific structure to the hydrogel polymer polymerized in the presence of an encapsulated foaming agent, followed by coarse pulverization.

The present invention relates to an expanded beads molded article containing a block copolymer of a polyethylene block and an ethylene-α-olefin copolymer block and having a density of 30 kg/m.sup.3 or more and less than 150 kg/m.sup.3 and a modulus of repulsion elasticity of 60% or more. The sole member of the present invention includes the expanded beads molded article of the present invention.

Components for articles of footwear and athletic equipment are provided including a foam. A variety of foams and foam components and compositions for forming the foams are provided. In some aspects, the foams and components including the foams can have exceptionally high energy return while also having improved durability and softness. In particular, midsoles including the foams are provided for use in an article of footwear. Methods of making the compositions and foams are provided, as well as methods of making an article of footwear including one of the foam components. In some aspects, the foams and foam components can be made by injection molding or injection molding followed by compression molding.

This invention relates to a foaming composition, comprising at least one ethylene-vinyl acetate (EVA) copolymer; at least one foaming agent; at least one peroxide compound; at least one polyamine; at least one crosslinking enhancer; at least one primary antioxidant; and at least one secondary antioxidant; the content of the crosslinking enhancer is from 0.1 to 3% by weight based on the total weight of the composition. A foaming article cured from the foaming composition under the temperature range of 80 to 120° C. according to the present invention exhibits high initial volume expansion ratio at the baking window from 130 to 200° C. and shows excellent stability after storage.