A composite article has an increased peel strength and includes a first layer including a low surface energy polymer. The composite article also includes a poly(meth)acrylate layer, an epoxide layer, and a polyurethane elastomer layer. The poly(meth)acrylate layer is disposed on and in direct contact with the first layer. Moreover, the poly(meth)acrylate layer includes a poly(meth)acrylate that includes the reaction product of at least one (meth)acrylate that is polymerized in the presence of an or -ganoborane initiator. The epoxide layer is disposed on and in direct contact with the poly(meth)acrylate layer. The polyurethane elastomer layer is disposed on and in direct contact with the epoxide layer. The composite article has a 90 peel strength of at least 50 pli measured using ASTM D6862.

A composite article includes a low surface energy polymer layer, a poly(meth)acrylate layer, an epoxide layer, and a hydrolytically resistant layer. The poly(meth)acrylate layer is disposed on and in direct contact with the low surface energy polymer layer and includes the reaction product of at least one acrylate that is polymerized in the presence of an organoborane initiator, such that the poly(meth)acrylate includes boron. The epoxide layer is disposed on and in direct contact with the poly(meth)acrylate layer. The hydrolytically resistant layer is disposed on and in direct contact with the epoxide and is the reaction product of an isocyanate component and an isocyanate-reactive component reacted in the presence of a curing agent. The isocyanate-reactive component includes a polydiene polyol and the curing agent crosslinks the carbon-carbon double bonds of the polydiene polyol.

A composite article is formed by disposing a poly(meth)acrylate layer, formed as the reaction product of at least one acrylate that is polymerized in the presence of an organoborane initiator, on and in direct contact with a low surface energy polymer layer, disposing an epoxide layer on and in direct contact with said poly(meth)acrylate layer, and disposing a hydrolytically resistant layer on and in direct contact with said epoxide layer. The hydrolytically resistant layer is a hydrolytically resistant polyurethane elastomer that is the reaction product of an aliphatic isocyanate component and an isocyanate-reactive component that retains at least 90% of its initial tensile strength after submersion in standardized seawater for 24 weeks. The isocyanate-reactive component is a hydroxyl-functional polymer having an average hydroxy functionality ranging from 2 to 3, wherein the hydroxyl-functional polymer is a dimer diol, a trimer triol, or a combination thereof.

The present invention provides: an assembly obtained by bonding a sheet made of a modified hydrogenated block copolymer having an alkoxysilyl group introduced therein with a thermoplastic resin sheet, wherein a peel strength of the adherend surface is 4 N/cm or higher; a method for producing an assembly by bonding a sheet made of a modified hydrogenated block copolymer having an alkoxysilyl group introduced therein with a thermoplastic resin sheet, the method comprising steps of: (1) activating an adherend surface of the thermoplastic resin sheet with at least one selected from plasma exposure, excimer UV exposure and corona discharge; and (2) superposing the sheet made of the modified hydrogenated block copolymer having the alkoxysilyl group introduced therein with the adherend surface of the thermoplastic resin sheet to be subjected to thermally press-bonding; and a sheet made of a modified hydrogenated block copolymer, comprising at least one surface activated.

A composite article has increased pull-off strength and includes a first layer including a low surface energy polymer, a poly(meth)acrylate layer, and an epoxide layer. The poly(meth)acrylate layer is disposed on and in direct contact with the first layer. Moreover, the poly(meth)acrylate layer includes a poly(meth)acrylate that includes the reaction product of at least one (meth)acrylate that is polymerized in the presence of an organoborane initiator. The epoxide layer is disposed on and in direct contact with the poly(meth)acrylate layer. The epoxide layer includes an epoxide. The composite article has a pull-off strength of greater than zero pli measured using ASTM D4541.

A ceramic resin is provided, along with its methods of formation and use. The ceramic resin may include a crosslinkable precursor, a photoinitiator, ceramic particles, and pore forming particles. The ceramic resin may be utilized to form a ceramic casting element, such as via a method that includes forming a layer of the ceramic resin; applying light onto the ceramic resin such that the photoinitiator initiates polymerization of the crosslinkable precursor to form a crosslinked polymeric matrix setting the ceramic particles and the pore forming particles; and thereafter, heating the crosslinked polymeric matrix to a first temperature to burn out the pore forming particles.

The present disclosure provides a thermally-conductive and sound-absorbing composite material and a preparation method thereof and a speaker. The thermally-conductive and sound-absorbing composite material includes the following components by mass percent: 10-80% of an activated carbon felt, 5-75% of zeolite particles, 1-80% of graphene particles and 5-40% of an adhesive, where the activated carbon felt serves as a skeleton; the graphene particles are bonded to an activated carbon fiber surface of the activated carbon felt through the adhesive; and the zeolite particles are bonded to surfaces of the graphene particles and the activated carbon fiber surface of the activated carbon felt through the adhesive. The thermally-conductive and sound-absorbing composite material provided by the present disclosure has excellent heat conductivity, excellent sound absorption performance, and a desirable mechanical strength.

Vulcanized tube having at least one foamed layer of elastomer material with a cellular structure with an average cell size in a range between 5 and 200 microns and the number of cells per unit of volume in a range between 1.9?10.sup.5 and 1.4?10.sup.9 cells/cm.sup.3. To form the tube, a forming device is inserted into an unvulcanized tube obtained in a prior initial stage of extrusion. At least one foaming agent is added to the elastomer material of the foamed layer in the initial stage of extrusion, such that the tube is vulcanized and the foamed layer is also simultaneously foamed. The vulcanizing process is carried out under pressure. Finally, in a stage of removal, the already vulcanized and foamed tube is removed from the forming device.

Recovery times of flexible polyurethane foams are increased by treatment with a pressure sensitive adhesive. An emulsion or dispersion of the adhesive in an aqueous carrier liquid is impregnated into the foam, with subsequent removal of the carrier. This invention is of special interest when the glass transition temperature of the starting foam is 16? C. or lower.

A ceramic resin is provided, along with its methods of formation and use. The ceramic resin may include a crosslinkable precursor, a photoinitiator, ceramic particles, and pore forming particles. The ceramic resin may be utilized to form a ceramic casting element, such as via a method that includes forming a layer of the ceramic resin; applying light onto the ceramic resin such that the photoinitiator initiates polymerization of the crosslinkable precursor to form a crosslinked polymeric matrix setting the ceramic particles and the pore forming particles; and thereafter, heating the crosslinked polymeric matrix to a first temperature to burn out the pore forming particles.