Provided is an elastic heat spreader film comprising: a) a graphitic film prepared from graphitization of a polymer film or pitch film, wherein the graphitic film has graphitic crystals parallel to one another and parallel to a film plane, having an inter-graphene spacing less than 0.34 nm, and wherein the graphitic film alone, after compression, has a thermal conductivity at least 600 W/mK, an electrical conductivity no less than 4,000 S/cm, and a physical density greater than 1.7 g/cm.sup.3; and b) an elastomer or rubber that permeates into the graphitic film from at least a surface of the film; wherein the elastomer or rubber is in an amount from 0.001% to 30% by weight based on the total heat spreader film weight. The elastic heat spreader film has a fully recoverable tensile elastic strain from 2% to 100% and an in-plane thermal conductivity from 100 W/mK to 1,750 W/mK.

The present invention provides vinyl-based resin particles capable of forming uniform pores in a thermosetting resin film when the particles are used as a pore-forming material for a thermosetting resin. Specifically, the present invention provides vinyl-based resin particles for use in making a thermosetting resin porous, the particles having a temperature of 300 to 350 C. at 10% mass loss when heated at a rate of 10 C./min in an air atmosphere, and the particles having a mass loss percentage of 85 to 100% after being heated at 350 C. for 5 hours in an air atmosphere.

A membrane is provided, as well as membrane electrode assemblies and sensors utilizing the membrane of the present technology. The membrane includes a membrane material with a top surface and a bottom surface; and a protonic ionic liquid disposed at least between the top surface and the bottom surface of the membrane material where the protonic ionic liquid is of Formula I. ##STR00001##

Processing reinforcing fiber products to recover reinforcing fibers by removing other material, such fiber sizing material and/or matrix material from the reinforcing fibers. The processing includes cosolvent treating the reinforcing fiber product with a cosolvent composition including a normally-liquid first solvent portion and a normally-gaseous second solvent portion under conditions of temperature and pressure at which the cosolvent composition is in the form of a single fluid phase that is a liquid or a supercritical fluid. The processing may be performed in a continuous manner to recover the continuous reinforcing fibers in a continuous form.

The present invention relates to a self-humidifying ion-exchange composite membrane including an aromatic hydrocarbon polymer ion-exchange membrane formed on the surface of a porous polymer support and a thin hydrophobic coating layer having a nanocracked morphology pattern on the surface of the ion-exchange membrane. The self-humidifying ion-exchange composite membrane of the present invention has good thermal/chemical stability, high mechanical strength, high ion-exchange capacity, and good long-term operational stability. Particularly, the self-humidifying ion-exchange composite membrane of the present invention is able to self-hydrate even under high-temperature and low-humidity conditions. Due to these advantages, it is expected that the self-humidifying ion-exchange composite membrane of the present invention will be commercialized as an electrolyte membrane for a fuel cell or a membrane for water treatment.

Provided is a process for producing a polymer composite film, comprising the steps of: (a) mixing a phthalocyanine compound with a polymer or its precursor and a liquid to form a slurry and forming the slurry into a wet film on a solid substrate, wherein the polymer is preferably selected from the group consisting of polyimide, polyamide, polyoxadiazole, polybenzoxazole, polybenzobisoxazole, polythiazole, polybenzothiazole, polybenzobisthiazole, poly(p-phenylene vinylene), polybenzimidazole, polybenzobisimidazole, and combinations thereof; and (b) removing the liquid from the wet film and, in some embodiments, converting the precursor to the polymer to form the polymer composite film comprising from 0.1% to 50% by weight of the phthalocyanine compound dispersed in the polymer.

A black-color polymer composite film comprising a phthalocyanine compound dispersed in a polymer selected from the group consisting of polyimide, polyamide, polyoxadiazole, polybenzoxazole, polybenzobisoxazole, polythiazole, polybenzothiazole, polybenzobisthiazole, poly(p-phenylene vinylene), polybenzimidazole, polybenzobisimidazole, and combinations thereof, wherein the phthalocyanine compound occupies a weight fraction of 0.1% to 50% based on the total polymer composite weight. Preferably, the phthalocyanine compound is selected from copper phthalocyanine, zinc phthalocyanine, tin phthalocyanine, iron phthalocyanine, lead phthalocyanine, nickel phthalocyanine, vanadyl phthalocyanine, fluorochromium phthalocyanine, magnesium phthalocyanine, manganous phthalocyanine, dilithium phthalocyanine, aluminum phthalocyanine chloride, cadmium phthalocyanine, chlorogallium phthalocyanine, cobalt phthalocyanine, silver phthalocyanine, a metal-free phthalocyanine, or a combination thereof.

The present invention relates to a process for preparing a resin composition comprising benzoxazine, a prepreg and a laminate prepared therefrom. Said resin composition comprising benzoxazine is prepared by adding an acidic filler into the resin composition comprising benzoxazine, wherein said resin composition comprising benzoxazine comprises a benzoxazine resin, an epoxy resin A1 having an epoxy equivalent of 150-450, and an epoxy resin A2 having an epoxy equivalent of 451-1000. By adding an acidic filler into the resin composition, the present invention promotes the polymerization of benzoxazine and epoxy resins, and decreases the curing temperature needed for the polymerization of benzoxazine and epoxy resins. The laminates prepared from the resin composition added with an acidic filler have a high anti-stripping stability, a high glass transition temperature, a low water absorption, a high heat resistance, a high bending strength and a better processability, and achieves a low coefficient of thermal expansion.

A production method for a fiber-reinforced composite material comprises: a step of stacking a prepreg plurally to obtain a prepreg-stacked body; and a step of heating the prepreg-stacked body to cure a resin, wherein the prepreg comprises: a reinforcing fiber layer including reinforcing fibers and a resin composition with which the space between fibers of the reinforcing fibers is impregnated and which contains (A) a benzoxazine resin, (B) an epoxy resin, and (C) a curing agent having 2 or more phenolic hydroxy groups in a molecule; and a surface layer provided on at least one surface of the reinforcing fiber layer and containing (A) to (C) components, and (D) polyamide resin particles having an average particle size of 5 to 50 m.

The present disclosure provides a carbon fiber dome. The carbon fiber dome includes at least two carbon fiber prepreg layers. The at least two carbon fiber prepreg layers include carbon fiber prepregs made by at least two weaving methods. In addition, the present disclosure provides a method for manufacturing the carbon fiber dome as described above. The method includes the following steps: using prepreg resin to pre-impregnate carbon fiber materials made by at least two weaving methods; and pre-impregnating the carbon fiber materials made by at least two weaving methods for bonding each other.