The present invention discloses a film for a medicine packaging and a method of preparing the same. The film for the medicine packaging comprises a polymer film layer, a graphene composite layer and a light-curable adhesive, wherein the polymer film layer is bonded with a graphene composite layer by a light-curable adhesive, the graphene composite layer comprises multiple graphene layers bonded by the light-curable adhesive; and the light-curable adhesive comprises a hyperbranched cationic mussel-imitated polymer comprising a multi-hydroxylbenzoylbenzamide ene amide monomer, a cationic monomer and a photo-responsive monomer. The present invention provides strong adhesion with reduced adhesive layer, allowing greatly increasing the number of the graphene layers in the graphene composite layer without obvious increase in the total thickness and mass. This can meet the requirements of the medicine packaging material, as it obviously lowers the film's permeation to water vapor and oxygen and significantly enhances the tensile strength.

Disclosed are hot-melt, curl-free methods, structures, and compositions, which in flexible packaging applications, reduce mineral-oil, hydrocarbon migration into packaged food. One embodiment provides an optionally oriented base film having a first side and a second side that is a transparent or opaque film. Further, the composition comprises, consists essentially of, or consists of a water-based primer applied to the first side. Further still, the composition includes a barrier layer to mineral-oil migration, wherein the barrier layer is located between the adhesive-receptive layer and the polymeric substrate, and wherein the barrier layer consists essentially of: (i) polymers of polyvinyl alcohol, ethylene vinyl alcohol, polyester, polyamide, or combinations thereof; and (ii) optionally additives. The barrier layer provides a barrier to mineral-oil migration of 0.1 g/day*dm.sup.2 or less at 40 C. for 40 days, and the curl-resistant composition does not curl when heated for at least one hour at 60 C.

The disclosure provides a method for treating a surface of a carbon fiber composite material, comprising the steps of: (1) pretreating a carbon fiber reinforced resin-based composite material; (2) spraying transparent powder to the surface of the carbon fiber reinforced resin-based composite material and curing it; (3) polishing the surface of the carbon fiber reinforced resin-based composite material after the transparent powder is cured; (4) spraying transparent powder to the surface of the carbon fiber reinforced resin-based composite material after the transparent powder thereon is cured and curing it; (5) polishing, cleaning and baking; and (6) spraying a clear lacquer to the surface of the carbon fiber reinforced resin-based composite material after the transparent powder is cured and curing it.

The present invention relates to a cured product having excellent stain resistance and low gloss, a method of manufacturing the same, and an interior material including the cured product. The cured product according to the present invention is formed by sequentially applying light in different specific wavelength ranges to a composition to cure the composition, thereby being capable of realizing a low gloss of 9 or less, based on a 60 degree gloss meter, without use of a matting agent and excellent stain resistance and exhibiting excellent abrasion resistance. Accordingly, the cured product may be usefully used as an interior material such as a flooring material.

A separation composite membrane, including a porous support layer, and a separation layer provided on the porous support layer and contains the following polymer a1 and b1; a separation membrane module; a separator; and a composition for forming a membrane suitable for preparing the separation composite membrane.

Polymer a1: A polymer whose ratio of a permeation rate of carbon dioxide to a permeation rate of methane is 15 or greater, and the permeation rate of the carbon dioxide is smaller than that in the polymer b1 and which has a solubility parameter of 21 or greater

Polymer b1: A polymer whose permeation rate of carbon dioxide is 200 GPU or greater, and a ratio of the permeation rate of the carbon dioxide to methane is smaller than that in the polymer a1 and which has a solubility parameter of 16.5 or less

A method for forming a multilayer coating film is provided. The method includes coating at least one object with an aqueous primer coating composition, an aqueous first colored coating composition, an aqueous second colored coating composition, and a clear coating composition, in that order. The aqueous primer coating composition contains a component (A) which contains a polyolefin resin, a component (B) which contains a polyurethane resin, a curing agent (C) and electrically conductive carbon (D). The aqueous first colored coating composition and aqueous second colored coating composition each contain a core/shell emulsion. The clear coating composition contains a hydroxyl group-containing acrylic resin, a polyisocyanate and a melamine resin. The method improves the appearance, chipping resistance, adhesive properties and low temperature impact properties of a coating film.

The present invention relates to a shock-absorbing nanostructured polymer alloy, comprising: a (meth)acrylic polymer matrix comprising one or more (meth)acrylic polymer(s), said (meth)acrylic polymer matrix forming a (meth)acrylic network, and, at least one polyborodimethylsiloxane (PBDMS) distributed in the (meth)acrylic polymer matrix, the polyborodimethylsiloxane forming a network, the polyborodimethylsiloxane network and the (meth)acrylic network being intertwined.

The invention also relates to a chemical composition for the manufacture of such an alloy as well as a process for manufacturing a part made of such an alloy.

The present invention relates to a method for manufacturing an electronic component having an electromagnetic shield, comprising: a bonding step of bonding a temporary protective material on a workpiece with unevenness on the surface thereof; a photocuring step of curing the temporary protective material by light irradiation; a icing step of singulating the workpiece and the temporary protective material; a shielding step of forming a metal film on the portion of the singulated workpiece, the portion having no temporary protective material bonded thereon; and a peeling step of peeling the temporary protective material from the workpiece having the metal film formed, wherein the temporary protective material is formed from a resin composition for temporary protection with an elastic modulus at 25 C. of 3 MPa or less and an elastic modulus at 25 C. of 40 MPa or more after light irradiation with an exposure dose of 500 mJ/cm.sup.2 or more.

A copolymer includes a repeating unit of Formula (I) and a repeating unit of Formula (II), a composition includes the copolymer, and an optical film has a layer formed of the composition,

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in the Formulae (I) and (II), R.sup.1 and R.sup.2 represent a hydrogen atom or an alkyl group, L.sup.3 and L.sup.1 represent a divalent linking group, L.sup.2 represents a single bond or a divalent linking group, and L.sup.4 represents a single bond or a divalent linking group, L.sup.4 does not represent a linking group including O(CO)NH, X represents a perfluoropolyether group, an alkyl group having a branched structure in which hydrogen is all substituted into fluorine, an alkenyl group, or an alkynyl group, and Y represents a crosslinking group.

A composite film may include a first transparent substrate and a first anti-reflective coating overlying a first surface of the first transparent substrate. The first anti-reflective coating may include a first UV curable acrylate binder, a photo initiator component, and silica nanoparticles dispersed within the first anti-reflective coating. The first anti-reflective coating may further include a ratio AC1.sub.SiO2/AC1.sub.B of at least about 0.01 and not greater than about 1.3. The composite film may further have a VLT of at least about 93.0% and a haze value of not greater than about 3%.