Abstract: The present invention relates to a method for preparing hierarchically ordered structures of inorganic phosphate particles, homogeneously deposited on the surface of a phyllosilicate, which is characterized in that it comprises the following steps: a) obtaining an acid solution of precursor compounds of an inorganic phosphate; b) preparing a dispersion of particles of a phyllosilicate in aqueous medium and acidifying the phyllosilicate dispersion by adding at least one acid, thereby obtaining an acid dispersion; c) mixing the acid solution obtained in step a) with the dispersion obtained in step b); and d), with stirring, adding a base to the mixture obtained in step c) until the required pH value for precipitating the corresponding inorganic phosphate on the phyllosilicate particles has been achieved, resulting in a hierarchically ordered structure of homogeneously distributed submicrometric or nanometric inorganic phosphate particles supported on the phyllosilicate surface.

Abstract: Preparation of a rubber composition containing a dispersion of aligned exfoliated graphite platelets. Such rubber composition is prepared by a method comprised of a sequential combination of concentrated solvent or dry masterbatching of elastomer and exfoliated graphite platelets, followed by blending the masterbatch (after removing the solvent from the solvent based masterbatch) with additional elastomer(s) and then followed by processing the resulting rubber composition to align the dispersed exfoliated graphite platelets in a substantially parallel relation to each other. Such processing may comprise as least one of extrusion and calendaring the rubber composition. The invention further relates to a tire containing a component comprised of such rubber composition containing a dispersion of aligned exfoliated graphite platelets prepared by the aforesaid method.

Abstract: The present invention relates to a new and efficient toxicity and/or odor reducing method for ethyl acrylate and/or acrylonitrile contained aqueous polymer dispersion.

Abstract: A polycarbonate resin composition including 35 to 49% by weight of a polycarbonate resin; 41 to 55% by weight of a glass fiber having a rectangular or oval cross-sectional shape in the direction perpendicular to the longitudinal direction, in which its aspect ratio is 50 to 200; 1 to 10% by weight of an impact modifier having a core-shell structure; 1 to 10% by weight of an ethylene-(meth)acrylate-based copolymer; and 1 to 10% by weight of a rheology modifier containing a thermoplastic polyester-based polymer or a phosphate ester-based compound.

Abstract: A fly ash material or other filler or combination of the two having a particle size distribution is mixed with a liquid coupling agent in a sealed mixer that is heated to gasify the coupling agent for association with the varied particles of the filler. An acid scavenger, an antioxidant, a compatibilizer and an impact modifier may be mixed with a base resin or target resin to form a master batch or the final composition. Either the master batch or the final composition is mixed with a blend of a mineral oil and a styrenic block copolymer in addition to low melt or fractional melt resins.

Abstract: Carbon nanostructures free of an adhered growth substrate can include a plurality of carbon nanotubes that are branched, crosslinked, and share common walls with one another. Under applied shear, crosslinks between the carbon nanotubes in carbon nanostructures can break to form fractured carbon nanotubes that are branched and share common walls. Methods for making polymer composites from carbon nanostructures can include combining a polymer matrix and a plurality of carbon nanostructures that are free of an adhered growth substrate, and dispersing the carbon nanostructures in the polymer matrix under applied shear. The applied shear breaks crosslinks between the carbon nanotubes to form a plurality of fractured carbon nanotubes that are dispersed as individuals in the polymer matrix. Polymer composites can include a polymer matrix and a plurality of fractured carbon nanotubes dispersed as individuals in the polymer matrix.

Abstract: A process of preparing a polymer modified asphalt (PMA) comprising mixing a predetermined amount of a polymer-asphalt master batch with a predetermined amount of an asphalt-cross linking agent blend. The polymer-asphalt master batch comprises at least one polymer and a first asphalt. The asphalt-cross linking agent blend comprises a second asphalt and at least one cross linking agent. A predetermined amount of the polymer-asphalt master batch is blended with a predetermined amount of the asphalt-cross linking agent blend to form a PMA blend. Mixing of the PMA blend is performed without substantial delay following blending of the polymer-asphalt master batch with the asphalt-cross linking agent blend.

Abstract: A thermoplastic resin composition and a molded article using the same. The thermoplastic resin composition includes a base resin including a polycarbonate resin and a polysiloxane-polycarbonate copolymer resin, an impact modifier, a phosphorus flame retardant, and inorganic fillers, wherein the inorganic fillers include wollastonite and talc, and the wollastonite has an average diameter of 5 ?m to 10 ?m and an aspect ratio (diameter:length) of 1:7 to 1:9. The thermoplastic resin composition can exhibit excellent properties in terms of tensile elongation, flexural strength, impact resistance, and balance therebetween.

Abstract: A process for preparing a completely delaminated graphene oxide/rubber nanocomposite. The process combines emulsion compounding with flocculation or spray drying, retains the morphology of graphene oxide/rubber composite in a liquid state, and achieves highly dispersed and highly delaminated morphology dispersed on nano scale. Furthermore, a substance able to produce ionic bonding or chemical bonding with the surface functional groups of graphene oxide is added to graphene oxide/hydrosol, as a surfactant, thus the interfacial bonding between graphene oxide and the rubber is increased. The composite is subjected to subsequent compounding and vulcanization to prepare a vulcanizate with dynamic performance, such as a high tensile strength, stress at a definite elongation, tearing strength, etc.

Abstract: Disclosed is a fluorine-containing resin film which is formed from a fluorine-containing resin composition and has a thickness of 10 to 50 ?m, wherein the fluorine-containing resin composition is prepared by adding 10 to 30 parts by mass of titanium oxide or a composite-oxide-type inorganic pigment to 100 parts by mass of a resin component comprising 60 to 95 parts by mass of a vinylidene fluoride resin and 5 to 40 parts by mass of a methacrylic acid ester resin, and wherein the peak intensity ratio of a II-type crystal, which is expressed by (A)/((A)+(B))×100 wherein A represents the peak height at 840 cm?1 and B represents the peak height at 765 cm?1 in a measurement chart produced by an infrared absorption spectrum, is 60% or more and the total crystallinity is 30% or more as calculated from an X-ray diffraction profile.

Abstract: The present invention relates to the application of polymeric resins and TiO2 doped with polymeric resins as coatings for external metal surfaces for industrial use, by selecting the following metals: stainless steel, carbon steel and copper. Focuses specifically on the synthesis of a polymeric resin waterborne corrosion consisting of nano-structured polymer particles formed with two or more acrylic monomers, vinyl or styrenic a functionalizing agent and a crosslinking agent from 1.0 to 20% w each. Doping addition is made of the same polymeric resins, which are incorporated in nanotubes of titanium dioxide in concentrations ranging from 50 to 10,000 ppm. The polymeric resin is water based corrosion synthesized by emulsion polymerization techniques and is during the synthesis process is introduced nanotube loading of titanium dioxide, which allowing the dispersion in the polymer matrix. Polymer dispersions obtained in this way are used as anti-corrosion coatings 100% water based.

Abstract: A buffer material protects a microelectronic device in space constrained environments, for improved efficiency with respect to magnetostrictive materials therein, and includes a gas filled polymer shell microsphere carried in an elastomeric polymer binder. Expanded Expancel microspheres being less than 20 microns in diameter form 80% of the composition by volume. The polymer binder is a low viscosity dimethyl silicone with a hardness of less than 25. Coating thicknesses may be based upon the overall expected dimensional changes of the encapsulation material, due to its coefficient of thermal expansion and an expected operating temperature range of the component, plus the expected shrinkage of that encapsulation material during polymerization and the overall mass which shall be exerting a force upon the magnetic core, plus the dimensional changes of the component as a result of the flux density resulting in magnetostriction of the magnetic core.

Abstract: The present invention relates to a process for the production of powders redispersible in water comprising an organic component and a water-soluble organic polymeric protective colloid. The organic component is dispersed and stabilized with the protective colloid in water to form a stable dispersion which is dried to form the powder redispersible in water. The organic component comprises abietic acid, sylvic acid, neoabietic acid, levopinaric acid, pimaric acid, isopimaric acid and/or palustric acid and/or their derivatives. The water-soluble organic polymeric protective colloid comprises synthetic protective colloids and naturally and/or synthetically produced biopolymer which can be synthetically modified. The obtained powder reduces efflorescence in hydraulically set systems.

Abstract: Provided is a thermoplastic resin composition having high flame resistance and high fluidity during injection molding, and improved impact resistance in a molded article. A method for producing a thermoplastic resin composition, the method including the step (1) of obtaining a polyester resin mixture by melt-kneading 50 to 80 parts by weight of crystalline polyester resin and 20 to 50 parts by weight of amorphous polyester resin with an extruder, and the step (2) of mixing the polyester resin mixture, a polycarbonate resin, a flame retardant, a dripping inhibitor and a toughening agent, wherein the cylinder temperature of the extruder is 250 to 280° C.

Abstract: A rubber wet masterbatch obtained, using at least a carbon black, a dispersing solvent, and a latex solution of a rubber as raw materials, the carbon black being a carbon black having an iodine adsorption number of 41 mg/g or less, and the rubber wet masterbatch being obtained through the following process: a process in which at the time of dispersing the carbon black into the dispersing solvent, at least one portion of the rubber latex solution is added to the carbon-black-dispersed solvent to produce a slurry solution comprising the carbon black to which rubber latex particles adhere, subsequently the slurry solution is mixed with the rest of the rubber latex solution, and next the mixture is solidified and dried.

Abstract: The flexible packaging composites include one or more mineral-containing layers with a bonding agent. The composite structure is used as a primary or secondary packaging container or insulating material. In addition to the mineral-containing layer, the composite can contain one or more non-mineral containing layers, including various combinations of extruded resins, cast or blown films, and fibers. The mineral-containing layer is substantially and continuously bonded to the other layers. The present invention is an unexpectedly unique and environmentally friendly composite structure containing mineral layers with bonding agents as a key component. The material is designed to form flexible and semi-rigid storage articles at equal or lower costs to prior art solutions while providing a mineral containing layer that is a very smooth, has comparatively high plasticity, and having a high quality printing surface not requiring Corona Treatment.

Abstract: A pigment preparation is provided, said preparation comprises an organic pigment comprising a chromophore Q1 and a derivative thereof comprising specific organic substituents via an aliphatic carbon atom in an amount of from 0.1 to 30 mol, based on 100 mol of the organic pigment as well as a process for its preparation and to its use in coloring an organic material such as plastics, coatings or inks.

Abstract: A thermoplastic resin composition includes a thermoplastic resin including a polycarbonate resin; a siloxane compound represented by Formula 1; and surface-modified hydrophobic silica: wherein R1 and R2 are the same or different and are each independently C1 to C5 alkyl; R3 and R4 are the same or different and are each independently C2 to C10 alkylene; A1 and A2 are the same or different and are each independently a glycidoxy group, an epoxy group, an amine group, a hydroxyl group, a hydrogen atom, a vinyl group, a (meth)acryloyl group, or an aryl group; and n is an integer from 2 to 80. The thermoplastic resin composition can exhibit excellent properties in terms of impact resistance, heat resistance, scratch resistance, surface gloss, mar resistance, and the like.

Abstract: A resin composition includes a resin selected from a polylactic acid resin and a polycarbonate resin as a matrix resin, and surface-treated red phosphorus, wherein the surface-treated red phosphorus is contained in an amount of 10 parts by weight to 40 parts by weight, based on 100 parts by weight of the polylactic acid resin or the polycarbonate resin.

Abstract: A method of forming a desiccating part including the steps of: (a) blending a composition comprising: at least 60 wt % desiccant, up to 10 wt % wetting agent, up to 5 wt % processing aid, and 10-30 wt % thermosetting resin; (b) forming the composition blended in step (a) into a part or shape; and (c) heating the part or shape of step (b) to crosslink the resin. Also included is a desiccating part comprising at least 70 wt % desiccant and a thermosetting binder resin.