Abstract: The present invention relates to binder compositions with improved amine components, and a method of manufacturing a collection of matter bound by said binder compositions.

Abstract: A polyimide resin containing a repeating structural unit represented by the following formula (1) and a repeating structural unit represented by the following formula (2), a content ratio of the repeating structural unit of formula (1) with respect to the total of the repeating structural unit of formula (1) and the repeating structural unit of formula (2) being 20 mol % or more and less than 40 mol %, and the polyimide resin satisfying predetermined conditions; wherein R1 represents a divalent group having from 6 to 22 carbon atoms containing at least one alicyclic hydrocarbon structure; R2 represents a divalent chain aliphatic group having from 5 to 16 carbon atoms; and X1 and X2 each independently represent a tetravalent group having from 6 to 22 carbon atoms containing at least one aromatic ring.

Abstract: A poly(imide-amide) copolymer including a structural unit represented by Chemical Formula 1; a structural unit represented by Chemical Formula 2; and any one of a structural unit represented by Chemical Formula 3, an amic acid precursor of the structural unit represented by Chemical Formula 3, and a combination thererof; wherein a cured material of the poly(imide-amide) copolymer may have a tensile modulus of greater than or equal to about 5.5 GPa, and a yellowness index of less than or equal to about 5: wherein, groups and variables in Chemical Formulae 1 and 3 are the same as described in the specification.

Abstract: There is provided a polyarylene sulfide configured to satisfy (1) to (4): (1) having a weight-average molecular weight of not less than 10000; (2) having a polydispersity of not greater than 2.5, wherein the polydispersity is expressed by a ratio of the weight-average molecular weight to a number-average molecular weight; (3) having a weight reduction on heating that satisfies an expression of ?Wr=(W1?W2)/W1×100?0.18(%) (where ?Wr denotes a weight reduction ratio (%) and is a value calculated from a sample weight (W2) at temperature reaching 330° C. relative to a sample weight (W1) at temperature reaching 100° C. in thermogravimetric analysis at a temperature rise rate of 20° C./minute in a non-oxidizing atmosphere at ordinary pressure); and (4) having a nitrogen content of not greater than 200 ppm.

Abstract: The present invention addressed the problem of providing a highly reliable thermosetting resin composition which is suitable for use in a sealing material for a semiconductor device and in which warpings and cracks do not occur even when used in a power device, in particular. The problem is solved by a thermosetting resin composition that includes a thermosetting resin and a curing catalyst, wherein the cured product of the thermosetting resin composition has a storage modulus at 25° C. of 1.0×106 Pa to 1.0×1010 Pa and an average linear expansion coefficient at 70 to 210° C. of 100 ppm/K or less.

Abstract: In an embodiment of the present invention, a wet gel includes a crosslinked silicone resin in which a silicone resin composition is solidified; a first liquid capable of dissolving the silicone resin composition; and one of a solid capable of being dissolved in the first liquid, and a second liquid such that a degree of swelling, when the crosslinked silicone resin is immersed in the second liquid, is less than a degree of swelling when the crosslinked silicone resin is immersed in n-dodecane, wherein the second liquid is capable of being mixed with the first liquid.

Abstract: The present invention relates to a powder of polyamide PA (homopolyamide or copolyamide) derived at least partially from renewable materials, in which the particles have a nonspherical shape and a volume median diameter of less than or equal to 20 ?m. The present invention also relates to a process for preparing such a powder.

Abstract: To provide a method capable of producing, by means of mechanical pulverization, a resin powder having a high bulk density and an average particle size of at most 50 ?m from resin particles containing a fluorocopolymer as the main component and having a melting point of from 260 to 320° C., such as PFA. The method is to obtain a resin powder having an average particle size of from 0.02 to 50 ?m by subjecting resin particles (A) having an average particle size of at least 100 ?m to mechanical pulverization treatment. The resin particles (A) is made of a material (X) having a fluorocopolymer (X1) as the main component; and said fluorocopolymer (X1) has a unit (1) based on a monomer containing at least one type of functional group selected from the group consisting of a carbonyl group-containing group, a hydroxy group, an epoxy group and an isocyanate group, and a unit (2) based on tetrafluoroethylene, and has a melting point of from 260 to 320° C.

Abstract: A method for preparing a “preblend” of nano-structured carbon, such as nanotubes, fullerenes, or graphene, and a particulate solid, such as polymer beads, carbon black, graphitic particles or glassy carbon involving wet-mixing and followed by optional drying to remove the liquid medium. The preblend may be in the form of a core-shell powder material with the nano-structured carbon as the shell on the particulate solid core. The preblend may provide particularly improved dispersion of single-wall nanotubes in ethylene-?-olefin elastomer compositions, resulting in improved reinforcement from the nanotubes. The improved elastomer compositions may show simultaneous improvement in both modulus and in elongation at break. The elastomer compositions may be formed into useful rubber articles.

Abstract: Polycarbonate articles having improved properties due to their substantially cross-linked nature are disclosed. The substantially cross-linked articles are formed by forming a product from a polymeric composition comprising a cross-linkable polycarbonate resin containing a photoactive group derived from a benzophenone, and exposing the formed product to an effective dosage of ultraviolet radiation to cause substantial cross-linking throughout the article. Such cross-linking can also be used to obtain films having good scratch resistance properties.

Abstract: A composition includes a thermosetting resin and a plurality of polymer nanoparticles at least partially dissolved in the resin. The resin has a gradient of mechanical properties around each location of the at least partially dissolved polymer nanoparticles. Each gradient extends from a particle center toward the resin surrounding the polymer nanoparticle.

Abstract: PVC-free decorative surface covering comprising a reinforced layer, said layer comprising a carrier impregnated with a PVC-free paste, said paste comprising from 5 to 50% by weight of a PVC-free polymer blend, from 45 to 90% by weight of one or more fillers and from 0.5 to 12% by weight of one or more lubricants. The PVC-free decorative surface coverings are prepared by a calendering process.

Abstract: An aqueous adhesive composition for treating a reinforcing fiber for bonding to a thermosetting polymer matrix and products made therefrom such as power transmission belts. The adhesive composition includes: water as the solvent or dispersing medium; a polyelectrolyte co-curable with the polymer matrix; a primer material compatible with the fiber and co-curable with the polyelectrolyte; and optionally a rubber curative compatible with the polyelectrolyte and the polymer matrix. A fiber-reinforced, composite polymer system may thus include a thermosetting polymer matrix, a reinforcing fiber embedded therein, and an adhesive composition coating the fiber; the adhesive composition including a polyelectrolyte co-curable with the polymer matrix and a primer material compatible with the fiber and co-curable with the polyelectrolyte. The adhesive composition may include a curative compatible with the polyelectrolyte.

Abstract: A process includes combining a metallocene catalyzed polypropylene with a nucleator and a slip agent to form a composition, and forming a cast film from the composition. The slip agent may exhibit an increased slip bloom rate within the cast film relative to the slip bloom rate exhibited by the slip agent in an otherwise identical cast film in which the nucleator is not present in the cast film. The cast film may exhibit a coefficient of friction that is less than a coefficient of friction of an otherwise identical cast film in which the nucleator is not present in the cast film.

Abstract: A method for preparing a chitosan complex film comprises: (1) reacting polyvinyl alcohol-124 with butanedioic anhydride to obtain a modified polyvinyl alcohol; (2) formulating the modified polyvinyl alcohol-124 into a 0.4 wt % aqueous solution, then adding the aqueous solution containing 0.4 wt % of modified polyvinyl alcohol-124 dropwise into an acetic acid solution at a concentration of 0.4 wt % chitosan to obtain a mixed solution; (3) adjusting the pH value of the mixed solution with a 0.01 wt % NaOH solution to pH 5.5, and removing surface bubbles after standing for one hour to obtain a casting solution; (4) pouring the casting solution into a culture dish, placing the culture dish into an oven at 60° C. and drying to a constant weight to obtain the chitosan complex film. The materials used in the method are inexpensive, and the reaction is not complicated, so the cost of the product is not high.

Abstract: A tow prepreg, made by impregnating a reinforcing fiber bundle with a matrix resin composition that comprises component (A): epoxy resin, component (B): epoxy resin curing agent, and component (C?): pre-gelatinizing agent with a minimum viscosity temperature of 110° C. or lower, wherein, the temperature of minimum viscosity is determined to be the temperature obtained at the minimum viscosity that appears on the highest temperature side when a sample is prepared by adding and dispersing homogeneously 10 parts by mass of the component (C?) to 100 parts by mass of bisphenol-A epoxy resin with an epoxy equivalent weight of 190±6 g/eq, and by dissolving 10 parts by mass of a boron trichloride-octylamine complex into the mixture, and when the viscosity of the sample is measured by increasing the temperature at a rate of 2° C./min.

Abstract: This invention relates to an elastomeric article with improved lubricity and donnablity and reduced stickiness/tackiness. According to the methods of the invention, the internal surface of the elastomeric article is coated with a polyisoprene coating. The coating of the invention is formed from synthetic polyisoprene rubber that may or may not contain minor amounts of other components. The coating is preferably directly bonded to the underlying elastomeric article.

Abstract: The present invention relates to a process for preparing a polyurethane composite material, comprising steps of: I) preparing a premolded polyurethane molding body, wherein the premolded polyurethane molding body is prepared from a polyurethane composition under a condition that isocyanate groups and isocyanate-reactive groups comprised in the polyurethane composition undergo an addition reaction; II) curing the premolded polyurethane molding body to prepare the polyurethane composite material, wherein the premolded polyurethane molding body cures by the radical polymerization of active olefinic bonds. The process of the present application has a lower TVOC value and better processability.

Abstract: Disclosed are a dynamic non-wicking PU foam and preparation and application thereof The PU foam is prepared from polyether polyol, toluene-2,4-diisocyanate, non-wicking additive and auxiliary agent. The dynamic non-wicking additive is composed of carboxylic acids, amines and alkyl alcohols in any proportion. The auxiliary agent is composed of silicone surfactant, amine promoter, tin catalyst, pigment and water. The dynamic non-wicking PU foam has a high stability and an extremely non-wicking effect. The shoes made of the dynamic non-wicking PU foam also have extremely good dynamic non-wicking and waterproof effects, thus ensuring both comfort and stability of quality.

Abstract: A formamide-free foam prepared by using sodium bicarbonate as a foaming agent and electron-beam irradiation for crosslinking is revealed. After copolymer and sodium bicarbonate being mixed evenly, the mixture is heated and compounded to form an intermediate. Then the intermediate is pressed and injected to form a sheet. Next the intermediate is irradiated by an electron-beam to form crosslinks therein. At last the intermediate is heated and foamed to get a formamide-free foam. Compared with foam produced by using azodicarbonamide as the foaming agent available now, formamide-free foam not only causes no harm to human health but also gives no negative effect to the environment during recycling. Thus the formamide-free foam is really environmentally friendly.

Abstract: The present invention relates generally to the use of talc as a chemical foaming agent in perfluoropolymers to form foamable and foamed compositions. For example, in one aspect, a foamable composition is disclosed, which comprises (i) one or more base perfluoropolymers comprising at least 50 percent by weight of the composition, and (ii) talc blended with the one or more base perfluoropolymers, where the talc comprises 3 percent to about 15 percent by weight of the composition. Each of the perfluoropolymers is selected from the group consisting of tetrafluoroethylene/perfluoromethylvinyl ether copolymer (MFA), hexafluoropropylene/tetrafluoroethylene copolymer (FEP) and perfluoroalkoxy (PFA) and any blend thereof, where hydrogen-containing fluoropolymers are absent from the composition. The one or more base perfluoropolymers are melt-processable at one or more elevated processing temperatures of at least about 600° F.

Abstract: A method for producing a polymer nanofoam includes: immersing a polymer material in carbon dioxide at a pressure greater than 5 MPa and a temperature of ?30° C. to 40° C. to obtain a carbon dioxide-saturated polymer material, wherein the melt index of the polymer material measured at 230 ° C. and 3.8 kg is between 0.1 g/10 min and 8.0 g/10 min. Thereafter, the carbon dioxide-saturated polymer material is depressurized to atmospheric pressure, and then the carbon dioxide-saturated polymer material is heated to form the polymer nanofoam.

Abstract: Polyhexahydrotriazine (PHT) and polyhemiaminal (PHA) materials form highly cross-linked polymers which can be used as binder resins in composite materials. A filler element functionalized with a primary amine group can be covalently bonded to the PHA/PHT polymer resins. Example filler elements include, without limitation, carbon nanotubes, silica materials, carbon and glass fibers, and nanoparticles. Filler materials are incorporated into polymeric materials to improve the mechanical strength or other characteristics of the polymeric material for various applications. Typical composite materials use thermosetting materials that, once set, are intractable. PHT and PHA materials can be reverted to starting materials by exposure to acids. Thus, composite components formed using these materials are recyclable.

Abstract: A stator compound including an acrylonitrile butadiene isoprene rubber (NBIR) terpolymer elastomeric base.

Abstract: A gas barrier material includes an atomic sheet, such as graphene and/or an analog of graphene. The gas barrier material can be arranged as part of a component, such as a container or other vessel, to limit the flow or permeation of gas through the component. Where the component is a container or part of a container, the gas barrier material may be formulated and arranged to limit or prevent gas ingress or egress with respect to the internal volume of the container. The atomic sheet offers improved gas barrier properties compared to traditional polymeric barrier materials and is particularly useful in applications where it is desired to limit permeation of small gas molecules such as helium, such as airships or other lighter than air vehicles.

Abstract: A solid material including a matrix, dispersed in which are microparticles of at least one antimicrobial agent for preventing, limiting and/or eliminating the contamination of the material and/or the contamination of a composition which is in contact with the material for at least a given time, and/or preventing, eliminating and/or slowing down the formation of biofilms on the surface of the material, wherein the antimicrobial agent is an oxide of at least one positively charged metal ion and the antimicrobial agent does not migrate out of the material. Also, the use of such material for manufacturing an article, to the process for manufacturing the article, and to the article obtained.

Abstract: A rubber composition comprising a compound having one or more groups represented by formula (X) and a rubber component is provided. wherein ring W1 represents a cyclic group having at least one selected from the group consisting of —C(?O)— and —C(?S)—; N10 represents a nitrogen atom; the at least one selected from the group consisting of —C(?O)— and —C(?S)— in the ring W1 and N10 are conjugated; and Z1 represents —O— or —S—.

Abstract: The present invention relates to polysulfides of the formula (I) where the cations K1+ and K2+ are each independently any monovalent cation or the fraction of any polyvalent cation which corresponds to a positive charge of one, and n is 2, 3, 4, 5, 6, these having a low residual acidity, and to processes for producing these polysulfide mixtures, to the use of the polysulfides of the formula (I) in rubber mixtures, to the corresponding rubber mixtures, to rubber vulcanizates produced therefrom and to the use thereof.

Abstract: Halogen-free flame retarded unsaturated polyester (UPE) composites are described, where aluminum methyl methylphosphonate (AMMP) was added to a UPE matrix in order to obtain a UL94-V0 formulation. The combustion properties of AMMP are improved to that of aluminum trihydrates (ATH) in cone calorimetry. The use of AMMP prepared with phosphonium catalyst was also shown to be advantageous for retaining the gelation time of the UPE resins in a mold.

Abstract: This room-temperature-curable organopolysiloxane composition includes: component (A); 0.1-30 parts by mass of component (B) per 100 parts by mass of component (A); and 0.001-20 parts by mass of component (D) per 100 parts by mass of component (A). Component (A) is an organopolysiloxane represented by general formula (1) (in general formula (1): R1 represents hydrogen, or a substituted or unsubstituted C1-20 monovalent hydrocarbon group; the plurality of R1s may be the same or different; and n represents an integer of at least 1).

Abstract: An object of the present invention is to provide an HNBR composition and an HNBR crosslinked body excellent in abrasion resistance and pressure resistance. The object is achieved by an HNBR composition containing 3 to 20 parts by weight of carbon fibers or wollastonite as a hard filler per 100 parts by weight of a hydrogenated nitrile rubber and containing 72 to 87 parts by weight of a carbon black having an average particle diameter of 40 to 50 nm, an iodine adsorption of 35 to 49 g/kg, and a DBP oil absorption of 100 to 160 ml/100 g, as well as an HNBR crosslinked body acquired by crosslinking the HNBR composition.

Abstract: An inorganic filler included in an epoxy resin composition includes a coating layer formed on a surface thereof, and the surface of the coating layer includes at least two elements selected from the group consisting of C, N and O.

Abstract: The present invention relates to a 3D printer polymer filament improving strength of a polymer resin and providing durability by using graphene coated metal nanoparticles and carbon nanotubes, and expressing a function of the graphene coated metal nanoparticles and the carbon nanotubes as a filler, and a manufacturing method thereof. Accordingly, according to the present invention, the 3D printer polymer filament and the manufacturing method includes mixing the graphene coated metal nanoparticles, the carbon nanotubes, and the polymer, using the manufactured mixture to form a filament through extrusion, and forming a 3D printed article by using the filament, thereby improving the strength and the durability by using the graphene coated metal nanoparticles and the carbon nanotubes.

Abstract: Provided is a wavelength conversion material composed of resin particles comprising an acrylic resin and an organic rare earth complex contained in the acrylic resin, in which the acrylic resin is obtained from an acrylic resin composition comprising a cross-linking agent, and deterioration of the organic rare earth complex is prevented. A wavelength conversion material composed of resin particles comprising an acrylic resin and an organic rare earth complex contained in the acrylic resin, wherein the acrylic resin is a polymer which is a reaction product of an acrylic resin composition comprising a (meth)acrylate monomer, a crosslinking agent and an azo polymerization initiator, wherein the crosslinking agent is a compound represented by the following formula (I): where R1 and R2 each independently represent a hydrogen atom or a methyl group and n represents an integer of 2 to 14, and the content of the cross-linking agent is: 0.

Abstract: A rubber composition contains at least: a diene rubber, a silica, a silane coupling agent having a mercapto group, a plasticizer, and an oil and/or a resin; from 50 to 200 parts by mass of the silica per 100 parts by mass of the diene rubber and from 2 to 20 mass % of the silane coupling agent having a mercapto group relative to the amount of the silica being blended; and a total amount of the plasticizer and the oil and/or the resin being 60 parts by mass or greater per 100 parts by mass of the diene rubber.

Abstract: A rubber compound for tyres comprising at least one cross-linkable polymer base, a reinforcing filler, a vulcanization system, a reinforcing resin and a dithiol chemical with formula (I) SHRSH ??(I) wherein R is an aliphatic or aromatic group composed of 3-12 atoms.

Abstract: The invention relates to compositions comprising OH-functional polybutadiene and solvent and to the use thereof as release agents in the production of polyurethane moulded articles or as antisquawk agents in the processing of moulded polyurethane articles.

Abstract: A stator compound including an acrylonitrile butadiene isoprene rubber (NBIR) terpolymer elastomeric base.

Abstract: Barrier films are prepared from a blend of two high density polyethylene blend components and a high performance organic nucleating agent. The two high density polyethylene blend components have substantially different melt indices. Large reductions in the moisture vapor transmission rate of the film are observed in the presence of the nucleating agent when the melt indices of the two blend components have a ratio of greater than 10/1. The resulting barrier films are suitable for the preparation of packaging for dry foods such as crackers and breakfast cereals.

Abstract: Provided herein are membranes including a blend of a propylene-based elastomer and an ethylene copolymer, a thermoplastic resin, a flame retardant, and an ultraviolet stabilizer.

Abstract: The present technology is: a rubber composition for an outside hood, the rubber composition containing, per 100 parts by mass of one type or two or more types of ethylene-propylene-diene terpolymers, at least 5 parts by mass of silica, and sulfur and/or a peroxide compound, a Mooney viscosity of the one type of ethylene-propylene-diene terpolymer being 50 or greater, a diene amount in the one type of ethylene-propylene-diene terpolymer being at least 8 mass % of the one type of ethylene-propylene-diene terpolymer, an average Mooney viscosity of the two or more types of ethylene-propylene-diene terpolymers being 50 or greater, and an average diene amount in the two or more types of ethylene-propylene-diene terpolymers being at least 8 mass % of the two or more types of ethylene-propylene-diene terpolymers; and an outside hood for a railway vehicle produced using the same.

Abstract: A thermoplastic composition for overmolding of an elastomer on a substrate made of mineral glass includes: (1) from 50 to 70% by weight of at least one thermoplastic elastomer (TPE) chosen from copolymers comprising styrene blocks (TPE-Ss), (b) from 20 to 35% by weight of a polyolefin chosen from propylene homopolymers (PPs), ethylene homopolymers (PEs) and copolymers of propylene and ethylene, and (c) at least 7% by weight of a functional alkoxysilane. The percentages are expressed with respect to the sum of the components (a), (b) and (c).

Abstract: The present disclosure describes poly(styrene/acrylate)-polyester hybrid particles, wherein poly(styrene/acrylate) polymers are polymerized and entangled within a polyester seed particle in an interpenetrating polymer network.

Abstract: Solutions of polyvinylidene fluoride (PVDF) or copolymers of 1,1-difluoroethylene in a solvent which comprises N-formylmorpholine (NFM), N-acetylmorpholine (NAM) or mixtures thereof and additionally a cosolvent selected from alkylene carbonate, mono-, di- or polyalkylene glycol dialkyl ethers or mixtures thereof.

Abstract: The present invention provides a thermoplastic polyester elastomer composition which is flexible and exhibits excellent thermal aging resistance and water resistance. According to the present invention, there is provided a thermoplastic polyester elastomer composition wherein, to 100 parts by mass in total of a thermoplastic polyester elastomer (A) and a modified hydrogenated styrene-type elastomer (B), 0.1 to 10 part (s) by mass of a carbodiimide compound (C), 0.01 to 5 part (s) by mass of an antioxidant of a hindered phenol type (D) and 0.

Abstract: Even when a tin-based polymerization catalyst and a phosphorus-based compound are present in a poly-L-lactic acid (A) and a poly-D-lactic acid (B), by using a specific proportion of an organic acid metal salt or an organic metal salt for stereocomplex crystallization, a stereocomplex polylactic acid composition having a high stereocomplex crystallinity and a high stereocomplex crystal melting point, a small stereocomplex crystal melting point depression even after remelting, a small decrease in the molecular weight, excellent forming processability, and also heat resistance can be provided.

Abstract: A material composition, which may be a support material, for three-dimensional (3D) inkjet printing is disclosed. The material composition may comprise a glycol polymer, a low molecular weight polar substance and a surface-active agent. The glycol polymer may be polyethylene glycol (PEG) having a molecular weight between about 1000 and about 6000 and the low molecular weight polar substance may be dimethyl hexanediol.

Abstract: Provided is a polyamide molding composition comprising a) at least one semi-aromatic, semi-crystalline polyamide, at least flat glass fiber as reinforcing filler, c) at least one aliphatic polyamide comprising recurring units complying with the formula —NH—R2—NH—CO—R3—CO—, wherein R2 and R3, equal to or different from each other at each occurrence, are divalent aliphatic hydrocarbon groups, and d) at least one additive.

Abstract: The present invention provides novel compounds and methods for hydrocyanines derived from near-infrared cyanine dyes, as reactive oxygen species probes in imaging. In certain embodiments, the present invention provides reduced dyes as substrates for ELISA and Western blots.

Abstract: The present invention provides methods, compositions, mixtures and kits utilizing deoxynucleoside triphosphates comprising a 3?-O position capped by a group comprising methylenedisulfide as a cleavable protecting group and a detectable label reversibly connected to the nucleobase of said deoxynucleoside. Such compounds provide new possibilities for future sequencing technologies, including but not limited to Sequencing by Synthesis.