Abstract: A polymerizable composition according to the present invention includes a compound (A) including two or more allyloxycarbonyl groups represented by Formula (1); at least one kind of polymerization initiator (B) selected from the group consisting of a peroxyketal-based radical polymerization initiator, a peroxy monocarbonate-based radical polymerization initiator, and a peroxyester-based radical polymerization initiator; and at least one kind of photochromic compound (C) selected from a naphthopyran compound group.

Abstract: [Object] To provide a method for producing a vinyl ether polymer having a hydroxyl group on the side chain, wherein the vinyl ether polymer having a low viscosity and excellent workability and processability is produced in a simple and efficient method. [Means for solving problem] The present invention relates to a method for producing a vinyl ether polymer having a hydroxyl group on the side chain, characterized in that vinyl ether comprising a hydroxyl group is subjected to radical polymerization by using an oil-soluble azo polymerization initiator, in the presence of a mixed solvent comprising water and an organic solvent selected from alcohol or cyclic ether radical polymerization.

Abstract: A propylene 1-hexene copolymer containing from about 5.5 to about 9.0% by weight, based upon the total weight of the copolymer, of 1-hexene derived units having: a) two melting temperature peaks in the DSC plot having a difference in height ranging from 0 to 5 mW; b) the higher melting temperature, measured by DSC, ranging from about 141.0° C. to about 151.0° C.; and c) Melt Flow Rate (MFR, measured according to ASTM D 1238, 230° C./2.16 kg) from about 3.5 to about 8.0 g/10 min.

Abstract: The present invention provides a vinyl alcohol-vinyl acetate copolymer having excellent solubility and a method for producing a vinyl alcohol-vinyl acetate copolymer. Provided is a vinyl alcohol-vinyl acetate copolymer including a unit of vinyl alcohol and a unit of vinyl acetate, the vinyl alcohol-vinyl acetate copolymer having a randomness value R of 0.5 or higher, the randomness value R being obtained using the following equation (1): R = 1 L A + 1 L O ( 1 ) where LO represents a mean chain length of the unit of vinyl alcohol and LA represents a mean chain length of the unit of vinyl acetate.

Abstract: A near infrared absorbing colorant polymer has a maximal absorption in a wavelength range of 700 to 1200 nm. It is preferable that the near infrared absorbing colorant polymer includes at least one near infrared absorbing colorant structure selected from the group consisting of a pyrrolopyrrole colorant, a cyanine colorant, a squarylium colorant, a diimonium colorant, a phthalocyanine colorant, a naphthalocyanine colorant, a rylene colorant, a dithiol complex colorant, a croconium colorant, an oxonol colorant, a triarylmethane colorant, a pyrromethene colorant, an azomethine colorant, an anthraquinone colorant, and a dibenzofuranone colorant.

Abstract: The object of the present invention is to provide a novel adhesive. The characteristics of the present invention is an adhesive comprising an organic polymer having a main chain formed by a water-soluble polymer unit, and a hydrophilic organic group and a self-assembling group bonded to the water-soluble polymer unit; and a curing agent.

Abstract: The present invention is directed to a functionalized elastomer, wherein the functionalized elastomer is a copolymer of a first monomer and a second monomer, the first monomer selected from the group consisting of conjugated diene monomers and vinyl aromatic monomers, and the second monomer of formula 1 wherein R1=C1-C8 alkyl, aryl, substituted aryl, or —SiR3 where R3 are independently C1-C8 alkyl; R2=C1-C8 alkyl, aryl, or substituted aryl, or —SiR3; and n=0-3.

Abstract: A crosslinking agent includes a compound represented by the following formula (1). wherein R1, R2, and R3 are independently a hydrogen atom, a fluorine atom, an alkyl group, a fluoroalkyl group, or a substituted or unsubstituted aryl group, a plurality of R1 are identical to or different from each other, a plurality of R2 are identical to or different from each other, a plurality of R3 are identical to or different from each other, provided that at least one of R1, R2, and R3 is a hydrogen atom, and at least one of R1, R2, and R3 is a fluorine atom or a fluorine atom-containing group, m is an integer from 2 to 6, l is an integer from 0 to 2, and each hydrogen on the benzene ring(s) may be substituted.

Abstract: A composition includes a polyphosphoric acid-modified acrylic polyol, wherein the polyphosphoric acid-modified acrylic polyol has greater than zero, but less than 1.0 wt % modification with polyphosphoric acid.

Abstract: A process for producing a viscous epoxy syrup from at least one liquid multifunctional epoxy, comprising the steps of: adding an initiator selected from the group consisting of electron-poor monoisocyanate, photoinitiator and thermal initiator to at least one liquid multifunctional epoxy; mixing the components; polymerizing the multifunctional epoxy such that the viscosity of the resulting epoxy syrup is at least twice as high, preferably at least four times as high and in particular at least ten times as high as the viscosity of the employed epoxy in the unreacted state makes it possible to produce epoxy adhesives having pressure-sensitive properties.

Abstract: Provided is a resin composition that can provide a cured product of low dielectric tangent, high mechanical strength, and high adhesiveness. The resin composition contains (A) a resin having a thermosetting functional group FA, (B) a resin having a radical polymerizable functional group FB, and (C) a resin having a functional group FA? reacting with the thermosetting functional group FA and a functional group FB? reacting with the radical polymerizable functional group FB. A number na of the functional group FA? of the component (C) when the number of the thermosetting functional group FA of the component (A) is defined as 1 and a number nb of the functional group FB? of the component (C) when the number of the radical polymerizable functional group FB of the component (B) is defined as 1 satisfy 0.01?na?200 and 0.01?nb?400, respectively.

Abstract: A method for instillation molding UV epoxy resin includes: the UV epoxy resin preparation step: adding at least two photosensitizers to a single component epoxy resin and uniformly mixing them to obtain the UV epoxy resin, wherein the photosensitizer with the highest content in the UV epoxy resin is a photosensitive curing agent for curing the UV epoxy resin, and the rest photosensitizers are photosensitive viscosity regulating agents for regulating the viscosity of the UV epoxy resin to be suitable for instillation molding; and instillation step: dividing the instillation molding of the UV epoxy resin into N procedures performed in one work station, wherein zero, one or more photosensitive viscosity regulating agents are initiated in each procedure, so that the UV epoxy resin reaches a viscosity suitable for respective instillation procedure and is subsequently instillation molded; curing step: initiating the photosensitive curing agent to finally cure the UV epoxy resin.

Abstract: The present invention is directed to addressing one or more of the aforementioned concerns and relates to thermal insulation materials and thermal insulation material compositions and methods for thermally insulating pipelines and associated equipment, structures, and objects used in offshore drilling. The present invention is directed to articles of manufacture comprising the thermal insulation materials and/or thermal insulation material compositions of the invention. More particularly the present invention relates to the use of ring opening metathesis polymerization polymers (ROMP polymers) and/or ROMP polymer composites for thermally insulating pipelines and associated equipment, structures, and objects used in offshore oil drilling.

Abstract: Provided is a light-emitting device including an anode, a light-emitting layer, an electron-transporting layer and a cathode. The electron-transporting layer contains at least one electron-transporting material whose LUMO level is ?3.0 eV or more and at least one dopant material selected from the group consisting of a heterocyclic compound whose SOMO level is ?2.2 to ?1.5 eV and a derivative thereof. The LUMO level of the electron-transporting material is smaller than the SOMO level of the heterocyclic compound.

Abstract: The present invention provides novel methods and processes for polymerizing unsaturated substrates, such as alkyne bearing monomers, with arenes. The polymerizations are catalyzed by gold (Au) catalysts/complexes and/or other cocatalysts. The invention further provides novel structurally complex polymers prepared in high yield via an intermolecular polyhydroarylation mechanism. Such resulting products comprise oligomeric and polymeric materials with novel molecular architectures and microstructures, which subsequently impart unique properties. The invention includes both the synthesis methods and processes and the resulting compounds and compositions of matter.

Abstract: The present specification relates to an ion exchange membrane, an electrochemical cell, a flow battery and a fuel cell comprising the same, and a method for manufacturing the same.

Abstract: Embodiments of the present disclosure provide for conjugated polymer nanoparticle, method of making conjugated polymer nanoparticles, method of using conjugated polymer nanoparticle, polymers, and the like.

Abstract: Provided herein are systems, and methods of using such systems, for producing superabsorbent polymers from ethylene oxide and carbon monoxide. The production systems have various unit operations, including, for example, a (?-propiolactone production system configured to produce (?-propiolactone from ethylene oxide and carbon monoxide and a superabsorbent polymer production system configured to produce superabsorbent polymers from (?-propio lactone and/or acrylic acid.

Abstract: Aqueous compositions of carboxylic acids, carboxylate esters, and carboxylate salts are generally disclosed, including methods of using such compounds to make various polymers, including, but not limited to, polyesters, polyamides, and polycarbamates. In certain embodiments, the carboxylic acids, carboxylate esters, and carboxylate salts are derived from a renewable source, such as a natural oil.

Abstract: A polylactide derivative according to the present invention is expressed by the following general formula (1) or general formula (2): In general formula (1), one of X1-X5 is an aldehyde group, one of the other four is an alkoxy group, and the other three are hydrogen atoms. In general formula (2), one of R1-R3 is selected from a chlorine atom, fluorine atom, aldehyde group, alkoxy group, alkyl group and ester, while the other two are selected from the chlorine atom, fluorine atom, aldehyde group, alkoxy group, alkyl group, ester, and hydrogen atom.

Abstract: Provided is a process for the removal of tetrahydrofuran from polyesters or copolyesters comprising 1,4-butylene dicarboxylate repeating units and from compositions comprising the polyesters or copolyesters.

Abstract: The present invention addresses the problem of providing an optical use polycarbonate resin composition which exhibits good fluidity, has a high refractive index, is inexpensive and exhibits impact resistance. This problem can be solved by an optical use polycarbonate resin composition that contains a polycarbonate resin (A) which contains a constituent unit represented by formula (1) and has an intrinsic viscosity of 0.320-0.630 dL/g, and polycarbonate resin (B) which contains a constituent unit represented by formula (2) and has an intrinsic viscosity of 0.320-0.600 dL/g, wherein the polycarbonate resin that contains a constituent unit represented by formula (2) is contained at a proportion of 45-75 mass %.

Abstract: The present invention provides a method for producing a thermoplastic resin by reacting reactants comprising a dihydroxy compound.

Abstract: Provided are compositions comprising isotactic polyethers. Methods of making isotactic polyethers, and uses thereof are also disclosed. Also provided are bimetallic complexes that can be used as catalyst. Methods of making isotactic polyethers and bimetallic complexes and uses thereof are also disclosed. For example, a racemic bimetallic (salalen)CrCl polymerization catalyst was prepared and used alkyl diol, PO-oligomer triols, and aPPO and PCL diols as CSAs in order to produce ?,?-hydroxy telechelic iPPO. These telechelic polymers have controlled molecular weights and are semicrystalline. Amorphous ?,?-hydroxy telechelic PPO can also be produced by increasing the reaction temperature in conjunction with the use of CSAs.

Abstract: A method for isolating a phenylene ether oligomer composition includes feeding a solution including a solvent and a phenylene ether oligomer into a thin film evaporator, forming a film on an interior surface of the thin film evaporator, and heating to devolatilize the solvent from the film, to provide a phenylene ether oligomer composition. The thin film evaporator includes cylindrical heating chamber and a rotor having one or more rotor blades, wherein an edge of the one or more rotor blades and the interior surface of the cylindrical heating chamber are separated by a distance of 0.5 to 3.5 millimeters. Phenylene ether oligomer compositions are also described.

Abstract: A low-k, non-flammable dicyclopentdiene (DCPD)-derived polyether and a method of producing the same are introduced. Incorporation of a phosphorus group and a DCPD derivative into a low-k, non-flammable dicyclopentdiene (DCPD)-derived polyether enable the DCPD-derived polyether to not only serve as an epoxy resin curing agent but also cure itself such that the cured product not only features satisfactory thermal properties and low-k characteristics but is also non-flammable.

Abstract: The disclosure relates to an improved method of producing MPMD based amorphous, semi-aromatic polyamides in order to improve their mechanical properties. It also relates to improved formulations of these polyamides which have further improved mechanical properties by the incorporation of greater amounts of isophthalic acid. The disclosure relates to an improved method of producing MPMD based amorphous, semi-aromatic polyamides in order to improve their mechanical properties. It also relates to improved formulations of these polyamides which have further improved mechanical properties by the incorporation of greater amounts of isophthalic acid.

Abstract: This resin composition is characterized by comprising (a) 100 parts by mass of a polyimide precursor containing a structural unit represent by general formula (1) (wherein, R1 and R2 are each independently selected from a hydrogen atom, monovalent aliphatic hydrocarbons having 1-20 carbon atoms, and aromatic groups, and X1 is a tetravalent organic group having 4-32 carbon atoms), (b) 0.001-5 parts by mass of a silicone-based surfactant, and (c) an organic solvent.

Abstract: The present invention features linear and three-dimensional supramolecular materials self-assembled from block co-polymers comprising oligo(ethylene sulfide) (OES). The block copolymers assemble into fibrils, micelles, or matrices. The fibrillar materials are sensitive to oxidation, which leads to decreased OES block hydrophobicity and crystallinity, and increased water solubility of the polymer constituents. Molecular loading options, coupled with oxidative sensitivity, allow implantable or injectable fibrillar suspensions or cross-linked three-dimensional matrices to demonstrate significant biomedical potential, especially in the context of extracellular and intracellular molecular delivery and applications related to infection and disease.

Abstract: Provided are a siloxane composition, said siloxane composition showing physical properties between a dimethyl polysiloxane oil and a gelatinous crosslinked siloxane and being fluid or becoming fluid when dissolved in a solvent, and a method for producing the same. The siloxane composition, which is obtained by subjecting specific starting organopolysiloxane materials to an addition reaction in a large excess (i.e., 8 times by mass or greater as much as the starting materials) of a solvent, comprises a crosslinked organopolysiloxane, said crosslinked organopolysiloxane having a weight-average molecular weight of 5,000-300,000,000 and containing 0.1-50 mol of silethylene bond per 1,000 mol of siloxane unit, dissolved in the solvent.

Abstract: A process includes forming a bio-derived crosslinking material from biorenewable aconitic acid. The process includes initiating a chemical reaction to form a bio-derived crosslinking material that includes multiple functional groups. The chemical reaction includes converting each carboxylic acid group of a biorenewable aconitic acid molecule to one of the multiple functional groups.

Abstract: A semifinished product for making a composite fiber molded part is made by first spinning from a row of orifices of a spinning nozzle low-melting fibers of a thermoplastic. These low-melting fibers are then combined into a laminated semifinished product with high-melting reinforcement fibers of the same thermoplastic but having a melting temperature higher than the melting temperature of the low-melting fibers.

Abstract: The invention relates to a method for producing a thermoplastic fibre composite containing a thermoplastic moulding compound (A) as a polymer-matrix (M), reinforcement fibres (B), and optionally additive (C). Said method comprises the following steps: i) flat structures (F) made from reinforcing fibres (B) treated with a silane sizing material are provided, ii) the flat structures (F) are placed in a thermoplastic molding compound (A) which comprises at least 0.3 mol %, with respect to components (A), of a chemically reactive functionality, iii) chemically reactive groups of the thermoplastic molding compound (A) are reacted in the polymer matrix (M) with the polar groups of the treated reinforcing fibres (B), iv) the at least one additive (C) is optionally incorporated v) cooling. Said method is particularly suitable for producing fibrous composites.

Abstract: A method for forming an isoporous graded film comprising multiblock copolymers and isoporous graded films. The films have a surface layer and a bulk layer. The surface layer can have at least 1×1014 pores/m2 and a pore size distribution (dmax/dmin)) of less than 3. The bulk layer has an asymmetric structure. The films can be used in filtration applications.

Abstract: A differential density absorbent towel paper web having from about 45% to about 90% by weight of the dry fiber basis of the differential density absorbent towel paper web of a softwood pulp fiber mixture and from about 10% to about 55% by weight of the dry fiber basis of the differential density absorbent towel paper web of a hardwood pulp fiber mixture is provided. The softwood pulp fiber mixture has: 1) from about 20.0% to about 88.5% by weight of the dry fiber basis of softwood pulp fiber; and, 2) from about 0.05% to about 5.0% by weight of the dry fiber basis of strengthening additive. The hardwood pulp fiber mixture has: 1) from about 9.9% to about 54.9% by weight of the dry fiber basis of hardwood pulp fibers; and, 2) from about 0.05% to about 20.0% by weight of the dry fiber basis of cellulose nano-filaments.

Abstract: The present invention relates to the use of a polysaccharide adhesive containing cold water-soluble or cold water-swelling, covalently cross-linked starch as a binder together with a foam generator for producing an adhesive foam.

Abstract: A polymer positive temperature coefficient (PPTC) material. The PPTC material may include a polymer matrix, a conductive filler, and a thermal stabilizer.

Abstract: A process for extruding polypropylene comprising extruding a composition comprising a polypropylene and a second acid scavenger and less than about 10 ppm of a nucleating agent.

Abstract: Multi-component synthetic mortar fixing system, especially for fixing anchoring elements in building substrates, which comprises in one component reactive synthetic resins (i) based on urethane (meth)acrylate, (ii) based on epoxy resin or (iii) based on free-radical-hardening (or-hardenable) unsaturated reactive resins, in a further component hardener, and at least one filler selected from oxides of silicon and aluminium, or mixed oxides in the presence of further cations, the d50 average particle size of which is 50 ?m or less, and also especially a silane having at least one hydrolysable group, and also its use, methods including its use in fixing anchoring elements in building substrates and related subject-matter of the invention.

Abstract: The present invention relates to a composite material obtained by in situ polymerization of a thermoplastic resin with a fibrous material. More particularly the present invention relates to a polymeric composite material obtained by in-situ polymerization of a thermoplastic (meth)acrylic resin and a fibrous material containing long fibers and its use, a process for making such a composite material and manufactured mechanical or structured part or article comprising this polymeric composite material.

Abstract: The present invention relates to a polyarylene sulfide-based resin composition, which has excellent thermal conduction efficiency in the horizontal and vertical directions and excellent mechanical properties such as tensile strength and impact strength, and to a molded article thereof.

Abstract: Carrageenan-based compositions containing a carrageenan, a starch, a plasticizer, water, and an optional buffer are disclosed, in which the carrageenan has both a potassium content of less than 4 wt. % and a viscosity configured to produce capsules on pressure-free rotary die equipment. Films and capsules can be formed from the carrageenan-based compositions.

Abstract: The present invention is directed to a vulcanizable rubber composition comprising (A) 100 parts by weight of elastomer consisting of 70 to 100 parts by weight, er 100 parts by weight of the elastomer (phr), of an isoprene-butadiene rubber having a Tg ranging from ?100° C. to ?50° C., and 0 to 30 phr of a second elastomer selected from the group consisting of isoprene-butadiene rubber having a Tg ranging from ?49 to ?20° C., natural rubber, synthetic polyisoprene, and polybutadiene, (B) from 30 to 80 phr of a resin having a Tg of at least 20 C, (C) from 0 to 4 phr of an oil, and (D) from 80 to 180 of a filler selected from the group consisting of carbon black and silica.

Abstract: A rubber composition has: at least three types of diene polymers forming a plurality of polymer phases immiscible with each other; and silica, wherein: a diene polymer (B), of which glass transition temperature (Tg) is neither the highest nor the lowest among the diene polymers each having content of ?10% by mass with respect to the total mass of the diene polymers, has been modified by a compound containing silicon atom; the diene polymer (B) satisfies formula (i) shown below: St+Vi/2?33??(i) (In the formula, “St” represents content of bonded styrene (mass %) of the diene polymer (B) and “Vi” represents vinyl bond content (mass %) of a conjugated diene compound part of the diene polymer (B)); and the silica has content of ?25 parts by mass with respect to the total mass or 100 parts by mass of the diene polymers.

Abstract: Provided are a rubber composition for a tire tread having improved braking performance, abrasion performance, and anti-aging performance, and a tire manufactured using this rubber composition. Disclosed is a rubber composition for a tire tread, the composition including 100 parts by weight of raw material rubber, 60 to 130 parts by weight of a reinforcing filler, and 10 to 60 parts by weight of modified natural oil, wherein the modified natural oil includes 50% to 90% by weight of a first natural oil; and 10% to 50% by weight of a second natural oil having a weight average molecular weight that is 2 to 10 times the weight average molecular weight of the first natural oil, with respect to the total weight of the modified natural oil.

Abstract: Crumb rubber obtained from recycled tires is subjected to an interlinked substitution process. The process utilizes a reactive component that interferes with sulfur bonds. The resulting treated rubber exhibits properties similar to those of the virgin composite rubber structure prior to being granulated, and is suitable for use in fabricating new tires, engineered rubber articles, and asphalt rubber for use in waterproofing and paving applications.

Abstract: The instant disclosure relates to ethylene vinyl alcohol pellets including one or more fluorine-containing micro-particles having a particle size that is not greater than 20 ?m. The EVOH films formed from the EVOH pellets may have a Charpy impact strength of at least 2.45 KJ/m2 according to ISO 179-1 at 23° C. and an elongation at break of at least 17.8% according to ISO 527-2 at 23° C.

Abstract: The invention relates to a composition comprising (A) a heterophasic propylene copolymer and (B) a nucleating composition, wherein (A) the heterophasic propylene copolymer consists of (a) a propylene-based matrix, wherein the propylene-based matrix consists of a propylene homopolymer and wherein the propylene-based matrix is present in an amount of 83 to 88 wt %, preferably 84 to 88 wt %, based on the total heterophasic propylene copolymer and (b) a dispersed ethylene-?-olefin copolymer, wherein the dispersed ethylene-?-olefin copolymer is present in an amount of 12 to 17 wt %, preferably of 12 to 16 wt %, based on the total heterophasic propylene copolymer and wherein the sum of the total amount of propylene-based matrix and total amount of the dispersed ethylene-?-olefin copolymer in the heterophasic propylene copolymer is 100 wt %, wherein the amount of ethylene in the ethylene-?-olefin copolymer is 40 to 60 wt % and wherein the heterophasic propylene copolymer has a melt flow index of 35 to 50 g/10 min as

Abstract: Thermoplastic molding compositions can be used in hydrofluoro olefin containing areas, comprising components A, B, C and D: 10 to 35 wt.-% ABS graft rubber copolymer A obtained by emulsion polymerization; 50 to 70 wt.-% SAN copolymer B; 4 to 20 wt.-% elastomeric SBC block copolymer C, and 4 to 20 wt.-% ABS graft rubber copolymer D obtained by mass polymerization.

Abstract: The present invention encompasses chlorine-containing polymer compositions having a fraction consisting of oxidized hydrocarbons and a fraction consisting of non-oxidized hydrocarbons. Both fractions have an average number of carbon atoms per molecule between 40 and 100 carbon atoms and an amount of molecules in which the carbon chain is linear of more than 75 wt. %.