Abstract: Provided is a vinyl alcohol-based copolymer, obtained by saponifying a copolymer of vinyl acetate and a polyfunctional monomer, wherein the polyfunctional monomer contains two or more ethylenic double bonds in its molecule, the vinyl alcohol-based copolymer has a side chain containing an ethylenic double bond and a molar ratio (d) of the ethylenic double bond to a total of vinyl alcohol units and vinyl acetate units is from 0.05/100 to 2/100, and the vinyl alcohol-based copolymer is water soluble.

Abstract: The present invention relates to: a polymer composition; an article; a medical device; an article production method; and a cell cluster production method. The polymer composition contains a polymer having the following repeating units (A) and (B) and is one selected from the group consisting of a medical device composition, a cell adhesion inhibitor, and a silicone substrate treatment composition: (A) a hydrophilic repeating unit; and (B) a repeating unit which has a polyoxyalkylene group in a side chain whose terminal is constituted by an alkyl group having 5 to 30 carbon atoms, an alkanoyl group having 5 to 30 carbon atoms, or an aryl group having 6 to 30 carbon atoms.

Abstract: A silane-grafted polyolefin composition is disclosed, and includes a desired reduced specific weight material. The composition finds application in a wide array of uses, and in particular automotive and uses such as weatherstrips, where this composition is used in place of conventional materials such as TPV and EPDM rubber formulations.

Abstract: A process for making preseed particles comprising, consisting of, or consisting essentially of the steps of: mixing initial seed latex particles; a monomer mixture comprising at least one monomer and at least one copolymerizable surfactant, at least one initiator and a chain transfer agent, is disclosed. The preseed particles, a monomer mixture comprising at least one monomer and at least one copolymerizable surfactant, and at least one initiator can then be mixed to form oligomer seed particles. The oligomer seed particles can be used to produce acrylic beads.

Abstract: An object of the present invention is to provide an aqueous dispersion for use in a cosmetic, which has both the flexibility and hair styling properties (hair set retention properties), and which allows for easily re-styling hair when the hair style once set has been disturbed; and a cosmetic including the same. In the above mentioned aqueous dispersion and the cosmetic, a polyurethane is used, which is obtainable from a polyol component including at least one type of a polyether polyol and a polyester polyol, and a polyvalent isocyanate component, wherein the polyol component includes: a polyether polyol containing as a major component a structural unit derived from a polyalkylene glycol having from 2 to 4 carbon atoms, and having a number average molecular weight of 400 or more and 4,000 or less; or a polyester polyol containing a structural unit derived from at least one type of dicarboxylic acid selected from the group consisting of phthalic acid, isophthalic acid and terephthalic acid.

Abstract: A polycondensation product containing a phenolic copolymer useful for a hydraulic-composition dispersant that has stable dispersability and can obtain a prescribed fluidity, including a copolymer obtained by polycondensing a monomeric mixture including compounds A-D of formulas (A)-(D). A hydraulic-composition dispersant containing the product or copolymer. In the formulas, A1O, A2O, A3O, and A4O represent a C2-4 alkylene oxide group; m, n represent a number from 0 to 300 and m+n?1; p, q represent a number from 1 to 300; X represents a hydrogen atom, alkyl group, or C1-24 acyl group; R0, R1 represent a hydrogen atom, alkyl group or alkenyl group; Y1, Y2 represent a hydrogen atom, phosphoester group, or sulfate ester group; Y3 represents a phosphoester or a sulfate ester group; R2 represents a hydrogen atom, carboxyl group, C1-10 alkyl group, C2-10 alkenyl group, phenyl group, napthyl group, or heterocyclic group; r represents a number from 1-100.

Abstract: The invention relates to an in-situ process for preparing an alkylphenol-aldehyde resin. The process comprises the step of providing a raw alkylphenol composition. The raw alkylphenol composition comprises one or more alkylphenol compounds and at least about 1 wt % phenol. Each alkylphenol compound has one or more alkyl substituents. The raw alkylphenol composition is reacted directly, without pre-purification, with one or more aldehydes to form an in-situ alkylphenol-aldehyde resin. The invention also relates to an in-situ alkylphenol-aldehyde resin formed from the in-situ process, and its use in a tackifier composition and rubber composition. The tackifier composition and rubber composition containing the in-situ alkylphenol-aldehyde resin show, inter alia, improved tack performance.

Abstract: The object of the present invention concerns a method for producing flexible polyester urethane foam with increased compression hardness, as well as flexible polyester urethane foam obtainable from the same.

Abstract: An embodiment relates to a polythiol composition for a plastic lens. The polythiol composition for a plastic lens according to the embodiment can produce a clear and transparent plastic lens by way of polymerizing such raw materials as a polythiol compound, an isocyanate, a photoactive color correcting agent, and the like, followed by a simple post-process such as irradiation of ultraviolet rays. In addition, since the process for preparing the lens is simple and economical, the lens is advantageously used for manufacturing various plastic lenses such as eyeglass lenses and camera lenses.

Abstract: The invention relates to a process for preparing a flame-resistant polymer-modified polyol having a solids content of 1 to 65 wt. % wherein (i) at least one polyisocyanate and (ii) an olamine are reacted in (iii) a base polyol having at least two active hydrogen containing groups of which more than 50% are primary active hydrogen containing groups and wherein the olamine has at least one phosphonic ester group attached to a tertiary nitrogen atom and contains at least two hydroxyl groups. The invention further relates to a flame-resistant polymer-modified polyol obtainable with the process of the invention, to a process for preparing optionally foamed plastics using the polymer- modified polyol of the invention, and to the use of a polymer-modified polyol for the preparation of flexible polyurethane foams.

Abstract: An object of the present invention is to provide a crosslinkable composition as a new crosslinking precursor, comprising a multifunctional epoxy compound using a plant component as a raw material, and a cured product obtained by curing the crosslinkable composition. The present invention provides a crosslinkable composition comprising: a plant-based multifunctional epoxy compound; and a crosslinking agent, wherein the multifunctional epoxy compound is obtained by multifunctionalizing limonene oxide, and the crosslinking agent is a polyalkyleneimine.

Abstract: The present disclosure relates to a cyclic polysulfane-based polymer, a cyclic polysulfane-polynorbornene block copolymer, a method of preparing the cyclic polysulfane-based polymer, a method of preparing the cyclic polysulfane-polynorbornene block copolymer, and a film including the cyclic polysulfane-polynorbornene block copolymer.

Abstract: Conjugated copolymers are provided that can be processed in a variety of solvents and can be rendered solvent-resistant when needed. The copolymers can be solution cast from nonpolar, polar, and aqueous solvents. After casting a polymer layer, the polymer can be rendered solvent resistant, thereby providing for improved stability and multi-layer processing and in electrochromic devices where the polymer layer is in contact with a nonpolar or polar solvent or electrolyte. Methods of making the copolymers are also provided, as well as methods of solution casting the polymers from a variety of nonpolar organic, polar, and aqueous solvents. Electrochromic devices are demonstrated having electrode(s) containing these polymers, including a variety of supercapacitor devices capable of using organic, biological, and aqueous electrolytes. Some of these electrodes demonstrate superfast switching and large power densities, showing promise for applications in supercapacitor batteries.

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: A method of forming a crosslinked polymer and an anion, the method comprising the step of reacting a first polymeric substituent comprising a nucleophilic group and a second polymeric substituent comprising an electrophilic group wherein the first polymeric substituent is a substituent of a first polymer and the second polymeric substituent is a substituent of the first polymer or a second polymer. The first and second polymers may be non-conjugated or conjugated. The crosslinked polymers may be used in electrochemical devices, for example battery cells.

Abstract: A graphene nanoribbon has a chiral edge to which a dicarbimide structure is bonded. The dicarbimide structure is an electron-withdrawing group. The width and band gap of the graphene nanoribbon are controlled by a precursor molecule used for a polymerization reaction. Furthermore, n-type operation of the graphene nanoribbon is realized by the dicarbimide structure. In addition, with the graphene nanoribbon, an increase in ribbon length and suppression of a polymerization defect by the stabilization of a reaction intermediate of the precursor molecule, as well as improvement in orientation are realized by the dicarbimide structure.

Abstract: The present invention relates generally to accelerators for the curing of thermosetting resins in the presence of metal compounds, quaternary ammonium and/or phosphonium salts, tertiary amines and/or phosphines and peroxide initiators, and methods of curing thermosetting resins using these accelerators.

Abstract: A terminal modified polybutylene terephthalate resin has a weight average molecular weight Mw of 10,000 to 100,000, a melting point of 210° C. to 235° C., and a melt viscosity ? at 250° C. of not more than 10 Pa·s, and includes 90 to 300 mol/ton of a compound having a (poly)oxyalkylene structure, the compound being terminally bound in the resin, wherein the weight average molecular weight Mw represents a relative weight average molecular weight with respect to the molecular weight of a standard poly(methyl methacrylate) as determined by gel permeation chromatography using hexafluoroisopropanol (supplemented with 0.005 N sodium trifluoroacetate) as a mobile phase.

Abstract: The present invention relates to: a bio-based polycarbonate ester comprising: (i) repeat unit 1 obtained from a condensation reaction of 1,4:3,6-dianhydrohexitol and carbonate; and (ii) repeat unit 2 obtained from a condensation reaction of 1,4:3,6-dianhydrohexitol and 1,4-cyclohexanedicarboxylate; and a preparation method for the bio-based polycarbonate ester, comprising the steps of: (1) preparing a compound represented by formula 3 through a trans-esterification or esterification reaction of a compound represented by formula 2 and phenol; and (2) preparing a compound comprising a repeat unit represented by formula 1 through a polycarbonate melt polycondensation reaction of the compound represented by formula 3 prepared in step (1), a compound represented by formula 4, and 1,4:3,6-dianhydrohexitol.

Abstract: Provided is a method of preparing poly(alkylene carbonate) using a molecular weight regulator in a process of preparing a copolymer of carbon dioxide/epoxide using a novel complex synthesized from salen-type ligand including a quaternary ammonium salt as a catalyst. According to the present invention, even though the molecular weight regulator is used, an activity of the catalyst may be stably maintained, whereby the low molecular weight of poly(alkylene carbonate) having a desirable level may be effectively provided. In addition, it is expected that since the novel complex as the catalyst of the present invention has a simple structure as compared to the existing copolymerization catalyst, due to the economical preparation cost thereof, the novel complex may be effectively applied to a large-scale commercial process.

Abstract: The invention relates to a preparation method of green nylon poly butyrolactams, the biological materials of GABA in vacuum under the condition of high temperature melt decomposition and purified butyrolactams, then by vacuum polymerization of green nylon poly butyrolactams. Compared with the prior art, the invention is prepared by biological method for the synthesis of a wide range of sources, to solve the problem of raw material supply PA4 for mass production, reduce the cost of reaction, and the reaction condition is simple, easy to implement simplified synthesis steps, from the laboratory to the transformation of industrial production.

Abstract: A thermoplastic composition is described herein including a first polyetherimide sulfone having a glass transition temperature of 250 to 290° C., and a second polyetherimide sulfone having a glass transition temperature of 230 to 249° C. The composition has an advantageous combination of optical properties including improved yellowness index, transmission, and haze. A method of manufacturing the thermoplastic composition and articles including the thermoplastic composition are also described. A method for improving the optical properties of a thermoplastic composition is also disclosed, where the method includes melt mixing the first and second polyetherimide sulfones, each having a glass transition temperature as defined herein. The method provides a composition having at least one of improved yellowness, haze, and transmission.

Abstract: A polyimide precursor composition that exhibits excellent tensile strength and breaking elongation, and that provides a film containing an alicyclic polyimide resin; a method for producing a polyimide film using the polyimide precursor composition; and a permanent film that contains an alicyclic polyimide resin and that exhibits excellent tensile strength and breaking elongation. The polyimide precursor composition is a mixture of a resin precursor component which is a polyamic acid including an alicyclic backbone having a predetermined structure, a monomer component that includes an aromatic diamine compound having a predetermined structure or an alicyclic tetracarboxylic acid di-anhydride having a predetermined structure; an imidazole compound having a predetermined structure; and a solvent.

Abstract: A polyphenylene sulfide resin composition includes a polyphenylene sulfide resin (a) of 90 to 50% by weight and a polyphenylene sulfide resin (b) and/or a polyphenylene sulfide resin (c) of the total of 10 to 50% by weight blended with the polyphenylene sulfide resin (a), relative to the total of the polyphenylene sulfide resins (a) to (c) as 100% by weight, in which the polyphenylene sulfide resin composition has a change rate of viscosity of 1.5 times or less when the composition is heated at 320° C. for 5 hours.

Abstract: Amino-functionalized linear and cyclic oligosiloxanes, which have at least two silicon and two oxygen atoms as well as an organoamino group and methods for making the oligosiloxanes are disclosed. Methods for depositing silicon and oxygen containing films using the organoamino-functionalized linear and cyclic oligosiloxanes are also disclosed.

Abstract: A resin composition having lower dielectric constant Dk, lower dielectric loss Df, lower water absorption, higher surface impedance, and higher glass transition temperature includes resins. The resins have a chemical structure selected from a group consisting of or any combination thereof.

Abstract: A silicone-modified polybenzoxazole resin comprising repeating units of formulae (1a) and (1b) is prepared by addition polymerization. R1 to R4 are a C1-C8 monovalent hydrocarbon group, m and n are integers of 0-300, R5 is C1-C8 alkylene or phenylene, a and b are positive numbers of less than 1, a+b=1, and X1 is a divalent linker of formula (2). The resin is flexible, soluble in organic solvents, and easy to use.

Abstract: A hydrogel is dried by a critical point drying technique. The hydrogel may include indicator molecules embedded therein and may be part of a hydrogel-based device, such as, for example, an analyte sensor.

Abstract: A composite gel in one aspect of the present disclosure comprises a substance prepared by gelling a raw material composition that comprises, as main components, a hydroxyl group-containing organic polymer compound and one of a hydroxyl group-containing inorganic compound and an inorganic oxide. A method for manufacturing the composite gel in one aspect of the present disclosure comprises a first process of gelling a raw material composition that comprises, as main components, a hydroxyl group-containing organic polymer compound and at least one of a hydroxyl group-containing inorganic compound or an inorganic oxide; and a second process of drying and subsequently pulverizing a resulting product in the first process to thereby obtain a composite gel fine powder.

Abstract: A method for preparing a “preblend” of nanostructured 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 nanostructured carbon as the shell on the particulate solid core. The preblend may provide particularly improved dispersion of single-walled 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: A process for manufacturing a cross-linked hyaluronic acid (HA) gel product is comprising the steps of: (a) preparing an aqueous mixture of HA and a cross-linking agent selected from multiepoxides and diepoxides; wherein the HA is dissolved in an aqueous solution containing 1-10% (w/w) inorganic hydroxide; and wherein the dissolved HA constitutes more than 10% (w/w) of the final mixture; and (b) subjecting the aqueous mixture to cross-linking conditions to allow the dissolved HA to react with the cross-linking agent so as to obtain a cross-linked HA gel product.

Abstract: Provided is a thermoplastic resin composition which provides a molded body having excellent thermal conductivity and excellent mechanical characteristics. A thermoplastic resin composition which contains (A) a thermoplastic resin, (B) pitch carbon fibers and (C) graphite, and wherein: the content of the graphite (C) is from 1% by mass to 20% by mass (inclusive) relative to 100% by mass of the thermoplastic resin composition; and a molded body, which is obtained by molding this thermoplastic resin composition and has a thickness of 1 mm, has a thermal conductivity of 10 W/mK or more as determined by a hot wire method.

Abstract: Graphene fibers made from a graphene film formed into an elongated fiber-like shape and composite materials made from the graphene fibers. The elongated fiber-like shape may be the graphene film in a rolled spiral orientation or the graphene film in a twisted formation. The graphene film has benzoxazine groups formed on at least an outer surface of the graphene film and epoxide groups formed on at least one edge of the graphene film. Methods of increasing strength of a composite material include combining a resin matrix with a plurality of the graphene fibers to form a prepreg material and curing the prepreg material to form the composite material.

Abstract: A belt with a tensile cord embedded in an elastomeric body, having a polyurea-urethane adhesive composition impregnating the cord and coating the fibers. The composition is reaction product of a polyurethane prepolymer and a diamine curative. The prepolymer is a reaction product of a compact, symmetric diisocyanate and a polyester, polyether, or polycarbonate polyol. The belt body may be of cast polyurethane, vulcanized rubber, or thermoplastic elastomer. The cord may have an adhesive overcoat.

Abstract: Method for open-mold production of a semi-crystalline thermoplastic polyamide matrix fiber-reinforced composite. The matrix has Tg>80° C. and Tf between 280° C. and 200° C. The matrix is prepared in-situ by molten state bulk polycondensation of a reactive precursor composition including A: a first polyamide prepolymer A1 each carrying two identical functions and a second polyamide prepolymer A2 each carrying two identical functions different from and coreactive with those of A1. The reactive precursors may alternatively include B: a prepolymer carrying (on the same chain) two different functions coreactive with each other. The reactive precursors may alternatively include a precursor composition that is a mixture of (A+B). The method involves successive steps of i) preparing the reactive mixture, ii) continuously coating the fibers by deposition-impregnation with the reactive mixture, iii) in-situ bulk polycondensation in an open heated die, and iv) cooling the composite.

Abstract: A friction stir welding method using a resin composition including: a monomer (A) having an ethylenically unsaturated bond; a thermosetting resin (B); a radical polymerization initiator (C); and a fiber reinforcing material (D), wherein the thermosetting resin (B) is an unsaturated polyester resin or a vinyl ester resin.

Abstract: The present invention provides a film having excellent heat resistance and a small difference between the permittivity at low temperatures and the permittivity at high temperatures. The present invention provides a film having a relative permittivity of 8 or more at a frequency of 1 kHz at 30° C., wherein the rate of change is ?8 to +8% as calculated from a relative permittivity A at a frequency of 1 kHz at 30° C. and a relative permittivity B at a frequency of 1 kHz at 150° C. according to the following formula: Rate of change (%)=(B?A)/A×100.

Abstract: There is provided a composition for forming a heat shrinkable film capable of providing a heat shrinkable film capable of having an excellent shrinkage rate and being heat-shrunk at a low temperature. The composition for forming a heat shrinkable film includes a polyethylene terephthalate (PET) resin having an inherent viscosity of 0.50 to 1.2 dl/g, and a polyester based copolymer including a dicarboxylic acid-derived residue including a residue derived from an aromatic dicarboxylic acid and a diol-derived residue including a residue derived from 4-(hydroxymethyl)cyclohexylmethyl 4?-(hydroxymethyl)cyclohexane carboxylate represented by the following Chemical Formula 1 and a residue derived from 4,4-(oxybis(methylene)bis) cyclohexane methanol represented by the following Chemical Formula 2.

Abstract: The present invention is intended to provide a laminated film including a void-provided layer achieving both a high proportion of void space and a high film strength. The laminated film of the present invention includes a void-provided layer 21 and a resin film 10, the void-provided layer 21 being stacked on the resin film 10. The laminated film is produced by a production method, including steps of forming a void-provided structure 20?, which is a precursor of the void-provided layer 21 on the resin film; and causing a crosslinking reaction in the precursor 20? after the precursor forming step. The precursor 20? contains a substance that generates a basic substance by light irradiation or heating, the basic substance is not generated in the precursor forming step, the basic substance is generated by light irradiation or heating in the crosslinking reaction step, and the crosslinking reaction step has multiple stages.

Abstract: Organic infrared attenuation agents have been developed to improve the thermal insulation properties of polymeric foams such as polystyrene low density foams. The organic infrared attenuation agents can include polyols such as sorbitol, maltitol, and poly(ethylene glycol), polysaccharides such as starch or cellulose, and infrared attenuation polyesters such as polybutylene terephthalate. The organic attenuation agents include aromatic compounds or carbon oxygen bonds that are effective in absorbing infrared radiation at the desired wavelengths.

Abstract: Polymer foam contains a continuous matrix of styrenic polymer that has metal oxide particulates selected from a group consisting of alumina boehmite and magnesium oxide and brominate styrene/butadiene copolymer dispersed therein.

Abstract: The present invention refers to an expanded polymeric material which consists of at least 150 phr, preferably at least 180 phr, but less than 500 phr ingredients in total, comprising 100 phr of at least two polymers, of which at least 40 phr is at least one polyolefin homopolymer and at least 20 phr is at least one styrene butadiene thermoplastic elastomer (TPE-s), the process of manufacturing such a material and the use of such a material.

Abstract: A composition for an expandable sealant including at least one polymeric material selected from the group consisting of low density polyethylenes (LDPE), linear low density polyethylenes (LLPDE), ethylene vinyl acetate (EVA), ethylene methacrylate (EMA), and ethylene-butyl acrylate (EnBA); and a chemical blowing agent, wherein the composition is substantially free of a cross-linking agent.

Abstract: Disclosed are azeotropic or azeotrope-like compositions containing Z-1,1,1,4,4,4-hexafluoro-2-butene and methyl perfluoropropyl ether. Also disclosed is process of using the azeotropic or azeotrope-like composition as blowing agents for preparing a thermoplastic or thermoset foam. Also disclosed is a process of using the azeotropic or azeotrope-like composition as a refrigerant for producing cooling or heating. Also disclosed is a process of using such azeotropic or azeotrope-like compositions as solvents. Also disclosed is a process of using the azeotropic or azeotrope-like composition as propellants for producing an aerosol. Also disclosed is a process of using such azeotropic or azeotrope-like compositions as heat transfer media. Also disclosed is a process of extinguishing or suppressing a fire by using such azeotropic or azeotrope-like compositions. Also disclosed is a process of using such azeotropic or azeotrope-like compositions as dielectrics.

Abstract: The present invention provides porous particles uniform in shape and having through holes that are not closed. The porous particles according to the present invention are porous particles having a substantially spherical shape. Each of the porous particles has an interconnected pore structure in which through holes provided inside the porous particle communicate with each other, and ends of the through holes are open toward an outside of the porous particle.

Abstract: An unvulcanized liquid or solid silicone rubber containing a proportion of a filler material that expands at an increased temperature.

Abstract: The present invention relates to a novel silicone rubber syntactic foam and the silicone precursor of said foam.

Abstract: The present invention relates to a novel secondary battery pack with improved thermal management useful for an all-electric vehicle (EV), a plug-in hybrid vehicle (PHEV), a hybrid vehicle (HEV), or battery packs used for other vehicles batteries, and more particularly, to the use of a specific material for thermally insulating a secondary battery pack and further minimizing the propagation of thermal runaway within a battery pack.

Abstract: A reusable, fiber containing pulp product is described that is highly suited for use in the manufacture of paper products. The reusable, fiber containing pulp product provides a mixture of fibers and small, dense polymer/particle fragments. The polymer/particle fragments within the reusable, fiber containing pulp product have a size range and density that facilitates efficient removal of the polymer/particle fragments using pressure screens.

Abstract: A polyester material including a composite having a carbon nanostructure, which comprises carbon element, from 0.5 to 4 wt % of a first non-carbon non-oxygen element substance, and from 0 to 4 wt %, of a second non-carbon non-oxygen element. The first non-carbon non-oxygen element is selected from the group consisting of P, Si, Ca, Al and Na; the second non-carbon non-oxygen element is any one selected from the group consisting of Fe, Ni, Mn, K, Mg, Cr, S or Co, or a combination of at least two selected therefrom. The G peak and D peak of the carbon element in the Raman spectrum has a peak height ratio of 1-20 in the composite having a carbon nanostructure.