Abstract: Affinity purification of platelet-derived growth factor-binding heparan sulphate from porcine mucosa (HS6) is disclosed. Also disclosed is the use of HS6 in repair and regeneration of the skin for treating wounds, burns, ulcers and other skin injuries.

Abstract: The present invention provides a modified conjugated diene-based polymer which includes a functional group derived from a substituted styrene-based compound and a functional group derived from an aminosilane-based compound, a method for preparing the same, and a rubber composition including the same. The modified conjugated diene-based polymer includes the functional group derived from an aminosilane-based compound of Formula 1 and a functional group derived from a substituted styrene-based compound of Formula 2 at both terminals of a main chain, and thus, shows a high modification ratio. When applying the polymer in a rubber composition, excellent affinity with a filler may be shown, and as a result, agglomeration of a filler in the rubber composition may be prevented, and the dispersibility of the filler may be increased, thereby improving the processability of the rubber composition.

Abstract: Methods for the production of heterophasic polymers in gas and slurry phase polymerization processes, and polymer compositions made therefrom, are disclosed herein.

Abstract: A method for making a polyisobutylene diol from a polyisobutylene diallyl. The method includes hydroborating the polyisobutylene diallyl to produce a polyisobutylene dialkyl borane, and oxidizing the polyisobutylene dialkyl borane to form the polyisobutylene diol. The polyisobutylene diallyl is hydroborated by combining in situ the polyisobutylene diallyl with a borane-coordinating solvent, an alkaline metal salt of borohydride, and an acid. The alkaline metal salt of borohydride is combined with the polyisobutylene diallyl before the acid is combined with the polyisobutylene diallyl.

Abstract: A modified PVA that enables formation of a film superior in cold water solubility, mechanical strength, and chemical resistance is provided. The modified PVA comprises a monomer unit represented by formula (I), and a structural unit represented by formula (II): wherein: a content of the monomer unit (I) is from 0.05 mol % to 10 mol %, and a content of the structural unit (II) is from 0.001 mol % to 0.5 mol % with respect to the total monomer units in the modified PVA; a viscosity average degree of polymerization is from 300 to 3,000; and a degree of saponification is from 82 mol % to 99.5 mol %. In the formula (I): R1 represents a hydrogen atom, or a methyl group; and R2 represents —R3—SO3?X+, —R3—N+(R4)3Cl?, or a hydrogen atom, R3 representing an alkanediyl group, X+ representing a hydrogen atom, a metal atom, or an ammonium group, and R4 representing an alkyl group.

Abstract: Provided are a modified hydrocarbon resin that can provide a hot-melt adhesive composition with low odor, low Gardner color and high peel adhesion, a method for producing the resin, and the hot-melt adhesive composition. A modified hydrocarbon resin comprising a 1,3-pentadiene monomer unit, a C4-C6 alicyclic monoolefin monomer unit, a C4-C8 acyclic monoolefin monomer unit, an alicyclic diolefin monomer unit, and an aromatic monoolefin monomer unit, and containing a carboxyl group or acid anhydride group, wherein a weight average molecular weight (Mw), a Z average molecular weight (Mz), a ratio (Mz/Mw), a Gardner color scale of a 50 mass % toluene solution, a softening point, and an acid value are in specific ranges.

Abstract: A process for preparing a solid catalyst component for the homopolymerization or copolymerization of CH2?CHR olefins, wherein R is hydrogen or hydrocarbyl radical with 1-12 carbon atoms, including a step (a), at a temperature ranging from 0 to 150° C., of reacting a Mg based compound of formula (MgClmX2-m).nLB, wherein m ranges from 0 to 2, n ranges from 0 to 6, X is, independently R1, OR1, —OCOR1 or O—C(O)—OR1 group, wherein R1 is a C1-C20 hydrocarbon group and LB is a Lewis base with a liquid medium made from or containing a Ti compound, having a Ti—Cl bond, in an amount such that the Ti/Mg molar ratio is higher than 3 and a Bi compound dissolved or dispersed in the liquid medium, wherein the solid catalyst compound is made from or contains the Ti compound, the Bi compound and optionally an electron donor on a Mg chloride based support.

Abstract: The present invention relates to [1] a colored fine particle dispersion containing colored fine particles and a neutralizing agent, in which the colored fine particles are produced by subjecting a monomer mixture containing an acid group-containing polymerizable monomer to emulsion polymerization in the presence of a pigment; the neutralizing agent contains a water-soluble amine compound; and the colored fine particle dispersion has a pH value of from 6 to 11, and [2] a process for producing a colored fine particle dispersion containing colored fine particles and a neutralizing agent, said process including the step 1 of subjecting a monomer mixture containing an acid group-containing polymerizable monomer to emulsion polymerization in the presence of a pigment to obtain a colored fine particle dispersion (p); and the step 2 of mixing the colored fine particle dispersion (p) and the neutralizing agent containing a water-soluble amine compound to obtain the colored fine particle dispersion having a pH value of

Abstract: A polymeric foam precursor composition including the following components: (a) a di- or tri-functional (meth)acrylate oligomer (2); (b) a di- or higher-functional thiol compound (3); and (c) a borane compound (4) as initiator. The foam precursor composition can be isocyanate free, and the curing rate is largely moisture independent and can cure at low temperatures, below freezing point.

Abstract: A binder composition for a non-aqueous secondary battery electrode contains a water-soluble polymer including, in a proportion of at least 0.1 mass % and not more than 20 mass %, a monomer unit derived from a monomer represented by general formula (1): CH2?C(R1)—NH—R2—OH (R1 is hydrogen or an alkyl group and R2 is (CHR3)n(O(CHR3)m)l [n=1 to 10; m=1 to 4; l=0 to 3; and R3 is hydrogen or an alkyl group having a carbon number of 1 to 4]).

Abstract: Bimodal polypropylene compositions and a process to form melt blended bimodal polypropylene compositions comprising combining at least two polypropylenes in at least a two-pass process, and forming a bimodal polypropylene composition having a Flexural Modulus (190° C., 1% secant) of at least 1700 MPa, as well as one or more other selected properties. These compositions are suitable for thermoformed articles and injection molded articles, any of which may be foamed.

Abstract: Provided in the present invention are an olefin polymerization apparatus and an olefin polymerization process. The following operations and effects can be realized by the apparatus or method provided in the present invention: the gas material discharged from the polymerization reactor is condensed, after the gas-liquid separation, the resulting gas portion is recycled to the reactor to form a circulation loop; the condensate can be selectively introduced to the polymerization reactor, in order to achieve the free switch between the homopolymerization reaction and the copolymerization reaction or between different copolymerization reactions, and at the same time the condensate can absorb the heat generated by the reaction. By using the apparatus and method provided in the present invention, polyolefin products having excellent mechanical properties and processability can be prepared as needed.

Abstract: Disclosed herein are ethylene-based polymers generally characterized by a Mw ranging from 70,000 to 200,000 g/mol, a ratio of Mz/Mw ranging from 1.8 to 20, an 1B parameter ranging from 0.92 to 1.05, and an ATREF profile characterized by one large peak. These polymers have the dart impact, tear strength, and optical properties of a metallocene-catalyzed LLDPE, but with improved processability, melt strength, and bubble stability, and can be used in blown film and other end-use applications.

Abstract: The invention pertains to a fluoroelastomer composition comprising: (a) a vinylidene fluoride-based fluoroelastomer [fluoroelastomer (A)] comprising recurring units derived from vinylidene fluoride (VDF) and recurring units derived from at least one additional (per)fluorinated monomer; said fluoroelastomer (A): —possessing a polydispersity index (IMWD) of between 1.5 and 3.

Abstract: Polymers having mechanical properties approaching or exceeding commercial elastomers and engineering thermoplastics, but improved biostability, are described herein. In one embodiment, the polymers have a hard segment containing one or more disulfoxide or disulfone moieties and a soft segment connected to the hard segment to form an elastomeric polymer. The polymer is resistant to oxidation and/or hydrolytic degradation, particularly in vivo, which allows for the use of these materials in implants/devices which are implanted for an extended period of time. The ratio or percentage by weight of soft segment to hard segment can be varied based on the physical and mechanical properties of the desired device.

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 to form a first composition comprising a functionalized olefin-based polymer comprises: a) polymerizing a composition comprising an olefin to form a reaction product comprising an olefin-based polymer; b) subjecting at least a portion of the reaction product to at least one devolatilization to form a polymer-rich melt, wherein step b) occurs downstream from and in-line with step a); and c) reacting at least a portion of the polymer-rich melt with at least one functionalization agent and, optionally, at least one free-radical initiator to form the first composition, wherein step c) occurs downstream from and in-line with step b), wherein “the viscosity of the functionalized olefin-based polymer (177° C./350° F.)” to “the viscosity of the olefin-based polymer (177° C./350° F.)” is from 0.1 to 5.0.

Abstract: The nano-fibre derivative method includes polymerization of 3-methoxthiophene (MOT) monomer on Poly(acrylonitrile co-itaconic acid) matrix and by use of electro-spinning of the produced nano-particulate.

Abstract: The present invention relates to an initiator mixture, a composition, use thereof, a process of preparing polymer polyol, and a polymer polyol obtained by the process. The initiator mixture comprises: a first peroxide of formula (I) R1—O—O—R2, wherein R1 and R2 are independent an alkyl group or an alkanoyl group comprising 1 to 30 carbon atoms, preferably 3 to 20 carbon atoms, and more preferably 4 to 20 carbon atoms; and a second peroxide of formula (II) R3—O—O—R4—O—O—R5, wherein R3 and R5 are independently an alkyl group comprising 1 to 30 carbon atoms, preferably 3 to 20 carbon atoms, and more preferably 5 to 10 carbon atoms, and R4 is a cycloalkylene group comprising 3 to 30 carbon atoms, preferably 4 to 20 carbon atoms, and more preferably 5 to 10 carbon atoms.

Abstract: A molded product according to the present invention is a molded product obtainable by polymerizing and curing a polymerizable composition including: a polyisocyanate compound (A); a polyol compound (B) which is represented by Formula (1) and which has a number average molecular weight of equal to or greater than 100; a bifunctional or higher functional active hydrogen compound (C) (here, excluding the compound (B)); and a photochromic compound (D), in which a concentration of SH groups measured by an IR analysis method is less than 1.0 wt %.

Abstract: The present invention relates to methods for curing alkenyl ether groups-containing polyurethanes with moisture-reactive end groups by means of a two-stage curing process. The invention further relates to alkenyl ether group-containing polyurethanes with silicon-containing end groups as well as to the cured polymers which can be obtained by means of the method according to the invention and to the products containing them.

Abstract: A composition is provided for making a polyurethane that may be incorporated in various products, such as a sealant, a coating, a caulk, an electric potting compound, a membrane, a sponge, a foam, an adhesives, and a propellant binder. The composition includes one or more polyols, one or more isocyanate-group containing compounds having an isocyanate group functionality of at least two, and optionally one or more chain extenders. At least one of the polyols is a farnesene-based polyol having a number average molecular weight less than or equal to 100,000 g/mol and a viscosity at 25° C. less than 10,000 cP. The farnesene-based polyol may be a homopolymer or a copolymer of farnesene. The composition may also comprise additional polyols, such as a polyol of a homopolymer or copolymer of a polydiene. Methods of preparing a polyurethane are also provided.

Abstract: The present invention relates to an organic aerogel obtained by reacting an isocyanate compound having a functionality equal or greater than 2 and a cyclic ether compound having a functionality equal or greater than 2 in a presence of a solvent. An organic aerogel according to the present invention provides good thermal insulation and good mechanical properties.

Abstract: Polyurethane foams including a polyurethane prepolymer composition, a catalyst, and a propellant are provided. The polyurethane prepolymer composition is produced from a formulation that includes an isocyanate reactive component in an amount of from about 1% to about 70% by weight based on the polyurethane prepolymer composition and an isocyanate component in an amount of from about 1% to about 70% by weight based on the polyurethane prepolymer composition. The isocyanate component includes toluene diisocyanate biuret in an amount of from about 1 to about 100% by weight based on the isocyanate component. The isocyanate reactive component includes one or more polyols. The polyurethane prepolymer composition has a viscosity of less than about 10,000 mPa*s at 50° C. and is substantially free of monofunctional reactive components. The polyurethane prepolymer composition also includes a free isocyanate monomer content of the toluene diisocyanate biuret of less than about 1% by weight.

Abstract: The present invention provides soluble, stable singlet fission (SF) compounds, compositions, materials, methods of their use, and methods for their preparation that provide efficient intramolecular singlet fission (iSF) and multiple excitons. The SF compound may be a dimer, an oligomer, or a polymer of polyoligoacenes, where for example, the compound achieves a triplet yield reaching about 200% per absorbed photon. In this system, SF does not depend on intermolecular inter-actions. Instead, SF is an intrinsic property of the molecule and therefore occurs independent of intermolecular interactions. Singlet fission has the potential to significantly improve the photocurrent in single junction solar cells and thus raise the Shockley-Queisser power conversion efficiency limit from about 33% to about 46% or greater. Quantitative SF yield at room temperature has only been observed in crystalline solids or aggregates of higher acenes.

Abstract: A process of forming a flame retardant polylactide includes forming a flame retardant lactide monomer. The process also includes forming a lactide feedstock that includes at least the flame retardant lactide monomer. The process further includes polymerizing the lactide feedstock to form a flame retardant polylactide.

Abstract: A polyester including ethylene 2,5-furandicarboxylate units is prepared in a process, where in an esterification step a 2,5-furandicarboxylate compound is reacted with ethylene glycol to form an ester composition, including components with 2-hydroxyethyl and 2,5-furandicarboxylate moieties; where in a polycondensation step the ester composition thus obtained is subjected to polycondensation at reduced pressure in the presence of a polycondensation catalyst to obtain a polycondensate; and where during the polycondensation step 2,5-furandicarboxylic acid is added to the ester composition.

Abstract: The invention relates to a polyester resin for toner to be used in the development of an electrostatic image or magnetic latent image in electrophotography, electrostatic recording, electrostatic printing, or the like, a method for producing a polyester resin for toner, and a toner, and an object of the invention is to provide, with excellent productivity and stability, a polyester resin for toner having excellent storage stability, hot offset resistance, and low temperature fixing property as toner while still considering the environmental protection and safety. A polyester resin for toner contains 40 mol % or more and 60 mol % or less of structural units derived from tri- or higher hydric carboxylic acids based on 100 mol % of structural units derived from all acid components, and has a metal content of 100 ppm or less.

Abstract: A process of forming a lactide copolymer includes forming a dimethylidene lactide molecule from an L-lactide molecule. The process also includes forming a functionalized lactide monomer from the dimethylidene lactide molecule. The process includes forming a mixture that includes the functionalized lactide monomer and a bisphenol A (BPA) monomer or a BPA-derived monomer. The process further includes polymerizing the mixture to form a lactide copolymer.

Abstract: A process of forming a bottlebrush polymer includes forming a poly(methylidenelactide) (PML) material from an L-lactide molecule. The process also includes forming a lactide feedstock that includes a blend of a first amount of an L-lactide monomer and a second amount of the PML material. The process further includes polymerizing the lactide feedstock to form a bottlebrush polymer.

Abstract: Certain embodiments are directed to cyanate resin blends comprising, for example, a mixture of a cyanate monomer and a cyanate oligomer. The resin blends are effective to provide a dielectric constant of less than 2.7, a glass transition temperature of at least 150° C. and a moisture absorption of less than 1.5%. Radomes using the resin are also described.

Abstract: A process to prepare polycarbamate comprising adding urea to a polyol in the presence of at least one catalyst selected from the group consisting of compounds having the following formula MmZn; wherein M is a divalent metal, and Z is an anionic functionality or a functionality capable of forming a covalent bond with M and wherein n times a valence number of Z equals X and m times two equals Y wherein the absolute value of X equals the absolute value of Y is provided. Also provided are a polycarbamate produced according to the process and a coating composition comprising the polycarbamate.

Abstract: A method of manufacture of a polyetherimide composition includes contacting a substituted phthalic anhydride and an organic diamine in the presence of diphenyl sulfone, sulfolane, or a combination comprising at least one of the foregoing solvents at a temperature of greater than 130° C. to provide a bis(phthalimide) composition comprising diphenyl sulfone, sulfolane, or a combination comprising at least one of the foregoing solvents and a bis(phthalimide); and polymerizing the bis(phthalimide) and an alkali metal salt of a dihydroxy aromatic compound in the presence of diphenyl sulfone, sulfolane, or a combination comprising at least one of the foregoing to form a polyetherimide. The method does not require any catalyst either for the imidization or the polymerization.

Abstract: The invention relates to a method for producing polymers, particularly polyhydroxyurethanes (PHU) from alkenyl ether polyols or pre-polymers that contain monomer units derived from such alkenyl ether polyols, and polythiol compounds, as well as to a method for crosslinking compounds containing alkenyl ether groups, with polythiol compounds. The invention also relates to the polymers and crosslinked polymers that can be obtained using the method according to the invention.

Abstract: Provided is an addition-curable organopolysiloxane resin composition capable of forming a cured product having a superior transparency, heat resistance and light resistance. The addition-curable organopolysiloxane resin composition contains: (A) an organopolysiloxane having in one molecule at least two silicon-atom-bonded alkenyl groups each having 2 to 10 carbon atoms; (B) an organohydrogenpolysiloxane having in one molecule at least two silicon-atom-bonded hydrogen atoms; (C) a platinum group metal-based catalyst; and (D) a barium compound represented by the following formula (1) Ba(OR)2 ??(1) wherein R represents a monovalent hydrocarbon group having 1 to 10 carbon atoms; or an acyl group having 2 to 15 carbon atoms.

Abstract: The invention relates to a method for producing polymer materials (P), preferably polysiloxanes, having at least one carboxylic acid ester group, in particular (meth)acrylate-containing polysiloxanes, wherein the process is carried out in the presence of reaction products (U) of metal salts, in particular chromium(III) salts, and primary amines.

Abstract: Complex shaped bodies of silicone are produced by ballistic 3D DOD printing by employing a silicone resin-based composition curable by hydrosilylation, which exhibits a high shear thinning behavior and a rapid viscosity recovery rate alter removal of shear.

Abstract: In an aspect, a method of synthesizing a graft copolymer comprises the steps of: copolymerizing a first macromonomer and a first reactive diluent; wherein said first macromonomer comprises a first backbone precursor directly or indirectly covalently linked to a first polymer side chain group; wherein said reactive diluent is provided in the presence of the first macromonomer at an amount selected so as to result in formation said graft copolymer having a first backbone incorporating said diluent and said first macromonomer in a first polymer block characterized by a preselected first graft density or a preselected first graft distribution of said first macromonomer. In some embodiments of this aspect, said preselected first graft density is any value selected from the range of 0.05 to 0.75. In some methods, the composition and amount of said diluent is selected to provide both a first preselected first graft density and a first preselected first graft distribution.

Abstract: A process for preparing an algal powder containing a reduced content of proteins, a bioplastic composition formed from such a powder, a process for manufacturing a plastic product obtained from such an algal powder and also the plastic product obtained in this way. Process for preparing an algal powder, especially intended for the manufacture of a plastic product, including the successive steps of: culturing and/or harvesting an algal biomass; reducing by at least 10% the intrinsic amount of proteins of the algae, by weight relative to the weight of proteins of the harvested biomass; drying; and reducing to give powder or granules.

Abstract: The present invention relates to a method for manufacturing hydrophilic biopolymers, particularly hydrophilic cellulosic material, particularly cellulose nanofibers like micro- or nanofibrillated cellulose, as described in claim 1; to novel materials comprising hydrophilic biopolymers and to the use of such hydrophilic biopolymers.

Abstract: The present disclosure provides (block co-polymer)-(metal organic framework) conjugates (BCPMOFs), such as (block co-polymer)-(metal organic nanostructure) conjugates (BCPMONs), and thermoplastic elastomers, gels, and compositions thereof. Exemplary BCPMONs include (block co-polymer)-(metal organic cage) conjugates (BCPMOCs), (block co-polymer)-(metal organic paddlewheel) conjugates, and (block co-polymer)-(metal organic square) conjugates, such as BCPMONs of Formula (A), (B), or (C). Also described herein are macromonomers for preparing the BCPMONs; thermoplastic elastomers, gels, and compositions involving the BCPMONs; methods of preparing the BCPMONs, thermoplastic elastomers, gels, and compositions; and methods of using the BCPMONs, thermoplastic elastomers, gels, and compositions.

Abstract: The present disclosure provides a solvent for alignment film material including 1-Methyl-2-pyrrolidinone, 2-Butoxyethanol, and 1,2-diethoxy-ethan. The present disclosure also provides an alignment film solution and a manufacturing method for alignment film. Through the present disclosure, the uniformity of the alignment film solution's coating is enhanced.

Abstract: A composite material is provided including an elastomeric polymer matrix and undercooled liquid metallic core-shell particles disposed in the matrix, wherein the particles each have an outer shell and a liquid metallic material as a core contained within the outer shell. The outer shell is frangible such that the liquid metallic material is released from at least some of the particles in response to a mechanical load applied to the composite and solidifies in-situ in the polymer matrix. As a result, the composite material can be self-strengthening and self-healing and can be reconfigurable in shape at ambient temperature.

Abstract: A thermoplastic starch composition acquired from compounding a mixture comprises starch-containing agricultural waste in 45 to 70% by weight of total composition that the agricultural waste contains starch content less than 50% in dry weight; thermoplastic synthetic polymer in 25 to 50% by weight of total composition; plasticizer in 1 to 10% by weight of total composition; and coupling agent in 1 to 5% by weight of total composition; wherein the compounding is performed at a first temperature which is higher than room temperature.

Abstract: A highly loaded and well-dispersed masterbatch composition and process for making thereof from a split stream process. The masterbatch composition includes a colorant, a thermoplastic carrier, a metallocene polymer processing aid, and optionally an additive. The split stream may be formed of a primary feed and a secondary feed. The primary and second feeds are combined by at least one of the following: supplying the secondary feed in either the same feed port as the primary feed, in a stream located upstream the primary feed, in a stream located downstream the primary feed, or a combination thereof.

Abstract: A method of producing treated ion exchange resin material includes exposing an enclosed vessel containing ion exchange resin and a pre-treatment solution to high energy radiation. The treated ion exchange resin material has reduced organic impurities or total organic carbon (TOC).

Abstract: Provided is a composition capable of providing a formed article that, even when using continuous fibers, has excellent interfacial adhesion between the continuous fibers and a matrix resin, and as a result, has excellent mechanical strength (e.g., impact resistance and flexural strength). One aspect of a composition according to the present invention includes a polymer (A) including an amino group, fibers (B), and a thermoplastic resin (C), in which a content ratio of the fibers (B) is 70 parts by mass or more and 250 parts by mass or less based on 100 parts by mass of the thermoplastic resin (C). Another aspect of the composition according to the present invention includes a polymer (A) including an amino group, a non-woven fabric (B?), and a thermoplastic resin (C).

Abstract: (A) A reinforcing fiber, (B) a resin particle, and (C) a matrix resin are combined to prepare a resin composition which improves a reinforcing effect by the reinforcing fiber. The reinforcing fiber (A) contains a carbon fiber. The resin particle (B) contains a semicrystalline thermoplastic resin, the semicrystalline thermoplastic resin in the resin particle (B) has an exothermic peak in a temperature range between a glass transition temperature of the semicrystalline thermoplastic resin and a melting point of the semicrystalline thermoplastic resin, the peak being determined by heating the resin particle (B) at a rate of 10° C./min. by differential scanning calorimetry (DSC), and the resin particle (B) has an average particle size of 3 to 40 ?m. The semicrystalline thermoplastic resin may be a polyamide resin having a melting point of not lower than 150° C. (particularly, a polyamide resin having an alicyclic structure and a glass transition temperature of not lower than 100° C.

Abstract: A fiber reinforced polyester polymer composition is disclosed that contains at least one tribological modifier. The tribological modifier may comprise an ultra-high molecular weight silicone alone or in combination with polytetrafluoroethylene particles. The composition not only has excellent tensile properties but also can produce a low friction surface.

Abstract: A method for producing a lignocellulose plastic composite material, in particular a simpler and more cost-effective option for producing lignocellulose plastic composite materials. Thermoplastic particles and a mixture of water and lignocellulose-containing particles are supplied to a refiner, and the lignocellulose-containing particles are reduced to fibres in the refiner. The thermoplastic particles are supplied to the refiner in a melted or fused state, or are melted or fused in the refiner, so that the melted or fused thermoplastic particles and the lignocellulose-containing particles that are reduced to fibres form material composite particles in the refiner.