Abstract: Disclosed herein are solution polymerization processes for producing a high-cis polydiene. The processes include polymerizing at least one conjugated diene monomer in an organic solvent in the presence of at least one thiol compound and a lanthanide-based catalyst composition to produce a polydiene having a cis-1,4-linkage content of 90-99%. The at least one thiol compound is represented by the general formula R—S—H, where R is a hydrocarbyl group or a substituted hydrocarbyl group. The lanthanide-based catalyst composition comprises (a) a lanthanide compound, (b) an alkylating agent, and (c) a halogen source, where (c) may optionally be provided by (a), (b), or both (a) and (b). The molar ratio of the at least one thiol compound to the lanthanide compound used in the polymerization process ranges from 0.01:1 to 100:1. Improved solution polymerization processes regarding the same are also disclosed herein.

Abstract: To provide an industrially useful ?-olefin•((meth)acrylic acid)-based olefin copolymer having both a high molecular weight and a high comonomer content, a catalyst component capable of realizing a production of two different kinds of ?-olefin•((meth)acrylic acid)-based olefin copolymers, and a production process using the catalyst. An ?-olefin•((meth)acrylic acid)-based olefin copolymer is produced by using a metal complex complexed with a ligand represented by the following formula (Y is phosphorus or arsenic) for a catalyst composition.

Abstract: In some aspects, polymeric yarns and communications cables incorporating the same are provided herein. Additionally, in some aspects, methods of producing polymeric yarns and communications cables incorporating the same are provided.

Abstract: The present invention provides a crosslinkable prepolymer which can be used to produce crosslinked polymeric materials (or contact lenses containing the same) having a high strength and excellent durability. The present invention relates to a polyvinyl alcohol-based prepolymer containing a unit having a pendant 1,2-diol containing group and a unit having a specific crosslinkable functional group, as well as a molding using the same.

Abstract: A ?-conjugated aromatic/heteroaromatic oligomer-containing vinyl monomer is generally provided, which can include a polymerizable group, a linker group, and a ?-conjugated aromatic/heteroaromatic side chain. The ?-conjugated aromatic/heteroaromatic side chain includes a first cyclopentadiene ring covalently attached to the linder group, a set of second cyclopentadiene rings covalently attached to the first cyclopentadiene ring, and a third cyclopentadiene ring positioned at a terminal end of the ?-conjugated aromatic/heteroaromatic side chain such that the set of second cyclopentadiene rings is positioned between the first cyclopentadiene ring and the third cyclopentadiene ring. Methods are also provided for forming a polymer via polymerizing the ?-conjugated aromatic/heteroaromatic oligomer-containing vinyl monomer, and for grafting a ?-conjugated aromatic/heteroaromatic oligomer-containing polymer onto a surface of a nanomaterial.

Abstract: Disclosed are a method of preparing a rubber-reinforced graft copolymer and a rubber-reinforced graft copolymer prepared using the method. According to the present disclosure, provided are a method of preparing an ?-methylstyrene-based rubber-reinforced graft copolymer which may enhance polymerization productivity and heat resistance, and a rubber-reinforced graft copolymer prepared using the method.

Abstract: The present invention relates to a composition comprising a polymeric elastomeric phase and an odoriferous active compound. In particular the present invention relates to a composition comprising a polymeric elastomeric phase and an odoriferous active compound and releasing said odoriferous active compound over a given period of time. The present invention concerns also objects comprising a polymeric elastomeric phase and an odoriferous active compound and releasing said odoriferous active compound over a given period of time.

Abstract: Conjugated diene monovinylarene block copolymers having superior kink resistance properties are disclosed. These copolymers can be used to produce tubing and other end-use articles, and can be a replacement for flexible PVC.

Abstract: Stereoregular diblock polybutadiene composed of a polybutadiene block having a 1,4-cis structure and a polybutadiene block having a syndiotactic 1,2 structure. Said stereoregular diblock polybutadiene can be advantageously used in both the footwear industry (for example, in the production of soles for shoes) and in the production of tires for motor vehicles and/or trucks.

Abstract: Stereoregular diblock polybutadiene composed of a polybutadiene block having a 1,4-cis structure and a polybutadiene block having a syndiotactic 1,2 structure. Said stereoregular diblock polybutadiene can be advantageously used in both the footwear industry (for example, in the production of soles for shoes) and in the production of tires for motor vehicles and/or trucks.

Abstract: The present invention relates to a method to form a polyurethane material, a catalyst composition comprising metalized polyhedral oligomeric silsesquioxanes (POMS) compounds in combination with reactive compounds suitable to be used to provide a polyurethane material and the polyurethane material obtained using the catalyst composition.

Abstract: Novel polyurea prepolymer and quasi-prepolymers are contemplated, the compositions being the reaction products of various isocyanate components with various polyamine components. Isocyanate components contemplated include uretonimine-modified 4,4? methylene diphenyl diisocyanate (MDI) 4,4? MDI, 2,4? MDI, aliphatic hexamethylene diisocyanate (HDI) trimer, HDI allophanate, and aliphatic HDI biuret. Polyamine components contemplated include primary amine-terminated poly(oxypropylene), secondary isopropylamine-terminated poly(oxypropylene), tetraethyl N,N?-(methylenebis(2-methyl-4,1-cyclohexanediyl)) bisaspartate, and poly[(3-aminopropyl)methylsiloxane-co-diphenylsiloxane].

Abstract: The invention relates to stable silicon dioxide dispersions and also their use for producing polyurethanes. The silicon dioxide dispersions are largely or preferably completely free of water and comprise silicon dioxide particles having an average diameter of 1-150 nm and at least one chain extender. The silicon dioxide particles can be modified by means of a silane (S) which comprises groups which are reactive toward isocyanates. Furthermore, a polyol, in particular a polyesterol and/or an isocyanate-comprising compound can be comprised in the silicon dioxide dispersions.

Abstract: A process for production of polyurethane systems using polyether polycarbonate polyols with use of additives comprising i) ionic surfactant A selected from those of the formula A?M+ with A?=anion selected from the group comprising alkyl- and arylsulphates, polyethersulphates and -sulphonates, sulphonates, alkyl- and arylsulphonates, alkyl- and arylcarboxylates, saccharinates and polyetherphosphates, and M+=cation, b) ionic surfactant B selected from a quaternized ammonium compound, c) tertiary amine compound C having a molar mass of preferably at least 150 g/mol, and/or d) oxazasilinane D is described, as are correspondingly produced polyurethane systems, preferably polyurethane foams, and the use thereof.

Abstract: A polyurethane reaction system includes an isocyanate component having at least one polyisocyanate and an isocyanate-reactive component having a storage stable polyol component that is a single phase liquid mixture at 23° C. including a first polyether polyol and a second polyether polyol. The first polyether polyol is included in an amount from 20 wt % to 90 wt %, based on total weight of the polyol component, is a glycol based polyoxypropylene-polyoxyethylene polyether polyol having number average molecular weight from 1500 g/mol to 1975 g/mol, and has a polyoxyethylene content from 26 wt % and 34 wt % based on a total weight of the first polyether polyol. The second polyether polyol is included in an amount from 10 wt % to 80 wt %, based on total weight of the polyol component, has a number average molecular weight from 750 g/mol to 4000 g/mol, and has a melting point higher than 23° C.

Abstract: The present invention provides a polyol composition including a polyol having a polyester chain, wherein the polyol composition substantially contains no metal-base polymerization catalyst and an amount of phosphorus element derived from a polymerization catalyst is 1 to 1000 ppm. Furthermore, a method for producing a polyol composition is provided, including reacting a compound having an active hydrogen with a compound having at least one selected from the group consisting of carboxyl group, ester group and acid halide group in the presence of 0.0001-0.05 parts by mol of a phosphorus compound with respect to 1 part by mol of the active hydrogen without using a metal-based polymerization catalyst.

Abstract: A reaction system for forming polyurethane elastomers includes a cardanol modified epoxy polyol. In particular, the reaction system has an isocyanate-reactive component that includes the cardanol-modified epoxy polyol and an isocyanate component that includes at least one polyisocyanate. The cardanol-modified epoxy polyol is a reaction product of an epoxy component and an epoxy-reactive component ata ratio of epoxy groups to epoxy reactive groups from 1:1 to 1:5, and the epoxy-reactive component includes a cashew nutshell liquid having a cardanol content of at least 85 wt %, based on a total weight of the cashew nutshell liquid.

Abstract: The invention relates to a urethane (meth)acrylate not comprising caprolactone, which is the product of reaction of A) a monoalcohol bearing from 1 to 5 (meth)acrylates, B) an allophanate-modified polyisocyanate, C) optionally, in the presence of a saturated polyol of functionality 2 to 3, D) optionally, in the presence of an unsaturated polyol with a hydroxyl functionality of 2 to 4, said polyol being C3 to C18, E) optionally, in the presence of a reactive diluent. The invention also relates to a process for preparing said urethane (meth)acrylate, and also to its use in curable compositions for coatings, in particular for varnishes and inks, adhesives, adhesion primers, coatings for wood, metal or plastic and application by spray gun in particular. These coatings have a good compromise between reactivity, flexibility, adherence and hardness, while at the same time being easy to apply.

Abstract: Embodiments of the invention include a method of producing polymer polyol dispersions is. The method includes providing at least one reaction system, and the reaction system includes: a) at least one polyol, b) at least one seed population, c) at least one catalyst, at least one co-reactant having an equivalent weight of up to 400 and at least one active hydrogen attached to a nitrogen or oxygen atom, and e) at least one polyisocyanate. The at least one seed population includes less than about 5% by weight of the total weight of the at least one reaction system and includes seed particles having diameters of less than 5 ?m. The at least one reaction mixture reacts to form at least one of a polyurea and polyurethane-urea particle population in the at least one polyol without the addition of any catalysts comprising tin. The polymer polyol dispersion has a solids content of at least 15% of the weight of the polymer polyol dispersion.

Abstract: The present disclosure relates, in part, to an epoxy resin composition comprising: an epoxy resin; and an aliphatic polyamine (e.g., as a cross-linking agent), wherein the aliphatic polyamine comprises a compound having the structure of Formula (1): wherein each of R1 and R2 is independently selected from the group consisting of hydrogen, alkyl group, cycloalkyl group and aromatic group; or R1 and R2 together with the carbon atom to which they are attached form a cyclic ring; each of R3 and R4 is independently selected from the group consisting of hydrogen, alkyl group, cycloalkyl group and aromatic group.

Abstract: This invention provides, among others, curing agents of Formulae (I) and (II), methods for preparing these curing agents, prepreg materials, degradable cross-linked polymers and reinforced composites made from these curing agents and epoxy resins, and methods for degrading and/or recycling the degradable polymers and reinforced composites.

Abstract: An epoxy resin hardener composition including a reaction product of (i) a compound having at least one vicinal epoxy group, and (ii) an amino alcohol; an epoxy resin composition including the epoxy resin hardener composition and a compound having at least one vicinal epoxy group; and a powder coating composition including particles of the epoxy resin hardener composition and particles of a compound having at least one vicinal epoxy group.

Abstract: The present invention relates to a process for preparing polymers by polycondensation catalysed by transition metals. These polymers are of great importance in, in particular, the fast-growing field of organic semiconductors. The polymers obtained by the process of the invention can be prepared with greater reproducibility and in higher purity than polymers obtained according to the prior art.

Abstract: A hydrogenated norbornene-based ring-opening polymer having a syndiotacticity ((racemo diads)/(meso diads+racemo diads)×100) of more than 90% is disclosed. A method for producing the same is also disclosed. It is thus possible to provide a hydrogenated highly syndiotactic norbornene-based ring-opening polymer that is formed of a single material, and exhibits high solvent resistance, and a method for producing the same.

Abstract: A polymer is provided that preferably includes at least one unsaturated cycloaliphatic group. In one embodiment, the polymer is combined with an optional crosslinker and an optional carrier to form a coating composition suitable for use in coating articles such as packaging articles. In one embodiment, the polymer has at least one unsaturated cycloaliphatic group that is at least bicyclic.

Abstract: Provided is a two-part composition. The first part is an epoxy terminated polyester having the structure wherein R1- is G- is -A- is a divalent alkyl group, -CA- is a divalent cycloalkyl group, and -R2- is a divalent organic group. The second part is an epoxy curing agent.

Abstract: An epoxy terminated polyester having the structure wherein R1— is G- is j is 0 to 5, —R2— is a divalent organic group, —R22— is a divalent alkyl group, and —R22— is a divalent alkyl group.

Abstract: The invention is to provide polycarbonate resins having excellent light resistance, transparency, hue, heat resistance, thermal stability, and mechanical strength and to provide processes for efficiently and stably producing a polycarbonate resin which stably shows those performances. The invention includes: polycarbonate resins which at least contain structural units derived from a dihydroxy compound having the portion represented by formula (1) as part of the structure thereof and which have specific properties; and processes for producing the polycarbonate resins, where the case where the portion represented by formula (1) is part of —CH2—O—H is excluded.

Abstract: The present inventions provide a novel polycarbonate copolymer having high fluidity and high molecular weight which is formed of a structural unit derived from an aliphatic diol compound and a structural unit derived from an aromatic dihydroxy compound, having a structure represented by the formula (III): having the content of the structural unit derived from the aliphatic diol compound of 1-30 mol %, having the Q-value (280° C., 160 kg load) in the range from 0.02 to 1.0 ml/s, and having the weight average molecular weight (Mw) of 30,000 to 100,000, and an aromatic polycarbonate compound which is formed of a structural unit derived from an aromatic dihydroxy compound which is suitable for a prepolymer for producing a high fluidity polycarbonate copolymer.

Abstract: The invention relates to a process for producing polyether carbonate polyols through an addition reaction of alkylene oxides and carbon dioxide onto one or more H-functional starter substances in the presence of a couble metal cyanide catalyst or in the presence of a metal complex catalyst based on the metals zinc and/or cobalt, characterized in that one or more H-functionalstarter substances containing at least 1000 ppm of component (K) is/are continuously metered into the reactor during the reaction, where component (K) is selected from at least one compound containing a phosphorus-oxygen bond and a phosphorus compound that can form one or more P—O bonds through reaction with OH-functional compounds.

Abstract: In one aspect, the present disclosure encompasses polymerization systems for the copolymerization of CO2 and epoxides comprising 1) a catalyst including a metal coordination compound having a permanent ligand set and at least one ligand that is a polymerization initiator, and 2) a chain transfer agent having two or more sites that can initiate polymerization. In a second aspect, the present disclosure encompasses methods for the synthesis of polycarbonate polyols using the inventive polymerization systems. In a third aspect, the present disclosure encompasses polycarbonate polyol compositions characterized in that the polymer chains have a high percentage of —OH end groups and a high percentage of carbonate linkages. The compositions are further characterized in that they contain polymer chains having an embedded polyfunctional moiety linked to a plurality of individual polycarbonate chains.

Abstract: In an example of a method disclosed herein, a polycarbonate with a hydrophilic surface is formed. An ether substituted dichlorosilane, phosgene, and a Bisphenol reactant are polymerized to form a polycarbonate including a hydrolyzable silane in its backbone chain. The hydrolyzable silane includes an alkoxy group attached to a silicon atom. The alkoxy group on the hydrolyzable silane is converted to a more hydrophilic functional group to form the polycarbonate with the hydrophilic surface.

Abstract: A method of producing a medical polyoxypropylene polymer and a polyoxypropylene/polyoxyethylene block copolymer including (A) adding to a polyoxypropylene polymer which is obtained by ring-opening polymerization of propylene oxide to a starting substance having an active hydrogen reacting with the propylene oxide and contains allyl ether as an impurity, a tertiary alkoxide of alkali metal in an excess amount based on a molar number of the active hydrogen of the starting substance and heat treating at 115° C. or less to isomerize the allyl ether to propenyl ether; and (B) adding a mineral acid to the product obtained in step (A) to adjust pH to 4 or less and treating at 70° C. or less to hydrolyze the propenyl ether. Also disclosed is a method of producing a medical polyoxypropylene/polyoxyethylene block copolymer which includes performing ring-opening polymerization of ethylene oxide to the polyoxypropylene polymer obtained above.

Abstract: The present invention relates to a composition containing a particulate solid, an organic or aqueous medium and a dispersant that may be a reaction product of an organic di or polyepoxide with a primary amine, aminoalcohol, amino acid, hydroxyacid or alcohol containing a fused or non-fused aromatic imide group. The invention further provides compositions for coatings, inks, toners, plastic materials (such as thermoplastics), plasticisers, plastisols, crude grinding and flush.

Abstract: The present invention relates to the field of polymer chemistry and more particularly to multiblock copolymers and micelles comprising the same. Compositions herein are useful for drug-delivery applications.

Abstract: Alternating co-polymers of cyclic dicarboxylic acids and cyclic diamines may be used to produce nylon 6,6. Di-substituted furan compounds may be used as the raw material for producing furan-dicarboxylic acids and/or furan-diamines. The furan-dicarboxylic acids and furan-diamines may be copolymerized to produce polymer precursors for nylon 6,6. The polymer precursors may be hydrogenated and/or deoxygenated to produce nylon 6,6.

Abstract: Polyhemiaminal (PHA) and polyhexahydrotriazine (PHT) materials are modified by 1,4 conjugate addition chemical reactions to produce a variety of molecular architectures comprising pendant groups and bridging segments. The materials are formed by a method that includes heating a mixture comprising solvent(s), paraformaldehyde, aromatic amine groups, aliphatic amine Michael donors, and Michael acceptors, such as acrylates. The reaction mixtures may be used to prepare polymer pre-impregnated materials and composites containing PHT matrix resin.

Abstract: The invention relates to a curable mixture comprising: RM % of m-xylylene bismaleimide of formula (I) RP % of a polyimide component, and RC % of a comonomer component. Further, the invention relates to methods for the preparation of the curable mixture, methods for the preparation of a prepolymer, of a crosslinked polymer, and composite materials, in particular of fiber-reinforced composites. In addition, the present invention relates to a prepolymer, a crosslinked polymer and composite materials, in particular fiber-reinforced composites, obtainable by said methods.

Abstract: This present disclosure relates to fluorinated polysiloxane resin compositions, and method for making the same, without the need for using halogen acids, and that display excellent properties of impact resistance, flexibility, chemical resistance, corrosion resistance, weather resistance, heat and fire resistance, abrasion resistance, ultraviolet resistance, hydrophobicity, and substrate adhesion.

Abstract: Polymeric BODIPY dyes including light harvesting BODIPY unit-comprising multichromophores are provided. In some embodiments, the dyes are polymeric tandem dyes that include a light harvesting BODIPY unit-comprising multichromophore and an acceptor chromophore covalently linked to the multichromophore in energy-receiving proximity therewith. The polymeric tandem dyes may be covalently linked to a specific binding member. Also provided are methods of evaluating a sample for the presence of a target analyte and methods of labelling a target molecule using compositions including the polymeric tandem dyes. Kits and systems for practicing the subject methods are also provided.

Abstract: A method of manufacturing a crosslinked fluororesin powder includes forming a powder mixture by mixing a fluororesin powder as a first powder with a second powder not fusing to the fluororesin powder even under conditions for crosslinking of the fluororesin powder, and conducting a cross-linking treatment to the formed powder mixture.

Abstract: It is an object to provide a compound that can provide a molded article and a coating film excellent not only in solubility in an organic solvent, but also in miscibility with/dispersibility in a matrix resin, causing no aggregation in a matrix resin, excellent in surface modification property, and having high transparency. A fluorine-containing highly branched polymer obtained by polymerizing a monomer A having two or more radical polymerizable double bonds in the molecule thereof with a monomer B having a fluoroalkyl group and at least one radical polymerizable double bond in the molecule thereof in the presence of a polymerization initiator C in a content of 5% by mol or more and 200% by mol or less, based on the total molar amount of the monomer A and the monomer B; and a resin composition comprising the polymer.

Abstract: A fiber-reinforced resin composition includes a polyarylene sulfide (A), a carbodiimide compound (B) and carbon fibers (C) in specific blending amounts and in which the carbon fibers (C) are surface-treated with a sizing agent (D), the carbodiimide compound (B) is an aliphatic carbodiimide compound, and the sizing agent (D) is a compound having three or more specific functional groups in one molecule; and a fiber-reinforced composite material includes a thermoplastic resin (A?), an adhesive compound (B?) and reinforcing fibers (C?) and in which the adhesive compound (B?) is a compound having two or more specific structures in one molecule, the thermoplastic resin (A?) is a thermoplastic resin containing an element other than carbon in a repeating unit structure of a main chain, and an abundance ratio Rb of the adhesive compound (B?) is 1.2 or more.

Abstract: The present invention provides sizing compositions and methods of using the same for glass fibers used in reinforced polymeric composites produced by reactive processing techniques.

Abstract: A primary object of the present invention is to provide a film exhibiting high electrical insulation properties and excellent withstand voltage properties and a method for producing the film. As a means for achieving the object, the present invention provides a vinylidene fluoride-based polymer film in which the 99% voltage failure resistance value in a Weibull plot is 300 V/?m or more.

Abstract: Disclosed is a film composed of a resin having a thiourethane bond, wherein the molar ratio (S/N) of sulfur to nitrogen contained in the resin is equal to or more than 0.8 and less than 3. A method for manufacturing a film is also disclosed. The disclosed film is excellent in a balance among high refractive index, low birefringence and light transmittance, and further excellent in a balance of mechanical characteristics such as toughness, hardness and dimensional stability, so that effects of deformation and the like during processing are very small, and the film is further excellent in solvent resistance as well.

Abstract: Polyhemiaminal (PHA) and polyhexahydrotriazine (PHT) materials are modified by 1,4 conjugate addition chemical reactions to produce a variety of molecular architectures comprising pendant groups and bridging segments. The materials are formed by a method that includes heating a mixture comprising solvent(s), paraformaldehyde, aromatic amine groups, aliphatic amine Michael donors, and Michael acceptors, such as acrylates. The reaction mixtures may be used to prepare polymer pre-impregnated materials and composites containing PHT matrix resin.

Abstract: The present invention relates to a thermosetting resin composition. The composition comprises from about 20 wt. % to about 70 wt. % of a thermosetting resin, from about 1 wt. % to about 30 wt. % of a curing agent, from about 0 wt. % to about 10 wt. % of an accelerant, a tungsten compound, and an inorganic filler. A prepreg may be prepared in an impregnation manner or a coating product may be prepared in a coating manner. The composition may decrease the thermal expansion coefficient of laminates and may effectively block UV light and decrease the light transmissivity.

Abstract: A foam composite includes a matrix and a plurality of fibers embedded in the matrix. The matrix can include viscoelastic foam. Also disclosed herein are methods of manufacturing such a foam composite.

Abstract: Described is a mono-axially oriented polyolefin film including a core or base layer containing a plurality of voids formed by a cavitating agent, wherein the film is oriented at least 4 times in the machine direction, and exhibits excellent tear resistance in the transverse direction.