Abstract: A method of printing a 3D printing a photopolymer composite material includes providing a resin premix material including an acrylate monomer or an acrylate oligomer, an inorganic hydrate, a reinforcing filler, a co-initiator, and an ultraviolet (UV) initiator. A thermal initiator is mixed with the resin premix to form a photopolymer composite resin. The photopolymer composite resin is repeatedly extruded and dual-cured by a 3D printing system to create a photopolymer composite material. The 3D printing system includes a control system, a mixing system, a feeding system in fluid communication with the mixing system, a light curing module controlled by the control system, and a printing head controlled by the control system.

Abstract: A method of printing a 3D printing a photopolymer composite material includes providing a resin premix material including an acrylate monomer or an acrylate oligomer, an inorganic hydrate, a reinforcing filler, a co-initiator, and an ultraviolet (UV) initiator. A thermal initiator is mixed with the resin premix to form a photopolymer composite resin. The photopolymer composite resin is repeatedly extruded and dual-cured by a 3D printing system to create a photopolymer composite material. The 3D printing system includes a control system, a mixing system, a feeding system in fluid communication with the mixing system, a light curing module controlled by the control system, and a printing head controlled by the control system.

Abstract: The present invention relates to a thermoplastic resin. More particularly, the present invention relates to a thermoplastic resin that is a graft copolymer having a seed-shell structure and includes a bimodal seed including a large-diameter rubbery polymer having an average particle diameter of greater than 2,000 ? and 3,500 ? or less and a small-diameter rubbery polymer having an average particle diameter of 500 ? to 2,000 ?; and an aromatic vinyl-vinyl cyan shell, wherein the aromatic vinyl cyan compound is included in an amount of 5% by weight to 28% by weight based on a total weight of the aromatic vinyl-vinyl cyan shell. In accordance with the present invention, a thermoplastic resin having a composition capable of improving graft density, and a thermoplastic resin composition capable of increasing dispersion and having high gloss due to inclusion of the thermoplastic resin are provided.

Abstract: A thermoplastic resin composition containing 25 to 50 parts by mass of a rubber-containing graft copolymer (A) obtained by copolymerizing a monomer mixture containing an aromatic vinyl compound and a vinyl cyanide compound in the presence of a diene-based rubber-like polymer, and 50 to 75 parts by mass of a hard copolymer mixture (B) containing a hard copolymer (B-I) and a hard copolymer (B-II).

Abstract: A method of preparing a diene-based rubber latex, a method of preparing an ABS-based graft copolymer including the same, and a method of manufacturing an ABS-based injection-molded article include preparing an in-situ bimodal rubber latex, in which a small-diameter polymer and a large-diameter polymer are formed in a desired ratio, by controlling contents, addition time points, and types of reactants when a conjugated diene based monomer, a crosslinking agent with a long linear chain end, an emulsifier including a multimeric acid of an unsaturated fatty acid or a metal salt thereof, and a molecular weight regulator are polymerized.

Abstract: The present disclosure provides a polyester composition suitable for ultrasonic welding and preparation method thereof, the composition includes the following components in parts by weight: 30˜50 parts of poly(1,4-cyclohexylene dimethylene terephthalate), 40˜60 parts of ABS, 5˜10 parts of a melt enhancer, 0.1˜1 parts of an antioxidant, and 0.1˜1 parts of a lubricant. Compared with the existing technologies, the polyester composition provided by the present disclosure improves melt strength by using the melt enhancer. The melt enhancer used is an ultra-high density polyethylene resin having a glycidyl methacrylate group after an irradiation treatment, so that the compatibility of the melt enhancer to the poly(1,4-cyclohexylene dimethylene terephthalate) is improved. In addition, by controlling a glass-transition temperature of the composition, no chipping is generated during ultrasonic welding, and the composition has a high welding strength, which is suitable for ultrasonic welding.

Abstract: The present invention relates to a matte coating composition comprising an aqueous dispersion of a) polymer particles having an average particle size in the range of from 80 nm to 500 nm; b) polymeric organic crosslinked microspheres having a particle size in the range of from 1 ?m to 20 ?m; c) polyethylene wax particles having a particle size in the range of from 0.3 ?m to 30 ?m; and d) a rheology modifier. The composition of the present invention gives matte finish coatings with excellent burnish resistance.

Abstract: The invention relates to an aqueous dispersion for use as open time improver in a coating composition which aqueous polymer dispersion comprises a first polymer having a number average molecular weight (Mn) of from 2,000 to 120,000 (determined by gel permeation chromatography using a mixture of tetrahydrofurane and acetic acid as eluent), an acid value of from 30 to 150 mg KOH/g, and an ethylene-oxide wt % (on total solid polymer) of from 1 to 20 wt %, said first polymer dispersion being obtainable by free radical polymerization of a monomer mixture in the presence of at least one free-radical initiator and at least one surfactant, said monomer mixture comprising: a) 5 to 20 wt %, preferably 7 to 10 wt %, acid functional ethylenically unsaturated monomers or precursors thereof or ethylenically unsaturated monomers comprising ionic group precursors; b) 5 to 25 wt %, preferably 7 to 20 wt %, ethylenically unsaturated monomers containing polyethylene oxide, polyethylene glycol or mono-alkoxypolyethylene glycol m

Abstract: A composite manufacture includes an extrudable thermoplastic matrix and a photochromic colorant, the photochromic colorant conferring to the composite a reversible strain-induced color change property. Methods include adding photochromic colorant to an extrudable thermoplastic polymer matrix to form a mixture, heating the mixture to form a composite, the photochromic colorant conferring to the composite a reversible strain-induced color change property. The composite manufactures can be used in cable coatings permitting visual detection of mechanical stresses in a wire based on the reversible strain-induced color change property.

Abstract: Provided is a rubber composition for tires achieving a balanced improvement of fuel economy, abrasion resistance, and road noise-reducing properties. The present invention relates to a rubber composition for tires, containing a core-shell structured particle including a core and a shell, the core having a melt viscosity at 38° C. of 0.1 to 3,000 Pa·s, the shell being formed of a polymer of a conjugated diene compound and/or an aromatic vinyl compound.

Abstract: The present invention is a method to start-up a process to make expandable vinyl aromatic polymer pellets comprising, a) providing a pelletizer (S) containing means to introduce the molten vinyl aromatic polymer comprising the expandable agent and optionally additives, a die plate having a plurality of holes of small diameter, typically in the range 0.8 to 1.

Abstract: A biocompatible, human implantable apparatus and a method for fully encasing a circuit within a polymer housing. The method may include placing the circuit in a mold, injecting a formulation into the mold, and polymerizing the formulation. The formulation may include monomers and polymers. The apparatus may include a circuit in a polymerized formulation of monomers and polymers.

Abstract: Thermoplastic moulding composition (F), comprising: A) from 5 to 80% by weight of a graft polymer (A) having bimodal particle size distribution and a moisture content of 0 to 27% by weight, made, based on (A), a1) from 40 to 90% by weight of an elastomeric particulate graft base (a1), obtained by emulsion polymerization of, based on (a1), a11) from 70 to 100% by weight of at least one conjugated diene, or of at least one C1-8-alkyl acrylate, or of mixtures of these, a12) from 0 to 30% by weight of at least one other monoethylenically unsaturated monomer and a13) from 0 to 10% by weight of at least one polyfunctional, cross linking monomer; a2) from 10 to 60% by weight of a graft a2), made, based on a2), a21) from 64 to 76% by weight of at least one vinyl aromatic monomer, a22) from 24 to 36% by weight of acrylonitrile, a23) from 0 to 30% by weight of at least one other monoethylenically unsaturated monomer, and a24) from 0 to 10% by weight of at least one polyfunctional, cross linking monomer; B) from 10 to 9

Abstract: A process for producing rubber modified polymers having an increased rubber phase volume, including feeding a vinyl aromatic monomer and an elastomer to a polymerization reactor to form a reaction mixture, polymerizing the reaction mixture, combining a copolymer to the polymerized reaction mixture to form a combined mixture, subjecting the combined mixture to further polymerization, and obtaining a rubber modified polymer product from the further polymerization.

Abstract: The present invention provides a resin composition including: (a): 75 to 97% by mass of a polypropylene-based resin; (b): 1 to 15% by mass of a polyphenylene ether-based resin having a reduced viscosity (?sp/c: measured as a 0.5 g/dL chloroform solution at 30° C.) of 0.25 to 0.36 dL/g; and (c): 2 to 19% by mass of a hydrogenated block copolymer which is a hydrogenated product of a block copolymer including at least two polymer blocks A mainly including a vinyl aromatic compound and at least one polymer block B mainly including a conjugated diene compound, wherein the polymer block A has a number average molecular weight (MncA) of 4,000 to 8,000 excluding 8,000, and a mass ratio ((b)/(c)) of the component (b) to the component (c) is 10/90 to 60/40.

Abstract: Disclosed herein is a low gloss thermoplastic resin composition with a soft touch surface comprising (A) about 10 to about 80% by weight of a soft rubbery aromatic vinyl copolymer resin which comprises rubber particles with a graft ratio of about 40 to about 90% and an average particle diameter of about 6 to about 20 ?m as a dispersed phase; (B) about 4 to about 60% by weight of a rubber-modified aromatic vinyl copolymer resin; and (C) about 5 to about 80% by weight of an aromatic vinyl-vinyl cyanide copolymer resin. The molded article molded from the thermoplastic resin composition can have a soft touch surface as well as excellent low gloss and impact strength.

Abstract: Process for the preparation of vinyl aromatic (co) polymers grafted on an elastomer in a controlled manner, comprising: dissolving an elastomer functionalized with bromoalkanes and nitroxy radicals, soluble in non-polar solvents, in a liquid phase consisting of a mixture of vinyl aromatic monomer(s)/polymerization solvent; feeding at least one radical initiator to the mixture, containing the functionalized elastomer in solution, and polymerizing the mixture thus obtained at a temperature higher than or equal to 1200 C; recovering the vinyl aromatic (co) polymer obtained after devolatization; and recycling the solvent/monomer(s) mixture, coming from the devolatization, to step (a).

Abstract: A tapered triblock copolymer having controlled vinyl distribution, enlarged middle block with intermediate composition and microstructure, increased compatibility between its adjacent blocks, good processing characteristics and a peak average molecular weight between 25,000 and 300,000 is made by anionically polymerizing conjugated diene and monovinyl aromatic monomers, polar modifier and initiator to make a first block rich in conjugated diene, forming a second block that is a copolymer of the conjugated diene and the monovinyl aromatic monomer and which is less rich in the conjugated diene than the first block, and forming a third block that is a homopolymer of the monovinyl aromatic monomer. The first, second and third blocks comprise 30 to 60, 20 to 50 wt % and 10 to 40 wt % of the tapered triblock copolymer, respectively. The tapered triblock copolymers may be used as asphalt modifiers, adhesives, sealants, compatibilizers, reinforcing agents and impact modifiers.

Abstract: It is an object of the present invention to provide a copolymer for a cured product that is satisfactory in properties, such as adhesion properties, as a chip stacking adhesive or the like. The present invention is a star polymer comprising, as an arm portion, a polymer chain containing repeating units represented by formula (I) and formula (II), and comprising a core portion derived from a monomer represented by formula (III), wherein a molar ratio of the repeating unit represented by formula (I) to the repeating unit represented by formula (II) ((I)/(II)) in the arm portion is in the range of 60/40 to 95/5.

Abstract: A method for continuously producing a thermoplastic resin from a conjugated diene includes: primarily polymerizing a conjugated diene monomer with an aromatic vinyl monomer in a first solvent in a first reactor, and feeding a hydroxyl group-containing polymerization inhibitor and a polar hydrocarbon to the first reactor to prepare a rubber solution; and adding an aromatic vinyl monomer and a monomer copolymerizable with the aromatic vinyl monomer to the rubber solution, and subjecting the mixture to secondary polymerization in a second solvent of the same kind as the first solvent in a second reactor. The method can provide a thermoplastic resin that can have excellent color and low gloss characteristics.

Abstract: A mixture which contains a) a copolymer or block copolymer A comprising one or more copolymer blocks (B/S)A which are respectively composed of from 65 to 95% by weight of vinylaromatic monomers and of from 35 to 5% by weight of dienes, and whose glass transition temperature TgA is in the range from 40° to 90° C., b) a block copolymer B comprising at least one hard block S which is composed of vinylaromatic monomers, and comprising one or more copolymer blocks (B/S)B which are respectively composed of from 20 to 60% by weight of vinylaromatic monomers and of from 80 to 40% by weight of dienes, and whose glass transition temperature TgB is in the range from ?70° to 0° C., c) a polystyrene C, and its use for the production of packaging for electronics components.

Abstract: A block copolymer or graft copolymer with weight-average molar mass Mw of at least 100 000 g/mol, comprising a) at least one block S composed of from 95 to 100% by weight of vinylaromatic monomers and from 0 to 5% by weight of dienes, and b) at least one copolymer block (S/B)A composed of from 63 to 80% by weight of vinylaromatic monomers and from 20 to 37% by weight of dienes, with glass transition temperature TgA in the range from 5 to 30° C., where the proportion by weight of the entirety of all of the blocks S is in the range from 50 to 70% by weight, based on the block copolymer or graft copolymer, and also mixtures thereof, and their use.

Abstract: It is to provide a method for producing a polymer by a living anionic polymerization, wherein the number of functional groups and the introduction position are accurately specified in the polymer. For this purpose, a cinnamyl alcohol represented by the following formula [I] or a derivative thereof is subjected to a reaction when conducting a living anionic polymerization. In formula [I], R1 represents an alkyl group or alkoxy group; m represents an integer of 0 to 5 and when m is 2 or more, R1s may be the same or different; R5 represents a hydrogen atom, alkali metal atom, trialkylsilyl group or a substituent represented by the following formula [II]. In formula [II], R3 represents a hydrogen atom or a C1-C6 alkyl group; and R4 represents an alkyl group which may be substituted by an alkoxy group, a cycloalkyl group which may be substituted by an alkoxy group, a phenyl group which may be substituted by an alkyl group, or a phenyl group which may be substituted by an alkoxy group).

Abstract: Disclosed is a resin having excellent impact resistance and color, and a method of preparing the same, and more specifically, a resin having the excellent impact resistance and color, and a method of preparing the same, in which the resin includes (a) an occlusion seed consisting of i) a base seed including 99.95 to 99 wt % of alkyl methacrylate and 0.05 to 1 wt % of crosslinker, and ii) a copolymer of aromatic vinyl compound and alkyl acrylate occluding the base seed; (b) a polymer core surrounding the occlusion seed; and (c) a polymer shell surrounding the core, and according to the present invention, it is effective in providing a resin having superior impact strength, transparency, and color, in which the resin can be used as an excellent impact modifier when applying on a polymethylmethacrylate resin, and a method of preparing the same.

Abstract: We disclose a monovinylarene-conjugated diene block copolymer containing a plurality of monovinylarene-conjugated diene mixed blocks, wherein each mixed block contains conjugated diene units and monovinylarene units in a weight ratio of about 0.05 to about 0.33. We also disclose a composition containing (a) from about 50 parts by weight to about 95 parts by weight of the monovinylarene-conjugated diene block copolymer and (b) from about 5 parts by weight to about 50 parts by weight of polystyrene; wherein the monovinylarene-conjugated diene block copolymer and the polystyrene total 100 parts by weight.

Abstract: Butadiene is anionically polymerized (or block copolimerized with styrene) in a low-boiling non-polar solvent in presence of rganolithiura compounds. At the end of the polymerization, the non-polar solvent is switched with styrene and the new solution is stored in tanks in relation to the type of polybutadiene (or its block copolymer with styrene) obtained. The polybutadiene solution (and/or its block copolymer with styrene) with the desired set of properties is then fed to a production plant of high impact vinyl aromatic (co)polymers.

Abstract: A pre-cursor block copolymer for sulfonation which, prior to hydrogenation, has the general configuration A-B-A, A-B-A-B-A, (A-B-A)nX, (A-B)nX, A-D-B-D-A, A-B-D-B-A, (A-D-B)nX, (A-B-D)nX or mixtures thereof, wherein A, B and D blocks do not contain any significant levels of olefinic unsaturation. Each A and D block is a polymer block resistant to sulfonation, and each B block is a polymer block susceptible to sulfonation. Each A block is a segment of one or more polymerized para-substituted styrene monomers, each B block contains segments of one or more vinyl aromatic monomers selected from polymerized (i) unsubstituted styrene monomers, (ii) ortho-substituted styrene monomers, (iii) meta-substituted styrene monomers, (iv) alpha-methylstyrene, (v) 1,1-diphenylethylene, (vi) 1,2-diphenylethylene and (vii) mixtures thereof, and each D block contains polymers having a glass transition temperature less than 20° C. and a number average molecular weight of between 1,000 and 50,000.

Abstract: A sulfonated block copolymer which is solid and non-dispersible in water having at least two polymer end blocks A and at least one interior block B wherein each A block is a polymer block resistant to sulfonation and each B block is a polymer block susceptible to sulfonation, wherein the A and B blocks do not contain any significant levels of olefinic unsaturation. Each A block includes one or more segments selected from polymerized (i) ethylene, (ii) monomers of conjugated dienes having a vinyl content less than 35 mol percent prior to hydrogenation, and (iii) mixtures thereof; and each B block comprising segments of one or more polymerized vinyl aromatic monomers selected from (i) unsubstituted styrene monomers, (ii) ortho-substituted styrene monomers, (iii) meta-substituted styrene monomers, (iv) alpha-methylstyrene, (v) 1,1-diphenylethylene, (vi) 1,2-diphenylethylene and (vii) mixtures thereof.

Abstract: Provided is a thermoplastic resin composition having excellent flame resistance, colorability, and scratch resistance, including: A) 100 parts by weight of a basic resin comprising 10 to 89 wt % of acrylonitrile-butadiene-styrene copolymer, 89 to 10 wt % of styrene-acrylonitrile copolymer, and 1 to 40 wt % of methylmethacrylate polymer; B) 1 to 30 parts by weight of bromoalkyl or bromophenyl cyanurate compounds; and C) 1 to 20 parts by weight of antimony compound, thereby, making it possible to provide the thermoplastic resin composition having excellent flame resistance, impact strength, scratch resistance, colorability, and surface hardness as synergy effects.

Abstract: The present invention relates to a graft copolymer, a method for preparing the same and a thermoplastic resin composition comprising the same. The graft copolymer of the present invention comprises a composite rubber polymer (A-1) having an average particle diameter of 250-600 nm prepared by particle enlargement after mixing a diene rubber polymer (a-1) latex having an average particle diameter of 50-150 nm and a core-shell structured, cross-linked alkyl acrylate rubber polymer (b-1) latex having an average particle diameter of 50-250 nm. A thermoplastic resin composition prepared by mixing the graft copolymer of the present invention with a hard matrix (B) has very superior weathering resistance and superior pigmentation property, gloss, impact resistance and low-temperature impact strength.

Abstract: The present invention relates to superabsorbent polymer particles with improved surface cross-linking and their use in absorbent articles. Superabsorbent polymers of the invention comprise polymer chain segments, wherein at least a part of these polymer chain segments are cross-linked to each other through direct covalent bonds. Moreover, the invention relates to a process for making these superabsorbent polymer particles.

Abstract: A process for forming a nanoparticle composition is provided. The process includes polymerizing conjugated diene monomer in a hydrocarbon solvent to form a first reaction mixture, and charging excess alkenylbenzense monomer and anionic catalyst to form mono-block and diblock polymers. Micelles of said mono-block and diblock polymers are formed, and at least one crosslinking agent is added to cross-link the micelles and form nanoparticles. The nanoparticles preferably have a poly(alkenylbenzene) core and an outer layer including monomer units selected from the group consisting of conjugated dienes, alkenylbenzenes, alkylenes, and mixtures thereof, and a size distribution of between about 1 and 1000 nm.

Abstract: A sulfonated block copolymer which is solid and non-dispersible in water having at least two polymer end blocks A and at least one polymer interior block B wherein each A block is a polymer containing essentially no sulfonic acid or sulfonate functional groups and each B block is a polymer block containing 10 to 100 mol percent sulfonic acid or sulfonate functional groups based on the number of monomer units of the B block, and wherein said A and B blocks do not contain any significant levels of olefinic unsaturation. Also claimed are processes for making such block copolymers, and the various end uses and applications for such block copolymers.

Abstract: Process for the preparation of vinyl aromatic (co) polymers grafted on an elastomer in a controlled manner, comprising: dissolving an elastomer functionalized with bromoalkanes and nitroxy radicals, soluble in non-polar solvents, in a liquid phase consisting of a mixture of vinyl aromatic monomer (s)/polymerization solvent; feeding at least one radical initiator to the mixture, containing the functionalized elastomer in solution, and polymerizing the mixture thus obtained at a temperature higher than or equal to 1200C; recovering the vinyl aromatic (co) polymer obtained after devolatization; and recycling the solvent/monomer (s) mixture, coming from the devolatization, to step (a).

Abstract: A process for preparing sulfonated block copolymers that are solid in water having at least two polymer end blocks A and at least one polymer interior block B involving sulfonating the interior block B until substantially sulfonated. Each A block having one or more segments selected from polymerized (i) para-substituted styrene monomers, (ii) ethylene, (iii) alpha olefins of 3 to 18 carbon atoms; (iv) hydrogenated 1,3-cyclodiene monomers, (v) hydrogenated monomers of conjugated dienes having a vinyl content less than 35 mol percent prior to hydrogenation, (vi) acrylic esters, (vii) methacrylic esters, and (viii) mixtures thereof. Each B block having segments of one or more polymerized vinyl aromatic monomers selected from (i) unsubstituted styrene monomers, (ii) ortho-substituted styrene monomers, (iii) meta-substituted styrene monomers, (iv) alpha-methylstyrene, (v) 1,1-diphenylethylene, (vi) 1,2-diphenylethylene and (vii) mixtures thereof.

Abstract: A sulfonated block copolymer which is solid and non-dispersible in water having at least two polymer end blocks A and at least one interior block B wherein each A block is a polymer block resistant to sulfonation and each B block is a polymer block susceptible to sulfonation, wherein the A and B blocks do not contain any significant levels of olefinic unsaturation. Each A block having one or more segments selected from (i) acrylic esters, (ii) methacrylic esters, and (viii) mixtures thereof; and each B block comprising segments of one or more polymerized vinyl aromatic monomers selected from (i) unsubstituted styrene monomers, (ii) ortho-substituted styrene monomers, (iii) meta-substituted styrene monomers, (iv) alpha-methylstyrene, (v) 1,1-diphenylethylene, (vi) 1,2-diphenylethylene and (vii) mixtures thereof.

Abstract: Compositions comprising (a) a rubber-modified monovinylidene aromatic polymer, e.g., HIPS, and (b) a specified poly-alpha-olefin (PAO), e.g., an oligomer of hexene, octene, decene, dodecene and/or tetradecene, that has a dynamic viscosity value of from about 40 to about 500 centipoise (cP) at 40° C., exhibit improved combinations of environmental stress crack resistance, impact resistance and heat resistance as compared to compositions without such a PAO. The compositions are useful in the manufacture of articles, e.g., refrigerator liners and food packaging, which come in contact with the oils contained in various food stuffs.

Abstract: The present invention provides a process for preparing emulsion polymer particles of a hollow core/shell structure in the presence of a monomer plasticizer having a ceiling temperature less than 181° C. wherein a polymerization inhibitor or reducing agent is not added to the aqueous emulsion of the core shell particles during the neutralization and swelling stage. The obtained core shell particles are useful in paints, paper coatings, foams, and cosmetics.

Abstract: The invention relates to screw elements for multi-screw extruders with screws co-rotating in pairs and being fully self-wiping in pairs, to the use of the screw elements in multi-screw extruders and to a process for extruding plastic compositions.

Abstract: A composition having a sulfonated block copolymer which is solid and non-dispersible in water having at least two polymer end blocks A, at least one polymer interior block B, and at least one polymer block D. Each A block is a segment of one or more polymerized para-substituted styrene monomers, each B block contains segments of one or more vinyl aromatic monomers selected from polymerized (i) unsubstituted styrene monomers, (ii) ortho-substituted styrene monomers, (iii) meta-substituted styrene monomers, (iv) alpha-methylstyrene, (v) 1,1-diphenylethylene, (vi) 1,2-diphenylethylene and (vii) mixtures thereof, and each D block having a glass transition temperature of less than 20° C. and a number average molecular weight of between 1,000 and 50,000 Adhesives, coatings and membranes are formed from the composition. Various articles are formed with the composition including films, fibers, fabrics, laminates, and absorbent cores.

Abstract: The inventive composition includes a block copolymer which includes four blocks and has the following block arrangement: B-S-B-S. The two polymer blocks B comprise conjugated diene monomer constitutional units; and the two polymer blocks S comprise vinyl aromatic hydrocarbon monomer constitutional units. The invention also includes methods of making such inventive compositions as well as asphalt compositions and/or thermoplastic elastomers which include such block copolymer.

Abstract: The present invention provides a block copolymer or a hydrogenated product thereof excellent in low-temperature shrinkability, natural shrinkability, rigidity and the like, excellent in a balance of physical properties such as blocking resistance, resistance to fusion bonding in hot water, impact resistance and the like, and having a few fish eyes (FE's) caused by gels. Further, the invention provides a heat shrinkable film and a heat shrinkable multilayer film suitable for drink container packaging, cap seals and the like, using such a block copolymer or the hydrogenated product thereof.

Abstract: The present invention provides polymeric nanoparticles comprising triblock and optionally diblock copolymer chains. The architecture of the polymeric nanoparticles may be controlled, resulting in nanoparticles having non-spherical shapes. The present invention also provides a method of preparing the polymeric nanoparticles and a rubber article such as a tire manufactured from a formulation comprising the polymer nanoparticles.

Abstract: The present invention is a, solid block copolymer comprising at least two polymer end blocks A and at least one polymer interior block B wherein each A block is a polymer block resistant to sulfonation and each B block is a polymer block susceptible to sulfonation, and wherein said A and B blocks do not contain any significant levels of olefinic unsaturation.

Abstract: A nanoparticle which includes a multi-armed core and surface decoration which is attached to the core is prepared. A multi-armed core is provided by any of a number of possible routes, exemplary preferred routes being living anionic polymerization that is initiated by a reactive, functionalized anionic initiator and ?-caprolactone polymerization of a bis-MPA dendrimer. The multi-armed core is preferably functionalized on some or all arms. A coupling reaction is then employed to bond surface decoration to one or more arms of the multi-armed core. The surface decoration is a small molecule or oligomer with a degree of polymerization less than 50, a preferred decoration being a PEG oligomer with degree of polymerization between 2 and 24. The nanoparticles (particle size?10 nm) are employed as sacrificial templating porogens to form porous dielectrics. The porogens are mixed with matrix precursors (e.g., methyl silsesquioxane resin), the matrix vitrifies, and the porogens are removed via burnout.

Abstract: This invention discloses a process for synthesizing a modified crosslinked elastomeric particle which comprises a two-step polymerization of a conjugated diolefin monomer and a vinyl aromatic monomer by emulsion polymerization, wherein the particle is synthesized by the steps of (1) polymerizing a conjugated diolefin monomer, alone or in combination with a vinyl aromatic monomer, and optionally a crosslinking monomer, to create a crosslinked elastomeric core having residual double bonds and an outer surface; (2) polymerizing a monomer of a vinyl aromatic monomer, alone or in combination with a diolefin monomer, to create a polymeric shell, wherein the polymeric shell is grafted to the outer surface of the polymeric core by reacting with the residual double bonds of the polymeric core; and (3) coagulating the core-shell emulsion latex solution to recover the particles.

Abstract: A second-order modified block copolymer which can be obtained by reacting a first-order modified block copolymer with a second-order modifier, wherein the first-order modified block copolymer comprises a base block copolymer and a functional group-containing first-order modifier group bonded to the base block copolymer, wherein the base block copolymer comprises at least one polymer block comprised mainly of vinyl aromatic hydrocarbon monomer units and at least one polymer block comprised mainly of conjugated diene monomer units, and wherein the second-order modifier has a specific functional group which is reactive to the functional group of the first-order modifier group of the first-order modified block copolymer. A second-order modified block copolymer-containing polymer composition comprising the second-order modified block copolymer as well as a thermoplastic resin and/or a rubbery polymer.

Abstract: A second-order modified block copolymer which can be obtained by reacting a first-order modified block copolymer with a second-order modifier, wherein the first-order modified block copolymer comprises a base block copolymer and a functional group-containing first-order modifier group bonded to the base block copolymer, wherein the base block copolymer comprises at least one polymer block comprised mainly of vinyl aromatic hydrocarbon monomer units and at least one polymer block comprised mainly of conjugated diene monomer units, and wherein the second-order modifier has a specific functional group which is reactive to the functional group of the first-order modifier group of the first-order modified block copolymer. A second-order modified block copolymer-containing polymer composition comprising the second-order modified block copolymer as well as a thermoplastic resin and/or a rubbery polymer.

Abstract: This invention describes the obtainment of impact-resistant materials from a block copolymer that comprises as monomers an alkadiene (conjugated diene) and a vinyl aromatic compound, which is used as impact modifier to obtain such materials and in which, at least, one of the blocks of the vinyl aromatic compound is polydisperse. The invention allows obtaining morphologies such as rods, points or capsules by incorporating such copolymer into a polymeric matrix derived from vinyl aromatic monomers independently from other agents such as chain transfer agents, and achieving increases, in the impact values up to 50% through the use of the copolymer of this invention.

Abstract: The present invention relates to a novel process for the preparation of solid-supported scavenging reagents and solid-supported functional polymers. The invention further relates to novel solid-supported functional polymers and to their use in organic synthesis and combinatorial chemistry.