Abstract: Embodiments of the present disclosure are directed to polyolefin grafted polydiene polymers, wherein the polyolefin grafted polydiene polymers comprises a polydiene having a polydiene polymer backbone, a polyolefin, and at least one sulfur containing functionalizing agent which grafts the polyolefin onto at least one non-terminal position on the polydiene polymer backbone.

Abstract: According to an embodiment of the present invention, there is provided a method of preparing a rubber composition, which includes (a) synthesizing a living polymer by solution polymerization of a monomer mixture including a conjugated diene-based monomer in the presence of a first catalyst; (b) reacting some ends of the living polymer with a coupling agent; (c) reacting the remaining ends of the living polymer with an organotin halide compound to prepare an end-modified conjugated diene-based polymer solution; and (d) adding a second catalyst and a conjugated diene-based monomer to the end-modified conjugated diene-based polymer solution to induce solution polymerization.

Abstract: The present invention is directed to a rubber composition comprising: a functionalized elastomer comprising: a polymeric backbone chain derived from a monomer comprising at least one conjugated diene monomer and optionally at least one vinyl aromatic monomer; and a functional group bonded to the backbone chain, the functional group comprising a multidentate ligand capable of complexing with a metal ion; and a metal ion. The invention is further directed to a pneumatic tire comprising the rubber composition.

Abstract: The present invention provides a TFE/Pr type elastomer being excellent in not only amine resistance but also heat resistance and chemical resistance and having a small gel content, and a crosslinkable composition comprising the elastomer. The above-mentioned fluorine-containing elastomer is a fluorine-containing elastomer being crosslinkable with the compound (A), comprising 40 to 70% by mole of tetrafluoroethylene unit, 30 to 60% by mole of propylene unit and 0.1 to 2.5% by mole of a carboxyl group-containing vinyl monomer unit and having a Mooney viscosity at 121° C. of 5 to 100.

Abstract: A method of curing a compound having a cross-linkable, unsaturated-chain polymer base and a curing system; the method employing microwaves as a form of energy to promote curing reactions; and the curing system including compounds of general formula (I) ([R1R2R3NR5 (NR4R6R7)n](n+1)+) y(n+1)Xy? (I) where: X is an atom or anionic group; R1, R2, R3, which are the same or different, are each CmH2m+1, where m is 1 to 3, or CH2CHCH2 or CHCHCH3, R4, R6, R7, which are the same or different, are each CH2CHCH2 or CHCHCH3; n is 0 or 1; y is 1 when n is 1; y is 1 or 2 when n is 0; R5 is an aliphatic group C15-C22 when n is 0; is an aliphatic group C8-C16 when n is 1; when n is 0, at least one of R1, R2, R3, R5 has a double bond.

Abstract: Butadiene copolymers are brominated using certain quaternary ammonium or phosphonium tribromides as the brominating agent. The bromination is performed in solution in a mixture of n-butyl acetate and ethyl acetate. The bromination process proceeds easily under mild conditions, and produces a brominated product that has excellent thermal stability.

Abstract: Impact-modified polystyrene resins such as HIPS and ABS resins are blended with a brominated vinyl aromatic-butadiene copolymer. The brominated copolymer is an effective flame retardant in these compositions, allowing in many cases a V-1 rating to be achieved in the UL-94 vertical burn test.

Abstract: Brominated styrene-butadiene copolymers are useful gas transport films. The gas transport films are made by brominating a starting styrene-butadiene copolymer, and then forming the brominated styrene-butadiene copolymer into a film The film may contain a blend of the brominated styrene-butadiene copolymer with one or more other polymers. The films have excellent selectivities between certain pairs of gasses, and exhibit high gas transport rates for various gasses such as carbon dioxide and water vapor.

Abstract: Butadiene copolymers are brominated using certain quaternary ammonium or phosphonium tribromides as the brominating agent. The bromination is performed in solution in a mixture of n-butyl acetate and ethyl acetate. The bromination process proceeds easily under mild conditions, and produces a brominated product that has excellent thermal stability.

Abstract: There is provided herein a membrane or film comprising one or more aromatic ionomers covalently crosslinked through aryl-aryl (—Ar—Ar—), aryl-ether-aryl (—Ar—O—Ar—), aryl-sulfide-aryl (—Ar—S—Ar—), aryl-sulfone-aryl bonds, or any combination thereof, wherein said one or more aromatic ionomers further comprises at least one electron withdrawing group adapted to improve oxidant resistance of said membrane or film.

Abstract: The present invention discloses a non-aqueous solution process for making cross-linked polymers. The cross-linked polymers are characterized by a repeat unit that includes at least one amino group. Amino groups can be part of the polymer backbone (e.g., polyethyleneimine), pendant from the polymer backbone (e.g., polyallylamine), or both types of amino groups can exist within the same repeat unit and/or polymer. The present invention discloses more specifically non-aqueous solution cross-linking to prepare Sevelamer and its salts, Colesevelam and its salts.

Abstract: The present invention provides a method for producing a stabilized fluoropolymer which comprises producing the stabilized fluoropolymer by subjecting a treatment target substance containing a sulfonic-acid-derived-group-containing fluoropolymer to a fluorination treatment, wherein the sulfonic-acid-derived-group-containing fluoropolymer is a fluoropolymer containing —SO3M (in which M represents H, NR1R2R3R4 or M11/L; R1, R2, R3 and R4 are the same or different and each represents H or an alkyl group containing 1 to 4 carbon atoms; and M1 represents an L-valent metal), and the treatment target substance has a moisture content of not higher than 500 ppm by mass.

Abstract: A hole transport polymeric compound and a polymer light emitting diode using the same. The hole transport polymeric compound includes a hole transport material, a thermal cross-linking agent containing an ethynyl group, and a compound represented by [Formula 1], and can be applied to a polymer light emitting diode. In addition, the hole transport polymeric compound has excellent hole transport capabilities and has stability in solvents so as to be insoluble in a solvent used upon stacking other organic layers and blocking electrons well.

Abstract: Vinylamine-containing polymers are disclosed where the amine groups are substituted with (1) cationic functional groups, (2) anionic functional groups, (3) hydrophobic functional groups, (4) hydrophilic functional groups, (5) functional groups that impart amphoteric characteristics to the polymers, or (6) combinations thereof. Also disclosed are processes for preparing such polymers, as well as compositions comprising such polymers. Among other applications, these polymers can be used in papermaking applications as dry strength additives, wet strength additives, retention aids, drainage aids, and pitch and stickies control agents.

Abstract: There are provided herein selective membranes, such as composite membranes, and/or films and processes for their preparation. The membranes and/or films have a given morphology which may be stabilized, for example against swelling and chemical degradation, by covalent crosslinking and optionally, in addition, by hydrophobization. There is provided a membrane and/or film and a process for the preparation thereof, the membrane and/or film include an ionomer and/or polyelectrolyte crosslinked through aryl-aryl (—Ar—Ar—), aryl-ether-aryl (—Ar—O—Ar—) and/or aryl-sulfide-aryl (—Ar—S—Ar—) bonds.

Abstract: Butadiene copolymers are brominated using certain quaternary ammonium tribromides as the brominating agent in a first step, and then with elemental bromine in a second bromination step. The bromination process proceeds easily under mild conditions, and produces a brominated product that has excellent thermal stability. The bromination proceeds to high conversions in shorter reaction times, when the bromination is performed using only the first bromination step.

Abstract: Compounds or polymers that contain carbon-carbon unsaturation are brominated using a quaternary phosphonium tribromide as the brominating agent. The bromination process proceeds easily under mild conditions. The process can be highly selective. When the substrate is a butadiene polymer or copolymer, the brominated product tends to have excellent thermal stability.

Abstract: The invention provides a compound and tautomeric forms thereof having the formula: wherein Rf1 is selected from the group consisting of hydrogen, a straight chain, branched secondary or branched tertiary C1-C20 perfluoroalkyl group optionally containing ether or thioether linkages and C1-C10 perfluoroalicyclic group optionally containing ether or thioether groups; Rf2 is a straight or branched C1-C20 perfluoroalkylene group optionally substituted with ether and thiother linkages; and X is selected from the group consisting of fluorine and The invention also provides perfluoroelastomeric compositions cured with the perfluoroimidoylamidines of the invention as well as combinations of perfluoroimidoylamidines and other curing agents.

Abstract: This invention relates to curable fluoroelastomer compositions comprising a) fluoroelastomers having either nitrile, alkyne or azide cure sites and b) fluorinated curatives containing diazide, dinitrile or dialkyne groups for reacting with cure sites on the fluoroelastomer. Fluoroelastomers having azide cure sites form crosslinks with curatives having dinitrile or dialkyne groups. Fluoroelastomers having nitrile or alkyne cure sites form crosslinks with curatives having diazide groups.

Abstract: Butadiene copolymers are brominated using certain quaternary ammonium tribromides as the brominating agent. The bromination process proceeds easily under mild conditions, and produces a brominated product that has excellent thermal stability. A quaternary ammonium monobromide salt is produced as a reaction by-product. A solvent for the monobromide salt is added to the reaction after 25-90% bromination of the aliphatic carbon-carbon double bonds. This provides for significantly shorter reaction times while providing a product with few impurities.

Abstract: The present invention provides solvent- and water-based primer compositions that include at least one chlorinated carboxylated polyolefin that has been modified with one or more polyfunctional alcohols. The chlorinated carboxylated polyolefins are obtained by the reaction of polyolefins with at least one of unsaturated carboxylic esters, unsaturated carboxylic acids, unsaturated carboxylic anhydrides, acrylic monomers, and mixtures thereof then chlorinated. The chlorinated carboxylated polyolefins are then further modified by reaction with one or more polyfunctional alcohols. These polyfunctional alcohol-modified chlorinated carboxylated polyolefins may also contain pendant carboxyl groups, which have the propensity to form hydrophilic salts with amines or inorganic bases, thereby rendering the polyfunctional alcohol-modified chlorinated carboxylated polyolefins water-dispersible.

Abstract: Brominated polybutadiene polymers are recovered from a bromination reaction solution by forming the solution into droplets, thermally stripping the solvent from the droplets, and then washing the resulting particles. The washed particles are then recovered from the washing liquid. The droplets can be dispersed into a gaseous medium such as air and then transferred into a nonsolvent liquid for washing, or can be formed directly into the nonsolvent liquid. The process forms a particulate polymer material that is easily filterable and has low levels of volatile impurities and inorganic salts. Brominated polybutadiene polymers recovered in this manner are often very thermally stable.

Abstract: The present invention relates to a modified styrene-maleic acid copolymer obtained by reacting a carboxylic acid group in a styrene-maleic acid copolymer with a halogen and/or epoxy compound. The modified styrene-maleic acid copolymer is useful as a low profile additive for a thermosetting resin, a water-absorbing material, etc.

Abstract: The invention relates to novel polymers or oligomers containing at least sulfinate groups (P—(SO2)nX, X=1-(n=1), 2-(n=2) or 3-(n=3) valent metal cation or H+ or ammonium ion NR4+ where R=alkyl, aryl, H), which are obtained by completely or partially reducing polymers or oligomers containing at least SO2Y-groups (Y?F, Cl, Br, I, OR, NR2 (R=alkyl and/or aryl and/or H), N-imidazolyl, N-pyrazolyl) by means of suitable reducing agents in a suspension or in a solution form. Polymer and polymer(blend)membranes which are obtained by further reacting the received sulfinated polymers, especially by alkylation of the sulfinate groups with mono- di- or oligo functional electrophiles. The invention further relates to methods for producing the sulfinated polymers and for further reacting the sulfinated polymers with electrophiles by S-alkylation.

Abstract: A multi-functional polymer defined by the formula (Q-R¦n—Z—P2—Y where (Q-R)n is a functionality cluster, Q is a functional group, R is a multi-valent organic group, P2 is a long-chain polymer, n is an integer from about 2 to about 10, Y is a proton, a weak functional group, or a selective functional group, and Z is a branch point where the functionality clusters join the long-chain polymer.

Abstract: An organic polymer is transferred from one solvent to another. In a first step, a solution of the polymer in a first solvent is divided into droplets, dispersed into a liquid phase such as water bath, and the first solvent is re-moved from the droplets to produce a slurry in the liquid phase. Then, the second solvent is contacted with the slurry to dissolve the organic polymer and produce a second solution. The second solution is removed from the liquid phase. The process is especially suitable for transferring a butadiene polymer from a hydrocarbon solvent into a halogenated solvent for bromination.

Abstract: Butadiene copolymers are brominated using certain quaternary ammonium tribromides as the brominating agent in a first step, and then with elemental bromine in a second bromination step. The bromination process proceeds easily under mild conditions, and produces a brominated product that has excellent thermal stability. The bromination proceeds to high conversions in shorter reaction times, when the bromination is performed using only the first bromination step.

Abstract: This invention relates to a precipitated silica reinforced conjugated diene-based elastomer composition containing an alkoxysilane coupled, in-chain functionalized, conjugated diene-based elastomer and to a tire having at least one component thereof. Said in-chain functionalized conjugated diene-based elastomer is a conjugated diene-based elastomer which contains a plurality of at least one of in-chain p- and m-(2-pyrrolidinoethyl) styrene (PES) and m-(2-pyrrolidino-1-methylethyl) alpha-methylstyrene (PAMS) groups.

Abstract: The present invention provides a TFE/Pr type elastomer being excellent in not only amine resistance but also heat resistance and chemical resistance and having a small gel content, and a crosslinkable composition comprising the elastomer. The above-mentioned fluorine-containing elastomer is a fluorine-containing elastomer being crosslinkable with the compound (A), comprising 40 to 70% by mole of tetrafluoroethylene unit, 30 to 60% by mole of propylene unit and 0.1 to 2.5% by mole of a carboxyl group-containing vinyl monomer unit and having a Mooney viscosity at 121° C. of 5 to 100.

Abstract: Butadiene copolymers are brominated using certain quaternary ammonium tribromides as the brominating agent. The bromination process proceeds easily under mild conditions, and produces a brominated product that has excellent thermal stability. A quaternary ammonium monobromide salt is produced as a reaction by-product. A solvent for the monobromide salt is added to the reaction after 25-90% bromination of the aliphatic carbon-carbon double bonds. This provides for significantly shorter reaction times while providing a product with few impurities.

Abstract: Water-soluble functionalized cationic copolymers obtainable by a process which comprises reacting a cationic base polymer which contains amino groups with at least one functional compound reactive to at least a part of the amino groups on the base polymer, are useful in personal care and cosmetic formulations.

Abstract: This invention relates to curable fluoroelastomer compositions comprising a) fluoroelastomers having either nitrile, alkyne or azide cure sites and b) fluorinated curatives containing diazide, dinitrile or dialkyne groups for reacting with cure sites on the fluoroelastomer. Fluoroelastomers having azide cure sites form crosslinks with curatives having dinitrile or dialkyne groups. Fluoroelastomers having nitrile or alkyne cure sites form crosslinks with curatives having diazide groups.

Abstract: To provide a novel fluorinated compound, a fluoropolymer and a method for producing the compound. A compound represented by the formula CF2?CFCF2C(X)(C(O)OZ)(CH2)nCR?CHR (wherein X is a hydrogen atom, a cyano group or a group represented by the formula —C(O)OZ, Z is a hydrogen atom or a C1-20 monovalent organic group, n is 0, 1, or 2, and R is a hydrogen atom or a C1-20 monovalent organic group), a method for producing it, and a fluoropolymer obtained by polymerizing the compound.

Abstract: A thermally stable brominated butadiene copolymer, such as brominated styrene/butadiene block copolymer, brominated random styrene/butadiene copolymer or brominated styrene/butadiene graft copolymer, preparation of the brominated butadiene copolymers, use of the brominated butadiene copolymers as a flame retardant additive and polymeric compositions, both foamed and non-foamed, that incorporate a flame-retarding amount of brominated butadiene copolymer.

Abstract: Partially neutralized chlorosulfonated polyolefin elastomers containing 0.5-10 weight percent chlorine and 0.25 to 5 weight percent sulfur are prepared from polyolefin elastomer base resins selected from the group consisting of propylene/ethylene copolymers, ethylene/propylene/diene copolymers, isobutylene/diene copolymers, isobutylene homopolymers, hydrogenated styrene/butadiene block copolymers and hydrogenated styrene/isoprene block copolymers.

Abstract: A chlorinated propylene-based polymer of the present invention having a weight average molecular weight (Mw) as measured by gel permeation chromatography (GPC) of 5,000 to 100,000 and a chlorine content of 0.1 to 70% by mass has the following properties: (1) it has a high solubility in a non-aromatic solvent having a low environmental burden even when it has a low degree of chlorination, and (2) it can be inhibited from suffering a decrease in the properties inherent to polypropylenes, such as durability, mechanical properties, appearance and hydrophobicity, by regulating its degree of chlorination at a low value.

Abstract: Butadiene copolymers are brominated using certain quaternary ammonium tribromides as the brominating agent. The bromination process proceeds easily under mild conditions, and produces a brominated product that has excellent thermal stability.

Abstract: A higher olefin polymer having a polar group which is produced by subjecting to an incorporation reaction of a polar compound or halogen compound into a higher ?-olefin polymer satisfying the requirements of the following (1) and (2), which is obtained by polymerizing one or more higher ?-olefins having 10 or more carbon atoms or copolymerizing one or more higher ?-olefins having 10 or more carbon atoms with one or more other olefins and a method for producing a higher olefin polymer having a polar group which is obtained by polymerizing one or more higher ?-olefins having 10 or more carbon atoms or copolymerizing one or more higher ?-olefins having 10 or more carbon atoms with one or more other olefins to form a higher ?-olefins polymer satisfying the requirements of the following (1) and (2) and subsequently subjecting to an incorporation reaction of a polar compound or halogen compound into the higher ?-olefin polymer.

Abstract: The present invention provides novel, polymeric supports, methods of making, and methods of using the supports, that have a fluorinated, amidated surface. The supports include polymeric microbeads, thin layers or membranes, plates, monoliths and the like. The supports are useful as packing materials for normal phase, reverse phase, and size exclusion chromatography, and provide high speed separation of analytes with excellent resolution.

Abstract: Provided is a vinyl polymer of a sulfonated monomer having a basic skeleton represented by the following formula (1), wherein x is 1 to 20 and n is 10 to 10,000. Also provided is a novel hydrocarbon vinyl polymer aimed at providing a hydrocarbon solid polymer electrolyte which can become a substitute for a fluorine electrolyte, and which has chemical and physical properties sufficient for practical use, yet can be produced at a low cost. Additionally, provided is a polymer electrolyte membrane suitable as the ion-exchange membrane of a solid polymer fuel cell by employing the polymer of a sulfonated vinyl monomer which has excellent film-forming properties and a large ion-exchange capacity (EW).

Abstract: Bromination of styrenic polymer is carried out in a closed reaction system to retain HX coproduct (where HX is HBr or HCl, or both) in the bromination reaction mixture at superatmospheric pressure. Preferably, the reaction mixture which includes the brominated styrenic polymer and substantially all of the HX coproduct formed is discharged into an aqueous quenching medium. By operating in this manner, the reaction is terminated and the brominated styrenic polymer of desired bromine content and substantially all HX coproduct are captured in the same operation, process equipment costs are reduced, and processing of the reaction mixture is facilitated.

Abstract: Bottles made of metallocene polypropylene (mPP) for storage and dispensing reservoirs for fragrance compositions, in particular fragrance oils, are described. The mPP bottles can be used in warmer units for slow release dispensing of the fragrance therein. The metallocene polypropylene bottles can be produced by extrusion or injection blow molding, injection molding, injection stretch blow molding (single or two stage), or other suitable molding process. The mPP bottles may optionally have at least one barrier coating layer and/or adhering layer. The mPP bottles may optionally be fluorinated. The mPP bottles have good clarity and possess the required physical properties needed when the bottles are filled on a production line.

Abstract: The present invention provides novel, polymeric supports, methods of making, and methods of using the supports, that have a fluorinated, amidated surface. The supports include polymeric microbeads, thin layers or membranes, plates, monoliths and the like. The supports are useful as packing materials for normal phase, reverse phase, and size exclusion chromatography, and provide high speed separation of analytes with excellent resolution.

Abstract: The instant invention relates to a process for the preparation of hydroxy-vinyl-aromatic polymers in particular 4-hydroxystyrene polymers or copolymers by anionic or controlled radical polymerization of the respective monomer, wherein the hydroxy functionality is blocked with a protective group which is subsequently removed by reacting it with a halosilane reagent. The resulting (co)polymers have a narrow polydispersity and are useful for manufacturing photoresists.

Abstract: This method for preparing an acrylic-modified chlorinated polyolefin resin comprises graft-copolymerizing an acid-modified chlorinated polyolefin resin with a monomer mixture containing a (meth)acrylate ester monomer having one hydroxyl group and another vinyl monomer in the presence of a cyclic ether compound. Also, the cyclic ether compound may be added in an amount of 1 to 100 parts by weight based on 100 parts by weight of the acid-modified chlorinated ployolefin resin, and the cyclic ether compound may be dioxane and/or 1,3-dioxolane.

Abstract: The invention relates to polymers obtained by S-alkylation of sulfinated polymers with alkylation agents, and AB-cross-linked polymers obtained by reacting polymers containing alkylation groups with low-molecular sulfinates, under S-alkylation, or AB-cross-linked polymers obtained by S-alkylation of sulfinated polymers with polymers containing alkylation groups.

Abstract: Chemical reactions are carried out with molten fluoropolymer, most conveniently in an extruder, wherein the reaction zone in the extruder is isolated from the melting zone, and the molten fluoropolymer is subdivided in the reaction zone sufficiently that contact and reaction between the reactant and the molten fluoropolymer in the reaction zone is essentially free of mass transfer limitation, followed by devolatilization in isolation from the reaction zone, and cooling the devolatilized fluoropolymer.

Abstract: The invention pertains to a method for making a block or gradient final (co)polymer comprising a step of radically polymerizing a mixture of ethylenically unsaturated monomers in the presence of a) a radical precursor and b) an iodine atom-containing intermediate polymer or a mixture of iodine atom-containing intermediate polymers, wherein the iodine atom-containing intermediate polymer comprises at least 50 mole % of methacrylate monomers and is obtainable from a polymerization of ethylenically unsaturated monomers.

Abstract: The present invention relates to a process for preparing tritylated polystyrene resin. More particularly, the present invention is directed to a process for preparing tritylated polystyrene resins, comprising a step for tritylating polystyrene by reacting polystyrene resin with benzophenone dichloride or substituted benzophenone dichloride to introduce trityl group on the benzene moiety of the polystyrene.

Abstract: The present invention provides a coating composition for polyolefin resins, comprising a resin obtained by graft-copolymerizing at least one member selected from the group consisting of an ?,?-unsaturated carboxylic acid and an acid anhydride thereof with at least one member selected from the group consisting of polypropylene and a propylene-?-olefin copolymer, chlorinating the graft copolymer to give an acid-modified chlorinated polyolefin, linking a (meth)acrylic ester having one hydroxyl group to the polyolefin via an ester linkage, and then graft-copolymerizing (meth)acrylic acid monomers with the polyolefin; and a process for producing the composition.