Abstract: A latex composition including a latex (A) of a diene rubber (a) having a weight average molecular weight of 50,000 or more and 1,000,000 or less and containing an ethylenically unsaturated acid monomer unit; and a latex (B) of a diene rubber (b) having a weight average molecular weight of 500 or more and less than 50,000 and containing an ethylenically unsaturated acid monomer unit.

Abstract: Described herein are polymers and associated methods to occlude structures and malformations of the vasculature with polymers with delayed controlled rates of expansion. Methods of forming such devices are also disclosed.

Abstract: An anode includes a thin film of an anode material; and a protective layer that is formed on the thin film of the anode material, that is composed of functionalized metal oxide nanoparticles, which are lithium-terminated sulfonated metal oxide nanoparticles, and that has a thickness of 300-5000 nm. A method for manufacturing the anode includes dispersing the functionalized metal oxide nanoparticles into a dispersion medium to form a dispersion; dipping a substrate into water, and introducing the dispersion thereto so that the functionalized metal oxide nanoparticles form a self-assembled molecular film on the water surface; lifting the substrate over the water surface to transfer the self-assembled molecular film onto the substrate, thereby providing a substrate coated with a functionalized metal oxide film; and transferring the functionalized metal oxide film onto the thin film of the anode material to provide an anode coated with the functionalized metal oxide film.

Abstract: Described herein are polymers and associated methods to occlude structures and malformations of the vasculature with polymers with delayed controlled rates of expansion. Methods of forming such devices are also disclosed.

Abstract: A method for governing care of a person includes determining the importance of a candidate activity (84) relative to the importance of patient sleep continuity (104) and, if the candidate activity is more important than sleep continuity, carrying out the activity or indicating the acceptability of carrying out the activity (106) and, if the candidate activity is not more important than sleep continuity, refraining from carrying out the activity or indicating the unacceptability of carrying out the activity (108). A system for patient care governance comprises a decision engine (80) for determining the importance of the candidate activity relative to the importance of sleep continuity, and a controller (92) responsive to the decision engine for issuing a command to carry out the activity or indicate the acceptability of carrying out the activity (106), refrain from carrying out the activity or indicate the unacceptability of carrying out the activity (108).

Abstract: The invention relates to a process for preparing a dispersion-based or hotmelt pressure-sensitive adhesive based on at least one polymer, which involves crosslinking the at least one polymer, the polymer having functional groups Y, the polymer additionally being admixed with at least one kind of functionalized particles which have at least one polymeric base unit, characterized in that the particles have a monomer as base unit, the monomer having at least one kind of functional groups Z which are not able to enter into any reaction with the functional group Y and which, by thermal energy, electromagnetic radiation, particulate radiation and/or sound energy, are converted into the group X, the crosslinking of the polymer being brought about at least in part by a reaction of the functional groups X of the particles and of the functional groups Y of the polymer, and additionally to pressure-sensitive adhesives based on at least one crosslinked polymer component, wherein the crosslinking of the polymer component

Abstract: The present invention relates to a process for the modification of a polymer surface. The polymer surface is treated with (i) an organoborane-amine complex and subsequently with (ii) a radically polymerizable monomer compound and optionally a deblocking agent.

Abstract: The invention relates to a process for preparing a pressure-sensitive adhesive based on at least one polymer, in the course of which said at least one polymer is crosslinked, the polymer having functional groups Y and having been admixed, further, with at least one kind of functionalized particles which have at least one nonpolymeric base unit, wherein the particles having a surface modification of the base unit, the surface modification of the particles having at least one kind of functional groups Z, which can not undergo any reaction with the functional group Y and is converted into group X by thermal energy, electromagnetic radiation, particulate radiation and/or sound energy and the crosslinking of the polymer being brought about at least in part by a reaction of the functional groups X of the particles and the functional groups Y of the polymer, and further to pressure-sensitive adhesives based on at least one crosslinked polymer component, the crosslinking of the polymer component being brought about a

Abstract: A novel process for reducing the molecular weight of nitrile rubber in the presence of specific catalyst systems containing the metathesis catalyst and also a specific addition of fluorine-containing boron compounds is provided.

Abstract: The present invention relates to a process for preparing a high impact monovinylaromatic polymer comprising admixing a rubber, at least one monovinylaromatic monomer and optionally one or more comonomer in the presence of at least a borane complex of the L-BH3 type wherein L is a Lewis base and polymerizing the monovinylaromatic monomer. The borane complex initiator, L may be an ether (e.g THF, tetrahydrofurane), a thioether (e.g dimethylthioether) or an amine. A preferred complex is an amine borane such as by way of example triethylamine borane. The present invention also relates to a high impact monovinylaromatic polymer having a weight ratio of grafted monovinylaromatic monomer and optional comonomer to the initial monovinylaromatic monomer and optional comonomer above 0.1%, advantageously above 2% and preferably in the range 2 to 4%. The invention is of particular interest to make high impact polystyrene.

Abstract: The composition and preparation of multiple graft low molecular weight polymers useful as dispersants are described. The dispersants described are suitable for controlling sludge and varnish as well as soot. The product is useful as a lubricant additive and a fuel additive.

Abstract: A K type of copolyarylborane: wherein hydrogen atoms are bonded to the ends; Arn represents at least one of Ar1, Ar2, and Ar3; each of Ar1 and Ar2 represents an arylene radical; Ar3 represents an heteroaromatic arylene radical; Ar1 has a ? electron density of no less than that of benzene; Ar2 is capable of hole transport; Ar3 has a ? electron density of no greater than that of benzene and less than that of Ar1; x, y, and z respectively represent the molar parts of Ar1, Ar2, and Ar3; each of x, y, and z is in the range of 0-1, and x+y+z=1; and R represents an aryl radical. This K type of copolyarylborane may be of use for organic light-emitting diodes (OLEDs), organic solar cells, organic photodetectors, and organic field-effect transistors.

Abstract: A golf ball comprising a core, an outer cover layer, and, optionally, an intermediate layer disposed between the core and the outer cover layer is provided. The core, intermediate layer, or cover layer includes a composition formed from a base polymer blend, a crosslink initiator, and at least one additive. The outer cover layer may comprise a polyurethane or polyurea composition. The base polymer blend preferably includes two or more rubber materials. The additive has at least one C—O—B linkage, the carbon in the linkage being a secondary or tertiary carbon and is selected from the group consisting of boranes, borates, boronates, borinates, heterocylic compounds having at least one boron atom as a ring member, boron-containing organosulfides, salts of such additives, and metal salts, organometallic salts, and non-metal salts of boron complexes.

Abstract: The present invention relates to a process for preparing a high impact monovinylaromatic polymer comprising admixing a rubber, at least one monovinylaromatic monomer and optionally one or more comonomer in the presence of at least a borane complex of the L-BH3 type wherein L is a Lewis base and polymerizing the monovinylaromatic monomer. The borane complex initiator, L may be an ether (e.g THF, tetrahydrofurane), a thioether (e.g dimethylthioether) or an amine. A preferred complex is an amine borane such as by way of example triethylamine borane. The present invention also relates to a high impact monovinylaromatic polymer having a weight ratio of grafted monovinylaromatic monomer and optional comonomer to the initial monovinylaromatic monomer and optional comonomer above 0.1%, advantageously above 2% and preferably in the range 2 to 4%. The invention is of particular interest to make high impact polystyrene.

Abstract: A golf ball including a core and at least one layer disposed about the core, wherein the core or the layer includes a composition formed from a base polymer, a crosslink initiator, and at least one additive. The additive has at least one C—O—B linkage, the carbon in the linkage being a secondary or tertiary carbon. The additive is also selected from the group consisting of boranes, borates, boronates, borinates, heterocylic compounds having at least one boron atom as a ring member, boron-containing organosulfides, sulfur-containing silicocompounds, salts of such additives, and metal salts, organometallic salts, and non-metal salts of boron complexes.

Abstract: Embodiments of the present invention include a polypropylene homopolymer synthesized from a metallocene catalyst system and methods of forming the homopolymer, the homopolymer having an aluminum and chlorine recoverables value of less than 25 ppm and a xylene solubles of less than 1 wt % relative to the total weight of the homopolymer. The resulting homopolymer has other desirable properties such as a heat deflection temperature at 0.45 MPa of from 90° C. to 110° C., and a MWD value of from 1.7 to 5.0. These properties make embodiments of the homopolymer desirable for films, and in particular for capacitor films.

Abstract: An in situ controlled oxidation reaction of trialkylborane (BR3) in the presence of polyolefin and maleic anhydride produces mono-oxidized trialkylborane adducts, i.e., peroxyldialkylborane (R—O—O—BR2), that can undergo homolytic cleavage to form (R—O* *O—BR2) and activate the polyolefin chain by alkoxyl radical (R—O*) hydrogen-abstraction at ambient temperature. The formed polymeric radical (C*), associated with the oxidized borane moiety (*O—BR2), then reacts with maleic anhydride by addition reaction, without side reactions, to form functional polyolefins that contain incorporated maleic anhydride side groups.

Abstract: An in situ controlled oxidation reaction of trialkylborane (BR3) in the presence of polyolefin and maleic anhydride produces mono-oxidized trialkylborane adducts, i.e., peroxyldialkylborane (R—O—O—BR2), that can undergo homolytic cleavage to form (R—O* *O—BR2) and activate the polyolefin chain by alkoxyl radical (R—O*) hydrogen-abstraction at ambient temperature. The formed polymeric radical (C*), associated with the oxidized borane moiety (*O—BR2), then reacts with maleic anhydride by addition reaction, without side reactions, to form functional polyolefins that contain incorporated maleic anhydride side groups.

Abstract: Polyolefin diblock copolymers are prepared via a chain transfer reaction with a borane dimer compound during a transition metal-catalyzed olefin polymerization in a process that resembles a transformation from transition metal coordination polymerization to free radical polymerization via a borane end group. The polyolefin diblock copolymers may be represented by the following formula: (Transition Metal Prepared Polyolefin)-b-(Free Radical Prepared Polymer), wherein the polyolefin segment is a homo-, co- and ter-polymer prepared by transition metal (especially metallocene catalyst) coordination polymerization of at least one olefin, and the free radical prepared polymer segment is prepared by free radical polymerization of at least one vinyl monomer, such as styrene, maleic anhydride, acrylates, methacrylates and their mixtures. The resulting diblock copolymers are useful as the interfacial materials to improve the interaction between polyolefins and other materials.

Abstract: Herein disclosed are a block copolymer having an isobutylene-based polymer block and a vinylic aromatic hydrocarbon-based polymer block and containing a styrenic unit having a halogenated saturated aliphatic hydrocarbon group on the benzene ring at 0.01 to 2 mol % on a basis of the total structural units and being capable of markedly improving the performance of a synthetic resin when the block copolymer is blended with the synthetic resin; a process for producing the block copolymer; and a resin composition position containing the block copolymer.

Abstract: An isobutylene-based polymer as a polymer of cationically polymerizable monomers principally composed of isobutylene or a combination of isobutylene and a styrene-series monomer, generates a molded article with outstanding properties, the isobutylene-based polymer characteristically satisfying the following provisions;1. the isobutylene-based polymer has a substantially continuos molecular weight distribution on a gel-permeation chromatogram;2. the molecular weight at the highest peak on a gel-permeation chromatogram is within a range of 10,000 to 500,000; and3. the length (a) of the elution time in the lower molecular region of the mountain from the highest peak and the length (b) of the elution time in the higher molecular region of the mountain from the highest peak on a gel-permeation chromatogram, satisfy the provision represented by the formula (b)/(a).gtoreq.1.3.

Abstract: The invention is a process for the manufacture of six-armed radial asymmetric block copolymers, comprising of the steps of anionically polymerizing first polymer arms, contacting the first polymer arms with a non polymerizable coupling agent containing 6 functional groups, the amount of the first polymer arms being substantially stoichiometrically corresponding to 4 of the functional groups, anionically preparing second polymer arms, different from the first polymer arms, in the same reactor, adding a polar compound capable of increasing the reactivity of the residual functional groups of the coupling agent, reacting these residual functional groups with the second polymers arms, and recovering the asymetric polymer. The asymmetric polymers are useful in adhesive, coating, or sealant compositions and in bitumen blends for roofing, and in sound deadening or vibration dampening compositions.

Abstract: A process for preparing a controlled functional density poly(secondary amine) comprising: (a) contacting a polymer containing olefinic unsaturation with carbon monoxide in hydrogen under hydroformylation conditions in the presence of a hydroformylation catalyst to produce a controlled functional density polyaldehyde containing reactive carbon-carbon double bonds, and (b) contacting the polyaldehyde with hydrogen and a primary amine under reductive amination conditions in the presence of a ruthenium-containing imine hydrogenation catalyst or (b.sup.1) contacting the polyaldehyde with a sterically hindered aliphatic or cycloaliphatic primary amine or an aromatic primary amine under reductive amination conditions in the presence of an alkali metal borohydride to produce poly(secondary amine) having a substantially equivalent ratio of secondary amine groups to reactive carbon-carbon double bonds as the ratio of aldehyde groups to reactive carbon-carbon double bonds in the polyaldehyde.

Abstract: A process for preparing a controlled functional density poly(secondary amine) comprising: (a) contacting a polymer containing olefinic unsaturation with carbon monoxide in hydrogen under hydroformylation conditions in the presence of a hydroformylation catalyst to produce a controlled functional density polyaldehyde containing reactive carbon-carbon double bonds, and (b) contacting the polyaldehyde with hydrogen and a primary amine under reductive amination conditions in the presence of a ruthenium-containing imine hydrogenation catalyst or (b.sup.1) contacting the polyaldehyde with a sterically hindered aliphatic or cycloaliphatic primary amine or an aromatic primary amine under reductive amination conditions in the presence of an alkali metal borohydride to produce poly(secondary amine) having a substantially equivalent ratio of secondary amine groups to reactive carbon-carbon double bonds as the ratio of aldehyde groups to reactive carbon-carbon double bonds in the polyaldehyde.

Abstract: A method for producing asymmetric radial polymers which comprises anionically polymerizing an anionically polymerizable monomer to form a first set of living polymer arms, coupling the first set of living polymer arms with a silicon-based coupling agent, substantially completing the coupling reaction, anionically polymerizing, in the presence of the coupled first set of polymer arms, a different anionically polymerizable monomer(s) to form a second set of living polymer arms, and adding a coupling activator and coupling the second set of living polymer arms to the coupled first set of polymer arms to form the asymmetric radial polymer.

Abstract: A living carbocationic catalyst composition comprising an initiator of a tertiary alkyl halide, a tertiary aralkyl halide or polymeric halide a co-initiator of an alkyl aluminum or alkyl boron, a proton scavenger and a solvent medium with a dielectric constant between 2.5 and 3.25 is used to produce narrow molecular weight distribution polymers particularly isobutylene polymers.

Abstract: A dental or surgical adhesive filler containing (a) a polymerizable acrylic acid or methacrylic acid derivative, (b) a vinyl polymer powder, (c) an organic boron compound as a curing agent, and optionally, a polar organic compound and an inert diluent. The advantage of the above dental or surgical adhesive filler is that it is easy to handle due to stability in curing time and freedom of ignition.

Abstract: Novel styrene derivatives are disclosed of the formula: ##STR1## wherein R.sub.1 and R.sub.2 are the same or different and each represents a saturated aliphatic hydrocarbon group or an aromatic hydrocarbon group, and R.sub.3 is --OH, Cl, or a group of the formula --OR.sub.4 or ##STR2## wherein R.sub.4 represents a saturated aliphatic hydrocarbon group or an aromatic hydrocarbon groups. The functionalized styrene monomers I as well as polymers and copolymers incorporating such monomer units are useful as initiators, or precursors thereof, for the polymerization of isobutylene under cationic conditions to give graft copolymers containing both styrenic and isobutylenic units. These copolymers have commercial applications such as rubbers, coatings, and luricants.

Abstract: Hydrocarbons and polymers thereof, of the structure (I)R--C(CH.sub.3).sub.2 --CH.sub.2 --C(CH.sub.3).sub.2 --CH.sub.2 --CH.dbd.CH--CH.sub.2 --Cl (I)where R is a hydrocarbon radical, are prepared by reacting corresponding starting materials which contain chlorine bonded to tertiary carbon, of the structureR--C(CH.sub.3).sub.2 --CH.sub.2 --C(CH.sub.3).sub.2 --Cl (II)with from 1 to 10 moles of butadiene in the presence of a Friedel-Crafts catalyst in a solvent which is inert to the catalyst, and the hydrocarbons or polymers thereof can be reacted in a further step of the process with a compound from the group comprising ammonia, primary or secondary amine or polyamine, amino alcohol, amino ether, hydrazine or hydrazine which is substituted up to three times.

Abstract: Novel styrene derivatives are disclosed of the formula: ##STR1## wherein R.sub.1 and R.sub.2 are the same or different and each represents a saturated aliphatic hydrocarbon group or an aromatic hydrocarbon group, and R.sub.3 is --OH, Cl, or a group of the formula --OR.sub.4 or ##STR2## wherein R.sub.4 represents a saturated aliphatic hydrocarbon group or a n aromatic hydrocarbon group. The functionalized styrene monomers I as well as polymers and copolymers incorporating such monomer units are useful as initiators, or precursors thereof, for the polymerization of isobutylene under cationic conditions to give graft copolymers containing both styrenic and isobutylenic units. These copolymers have commercial applications such as rubbers, coatings, and lubricants.

Abstract: Novel block polymers which are thermoplastic elastomers which are thermoplastic elastomers are provided for use as binders in high-energy compositions such as propellants, explosives, gasifiers or the like. The block polymers have an ABA structure wherein the A blocks are crystalline at temperatures below 60.degree. C. and the B blocks are amorphous at temperatures above -20.degree. C. Both the A and B blocks are polyethers formed from monomers of oxetanes and/or tetrahydrofuran. The block polymers melt in the range of 60.degree. C. to 120.degree. C. and have low viscosities above their melting points due to mutual miscibility of the A and B blocks.

Abstract: This invention provides a novel catalyst composed of a complex of an organic acid or its ester and a Lewis acid, preferably boron trichloride that can add olefin monomers to increase the molecular weight of the complex from as low as 200 to in excess of a million, with the complex being active viz., living, until the complex dies, viz., is decomposed or destroyed so that polymers in the liquid or easily liquefiable range of 300 to about 10,000 can be made of those more difficult to be liquefied or unliquefiable, viz., those of over 10,000 up to 100,000 or in some cases 500,000 and then those in the range of the elastomers, or moldable or extrudable plastics range having very high molecular weights, generally in excess of 100,000 up to in excess of 500,000 and having useful end groups such as the halogens and specifically chloride, allyl, acryl or methacryl, acetate or formate to name some of the more useful ones.

Abstract: Block copolymers compose a polyisobutylene rubbery soft segment of M.sub.n of about 5,000 to above 500,000 and glassy hard segments of M.sub.n of about 5,000 or higher and usually about 10,000 to 35,000 or more, are made by preparing a living polymer block of the polyisobutylene and then polymerizing on said living polyisobutylene block the glassy hard segments by adding thereto an electron donor having a donor number of 15 to 50 and then adding and polymerizing the monomers for the glassy hard segments. The monomers for the glassy hard segments are styrene and its derivatives and indene and its derivatives and mixtures thereof.

Abstract: A polymerization process is provided for producing a terminally functional polymer which comprises introducing a monomer charge, a Lewis acid and an organic peroxy compound into a suitable reaction vessel and polymerizing the monomer charge at a temperature of from about 0.degree. to about -80.degree. C. to form the terminally functional polymer, wherein the monomer charge comprises isobutylene and the organic peroxy compound is charged in an amount of from about 10.sup.-4 to about 10.sup.-1 moles per mole of the isobutylene. In a preferred embodiment, the monomer charge additionally comprises vinylidene aromatic or diolefin monomers. In another preferred embodiment the monomer charge comprises the sequential addition of isobutylene and vinylidene aromatic or diolefin monomers. In a further preferred embodiment said reaction vessel is additionally charged with an electron door having an electron door number of from about 22 to about 50 the amount of said electron door being from about 10.sup.-4 to about 10.

Abstract: The invention relates to a method of preparing allyl-terminated polyisobutylene (PIB) by allylation with allyltrimethylsilane of tertiary chloro-capped PIB by electrophilic substitution. The synthesis begins with the BCl.sub.3, catalyzed mono- or oligo-tertiary chloride "inifer" initiated polymerization of isobutylene, followed in the same reaction vessel by the addition of hexane, allyltrimethylsilane, and TiCl.sub.4.

Abstract: This invention describes the preparation of reactive engineering thermoplastics containing arylcyclobutene groups pendant to an aromatic ring. The polymers are prepared by alkylation or acylation of an engineering thermoplastic which contains one or more aromatic groups capable of being alkylated or acylated with a suitable arylcyclobutene alkylating or acylating agent. The prepared reactive engineering thermoplastics containing pendant arylcyclobutene groups may be cross-linked and cured by heating above about 200.degree. C.

Abstract: The aerobically hardenable compositions which comprise polymerizable systems containing components having some degree of ethylenic unsaturation and an oxygen-stable polymerization initiator of at least one organo-boron compound containing at least a major portion of boron to carbon bonds and possibly some boron to hydrogen bonds in the molecule and the boron containing radials are bound to an organic polymer matrix which is oxygen stable, the compositions being useful as casting resins, fillers and adhesives.

Abstract: The invention relates to a process for preparing terpolymer polyblends having high gloss and ductility in formed articles, wherein, rubber particles in an aqueous latex are reacted with an alkenyl aromatic, alkenyl nitrile and alkyl acrylate monomer formulation such that said rubber particles become grafted with at least a portion of said monomers while said monomers form a matrix terpolymer phase of said monomers followed by separating said matrix phase terpolymer and said grafted rubber particles from said latex as a terpolymer polyblend. The invention also relates to a composition of said process.

Abstract: Novel telechelic halogenated polymers of cationically polymerizable olefin monomers are formed carrying from 2 to about 6 terminal halogens. The telechelic halogenated polymers are formed by reacting the monomer with an initiator transfer agent, carrying at least two tertiary halogens, and under cationic polymerization conditions. Additionally, novel thermoplastic elastomer block copolymers are formed from these telechelic halogenated polymers by reacting the latter with vinyl aromatic monomers in the presence of a coinitiator.

Abstract: Coating compositions which are free of volatile organic solvents and curable under the action of heat or radiation without undesirable evaporation of organic solvents, prepared by reacting a copolymer resin of a cyclopentadiene type compound such as dicyclopentadiene and maleic anhydride, with at least one compound represented by the formula ##STR1## or the like wherein X is H or --CH.sub.3 and R is --CH.sub.2 CH.sub.2 OH or the like to produce a resin which is then dissolved in a reactive solvent such as a (meth)acrylate type monomer or ammonia water; and a process for preparing the coating compositions.

Abstract: A process for production of the maleic anhydride adduct of a liquid polymer having a maleic anhydride addition amount of 2 to 70% by weight, which comprises reacting a liquid polymer having a molecular weight of 150 to 5,000 and a viscosity of 2 to 50,000 cp at 30.degree. C. in the presence of at least one compound, as a gelation inhibitor, selected from the group consisting of imidazoles, thiazoles, metallic salts of mercaptothiazoles, urea derivatives, naphthylamines, nitrosamines, iron, iron compounds and specific halogen compounds, said liquid polymer being selected from the group consisting of liquid polybutadienes, liquid polyisoprenes and liquid copolymers comprising units of butadiene or isoprene and units of at least one compound selected from the group consisting of other diolefins, olefins and aromatic vinyl compounds.

Abstract: Block copolymers compose a polyisobutylene rubbery soft segment of M.sub.n of about 5,000 to above 500,000 and glassy hard segments of M.sub.n of about 5,000 or higher and usually about 10,000 to 35,000 or more, are made by preparing a living polymer block of the polyisobutylene and then polymerizing on said living polyisobutylene block the glassy hard segments by adding thereto an electron donor having a donor number of 15 to 50 and then adding and polymerizing the monomers for the glassy hard segments. The monomers for the glassy hard segments are styrene and its derivatives and indene and its derivatives and mixtures thereof.