Abstract: Process for the continuous bulk production of high impact vinylaromatic copolymers in which the vinylaromatic monomer, and if present, a comonomer selected from the group consisting of acrylonitrile, methacrylonitrile, acrylic acid, methacrylic acid and their alkyl- or cyclo-alkyl-esters containing from 1 to 8 carbon atoms in the alkyl group, the rubber, a part of the diluent solvent and the catalyst are premixed in a premixer at a temperature under 100.degree. C. and fed to a plug-flow agitated tubular reactor, which is divided into several stages or zones. The excess mixture is recycled to the premixer and the remaining part of the diluent solvent is injected into the top of the reactor to prevent the formation of incrustations. In the first zone of the reactor, the temperature and the residence time of the mixture are regulated so to have the halving the catalyst life.

Abstract: Novel diene/methacrylate ester block polymers, especially tertiary butyl methacrylate ester block polymers are uniquely prepared at near ambient temperatures and capable of being hydrolyzed and neutralized to yield the corresponding methacrylic acid and methacrylic acid salt (ionomer) derivatives. The compositions are usefully employed in the preparation of thermoplastic elastomers, adhesives and laminating films.

Abstract: Polyolefin-vinyl polymer composites are produced by impregnating polyolefin particles with vinyl monomer and free radical polymerization initiator in the ratio of about 10-200 parts by weight of vinyl monomer and 0.01-4.0 parts by weight free radical polymerization initiator per 100 parts by weight polyolefin, the impregnation being effected by slowly mixing the components at room temperature or at an elevated temperature below the decomposition temperature of the free radical polymerization initiator. After the impregnation is completed, an aqueous suspension of the mixture is formed by adding the same to water in a ratio of about 100 parts by weight of mixture per 80-1000 parts by weight of water, after which the aqueous suspension is heated to a temperature sufficiently high to polymerize the vinyl monomer.

Abstract: The maleimide copolymer of the invention is of the class of N-substituted maleimide copolymer such as N-alkyl or N-aromatic maleimide copolymer having peroxy bonds in a molecule, utilizable as a precursor for preparing a maleimide block copolymer and as a modifier for other resins. The maleimide block copolymer, which is useful as a molding material or a thermal resistance improver, is obtained by polymerizing maleimide monomers in the presence of a polymeric peroxide followed by polymerizing vinyl monomers.

Abstract: Curing product based onA) compounds having at least two R.sup.1 R.sup.2 C.dbd.CR.sup.3 --X groups (I) andB) compounds having methanetricarboxamide units of the formula ##STR1## these compounds B) containing at least two groups having active H atoms of the type ##STR2## In order to prepare this curing product, the compounds A) and B) of an oligomeric and/or polymeric reaction product are reacted in the presence of at least one catalyst. The mixtures of A) and B) can be used as two-component lacquers on their own or together with customary additives.

Abstract: Elastomers based on acrylates, which are comprised, in the amount of at least 40 wt. % and as much as 100 wt. %, of one or more copolymers having a molecular weight>50,000 daltons and comprised of units of:i) acrylate monomers in the amount of 50-95 wt. %, andii) macromonomers comprised of a vinylic group and, covalently bonded with such group, a polyvinyl unit selected from the group of acrylates and methacrylates and having a glass transition temperature Tg at least 60.degree. C. and molecular weight 500-100,000 dalton.

Abstract: A composition comprising (i) a copolymer of ethylene; one or more polar unsaturated alcohols, acids, or esters; and a N-substituted maleimide or (ii) a copolymer of ethylene and one or more polar unsaturated alcohols, acids, or esters grafted with an N-substituted maleimide.

Abstract: Disclosed is a method of making graft copolymers of olefin polymers by contacting a particulate olefin polymer with a free radical polymeriztion initiator, e.g., a peroxide, and a vinyl monomer at about from 60.degree. to 125.degree. C., while controlling the monomer addition rate so that it does not exceed about 4.5 pph/min, and most preferably does not exceed about 3.0 pph/min, at any monomer feed level. To prevent polymer degradation, a non-oxidizing environment is maintained throughout the process, and residual free radicals are deactivated, and unreacted initiator is decomposed, before the graft copolymer is exposed to air.

Abstract: Ethylene/vinyl acetate copolymers containing very high molecular weight components and having a reduced tendency to tackiness may be obtained by a further addition of ethylene during the process of solution polymerization at a moderate pressure.

Abstract: A methacrylimide-containing polymer comprising a polymer (A) comprised of 5-100 weight % of units represented by the formula (I): ##STR1## wherein R is H or C1-20 hydrocarbon group, and 0-95 weight % of units derived from an ethylenic monomer, wherein a polymer derived from at least one ethylenic monomer has been grafted onto the polymer (A). The methacrylimide-containing polymer is used as a blend with another thermoplastic polymer.

Abstract: Graft polymers are prepared by the free radical reaction of a base polymer such as polyethylene or polypropylene with an olefinic compound containing a tertiary alkyl ester group, which may be a simple carboxylic acid or a carbamic acid ester group. Upon melt blending or the like with polymers containing other functional groups, such as carboxy- or epoxy-functionalized polyphenylene ethers, the t-butyl groups are removed by thermal degradation and there are obtained copolymers which are useful to compatibilize blends of the corresponding polymeric constituents.

Abstract: This invention relates to a process for the catalytic grafting of an ethylenically unsaturated monomer onto a copolymer in the presence of a catalyst. The monomer is selected from the group consisting of ethylenically unsaturated carboxylic acids, anhydrides esters and other derivatives thereof. The copolymer is selected from the group consisting of certain copolymers of ethylene and ionomers of such copolymers. The catalyst is a mixture of (a) a certain amount of water and (b) at least one of certain phosphorus-containing compounds. The process comprises admixing copolymer, monomer, catalyst and an organic peroxide at a temperature above the melting point of the copolymer for a period of time so as to obtain a uniform distribution of monomer, catalyst and peroxide in the copolymer. The resultant grafted copolymer has improved color, and is useful in adhesive systems and as a compatibilizer for polymers and other materials.

Abstract: A graft copolymer produced by polymerizing an ethylenically unsaturated monomer in the presence of a fluorine-containing resin having reactive double bonds via a urethane linkage is excellent in transparency and pigment dispersibility and can provide a coating composition excellent in weather resistance.

Abstract: Disclosed is a graft copolymer resin prepared by graft polymerizing a vinyl compound onto a composite-structured acrylic rubber whose particles are composed of a core consisting of a diene rubber enlarged by treatment with an acid group-containing copolymer latex, and an outer layer consisting of an acrylate polymer having a crosslinked structure formed by the combined use of a graft-linking agent and a cross-linking agent. This graft copolymer resin may be blended with a rigid thermoplastic resin in a specific proportion. This resin composition imparts a good gloss to the molded articles formed therefrom, while retaining excellent impact resistance and weather resistance.

Abstract: Group Transfer Polymerization (GTP) process for preparing a "living" polymer, the process comprising contacting under polymerizing conditions in a polymerization medium, at least one acrylic or maleimide monomer with an initiator which is a tetracoordinate organosilicon, organotin or organogermanium compound having at least one GTP initiating site and a catalyst which is or is a source of an anion selected from the group consisting of bifluoride, fluoride, cyanide, azide or a selected oxyanion, or a selected Lewis acid or Lewis base, the process further characterized in that the initiator or the anion or Lewis acid catalyst is chemically attached (grafted) to a solid support that is insoluble in the polymerization medium.

Abstract: An electrophotographic toner composition is provided. It contains a vinyl polymer having a number average molecular weight of 1,000-10,000, a weight average molecular weight/number average molecular weight ratio of 41-200, a glass transition temperature of 50.degree.-70.degree. C., and specific shear rates at 110.degree. C. and 190.degree. C. respectively. The toner composition affords vivid copy marks even when used in a small amount, and exhibits good fixing property even at low temperatures.

Abstract: Composite resin particles each comprising a particulate crosslinked polymer to which a number of substantially linear, metal-containing polymer chains are chemically bonded. The invention also provide methods for the preparation of said composite resin particles. The present composite resin particles have self-film forming properties, can give a stable dispersion in an organic solvent or a resinous varnish and are specifically useful in paint industries. The particles are further characterized by having the desired properties of the metal element contained therein, as, for example, self-catalytic function in crosslinking, excellent biological activities and the like.

Abstract: Composite resin particles each comprising a particulate crosslinked polymer to which a number of substantially linear, metal-containing polymer chains are chemically bonded. The invention also provide methods for the preparation of said composite resin particles. The present composite resin particles have self-film forming properties, can give a stable dispersion in an organic solvent or a resinous varnish and are specifically useful in paint industries. The particles are further characterized by having the desired properties of the metal element contained therein, as, for example, self-catalytic function in crosslinking, excellent biological activities and the like.

Abstract: Composite acrylic acrylic resin particles each comprising a particular metal-containing crosslinked acrylic polymer to which a number of substantially linear acrylic polymer chains are chemically bonded are provided. Such particles are specifically useful as resinous filler in curing type coating compositions because of having curing catalytic activities.

Abstract: Polymer powders and thermoplastic moulding materials with improved properties are obtained if graft polymers and/or resins in particle form are used and small amounts of rubber-like polymers are polymerized or graft-polymerized onto their particle surfaces.

Abstract: "Living" polymers and their preparation in the absence of a co-catalyst at a pressure greater than about 50 MPa, from polar acrylic or maleimide monomers and organosilicon, -tin or -germanium initiators.

Abstract: An oxidized halogenated polymer is prepared by a process comprising (a) forming an admixture of an acidic oxidizing agent and a suspension of a particulate halogenated polymer in a polar liquid; (b) heating the admixture to a temperature sufficient to initiate the reaction between the polymer and the oxidizing agent; and (c) continuing the reaction until an oxidized polymer having a preselected extent of oxidation is obtained. At least one addition polymerizable compound is, optionally, grafted to the oxidized halogenated polymer. The oxidized halogenated polymer and graft copolymers thereof have physical properties different from the halogenated polymer and graft copolymers thereof. Certain graft copolymers are non-caking or free flowing.

Abstract: A polymer prepared by subjecting to conditions of radical graft polymerization a copolymer of an .alpha.-olefin and an aliphatic nonconjugated diene and a monomer that is capable of radical polymerization with said copolymer is described. This polymer has high miscibility with a dissimilar resin and has a high practical value for use as a compatibilizing agent in blending two or more resins.

Abstract: Polymers obtainable by subjecting at least one monomer, polymerizable by free radicals, to a free-radical emulsion polymerization in the presence of a polymer of the formulae I and/or II ##STR1## in which M, n, R, R.sup.1, R.sup.2, x and y have the meanings mentioned in the description, the use of the polymers obtained for surface-sizing of paper or paper-like materials and also novel polymers of the formulae I and/or II.

Abstract: A modified ethylenic random copolymer derived from 100 parts by weight of base ethylenic random copolymer composed of 25 to 75 mole % of ethylene and 75 to 25 mole % of an alpha-olefin having 3 to 20 carbon atoms and grafted thereto, (a) 0.2 to 50 parts by weight of an unsaturated carboxylic acid having 3 to 10 carbon atoms or an anhydride or ester thereof, (b) 0.2 to 200 parts by weight of a styrene-type hydrocarbon having 8 to 12 carbon atoms, or (c) 0.2 to 300 parts by weight of an unsaturated silane compound having 2 to 20 carbon atoms, said modified ethylenic random copolymer having an intrinsic viscosity [.eta.], measured in decalin at 135.degree. C., of 0.01 to 1.5 dl/g and a molecular weight distribution (Mw/Mn), measured by gel permeation chromatography, of not more than 4.

Abstract: Polymeric materials useful as positive resists comprise a backbone formed from an addition polymer which is degradable by radiation and at least 3 pendant polymeric groups which show no appreciable positive resist characteristics. Preferably these materials comprise a backbone which is a polymethacrylate ester and from 3 to 5 pendant polystyrene groups. These polymers exhibit increased sensitivity and resistance to plasma processing and provide resists which are useful as components of integrated circuits.

Abstract: Hydroperoxidized rubber-containing polymers are prepared in a process wherein a rigid phase polymer is prepared by polymerization of one or more free radically polymerizable monomers in the presence of a hydroperoxidized rubbery intermediate in a well stirred back-mixed reactor operating under essentially homogeneous conditions at a solids content of from about 30 to about 75 percent by weight, and an initial rubber content in the feed of from about 5 to about 12 percent by weight.

Abstract: Polymer blend compositions comprise a polyphenylene ether polymer, a styrene-acrylonitrile polymer and a copolymer compatiblizing agent in an amount sufficient to effect improved compatability between the polyphenylene ether polymer and the styrene-acrylonitrile polymer. The copolymer compatabilizing agent comprises a graft copolymer of A graft polymerized to B or a block copolymer of A block polymerized with B. A and B comprise polymers which are immiscible with one another, and one of A and B is miscible with the polyphenylene ether polymer while the other of A and B is miscible with the styrene-acrylonitrile polymer.

Abstract: Stable dispersion of addition (co)polymers in an inert relatively non-polar organic hydrocarbon liquid, the dispersed particles embracing both a (co)polymer and a polymer containing an ethylenically unsaturated monomer. The (co)polymers are substantially composed of:(a) 5 to 100 mole % of styrene and/or methyl styrene;(b) 0 to 95 mole % of alkyl methacrylate having 1 or 2 carbon atoms in the alkyl group and/or alkoxyalkylene methacrylate having 1 or 2 carbon atoms in the alkoxy group and the alkylene group;(c) 0 to 40 mole % of alkyl methacrylate having 3 to 12 carbon atoms in the alkyl group;(d) 0 to 40 mole % of hydroxalkyl methacrylate having 2 to 12 carbon atoms in the alkyl group and/or glycidyl methacrylate; and(e) 0 to 20 mole % of m methacrylic acid.The (co)polymers are grafted to a polymer of a number average molecular weight of 2000 to 10.

Abstract: Metal drier moderated to provide compositions of extended pot life by at least one compound of niobium, zirconium, titanium, tungsten, boron, silicon, phosphorus or aluminum. Coating compositions of free radical polymerizable compounds and moderated metal drier exhibit lower propensity to yellowing.

Abstract: Radiation curable compositions useful as coatings for wood, metal, glass, fabric, paper, fiber and plastics are made from copolymers of dialkyl muconates and p-acetoxystyrene blended with ethylenically unsaturated compounds.

Abstract: Metal drier moderated to provide compositions of extended pot life by at least one molybdenum compound. Coating compositions of free radical polymerizable compounds and moderated metal drier exhibit lower propensity to yellowing.

Abstract: Graft polymers are prepared by reacting an ethylenically unsaturated polymerizable monomer with a polymer of an olefin of 2 to about 8 carbon atoms in a process wherein the olefin polymer is substantially insoluble in the monomer but is capable of absorbing the monomer. In a preferred aspect, a vinyl halide polyolefin graft polymer is produced by reacting a solid polyolefin particle with a vinyl halide monomer in which the polyolefin is substantially insoluble, but is capable of absorbing the monomer. The solid particles can be contacted with the monomer in one step or in stages. When the stage-wise reaction is continued until the proportion of polyolefin in the polymer product is about 2 to about 20 weight percent, the resulting product can be formed to a transparent or translucent article.

Abstract: The invention relates to ABS molding compositions having a markedly reduced residual butadiene content, even at high processing temperatures.

Abstract: Large acrylic star polymers containing multifunctional monomers in the core are made by group transfer polymerization techniques, preferably by arm-first, core-first, or arm-core-arm approaches.

Abstract: Unique Diels-Alder adducts of an activated olefin and an alloocimene polymer containing pendant conjugated double bonds were prepared. These adducts are useful as binders in adhesive, printing ink and coating formulations.

Abstract: A process for the production of a nonaqueous stable emulsion feedstock comprising a rubber, a block copolymer having at least one component miscible with the rubber and at least one component miscible with the monomer, and at least two unsaturated organic monomers capable of free radical polymerization is disclosed. At least one of the monomers must be miscible with the rubber and the mixture of the monomers is substantially a nonsolvent for the rubber. The block copolymer maintains the rubber or rubber-rich particles in emulsified form within the mixture of monomers. In general, the process comprises (1) mixing the rubber, block copolymer and at least a portion of the rubber miscible monomers to form a first nonaqueous solution, (2) mixing the remaining monomers and the remaining portion of the rubber miscible monomers to form a second solution, and (3) combining the two solutions to form the nonaqueous stable emulsion feedstock.

Abstract: A method is provided for preparing a polymer bound stabilizer which comprises reacting a stabilizer precursor molecule containing a reactive double bound which is not readily homopolymerizable with a pre-formed polymer in the presence of a free radical.

Abstract: Stable dispersion of addition (co)polymers in an inert relatively non-polar organic hydrocarbon liquid, the dispersed particles embracing both a (co)polymer and a polymer containing an ethylenically unsturated monamer. The (co)polymers are substantially composed of:(a) 5 to 100 mole % of styrene and/or methyl styrene;(b) 0 to 95 mole % of alkyl methacrylate having 1 or 2 carbon atoms in the alkyl group and/or alkoxyalkylene methacrylate having 1 or 2 carbon atoms in the alkoxy group and the alkylene group;(c) 0 to 40 mole % of alkyl methacrylate having 3 to 12 carbon atoms in the alkyl group;(d) 0 to 40 mole % of hydroxyalkyl methacrylate having 2 to 12 carbon atoms in the alkyl group and/or glycidyl methacrylate; and(e) 0 to 20 mole % of methacrylic acid.

Abstract: Cross-linking type adhesive compositions comprising (A) polymers having .alpha.,.beta.-unsaturated carboxylate groups, (B) materials having polymerizable vinyl groups, which contain an acrylic and/or methacrylic acid, (C) thermoplastic resins and (D) catalysts of organic peroxides and/or photosensitizers. The adhesive compositions have good adhesive properties together with an excellent heat aging resistance, and can be applied for adhesion to organic and inorganic substrates.

Abstract: Composition for preparing a polymer concrete, a method of protecting or reconditioning surfaces by treatment with the composition, the protected or reconditioned surfaces thus-treated, and multi-package systems for bringing the components of the composition to an application site, wherein the composition comprises a substantially non-aqueous slurry of (1) an aggregate material and (2) a monomer binder system effective to bind the aggregate, upon curing, into a polymer concrete, the binder system comprising (a) a liquid comonomer component, (b) a solid, thermoplastic macromonomer component dissolved in the comonomer and comprising a linear polymer terminated at one or both ends with a polymerizable end group, and (c) a polymerization catalyst.

Abstract: This invention relates to vinyl monomer compositions exhibiting accelerated surface cure characteristics. These compositions are prepared from a vinyl monomer or monomer mixtures such as a blend of dicyclopentenyloxyethyl methacrylate and hydroxypropyl methacrylate, a bulk phase polymerization catalyst system, a polyvalent metal oxidative surface phase catalyst, and a diolefin rubber dispersed in the vinyl monomer as a surface cure accelerator. These compositions are useful as binders for polymer concrete and as impregnants for porous surfaces. The accelerated surface cure is particularly advantageous with monomer mixtures containing low volatility vinyl monomers.

Abstract: The present invention relates to a polymer having a thiol group at one end of the molecule, which is obtained by subjecting the monomers capable of radical polymerization to radical polymerization in the presence of a thiolcarboxylic acid and then treating the resulting polymer with an alkali or acid; to a process for producing the same; and to a block copolymer based on the polymer having a thiol group at the end.The polymer having a thiol group at one end is difficult of forming disulfide linkages by oxidation and thus difficult of becoming insoluble. It is also a highly reactive material that will find wide use in varied application areas. The block copolymer based on the polymer having a thiol group at the end is superior in compatibility and will find wide use in varied application areas.

Abstract: Large acrylic star polymers, are made by group transfer polymerization techniques by arm-first, core-first, or arm-core-arm approaches.

Abstract: Non-aqueous dispersions of polymeric microparticles are disclosed. The dispersions are prepared by free radical initiated addition polymerization of a polymerizable monomer in the presence of a dispersion stabilizer in an organic liquid. The dispersion stabilizer is a styrene polymer terminated with an alpha, beta-ethylenically unsaturated group. The polymeric microparticles are useful as rheology modifiers in coating compositions.

Abstract: The invention relates to a thermoplastic molding material of an elastomeric polymer A, a shell B grafted to the polymer A, and a copolymer C as rigid matrix. The amount of polymer A is 1 to 25 percent by weight based on the weight of A+B+C. It has a glass transition temperature, Tg, of less than 0.degree. C. and an average particle size of 200 to 750 nanometers (d.sub.50 value of the integral mass distribution) and is composed of: 50 to 99.9 percent by weight of at least one alkylacrylate with 1 to 8 carbon atoms in the alkyl radical and 0.1 to 5 percent by weight of a polyfunctional monomer which has a crosslinking action. Grafting shell B represents 5 to 40 percent by weight based on A+B+C and is composed of at least one of the monomers of the group of(b.sub.1) vinylaromatic monomers, and(b.sub.2) the ethylenically unsaturated monomers.Grafting shell B is prepared in two stages with 30 to 70 percent by weight of the monomers b.sub.

Abstract: A thermoplastic, melt-processible, elastomeric composition based on partially crosslinked compatible blends of an ethylene copolymer and a vinyl or vinylidene halide polymer.

Abstract: Polymeric dyes having pendent chromophore groups which are selected from azo, tricyanovinyl, anthraquinone, methine, and indoaniline groups fall into two classes, [A] condensation polymers, and [B] polymers derived from copolymerized ethylenically-unsaturated monomers, the dyes being capable of undergoing thermoplastic deformation by a focused laser beam when in a layer of thickness in the range of 0.1 to 100 micrometers and having an absorptivity in the range of 10 to 250 Lg.sup.-1 cm.sup.-1. They are film-forming, thermally- and light-stable, and solvent-coatable. These compounds are useful as coloring and light-absorbing agents, particularly as the light-absorbing agents in thin optical recording layers.

Abstract: A polyphenylene ether resin composition which possesses out standing impact resistance and weatherability and retains the advantageous properties inherent in a polyphenylene ether, which comprises:(A) 10 to 90 parts by weight of polyphenylene ether resin which is selected from the group consisting of phenylene ether homopolymer and phenylene copolymer,(B) 5 to 88 parts by weight of polystyrene resin which is selected from the group consisting of polystyrene rubber-modified polystyrene, styrene-butadiene copolymer, styrene/butadiene/acrylonitrile copolymer, styrene/.alpha.-methylstyrene copolymer, poly-.alpha.-methylstyrene, rubber-modified styrene/.alpha.

Abstract: Adhesive compositions with thermoreversible crosslinking resulting from the reaction of a divinyl ether having the formula CH.sub.2 .dbd.CH--O--R--O--CH.dbd.CH.sub.2, R being aliphatic, aromatic or cycloaliphatic, with a copolymer resulting from the copolymerization of an olefin with an ethylenically unsaturated monocarboxylic acid and, optionally, an ester of an ethylenically unsaturated monocarboxylic acid, the proportion being 0.1 to 5 percent by weight of the divinyl ether to 99.9 to 95 percent by weight of the copolymer.