Abstract: The present invention relates to an improved packaging composition comprising an ethylene copolymer selected from ethylene acid or ester copolymers such as ethylene vinyl acetate, ethylene/acrylic acid or methacrylic acid copolymers which optionally contain a third comonomer such as an alkyl acrylate and the corresponding ionomers of said copolymers which are blended with a hydrophilic zeolite to form a composition which removes residual acids or small esters from the polymeric or ionomeric composition containing such residual acids. The acids may be present as initial by products in the copolymerization process or may be degradation products. The use of these compositions is particularly important when the resins are formed into packages or other fabricated material which are exposed to acid sensitive material.

Abstract: An acrylic rubber composition comprising 100 parts by weight of (a) an acrylic rubber having carboxyl groups, 0.3 to 8 parts by weight of (b) an aromatic secondary amine compound, and 0.3 to 8 parts by weight of (c) nickel dialkyldithiocarbamate. A crosslinkable acrylic rubber composition further comprising 0.1 to 10 parts by weight of a crosslinking agent in addition the ingredients (a), (b) and (c). By crosslinking the crosslinkable acrylic rubber composition, a crosslinked article having high heat resistance and exhibiting especially a reduced variation in elongation by heat load can be obtained.

Abstract: The process of this invention can be utilized to stabilize tin-coupled rubbery polymers. It is particularly useful for stabilizing rubbery polymers that do not contain bound styrene. This invention more specifically discloses a process for improving the stability of a tin-coupled rubbery polymer which comprises (1) adding 0.1 phr to about 4 phr of styrene to a living rubbery polymer to produce a styrene capped rubbery polymer, (2) adding a tin halide to the styrene capped living rubbery polymer to produce the tin-coupled rubbery polymer, and (3) optionally, adding a tertiary chelating alkyl 1,2-ethylene diamine or a metal salt of a cyclic alcohol to the tin-coupled rubbery polymer. The use of metal salts of cyclic alcohols is preferred because they do not lead to recycle stream contamination. This is because cyclic alcohols do not co-distill with hexane or form compounds during steam-stripping which co-distill with hexane.

Abstract: Novel compounds derived from traditional semi- drying and non-drying oils featuring internally plasticizing and crosslinkable properties are disclosed and claimed. Preferred embodiments include acrylate or methacrylate esters of hydroxy long-chain olefinic compounds derived from castor oil or lesquerella oil. A process for the preparation of the novel compounds is also disclosed, which involves esterification reaction of ethylenically unsaturated carboxylic acids or its derivatives with substituted hydroxy long-chain olefinic compounds. These compounds are suitable for forming latices, which form films at low minimum film forming temperatures (MFT) ranging from −5 to 10 ° C. and cure to above ambient glass transition (Tg polymers without the use of traditional organic cosolvents which contribute to environmental pollution via volatile organic compounds (VOCs) emissions. These latices are therefore useful in waterborne coatings, contact and pressure sensitive adhesives, and inks.

Abstract: In one embodiment, this invention provides a composition comprising a functionalized block copolymer crosslinked with acetylacetonate. The crosslinked block copolymer has improved solvent resistance and improved cohesive strength at high temperatures. The crosslinked block copolymer comprises preferably an acid functionalized, hydrogenated block copolymer having an ABA or similar structure wherein the block comprises at least 80 wt % of a vinyl-aromatic hydrocarbon, preferably styrene, and wherein the B block comprises at least 80 wt % of a hydrogenated and conjugated diene, preferably butadiene, isoprene or a mixture thereof. In another embodiment, this invention provides an adhesive, sealant, oil gel, asphalt composition, or wax composition comprising the acid functionalized, hydrogenated block copolymer.

Abstract: Perfluoroelastomers, curable by peroxidic route, obtainable by polymerizing the following monomers: a) tetrafluoroethylene (TFE); b) fluorovinylethers of general formula: CFX═CXOCF2OR  (I) c) bis-olefins having general formula: RI1RI2C═CRI3—Z—CRI4═CRI5RI6  (IA) d) optionally, one or more fluorinated olefinic comonomers selected from C2-C8 perfluoroolefins, perfluoroalkylvinylethers (PAVE) CF2═CFOR2f, perfluoro-oxyalkylvinylethers CF2═CFOXa, said perfluoroelastomers comprising iodine and/or bromine atoms in the chain and/or in end position, said halogen atoms deriving from “cure site” comonomers and/or from chain transfer agents used in polymerization.

Abstract: A process for reducing the residual monomer amount in aqueous polymer dispersions comprises aftertreating with a redox initiator system.

Abstract: The present invention relates to a molecular weight-enlarged, homogeneously soluble ligand, which includes: an average molecular weight of at least 1000 g/mol; a molecular weight-enlarging polymer; optionally, a linker; and at least one homochiral active center; wherein the active center is bound to the molecular weight-enlarging polymer through the linker or is bound directly to the molecular weight-enlarging polymer, methods of preparing, catalysts containing same, and methods of using same.

Abstract: The oxygen resin composition of the present invention includes: a thermoplastic resin (a) having carbon-carbon double bonds; a gas barrier resin (b) having an oxygen transmission rate of 500 ml·20 &mgr;m/m2·day·atm or less (20° C. 65% RH); and a transmission matel salt (c). This resin composition and molded articles formed using the resin composition effectively absorb and scavenge oxygen when used to package products susceptible to degradation by oxygen, such as foods and drinks.

Abstract: A bifunctional phenylene ether oligomer of the formula (1), obtained by oxidation polymerization of abivalent phenol of the formula (2) and a monovalent phenol of the formula (3),

Abstract: Metal salts of cyclic alcohols can be used as modifiers in lithium initiated solution polymerizations of diene monomers into rubbery polymers having a low vinyl content. For instance, such initiator systems can be used in the copolymerization of styrene and isoprene to produce low vinyl styrene-isoprene rubber having a random distribution of repeat units that are derived from styrene. It is important for such polymerizations to be conducted in the absence of polar modifiers, such as Lewis bases. The subject invention more specifically discloses an initiator system which is comprised of (a) a lithium initiator and (b) a metal salt of a cyclic alcohol, wherein said initiator system is void of polar modifiers. The present invention also discloses a process for preparing a rubbery polymer having a low vinyl content which comprises: polymerizing at least one diene monomer with a lithium initiator at a temperature which is within the range of about 5° C. to about 100° C.

Abstract: A method of manufacturing a support media from a cross-linked polymerisate based on vinyl compounds, and exhibiting residual vinyl groups. The characteristic feature of the method is that the polymerisate is subjected to a heating step that preferably is carried out under reduced access of oxygen. The use of the support media is also described.

Abstract: A current limiting device comprises at least two electrodes; an electrically conducting composite material between the electrodes; interfaces between the electrodes and electrically conducting composite material; an inhomogeneous distribution of resistance at the interfaces whereby, during a high current event, adiabatic resistive heating at the interfaces causes rapid thermal expansion and vaporization and at least a partial physical separation at the interfaces; and a structure for exerting compressive pressure on the electrically conducting composite material, wherein the electrically conducting composite material comprises at least one polymer matrix and at least one conductive filler.

Abstract: A process for reducing the carbonyl group of a polyketone consisting of a carbon monoxide ethylene-based copolymer, comprising reacting a blend of carbon monoxide ethylene-based polymer with a metal alkoxide in a molten condition in proportions to provide a novel polyalcohol. This chemical modification changes the properties of the carbon monoxide ethylene-based polymers and renders them eligible for uses for which the original polymers were not or not very suitable.

Abstract: A continuous process for manufacture of a polymer including branched and linear components comprising first polymerizing conjugated diene(s) in the presence of an organometallic initiator to a conversion that is at least 90% complete. A coupling agent is added to obtain a polymer including branched and linear components. The coupling agent is added at a ratio of about 0.3 to about 0.6 coupling equivalents to initiator equivalents.

Abstract: This invention relates to a method of producing modified vinyl ether polymers, wherein vinyl ether polymers comprising recurring units of general formula (I) where R represents a C2-C4 alkyl group and x denotes an integer from 10 to 1000, are partially transetherified with compounds of general formula Y—OH, wherein Y represents aliphatic and/or cycloaliphatic hydrocarbon groups comprising 5 to 30 carbon atoms, the hydrogen atoms of which can be replaced at least in part by halogen atoms and/or aryl radicals, and/or represents aliphatic, cycloaliphatic and/or aromatic groups with a molecular weight of up to 6000 which contain at least one ether group —O— or an ester group —COO— within the molecule, in the presence of compounds of the platinum metals with the release of the corresponding C2-C4 alcohols, wherein statistically at least one R radical is replaced by a Y radical per molecule of vinyl ether polymer.

Abstract: The present invention is an improvement upon the known method of anionically polymerizing monomers by contacting the monomers with an anionic polymerization initiator which is an organo-substituted alkali metal compound. The improvement comprises decreasing the viscosity of the polymer cement by adding at least 0.01 equivalent of a metal alkyl compound per equivalent of alkali metal initiator if the metal alkyl is added before or at the beginning of polymerization. If the metal alkyl is added during the polymerization or after but before the living polymer is terminated, then at least 0.01 equivalent of the metal alkyl compound per equivalent of living polymer chain ends is should be used. The alkyl groups of the metal alkyl are chosen such that they do not exchange with the organo substituents of the alkali metal, which can be the living polymer chain ends or the organo substituents of the initiator.

Abstract: (Meth)acrylic polymers having alkenyl or curable silyl groups at the chain ends in high functionality ratios are prepared by a process which comprises (i) preparing a (meth)acrylic polymer having halogen atoms at the chain ends, using an organohalogenated compound or a halosulfonyl compound as an initiator and a metal complex catalyst wherein the central metal atom is selected from the group consisting of the elements of Groups 8, 9, 10 and 11 of the periodic table; and (ii) transforming the halogen atom into an alkenyl group or a curable silyl group-containing substituent.

Abstract: A process for preparing a solution of high molecular weight polymers of conjugated dienes in a vinylaromatic hydrocarbon by anionic polymerization of the diene in the presence of an alkyllithium as catalyst and a process for preparing impact-modified polymers of vinylaromatic compounds is described. The first process comprises firstly polymerizing the diene in solution in an aromatic hydrocarbon which is free of ethylenic double bonds to a molecular weight below about 105, then adding a trialkylaluminum in a molar excess relative to the alkyllithium, diluting the solution obtained with the vinylaromatic compound and then coupling the polydiene with a polyepoxide or an alkyl (meth)acrylate to give a high molecular weight polymer. The solution obtained in this way is further processed to give an impact-modified polymer of a vinylaromatic hydrocarbon by polymerizing the solution prepared as described, if desired after addition of further amounts of a vinylaromatic compound, in a manner known per se.

Abstract: The present invention is an improvement upon the known method of anionically polymerizing monomers by contacting the monomers with an anionic polymerization initiator which is an organo-substituted alkali metal compound. The improvement comprises decreasing the viscosity of the polymer cement by adding at least 0.01 equivalent of a metal alkyl compound per equivalent of alkali metal initiator if the metal alkyl is added before or at the beginning of polymerization. If the metal alkyl is added during the polymerization or after but before the living polymer is terminated, then at least 0.01 equivalent of the metal alkyl compound per equivalent of living polymer chain ends is should be used. The alkyl groups of the metal alkyl are chosen such that they do not exchange with the organo substituents of the alkali metal, which can be the living polymer chain ends or the organo substituents of the initiator.

Abstract: A process is described for reducing the residual monomer content in a liquid solution, mixture, melt, suspension or dispersion of a polymer by postpolymerization with addition of a redox initiator system at a reaction temperature appropriate to it and with an extremely short mixing time of the liquid system in the production reactor by metering—gradually, in portions or continuously—at least one of the redox initiator components required to initiate polymerization of the residual monomers over a period (metering time) which is from about 10 to 250 times the mixing time of the liquid system in said reactor.

Abstract: This invention relates to a gel-free process for making functionalized polymers. When multi-alkali metal initiators are used to make these polymers anionically, the process comprises anionically polymerizing at least one monomer with a multi-alkali metal initiator in a hydrocarbon solvent, capping the polymer by adding to the polymer a capping agent that reacts with the ends of the polymer chains such that strongly associating chain ends are formed wherein a strongly associating gel is formed, and, finally, adding a trialkyl aluminum compound to the gel. The important characteristic of the capping agent herein is that it will cap the living polymer and will add a functional group to the polymer chain end which will be strongly associating in the hydrocarbon solvent.

Abstract: The present invention is an improvement upon the known method of anionically polymerizing monomers by contacting the monomers with an anionic polymerization initiator which is an organo-substituted alkali metal compound. The improvement comprises decreasing the viscosity of the polymer cement by adding at least 0.01 equivalent of a metal alkyl compound per equivalent of alkali metal initiator if the metal alkyl is added before or at the beginning of polymerization. If the metal alkyl is added during the polymerization or after but before the living polymer is terminated, then at least 0.01 equivalent of the metal alkyl compound per equivalent of living polymer chain ends is should be used. The alkyl groups of the metal alkyl are chosen such that they do not exchange with the organo substituents of the alkali metal, which can be the living polymer chain ends or the organo substituents of the initiator.

Abstract: A method for regenerating strong-base anion exchange resins utilizing a sequential chemical displacement technique with new regenerant formulation. The new first regenerant solution is composed of a mixture of ferric chloride, a water-miscible organic solvent, hydrochloric acid, and water in which tetrachloroferrate anion is formed and used to displace the target anions on the resin. The second regenerant is composed of a dilute hydrochloric acid and is used to decompose tetrachloroferrate and elute ferric ions, thereby regenerating the resin. Alternative chemical displacement methods include: (1) displacement of target anions with fluoroborate followed by nitrate or salicylate and (2) displacement of target anions with salicylate followed by dilute hydrochloric acid. The methodology offers an improved regeneration efficiency, recovery, and waste minimization over the conventional displacement technique using sodium chloride (or a brine) or alkali metal hydroxide.

Abstract: A process is described for effectively reducing the residual monomer content of an aqueous polymer dispersion by aftertreatment at atmospheric pressure or above with an initiator system comprising a) a hydroperoxide, hydrogen peroxide or a peracid, and b) an &agr;-hydroxy carboxylic acid, such as tartaric acid, or with a salt thereof.

Abstract: A curing catalyst comprising at least one of a cationic curing catalyst component and an organo-metallic compound component. At least one of these components is capable of reversibly repeating the dissolution and precipitation through heating and cooling. The cationic curing catalyst component includes in its molecule at least one substituted or unsubstituted hydrocarbon group having 10 or more carbon atoms, or at least one cyclic organic structure having a substituted or unsubstituted hydrocarbon group having 10 or more carbon atoms.

Abstract: A butadiene-type polymer suitable for use as a processing aid in a rubber composition is formed by polymerizing butadiene or other conjugated diene monomers in a solvent, such as hexane, to form a polymer of relatively low molecular weight (around 30-40,000 g/mole). The polymer is coupled with a coupling agent, such as tin tetrachloride, to increase its molecular weight to a level at which conventional desolventizing processes may be used to remove the solvent from the mix. After desolventizing, the polymer is decoupled, by heating, to return the polymer to its original molecular weight.

Abstract: The present invention provides an effective process for removal of the residual metal catalyst from a polymer solution using water and alcohol containing an inorganic acid after selective hydrogenation of the unsaturated olefinic double bonds in a polymer of a conjugated diene monomer or a copolymer of a conjugated diene monomer and an aromatic vinyl monomer in the presence of a homogeneous organotitanium catalyst, which is an economical and simple process especially for the purpose of an industrial use for effectively removing the residual titanium compounds and lithium salts from the hydrogenated polymer solution.

Abstract: (Meth)acrylic polymers having alkenyl or curable silyl groups at the chain ends in high functionality ratios are prepared by a process which comprises (i) preparing a (meth)acrylic polymer having halogen atoms at the chain ends, using an organohalogenated compound or a halosulfonyl compound as an initiator and a metal complex catalyst wherein the central metal atom is selected from the group consisting of the elements of Groups 8, 9, 10 and 11 of the periodic table; and (ii) transforming the halogen atom into an alkenyl group- or a curable silyl group-containing substituent. The obtained (meth)acrylic polymers form homogeneous curing materials.

Abstract: Disclosed is a metal containing polymer composition comprising; a metal overbased imide or ester functionalized polymer prepared by reacting (A) a polymer comprising (A1) an acidic functionalized polymer or ester functionalized polymer; (A2) an acidic mixed ester-acid of a carboxy containing interpolymer; or (A3) an ester functionalized polymer comprising a lactone and (B) a metal overbased composition that contains a reactive basic functionality comprising (B1) a metal overbased amine wherein the reactive basic functionality is a primary or secondary amino group; (B2) a metal overbased hydroxy substituted carboxylic acid wherein the reactive basic functionality is a hydroxy group; or (B3) a metal overbased dispersant wherein the reactive basic functionality is a primary or secondary amino group.

Abstract: The present invention is an improvement upon the known method of anionically polymerizing monomers by contacting the monomers with an anionic polymerization initiator which is an organo-substituted alkali metal compound. The improvement comprises decreasing the viscosity of the polymer cement by adding at least 0.01 equivalent of a metal alkyl compound per equivalent of alkali metal initiator if the metal alkyl is added before or at the beginning of polymerization. If the metal alkyl is added during the polymerization or after but before the living polymer is terminated, then at least 0.01 equivalent of the metal alkyl compound per equivalent of living polymer chain ends is should be used. The alkyl groups of the metal alkyl are chosen such that they do not exchange with the organo substituents of the alkali metal, which can be the living polymer chain ends or the organo substituents of the initiator.

Abstract: An aqueous leather coating composition and a method for coating leather with the aqueous coating composition are provided. The aqueous coating composition contains an aqueous emulsion polymer which includes from 0.4% to 10% by weight of a copolymerized acetoacetate or acetoacetamide monomer and has a glass transition temperature from −20° C. to 10° C. In an alternative embodiment the aqueous coating composition contains an aqueous emulsion polymer which includes from 0.1% to 6% by weight of a copolymerized acetoacetate or acetoacetamide monomer and from 2% to 15% by weight of copolymerized carboxylic acid monomer and has a glass transition temperature from −40° C. to 0° C., the polymer having been contacted with a transition metal oxide, hydroxide, or carbonate at a pH less than 9 in an amount greater than 0.20 equivalent of transition metal per equivalent of copolymerized carboxylic acid monomer.

Abstract: The present invention describes the preparation of copolymers grafted by the so-called “grafting from” method, comprising two steps. In the first step, a polymer of a variable type referred to as poly(M1) is reacted with persistent free radicals of the type diphenyltrialkylsilyloxymethyl to form a reactive polymer poly(M1)F, containing a variable number F of these groups attached to the chain. F represents the average functionality of the reactive polymers and may be predetermined by controlling the ratio of poly(M1) and the free radical generator or TPES. In the second step, poly(M1)F is dissolved in a monomer M2 and then redissociated by heating to temperatures of 110-130° C. to produce the macroradical poly(M1) and the persistent radicals. The macroradical poly(M1) rapidly initiates polymerization whereas the diphenyltrialkylsilyloxymethyl radical stays temporarily on the sideline of the initiation reaction.

Abstract: A composition of matter, comprising: a chemically functionalized carboxylate-alumoxane that is functionalized with a chemically reactive substituent, and a reactive compound, wherein the chemically reactive substituent reacts with the reactive compound so as to link the carboxylate-alumoxane to the reactive compound and form a polymer matrix. The functional groups on the carboxylate-alumoxane can vary depending on the desired properties of the matrix. Also, the composition of matter may comprise a cross-linked matrix in which the cross-linked components consist of functionalized alumoxanes.

Abstract: A method for reducing the molecular weight of olefin copolymers comprises contacting an olefin copolymer and a base oil containing less than about 0.05 wt. % sulfur in the presence of oxygen and at a temperature of at least about 60° C.

Abstract: Perfluoroelastomer compositions comprising perfluoroelastomers having copolymerized units of tetrafluoroethylene, a perfluoro(vinyl ether), and a nitrile-containing cure site monomer are cured with certain nitrogen-containing nucleophilic compounds. The nucleophilic compounds also act as dual curatives in perfluoroelastomer compositions which incorporate other curing agents.

Abstract: The present invention relates to a process for preparing functionalized polymers having at least one double bond and functional groups containing a carbonyl radical along their chains. The process involves (a) subjecting a starting polymer comprising at least one double bond, in an inert hydrocarbon solvent, to a hydroalumination or carboalumination reaction along its chain by adding an agent derived from aluminum to the starting polymer, (b) adding to the product obtained in (a) at least one electrophilic agent that reacts with said agent derived from aluminum and (c) stopping the functionalization reaction of (b) and recovering the functionalized polymer.

Abstract: A superabsorbent resin composition comprising the following components

Abstract: A method of preparing a carbamate-functional polymer comprising the steps of providing a hydroxy-functional polymer and reacting a carbamate compound with the hydroxy-functional polymer in the presence of a transcarbamation catalyst, thereby forming a carbamate-functional polymer. The transcarbamation catalyst may be Bi(III) compounds, Zr(IV) compounds, or mixtures of these.

Abstract: Disclosed is a process for esterifying and/or transesterifying a polymer having a polyethylenic backbone and pendant acid and/or ester moieties comprising contacting a melt of the polymer with a transesterifying compound so that the polymer undergoes esterification and/or transesterification but not alcoholysis. The esterified or transesterified polymer also has pendant ester moieties which differ in kind and/or number from the unreacted polymer. In one embodiment, the process also comprises adding an amount of a transition metal salt that is effective to promote oxygen scavenging. Also in a further embodiment, the process comprises irradiating the transesterified polymer with actinic radiation to reduce the induction period before oxygen scavenging commences. Also disclosed are compositions comprising a component which comprises an ethylenic or polyethylenic backbone and a pendant or terminal moiety comprising a benzylic, allylic, or ether-containing radical.

Abstract: A superabsorbent resin composition comprising the following components (A), (B) and (C), wherein (A) is a superabsorbent resin, (B) is a metal compound containing at least one metal A selected from the group consisting of titanium and zirconium and (C) is a chelating agent.

Abstract: A method of continuously polymerizing a conjugated diene monomer and a vinyl aromatic hydrocarbon monomer in a hydrocarbon solvent by using an organolithium initiator, adding to the polymerization mixture a tin compound and again adding a tin compound after the polymerization mixture has been withdrawn from the polymerization vessel. The resulting diene polymers possess a significantly reduced Payne Effect and a substantial reduction (over 10%) in tan delta at 50° C. which results in tires having decreased hysteresis loss, excellent wear resistance and rolling resistance and good wet skid resistance.

Abstract: Fluoropolymers comprising a fluoroelastomer matrix incorporating therein particles of a semicrystalline fluoropolymer containing iodine and/or bromine and formed of tetrafluoroethylene (TFE) homopolymers or copolymers wherein the average particle sizes of the semicrystalline fluoropolymer latex range from 10 to 100 nm.

Abstract: An aqueous leather coating composition and a method for coating leather with the aqueous coating composition are provided. The aqueous coating composition contains an aqueous emulsion polymer which includes from 0.4% to 10% by weight of a copolymerized acetoacetate or acetoacetamide monomer and has a glass transition temperature from −20° C. to 10° C. In an alternative embodiment the aqueous coating composition contains an aqueous emulsion polymer which includes from 0.1% to 6% by weight of a copolymerized acetoacetate or acetoacetamide monomer and from 2% to 15% by weight of copolymerized carboxylic acid monomer and has a glass transition temperature from −40° C. to 0° C., the polymer having been contacted with a transition metal oxide, hydroxide, or carbonate at a pH less than 9 in an amount greater than 0.20 equivalent of transition metal per equivalent of copolymerized carboxylic acid monomer.

Abstract: Perfluoroelastomer compositions comprising perfluoroelastomers having copolymerized units of tetrafluoroethylene, a perfluoro(vinyl ether), and a nitrile-containing cure site monomer are cured with compounds that are capable of generating ammonia at temperatures of 40° C.-330° C. to produce cured compositions having excellent thermal stability. The ammonia-generating compounds also act as cure accelerators in perfluoroelastomer compositions that incorporate other curing agents.

Abstract: The present invention provides a solid golf ball which attains long flying distance and is superior in hit feeling and durability. The present invention provides a solid golf ball in which at least a portion thereof is made of rubber, wherein the rubber portion is a crosslinked, molded rubber composition comprising a base rubber, a co-crosslinking agent and peroxides, the base rubber comprising a polybutadiene modified with a tin compound and having a cis content of 40% or more.

Abstract: The present invention is directed to new metal cation neutralized high acid ionomer resins and to golf ball cover compositions containing these new resins. When the new high acid ionomer resins are utilized to manufacture a golf ball, the golf ball produced thereby exhibits properties of improved distance without sacrificing characteristics such as playability and/or durability when compared to low acid ionomer and/or low acid/high acid ionomer blends.

Abstract: Novel modifying agents contain a sharply-melting crystalline polymer ingredient, preferably a side chain crystalline (SCC) ingredient, and an active chemical ingredient. Such modifying agents, especially when in the form of particles, can be placed in contact with a matrix, will not modify the mix below the crystalline melting point Tp, but will rapidly modify the matrix above Tp. The active chemical ingredient can react with the matrix, catalyze a reaction of the matrix, or inhibit a reaction of the matrix. Particularly useful compositions are polymer precursors which are storage-stable at low temperatures but which are rapidly converted to crosslinked resins when heated to temperatures above Tp, optionally in the presence of light.

Abstract: Curable perfluoroelastomer compositions are disclosed that comprise ammonia and uncured perfluorinated elastomers having copolymerized units of nitrile-containing cure site monomers. Such compositions are curable at low temperatures. In addition, curable perfluoroelastomer compositions are disclosed wherein ammonia functions as a cure rate accelerator in the presence of other curing agents.

Abstract: Solutions of graft polymers of a polymer having reactive hydrogen groups and grafted through reactive hydrogen groups an alkoxy metallic compound wherein the metal is titanium, zirconium and/or hafnium are useful as photoresist materials which are resistant to plasma. Also, compounds and graft polymers wherein the alkoxy metallic compound also contains silicon, tin or germanium are provided.