Abstract: A curable resin composition comprising (a) an acrylic polymer having a plurality of alicyclic epoxide functions, and (b) an amount effective to initiate the curing reaction of the acrylic polymer (a) upon heating of a heat-latent cation polymerization initiator. The composition finds its uses in coating compositions, sealants, potting and casting compositions.

Abstract: Ion exchange fibers comprising a polymer component having a main chain of a syndiotactic poly(1,2-butadiene) structure and containing ion exchange functional groups introduced at least part of side chain ethylene groups. These fibers may be suitably formed into a non-woven fabrics, and thus an ion exchange cloth can be obtained, which has excellent ion exchange capacity, flexibility excellent processing capacity, high mechanical strength and elongation. The ion exchange fibers have excellent ion exchange capacity with respect to fluid such as water or gas and thus can be used as cartridge filters and fiber-filled filters.

Abstract: The present invention provides a process for the production of polymers with an optical position in diagram where refraction index n.sub.D is plotted against optical dispension v.sub.D expedient for an optical use by metathetic counterion exchange, wherein, in a polymer of the general formula: ##STR1## R.sub.1 and R.sub.2, which can be the same or different, are divalent organic radicals, R.sub.3 and R.sub.4, which can be the same or different, are monovalent organic radicals, n is a whole number greater than 2 and y is 0 or 1. R.sub.1, R.sub.2, R.sub.3, R.sub.4, y and n are so chosen that together they form a polymeric basic structure which promotes glass formation and prevents crystallisation, and X.sup.- is a halogen atom. The halogen ion is replaced by an equivalent of a mono- or polyvalent organic or inorganic counterion different from the halogen ion and suitable for the adjustment of the desired solid body properties.

Abstract: Crosslinked styrenic polymers may be sulphonated in a controlled manner in an organic solvent at elevated temperature using SO.sub.3 in the presence of a trialkyl phosphate. The process does not introduce further crosslinking into the polymer permitting it to have an extremely high water uptake. The resulting polymer is useful as a hydrogel.

Abstract: Polymer compositions useful for the production of articles of biodegradable plastics material with improved biodegradability include destructed starch and a polymer selected from the group consisting of ethylene-vinyl alcohol, polyvinyl alcohol and mixtures thereof wherein at least a portion of the said polymer is modified by the substitution of from 0.1 to 5 molar % of the functional alcohol groups in the polymer chain by X groups in which X is an oxo or an alkyl carbonyl group in which the alkyl group contains from 1 to 4 carbon atoms.

Abstract: Succinimides, succinic esters, and succinic ester-amides are formed by (A) reacting (i) at least one substantially aliphatic polymer of at least one lower olefin, and (ii) an acidic reactant or a mixture of two or more acidic reactants represented by the general formulaR--CO--CH.dbd.

Abstract: The present invention pertains to a process for the preparation of polymers comprising poly(4-hydroxystyrene) or substituted poly(4-hydroxystyrene) or both. The polymers have low optical density (absorbance) over a wavelength range from about 240 to about 260 nm, as well as low optical density over the near UV and visible spectrum (310 to 800 nm). Such polymers are produced by polymerizing 4-acetoxystyrene and/or substituted 4-acetoxystyrene monomers, with or without other comonomers, and subsequently performing transesterification. In the most preferred embodiment of the present invention, the polymers are produced using at least one alcohol as a reaction medium, a chain transfer agent and a transesterification reactant, providing an unusually economic process. These polymers are particularly useful as photoresist components for use in combination with deep UV, X-ray, and E-Beam imaging systems.

Abstract: A radiation-sensitive compound, which comprises a polymer including a plurality of azide-substituted aromatic ester groups and a plurality of carboxylic or sulphonic acid groups capable of imparting to the compound solubility in aqueous or alkaline medium. After image-wise exposure, the compound can be developed using an aqueous or alkaline developer. The compound is useful in the production of radiation sensitive plates for the manufacture of lithographic printing plates which can be baked to improve printing life.

Abstract: A method for preparing a sulfonated compound with minimal or no waste products using a porous inorganic material absorber. The absorber is saturated with a compound to be sulfonated and then contacted with a sulfonating gas mixture to form a sulfonated product. After forming the sulfonated product, excess sulfonating gas is removed by contacting the sulfonated product with warm air. The sulfonated product is then neutralized and the product is removed with water from the inorganic material absorber. The absorber is then dried with hot air so that it may be reused for future sulfonation processes. The process results in preparation of a sulfonated compound having inorganic salts present in an amount less than about 1.0 percent by weight based on total sulfonated product weight. The process results in highly effective sulfonation of a compound with formation of little or no waste materials, particularly waste materials such as solvents and undesirable inorganic salts.

Abstract: A process for anionic polymerization of polymerizable monomers with an organo lithium initiator followed by polymerization termination characterized in that terminated reaction products are neutralized by contacting with sulfuric acid, phosphoric acid or a mixture thereof.

Abstract: Monochloromonofluorobenzene provides a reaction medium for chlorination of C.sub.2 -C.sub.8 olefin polymers which is inert to chlorination and does not function as a stratospheric ozone depleter.

Abstract: A process for producing a chlorinated polyolefin is disclosed, which comprises dissolving or suspending a polyolefin in a solvent and conducting chlorination reaction of the dissolved or suspended polyolefin, said solvent being a chloroform-based solvent comprising a mixture of 100 parts by weight of chloroform containing no alcohol and from 0.0005 to 15 parts by weight of a compound having from 4 to 10 carbon atoms and containing one or more double bonds per molecule. A process for producing a chlorosulfonated polyolefin is also disclosed, which comprises dissolving or suspending a polyolefin in a solvent and conducting chlorination and chlorosulfonation reaction of the dissolved or suspended polyolefin, said solvent being a chloroform-based solvent comprising a mixture of 100 parts by weight of chloroform containing no alcohol and from 0.0005 to 15 parts by weight of a compound having from 4 to 10 carbon atoms and containing one or more double bonds per molecule.

Abstract: An encapsulated breaker chemical composition used in a fracturing process in an oil or gas stimulation operation which comprises: (a) a breaker chemical; (b) a water soluble sealing layer, such as urea, having a thickness within the range of about 1 to about 30 microns deposited on the surface of said breaker chemical and encapsulating said breaker chemical; and (c) a pinhole free coating of a neutralized sulfonated elastomeric polymer of about 2 to about 80 microns thick deposited onto the surface of the coated breaker chemical, wherein said neutralized sulfonated polymer encapsulates the breaker chemical and is permeable to the breaker chemical.

Abstract: An encapsulated breaker chemical composition used in a fracturing process in the protection of an oil or gas stimulation operation which comprises: a breaker chemical; and a pinhole free coating of a neutralized sulfonated elastomeric polymer of about 2 to about 80 microns thick deposited onto the surface of the breaker chemical, wherein said neutralized sulfonated polymer encapsulates the breaker chemical, wherein the neutralized sulfonated polymer is permeable to the breaker chemical and the neutralized sulfonated polymer is non-reactive to the breaker chemical.

Abstract: An encapsulated breaker chemical composition used in an oil or gas stimulation operation which comprises: a breaker chemical; and a pinhole free coating of an ionically and covalently crosslinked neutralized sulfonated elastomeric polymer of about 2 to about 80 microns thick deposited onto the surface of the breaker chemical, wherein said polymer encapsulates the breaker chemical, wherein the polymer is permeable to the breaker chemical and the polymer is non-reactive to the breaker chemical.

Abstract: A process for anionic polymerization of polymerizable monomers with an organo lithium initiator followed by polymerization termination characterized in that terminated reaction products are neutralized by contacting with sulfuric acid, phosphoric acid or a mixture thereof.

Abstract: A surface-modified fibrillated fiber composition is disclosed herein which comprises polyacrylonitrile homopolymer or copolymer and a surface of pendant N-haloamide groups. Also disclosed is a process for the production of said composition.

Abstract: Polymers of olefin monomers and a substantially uniform concentration of carboxyl, hydroxyl, thio, amino, carbonyl and imino functional group-containing monomers. Polymers of olefin monomers and carboxyl, hydroxyl, thio, amino, carbonyl and imino functional group-containing monomers substantially devoid of halogen. Method for preparing polymers by reacting carboxyl, hydroxyl, thio, amino, carbonyl and imino functional group-containing monomers with non-halogenated organometallic compounds to form masked, functional group-containing monomers and polymerizing polymer chain monomers with the masked, functional group-containing monomers to produce a polymer chain. Method for forming masked, functional group-containing monomers by reacting carboxyl, hydroxyl, thio, amino, carbonyl and imino functional group-containing monomers with non-halogenated organometallic compounds. Masked, carboxyl, hydroxyl, thio, amino, carbonyl and imino functional group-containing monomers.

Abstract: A process for preparing a functionalized petroleum resin which comprises the steps of: dissolving a petroleum resin having a norbornene moiety with a double bond in a solvent to form a solution; adding to the solution a borane compound having the formula: ##STR1## wherein R.sub.1 and R.sub.2 are alkyl or cycloalkyl groups having about 1 to about 10 carbonations; reacting said petroleum resin with said borane compound at about room temperature for a sufficient period of time to form a borane intermediate; and reacting said borane intermediate with a chemical agent to convert said borane intermediate into said functionalized petroleum resin.

Abstract: A surface treatment agent for paper comprising a quaternized product of a copolymer containing at least (a) styrene and/or a styrene derivative and (b) N,N-dialkylaminoalkyl (meth) acrylamide is disclosed. This surface treatment agent is excellent in slip prevention and sizing effect, the sizing effect not being impaired at a pH over 7.

Abstract: Disclosed herein is a vinylamine copolymer having the structural units represented by the following formulas (I), (II), (III), (IV) and (V): ##STR1## wherein x.sup..crclbar. represents an anion or hydroxyl ion, R represents a hydrogen atom or a methyl group, M.sup..sym. represents a hydrogen ion or a monovalent cation, in which the molar fraction of the structural unit (I) is 5 to 85% by mole, the molar fraction of the structural unit (II) is 2 to 85% by mole, the molar fraction of the structural unit (III) is 5 to 80% by mole, the molar fraction of the structural unit (IV) is 0 to 40% by mole, all of said molar fractions being based on the vinylamine copolymer, and the molar fraction of the structural unit (V) is 0 to 8% by mole which is based on the total content of the structural units (III), (IV), and (V), a flocculating agent and a paper strength increasing agent using the vinylamine copolymer, and a process for producing the vinylamine copolymer.

Abstract: This invention provides cationic acrylamide polymers which are highly effective as paper strength agents, drainage agents and suspension flocculants, and which do not show much temporal deterioration; it also provides a method of manufacturing said polymers wherein the manufacturing equipment is compact and can be installed on site, and the cationicity of the polymers can be modified in a short time.This invention comprises a method of manufacturing cationic acrylamide polymers by reaction, with a hypohalogenite, of a (meth)acrylamide homopolymer, a copolymer of (meth)acrylamide and acrylonitrile, a copolymer of (meth)acrylamide and N,N-dimethylacrylamide, in a high temperature range of 50.degree.-110.degree. C. for a short time; the polymers manufactured by said process; and paper strength agents, drainage agents and flocculants having these polymers as their principal constituent.

Abstract: An in-mold sulfonation system for sulfonating the surface of plastic articles such as plastic containers during molding. Sulfur trioxide is introduced into a pre-mold chamber, converted to a relatively high pressure gaseous sulfur trioxide, and then injected into a mold such as a blow mold immediately before or immediately following full expansion of the formed plastic article in the mold cavity. Neutralization with a gaseous neutralizing agent follows. By controlling the timing and temperature of the in-mold sulfonation step it is possible to produce a plastic article having an effective barrier layer but containing a minimum of undesirable rinseable salts.

Abstract: Ziegler-Natta catalyzed polymer chains are end capped with at least one functional group-containing unit which is otherwise essentially absent from said polymer chain. The chains can be grafted to form graft copolymers and star copolymers. The compositions are useful as oil additives and in general purpose elastomer as well as thermoplastic polymer compositions.

Abstract: A water soluble polymer which is characterized by the formula: ##STR1## wherein x is 50 mole percent or 662/3 mole percent or 75 mole percent and y+z is 50 mole percent, when x is 50 mole percent, y+z is 331/3 mole percent, when x is 662/3 mole percent, and y+z is 25 mole percent, when x is 75 mole percent, wherein the molar ratio of y to z is about 100:1 to 1:100, and M.sup.+ is hydrogen or a metal cation selected from the group consisting of lead, aluminum, iron and Groups IA, IIA, IB and IIB of the Periodic Table of Elements and the level of sulfonation based upon the styrene monomer is about 75 to about 100 mole percent.

Abstract: Use of strong acidic materials, such as molecular sieves, reduces the level of t-butyl alcohol (TBA) produced during the visbreaking of polyolefins.

Abstract: Polyacrylamide is reacted with formaldehyde and bisulfite at a temperature of at least about 100.degree. C. and at an initial reaction mixture pH of less than about 12, preferably about 3 to about 8, to produce sulfomethylpolyacrylamide.

Abstract: Improved methods are provided for the sulfomethylation of high molecular weight polyacrylamide polymers which reduce or minimize cross linking and result in polymers which have a reduced specific viscosity (RSV) greater than the polyacrylamide polymer used as the starting material polymer in the process.

Abstract: Homopolymers or block copolymers of vinylaromatics and/or dienes and hydrogenated derivatives thereof, which contain end groups of the general formula (I):NH--(A).sub.x --NR.sup.1 R.sup.2 .multidot.n H.sub.m S (I)where A is a substituted or unsubstituted bridge which, in addition to carbon, may contain nitrogen or oxygen, X is 0 or 1, S is an inorganic or organic acid radical, n is an integer from 1 to 12 and indicates the number of moles of acid used per chain end, R.sup.1 and R.sup.2 are each hydrogen, aliphatic or aromatic radicals or a bridge of 3 to 12 carbon members which may be substituted by aliphatic or aromatic radicals, and m is the number of hydrogen ions of the acid used, are prepared from polymers having amino end groups of the general formula (II):NH--(A).sub.x --NR.sup.2 R.sup.3 (II)where R.sup.1, R.sup.

Abstract: This invention provides a pressure sensitive adhesive composition comprising an acrylic copolymer component (A) which is at least in part an acetoacetyl group-containing acrylic copolymer and at least one curing component (B) selected from the class consisting of isocyanate compounds, epoxy compounds, aldehyde compounds, non-amino resin amine compounds, metal salts, metal alkoxides, metal chelate compounds, ammonium salts and hydrazine compounds.This adhesive composition is well-balanced in the triad of tack, adhesion, cohesion in adhesion technology and can be advantageously used in various applications such as adhesive tapes and labels.

Abstract: A method for reconstituting superabsorbent polymer fines which comprises the following steps: wetting the superabsorbent polymer fines with an aqueous solution sufficient to form an amorphous gel of the fines, grinding the gel, and drying the ground gel product; wherein the improvement is characterized by the addition of an aqueous solution containing a persulfate salt.

Abstract: A photosensitive and heat-sensitive polymer having conjugated polyenes and sulfonic acid groups and an absorbance ratio of a strong band in the region of 1200 cm.sup.-1 to 1300 cm.sup.-1 assignable to sulfonic acid groups adjacent to conjugated polyenes of at least 3 sequence lengths to a strong band near 1050 cm.sup.-1 assignable to sulfonic acid groups in the IR spectrum of at least 0.6. The photosensitive and heat-sensitive polymer is obtained by the sulfonation of a polymer of an ethylenically unsaturated monomer having a number average molecular weight of at least 10,000 or a polymer having conjugated polyenes and a number average molecular weight of at least 10,000 and selected from specified polymers and copolymers. The photosensitive and heat-sensitive polymer is useful for information recording materials capable of being recorded by a laser beam or a thermal head for preparing printing plates, especially offset printing plates.

Abstract: A method of introducing acrylamido methane sulfonic acid groups into acrylic acid or methacrylic acid polymers which comprises reacting the carboxylic acid groups in such polymers with from 2-100 mole % of an ammonia, formaldehyde and a water-soluble bisulfite mixture.

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 method is disclosed for preparing polyacrylonitrile copolymers by Heterogeneous reaction of polyacrylonitrile aquagel. Generally, the method includes the steps of preparing a solution of polyacrylonitrile by dissolving the polyacrylonitrile in a water-miscible solvent which is capable of dissolving the polyacrylonitrile but incapable of hydrolyzing the nitrile groups of the polyacrylonitrile under the dissolution conditions. Coagulating the polyacrylonitrile solution by replacing the solvent with a coagulating fluid such as water or a water-miscible fluid incapable of dissolving polyacrylonitrile at temperatures below 80.degree. C. and incapable of reacting with the nitrile groups of the polyacrylonitrile, thus obtaining the polymer in the aquagel state. Replacing the coagulating fluid with a fluid reagent capable of reacting with the nitrile groups of the polyacrylonitrile aquagel but incapable of dissolving the polyacrylonitrile aquagel at the selected reaction temperature.

Abstract: The present invention relates a cement composite containing glass fibers encapsulated with a polymeric coating which is formed from an organic solution of an interpolymer complex of an anionic polymer and a cationic polymer.

Abstract: The present invention relates to poly-(C.sub.2 -C.sub.10 -.alpha.-olefine)-carboxylic acids of Mw (weight average) 2000 to 350,000, to their preparation by oxidative degradation of polyolefines or by reaction of "Living" polyolefines with CO.sub.2, to their conversion into poly-(C.sub.2 -C.sub.10 -.alpha.-olefine)-carbonyl halides and to their use for preparing polyolefine/polycarbonate block copolymers and the block copolymers obtainable by the process according to the invention.

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.

Abstract: Sulphosuccinamide acids and their salts corresponding to the following general formula ##STR1## wherein X denotes the residue of a hydrophobic, optionally branched vinyloligomer having an average molecular weight M.sub.n of from 200-5,000, preferably from 300-3,000,of the groups denoted byR.sup.1 R.sup.2, one is hydrogen and the other is --SO.sub.3 M, andn represents a number with a value of from 1.4-3.0, preferably form 1.6-2.3. andM denotes hydrogen, an alkali metal, or an ammonium, C.sub.1 -C.sub.4 -alkyl-ammonium or C.sub.2 -C.sub.3 -hydroxy alkyl-ammonium group.

Abstract: This invention relates to a p-methyl styrene polymer represented by the following formula: ##STR1## Z denotes a group such as a functional group. Poly p-methylstyrene (PPMS) is lithiated by reaction with n-butyllithium. The lithiated PPMS is used to prepare polymers containing functional groups. As an example, a solution of PPMS (MW 260,000), 1.0 g in 20 ml of cyclohexane, was reacted with n-butyllithium, 8.5 mmol, and tetramethylethylenediamine, 8.7 mmol, for 20 hours to obtain a precipitate. The precipitate was dissolved in THF, and CO.sub.2 was blown into the solution. The solution was washed with an aqueous solution of HCl and dropped into methanol to obtain a solid polymer having carboxyl group functionality.

Abstract: A process for the preparation of hydroxamated polymers of acrylamide is disclosed whereby the polymer is reacted with a hydroxylamine salt at pH of at least about 8.0.

Abstract: Polymers of 4-vinylphenol are made by the acid catalyzed transesterification of polymers of 4-acetoxystyrene in an alcohol. The 4-vinylphenol polymers are useful as epoxy resins curing agents and as the phenolic base for epoxy resin per se.

Abstract: Copolymers of p-acetoxystyrene and allyl esters of ethylenically unsaturated acids are selectively hydrolyzed to copolymers of p-vinylphenol and allyl esters of ethylenically unsaturated acids using acid or base catalysis in an alcohol or water.

Abstract: An excellent cold-proof chlorosulfonated polyethylene and a method of manufacturing the same featured in that a polyethylene is once dissolved in a solvent by heating up them over a dissolution temperature of the polyethylene, then cooled and thus obtained homogeneous solution of the polyethylene is allowed to react with a sulfuryl chloride in the presence of a catalyst of a radical generating agent in the dissolution temperature region of the polyethylene or in a temperature region lower than the former one.

Abstract: Copolymers of p-acetoxystyrene and dialkyl muconates or alkyl sorbates are selectively hydrolyzed to copolymers of p-vinylphenol and dialkyl muconates or alkyl sorbates using acid or base catalysis in an alcohol or water.

Abstract: Dehydrogenated poly(spiro[2,4]hepta-4,6-diene) which is insoluble in organic solvents, has an electrical conductivity of at least 10.sup.-10 S.times.cm.sup.-1, and contains, relative to the total number of recurring structural units in the polymer, 0-90 mol % of the recurring structural units of the formulae I and II ##STR1## in which R.sup.1 is in each case a hydrogen atom or an alkyl group having 1 to 4 C atoms, and 10-100 mol % of at least one of the recurring structural units of the formulae III to VI ##STR2## in which R.sup.1 is as defined in formula I or II and X.sup.- is a bromide or iodide ion or an anion of a Lewis or protonic acid, is obtained by treating poly(spiro[2,4]-hepta-4,6-diene) with bromine, iodine or a Lewis or proton-donating acid, and can be used in an electrically conducting material for the production of, for example, conductors, electrodes, batteries or semiconductor components.

Abstract: The present invention relates to a rubber-like polybutadiene or a rubber-like butadiene-styrene copolymer suited for use in tire treads which are obtained by polymerization of the monomer(s) in the presence of an organolithium catalyst, followed by reacting a carbodiimide with the reactant product thereof so as to subject it to reaction at its living point, and if necessary, further reacting the product thus obtained with a trifunctional or higher-order coupling agent. The invention further relates to a process for the production thereof, and a rubber composition containing more than a definite amount of said polymer.

Abstract: An acrylic or methacrylic resin emulsion coating composition comprising a blended mixture composed of(1) 100 parts by weight as solid resin content of a copolymer resin emulsion [A], the copolymer resin therein having a glass transition temperature Tg(A), determined by the DSC method, of about -10.degree. to about -55.degree. C., and said copolymer resin emulsion [A] being an aqueous emulsion-copolymerization product being free from a copolymerizable diallyl component and derived from acrylic and/or methacrylic monomers (a) and (b) specified in the claims in the presence of a polyoxyethylene/polyoxypropylene block copolymer,(2) 20 to 300 parts by weight as solid resin content of a copolymer emulsion [B], the copolymer resin therein having a glass transition temperature Tg(B), determined by the DSC method, of less than 0.degree. C., and satisfying the following equationTg(B)-Tg(A)=10.about.55.degree. C.

Abstract: Disclosed herein is a process for preparing a water-soluble polymer, which comprises granulating a hydrous gel-like polymer obtained by polymerizing N-vinylformamide in the form of an aqueous solution of which a monomer concentration is 20 to 60% by weight, dispersing the formed polymer particles in methanol and contacting them with an aqueous solution of ammonium salt of a monovalent acid in an amount of 1 to 200% by mole based on the formamide groups in said polymer, thereby partially modifying the formamide groups in the polymer.

Abstract: A composition comprising (a) at least one oxidized polycationic polyheteroaromatic compound and (b) at least one polyanion of a film-forming thermoplastic polymer containing sulfated alcohol groups ##STR1## in repeating structural units. The composition has high electrical conductivity and good mechanical properties, especially after drawing at temperatures below the melt/decomposition temperature. The material may be used as electrodes, electrically conductive filaments or components for electromagnetic screening.