Abstract: A negative-working radiation-sensitive mixture comprising a binder and a polymer containing 1,2,3-thiadiazole groups is disclosed. The binder is a polyfunctional compound having functional groups that react with ketene. The polymer is a compound obtained by polymerization of a compound of the general formula I ##STR1## in which R is a polymerizable group. If the polymer is a copolymer containing comonomers having functional groups capable of reacting with ketene, the binder can be omitted. The negative-working radiation-sensitive mixture is particularly suitable for UV, electron beam and X-ray lithography.

Abstract: An improved adhesive composition comprising a nonacidic aqueous latex copolymer of a lower acrylate, an acrylic nitrile and a glycidyl acrylate having a crosslinking agent dissolved in the aqueous phase.

Abstract: The weather and UV-light resistance of polyacetal resin compositions is improved by incorporating into polyacetal resin a stabilizing package comprised of at least one stabilizing agent selected from benzotriazoles, benzophenones, aromatic benzoates, cyanoacrylates, oxalanilides, and hindered amines, and an acylate resin selected from homopolymers or copolymers of acrylic or methacrylic acid, and ester derivatives thereof.

Abstract: Polymer bound hindered amine light stabilizers are prepared by reacting hindered amine light stabilizers containing reactive hydrazide functionalities with anhydride containing polymers or copolymers. The reactions may be carried out in an inert solvent or in a melt blending step. The polymer bound hindered amine light stabilizers are useful alone or may also be used to stabilize other polymers, copolymers or polymer blends against the deleterious effects of heat and/or light.

Abstract: A composition for closing pores in a formation following a steam-flooding enhanced oil recovery process. The composition comprises an aqueous temperature activated gellable mixture. This mixture is comprised of water, water dispersible polymers, phenolic compounds, and aldehyde producing compounds. Polymers which can be utilized herein include polyvinyl alcohol, polyacrylamide and poly(acrylamide-coacrylamido-2-methylpropane sulfonate). Phenol is the phenolic compound of choice. At a formation temperature greater than 300.degree. F., trioxane, the preferred aldehyde producing compound decomposes to yield formaldehyde which reacts with phenol to form phenolic resin in situ. The resin gels the polymer and forms a solid gel in a heated zone of the formation.

Abstract: Gelable acid compositions containing novel crosslinkable copolymers and the novel copolymers. The copolymers contain an N-(alkoxymethylene)acrylyl moiety. In addition there are provided gelable acid compositions containing a group of polyfunctional reactants that contain a plurality of --CH.sub.2 OH and/or --CH.sub.2 CH.sub.2 OH groups in the molecule.

Abstract: Ultraviolet light stabilizers are chemically bound to anhydride containing polymers or copolymers. The polymeric stabilizers are prepared by the reaction of primary amino or hydrazido-substituted UV absorbers with some or all of the anhydride groups of the polymer or copolymer to form pendant stabilizer substituted imide or amic acid groups. The polymer bound stabilizers are not lost from the polymer system by volatilization, migration, or extraction, even at high temperature. The polymer of this invention may be used as they are or as concentrates to stabilize other polymer systems.

Abstract: Polymer bound stabilizer compounds are provided in which two or more different classes of stabilizers are chemically bound to anhydride containing polymers or copolymers. The polymeric stabilizers are prepared by the reaction of primary amino or hydrazido substituted stabilizers (i.e., antioxidants, light stabilizers, etc.) with some or all of the anhydride groups of the polymer or copolymer to form pendant stabilizer substituted imide or amic acid groups. The polymer bound stabilizers are not lost from the polymer system by volatilization, migration or extraction, even at high temperatures. The polymer bound stabilizer compounds may be used as concentrates to stabilize other polymer systems.

Abstract: Polymer bound antioxidants are provided in which the antioxidant stabilizer groups are chemically bound to polymers or copolymers by an acylaminoimide or diacylhydrazide function. The polymer bound antioxidants are prepared by reacting hydrazido substituted antioxidants with some or all of the anhydride groups of anhydride containing polymers or copolymers. The concentration of the stabilizers bound to the polymer may be readily varied depending upon the particular end-use of said polymer. Polymer with high concentrations of bound antioxidants can be used as masterbatches to stabilize other polymer systems.

Abstract: Polymer bound hindered amine light stabilizers are prepared by reacting hindered amine light stabilizers containing reactive hydrazide functionalities with anhydride containing polymers or copolymers. The reactions may be carried out in an inert solvent or in a melt blending step. The polymer bound hindered amine light stabilizers are useful alone or may also be used to stabilize other polymers, copolymers or polymer blends against the deleterious effects of heat and/or light.

Abstract: A Mannich base of a high molecular weight acrylamide polymer can be made by reacting, in aqueous solution, the polymer with a Mannich base of a low molecular weight compound such as urea. A composition of the polymer and the Mannich base is preferably substantially non-aqueous.

Abstract: A high solids coating composition comprises a low molecular weight polymeric blend of acrylic polymer, polyester polymer, and amine cross-linking resin. The acrylic and polyester polymers contain primary hydroxyl groups adapted to coreact and cross-link with active amine cross-linking resin such as aminoplast resins. All of the polymers have a number average molecular weight below about 3000.

Abstract: A thermoplastic resin composition containing polyphenylene oxide resin is provided, which is superior in processability and impact resistance as well as heat resistance, chemical resistance and hardness, said thermoplastic resin composition comprising(A) polyphenylene oxide resin or a resin composition containing the same, and(B) ethylene copolymer comprising 50-90% by weight of ethylene, 5-49% by weight of alkyl ester of .alpha.,.beta.-unsaturated carboxylic acid and 0.5-10% by weight of maleic anhydride.

Abstract: A high solids coating composition comprises a low molecular weight polymeric blend of acrylic polymer, polyester polymer, and amine cross-linking resin. The acrylic and polyester polymers contain primary hydroxyl groups adapted to coreact and cross-link with active amine cross-linking resin such as aminoplast resins. All of the polymers have a number average molecular weight below about 3000.

Abstract: Ionene elastomers are prepared by reaction of polymeric diamines and certain dihalide linking agents. These elastomers have utility in coating compositions, adhesive compositions, and in the fabrication of elastomeric articles. Certain novel dihalide linking agents are also claimed.

Abstract: A non-asbestos clutch facing has an actual density such that the facing is permeable to air. The clutch facing is preferably a moulded facing containing short reinforcing fibres and having an actual density not greater than 90% of theoretical.The facing may be made by a technique in which a pre-form is prepared, moulded to the desired density and then cured under a pressure such as not to cause substantial further density change.

Abstract: Low density friction products composed of non-asbestos reinforcing fibers embedded in a matrix of binder material, optionally including friction and wear modifiers, are described in which the actual density of the product is less than 72% of the theoretical density. Clutch facings of this density exhibit improved wear characteristics, lower inertia and increased burst strength.

Abstract: A resin composition comprising 100 parts by weight of a thermosetting resin and 1 to 100 parts by weight of a functional, rubbery copolymer containing among the monomer units which constitute the copolymer, at least one monomer containing a substituent selected from the group consisting of epoxy, hydroxyl, carboxyl and amino groups, said copolymer being prepared by one of three emulsion polymerization processes in which a nonionic surface active agent and/or ionic surface active agent is employed as the emulsifying agent.

Abstract: A binder which is suitable for coating agents and is based on a combination which is essentially free of protective colloids and consists of an aqueous primary dispersion of a synthetic polymer and a water-insoluble polycondensate of phenols and aldehydes, some of which may be replaced by ketones, is prepared by a process in which the phenolic components for the polycondensate are first mixed with an aqueous primary dispersion of a synthetic polymer which contains glycidyl, carbonyl, N-methylol, N-alkoxymethyl, ether, amino and/or hydrazo groups and may furthermore contain carboxyl or hydroxyl groups, and the polycondensation with the aldehydes (and ketones) is then carried out in this mixture, under conventional conditions.The binders prepared according to the invention are useful as binders for dispersion paints and coatings, in particular as heat-curable binders for metal finishes.

Abstract: A rubber composition consisting essentially of 5-99 parts by weight of a thermosetting resin and 94-1 parts by weight of one of the following functional rubber-like copolymers (I) to (III) having a Mooney viscosity ML.sub.1+4.sup.

Abstract: An impact-resistant phenolic resin composition comprising 99 to 25% by weight of a phenolic resin and 1 to 75% by weight of a nitrile group-containing highly saturated polymer rubber whose amount of bound nitrile ranges from 10 to 60% by weight and having an iodine value not exceeding 120.

Abstract: Polyphenylene ether compositions having enhanced commercial value as engineering resin, which are excellent in the appearance characteristics, such as surface gloss and weld part beauty, and stress crack resistance. The present resin composition is composed of a polyether resin (PPE) and a rubber reinforced high impact polystyrene (HIPS), if desired, together with a vinyl aromatic compound resin, wherein the PPE has specific characteristics with respect to the intrinsic viscosity, the eluting amount, and others.

Abstract: A rubber mixture is provided for direct bonding to metal surfaces, and includes a base of natural and/or synthetic rubber which contains fillers, processing aids, vulcanizing agents, a bonding agent in the form of a phenol, or derivatives thereof, which form phenolic resins with formaldehyde, a source of formaldehyde, and metallic compounds, preferably oxides of metals, the outer electron shell of which has 2s electrons. The metallic compounds are present in a measured quantity which is about 30 to 400 mMol above the conventional dosage of 40 to 60 mMol for activating the polymerization, with this measured quantity being applicable to each 100 g of rubber. The measured quantity of bonding agent ranges from two to four times the conventional quantity of 40 mMol per 100 g rubber.

Abstract: A friction material suitable for use as a bearing, comprising:(a) 20-40 weight percent phenolic resin;(b) 5-15 weight percent graphite;(c) 0.5-3.5 weight percent carbon black;(d) 40-60 weight percent of a non-asbestos containing refractory fiber comprising at least 25 wt. % CaO and 35 wt. % SiO.sub.2 ; and(e) 4-10 weight percent acrylic fiber.

Abstract: A resin composition comprising(I) a granular or powdery resin which is a condensation product of a phenol, an aldehyde and optionally a nitrogen-containing compound having at least two active hydrogens and is characterized by (A) containing spherical primary particles and their secondary agglomerated particles each having a particle diameter of 0.1 to 150 microns, (B) having such a size that at least 50% by weight thereof can pass through a 100 Tyler mesh sieve, and (C) having a free phenol content, determined by liquid chromatography, of not more than 500 ppm, and(II) at least one member selected from the group consisting of (1) a rubbery elastic material, (2) a thermoplastic resin and (3) a curable reisn other than said granular or powdery resin (I) and/or a filler material other than said granular or powdery resin (I).

Abstract: An aramid reinforcing element is treated with a cold gas plasma of air, N.sub.2, He, Ne or Ar or mixture thereof at up to 300 watts power for a few seconds to several minutes to improve its adhesion to rubber compounds.

Abstract: A novel bis-imide matrix resin system especially useful for high temperature, high performance, graphite fiber composites is disclosed. Microcracking of composites is reduced and transverse strength is increased by the addition to the resin system of 1 to 15 percent of compatible elastomers, such as polyether sulfones, bis-phenol linear homopolymeric epoxies or polyacrylic esters. The resin system comprises 50 to 95 percent by weight of ethylenically unsaturated bis-imides, preferably a low melting mixture of a major portion of maleimides of aromatic amines with a minor portion of maleimides of an aliphatic amine and 5 percent to 35 percent by weight of a diunsaturated low-temperature cross-linking agent such as divinyl benzene which gels the bis-imide at low temperatures. Room temperature tackiness, heat resistance and cross-link density are improved by the presence of 1 to 10 percent of a trifunctional curing agent.

Abstract: An aromatic polyester copolymer consisting of 10 to 90 mol % of a recurring unit of the formula: ##STR1## and 90 to 10 mol % of a recurring unit of the formula: ##STR2## and having a logarithmic viscosity number of at least 0.3 as measured in a mixture of phenol and tetrachloroethane (6:4 in weight ratio) at a concentration of 1 g/100 cc at 25.degree. C. and having a terminal carboxyl content of about 80 mol eq./ton or less. This aromatic polyester copolymer has high durability under dry and moist heat as well as high resistance to water crazing and hence can be fabricated into useful articles by various molding techniques.

Abstract: Resinous coating compositions can be expediently heat cured by phenol compounds containing at least two methylene amine groups which are conjugated with the aromatic alcohol group or phenol group. The hydroxyl group substantially increase the reactivity of the aminomethyl functionality whereby active hydrogen containing resins can be effectively cross-linked.

Abstract: A novel bis-imide matrix resin system comprising 50 to 95 percent by weight of ethylenically unsaturated bis-imides, preferably a low melting mixture of a major portion of maleimides of aromatic amines with a minor portion of maleimide of an aliphatic amine and 5 percent to 35 percent by weight of a diunsaturated low-temperature cross-linking agent such as divinyl benzene which gels the bis-imide at low temperatures. This reduces stress between the matrix resin and the surface of the reinforcing fiber, thus reducing the tendency to form microcracks. Microcracking is further reduced and transverse strength is increased by the addition of 0 to 15% of compatible elastomers to the resin and cross-linking agent. Room temperature tackiness, heat resistance and cross-link density are improved by the presence of 0 to 10% of a trifunctional curing agent.

Abstract: Compositions useful as frictions particles comprised of tri- and/or tetrafunctional phenol, rubber, aldehyde, protective colloid and a reaction promoting compound. The friction particles are formulated into friction elements. A process for producing the friction particles in particulate form.

Abstract: Cationic amine-functional copolymer mixtures with aminoplast resins which are stably dispersible in water with the aid of a solubilizing acid and water miscible organic solvent, and which cure to possess superior detergent and corrosion resistance are provided by forming a solution copolymer of monoethylenically unsaturated monomers including from 3% to 35% of monomer having a basic amino group and from 20% to less than 35% of isobutoxymethyl acrylamide or methacrylamide. The copolymer preferably includes from 20% to 45% of styrene and/or vinyl toulene in admixture with from 15% to 40% of 2-ethylhexyl methacrylate and the preferred aminoplast resins are benzoguanamine-formaldehyde and bisphenol-formaldehyde.

Abstract: Water dispersible cationic amine-functional copolymer condensates are prepared by heat reacting in solution in water miscible organic solvent a solution copolymer containing from 3% to 35% of monomer having a basic amino group and from 20% to 50% of isobutoxymethyl acrylamide or methacrylamide, the amine groups in the copolymer being at least partially neutralized by a solubilizing acid, with from 5% to 40% of a solvent-soluble, heat-hardening condensate of a phenol having at least two aldehyde-reactive positions with at least two mols of formaldehyde per mol of the phenol, the phenolic condensate being poorly dispersible in water until after condensation with the copolymer.

Abstract: This invention relates to fiber blends, yarns and fabrics for use in lightweight garments offering protection against brief exposure to extreme thermal fluxes, the fiber blend comprising a component that fuses within 10 seconds upon exposure to a heat flux of 2 cal./cm..sup.2 /sec. and a component that in fabric form exhibits a flame strength of at least 20 mg. per denier for at least 10 seconds during exposure to a heat flux of 2 cal./cm..sup.2 /sec.

Abstract: Elastoplastic compositions are described comprising blends of cross-linked rubber and thermoplastic polyamide.

Abstract: This invention is directed to low molecular weight, solid addition products having a softening point above 100.degree. F. and the method of preparing same and more particularly to the use of said addition products as crosslinking agents in various polymeric powder coatings, e.g. polyesters. The solid, low molecular weight products are derived from the addition reaction of at least one monohydroxy, single-ring aromatic carbon compound and hexakis (alkoxymethyl) amino-triazine.