Abstract: A low surface gloss polyacetal resin composition includes (A) 100 parts by weight of a polyacetal base resin and (B) between about 0.1 to 40 parts by weight of a silicon graft copolymer which is the radical copolymerization product of (a) an acrylic-modified silicone with (b) a radical-polymerizable monomer. Optionally, the compositions may have a weathering (UV-light) stabilizer. Molded articles formed of the compositions exhibit low surface gloss and weather-resistance properties and are thus usefully employed in end-use applications where such attributes are required (e.g. automotive trim parts, electronic components, and the like).

Abstract: Amino resins, e.g., urea-formaldehyde and melamine-formaldehyde thermosetting resins, are cured with a latent catalyst which is a thermally-decomposable adduct of an aromatic sulfonic acid (e.g., p-toluene sulfonic acid) and a bicyclic oxazolidines (e.g., 1-aza-3,7-dioxa-5-ethylbicyclo (3.3.0) octane. The coating compositions can contain other conventional co-reactants, such as polyols, polyacids, alkyd resins, polyester resins, epoxies, acrylics and the like. Coatings containing the amino resin, co-reactant, and latent catalyst have an acceptable viscosity stability, cure rapidly at temperatures lower than some other latent catalysts, and produce films with no wrinkles.

Abstract: This invention relates to a core-shell polymer which is useful for polyoxymethylene resin, a polyoxymethylene resin composition containing the core-shell polymer and a molded article made of the polyoxymethylene resin composition.The core-shell polymer comprises a rubbery polymer core and a glassy polymer shell and has substantially no detectable anion.This core-shell polymer makes the molded articles be improved on the impact strength, elongation at the weld line, etc. The molded articles is used as various products (such as gears, reels, etc.).

Abstract: A compatible polymer blend consisting essentially of:a) 0.5-99.5 wt. % of homopolymer or copolymer polyoxymethylene component, andb) 99.5-0.5 wt. % of a polymer component which comprises 40-100% of at least one monomer of formula ##STR1## in which R.sub.1 is methyl or ethyl. The blends are suitable for use as engineering plastics.

Abstract: A polyacetal resin composition is improved in the weather-resistance and comprises:(A) a polyacetal resin,(B) 0.01 to 5% by weight (based on the whole composition) of a weathering (light) stabilizer and(C) 0.01 to 10% by weight (based on the whole composition) of an acrylic oligomer of a polyester type.

Abstract: A stain resistant composition for fibers having polyamide linkages prepared by polymerizing an .alpha.-substituted acrylic acid or ester in the presence of a sulfonated aromatic formaldehyde condensation plymer, or by polymerization of a sulfonated hydroxyaromatic ester of an .alpha.-substituted acrylic acid or acrylic acid, and methods for making and applying the composition.

Abstract: The invention relates to a mixture composed of polyoxymethylene (component A), a rubber-elastic graft copolymer in which the particles have been formed from a rubber-elastic, single-phase core based on polydiene and a hard graft shell (component B) and a polymeric third component (component C).The invention also relates to a three-component mixture of the components A, B' and C, the core, in the case of B' being preponderantly or entirely composed of poly(meth)acrylic acid ester or silicone rubber instead of polydiene.The shaped articles produced from these mixtures are particularly distinguished by good low-temperature impact strength.

Abstract: There are provided new moldable blends of a normally crystalline acetal polymer and a normally non-crystalline elastomeric copolymer of about 15 to 45 mol %, preferably about 25 to 35 mol % of trioxane, about 55 to 85 %, preferably about 65 to 75 mol % of 1,3-dioxolane, said mol percents based on the total of trioxane and 1,3-dioxolane, and about 0.005 to 0.15 wt. %, preferably about 0.05 to 0.12 wt. % of 1,4-butanediol diglycidyl ether or butadiene diepoxide as a bifunctional monomer, based on the total weight of copolymer.

Abstract: A curable polyester composition having improved properties is described, and the curable polyester composition comprises:(A) at least one unsaturated polyester resin;(B) at least one hydrocarbon monomer copolymerizable with the polyester; and(C) at least one aryl sulfonamide-aldehyde resin.When the curable polyester composition is to be used as a plastic body filler, the curable polyester composition generally will be modified to include (D) at least one inorganic filler which may comprise a mixture of an inorganic powder and inorganic hollow microspheres.The curable polyester resin compositions of the invention are useful as plastic body fillers for repairing metal surfaces, and the curable compositions have been found to be particularly useful and advantageous as plastic body fillers for galvanized steel.

Abstract: A stain resistant composition for fibers having polyamide linkages prepared by polymerizing an .alpha.-substituted acrylic acid or ester in the presence of a sulfonated aromatic formaldehyde condensation polymer, and methods for making and applying the composition.

Abstract: Incorporation into polyacetal molding compositions of 0.05-3 weight percent of certain non-meltable polymers containing formaldehyde reactive hydroxyl groups, formaldehyde reactive nitrogen groups, or formaldehyde reactive hydroxyl and formaldehyde reactive nitrogen groups, wherein the polymer has an average particle size, both prior to melt processing with the polyacetal and after melt processing with the polyacetal, of less than 10 microns, results in improved thermal stability of such compositions.

Abstract: Highly conjugated organic polymers typically have large non-resonant electronic susceptibilities, which give the molecules unusual optical properties. To enhance these properties, "defects" are introduced into the polymer chain. Examples include light doping of the conjugated polymer and synthesis, conjugated polymers which incorporate either electron donating or accepting groups, and conjugated polymers which contains a photoexcitable species capable of reversibly transferring its electron to an acceptor. Such defects in the chain permit enhancement of the second hyperpolarizability by at least an order of magnitude.

Abstract: A stain resistant composition for fibers having polyamide linkages prepared by polymerizing an .alpha.-substituted acrylic acid or ester in the presence of a sulfonated aromatic formaldehyde condensation polymer, and methods for making and applying the composition.

Abstract: This invention relates to novel forms of poly(heteroaromatic vinylenes), and poly(aromatic vinylenes) and to solutions thereof, either in the conductive form or non-conductive form.

Abstract: There is disclosed a novel poly-.beta.-alanine compound comprising monomeric units of the formula (CH.sub.2 CH.sub.2 CONH) and monomeric units of the formula ##STR1## in a specific proportion, having a high degree of polymerization and which is essentially free from metal contamination. The novel poly-.beta.-alanine is produced by polymerizing acrylamide using an alkaline earth metal alcoholate catalyst in an extremely limited amount. The novel compound has a wide variety of uses, and is especially useful as a thermal stabilizer for a polyacetal resin.

Abstract: Incorporation of 0.1-10 weight percent of certain polymers and/or oligomers containing both hydroxy groups and at least one other functional group that is a stronger Lewis base than the hydroxy groups into polyacetal molding compositions results in improved thermal stability of such compositions.

Abstract: The modification of thermoplastic polymers with a combination of azidosilanes and monolefinically unsaturated monomers and subsequent crosslinking by moisture.

Abstract: Incorporation of 0.1-10 weight percent of certain hydroxy containing polymers and/or oligomers into polyacetal molding compositions results in improved thermal stability of such compositions.

Abstract: Ultraviolet curable terpolymers of trioxane, from at least 65 weight percent to about 75 weight percent of 1,3-dioxolane and from about 2 weight percent to about 20 weight percent of a monoethylenically unsaturated aliphatic diol formal having at least 4 carbon atoms in its main chain, e.g., 4,7-dehydro- 1,3-dioxepin, which are non-crystalline at room temperature or above are disclosed. These terpolymers, when admixed with a multifunctional crosslinking monomer, e.g., a multifunctional acrylate such as 1,6-hexanediol diacrylate, and a photosensitizer, e.g., a benzoin compound such as benzoin isobutyl ether, can be cured to an insoluble, non-tacky, rubbery state using UV radiation. The thus-cured polymeric materials form useful crosslinked films, and when cryogenically ground to a suitable small particle size can be blended with conventionally prepared crystalline oxymethylene homo-, co- and terpolymers to improve the latters' impact properties.

Abstract: Electroactive polymers of the structure and formula ##STR1## in their neutral and ionized forms, where the backbone group R.sub.b is selected from or is a combination of five- and six-membered rings capable of aromatic and quinonoid bonding structures, R.sub.s is selected from aliphatic, aromatic and heterocyclic groups and x, y are positive integers from 1 to 5 and m is a positive integer from 2 to about 10,000, together with a method of making them are disclosed.

Abstract: Solid state compositions having improved storage stability are provided by reacting an aqueous solution or slurry of polymeric acetal carboxylate and alkali metal hydroxide with carbon dioxide to form alkali metal carbonate in intimate admixture with the polymer and recovering the admixture in solid form. The compositions are useful as builders in detergent formulations.

Abstract: Allyl ether capped styryl pyridines and styryl pyrazines are prepared by allylating with an allylating agent such as allyl halide or allyl methyl carbonate the reaction product of (A) a substituted pyridine and/or pyrazine with (B) a substituted aromatic aldehyde with the proviso that at least one of the components (A) or (B) contains a hydroxyl group which is susceptible to allylation. These allylated styryl pyridines and pyrazines can be homopolymerized or copolymerized with other materials to produce polymers having excellent high temperature resistance, good mechanical strength and excellent processability and are used to make cured composites with heat resistant fibers that have applications in high temperature environments such as engine compartments and/or fire walls.

Abstract: Alkenylphenylglycidyl ether capped styryl pyridines and styryl pyrazines are prepared by etherifying with an alkenylphenylglycidyl ether the reaction product of (A) a substituted pyridine and/or pyrazine with (B) a substituted aromatic aldehyde with the proviso that at least one of the components (A) or (B) contains a hydroxyl group which is susceptible to etherification by an alkenylphenylglycidyl ether. These alkenylphenylglycidyl ether capped styryl pyridines and pyrazines can be homopolymerized or copolymerized with other materials to produce polymers having excellent high temperature resistance, good mechanical strength and excellent processability and are used to make cured composites with heat resistant fibers that have applications in high temperature environments such as engine compartments and/or fire walls.

Abstract: A polyacetal copolymer composed of an acetal polymer portion and a thermoplastic elastomer portion having soft segments and hard segments, the second-order transition temperature of said elastomer portion being in the range of -120.degree. to 40.degree. C. A process for producing such a polyacetal copolymer is also described.

Abstract: Storage stable curing agents for acrylate adhesives, which curing agents are miscible with an acrylate resin adhesive, are produced by the mixing together of a polymerizable monomer, a thermoplast or elastomer soluble therein, and a liquid aldehyde/amine condensation product, and subsequent homogenisation of the mixture at elevated temperature. The curing agents, which optionally contain also stabilizers and curing accelerators, can be mixed with acrylate resin adhesives in any chosen quantity ratio between 2:1 and 1:2.

Abstract: Cementitious resin solutions for chemicals-resistant cements are prepared by dissolving a resin in furfuryl alcohol or preparing a resin solution by acidic condensation with the use of furfuryl alcohol. 0.01 to 0.1 equivalents of a primary amine per liter are added to the resin solution.

Abstract: A process for the preparation of a modified aromatic hydrocarbon resin which comprises reacting an aromatic hydrocarbon-formaldehyde resin with an unsaturated polybasic acid or an anhydride thereof, together with a saturated polybasic acid or an anhydride thereof if necessary, in the presence or absence of water, while introducing steam into the reaction system to remove by-produced formaldehyde out of the reaction system, and reacting the formed reaction product with at least one dihydroxy compound selected from the group consisting of (A) a glycol and (B) a hydroxy-terminated oligomer obtained by reacting a glycol with an unsaturated polybasic acid or an anhydride thereof; the cured product of the modified aromatic hydrocarbon resin being excellent in mechanical strength and resistance to water and alkalis.

Abstract: This invention relates to "comb" polymers having high molecular weight and related structurally to polyoxymethylene, but having improved thermal stability. In addition, this invention relates to a method for preparing these high molecular weight "comb" polymers and teaches a process which exhibits reduced reactor fouling and produces a free-flowing powder. Generally the improved polymer is made by copolymerizing trioxane with polyanhydride or copolymerizing trioxane with copolymers of olefins and anhydrides. The improved polymer can optionally be reacted with agents known to react with terminal hydroxy groups to end-cap the polymer.

Abstract: Polymer compositions comprising adducts of acrolein and isocyanuric acid and polyfunctional compounds containing aldehyde-reactive groups such as amines, amides, alcohols, thiols and oxiranes. The compositions are useful in molding, laminating, coating and adhesive applications.

Abstract: Polymer compositions comprising acetals of acrolein-isocyanuric acid adducts and polyfunctional compounds containing acetal-reactive groups such as alcohols, thiols oxiranes and amides. The compositions are useful in molding, laminating, coating and adhesive applications.

Abstract: Polymer compositions comprising hemiacetals of acrolein-isocyanuric acid adducts and polyfunctional compounds containing hemiacetal-reactive groups such as amines, amides, alcohols, thiols and oxiranes. The compositions are useful in molding, laminating, coating and adhesive applications.

Abstract: The invention is for the preparation and use of novel compositions and formulations of pressure sensitive adhesives for solid surfaces and which are especially adapted for use on both flexible and rigid plastic surfaces. Both the compositions and the adhesive formulations are considered to be novel and contain, among other components and ingredients, acrylic and methacrylic ester formals. The new formulations have been shown to have superior properties in a number of critical areas all of which are of great importance and provide advantages for the pressure sensitive adhesives.

Abstract: The alkali metal, ammonium and alkanol ammonium salts of polymeric acetal carboxylates are stable detergent builders under laundry use conditions but depolymerize in acid media, making the polymer fragments more readily biodegradable in waste streams.

Abstract: The alkali metal, ammonium and alkanol ammonium salts of polymeric acetal carboxylates are stable detergent builders under laundry use conditions but depolymerize at lower pH, making the polymer fragments more readily biodegradable in waste streams. Such polymeric acetal carboxylates can now be made by an improved process which includes the steps of bringing together in a reaction zone under polymerization conditions an ester of glyoxylic acid and a polymerization initiator, and adding an alkyl vinyl ether to the resulting polymer in the presence of a solvent having a dielectric constant of at least 15, such as an alkyl nitrile and a haloacetic acid catalyst, such as trifluoroacetic acid, to stabilize the polymer against rapid depolymerization in alkaline solution. The preferred solvent is acetonitrile.

Abstract: The alkali metal, ammonium and alkanol ammonium salts of polymeric acetal carboxylates are stable detergent builders under laundry use conditions but depolymerize in mildly acidic media, making the polymer fragments more readily biodegradable in waste streams. Such polymeric acetal carboxylates can now be made by a process which comprises bringing together in a reaction zone under polymerization conditions an ester of glyoxylic acid and a polymerization initiator, and adding to the resulting polymer an alkyl vinyl ether and an organoaluminum compound to stabilize the resulting polymer against rapid depolymerization in alkaline solution. The preferred alkyl vinyl ether is ethyl vinyl ether, and the preferred organoaluminum compounds are alkyl aluminum halides and trialkyl aluminum.

Abstract: The alkali metal, ammonium and alkanol ammonium salts of polymeric acetal carboxylates are stable detergent builders under laundry use conditions but depolymerize in acid media, making the polymer fragments more readily biodegradable in waste streams. Such polymeric acetal carboxylates can now be made by a process which comprises bringing together in a reaction zone under polymerization conditions an ester of glyoxylic acid and a molecular sieve, and adding an alkyl vinyl ether to the resulting polymer in the presence of the molecular sieve to stabilize the polymer against rapid depolymerization in alkaline solution. The preferred alkyl vinyl ether is ethyl vinyl ether.

Abstract: An acetal resin composition comprising an admixture of 100 parts by weight of an acetal resin and 0.01 to 15 parts by weight of a petroleum resin, said petroleum resin being prepared by polymerizing a cracked petroleum fraction boiling between -15.degree. C. and 200.degree. C. and containing unsaturated hydrocarbons, and having a molecular weight in the range of 400 to 2500 and a second order transition temperature in the range of 35.degree. to 90.degree. C.