Abstract: A process for producing large-size formed articles consisting of a modified polyamide, by polymerization of a mixture containing, besides the omega-lactam corresponding to the polyamide, the following reagents:a) a polymerization catalyst selected from the sodium salt and the potassium salt of said omega-lactam;b) a polyoxyalkylene polyamine having a molecular weight ranging from 400 to 5,000 and an amine functionality ranging from 1.9 to 2.5;c) an activator consisting of a polyisocyanate having all the isocyanic groups blocked with a lactam;said reagents being fed, at a temperature of from 105.degree. to 125.degree. C., to a mold heated to 130.degree.-170.degree. C.

Abstract: The present invention provides an oligomer having an inherent viscosity .eta. of 0.001-0.5 dl/g as measured at a concentration of 0.5 g/dl in N-methyl-2-pyrrolidone at 30.degree. C., which has been obtained by subjecting to polymerization and imidization (a) an acid component consisting of an aromatic tetracarboxylic acid dianhydride and/or a derivative thereof and (b) a diamine component consisting of 5-100 mole % of a diaminosiloxane represented by the undermentioned formula (I) and 95-0 mole % of an organic diamine other than the formula (I): ##STR1## wherein R.sub.1 is a divalent aliphatic group of 1-5 carbon atoms or a divalent aromatic group of 6 or more carbon atoms; R.sub.2 and R.sub.3 are each a monovalent aliphatic or aromatic group and may be the same or different; and m is an integer of 1-100, as well as an oligomer solution obtained by dissolving the above oligomer in an organic solvent.

Abstract: Lactam-lactone copolymers are provided that range in properties from plastic to elastomer which are formed by reacting components of a polymerizable composition comprising: a lactam monomer; a lactone monomer; a C.sub.3 to C.sub.12 lactam magnesium halide catalyst; and an initiator.

Abstract: An addition type imide resin prepolymer is obtained by a reaction of unsaturated bisimide of 1.0 mol to diamine of 0.25 to 0.43 mol and an addition of polyamine having three or more benzene rings. The prepolymer is thereby made to contain substantially no unreacted diamine component which affects human body of operators, and to have remarkably excellent heat resistance and adhesive properties, while effective to restrain a production of any component of a molecular weight exceeding 15,000.

Abstract: A method for producing a sliding coupling, w hich comprises injecting a casting material comprising the following components (A) and (B) into a clearance between a bearing and a shaft fitted in and rotatably or reciprocatively supported by the bearing, wherein a primer is preliminarily applied to either the shaft or the bearing and a releasing agent is preliminarily applied to the other; followed by polymerization and curing to form a resin lining on the surface of the shaft or the bearing:(A) a .OMEGA.-lactam liquid containing a polymerization catalyst of an alkali metal or alkaline earth metal compound; and(B) a .OMEGA.-lactam liquid containing at least one polymerization initiator.

Abstract: Polyimide precursor compositions incorporating at least one compound of fula (1), at least one compound of formula (2), at least one compound of formula (3) and at least one compound of formula (4) ##STR1## in which one of the groups R.sup.3 and R.sup.4 represents a hydrogen atom and the other, in the same way as the groups R.sup.1 and R.sup.2, which can be the same or different, in each case represent a hydrocarbon group having 1 to 16 carbon atoms, m is a number between 5 and 20, n is an integer between 1 and 5 and R.sup.5 represents a hydrogen atom, a halogen atom, a hydrocarbon group with 1 to 16 carbon atoms, or a group of formula R.sup.6 --O-- in which R.sup.6 represents a hydrocarbon group having 1 to 16 carbon atoms. The preferred composition contains 30 to 70% by weight of dry matter of compounds of formulas (1), (2) and (3), in which the groups R.sup.1, R.sup.2 and one of the groups R.sup.3 and R.sup.4 is a methyl or ethyl group and the compound of formula (4) is benzyl alcohol.

Abstract: New wholly aromatic polyamides are provided. This polymers are prepared by a mixture of N,N'-bis(4-aminophenyl)-isophthalamide and p-phenylenediamine in a tertiary amide solvent containing an alkali metal salt such as LiCl and a tertiary amine as an acid acceptor. The polymers are easily dry-jet spun to form a fiber and cast to form a film. The fiber and film so obtained have ultrahigh tenacity, elasticity and elongation.

Abstract: A denatured bismaleimide resin of repeating units represented by the following formula (I) and process for preparing same which comprises the Michael addition reaction of a bismaleimide and an aromatic secondary diamine: ##STR1## wherein, n represents an integer of 1 to 3, A represents a divalent group having from 2 to 20 carbon atoms,A' represents a divalent group having less than 20 carbon atoms which includes at least one or more aromatic groups, andR represents aliphatic having from 1 to 10 carbon atoms.

Abstract: The invention relates to high molecular weight thermoplastically deformable branched aliphatic polyamides prepared by polycondensation of lactams and/or polyamide-forming diamine/dicarboxylic acid reaction mixtures and/or amino acids in the presence of small amounts of specific diamino-alcohols and approximately equivalent amounts of polycarboxylic acids (preferably dicarboxylic acids), and to a process for their preparation, which is distinguished by considerably shortened polycondensation times, without crosslinked products being formed. If appropriate, the process additionally utilizes a solid phase after-condensation, in which rapid further condensation to products which are indeed branched but are soluble in m-cresol and have an increased melt viscosity takes place.

Abstract: High molecular weight aromatic polyamides with pendant carboxyl groups.

Abstract: The condensation of .beta.-dicarbonyl compounds with .alpha.,.beta.-unsaturated compounds is promoted by amidine and guanidine compounds.

Abstract: A molecular weight controller having particular application in the polymerization of a lactam, i.e., epsiloncaprolactam, to a polyamide, i.e., poly(epsiloncaprolactam). The molecular weight controller comprises a primary monofunctional amine, i.e., benzylamine, a primary monofunctional acid, i.e., acetic acid, and a salified aminoacid containing an aromatic, a cyclohexane, or cyclopentane moiety, i.e., 4-(aminomethyl)benzoic acid salified with p-toluenesulfonic acid. The resulting polyamide has a reduced water extractable content.

Abstract: Imide prepolymer compositions containing an unsaturated component (A) and diamine component (B) at the (A)/(B) molar ratio of 0.9-1.5 and 0.01-5.0% by weight, based on the sum of said components (A) and (B), of at least one radical polymerization inhibitors, and preferably further 0.01-5.0% by weight, based on the sum of said components (A) and (B), of at least one compound selected from the group of carboxylic acid and carboxylic acid anhydride.The imide prepolymer compositions of the present invention which contain the above-defined components in specific proportions are tough and excellent in adhesive strength to glass cloths and metals and in heat resistance.

Abstract: There is provided the process for producing an imide-based prepolymer having high solvent solubility by reacting an unsaturated bisimide of formula (I): ##STR1## wherein D is a divalent group having a carbon-to-carbon double bond, and A is a divalent group having at least two carbon atoms, with a diamine in the presence of a radical scavenger.

Abstract: The present invention relates to polymaleimide compounds having the following chemical structure: ##STR1## wherein n represents an integer of from 0 to about 50 and to a process for preparing the same.

Abstract: Polyamides are prepared from a carbonitrile and an amine by reacting by heating a mixture of a carbonitrile which is a dinitrile, an equivalent amount of a primary or secondary amine which is a diamine, and at least a stoichiometric amount of water in the presence of an effective amount of a catalyst. The catalyst is a complex containing at least one metal selected from the group consisting of ruthenium, rhodium and molybdenum, and at least one group selected from the group consisting of hydride, phosphine, carbonyl, ammonia, and hydroxyl.

Abstract: A process for producing modified, impact-resistant polyamides showing an increased polymerization rate, which consists in polymerizing an .omega.-lactam in the presence of:(a) a mixture of an organic di-isocyanate and an organic mono-isocyanate, the isocyanate groups of both of which are blocked with an .omega.-lactam;(b) a poly-oxy-alkylene-amine having an aminic functionality lower than 3, and(c) an alkaline catalyst.

Abstract: Process of preparing modified polyamides endowed with improved mechanical properties, which process resides in polymerizing an .omega.-lactam in the presence of(a) a polyisocyanate having the isocyanate groups blocked by an .omega.-lactam,(b) a poly-oxy-alkylene-amine, and(c) an alkali metal catalyst.A further object of the invention is the products obtained by means of such a process.

Abstract: Disclosed herein is a process for producing a polyamide comprising polymerizing at least one monomer of polyamide in the presence of(1) a hydrocarbon polymer having at least one group selected from the group consisting of a carboxyl group, a derivative group of carboxylic acid, an amino group, and a hydroxyl group, or(2) a polymer produced by reacting the hydrocarbon polymer with a polyamide, or polymerizing at least one monomer of polyamide in the presence of the hydrocarbon polymer.

Abstract: A method for synthetizing polyanhydrides in solution using coupling agents and a removable acid acceptor to effect a one-step polymerization of dicarboxylic acids. As used in the method, these coupling agents include phosgene, diphosgene, and acid chlorides. Insoluble acid acceptors include insoluble polyamines and crosslinked polyamines such as polyethyleneimine and polyvinylpyridine and inorganic bases such as K.sub.2 CO.sub.3, Na.sub.2 CO.sub.3, NaHCO.sub.3, and CaCO.sub.3. The only byproduct formed is a removable hydrochloric acid-acid acceptor.Examples are provided of the polymerization of highly pure polyanhydrides using phosgene, diphosgene or an acid chloride as the coupling agent, in combination with either an insoluble acid acceptor or a soluble acid acceptor in a solvent wherein the polymerizaiton byproduct or polymer is insoluble.A particularly important application of these polyanhydrides is in the formation of drug delivery devices containing bioactive compounds.

Abstract: A polyamide powder consisting essentially of elementary porous particles having a "gypsum rose" structure and a process for preparing a polyamide powder comprising polymerizing by anionic polymerization lactam in a solvent medium in the presence of a catalyst, an activator, and at least one amide; one of which is N,N'-alkylene bisamide; said polymerization being initiated with said lactam and said amide used in an amount such that the solvent is in the supersaturated state at the polymerization initiation temperature.

Abstract: A process for tempering unextracted polycaprolactam is disclosed which results in polycaprolactam having suitable physical and chemical properties for melt extrusion and spinning, without the need for conventional solvent/water extraction and drying of crude granules.

Abstract: Acetylene terminated aspartimides are prepared using two methods. In the first, an amino-substituted aromatic acetylene is reacted with an aromatic bismaleimide in a solvent of glacial acetic acid and/or m-c=resol. In the second method, an aromatic diamine is reacted with an ethynyl containing maleimide, such as N-(3-ethynylphenyl) maleimide, in a solvent of glacial acetic acid and/or m-cresol. In addition, acetylene terminated aspartimides are blended with various acetylene terminated oligomers and polymers to yield composite materials exhibiting improved mechanical properties.

Abstract: A polyamide powder consisting essentially of elementary porous particles having a "gypsum rose" structure and a process for preparing a polyamide powder comprising polymerizing by anionic polymerization lactam in a solvent medium in the presence of a catalyst, an activator, and at least one amide; one of which is N,N'-alkylene bisamide; said polymerization being initiated with said lactam and said amide used in an amount such that the solvent is in the supersaturated state at the polymerization initiation temperature.

Abstract: Thermosetting mixtures which contain (a) 10 to 90% by weight of at least one aromatic di- or polycyanate compound or a prepolymer thereof,(b) 90 to 10% by weight of at least one compound of the formula I or II ##STR1## or of a prepolymer of a compound of the formula I or II and, based on the sum of (a) and (b),(c) 0 to 50% by weight of at least one compound of the formula III ##STR2## in which R.sub.1, R.sub.2 and R.sub.3 independently of one another are each a hydrogen atom or methyl, n is 1 or 2 and m is 2 or 3, R is hydrogen or an aliphatic, cycloaliphatic or aromatic radical, R' is an aliphatic radical, m- or p-phenylene or m- or p-phenylenoxy and R" is an m-valent organic radical with 2-14 30 C atoms, are suitable for the production of shaped articles, such as prepregs or laminates, coatings and glueings.

Abstract: Biuret-group-containing polyisocyanates based on non-aromatic diisocyanates, possibly mixed with liquid N-alkyl-lactams, as activators for activated anionic polymerization of lactams.

Abstract: This invention relates to a curable resin composition comprising (a) a component selected from the group consisting of a dicyanate-terminated aromatic polysulfone oligomer, a dicyanate-terminated aromatic polyketone oligomer and mixtures thereof, (b) a cyanate ester component selected from the group consisting of polyfunctional aromatic cyanate ester monomers having at least two cyanate groups bonded to their aromatic ring, prepolymers of the cyanate esters and prepolymers of the cyanate ester monomers and amines, and (c) a bismaleimide component selected from the group consisting of bismaleimides, bismaleimides prepolymers and prepolymers of the bismaleimides and amines.

Abstract: The invention relates to a process for the preparation of a caprolactam that is not appreciably subject to re-equilibration during melt spinning of textile fibres. In the process such an amount of chain length regulating agent is used that the relative viscosity of the polyamide increases by not more than 0.5 units after 20 hour heat treatment in the solid phase in an inert gas atmosphere at between 110.degree. C. and 190.degree. C., after extraction.

Abstract: Nylon-type polyamides are produced from a diamine and a diamide in contact with a catalyst comprising a urea, thiourea, or derivatives thereof. For example, high quality nylon-6,6 is manufactured by contacting hexamethylenediamine and adipamide in water with urea, thiourea, or derivatives thereof catalyst, at an elevated temperature and pressure.

Abstract: Disclosed herein is an under-hood material for motorcars, prepared by molding a polymide resin comprising a caproamide component and/or a hexamethylene adipamide component as the major component thereof and having hydrocarbon groups of 6 to 22 carbon atoms as the end groups thereof, wherein (a) the number of the hydrocarbon groups is 5 to 100% of the total number of the end groups of the polyamide and (b) a relative viscosity of the polyamide is 2 to 6.

Abstract: The invention relates to polyimides of the general formula ##STR1## wherein R.sub.1, R.sub.2 =H, C.sub.1-3 -alkyl, halogen,R.sub.3 =C.sub.2-12 -alkylene or ##STR2## m=0, 1, X=CH.sub.2, C(CH.sub.3).sub.2, CO, O, S, SO.sub.

Abstract: A polyamide is produced by polymerizing at least one of an alpha, beta-unsaturated carboxylic acid and ammonia, an ammonium salt of an alpha, beta-unsaturated carboxylic acid, an alpha, beta-unsaturated nitrile and water, a beta-amino propionic acid or alkyl derivative thereof and an alpha, beta-unsaturated amide and ammonia in the presence of a catalyst comprising a pentaammine cobalt (III) complex.

Abstract: This invention relates to the use of compositions of the formula: ##STR1## wherein n is 2 to 4 and X is --O--, --S-- or ##STR2## wherein R.sub.1 is an aliphatic or aromatic moiety as a curing agent for epoxy resins to form a thermoset material which has a reduced shrinkage.

Abstract: A process for the manufacture of a polyamide powder comprising polymerizing in solution a reaction mixture comprising a monomer lactam or lactams capable of generating said polyamide in the presence of an N,N'-alkylene bisamide.

Abstract: A process for producing a lactam copolymer, which comprises copolymerizing an omega-lactam and a diene polymer having an amino or imino group at molecular ends by the action of an alkaline catalyst and a polyfunctional co-catalyst, the proportions of the components satisfying the following equations (I) and (II)a/c>1/4 (I)b/c>1 (II)wherein a, b and c represent the equivalent weights of the alkaline catalyst, the polyfunctional co-catalyst and the diene polymer, respectively, per equivalent of omega-lactam.

Abstract: Disclosed herein are a polyamide resin of a relative viscosity of from 2.5 to 6, having hydrocarbon group(s) of 6 to 22 carbon atoms as the end group(s) thereof, the number of the hydrocarbon group(s) being 40 to 100% of the total number of the end groups of the polyamide, and a process for producing the polyamide resin.

Abstract: The invention relates to a process for preparing an acyl-lactam compound characterized in that the reaction product of a lactam with a dicarboxylic acid anhydride is reacted with a polyol at a temperature of 150.degree. C. at most. These acyl-lactam compounds are very suitable as activator in the preparation of nylon block copolymers, more specifically in the RIM or RRIM systems.

Abstract: Methods of making modified polyimide adhesives and laminating compositions. These adhesives are also particularly useful as the matrix material in high strength fiber reinforced composites. The adhesive compositions are prepared by initially reacting an oxoimine with one or more tetracarboxylic acid dianhydrides, which is primarily 1, 2, 3, 4-butanetetracarboxylic acid dianhydride. The resulting bisimide is dissolved in a non-reactive solvent and a suitable diamine is added to react with the bisimide, producing a liquid resin solution which is essentially a polyamide resin solution. This solution is useful as an adhesive or a fiber composite matrix which can be cured to a polyimide at moderate processing temperatures. The final adhesive bond or matrix is found to be flexible, strong and very resistant to flame, high temperatures, oils and solvents.

Abstract: Described are novel thermosetting epoxy resin compositions suitable for making cured resins, prepregs and stiff, tough thermoset composites. The thermosetting compositions comprise a polyepoxide component, an amine hardener and a specified amount of certain aromatic oligomers containing functional groups which are reactive with the polyepoxide and/or hardener under curing conditions for the composition. The cured resins have a multiphase morphology which comprises at least one glassy continuous phase and at least one glassy discontinuous phase and have a fracture toughness, K.sub.IC, of at least 1.0 MPam.sup.1/2.

Abstract: Disclosed is a stiff, tough thermoset composite, the composite comprising a crosslinked epoxy resin matrix and high strength filaments. The resin matrix comprises a glassy discontinuous phase dispersed in a glassy continuous phase that continues throughout the resin matrix. Volume fractions of the discontinuous phase are at least about 35% of the total volume of the continuous and discontinuous phases combined in exceptionally tough composites.Also disclosed are novel resin compositions suitable for making these thermosets.

Abstract: A process for preparing polyamides which comprises polycondensing dicarboxylic acids having the following general formula and diamines by using carbodiimides as the condensing agent. ##STR1## wherein X is a group having a valence of (m+2), and C.sub.6-20 carbocyclic group, C.sub.3-20 heterocyclic group, C.sub.2-20 alkyl group, or C.sub.2-20 alkenyl group, the group having at least one carbon-carbon double bond in the position of conjugating to carboxylic acid radical or the group having an .alpha.,.beta.-unsaturated ketone structure;Y is --OR or --NRR' wherein R and R' each independently is C.sub.5-20 carbocyclic group, C.sub.1-20 heterocyclic group, C.sub.1-20 alkyl group or substituted group thereof having at least one substituent selected from the group consisting of --OW (wherein W is C.sub.1-12 alkyl group), C.sub.2-12 saturated acyl group, C.sub.2-12 saturated acyloxy group, C.sub.2-12 saturated acylamino group, C.sub.2-12 dialkylamino group, --SW (wherein W is the same as defined above), C.sub.

Abstract: An N-substituted carbamoyl-lactam compound of the formula ##STR1## wherein R is a di-valent radical derived from polytetramethylene glycol, R' is an at least divalent radical derived from a diisocyanate, Y is a C.sub.3 -C.sub.14 ring-forming alkylene group, and a has a value of at least 1 and is a number corresponding to the mean functionality of the aforesaid polyisocyanate minus 1. A process for preparing the N-substituted carbamoyl-lactam compound is also described.

Abstract: Process for preparing polyamide by anionically polymerizing lactam in the presence of an alkaline metal catalyst, an activator and at least one low molecular weight ester compound. The polymerization process is rapid and yields polyamides having good impact strengths. The process significantly reduces moulding time in reaction injection moulding.

Abstract: The invention relates to a process for the preparation of a nylon block copolymer composition by polymerization of lactam in the presence of a lactam-polymerization catalyst and an activator, characterized in that the activator used is a combination of:1. a high molecular weight lactam-terminated activator with a molecular weight of at least 1500, and2. a low molecular weight lactam-terminated activator with a molecular weight of at most 750.The process according to the invention can, in particular, be used in a reaction injection moulding process, in which liquid reaction component are introduced into a mould where fast polymerization to a moulded object takes place.

Abstract: N-alkylamide-substituted amines, such as nitrilotripropionamide, are either self-polymerized or copolymerized with other monomers, such as amino acids, in the presence of a stoichiometric amount of aqueous ammonia and at a temperature of at least 200.degree. C. and autogenous pressure to form substantially linear polyamides, such as poly-.beta.-alanine and nylon-3/6.

Abstract: Described herein are compositions which contain a specific group of oligomeric diamine hardeners and epoxy compounds which when combined with structural fibers produce composites which have improved tensile properties, high compressive strengths, and improved impact resistance. These compositions also exhibit low moisture absorption.

Abstract: Methods of making water soluble polyimide resin compositions. A carboxy terminated bisimide is prepared by reacting a suitable aromatic dianhydride with a suitable oxoimine. The bisimide is then mixed with a sufficient quantity of a water soluble solvent to dissolve the bisimide. Water is added to make a solution of the desired viscosity. An aromatic diamine is added to this water solution. To the mixture is added a suitable quantity of a tertiary amine to stabilize the resin. The solution is coated onto a surface and dried to produce a smooth, flexible coating. The coating can then be heated to an appropriate temperature to produce a fully polymerized coating which is thermally stable and resistant to oils and solvents.

Abstract: An improved method of molding involves utilizing as the catalyst and initiator components of a polymerizable composition, a Grignard catalyst and a dual initiator system.

Abstract: A process for polymerizing .epsilon.-caprolactam to form a nylon-6 block copolymer in which a reactant stream containing .epsilon.-caprolactam, and a lactam polymerization initiator is brought into polymerizing admixture with a reactant stream containing .epsilon.-caprolactam and a lactam magnesium halide, wherein sufficient 2-oxo-1-pyrrolidinyl compound is added to the admixture either as 2-pyrrolidinone, 2-oxo-pyrrolidinyl magnesium halide or 2-oxo-1-pyrrolidinyl capped initiator compound to enhance the rate of polymerization of the .epsilon.-caprolactam. The lactam polymerization initiator is a telechelic oligomer or polymer containing a backbone which provides elastomeric segments in the nylon-6 block copolymer, and attached to the backbone are activated initiator groups which initiate the polymerization of .epsilon.-caprolactam in the presence of the lactam magnesium halide.

Abstract: Compositions for the preparation of block copolylactams comprising lactam, lactam polymerization initiator and an effective amount of a viscosity enhancing compound selected from the group consisting of the lactamates and .omega.-amino acid salts of barium, calcium and strontium.