Abstract: The invention disclosed is an improved process for the preparation of high molecular weight poly(arylcarbonate), the molecular weight ranging from 45,000-60,000 (corresponding to n.sub.inh 0.8 to 1.0) The process involves heating in a controlled manner, a BPA-polycarbonate oligomer in the presence of a catalyst selected from alkali metal aryl acid, alkali metal borohydrial and a quarternary ammonium salt of bioxiyanion derived from a carboxylic acid poly(arylcarbonate)s of high molecular weight produced by the process of present invention show enhanced crystallinity.

Abstract: A crystallizable thermoplastic polymer composition is prepared by adding a small amount of a substantially graphitic non-turbostratic carbon to a polyketone polymer. The graphitic carbon acts as a nucleating agent, increasing the crystallization rate of polyketone polymer.

Abstract: A hydroxy-substituted poly(phenylene ether) resin can be produced by copolymerizing from 1.5 to 8 mol % of a phenol compound selected from those represented by the following formulae (a), (b), (c), (d), and (e): ##STR1## and from 98.5 to 92 mol % of a phenol compound of the following formula (f): ##STR2## The hydroxy-substituted poly(phenylene ether) resin shows excellent compatibility with a polyamide, a polycarbonate, a poly(butylene terephthalate), a poly(phenylene sulfide), and is useful as a copatibilizer or a modified resin for engineering plastics.

Abstract: Process for producing polybutylene terephthalate with less than 1.0 wt % units derived from ethylene glycol from polyethylene terephthalate scrap by diolysis and ester exchange with 1,4-butanediol and subsequent polycondensation.

Abstract: A method for preparing a polymer including the step of reacting carbon monoxide and a reactant pair having respective general formulas ##STR1## a reactant having the general formula ##STR2## in the presence of catalyst and free iodo or bromo ions. X is --Br or --I. n is an integer from 0 to 4. R.sup.1 is selected from the group consisting of alkyl, arylalkyl, aryl, heteroaryl, and cycloalkyl. R.sup.2 is selected from the group consisting of ##STR3## wherein each R.sup.5 is independently selected from the group consisting of alkyl and aryl, m is an integer from 1-12, and j is an integer between 0 and 300.

Abstract: A method for preparing a polymer including the step of reacting carbon monoxide and a reactant pair having respective general formulas ##STR1## and or a reactant having the general formula ##STR2## in the presence of catalyst and free iodo or bromo ions. X is a nonortho halide selected from --Br and --I. n is an integer from 0 to 4. R.sup.1 is selected from the group consisting of alkyl, arylalkyl, aryl, heteroaryl, and cycloalkyl. R.sup.2 is selected from the group consisting of ##STR3## and Each R.sup.5 is independently selected from the group consisting of alkyl and aryl, m is an integer from 1-12, and j is an integer between 0 and 300. R.sup.3 is selected from the group consisting of substituted aryl, unsubstituted aryl, substituted heteroaryl, and unsubstituted heteroaryl.

Abstract: A cyclic polycarbonate oligomer having a low melting point useful in the preparation of high molecular weight resins. The cyclic polycarbonate oligomers have structural units with long alkyl chains which may contain ester substituents.

Abstract: Hyperbranched aramids, made from an aromatic aminodicarboxylic acid or an aromatic aminodicarboxylic acid, and optionally an aromatic aminocarboxylic acid are disclosed. The hyperbranched aramids are useful as aids for the processing of aramid solutions. Also disclosed are novel monomers used to make the hyperbranched aramids.

Abstract: The present invention relates to a process for the preparation of N-(hydroxyphenyl)maleamic acid and various dimers and oligomers thereof. The process is characterized by heating, in the absence of any solvent, N-(hydroxyphenyl)maleamic acid at a temperature ranging from about 150.degree. to about 250.degree. C. in the presence of an acid catalyst. This unique process avoids the need to recover expensive highly polar solvents. The present invention also relates to use of these maleimide containing compounds in rubber. The use of the blend of hydroxyphenyl maleimide and the various dimers and low molecular weight oligomers impart superior properties to rubber when compared to the use of hydroxyphenyl maleimide alone in rubber.

Abstract: Novel polyiminocarbonates having molecular weights exceeding 70,000 daltons. Novel solution polymerization and interfacial polymerization processes for the preparation of polyiminocarbonates in which cyanate compounds are reacted with diphenol compounds in the presence of a strong base catalyst.

Abstract: A method for the polymerization of Nylon 6 from caprolactam and water using a catalyst composition comprising a primary catalyst, which can be an alkali metal hypophosphite or an alkali-earth metal hypophosphite, and an amine cocatalyst. The amine cocatalyst can be selected from the group consisting of phenylene diamines, hindered amines, poly(hindered amines), Group I benzotriazoles, and Group II benzotriazoles. The catalyst composition used in this invention is most useful when used in conjunction with the reactive extrusion technology which requires a very fast polymerization rate to take full advantage of this evolving technology.

Abstract: Hydroxy group-containing polymers, particularly polyphenylene ethers, are capped by reaction with a chlorotriazine in the presence of a substantially inert organic liquid such as toluene, water, a phase transfer catalyst and a tertiary amine from a specific class, preferably a trialkylamine such as triethylamine or dimethyl-n-butylamine. The reaction proceeds rapidly and in good yield.

Abstract: Amorphous polyamide compositions are provided which are transparent and have improved glass transition and thermal decomposition temperatures. The polyamide compositions of the present invention can be prepared as the polymeric condensation product of a diamine component comprising neopentyldiamine, and a diacid component comprising an aromatic dicarboxylic acid.

Abstract: Substituted and unsubstituted di-phthalonitrile monomers devoid of ether /or phenoxy groups are solid at room temperature and which monomers are defined by the following general formula: ##STR1## where R is an aromatic tetravalent radical, thermoplastic prepolymers and thermosetting polymers which polymers are solid at room temperature and have a defined glass transition temperature if said polymers are cured at a temperature below a critical temperature or are devoid of a glass transition temperature if said polymers are postcured at a temperature exceeding said critical temperature.

Abstract: A biguanide group-containing polymer having repeat units of the following general formula (I): ##STR1## wherein A represents a radical selected from the group consisting of ##STR2## where R.sup.1, R.sup.2 and R.sup.3 independently from each other represent a hydrogen atom, an alkyl group having 1-18 carbon atoms, an alkoxycarbonylalkylene group having 3-18 carbon atoms, an alkylenecarboxylic acid group having 2-18 carbon atoms or an aryl group having 6-8 carbon atoms, and ##STR3## where R.sup.1, R.sup.2 and R.sup.3 have the same meaning as above and X represents an acid,B represents a radical selected from the group consisting of --NH.sub.2 and --NH.sub.2 Y where Y represents an acid, and m and n independently from each other are integers of 1 or more with the proviso that (m+n) is 10 or more.The polymer may be prepared by reacting polyallylamine with a guanyl-O-alkylisourea compound to convert a portion of the amino groups of the polyallylamine to biguanido groups.

Abstract: Radiation-sensitive polymers contain, in the polymer main chain, both acid-labile groups and onium salt groups with nonnucleophilic counterions and are suitable for the production of semiconductor structural elements.

Abstract: A continuous process for the removal of electrolytes and catalysts from organic polycarbonate solutions is disclosed. Accordingly, a solution obtained in the course of the two-phase interfacial reaction for the preparation of polycarbonate, containing thermoplastic aromatic polycarbonate and an organic solvent and up to 10 parts by weight water as well as residues of chain terminators, branching agents and diphenols is washed with water and/or hydrochloric acid through a cascading train of centrifuges. The resulting polycarbonate resin is characteristically of extremely low iron content.

Abstract: Aluminum-nitrogen polymers comprising a backbone of alternating aluminum and nitrogen atoms both having pendant organic groups, wherein some of the pendant organic groups are unsaturated, are prepared by reacting an unsaturated organic nitrile with a dialkylaluminum hydride. The polymers are crosslinked by supplying energy to generate free radicals. The crosslinked polymers can be pyrolyzed to form an aluminum nitride ceramic.

Abstract: A polymer having repeating units corresponding to the structure ##STR1## wherein R is selected from the group consisting of ##STR2## where z is 1, 2, 3, or 4, A is a divalent substituted or unsubstituted aromatic radical, y is in the range of 0.10 to 0 and x is in the range of 0.02 to 0.90 and n is at least 50.

Abstract: Novel crystalline polyamides having high heat deflection temperatures when filled are prepared from aliphatic diamines and either mixtures of terephthalic acid and adipic acid or mixtures of terephthalic acid, isophthalic acid and adipic acid. The mole ratio of aliphatic diamine to terephthalic acid, isophthalic acid, and adipic acid is in the range of about 100:65-95:25-0:35-5. The polyamides can be filled with about 10 to about 60 parts by weight of a filler. The mechanical properties of these polyamides are largely unaffected by absorbed water.