Abstract: A process for forming a built-up film with logic polymers whose film inherently cannot be readily obtained by LB technique comprises modifying the high polymers, and if required, further cyclizing the product partially or wholly. The produced thin films have extremely excellent heat resistance, good chemical resistance and mechanical characteristics and their thickness is so small that it is generally hardly attainable, that is, less than 10,000 .ANG., or if desired, 10 to 1000 .ANG..

Abstract: Aromatic polyesteramides exhibiting melt processability are disclosed. The polyesteramides comprise certain essential repeating units of the formulas ##STR1## wherein X is alkyl, alkoxy, trifluoromethyl, halogen or nitro. The polyesteramides exhibit melt anisotropy. Films and fibers combining a balance of properties suited to high strength service can be provided from the melt-processable polyesteramides.

Abstract: A curable composition comprising (a) a curable polyimide soluble in organic solvents and (b) a polymerization initiator as essential components, said polyimide consisting of recurring units represented by the formula ##STR1## wherein, each of X, X.sub.1, X.sub.2, X.sub.3 and X.sub.4 is a tetravalent carbocyclic or heterocyclic residue, each of Y.sub.1, Y.sub.2, and Y.sub.3 is a divalent carbocylic or heterocyclic residue, at least one of Z.sub.1 and Z.sub.2 is a residue having a reactive carbon-carbon double bond, and each of l, m, and n is an integer from 0 to 20, preferably from 0 to 10. The polyimide may include (a) polyacrylate compounds (b) bis-imide compounds (c) photosensitive polyimide precursors (d) oxime initiators (e) a 3 component sensitizer of a phenone compound, a mercapto compound, and an arylamine-alkanol, or mixtures of a,b,c,d, and e.

Abstract: Described herein are novel crystalline chain extended poly(aryl ether ketones) which display excellent toughness, fabricability and very good high temperature and solvent resistance.

Abstract: Cyclic polyester and especially polyarylate oligomers, typically having degrees of polymerization from 2 to about 7, are prepared by reacting a bisphenol such as bisphenol A or 6,6'-dihydroxy-3,3,3',3'-tetramethylspiro(bis)indane with a dicarboxylic acid chloride such as isophthaloyl or terephthaloyl chloride in the presence of a catalyst, under conditions of low concentration. The cyclic oligomers may be polymerized to linear polyesters by contact with a transesterification catalyst at a temperature in the range of about 200.degree.-300.degree. C.

Abstract: Novel polymers and molding compositions are prepared from acyl halide derivatives of tricarboxylic acids and diamines and about 1 to about 10 percent by weight of phthalic anhydride, trimellitic anhydride or aniline moieties. The polymers are useful in engineering plastics.

Abstract: A liquid crystal aligning agent consisting essentially of a polyimide resin obtained by the polymerization of a diamine, a tetracarboxylic acid dianhydride and a monoamine of the formula:R.sup.2 (R.sup.1).sub.n NH.sub.2 (I)wherein R.sup.1 is a divalent organic group, R.sup.2 is an alkyl group having from 6 to 20 carbon atoms, and n is 0 or 1.

Abstract: An organic silicon-terminated polyimide precursor having a very stable solution viscosity is produced by polycondensing 100 parts by weight of a mixture composed of 90 to 99.5% by mole of an organic diamine represented by the following general formula (I) and 10 to 0.5% by weight by mole of an organic silyl represented by the following general formula (II): ##STR1## wherein R.sup.1 and R.sup.2 are divalent organic groups; R.sup.3 and R.sup.4 are monovalent organic groups; m is 0, 1, 2, or 3, with an organic tetracarboxylic acid dianhydride represented by the following general formula (III) in a molar amount corresponding to the 100 parts by weight of the mixture of the organic diamine and the organic silyl represented by the said general formulae (I) and (II), respectively, in an organic polar solvent at 0.degree. to 40.degree. C., thereby obtaining a solution of organic silicon-terminated polyimide precursor, and heating the solution at 50.degree. to 80.degree. C.: ##STR2## wherein R.sup.

Abstract: This invention relates to a method of manufacturing aromatic polyamides having general formula(--CO--Ar--CO--NH--Ar'--X--Ar"--Y--Ar"--X--Ar'--NH--).sub.mwhere Ar, Ar', and Ar" each represent an m- or p-phenylene group, possibly substituted with alkyl groups having 1 to 4 carbon atoms; and X is O and Y is SO.sub.2 or X is SO.sub.2 and Y is O. In the present method, isophthalic and/or terephthalic acids are reacted with diamines of the formulaH.sub.2 N--Ar'--X--Ar"--Y--Ar"--X--Ar--NH.sub.2in the presence of a catalytic amount of an acid derived from phosphorus and having formula H.sub.3 PO.sub.n (where n=2, 3 or 4), or in the presence of triphenyl phosphite, and possibly in the presence of a 4-dialkylaminopyridine, in a polar, aprotic, organic solvent, at temperatures between 160.degree. and 300.degree. C.

Abstract: Described herein is a process for preparing polyesters which comprises reacting a dihydric phenol with a diester derivative of an aromatic diacid in the presence of from about 10 to about 60 weight percent of a processing aid having a boiling point of greater than about 200.degree. C., under polyester forming conditions.

Abstract: A method of manufacturing polyamides from aromatic dicarboxylic acids and aromatic diamines in the presence of catalytic amounts of a phosphorous-containing catalyst and a 4-diakylaminopyridine as cocatalyst, at temperatures above 180.degree. C., is described.

Abstract: Novel branched copolyetherketones comprising condensation products of diphenyl ether, aromatic acid halides and trifunctional comonomers are disclosed.

Abstract: Described herein is an improved process for preparing poly(aryl ether ketones) by reacting nucleophilic coreactants with electrophilic coreactants under Friedel Crafts polymerization conditions, wherein the improvement comprises carrying out the polymerization in a solvent comprising 1,2-dichlorethane.

Abstract: Described herein is a process for stabilizing a poly(aryl ether ketone) produced by a Friedel-Crafts polymerization process which comprises adding a nucleophilic and/or an electrophilic capping agent during the polymerization.

Abstract: Novel copolyetherketones derived from diphenyl ether and aromatic diacids or diacid halides are disclosed where the diphenyl ether is present in a molar excess relative to the diacid or diacid halide chlorides of about 2 to 8%.

Abstract: Described herein are novel crystalline chain extended poly(aryl ether ketones) which display excellent toughness, fabricability and very good high temperature and solvent resistance.

Abstract: An aromatic polyester composition comprising an aromatic polyester derived from terephthalic acid and/or isophthalic acid and a bisphenol and a stabilizer comprising dimercaptothiadiazole.

Abstract: The preparation of poly(arylene ketones) and in particular all para-linked poly(arylene ether ketones) by Friedel-Crafts polymerization in the presence of a Lewis acid generally results in an intractible reaction product difficult to remove from the reaction vessel and difficult to purify. The addition of a liquefaction agent, such as a hydrogen halide and in particular hydrogen chloride, to the reaction mixture, results in a tractible gel or a liquid which can be readily handled. The hydrogen halide is preferably under pressure and a diluent may also be added along with the hydrogen halide.

Abstract: Polyarylates having amide terminal groups are prepared using a terminating amount of ammonia, ammonium compounds, primary amines, secondary amines, hydrogen ammonium salts of secondary amines, or hydrogen ammonium salts of primary amines. These amide terminated polyarylates exhibit improved thermal properties and are useful in the production of films and molded articles.

Abstract: The present invention relates to aromatic polyester(carbonate)s with end groups of the formula (Ib) ##STR1## optionally mixed with known aromatic polyester(carbonate)s, their preparation by the phase boundary process or in homogeneous solution and their modification by irradiation.

Abstract: The invention relates to completely aromatic polyesters in which at least one end of the molecular chains is composed of the radicals ##STR1## The invention also relates to a process for the preparation of polyesters of this type and to the shaped articles produced therefrom.The polyesters according to the invention are also open to subsequent solid-phase condensation.

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: Polyesters having at least 90%, by weight, of recurrent structural units corresponding to the following formula: ##STR1## and characterised by a relative viscosity.eta..sub.rel of from 1.6 to 4.5 (determined at 25.degree. C. in CH.sub.2 Cl.sub.2, c=5 g/l) are suitable for the production of films having highly advantageous performance characteristics, in particular high heat resistance.

Abstract: A method of producing aromatic polyesters by polycondensation of diols and carboxylic acids, comprising polycondensating said diols and said dicarboxylic acids in the presence of a sulfur compound of a general formula: ##STR1## wherein R.sub.1 represents a substituted or unsubstituted aryl, alkyl or aralkyl group, X represents a halogen atom.

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: Oligomeric and/or polymeric polyoxazole and polythiazole precursors can be prepared with high purity, i.e., especially without chloride, in a simple manner if an aromatic and/or heterocyclic dihydroxy, dialkoxy or diaryloxydiamino compound or a corresponding dithio compound is reacted with a dicarboxylic acid in the presence of a carbodiimide. The precursors prepared in this manner are suitable, for instance, for the manufacture of protection and insulating layers.

Abstract: The invention relates to a process for the production of colorless, heat-stable and hydrolysis-stable aromatic polyesters and polyester carbonates by conventional interfacial polycondensation of aromatic dicarboxylic acid dichlorides and diphenolates in which dicarboxylic acid dichlorides are used which have been obtained by chlorination from the dimethyl esters of the corresponding acids, and tertiary cycloaliphatic amines are used as catalysts.

Abstract: A copolymer formed from an isoimide oligomer and another compound, such as an aryl sulfone, each of which has reactive functional terminal groups, such as ethylenic or acetylenic groups. The isoimide oligomer is soluble in the other compound, unreactive with the compound below a certain temperature and forms a liquid blend therewith. Upon heating the liquid blend above that certain temperature, the terminal groups on the isoimide oligomer and the other compound react with each other to form a copolymer. The liquid blends may be used to form encapsulants, coatings, films, and resin matrices for composites to provide resins with excellent high temperature properties.

Abstract: Melt preparation of polyarylate with catalyst system comprising an imidazole.

Abstract: Polycarbonates exhibiting improved heat resistances comprised of the reaction products of (i) a carbonate precursor and (ii) at least one dihydric phenol represented by the general formula ##STR1## wherein: R and R.sup.1 are independently selected from alkyl radicals;A is selected from divalent hydrocarbon radicals, ##STR2## and n is either zero or one.

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: The invention relates to a process for the preparation of aromatic polyester-carbonates wherein, in a first stage, aromatic oligo-esters or oligo-ester-carbonates having hydroxyl end groups are prepared from diaryl esters of aromatic dicarboxylic acids (or their starting materials) and diphenols and, optionally, a diaryl carbonate, by trans-esterification in the melt, and in a second stage these oligo-esters or oligo-ester-carbonates are condensed with phosgene by the phase boundary process to give the polyester-carbonate.

Abstract: Boron- and nitrogen-containing compositions prepared by the reaction of a quaternary ammonium hydroxide with a trialkyl or triaryl borate are useful for the preparation of the active catalyst species in the transesterification of reaction for the production of polycarbonates or polyester-polycarbonates from diaryl carbonates (optionally in admixture with diaryl dicarboxylates) and dihydroxyaromatic compounds.

Abstract: A new class of ethynyl-terminated oligomers and the process for preparing same are disclosed. Upon the application of heat, with or without a catalyst, the ethynyl groups react to provide crosslinking and chain extension to increase the polymer use temperature and improve the polymer solvent resistance. These improved polyesters are potentially useful in packaging, magnetic tapes, capacitors, industrial belting, protective coatings, structural adhesives and composite matrices.

Abstract: In the method for producing aromatic polyesters having excellent moldability, good thermal resistance and little dependence on molding temperature and providing molded products having little anisotropy, obtained from (A) one or more compounds selected from aromatic dicarboxylic acids and their derivatives and (B) one or more compounds selected from aromatic dihydroxy compounds and their derivatives, or (A), (B) and (C) one or more compounds selected from aromatic hydroxycarboxylic acids and their derivatives, a method characterized in that polymerization is carried out in a reaction system containing, together with (A), (B) and optionally (C), a quinone compound (D) and/or a complex obtained from (B) and (D) as well as an organic carboxylic acid anhydride, or a reaction product thereof.

Abstract: An aromatic polyester having improved heat resistance, hydrolysis resistance and alkali resistance which comprises recurring units of the general formula: ##STR1## and recurring units of the general formula: ##STR2## wherein R.sup.1 and R.sup.2 are an alkyl or alkoxyl group having 1 to 4 carbon atoms, R.sup.3, R.sup.4, R.sup.5 and R.sup.6 are the same or different and each is an alkyl or alkoxyl group having 1 to 4 carbon atoms, Cl or Br, x and y are an integer of 1 to 4, z, x', y' and z' are 0 or an integer of 1 to 4, and X is an alkylidene or cycloalkylidene group having 1 to 8 carbon atoms, --O--, --S--, --SO.sub.2 -- or --CO--.

Abstract: A process of endcapping a polyimide system with an endcapping agent in order to achieve a controlled decrease in molecular weight and melt viscosity along with predictable fracture resistance of the molded products is disclosed. The uncapped system is formed by combining an equimolar ratio of 4,4'-bis(3,4-dicarboxyphenoxy) diphenylsulfide dianhydride (BDSDA) and 1,3-bis(aminophenoxy)benzene (APB) dissolved in bis(2-methoxyethyl)ether. The endcapped system is formed by dissolving APB in bis-(2-methoxyethyl)ether, adding the endcapping agent, and then adding the BDSDA. By varying the amount of endcapping from 0 to 4%, molecular weight is decreased from 13,900 to 8660. At a processing temperature of 250.degree. C., there is a linear relationship between molecular weight and viscosity, with the viscosity decreasing by two orders of magnitude as the molecular weight decreased from 13,900 to 8660. A greater drop in viscosity is noted at higher temperatures.

Abstract: A process for the synthesis of the photosensitive polyamic acid derivatives which are polyimide precursors, comprising the sequential steps:(1) Partially derivatizing an aromatic dianhydride with a reactive monomer containing a photosensitive moiety;(2) Condensation polymerizing the partially derivatized aromatic dianhydride with aromatic diamine to form polyamic acid;(3) Isoimidization of the polyamic acid;(4) Condensation of the polyisoimide to polyamic acid derivative by reaction with additional reactive monomer; and(5) Separation of the polyamic acid derivative.

Abstract: In a process for preparing aromatic polyesters (polyarylates) by heating a bisphenol (e.g., Bisphenol-A), at least one dicarboxylic acid (e.g., terephthalic acid and isophthalic acid) and acetic anhydride, a gamma-butyrolactone, such as gamma-butyrolactone, is employed a diluent, reducing sublimation of reactants, and resulting in higher molecular weight of the polymer.

Abstract: Color improved polyarylates having a reduced viscosity of from about 0.1 to greater than 1.0 dl/gm produced by a process comprising the following steps:(a) reacting an acid anhydride derived from an acid containing from 2 to 8 carbon atoms with at least one dihydric phenol to form the corresponding diester; and(b) reacting said diester with at least one aromatic dicarboxylic acid at a temperature sufficient to form the polyarylate, wherein the improvement comprises carrying out said process in the presence of a particular solid adsorbent.

Abstract: Copolyester-carbonates having amide and carbamate terminal groups. These copolyester-carbonates are prepared by reacting (i) a carbonate precursor, (ii) at least one difunctional carboxylic acid or an ester forming reactive derivative thereof, (iii) at least one dihydric phenol, and (iv) a chain terminating amount of at least one carbamate-amide precursor. These copolyester-carbonates exhibit improved thermal stability.

Abstract: Processes for forming a class of relatively low molecular-weight oligomers containing at least one isoimide group and terminal groups capable of undergoing an addition polymerization reaction are provided. These oligomers are characterized by excellent solubility in common solvents and a melting temperature considerably lower than their cure temperature, thus enabling the oligomers to be formed into cured polymers more slowly and at lower temperatures, all without the evolution of deleterious gases. The process for forming these oligomers includes the formation of a polyamic acid and dehydration thereof under specified conditions to effect cyclization of the polyamic acid to form the isoimide-containing oligomer, without the formation of undesired side-reaction products.

Abstract: High molecular weight aromatic polyesters having a low content of end groups and a very slight inherent color can be obtained according to the phase interfacial process wherein particular amines and a slight alkali excess are used.

Abstract: A polyesteramide having structural units of the general formula: ##STR1## wherein Ar is a bivalent aromatic group comprising at least 10% by mole of a group having the following formula: ##STR2## in which R.sup.1, R.sup.2, R.sup.3 and R.sup.4 are the same or different and each is methyl group or ethyl group, and structural units of the general formula: ##STR3## wherein R is a bivalent organic group. At least 10% by mole of a bifunctional phenol compound to be used is a tetraalkylbisphenol-F, and whereby the obtained polyesteramide has improved hydrolysis resistance and electric characteristic with an excellent heat resistance.

Abstract: Spherical porous polyimide powder having an average particle diameter of 1 to 20 .mu.m which is infusible and insoluble in organic solvents is produced by polymerizing an aromatic tetracarboxylic acid dianhydride and an aromatic polyisocyanate in an organic solvent at a temperature of 100.degree. to 200.degree. C. and in the presence of a tertiary amine catalyst to form polyimide particles in the form of slurry, filtering or centrifuging said polyimide particles, and washing the resulting polyimide particles with an organic solvent.

Abstract: Described herein is a process for preparing a polyester or a poly(ester carbonate) which comprises reacting a dihydric phenol with an aromatic diacid and a diaryl carbonate in the presence of from about 10 to about 60 weight percent of a processing aid under polyester or poly(ester carbonate) forming conditions.

Abstract: A polyamide acid composition for preparing a polyimide which can extend the pot life of the composition comprising a solution of a polyamide acid in an organic solvent, the polyamide acid being a precursor of the polyimide, a dehydrating agent, a catalyst and a pot life extending agent which can lower a rate of conversion of the polyamide acid to the polyimide, and the process for preparing the polyimide from said polyamide acid composition. According to the present invention the pot life can be extremely extended to give the composition an enough flowability for a long time without reducing the excellent properties such as a heat resistance and an electric insulation of the obtained polyimide.

Abstract: A process for producing polycarbonate is described, comprising reacting a chloroformate group-containing polycarbonate oligomer with an aqueous alkaline solution of a compound containing at least three functional groups and, thereafter, interfacial polycondensing the above-obtained reaction product with an aqueous alkaline solution of a dihydric phenol compound. The thus-produced polycarbonate has good melt characteristics compared with conventional polycarbonates, and the dependence of melt viscosity on a rate of shear is large. Thus, the polycarbonate of the invention is suitable for extrusion molding, particularly for blow molding using an extrusion molding machine, and can provide good quality sheets or molds.

Abstract: A method for determining the concentration of ingredients and other process variables in a polymerization process by measuring the capacitance and dissipation factor of the mixture and determining its dielectric constant at various stages of the process. By the use of an automatic capacitance bridge and a computer, the process variables can be determined and controlled in a matter of seconds.

Abstract: A method for determining the concentration of additives in a compounding process by measuring the capacitance and dissipation factor (tan.delta.) of the mixture and converting such values to the concentrations of the additives. This method may also be utilized to determine the concentration of the polymers in the mixture. This method is preferably applied to a compounding process of blending polyphenylene oxide and polystyrene thermoplastic resins and is preferably applied to a continuous compounding process of these resins to determine therein the concentration of an aryl phosphate ester flame retardant.