Abstract: An aromatic polyamide having a high molecular weight is produced by a polycondensation reaction of an aromatic aminocarboxylic acid and/or a mixture of an aromatic dicarboxylic acid and an aromatic diamine in a polar solvent in the presence of a dehydrating catalyst with heating at a temperature of about 160.degree. C. or higher.

Abstract: Aromatic oligomers, in particular arylene ketone and arylene sulfone oligomers, are prepared by reacting an appropriate monomer system in the presence of free Lewis acid and a complex between a Lewis acid, for example, aluminum trichloride, and a Lewis base, for example, N,N-dimethylformamide, and, optionally, a diluent, such as methylene chloride. The process is particularly advantageous for the preparation of substantially or all paralinked arylene ether ketone oligomers as the presence of the Lewis acid/Lewis base complex markedly reduces alkylation and ensures the substantial absence of ortho substitution. The monomer system can be, for example, a self-reacting monomer such as p-phenoxy-benzoyl chloride or a two-monomer system such as 1,4-diphenoxybenzene and terephthaloyl chloride.

Abstract: Crystalline polyimides having low glass transition temperatures and high solvent resistance are obtained by reacting diamino-oligo-phenylene sulfides with aromatic tetracarboxylic acids or their anhydride derivatives. The diamino-oligo-phenylene sulfides can be of varying length and can be reacted with the dianhydride by conventional processes.

Abstract: A process for producing an aromatic polyketone which comprises polymerizing an appropriate monomer or monomers by a Friedel-Crafts polymerization reaction using a Lewis acid catalyst. A controlling agent such as a Lewis base may be added to the reaction medium and/or the reaction is conducted under specified conditions to control the reaction. The reaction medium comprises, for example, aluminum trichloride as the Lewis acid, an organic Lewis base such as N,N-dimethylformamide or an inorganic Lewis base such as sodium or lithium chloride, and a diluent such as methylene chloride or dichloroethane. The amount of Lewis acid, the amount of Lewis base, the temperature of the reaction and the monomer to diluent molar ratio are varied depending on the monomer system to obtain melt-processable, high molecular weight, substantially linear polymers, for example poly(carbonyl-p-phenylene-oxy-p-phenylene), poly(carbonyl-p-phenylene-oxy-p-phenylene-oxy-p-phenylene), and the like.

Abstract: The preparation of poly(arylene ether ketones) by Friedel-Crafts polymerization, in the presence of a Lewis acid catalyst and a diluent, is conducted under conditions in which the polymer and/or its complex with the catalyst is suspended in the diluent during at least part of the polyreaction mixture if desired. The dispersant may be a polymer or an organic compound containing at least eight carbon atoms and is preferably a Lewis base. The dispersant preferably contains at least one molecular segment substantially compatible with the poly(arylene ether ketone) or its complex with the Lewis acid and substantially incompatible with the diluent and at least one molecular segment substantially compatible with the diluent and substantially incompatible with the poly(arylene ether ketone) or its complex with the Lewis acid.

Abstract: Aromatic N-glycidylamines are prepared by treatment of an amine having at least one, and preferably two or more aromatic amino hydrogen atoms, with epichlorohydrin in the presence, as catalyst, of a di- or higher-valent metal salt of nitric or perchloric acid, or of a carboxylic or sulphonic acid substituted by fluorine, chlorine or bromine on the carbon atom alpha to the carboxylic or sulphonic acid group, and dehydrochlorinating the product. The presence of the metal salt gives a product having a higher glycidyl content and a lower viscosity than does the same reaction in the absence of such a salt.Suitable aromatic amines include aniline, phenylene diamines, phenylene diamines substituted on the aromatic ring and bis(4-aminophenyl)methane. The metal salt may be of, for example, magnesium, calcium, zinc, manganese, nickel, iron, lanthanum, vanadium, ytterbium or uranium.

Abstract: A process is described for the preparation of predominantly linear polyurethane solutions which comprises(a) reacting(A) an organic diisocyanate or diisocyanate mixture optionally containing small portions of a triisocyanate with(B) one or more polyhydroxyl compounds which are predominantly bifunctional and generally have molecular weights of from about 400 to 5000 and(C) optionally one or more chain lengthening agents having at least two isocyanate reactive hydrogen atoms and molecular weights of from about 32 to 399,wherein the proportion of isocyanate groups to the number of isocyanate-reactive hydrogen atoms is in the range of from about 0.9:1 to 1:0.9, and(b) when the polyurethane formed has reached the required viscosity, adding a monofunctional, low molecular weight oxime having a molecular weight of from about 73 to 325, preferably butanone oxime, to the reaction mixture as chain breaking agent in a quantity equivalent to or in excess of the equivalents of unreacted isocyanate groups.

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: Biphenylene end-capped low molecular weight thermally stable aromatic polymers and the process for their preparation. The invention is further directed to crosslinked biphenylene end-capped aromatic polymers and to the process for their preparation. The process for preparing the biphenylene end-capped low molecular weight thermally stable aromatic polymers comprises carrying out a misbalanced polymerization reaction of a suitable aromatic aminoketone compound and a suitable aromatic ketomethylene compound and thereafter adding a monofunctional biphenylene compound.

Abstract: An improved process for preparing a polyarylate having a reduced viscosity of from about 0.1 to greater than 1.0 dl/gm 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: Described herein is a process for preparing polyarylates which comprises reacting a diester derivative of a dihydric phenol with an aromatic dicarboxylic acid in the presence of from about 10 to about 60 weight percent of at least one particular halogenated and/or etherated substituted aromatic or heteroaromatic compound, at a temperature of from about 260.degree. to about 350.degree. C.

Abstract: A process for the production of polyquinazolone-based polymers by reacting bisquinazolone with a diamine or a diamine substituted with a carboxylic acid, sulfonic acid or metal salt thereof in the presence of a Lewis acid catalyst or a phosphorus-containing dehydrating agent, where the polymers are useful to produce permselective membranes.

Abstract: In the production of an aromatic polyester by reacting at least one aromatic diester of the formula ##STR1## wherein R is a hydrogen atom, an alkyl group having 1 to 6 carbon atoms or a cycloalkyl group having 3 to 8 carbon atoms; andAr.sub.2 is an arylene group,with at least one aromatic dicarboxylic acid of the formula ##STR2## wherein Ar.sub.2 is an arylene group,in the presence of a catalyst, the improvement which comprises employing a transition metal salt of naphthenic acid as the catalyst.

Abstract: Described herein is a process for preparing crystalline polyarylates which comprises (a) forming a crystalline polyarylate prepolymer having a reduced viscosity of from 0.05 to about 0.4 dl/g by reacting at least one diester derivative of a dihydric phenol with at least one aromatic dicarboxylic acid in the presence of a solvent, at a temperature of from about 250.degree. to about 300.degree. C., and (b) heating the prepolymer so formed below its melting point to form a crystalline polyarylate having a reduced viscosity of from about 0.45 to about 1.2 dl/g.

Abstract: Described herein is a process for preparing polyarylates which comprises reacting a diester derivative of a dihydric phenol with an aromatic dicarboxylic acid in the presence of from about 10 to about 60 weight percent of a diphenyl ether compound at a temperature of from about 260.degree. to about 350.degree. C. and in the presence of a magnesium catalyst.

Abstract: Described herein is a process for preparing polyarylates which comprises reacting a diester derivative of a dihydric phenol with an aromatic dicarboxylic acid in the presence of from about 10 to about 60 weight percent of a diphenyl ether compound at a temperature of from about 260.degree. to about 350.degree. C.

Abstract: A method for preparing an aluminum ion-filled polyimide adhesive wherein a meta-oriented aromatic diamine is reacted with an aromatic dianhydride and an aluminum compound in the presence of a water or lower alkanol miscible ether solvent to produce an intermediate polyamic acid; and thereafter converting the polyamic acid to the thermally stable, metal ion-filled polyimide by heating in the temperature range of 300.degree. C. to produce a flexible, high temperature adhesive.

Abstract: A polymer of the general formula: R'--M--Ar--B--Ar'--MArBAr'--.sub.k-2 M--Ar--B--Ar'--R wherein M and D, which can be the same or different, are independently ##STR1## wherein each Ar is independentlyR'--M--Ar--D--Ar'[--MArDAr'--].sub.k-2 M--Ar--D--Ar'--R"wherein L is ##STR2## phenyleneoxy, ##STR3## a covalent bond or T, wherein T is as defined belowand each Ar' is independently ##STR4## wherein T is O, S, phenyleneoxy, or --CR.sub.2 -- wherein R is as defined below, or --O--Ar--O-- wherein Ar can have any of the values set forth above and wherein R' and R" are independently ##STR5## wherein X is a covalent bond, --O--, --S--, or --CR.sub.2 -- wherein each R is independently hydrogen, an alkyl or fluoroalkyl group, preferably of 1 to 10 carbons, phenyl or an electron withdrawing group substituted phenyl, Y is CN, NO.sub.2, ##STR6## or if X is a covalent bond, Y can be hydrogen as well as any of the foregoing; or Ar"CO-- or Ar"SO.sub.

Abstract: The molecular weight of highly aromatic polymers made by the Friedel-Crafts polymerization of EN monomers of the formula Ar--L--Ar.sup.1 --X, wherein X is selected from SO.sub.2 Y or COY, Y being a radical selected from --OH, halogen, or alkyl, wherein Ar and Ar.sup.1 are independently ##STR1## wherein L is --CO--, --SO.sub.2 --, phenyleneoxy, --NHCO--, a covalent bond, --O--, or --CR.sub.2 --, wherein each R is independently hydrogen, an alkyl or fluoroalkyl group, phenyl or a phenyl group substituted by an electron withdrawing group such as halogen, NO.sub.2 or --CN, is controlled by including in the reaction mixture an acylatable aromatic compound whose rate of acylation under Friedel-Crafts conditions is at least about 150 times that of benzene. The molecular weight of other polymers made from EN type monomers by Friedel-Crafts catalysis can also be controlled in this way.

Abstract: The products of the invention are vinyl end-capped oligomers which are prepared from 2,4-bis (p-aminobenzyl) aniline and a vinyl substituted aromatic monoamine, the principal component of which is the compound whose structure is shown in FIG. 3. The products are prepared from either of two (2) precursors. The first precursor is a compound whose structure is shown in FIG. 2 and which is prepared from 2,4-bis (p-aminobenzyl) aniline, a dianhydride of an aromatic tetracarboxylic acid such as 3,3'4,4'-benzophenonetetracarboxylic acid (BTDA) and a vinyl substituted aromatic monoamine, such as 3-aminophenyl-ethylene (APE). The second precursor is a complex amine salt having the structure shown in FIG. 6 and which is prepared from 2,4-bis-(p-aminobenzyl) aniline, a dialkyl ester of BTDA and APE.

Abstract: Stable paramagnetic alkali radical cationic triple ions of selected 1,2 and 1,4 dicarbonyl compounds and their nitrogen-containing analogs have been produced by both conventional alkali metal reduction of an appropriate organic compound and by a novel process in which the selected 1,2 or 1,4 dicarbonyl compound or the nitrogen containing analog thereof is mixed with an alkali tetraphenylborate and irradiated under ultraviolet light.

Abstract: The present invention relates to novel, substantially insoluble and infusible plastics which are cross-linked by way of triazine rings and, optionally, by way of tri-substituted bis-oxymethylene urea groups or urethane groups.

Abstract: Triazine compounds and cross-linked polymer compositions are made by heating aromatic nitriles to a temperature in the range of from about 100.degree. C. to about 700.degree. C., and preferably in the range of from about 200.degree. C. to about 350.degree. C. in the presence of a catalyst or mixture of catalysts selected from one or more of the following groups: (A) organic sulfonic and sulfinic acids, (B) organic phosphonic and phosphinic acids, and (C) metallic acetylacetonates, at a pressure in the range of from about atmospheric pressure to about 10,000 p.s.i., and preferably in the range of from about 200 p.s.i. to about 750 p.s.i.

Abstract: Disclosed are monomers of the formula: ##STR1## WHEREIN R is ##STR2## R' is hydrogen or methyl; R" is alkyl of 1-10 carbon atoms;X and Y are independently selected from the group consisting of NO.sub.2, halogen, cyano and --CF.sub.3 ;Z is oxygen or dicyanomethylene;a and a' can range from 0-3; andn is 1-10.These monomers can be readily polymerized to polymers suitable for use in electrophotographic imaging members and methods.

Abstract: The products of the invention are vinyl end-capped oligomers which are prepared from 2,4-bis (p-aminobenzyl) aniline and a vinyl substituted aromatic monoamine, the principal component of which is the compound whose structure is shown in FIG. 3. The products are prepared from either of two (2) precursors. The first precursor is a compound whose structure is shown in FIG. 2 and which is prepared from 2,4-bis (p-aminobenzyl) aniline, a dianhydride of an aromatic tetracarboxylic acid such as 3,3'4,4'-benzophenonetetracarboxylic acid (BTDA) and a vinyl substituted aromatic monoamine, such as 3-aminophenyl-ethylene (APE). The second precursor is a complex amine salt having the structure shown in FIG. 6 and which is prepared from 2,4-bis-(p-aminobenzyl) aniline, a dialkyl ester of BTDA and APE.