Abstract: There are disclosed a method for drying and a method for solid-phase polymerizing a crystallizable polyamide being in an amorphous state which comprises regulating the moisture concentration in the polyamide at its glass transition temperature to at least 0.15% by weight as determined by Karl Fisher titration; heating the polyamide thus regulated at a pressure of at least one arm without reducing the moisture to crystallize the same up to a crystallinity of at least 15% and; further heating the polyamide thus crystallized at a temperature lower than its melting point under reduced pressure with a batchwise heating apparatus.

Abstract: Aromatic copolyamides, production thereof, formed structures and production thereofDescribed are aromatic copolyamides comprising the structural repeat units of the formulae I, II and III ##STR1## where Ar.sup.1, Ar.sup.2, Ar.sup.3 and Ar.sup.

Abstract: Described is a method for preparing a polybenzazole filament which comprises extruding a polybenzazole dope filament, drawing the filament across an air gap, coagulating and washing the filament, and drying the filament, characterized in that a solution of a compound selected from the group consisting of ferrocenes, ruthocene, iodide-, cobalt-, and copper-containing compounds, dyes, and mixtures thereof is contacted with a filament subsequent to the washing step and prior to the drying step. This method provides a means to improve the tensile strength retention of damaged polybenzazole filaments following exposure to sunlight.

Abstract: Aramid polymers with small amounts of alkyl- and/or alkoxy-substitution on their aromatic diamine and/or aromatic diacid monomeric units are disclosed. Such aramid polymers show improved properties compared to similar aramids without the substitution. The aramids described herein are useful for films or fibers, for example, as employed in the manufacture of packaging, ropes, filter bags, or composites. The invention also includes a process for making such polymers, involving subjecting fibers or films made from such aramid polymers to heat treatment under tension.

Abstract: This invention relates to a branched fractal three dimensional porous polymer species which comprises rigid aromatic recurring units having electrophilic or nucleophilic reactive moieties on the exterior thereof. Another aspect of this invention relates to a star polymer comprising a polymeric core formed of the fractal polymers (FPS) of this invention having linear polymeric moieties grafted to the exterior thereof by way of residues formed by reaction between the reactive moieties on the exterior of the fractal polymer (FP) and complimentary reactive moieties on a linear polymer. Yet another aspect of this invention relates to polymeric composites comprising a polymer matrix having dispersed therein the star polymers of this invention.

Abstract: Cyclic imides are inhibitors of tumor necrosis factor .alpha. and can be used to combat cachexia, endotoxic shock, and retrovirus replication. A typical embodiment is 2-(2,6-dioxo-3-piperidinyl)-4-azaisoindoline-1,3-dione.

Abstract: Aramids which after drawing have high tensile strengths and tensile moduli are made from units derived from selected 2,2'-disubstituted-4,4'-diaminobiphenyls, p-phenylenediamine, oxydianiline and terephthalic acid. Also disclosed is a process for drawing such aramids at least 1.5%, which results in the drawn aramid having significant crystallinity and higher tensile strength. The aramids are useful for ropes and composites.

Abstract: The present invention relates to new polyamides comprising, on a mass basis:(a) 45 to 75% of an x,T unit, x being between 4 and 12 inclusive, the x,T unit being the condensation product of a diamine having x carbon atoms and of terephthalic acid, and(b) 55 to 25% of an aliphatic unit -HN-(CH.sub.2).sub.n -CO, n being between 6 and 14 inclusive. and the terpolyamides obtained by including a monomeric unit (c) such as the unit 6 or 6,I as a replacement for part of the aliphatic unit (b).The polyamide compositions thus obtained exhibit a Tg lower than 130.degree. C., a Tm higher than 230.degree. C. and a good crystallizability.

Abstract: Polyamides and polyamide fibers having a major proportion of hexamethyleneadipamide units and minor proportions of at least two other amide units, one of those other amide units being those of 2-methylpentamethylenediamine are disclosed.

Abstract: Poly(arylene ether)ketones, polyamides, and poly(benzoxazoles) that contain thiophene rings within the aromatic polymer backbone are disclosed, along with fibers, films, and other articles of manufacture formed therefrom.

Abstract: The invention relates to readily processible polyamide molding compounds which have very good mechanical and electrical properties as well as high surface quality and are based on polyamide, magnesium hydroxide and polyhydroxy compounds of the Novolak type.

Abstract: The invention provides copolymers having magnetic properties, said copolymers containing aminoaromatic groups, and being based on a structural unit comprising:a first group of aminoaromatic compounds chosen from aniline derivatives and the corresponding iminoquinone forms; anda second group of substituted aminoaromatic compounds chosen from substituted amino compounds containing at least two condensed benzene rings, substituted polycyclic compounds containing at least one aniline structural unit in their structure, compounds derived from aniline and carrying a substituent bonded to the ring by means of an ethynylidene or paraphenylene link, and the corresponding iminoquinone compounds.

Abstract: A structural panel for a vehicle or building contains a substrate and a layer of flame resistant polybenzazole polymer. If the substrate is heat resistant, the panel can serve as a fire barrier. If the substrate is not heat resistant, the polybenzazole layer can still serve to delay ignition and contain any volatile gases and molten polymer that forms when the panel is subjected to heat.

Abstract: Thermoplastic poly(imide-esters) and poly(imide-amides) with repeat units derived from the title amino acid. In the polymer the amino group becomes part of an imide group and the carboxyl group becomes part of an ester or amide group. The polymers have a good balance of properties, making them useful for melt forming shaped articles, films and fibers.

Abstract: This invention relates to a sheetlike wholly aromatic polyamide shaped article useful as electrical insulating materials excellent in corona resistance (corona durability) and in surface smoothness. The corona durability of said sheetlike shaped article is increased to 150 minutes or above by adding a nonionic polymer flocculant to an aqueous dispersion comprising 10 to 90% by weight of mica particles, preferably treated with a silane coupling agent and 90 to 10% by weight of a wholly aromatic polyamide stock (fibrids and fibers) in obtaining the sheetlike shaped article from the aqueous dispersion by wet shaping.

Abstract: A novel aromatic diamino amide monomer of the structural formula (I), a novel aromatic polyamide of the structural formula (II) prepared by polycondensation of the monomer and an aromatic diacid halide, and an aromatic polyamide film produced from the polyamide which has high strength as well as high modulusity. ##STR1## wherein, each of two NH.sub.2 groups may be in meta or para-position to the amide bond. ##STR2## wherein, Ar represents a phenyl group, X represents CONH.sub.2 group in ortho-position to the amide bond, Y represents H, Cl, Br, I, NO.sub.2 or an alkyl or alkoxy group having 1 to 4 carbon atom, and n represents an integer between 10 and 100,000.

Abstract: Heat-stable polyimides and polyamideimides with modified benzhydrol structural elements and a process of preparing thereof; wherein the polyimides and polyamideimides are obtained by reacting 3,3'4,4'-benzhydroltetracarboxylic acid dimethyl ester a) with only a diamine and then cyclized to give polyimides or b) with a diamine and with trimellitic, phthalic-or isophthalic acid (or the anhydrides, acid chlorides, anhydride chlorides or esters) and is then cyclized to give polyamideimides.

Abstract: A method is disclosed for significantly diminishing the rate of degradation of naturally-produced .gamma.-PGA in a .gamma.-PGA-producing cell culture. Also, a method is disclosed for significantly decreasing the water solubility coefficient of naturally-produced .gamma.-PGA by forming derivatives of .gamma.-PGA. In addition, a polymer solution is disclosed which includes a polysaccharide component and a .gamma.-PGA component.

Abstract: Memory enhancing thermal proteins were synthesized from heating aspartic acid, glutamic acid, proline and tryptophan above 100.degree. C. Two hydrophobic and one non-hydrophobic polymer were injected intracerebroventricularly into the brains of mice after the mice had undergone partial training in footshock avoidance conducted in a T-maze. When retention of footshock avoidance was tested one week later, the hydrophobic polymers enhanced retention while the non-hydrophobic polymer did not.

Abstract: A stepwise linear polymer composition having intense magnetic properties and a method for preparation of same. A phthalimide compound and an aromatic dialiphatic acid are reacted in the presence of an acetate of monovalent metal at elevated temperatures to form a phenylenebis diphthalimidine compound. The phenylenebis diphthalimidine compound is then reacted with 3-benzylidine phthalimidine and a metal salt of an aliphatic acid at elevated temperatures under an inert gas to form the intensely magnetic polymer. The reactions may be carried out in the presence of a solvent.

Abstract: Aramids, which in the drawn state have high tensile strengths tensile elongations, and tensile moduli, are made from units derived from selected 2,2'-disubstituted-4,4'-bibenzoic acids, 3,4'-oxydibenzoic acid or 3,4'-dicarboxybenzophenone, p-phenylenediamine, and optionally terephthalic acid. The aramids are useful for ropes and composites.

Abstract: A crosslinked polymer composition having intense magnetic properties and a method for preparation of same. A phthalimide compound and an aromatic dialiphatic acid are reacted in the presence of an acetate of a monovalent metal at elevated temperatures to form a phenylenebis diphthalimidine compound. The phenylenebis diphthalimidine compound is then reacted with a metal salt of an aliphatic acid at elevated temperatures under an inert gas to form the intensely magnetic crosslinked polymer. The reactions may be carried out in the presence of a solvent.

Abstract: Novel cyclic imino ether compositions containing one or more mesogenic moieties, when polymerized, result in products having improved properties.

Abstract: Aromatic copolyamides are described which are soluble in organic polyamide solvents and which comprise the recurring structural units of the formulae Ia, Ib, Ic and Id[--OC--R.sup.1 --CO--NH--R.sup.2 --NH--] (Ia),[--OC--R.sup.1 --CO--NH--R.sup.3 --NH--] (Ib),[--OC--R.sup.1 --CO--NH--R.sup.4 --NH--] (Ic),[--OC--R.sup.1 --CO--NH--R.sup.5 --NH--] (Id)in whichR.sup.1 and R.sup.2 are mainly unsubstituted divalent aromatic radicals, the valency bonds of which are in the para-position or in a comparable coaxial or parallel position with respect to one another,R.sup.3 is a radical of the formula II ##STR1## R.sup.4 is a radical of the formula III--Ar.sup.1 --O--Ar.sup.1 --O--Ar.sup.1 -- (III), andR.sup.5 is a radical of the formula IV and/or V ##STR2## in which Ar.sup.1 has one of the meanings defined for R.sup.

Abstract: Use of fluorinated aromatic polyamides as orientation layer for liquid crystal switching and display devicesUse of substituted aromatic polyamides as orientation layer in liquid crystal switching and display elements is described, in which the polyamides contain structural units of the formula (I) ##STR1## in which in formula I the symbols have the following meaning: ##STR2## in which R.sup.1 and R.sup.2 are identical or different and are perfluorinated alkyl having 1 to 4 carbon atoms, R.sup.3 and R.sup.4 are identical or different and are H or CF.sub.3, and in which --W-- is, for example, --O--, --C(CH.sub.3).sub.2 --, --C(CF.sub.3).sub.2 --.Orientation layers made of these polyamides can be cured at low temperatures, have good adhesion and high transmittance and allow for a high surface tilt angle.

Abstract: A thermoplastic resin composition comprise 99.9.about.50 parts by weight of one or more thermoplastic resin selected from the group consisting of aromatic polyimide, aromatic polyetherimide, aromatic polyamideimide, aromatic polyethersulfone and aromatic polyether ketone and 0.1.about.50 parts by weight of one or more liquid crystal type aromatic polyimide having recurring structural units represented by the formula (1): ##STR1## wherein R.sub.1 .about.R.sub.5 is a hydrogen atom, fluorine atom, trifluoromethyl, methyl, ethyl or cyano and may be the same or different, and R is a tetravalent radical having 6.about.27 carbon atoms and being selected from the group consisting of a monoaromatic radical, condensed polyaromatic radical and noncondensed aromatic radical connected each other with a direct bond or a bridge member.

Abstract: A process for the manufacture of polyamides consisting essentially of the stages of:(i) reacting 10 to 90% by weight of the aliphatic and/or cycloaliphatic and/or aromatic-aliphatic diamines (c) with a lactam and/or corresponding amino acid (a) or the substantially stoichiometric combination of one or more aliphatic diamine(s) and of one or more dicarboxylic aliphatic acid(s) and with the aromatic diacid (b); and(ii) reacting the remainder of the aliphatic and/or cycloaliphatic and/or aromatic-aliphatic diamine (c) with the oligomer produced in stage (i) in one or more substages.

Abstract: Partly aromatic copolyamides contain as essential componentsA) 40-90% by weight of units derived from terephthalic acid and hexamethylenediamine,B) 0-50% by weight of units derived from .epsilon.-caprolactam andC) 0-60% by weight of units derived from adipic acid and hexamethylenediamine,the components B) and/or C) accounting for a total of not less than 10% by weight of the total units and the copolyamide having a triamine content of less than 0.5% by weight.

Abstract: This invention concerns new molecules with active, non-linear optical properties and which can be thermally reticulated (more precisely, these molecules include terminal functions which can be reticulated, attached to either side of the groups active in non-linear optics, which can be oriented under an electrical field). When reticulated and oriented under an electrical field, these materials are particularly stable and can be employed for industrial applications, using non-linear optics (electrooptical modulators, frequency doublers, etc.).

Abstract: High molecular weight polyamides having benzidine linkages are prepared using certain substituted benzidine monomers.

Abstract: A process for making PBZ fibers of ultra-high physical properties is given. Polybenzoxazole fibers made by the process of this invention have tensile strengths nearly double in value from what has been reported previously.

Abstract: Thermotropic liquid crystalline copolyamides comprise: (a) a thermoplastic, aliphatic polyamide, such as nylon-6,6; and (b) a mesogen comprising an amide-linked aromatic group segment which is not completely para-linked (namely, is substantially ortho- or meta-linked or a mixture of ortho- and meta-linked) by an amide linkage to an alkylene amide group contained in the mesogen.

Abstract: A preferred class of polyimide oligomers include (1) linear, difunctional crosslinking oligomers prepared by condensing an imidophenylamine end cap with a lower alkylene diamine or a polyaryldiamine such as 3,3'-phenoxyphenylsulfone diamine and with a dianhydride, particularly 4,4'-phenoxyphenylsulfone dianhydride; and (2) multidimensional, crosslinking, polyimide oligomers having an aromatic hub and at least two radiating arms connected to the hub, each arm including a crosslinking imidophenylamine end cap at its distal end and at least two imide linkages.Blends, prepregs, and composites can be prepared from the oligomers.

Abstract: A wholly aromatic polyamide capable of being dissolved in organic solvents to form an isotropic dope solution and having an excellent chemical resistance, heat resistance, processability and mechanical strength and a high modulus, comprises recurring aromatic dicarbonyl units of the formulae: ##STR1## and recurring aromatic diamine units of the formulae: ##STR2## wherein R and R' are a hydrogen or halogen atom or an alkyl or alkoxyl radical, n is 1 to 3, and p and q are 1 to 4.

Abstract: Aromatic copolyamides are described which are soluble in organic polyamide solvents and which essentially consist of the recurring structural units of the formulae Ia, Ib and Ic ##STR1## wherein R.sup.1 and R.sup.4 are divalent aromatic radicals, the valency bonds of which are in the para position or in a comparable coaxial or parallel position relative to one another, R.sup.2 is a radical of the formula III ##STR2## and R.sup.3 is a radical of the formula IV ##STR3## The mole fractions of the individual structural features in the copolyamides are fixed within selected limits. Fibers composed of the copolyamides claimed are distinguished by a high stretchability.

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: A process for preparing shaped polybenzimidazole sintered products having increased resistance to dimensional modification by absorption of water and the products prepared therefrom.

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: The present invention discloses new polymers which can assume an accordion-like conformation of the backbone. These polymers are prepared by the copolymerization of two difuntional, chemically precoupled precursors to chromophoric units. The resulting polymers have a head-to-head, tail-to-tail topology (a syndioregic arrangement of rigid units along the polymer backbone), and the molecular units are designed to fold into an "accordion" conformation. This useful microstructure (a three-dimensional conformation) forms spontaneously (self-assembles); or, it can be brought about by field-assisted processing. Films and fibers of these polymers have useful second-order nonlinear optical properties, and may be used for the modulation and switching of optical communications signals.

Abstract: New, thermooxidatively stable polyimides have been prepared from the reaction of aromatic dianhydrides containing isopropylidene bridging groups with aromatic diamines containing amide connecting groups between the rings. Several of these polyimides were shown to be semi-crystalline as evidenced by wide angle xray scattering and differential scanning calorimetry. Most of the polyimides form tough, flexible films with high tensile properties. These polyimide films exhibit enhanced solubility in organic solvents.

Abstract: An N-substituted polyamide-imide essentially composed of identical or different repeating units of the formula I ##STR1## where R.sup.1 is one of the following tetravalent aromatic radicals ##STR2## and X is a bond or one of the following linkers ##STR3## where R.sup.2 and R.sup.4 are each, independently of one another, one of the following divalent aromatic radicals ##STR4## and where X has the abovementioned meanings and where R.sup.3 is hydrogen or a monovalent radical such as C.sub.1 -C.sub.6 -alkyl or phenyl, and the C.sub.1 -C.sub.6 -alkyl-, C.sub.1 -C.sub.6 -alkoxy-, aryl- or halogen-substituted derivatives thereof, and precursors (monomers) therefor, are described.

Abstract: A process for the production of a fiber-reinforced composite material, which comprises the steps of(1) preparing a polymeric composition containing a substantially linear aromatic oligomer having a terminal aliphatic hydroxyl group, bis(acylcaprolactam) and a catalyst which promotes a ring opening-addition reaction of a hydroxyl group and a caprolactam ring,(2) melting the polymeric composition and impregnating it into a fibrous reinforcing material to form a impregnated product, and(3) heating the impregnated product up to a temperature sufficient to open the caprolactam ring while inhibiting elimination of caprolactam thereby to form, as a matrix resin, a thermoplastic copolymer having an ester group and an amide group in its main chain;and a fiber-reinforced composition material produced by the above-mentioned process.

Abstract: Azole rings, such as oxazole and thiazole rings, can activate an aromatic ring bonded to a leaving group such as a halogen atom so that the aromatic ring will undergo aromatic nucleophilic substitution. The reaction is useful for making ethers, thioethers and amines containing azole rings. In particular, monomers having azole rings, activated aromatic rings with leaving groups and nucleophilic moieties can react under conditions of aromatic nucleophilic displacement to form non-rigid rod PBZ polymers. The non-rigid rod PBZ polymers can be used to form molecular composites with rigid rod PBZ polymers which molecular composites are not substantially phase separated.

Abstract: Processible chromophoric polymers having nonlinear optical properties and wherein the chromophore is present in and is a part of the polymer backbone, including substantially all of the monomer or repeat units, with the dipole moments pointing in the same direction (head-to-tail) along the polymer backbone. Such polymers include phenylene, phenylene vinylene, stilbenylene, phenyl piperdine, and coumarin polymers.

Abstract: A hot-melt adhesive comprising a special polyamideimide or polyamide is excellent in heat resistance and adhesive strength and usable for providing substrates for printed circuit boards.

Abstract: Certain substituted benzidines enable the preparation of linear chain, high molecular weight polyimides based on benzidine.

Abstract: Preparation of specially substituted aromatic polyamides containing structural units of the formula I mentioned and copolyamides containing at least 10 mol % of structural units of the formula I and structural units of the formula II mentioned and their use as orientation layer in liquid crystal display elements and/or liquid crystal switching elements.

Abstract: In one embodiment this invention provides polymalonamide polymers with side chains which exhibit nonlinear optical response.

Abstract: It is advantageous to prepare oligomers of polybenzazole polymers by reaction of AA-PBZ monomer with an excess of BB-PBZ monomer. The resulting oligomer dopes may be stored at a temperature at which they remain pumpable until such time as the dope can be advanced to higher molecular weight by adding additional AA-PBZ monomer. The molecular weight of the polymer may be adjusted by controlling the amount of chain extender and/or chain terminator added to oligomer mixtures as they are advanced to final molecular weight.

Abstract: Azole rings, such as oxazole and thiazole rings, can activate an aromatic ring bonded to a leaving group such as a halogen atom so that the aromatic ring will undergo aromatic nucleophilic substitution. The reaction is useful for making ethers, thioethers and amines containing azole rings. In particular, monomers having azole rings, activated aromatic rings with leaving groups and nucleophilic moieties can react under conditions of aromatic nucleophilic displacement to form non-rigid rob PBZ polymers. The non-rigid rod PBZ polymers can be used to form molecular composites with rigid rod PBZ polymers which molecular composites are not substantially phase separated.