Abstract: The present invention relates to a process for the preparation of polyamide-12 powder by anionic polymerization of lauryllactam in solution in a solvent of the lactam, the polyamide-12 powder being insoluble in this solvent, the polymerization being carried out: in the presence of a catalyst and of an activator; in the presence of a finely divided organic or inorganic filler, the proportion of this filler being less than or equal to 1.5 g per 1000 g of lauryllactam; and in the presence of an amide of formula R1—NH—CO—R2 in which R1 can be replaced by an R3—CO—NH— or R3—O— radical and in which R1, R2 and R3 denote an aryl, alkyl or cycloalkyl radical, the proportion of this compound being between 0.001 mol and 0.030 mol per 1000 g of lauryllactam.

Abstract: A film and a magnetic-recording medium using the film, where the heat shrinkage ratio in the transverse direction of the film subjected to heat treatment under no tension for 30 min. at 180° C. is from 1.0 to 2.5%, and where the film satisfies the following equations (1)-(4) simultaneously, with ?MD (×10?6/° C.) and ?TD (×10?6/° C.) being coefficient of thermal expansion in the longitudinal and the transverse direction, respectively, and ?MD (×10?6/% RH) and?TD (×10?6/% RH) being coefficient of hygroscopic expansion in the longitudinal and the transverse direction, respectively. In the film, by controlling the dimensional changes by temperature and humidity within specific ranges, it becomes possible to control the dimensional change and the difference in dimensional changes between the longitudinal and the transverse direction of the film used as a magnetic-recording medium to be extremely small. ?10??MD?10 (1), ?MD?10??TD??MD?3 (2), ?10??MD?10 (3), ?MD?10??TD??MD?3 (4).

Abstract: A process for preparing a polyamide by reacting a mixture which comprises a monomer which has a nitrile group and has at least one other functional group capable of forming a carboxamide group, and comprises water, in the presence of titanium dioxide as catalyst, which comprises using titanium dioxide whose BET surface area, determined to the German standard DIN 66 131 volumetrically by the multipoint method, is in the range from 5 to 35 m2/g.

Abstract: The present invention provides hydroxy-functional esters having at least one terminal acrylate-functional group. Preferred esters include those represented by the following formula (1): wherein each R1 independently represents a substituted or unsubstituted aliphatic group; R represents hydrogen or methyl; a represents an integer of 0 to 5; b represents an integer of 0 to 5; a+b=at least 1; c represents an integer of 0 to 3; and A represents an alkylene, heteroalkylene, or arylene segment.

Abstract: Polyamides are prepared from aminonitriles and water by (1) reacting the aminonitriles with water at from 180 to 350° C. and such a pressure in the range from 30 to 120 bar that a gaseous phase is present as well as a liquid phase, in a first reaction stage, (2) expanding the reaction mixture obtained in the first reaction stage via an evaporator zone or adiabatically with removal of water and ammonia into a second reaction stage, and (3) postcondensing in the second reaction stage at from 0.1 mbar to 5 bar and from 230 to 320° C.

Abstract: The invention is a composition made by mixing a multifunctional acrylate with an aminofunctional silane and an ethylenically unsaturated acid to form a reaction product, optionally dissolved in a solvent, characterized in that the multifunctional acrylate has a molecular weight of from about 100 to about 3000. The composition can be coated on a substrate, then optionally exposed to moisture and treated to initiate a free radical reaction. The invention can be applied to a variety of substrates used in packaging applications. The reaction mixture can further be cured by heating in the presence of moisture. The free radical reaction can be initiated by electron beam irradiation, ultraviolet radiation, gamma radiation, and/or heat and chemical free radical initiators.

Abstract: Described is the use of metal oxides as heterogeneous catalysts in a process for producing polyamides by polymerization of lactams and optionally further polyamide-forming monomers wherein the metal oxides are used in a form which permits mechanical removal from the reaction mixture and are removed from the reaction mixture during or after the polymerization, to reduce the extractables content of the polyamide obtained.

Abstract: In a process for producing polyamides, a mixture comprising hexamethylenediamine and aminocapronitrile and obtained from the hydrogenation of adiponitrile is reacted with water and a dicarboxylic acid.

Abstract: The continuous process for producing polyamides by reacting at least one aminonitrile with water comprises the following steps: (10) reacting at least one aminonitrile with water at a temperature of from 200 to 290° C. at a pressure of from 40 to 70 bar in a flow tube containing a Brönsted acid catalyst selected from a beta-zeolite, sheet-silicate or metal oxide catalyst in the form of a fixed bed, (11) diabatically or adiabatically expanding the reaction mixture from step (1) into a first separation zone to a pressure of from 20 to 40 bar, the pressure being at least 10 bar lower than the pressure in step (1), and to a temperature within the range from 220 to 290° C. by flash evaporation and removal of ammonia, water and any aminonitrile monomer and oligomer, (12) further reacting the reaction mixture from step (2) in the presence of water at a temperature of from 200 to 290° C.

Abstract: Process for making nylon 6 in which a feed stream containing a major portion of caprolactam and/or nylon 6 prepolymer and a minor portion of aminocapronitrile is fed to a multistage reactive distillation column in which the feed stream flows countercurrently to a steam stream.

Abstract: In a process for producing polyamides by polymerization of lactams in the presence of metal oxides as heterogeneous catalysts, the metal oxides are used in a form which permits mechanical removal from the reaction mixture and are removed from the reaction mixture in the course of or on completion of the polymerization.

Abstract: A process for producing glucoprotamines by condensation of N-substituted propylene diamines with 2-aminoglutaric compounds in which the reaction is carried out in the presence of aminosilicones is disclosed. Glucoprotamines produced in accordance with the disclosed process exhibit improved color quality and longer storage stability.

Abstract: The continuous process for producing a polyamide by reacting at least one aminonitrile with water comprises the following steps: (1) reacting at least one aminonitrile with water at a temperature from 90 to 400° C. and a pressure from 0.1 to 15×106 Pa in a flow tube containing packing elements of a Brönsted acid catalyst selected from beta-zeolite, sheet-silicate or titanium dioxide packing elements and metallic packing elements to obtain a reaction mixture, (2) further reacting the reaction mixture at from 150 to 400° C.

Abstract: Prepolymers of Formula (I) are useful in hydrogel materials wherein M is a hydrophilic radical derived from at least one hydrophilic ethylenically unsaturated monomer and having a molecular weight of about 500 to 5000; each R is independently selected from an alkylene group having 1 to 10 carbon atoms wherein the carbon atoms may include ether, urethane or ureido linkages therebetween; each R′ is independently selected from hydrogen, monovalent hydrocarbon radicals or halogen substituted monovalent hydrocarbon radicals wherein the hydrocarbon radicals have 1 to 18 carbon atoms which may include ether linkages therebetween; a is an integer equal to or greater than 1; each U is independently a divalent urethane or ureido segment; x is greater than or equal to 1, y is greater than or equal to 1; and z is greater than or equal to 1; and each E is independently a polymerizable, ethylenically unsaturated radical.

Abstract: Disclosed is a process for preparing spherical polyamide having an average grain diameter of 100 .mu.m or less which comprises polymerizing monomers for preparing the polyamide under heating at a temperature higher than the melting points of the monomers and the polyamide while melting the monomers in a polymerization medium under stirring whereby dispersing the formed polyamide with fine particles in the polymerization medium and then cooling the resulting mixture.

Abstract: There is disclosed an organic optical component prepared from a resin essentially comprising one or more repetitive structural units selected from the group consisting of structures represented by general formula (1); ##STR1## wherein A is either of the groups below. ##STR2## This invention provides an organic optical component with excellent transparency, heat resistance and mechanical strength as well as a low birefringence. This invention also provides a novel aromatic polyamide with a low permitivity and excellent transparency, processability and thermal stability, besides excellent heat resistance inherent in an aromatic polyamide.

Abstract: Formulations including a high density polyester and a density reducing component. The formulations are useful for facilitating the separation of blood serum or plasma from the cellular portion of blood in blood collection applications.

Abstract: Formulations including a high density polyester and a density reducing component. The formulations are useful for facilitating the separation of blood serum or plasma from the cellular portion of blood in blood collection applications.

Abstract: Aminoxyl-containing radical is provided in polymers and copolymers by replacing a hydroxyl moiety in a carboxyl group at a chain end of a starting material biodegradable polymer or copolymer with imino or oxy linked to aminoxyl-containing radical to form an amide linkage or an oxycarbonyl linkage at the chain end of biocompatible polymers or copolymers to the aminoxyl-containing radical. Preferred starting material polymers and copolymers are prepared from the hydroxy alkyl carboxylic acid monomers glycolic acid and lactic acid. Preferred aminoxyl-containing radical is 2,2,6,6-tetramethylpiperidine-1-oxy. Product polymers are useful for aminoxyl-containing radical treatment of tumors, and to increase the efficiency of chemotherapy and ionizing radiation therapy of tumors and for the reconstruction of injured, diseased, or aged human blood vessels.

Abstract: A crosslinked poly(ethylene or propylene)glycol-containing polymer which has a unique spatial structure and can be designed especially for application as a chromatographic resin or as a solid support for the synthesis of peptides, oligonucleotides or oligosaccharides or as a substrate for the immobilization of proteins. The polymer is formed by radical copolymerization of derivatized poly(ethylene or propylene) glycol bis-end substituted with a moiety selected from the group consisting of acryloylalkyl, acryloylaryl, acrylamidoalkyl and acrylamidoaryl with an acrylic amide, nitrile or ester. When it is to be used as a solid support or immobilization substrate, the polymer will incorporate a spacer comprising functional groups for the attachment of peptides, proteins, nucleotides or saccharides such as those selected from the group consisting of amino, alkylamino, hydroxy, carboxyl, mercapto, sulfeno, sulfino, sulfo and derivatives thereof.

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: An improved liquid crystal-aligning coating composed mainly of a specified high molecule, mainly a polyether polyimide or a polyimide, and capable of controlling the alignment and pretilt angle of liquid crystals; a liquid crystal display element using the coating; and a dinitro compound and a diol compound each as an intermediate of a diamino compound constituting the polyimide ether, are provided, which specified high molecule contains in its molecular long chain, a substituted cyclohexylidene group or a cyclohexylidene group expressed by the formula ##STR1## wherein R.sub.1 to R.sub.6 of the cyclohexyl group each represent H, 1-15C alkyl group, a cyclohexyl group or a cyclohexyl group having 1-15C alkyl group, and may be each the same or partly or totally different.

Abstract: The invention relates to a process for the production of poly-(1,4-benzamide) in admixture with SiO.sub.2 by polycondensation of 4-aminobenzoic acid in the presence of SiCl.sub.4 in 1,3-dimethyltetrahydro-2(1H)-pyrimidinone in the presence of salts, such as lithium chloride or calcium chloride.

Abstract: The present invention provides polyamide-polyimide and polybenzoxazole-polyimide polymers derived therefrom with improved processing and film characteristics having incorporated into the polymeric backbone the polymeric condensation residuum of novel aromatic diamino compounds having the formula: ##STR1## wherein A is selected from the group consisting of SO.sub.2, O, S, CO, C.sub.1 to C.sub.6 alkyl, perfluoroalkyl or perfluoroarylalkyl having from 1 to 10 carbon atoms and a carbon-carbon double bond directly linking the two aromatic groups, and R is selected from the group consisting of hydrogen, hydroxy and C.sub.1 to C.sub.4 alkoxy.The polyamide-polyimide polymers of this invention are prepared by reacting compounds of the above formula, alone or admixed with other aromatic diamines, with one or more aromatic tetarcarboxylic acids or anhydrides thereof. Polybenzoxazole-polyimide derivatives of such polyamide-polyimide polymers are prepared utilizing compounds of the above formula wherein R is hydroxy or C.

Abstract: The present invention provides polyamide-polyamide and polybenzoxazole-polyamide polymers derived therefrom with improved processing and film characteristics having incorporated into the polymeric backbone the polymeric condensation residuum of novel aromatic diamino compounds having the formula: ##STR1## wherein A is selected from the group consisting of SO.sub.2, O, S, CO, C.sub.1 to C.sub.6 alkylene, perfluoroalkylene or perfluoroalkylene having from 1 to 10 carbon atoms and a bond directly linking the two aromatic groups and R is selected from the group consisting of hydrogen, hydroxy and C.sub.1 to C.sub.4 alkoxy.The polyamide-polyamide polymers of this invention are prepared by reacting compounds of the above formula, alone or admixed with othr aromatic diamines, with one or more aromatic or aliphatic dicarboxylic acid or amide-forming derivatives thereof.

Abstract: The invention relates to a process for the production of polybenzamides from amino benzoic acids in the presence of metal halides.

Abstract: The invention concerns a simple process for preparing an ester acyllactam and/or esteramide acyllactam by the catalytic condensation of imide and alcohol, characterized in that a polyol and an acyllactam compound are reacted in the liquid state in the presencce of a halide, carboxylate or acetylacetonate from beryllium, magnesium, calcium, strontium, barium, boron, aluminium, zinc or cadmium.The invention is important for the preparation of compounds which may be used in the preparation of nylon block copolymers, more in particular in RIM-nylon systems (Reaction Injection Moulding), since when the compounds obtained according to the present invention are used in a RIM system, a very fast lactam polymerization takes place, and it therefore also relates to the preparation of nylon block copolymers.

Abstract: The present invention relates to a process for the preparation of aromatic polyamides mixed with SiO.sub.2, which is characterized in that terephthalic (isophthalic) acid is subjected to polycondensation with aromatic diamines in the presence of SiCl.sub.4 and tertiary aromatic nitrogen heterocyclic compounds, to the polyamides which are produced as a mixture with SiO.sub.2 and to a process for their isolation.

Abstract: Copolyester polyol resins comprising the reaction product of an aromatic component selected from phthalic derivatives, polyethylene terephthalate, or dimethyl terephthalate, an aliphatic component selected from certain dibasic compounds, at least one primary hydroxyl glycol, and at least small amounts of a secondary hydroxyl glycol, the mole ratios of the components being:(a) glycols to aromatic plus aliphatic component of from about 1.3 to 2:1;(b) aromatic component to aliphatic component of from about 0.6 to 4.0:1;(c) a secondary to primary hydroxyl glycol of from 0.05 to 0.4:1; and(d) ethylene glycol content to aromatic component of from about 0.01 to 0.5:1.0.The invention also comprises polyol blends utilizing from 30 percent up to 90 percent of such resins and resultant polyurethane modified polyisocyanurate foams made by reacting such polyol blends with polymeric polymethylene polyphenylisocyanate.

Abstract: This invention provides a single stage melt polymerization process for the production of an improved type of high molecular weight polybenzimidazole, which involves the use of an organosilicon halide polymerization catalyst.The process provides poly-2,2'-(m-phenylene)-5,5'-bibenzimidazole of improved color and Plugging Value, and is further characterized by an Inherent Viscosity of at least about 0.7 dl/g, and a weight average molecular weight of at least about 100,000.

Abstract: This invention provides a single stage melt polymerization process for the production of an improved type of high molecular weight polybenzimidazole, which involves the use of an organosilicon halide polymerization catalyst.The process provides poly-2,2'-(m-phenylene)-5,5'-bibenzimidazole of improved color and Plugging Value, and is further characterized by an Inherent Viscosity of at least about 0.7 dl/g, and a weight average molecular weight of at least about 100,000.

Abstract: Poly(.epsilon.-caprolactam) is prepared with less than 3 percent water-extractable material by carrying out the polymerization reaction in a vessel, the interior surfaces of which are coated with an inert adherent coating of an organic polymer.

Abstract: Novel polyamides are prepared having end groups especially selected to impart special properties to the polymer. These polyamides are prepared by utilizing anionic polymerization processes and the end groups can be of a type that, under existing methods, normally will hinder or completely stop the anionic polymerization reaction. The hindering effect of these end groups is largely overcome through the formation of novel initiator compounds that enables the polymerization reaction to proceed with extreme rapidity at comparatively low temperatures despite the presence of these end groups.

Abstract: Novel compounds of the general formula ##STR1## (m = 0 or 1; n = 2 or 3 and R = H or CH.sub.3) are produced by reacting a 2-aminoalkyl alkylene urea with an allyl ester of a carbonylic acid. Among the particular allyl esters disclosed as reactants are diallyl carbonate, allyl and methallyl chloroformate, diallyl and dimethallyl oxalate. The recovered allyl esters of the alkyleneureido amic acid compounds find particular use as functional comonomers for imparting wet adhesion properties to emulsion systems containing vinyl ester polymers used in paints and coating compositions.

Abstract: The invention relates to a method for the cationic polymerization of lactams either substituted or unsubstituted on the lactam ring, which contain 6-16 carbon atoms, in the presence of 0.05 - 10 mol. % based on the lactam of an anhydrous salt of Cu, Zn, B, Al, Ti, Si, V, Sb, Bi, Cr, Mo, W, Mn, Fe, Co, Ni and an inorganic or organic anion such as phosphate, pyrophosphate, phosphite, sulfate, halide, carboxylate and sulfonate in the presence of 0.05 - 5 mol. % of a protic organic or inorganic acid such as pyrophosphoric, phosphorous, hydrohalic carboxylic and sulfonic. These additives can be added to lactam below 180.degree. C and the polymerization is carried out at 150.degree. - 320.degree. C for 0.1 - 200 hr. The above-specified salts, also their mixtures, can be used. The polymerization can be carried out with mixtures containing two or more lactams.