Abstract: Composite materials are described herein. An example composite material may comprise a shell fiber layer. The example composite material may comprise a membrane disposed adjacent the shell fiber layer.

Abstract: An object of the present invention is to provide an environmentally friendly drilling fluid that has excellent cuttings transport capability and excellent hole cleaning capability. A drilling fluid according to the present disclosure is a drilling fluid containing water, biodegradable fibers, and a thickener. The thickener contains a biodegradable polysaccharide. The content of the biodegradable polysaccharide in the drilling fluid is greater than or equal to 0.01 g/L and less than or equal to 5 g/L.

Abstract: The present invention provides a process of using an alloy nanoparticle catalyst to catalyze one pot chemical reactions for synthesizing functional polymers with controlled polymerization and properties. In particular, the present invention provides a process of using an AuPd NP catalyst to catalyze one pot chemical reactions for synthesizing polybenzoxazole with controlled polymerization and improved chemical stability.

Abstract: The invention relates to the on-line control of the molecular weight in continuous solid state polymerization processes. In particular it is directed to a polyester process or to a polyamide process, and more specifically to a poly(ethylene terephthalate) (PET) or a poly(butylene terephthalate) (PBT) or a nylon 6,6 continuous solid-state polymerization (SSP) process. An in-line viscometer melts and measures the molecular weight of the SSP resin and adjusts one or more of the process variables, i.e. reactor time, inert gas purity and inert gas temperature to maintain a constant resin molecular weight.

Abstract: Copolymers containing at least one perfluoropolyether segment and multiple aminooxalylamino groups are described. Methods of making the copolymers are also described. The copolymers can be prepared by reacting an oxalylamino-containing compound and an amine compound having at least two primary amino groups, at least two secondary amino groups, or at least one primary amino group plus at least one secondary amino group.

Abstract: Copolymers containing at least one perfluoropolyether segment and multiple aminooxalylamino groups are described. Methods of making the copolymers are also described. The copolymers can be prepared by reacting an oxalylamino-containing compound and an amine compound having at least two primary amino groups, at least two secondary amino groups, or at least one primary amino group plus at least one secondary amino group.

Abstract: Copolymers exhibiting the following combinations of properties, including without limitation, ?-caprolactone in an amount ranging from about 12 to about 70 mole percent, glycolide in an amount ranging from about 30 to about 88 mole percent, crystallinity ranging from about 10 to about 50% as measured by WAXD or about 10 to about 50 J/g as measured by DSC, and an inherent viscosity ranging from about 0.5 to about 1.45 dL/g as measured in a 0.1 g/dl solution of HFIP at 25° C.; a method for melt blowing such copolymers and nonwoven constructs produced therefrom are described herein.

Abstract: The present invention generally relates to a poly(bisoxalamide) and a process for preparing and article comprising the poly(bisoxalamide).

Abstract: The disclosures herein relate to a polymer such as nylon 66, having low yellowness and excellent whiteness retention for applications in melt extrusion and injection molding where an increase in molecular weight is not desirable. The polymer is prepared with a phosphorus compound content, e.g., a sodium hypophosphite (SHP) content, in an amount of 150 to 300 ppm by weight. The presence of an “end cap” additive such as one selected from acetic acid, propionic acid, benzoic acid, or succinic acid, added at the start of polymerization, effectively mitigates undesired molecular weight gain.

Abstract: Provided is a polyoxamide resin which has excellent impact resistance and is characterized in that the polyoxamide resin is obtained from a diamine in which the diamine component has 10 to 18 carbons and in that the polyoxamide resin has a relative viscosity (?r) of 2.1 or greater as determined at 25° C. using 96% sulfuric acid as a solvent and a solution having a concentration of 1.0 g/dL, and also provided is an impact-resistant part comprising this resin. The polyoxamide resin has a higher molecular weight than a conventional polyoxamide resin, a large moldable temperature range as estimated from the difference between the melting point and the thermal decomposition temperature and therefore excellent molten moldability, and furthermore excellent impact resistance when compared to a conventional aliphatic polyoxamide resin without losing the low water absorbency, chemical resistance, hydrolysis resistance, high elasticity, and high strength seen with aliphatic straight-chain polyoxamide resins.

Abstract: A process for preparation of a polyamide PA-4X containing monomer units of 1,4-diaminobutane and an aliphatic linear dicarboxylic acid X with at least 8 carbon atoms, which contains the following steps: 1) making a solution comprising a salt of 1,4-diaminobutane and the aliphatic linear dicarboxylic acid and water, at a temperature at which the salt dissolves; 2) concentrating the solution of the salt at a temperature above the crystallization temperature of the salt, at a pressure of at most 7 barA to a water content of between 0 and 30 wt % based on the total amount of solution, 3) producing a polymer from the solution obtained by step 2, while keeping the polymer in a melt and at a pressure of less than 18 barA, 4) depressurizing the polymer obtained at step 3 while keeping the polymer in the melt to further polymerize the polymer. In an preferred embodiment the aliphatic linear dicarboxylic acid is 1,10-decanedioic acid.

Abstract: A copolyamide resin for molding including a diamine component which includes two or more diamines and a dicarboxylic acid component. The diamine component includes 70 mol % or more of a xylylenediamine which includes 20 mol % or more of p-xylylenediamine and the dicarboxylic acid component includes 70 mol % or more of a straight-chain aliphatic dicarboxylic acid having 6 to 18 carbon atoms. The copolyamide resin contains particles having a major diameter of 50 ?m or more in an amount of 1000 particles/g or less, the particles being made of a polyamide having a melting point higher than that of the copolyamide resin by 20° C. or more when measured by a differential scanning calorimetry. The copolyamide resin has very uniform and stable properties and is excellent in any of mechanical properties, heat resistance, chemical and physical properties, and molding properties. An efficient production method of the copolyamide resin, its resin composition, and its molded article are also described.

Abstract: Copolymers containing at least one perfluoropolyether segment and multiple aminooxalylamino groups are described. Methods of making the copolymers are also described. The copolymers can be prepared by reacting an oxalylamino-containing compound and an amine compound having at least two primary amino groups, at least two secondary amino groups, or at least one primary amino group plus at least one secondary amino group.

Abstract: Copolymers exhibiting the following combinations of properties, including without limitation, ?-caprolactone in an amount ranging from about 12 to about 70 mole percent, glycolide in an amount ranging from about 30 to about 88 mole percent, crystallinity ranging from about 10 to about 50% as measured by WAXD or about 10 to about 50 J/g as measured by DSC, and an inherent viscosity ranging from about 0.5 to about 1.45 dL/g as measured in a 0.1 g/dl solution of HFIP at 25° C.; a method for melt blowing such copolymers and nonwoven constructs produced therefrom are described herein.

Abstract: Degradable polymers were synthesized that self-assemble with DNA to form particles that are effective for gene delivery. Small changes to polymer synthesis conditions, particle formulation conditions, and polymer structure provides significant changes to efficacy in a cell-type dependent manner. Polymers presented here are more effective than commercially available materials, such as LIPOFECTAMINE 2000™, FUGENE®, or polyethylenimine (PEI), for gene delivery to cancerous fibroblasts or human primary fibroblasts. The presently disclosed materials may be useful for cancer therapeutics and regenerative medicine.

Abstract: The present invention generally relates to a poly(bisoxalamide) and a process for preparing and article comprising the poly(bisoxalamide).

Abstract: The epoxy resin molding material of the invention comprises (A) an epoxy resin and (B) a curing agent, wherein the (B) curing agent contains a polyvalent carboxylic acid condensate. The thermosetting resin composition of the invention comprises (A) an epoxy resin and (B) a curing agent, wherein the viscosity of the (B) curing agent is 1.0-1000 mPa·s at 150° C., as measured with an ICI cone-plate Brookfield viscometer.

Abstract: The present invention concerns monomeric or polymeric linker molecules useful in biological and chemical applications, their synthesis, and the synthesis and use of derivatives of the linkers conjugated to a variety of detectable labels and other substances. The linkers may be used, for example, in conjunction with fluorescent labels, nucleic acid or nucleic acid analog probes, and solid phase systems, and to enhance the solubility of the conjugated molecules.

Abstract: A molding material for fuel parts (particularly a molding material for fuel parts of automobiles), ensuring excellent fuel barrier property against not only gasoline fuel, but also an alcohol mixed fuel, is provided. A molding material for fuel parts and a fuel part, comprising a polyamide containing an oxamide bond unit represented by —NH—R—NHC(?O)C(?O)—.

Abstract: There is provided a polyamide resin that can achieve a sufficiently high molecular weight compared to conventional polyamide 92, has a broad moldable temperature range or width estimated from a difference between melting point and thermal decomposition temperature, exhibits excellent melt moldability and has excellent chemical resistance and hydrolysis resistance compared to conventional aliphatic polyamide resins without impairing low water absorption property of an aliphatic linear polyoxamide resin. A polyamide resin in which the dicarboxylic acid component is oxalic acid and the diamine component is a diamine component composed of 1,9-nonanediamine and 2-methyl-1,8-octanediamine, with the molar ratio between 1,9-nonanediamine and 2-methyl-1,8-octanediamine being from 6:94 to 99:1.

Abstract: The invention relates to an airdrying resin suitable for a coating composition characterized in that the resin is a polyesteramide prepared from: A) at least one anhydride chosen from the list containing succinic, glutaric, citraconic, itaconic or maleic anhydride or a combination of any of them, and B) at least one alkanol-amine, and C) at least one fatty acid, wherein the fatty acid is incorporated in the resin in an amount equivalent to an oil-length between 15 and 40%. This airdrying resin is both water- and solvent-soluble, having a combination of properties desirable for different types of applications. The invention relates also to a method for preparing such a polyesteramide resin, to a composition comprising at least one polyesteramide resin and a method for preparing such a composition, to a substrate fully or partially coated with this composition, a method for curing the coated substrate, the cured and coated substrate and the use of resin in various applications.

Abstract: A binder composition for glass fiber mats or the like, where the binder composition includes a carboxylated emulsion resin and a polyfunctional aziridine crosslinking agent. The binder composition is formaldehyde free, exhibits good crosslinking density, and enables the economical production of strong, flexible fiberglass mats which may be used as thermal and acoustic insulation.

Abstract: The present invention contemplates a process for forming polyaminoamide polymers formed by the reaction of a dibasic acid/ester with excess amounts of an amine; the intermediate polymer resulting therefrom; a process for synthesizing effective, high solids resins resulting from the reaction of intermediate polymers with an epihalohydrin; and the resultant high, solids resin. These resins may be used as wet strength resins in the papermaking industry.

Abstract: Chemically different cyclic ester oligomers can be copolymerized to form copolyesters whose properties can be tailored by the choice of cyclic ester oligomers used. The copolyesters formed are especially useful as encapsulants and as coatings. In many instances the copolyesters, assuming they are not randomized in later transesterification reactions, have unique microstructures related to the sequencing of repeat units the their polymer chains.

Abstract: A curable composition is placed on a candle, and then the composition is exposed to curing conditions such as ultraviolet light, to thereby cure the coating composition and provide a candle having a cured coating. The curable composition may be the reaction product of TMPTA (trimethylolpropanetriacrylate), itself the reaction product of trimethylolpropane and acrylic acid) and oleyl amine (an unsaturated primary amine having eighteen carbons). The candle may be made of wax or a gelled solvent, i.e., a mixture of gellant and solvent, particularly a hydrocarbon or other low polarity solvent. The undiluted coating may be applied by spraying on the oily surface of the candle. Ultraviolet cure of the coating occurs in 1-2 seconds.

Abstract: An adhesive tape comprising: (a) a polymer film; (b) a primer coat on said polymer film; and (c) an adhesive layer on the primer coat comprising: (i) a natural rubber latex; and (ii) a tackifier.

Abstract: A method of production of a homopolymer or copolymer or homo-oligomer or co-oligomer product characterised in that the product is obtained by condensation reaction of a diaminoanthracene, substituted or not, optionally with a diiminoanthracene substituted or not in the absence of anthraquinone substituted or not.

Abstract: A curable composition is placed on a candle, and then the composition is exposed to curing conditions such as ultraviolet light, to thereby cure the coating composition and provide a candle having a cured coating. The curable composition may be the reaction product of TMPTA (trimethylolpropanetriacrylate), itself the reaction product of trimethylolpropane and acrylic acid) and oleyl amine (an unsaturated primary amine having eighteen carbons). The candle may be made of wax or a gelled solvent, i.e., a mixture of gellant and solvent, particularly a hydrocarbon or other low polarity solvent. The undiluted coating may be applied by spraying on the oily surface of the candle. Ultraviolet cure of the coating occurs in 1-2 seconds.

Abstract: The present invention relates to fibers, and nonwovens comprising said fibers, comprising a biodegradable copolymer, wherein the copolymer comprises at least two randomly repeating monomer units (RRMU) wherein the first RRMU monomer unit has the structure ##STR1## and the second RRMU has the structure ##STR2## wherein at least 50% of the RRMUs have the structure of the first RRMU. The present invention further relates to an absorbent article comprising a liquid pervious topsheet, a biodegradable liquid impervious backsheet comprising the above fibers and/or nonwovens, and an absorbent core positioned between the topsheet and the backsheet.

Abstract: In process for making a polyesteramide composition, an alkyl aryl terephthalate ester is formed from a dialkyl terephthalate by transesterification and then reacted with an alkyl diamine to form a bis-ester amide wherein the reaction product containing the bis-ester amide may be directly contacted with an alkyl diamine without the need for purification steps.

Abstract: A process for the preparation of tetraazamacro-cycles of general formula (I) ##STR1## wherein n, p and q can independently be 0 or 1, comprising the following steps:a): condensation of polyamines with a glyoxal derivative;b): condensation of the resulting compound with an alkylating agent;c): oxidation of the resulting compound with an oxidizing agent, to give a mixture of oxidated products which is submitted tod): hydrolysis in acid aqueous solution, to give the compound of formula (I).

Abstract: Disclosed are novel crosslinked polymeric ammonium salts wherein in said polymeric salt: about 25% or more of the segments which link ammonium nitrogen atoms are group Y wherein Y is an n-alkylene group or alkyl substituted n-alkylene group, wherein said n-alkylene group has 7 to about 20 carbon atoms; zero to about 75% of segments which link ammonium nitrogen atoms are group Z wherein Z is a hydrocarbylene radical containing 2 or more carbon atoms, said hydrocarbylene radical optionally containing one or more hydroxyl, ether, amino, thioether, keto, or silyl groups or heterocyclic rings; and about 25% or more of the ammonium atoms are secondary ammonium atoms.

Abstract: Disclosed are polyesteramide resin compositions having amide units of formula (I): ##STR1## and the units of the formula (II): ##STR2## wherein the polyesteramide is substantially devoid of units derived from butane diol. The ratio of (I) to (II) in the polyesteramide is preferably less than 1:3. Preferred polyesteramides have at least 80% of units of formula (I) separated by at least one of the units of formula (II).

Abstract: A process is provided for preparing a dispersion of a polyamide in water, said process comprising:forming a solution of a polyamide having an acid value of greater than about 2 in an organic solvent to form a solution of said polyamide in said solvent, said polyamide and said solvent being at a temperature below the softening point of said polyamide during said dissolving, said solution further comprising a surfactant, wherein at least a portion of the acid value of said polyamide is neutralized,adding sufficient water to said solution with mixing to form an oil-in-water dispersion, the temperature of said solution and said water being below the softening point of said polyamide during said adding, andremoving at least a major amount of said organic solvent from said oil-in-water dispersion. The resulting dispersion is useful in preparing a coating of the polyamide, which coating is useful as an adhesive.

Abstract: Shaped articles are obtained from a polymerization mixture of soluble wholly aromatic polyamides in a gel state.

Abstract: Disclosed are polymers and copolymers containing at least one repeating unit of the formula ##STR1## in which X is O or NH; R is a single bond or a hydrocarbon chain; R' is a hydrocarbon chain containing one or two carbon atoms, and P is the residue of an oligomer HX--P--XH whose solution viscosity determined in meta-cresol at 30.degree. C. at concentrations of 0.5 g/dl is lower than 0.50 dl/g.sup.-1. Also disclosed is a process for obtaining the polymers and copolymers.

Abstract: There is disclosed a method for producing aromatic polyamides represented by the following formula (III), which comprises reacting an aromatic dihalogen compound represented by the following formula (I) with a diamine compound represented by the following formula (II) in the presence of cobalt/phosphine complex and a basic substance under carbon monoxide atmosphere:X.sub.1 --Ar--X.sub.2 formula (I)wherein Ar represents an aromatic residue and X.sub.1 and X.sub.2 each represent a bromine or iodine atom,H.sub.2 N--R--NH.sub.2 formula (II)wherein R represents a divalent hydrocarbon group, andformula (III) ##STR1## wherein Ar and R each have the same meaning as the above, and n is a positive integer.

Abstract: Disclosed is the use of a laminate of a textile material covered with a copolyetherester film having a water vapor transmission rate of at least 1000 g/m.sup.2 /day for the manufacture therefrom of waterproof rainwear, shoes, tents, and mattress covers, and for the complete covering therewith of molded articles of foam rubber for use in chairs or mattresses, the copolyetherester being composed of a plurality of recurrent intralinear long-chain ester units and short-chain ester units which are randomly joined head-to-tail through ester bonds, with at least 20 wt. % of the long-chain ester units being prepared from a long-chain glycol having a carbon to oxygen ratio in the range of 2.0 to 2.4, which glycol constitutes 15-45 wt. % of the copolyetherester, and with at least 70 wt. % of the short-chain ester units consisting of butylene naphthalate units constituting 20-80 wt. % of the copolyetherester.

Abstract: This invention provides hydrolytically labile polyamide compositions and articles containing an ester derived moiety in the polymer backbone which will degrade after exposure to water over long periods of time.

Abstract: A multicomponent film structure having at least three layers the outer layers of which are each a continuous layer of a hydrophobic copolyetherester elastomer and an inner layer of which is a continuous layer of a hydrophilic copolyetherester elastomer, said film structure having good resistance to water absorption.

Abstract: The present invention relates to a process for the manufacture of a crosslinked polymer, wherein a crosslinking reaction is carried out between an organic crosslinking agent which is a polyacid or a derivative of a polyacid, and a long chain alkylpolyamine having at least two amine functional groups which may be primary and/or secondary and which is not a succinimide. The long chain alkylpolyamine can be obtained by a method comprising reacting a corresponding long chain alkylcarbonyl compound with an amine. The long chain carbonyl compound is for example prepared by ozonolysis of a polyolefin which can be a polybutene. The obtained crosslinked polymer can be used as an additive in lubricant compositions.

Abstract: Block polyamido polyamine condensation products of an aromatic polycarboxylic acid component with a polyoxyalkylene polyamine component prepared by reacting the polycarboxylic acid component with an amount of the polyoxyalkylene polyamine component sufficient to react each carboxyl group with 1 mole of the polyoxyalkylene polyamine component.The polyoxyalkylene polyamine being selected from the group consisting of polyoxypropylene diamines, polyoxyethylene diamines, polyoxyethylene/oxypropylene diamines and polyoxypropylene triamines, and the aromatic polycarboxylic acid component being selected from the group consisting of C.sub.8 to C.sub.28 benzene dicarboxylic acids, benzene tricarboxylic acids, naphthalene carboxylates, hemimellitic acid, 1,1,3-trimethyl-3-phenylindan-4',5-dicarboxylic acid, trimellitic acid, and anhydrides and C.sub.1 to C.sub.4 alkyl esters thereof.

Abstract: Oxygen barrier structures such as packages, laminated films, etc. are disclosed. The oxygen barrier has at least one layer comprising a polymer having oxamide units of the formula: ##STR1## and may further include amide units selected from the formulae: ##STR2## wherein R and R' are independently hydrocarbyl radicals of from 2 to 20 carbon atoms, and R" is a hydrocarbyl radical of from 1 to 18 carbon atoms. The polyoxamide or copoly(amide-oxamide) layer has an oxygen permeability which, at a high relative humidity, is less than or about the same as the oxygen permeability at a low relative humidity. Also disclosed is a method of protecting an article such as a foodstuff against oxidation by packaging the article with the oxygen barrier structure.

Abstract: A block polyamido primary amine condensation product prepared by reacting a defined polyoxyalkylene polyamine having terminal primary amine groups with an amount of a defined dicarboxylic acid or an anhydride or a C.sub.1 to C.sub.4 alkyl ester thereof, sufficient to react one mole of the dicarboxylic acid reactant with each primary amine group of the polyoxyalkylene polyamine to thereby prepare an intermediate condensation reaction product containing terminal carboxyl groups, and reacting one mole of a defined organic di-primary amine with each terminal carboxyl group of the said intermediate condensation reaction product to thereby provide, as the principal product of the reaction a block polyamido primary amine condensation product.

Abstract: Oxygen barrier structures such as packages, laminated films, etc. are disclosed. The oxygen barrier has at least one layer comprising a polymer having oxamide units of the formula: ##STR1## and may further include amide units selected from the formulae: ##STR2## wherein R and R' are independently hydrocarbyl radicals of from 2 to 20 carbon atoms, and R" is a hydrocarbyl radical of from 1 to 18 carbon atoms. The polyoxamide or copoly(amide-oxamide) layer has an oxygen permeability which, at a high relative humidity, is less than or about the same as the oxygen permeability at a low relative humidity. Also disclosed is a method of protecting an article such as a foodstuff against oxidation by packaging the article with the oxygen barrrier structure.

Abstract: Polyamides having improved solubility and processing characteristics are provided having incorporated into the polymeric chain a novel aromatic diamine compound, 2-(3-aminophenyl)-2-(4-aminophenyl) hexafluoropropane (3-4'-6F Diamine). The polyamides are prepared by reacting the 3,4'-6F Diamine with an aliphatic or aromatic di-acid or acid halide. It has been found that the polyamides of this invention have improved solubility characteristics, low dielectric constants and improved thermal flow properties as a consequence of the meta/para positioning of the amino groups on the daimine, which renders these polymers more readily melt spinnable for the production of fibers. The polymers may also be compression molded and fabricated into composites at moderate temperatures and pressures.

Abstract: (A) A continuous layer of a hydrophobic elastomer having a water vapor transmission rate of 400-2500 gm.mil/m.sup.2 /24 hrs.

Abstract: An ungelled composition is prepared as the half-amide reaction product of a diester of oxalic acid and a material containing one or more primary and/or secondary amino groups and one or more different functional groups. The ungelled composition is useful as a crosslinking agent for amine group containing materials and as an intermediate in the preparation of resinous compositions for fire protective coatings.

Abstract: Disclosed are novel wet strength resins for paper, said resins being derived by reacting an epihalohydrin, such as epichlorohydrin, with a polyamino-copolyamide derived by reacting methylbisaminopropylamine with (a) a diester of oxalic acid and (b) a diester of a saturated dicarboxylic acid containing at least 4 carbon atoms, the mole ratio of (a) to (b) being from about 0.25:1 to about 10:1.

Abstract: Hydrophosphonylated derivatives of homopolymers and copolymers of poly allyl glycidyl ethers are formed by reacting said polymers with sodium hypophosphite (NaH.sub.2 PO.sub.2). The novel polymers of this invention may be represented by the general formula: ##STR1## wherein x ranges from about 5 to about 10.sup.6, y ranges from 0 to about 10.sup.6, A is interpolymerized units of one or more epoxides having the oxirane group ##STR2## and R is ##STR3## n is 0 to 19, and m is 0 to 20. y Preferably is zero, and x preferably ranges from about 5 to about 10.sup.6, and most preferably from 5 to 10.