Abstract: A method for quantitative detection of trace polylactic acid microplastics (PLA MPs) in an environmental sample is disclosed, where the PLA MP in the environmental sample is depolymerized in an alkaline alcohol phase system, and the monomers thereof, i.e., lactic acid molecules were separated and recovered. Mass concentrations of lactic acid before and after reaction are quantitatively detected by HPLC-MS, and the initial mass concentration of PLA MPs in the sample is calculated using a formula. The minimum detectable concentration may be as low as 0.05 mg/kg. This method can quantify the trace PLA in water body, sludge, sediment, dust, and soil samples; no special treatment is required before heating in pentanol; use of such reaction conditions as heating and alkaline alcohol phase reduces reaction time substantially.

Abstract: A method for using citraconic anhydride and itaconic anhydride as addition cure end caps in reactions for forming polyamic acid oligomers and polyimide oligomers, is provided. Prepregs and high temperature adhesives made from the resulting oligomers, as well as, high temperature, low void volume composites made from the prepregs, are also provided.

Abstract: PSA-PCL micelles were developed as carrier systems for pharmaceutical drugs. As an example, cyclosporine A (CyA) was encapsulated in the micelles and physical characterization, including size and zeta potential, demonstrated that the micelles possess favorable properties for drug delivery. In vitro studies verified that rheumatoid arthritis synovial fibroblasts are able to internalize the CyA-loaded micelles. CyA was released from the PSA-PCL micelle upon uptake and subsequently, partitioned into the phospholipid membrane. The PSA-PCL micelles also demonstrated improved therapeutic efficacy in drug delivery when used to deliver statins and disease modifying anti-rheumatic drugs (DMARDs).

Abstract: The present technology provides a rubber composition for a conveyor belt. The rubber composition comprises: a rubber component containing butadiene rubber and/or styrene butadiene rubber, carbon black, sulfur, and a vulcanization accelerator; the glass transition temperature of the butadiene rubber and the styrene butadiene rubber being ?65° C. or lower; the nitrogen adsorption specific surface area of the carbon black being 90 m2/g or less; the total content of the butadiene rubber and the styrene butadiene rubber being 50% by mass or greater relative to the content of the rubber component; the content of the carbon black being from 30 to 50 parts by mass per 100 parts by mass of the rubber component; and the mass ratio (sulfur/vulcanization accelerator) of the content of the sulfur to the content of the vulcanization accelerator being 1.5 or less.

Abstract: Disclosed herein are a homogeneous sulfur-modified polymer composition, a method of preparing sulfur-modified polymer, and an asphaltic concrete mixture.

Abstract: A method for making an electrode active material of a lithium ion battery is disclosed. In the method, elemental sulfur is mixed with a polyacrylonitrile to form a mixture. The mixture is heated in vacuum or a protective gas at a heating temperature of about 250° C. to about 500° C., to form a sulfur containing composite. The sulfur containing composite is reacted with a reducing agent for elemental sulfur in a liquid phase medium to remove part of the elemental sulfur from the sulfur containing composite.

Abstract: The invention provides a rubber composition for golf balls which includes: (A) a base rubber containing a polybutadiene having a cis-1,4 bond content of at least 60 wt %; (B) an unsaturated carboxylic acid and/or a metal salt thereof; (C) an anthranilic acid derivative of the general formula wherein R1 and R2 are each independently a hydrogen atom or a hydrocarbon group of 1 to 20 carbons, m is an integer from 1 to 4, and n is an integer from 1 to 3, with the proviso that if m and/or n is 2 or more, each occurrence of R1 and R2 may be the same or different; and (D) sulfur. The rubber composition for golf balls of the invention enables a high-quality molded and crosslinked product having a suitable hardness and a high resilience to be obtained.

Abstract: The invention relates to a method for preparing a polyacrylonitrile-sulfur composite material, in which, polyacrylonitrile is converted to cyclized polyacrylonitrile, and the cyclized polyacrylonitrile is reacted with sulfur to form a polyacrylonitrile-sulfur composite material. By a separation of the preparation method into two partial reactions, the reaction conditions are advantageously able to be optimized for the respective reactions and a cathode material is able to be provided for alkali-sulfur cells with improved electrochemical properties. In addition, the invention relates to a polyacrylonitrile-sulfur composite material, a cathode material, an alkali-sulfur cell or an alkali-sulfur battery as well as to an energy store.

Abstract: The present disclosure relates to a sulfurized polyacrylonitrile and a lithium-ion battery cathode active material. The sulfurized polyacrylonitrile includes a structural unit. A general molecular formula of the structural unit is C3HNSn, in which n is a positive integer. The lithium-ion battery cathode active material includes sulfurized polyacrylonitrile and a sulfurized polyacrylonitrile with inserted ions.

Abstract: The invention provides methods for making copolymers and multi-arm block copolymers useful as drug delivery vehicles. The multi-arm block copolymers comprise a central core molecule, such as a residue of a polyol, and at least three copolymer arms covalently attached to the central core molecule, each copolymer arm comprising an inner hydrophobic polymer segment covalently attached to the central core molecule and an outer hydrophilic polymer segment covalently attached to the hydrophobic polymer segment, wherein the central core molecule and the hydrophobic polymer segment define a hydrophobic core region. The solubility of hydrophobic biologically active agents can be improved by entrapment within the hydrophobic core region of the block copolymer. The invention further includes pharmaceutical compositions including such block copolymers, pharmaceutical compositions, and methods of using the block copolymers as drug delivery vehicles.

Abstract: A rubber composition comprising 0.3 to 10 parts by mass of sulfur and 0.1 to 10 parts by mass of a sulfeneamide base vulcanization accelerator represented by the following Formula (I) based on 100 parts by mass of a rubber component: (wherein R1 to R10 are a hydrogen atom, a linear alkyl group having 1 to 4 carbon atoms or a branched alkyl group having 3 to 4 carbon atoms, and they may be the same or different; R11 is a hydrogen atom, a linear alkyl group having 1 to 10 carbon atoms or a branched alkyl group having 3 to 10 carbon atoms; R12 to R15 are a hydrogen atom, a linear alkyl group or alkoxy group having 1 to 4 carbon atoms or a branched alkyl group or alkoxy group having 3 to 4 carbon atoms, and they may be the same or different; and x represents an integer of 1 or 2).

Abstract: In a method for making sulfurized polyacrylonitrile, polyacrylonitrile, a first solvent, a catalyst, and sulfur or sodium thiosulfate are provided. The polyacrylonitrile is dissolved in the first solvent to form a polyacrylonitrile solution. The catalyst is uniformly dispersed in the polyacrylonitrile solution. The polyacrylonitrile solution with the catalyst is heated to induce a cyclizing reaction of the polyacrylonitrile, thereby forming a first conjugated polymer solution with a conjugated polymer. The sulfur or sodium thiosulfate is uniformly mixed with the conjugated polymer to form a mixture. The mixture is heated to form sulfurized polyacrylonitrile.

Abstract: The invention provides methods for making copolymers and multi-arm block copolymers useful as drug delivery vehicles. The multi-arm block copolymers comprise a central core molecule, such as a residue of a polyol, and at least three copolymer arms covalently attached to the central core molecule, each copolymer arm comprising an inner hydrophobic polymer segment covalently attached to the central core molecule and an outer hydrophilic polymer segment covalently attached to the hydrophobic polymer segment, wherein the central core molecule and the hydrophobic polymer segment define a hydrophobic core region. The solubility of hydrophobic biologically active agents can be improved by entrapment within the hydrophobic core region of the block copolymer. The invention further includes pharmaceutical compositions including such block copolymers, pharmaceutical compositions, and methods of using the block copolymers as drug delivery vehicles.

Abstract: A water-base adhesive mix for producing tires and containing, by weight, 20 to 80% water, 10 to 40% of a cross-linkable unsaturated-chain polymer base, 0.2 to 1% sulphur, 1 to 25% of a reinforcing filler, 1 to 10% of emulsifiers, 2 to 8% of a resin which cross-links by reaction with polyisocyanates, and 0.5 to 5% of an aqueous dispersion having blocked aromatic polyisocyanates with an activation temperature of 120 to 160° C. The blocked aromatic polyisocyanates are produced by reaction of an aromatic polyisocyanate (a), a blocking agent (b), and a nonionic diol alkoxylate (c) of the general formula (I) R1CH2O(CH2CH2O)n(CH2CHCH3O)mR2??(I) where R1 is R2 and R3 are the same or different, and are selected from methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl; n is a whole number from 0 to 40 m is a whole number from 0 to 40 n+m is a whole number from 20 to 80.

Abstract: The invention pertains to a particle comprising a composition containing a matrix and a peroxide or azo radical initiator, wherein the particle is a fiber or fibrid selected from aramid, polyester, polyamide, cellulose, and glass. The invention further relates to particle-elastomers comprising said composition, and skim products, tires, tire treads, and belts comprising these particle-elastomers.

Abstract: The invention relates to a polymer comprising structural units of formula and formula wherein R1, R2, R5 and R6 are independently hydrogen, a methyl group, or —COOH, only one of R1 and R2 or R5 and R6 is —COOH; R3 and R7 are independently hydrogen, or a methyl group; R4 is —COOH, —CONH2 or —OH, when R4 is —OH, R1, R2 and R3 are respectively hydrogen; and R8 is —COO, —CONH, or —O—, when R8 is —O—, R5, R6 and R7 are respectively hydrogen. Methods for preparing and using the polymer are also described herein.

Abstract: The invention provides methods for making copolymers and multi-arm block copolymers useful as drug delivery vehicles. The multi-arm block copolymers comprise a central core molecule, such as a residue of a polyol, and at least three copolymer arms covalently attached to the central core molecule, each copolymer arm comprising an inner hydrophobic polymer segment covalently attached to the central core molecule and an outer hydrophilic polymer segment covalently attached to the hydrophobic polymer segment, wherein the central core molecule and the hydrophobic polymer segment define a hydrophobic core region. The solubility of hydrophobic biologically active agents can be improved by entrapment within the hydrophobic core region of the block copolymer. The invention further includes pharmaceutical compositions including such block copolymers, pharmaceutical compositions, and methods of using the block copolymers as drug delivery vehicles.

Abstract: There is provided a rubber composition for a tread having excellent hardness and improving the processability and grip performance of a tire, and a tire comprising thereof. A rubber composition for a tread comprising 30 to 80 parts by weight of silica having a BET specific surface area of less than 150 m2/g and 10 parts by weight or less of carbon black based on 100 parts by weight of a rubber component comprising an epoxidized natural rubber, and a tire comprising thereof.

Abstract: At least partially hydrolyzed chlorosulfonated polyolefin elastomers containing 0.5-10 weight percent chlorine and 0.25 to 5 weight percent sulfur are prepared from low density polyethylene or from linear ethylene/alpha-olefin copolymer base resins having a ratio of weight average molecular weight (Mw) to number average molecular weight (Mn) less than 3.5.

Abstract: A core-first method is provided for making a core-shell nanoparticle that includes the following steps: adding to a solvent, a mono-vinyl monomer cross-linked with a cross-linking agent to form the core of the nanoparticle, the core having an average diameter of 5 nanometers to about 10,000 nanometers, and the core having polymer chains with living ends; adding a charge agent comprising a fixed formal charge group onto the living ends of the core to form the shell of the nanoparticle; controlling the charge of the nanoparticle based on the type of charge agent, the quantity of the charge agent, or both the type of charge agent and the quantity of the charge agent. A core-shell nanoparticle is also provided.

Abstract: Disclosed herein are a homogeneous sulfur-modified polymer composition, a method of preparing sulfur-modified polymer, and an asphaltic concrete mixture.

Abstract: The invention provides methods for making copolymers and multi-arm block copolymers useful as drug delivery vehicles. The multi-arm block copolymers comprise a central core molecule, such as a residue of a polyol, and at least three copolymer arms covalently attached to the central core molecule, each copolymer arm comprising an inner hydrophobic polymer segment covalently attached to the central core molecule and an outer hydrophilic polymer segment covalently attached to the hydrophobic polymer segment, wherein the central core molecule and the hydrophobic polymer segment define a hydrophobic core region. The solubility of hydrophobic biologically active agents can be improved by entrapment within the hydrophobic core region of the block copolymer. The invention further includes pharmaceutical compositions including such block copolymers, pharmaceutical compositions, and methods of using the block copolymers as drug delivery vehicles.

Abstract: At least partially neutralized chlorosulfonated ethylene/alpha-olefin elastomers containing 0.5-10 weight percent chlorine and 0.25 to 5 weight percent sulfur are prepared from ethylene/alpha-olefin copolymer base resins having a ratio of weight average molecular weight (Mw) to number average molecular weight (Mn) less than 3.5.

Abstract: An easily recyclable cross-linked isotactic polypropylene that is additionally miscible with polyethylene is formed from a chemical reaction of combining a polymer, sulfur, peroxide, an accelerator, and at least one additive. The polymer can be mixtures of isotactic polypropylene homopolymer with an elastomer; mixtures of isotactic polypropylene homopolymer with thermoplastic-based mixes; mixtures of isotactic polypropylene copolymer with an elastomer; mixtures of isotactic polypropylene copolymer with thermoplastic-based mixes; or combinations thereof. The accelerator can be a sulfur accelerator.

Abstract: A method for preparing reversibly cross-linked isotactic polypropylene having a degree of crystallinity substantially identical to a degree of crystallinity of a starting polypropylene by mixing in the presence of heat, a polymer of isotactic polypropylene homopolymer; isotactic polypropylene copolymer; mixtures of isotactic polypropylene homopolymer and copolymer with an elastomer, an organic peroxide, and an accelerator, forming macro-radicals; the simultaneously coupling the macro-radicals with a sulfur obtaining an optimum cross-linking degree and a product made by the method.

Abstract: An article of manufacture made of an isotactic polymer, a cross-linking agent, and an accelerator. The cross-linking agent includes a peroxide and a sulfur. The peroxide has an activity ranging from about 40% to about 100%. The ratio of the accelerator to the sulfur ranges from about 1:4 to about 1:10 depending on the activity, and the ratio of the accelerator to the peroxide ranges from about 1:4 to about 1:10 depending on the activity. The article is formed by mixing the polymer, the cross-linking agent, and the accelerator at high shear rates forming a blend. The blend is heated and sent through an extruder at a temperature less than 140 degrees Celsius for less than one minute. The blend is then inserted into a molding, wherein the formed article comprises a resilience value up to about 50 KJ/m2.

Abstract: The invention provides methods for making copolymers and multi-arm block copolymers useful as drug delivery vehicles. The multi-arm block copolymers comprise a central core molecule, such as a residue of a polyol, and at least three copolymer arms covalently attached to the central core molecule, each copolymer arm comprising an inner hydrophobic polymer segment covalently attached to the central core molecule and an outer hydrophilic polymer segment covalently attached to the hydrophobic polymer segment, wherein the central core molecule and the hydrophobic polymer segment define a hydrophobic core region. The solubility of hydrophobic biologically active agents can be improved by entrapment within the hydrophobic core region of the block copolymer. The invention further includes pharmaceutical compositions including such block copolymers, pharmaceutical compositions, and methods of using the block copolymers as drug delivery vehicles.

Abstract: The instant invention provides a two-step polymerization process for preparing amphiphilic poly(N-vinyl-2-pyrrolidone), (PVP)-block-polyester copolymers and other diblock and triblock copolymers consisting of PVP as one block. The block copolymers of the invention can be used as vehicles for drug delivery.

Abstract: According to the present invention, a water absorbent material and materials to be sucked included in a water permeable bag type member form a water absorber. Thus, the water absorber is small both in weight and volume upon its transportation, and accordingly, the water absorber can be rapidly conveyed in large quantities without depending on a human power. The water absorber absorbs water upon its use to adequately satisfy a function of a form traceability for weight, volume and outline.

Abstract: A method for making isotactic polymer using a cross-linking agent entails introducing the cross-linking agent to a polymer and an accelerator. The cross-linking agent includes a peroxide and a sulfur. The peroxide has an activity ranging from about 40% to about 100%. The ratio of the accelerator to sulfur or peroxide ranges from 1:4 to 1:10 depending on the activity of the peroxide. The method further entails shearing the polymer in a high shear rate mixer and initiating cross-linking with the peroxide, wherein the accelerator partially inhibits the cross-linking of the peroxide. The method ends by forming macro radicals during the cross-linking; and forming macromolecular chains of polymer with sulfur bridges without the need for high torque. The accelerator ensures that the cross-linking and the formation of sulfur bridges occur simultaneously.

Abstract: The invention relates to a method for vulcanizing caoutchouc or latex by adding a mixture M which contains a component a) from a1) 20 to 96% by weight of sulfur, a2) 4 to 80% by weight of a complexing agent, and optionally other additives b) to caoutchouc or latex and then vulcanizing the mixture. The inventive method is characterized in that the average particle size of the primary particles of component a) ranges from 0.05 to 20 ?m.

Abstract: This invention concerns the crosslinking of isotactic polypropylene, which has always been considered a non-crosslinkable polymer. Isotactic polypropylene crosslinking not only generates new uses but also the prospects of both economic and environmentally friendly mixing and recovery operations with other polymers. The crosslinking and interpenetrating polymer network (IPN) (as is the case with polypropylene/polyethylene mixture) provides both interesting properties and significant economic and environmentally friendly interest. The principle of the crosslinking mechanism is to create macro radicals and cause them to act immediately on sulphur before the reaction of peroxide termination. The mixing process used is extrusion; however, all other processes of transformation used for thermoplastics would be useful for subsequent industrial use.

Abstract: According to the present invention, a water absorbent material and materials to be sucked included in a water permeable bag type member form a water absorber. Thus, the water absorber is small both in weight and volume upon its transportation, and accordingly, the water absorber can be rapidly conveyed in large quantities without depending on a human power. The water absorber absorbs water upon its use to adequately satisfy a function of a form traceability for weight, volume and outline.

Abstract: A process for reducing odor emission in aqueous polymer dispersions and in polymer powders comprises admixing an aqueous dispersion of a polymer obtained by free-radical polymerization of one or more ethylenically unsaturated monomers, after conclusion of the polymerization, with an odor-reducing composition containing a) one or more water-soluble compounds selected from metal salts of copper(II), silver, aluminum, zinc and iron(III), potassium permanganate, imidazoline, and imidazoline derivatives, optionally in combination with b) one or more water-soluble reducing agents selected from ascorbic acid, isoascorbic acid, iron(II) salts, zinc formaldehydesulfoxylate and alkali metal formaldehydesulfoxylate, and optionally drying the thus treated aqueous polymer dispersion to form a polymer powder.

Abstract: Hetero-telechelic polymers having the formula: FG—(Q)d—Z—J—[A(R1R2R3)]x  (I) wherein FG is a protected or non-protected functional group; Q is a saturated or unsaturated hydrocarbyl group derived by incorporation of a compound selected from the group consisting of conjugated diene hydrocarbons, alkenylsubstituted aromatic hydrocarbons, and mixtures thereof; d is an integer from 10 to 200; Z is a branched or straight chain hydrocarbon group which contains 3-25 carbon atoms, optionally containing aryl or substituted aryl groups; J is oxygen, sulfur, or nitrogen; [A(R1R2R3)]x is a protecting group, wherein A is an element selected from Group IVa of the Periodic Table of Elements; R1, R2, and R3 are each independently selected from the group consisting of hydrogen, alkyl, substituted alkyl groups containing lower alkyl, lower alkylthio, and lower dialkylamino groups, aryl or substituted aryl groups containing lower alkyl, lower alkylthio, and lower dialkylam

Abstract: Hetero-telechelic polymers having the formula: FG—(Q)d—Z—J—[A(R1R2R3)]x  (I) wherein FG is a protected or non-protected functional group; Q is a saturated or unsaturated hydrocarbyl group derived by incorporation of a compound selected from the group consisting of conjugated diene hydrocarbons, alkenylsubstituted aromatic hydrocarbons, and mixtures thereof; d is an integer from 10 to 200; Z is a branched or straight chain hydrocarbon group which contains 3-25 carbon atoms, optionally containing aryl or substituted aryl groups; J is oxygen, sulfur, or nitrogen; [A(R1R2R3)]x is a protecting group, wherein A is an element selected from Group IVa of the Periodic Table of Elements; R1, R2, and R3 are each independently selected from the group consisting of hydrogen, alkyl, substituted alkyl groups containing lower alkyl, lower alkylthio, and lower dialkylamino groups, aryl or substituted aryl groups containing lower alkyl, lower alkylthio, and lower dialkylam

Abstract: The present invention involves a method of making a multiblock copolymer containing two or more types of sequences of derivatives of acrylic acid with at least one derivative being acrylic acid salt and at least one being acrylamide. The method includes: (e) in sequence, a first step being a catalytic reaction of nitrile groups in polyacrylonitrile dissolved in an inorganic aqueous solvent of polyacrylonitrile; and, (f) at least one subsequent step being at least one catalytic reaction of nitrile groups in absence of polyacrylonitrile solvents. The present invention also pertains to the products resulting from the method.

Abstract: Disclosed are sulfonated aromatic perfluorocyclobutane polymers meeting a condition selected from: a) the equivalent weight of the polymer is 5000 or less, and b) the proton conductivity of the polymer at 25° C. is 0.

Abstract: An elastomer composition including an elastomer having a functional group, and a compound having a functional group, in which corresponding functional groups form a cross-link by at least one of an ionic bond, a hydrogen bond, and Diels-Alder reaction with temperatures, i.e., by heating, while the cross-link is cleaved at around room temperature, forming and cleaving of the cross-link being reversible.

Abstract: The present invention involves a method of making a multiblock copolymer containing two or more types of sequences of derivatives of acrylic acid with at least one derivative being acrylic acid salt and at least one being acrylamide.

Abstract: A method of crosslinking polystyrene polymers and co-polymers for the formation of macroreticular materials of an Mc 30,000 to 50,000 is described. The materials forming an insoluble gel which is shaped in an extruder to 3 to 5 cm pieces and is subject to sulphonation with dense sulphuric acid, with oleum sulphuric acid with sulphur trioxide and with chlorosulphonic acid, and the introduction of sulphonic groups to a high density and with the introduction of nitric group and with the introduction of carboxylic group with the copolymer styrene-acrylonitrile.

Abstract: The present invention involves a method of making a multiblock copolymer containing two or more types of sequences of derivatives of acrylic acid with at least one derivative being acrylic acid salt and at least one being acrylamide. The method includes: (e) in sequence, a first step being a catalytic reaction of nitrile groups in polyacrylonitrile dissolved in an inorganic aqueous solvent of polyacrylonitrile; and, (f) at least one subsequent step being at least one catalytic reaction of nitrile groups in absence of polyacrylonitrile solvents.The present invention also pertains to the products resulting from the method.

Abstract: Elastomeric polymers that have been functionalized are shown to provide superior extruded profiles for use in vehicle sealing systems. Generally the polymers functionalized are the ethylene, -alpha-olefin, non-conjugated diene monomer terpolymers or ethylene, -alpha-olefin copolymers. The elastomeric polymers are functionalized with one or more of carboxylic acids, anhydrides, hydroxyl, epoxide or amine functionality. The functionalized elastomeric polymers are generally used in conjunction with non-functionalized elastomeric polymers. The functionalized elastomeric polymers provide superior adhesion to the additional components used to enhance functionality and/or aesthetics. Among the vehicle sealing systems discussed are glass run channels, inner belt line seals, outer belt line seals and door seals.

Abstract: New sulfur-vulcanizable, silica-reinforced tire rubber compositions and tires and tire parts, vulcanized and unvulcanized, made employing them are made with coupling agent compositions comprising a sulfur-containing norbornanyl silicon compound of the structure [Sy—R]n—SiX4−n wherein each X is chosen from monovalent hydrocarbon groups or hydrolyzable groups; y is 1 to 5 when y is 1 the compound is an episulfide, and when y is 2 to 5 the sulfur atoms form a polysulfide wherein each sulfur atom is bonded to another sulfur atom and the terminal valences of the polysulfide are bonded to vicinal carbon atoms; n is 1, 2 or 3; R is a polyvalent polycycloaliphatic hydrocarbon radical. Tires made with these compositions exhibit a desirable combination of properties, including reduced rolling resistance and road noise and maintained or improved modulus, wet traction and abrasion resistance.

Abstract: The present invention involves a method of making a multiblock copolymer containing two or more types of sequences of derivatives of acrylic acid with at least one derivative being acrylic acid salt and at least one being acrylamide.

Abstract: The invention relates to preparation of EPDM-based and EPR-based rubber compositions which are vulcanized with peroxide together with a specified combination of sulfur and acrylate co-agents. The invention further relates to articles having at least one component thereof.

Abstract: Perfluoroelastomer compositions comprising perfluoroelastomers having copolymerized units of tetrafluoroethylene, a perfluoro(vinyl ether), and a nitrile-containing cure site monomer are cured with compounds that are capable of generating ammonia at temperatures of 40° C.-330° C. to produce cured compositions having excellent thermal stability. The ammonia-generating compounds also act as cure accelerators in perfluoroelastomer compositions that incorporate other curing agents.

Abstract: The present invention is a method of making acrylonitrile copolymers having multi block structure comprising acrylic acid, acryl amids and acrylamidine hydrophilic groups in hydrophilic blocks and residual nitrile groups in hydrophobic blocks, by partial hydrolysis of polyacrylonitrile to a predetermined hydrolysis conversion at which the hydrolysis is self terminating by a process that improves quality and reduces product heterogeneity.

Abstract: Polar polymers having the following formula: FG-(Q)d-Rn-Z-J-[A(R1R2R3)]x   (I) wherein FG is H or a protected or non-protected functional group; Q is a polar hydrocarbyl group derived by incorporation of a polar compound selected from group consisting of esters, amides, and nitrites of acrylic and methacrylic acid, and mixtures thereof; d is an integer from 10 to 2000; R is a saturated or unsaturated hydrocarbyl group derived by incorporation of a compound selected from the group consisting of conjugated diene hydrocarbons, alkenylsubstituted aromatic hydrocarbons, and mixtures thereof; n is an integer from 0 to 5; Z is a branched or straight chain hydrocarbon group which contains 3-25 carbon atoms, optionally containing aryl or substituted aryl groups; J is oxygen, sulfur, or nitrogen; [A(R1R2R3)]x is a protecting group, in which A is an element selected from Group IVa of the Periodic Table of Elements; R1, R2, and R3 are each independently selected from the group consisting

Abstract: Hetero-telechelic polymers having the formula:FG--(Q).sub.d --Z--J--[A(R.sup.1 R.sup.2 R.sup.3)].sub.x (I)wherein FG is a protected or non-protected functional group; Q is a saturated or unsaturated hydrocarbyl group derived by incorporation of a compound selected from the group consisting of conjugated diene hydrocarbons, alkenylsubstituted aromatic hydrocarbons, and mixtures thereof; d is an integer from 10 to 200; Z is a branched or straight chain hydrocarbon group which contains 3-25 carbon atoms, optionally containing aryl or substituted aryl groups; J is oxygen, sulfur, or nitrogen; [A(R.sup.1 R.sup.2 R.sup.3)].sub.x is a protecting group, wherein A is an element selected from Group IVa of the Periodic Table of Elements; R.sup.1, R.sup.2, and R.sup.