Abstract: Processes and systems for making a poly(vinyl acetal) resin particles are provided. The processes and systems described herein utilize one or more methods, including, for example, slurry dilution and/or filtration of various process streams, to optimize the transport and recovery of the poly(vinyl acetal) resin particles. Systems and processes described herein facilitate increased production of the final resin product by minimizing product loss and maximizing on-line operation time and production flexibility.

Abstract: Processes and systems for making a poly(vinyl acetal) resin particles are provided. The processes and systems described herein utilize one or more methods, including, for example, slurry dilution and/or filtration of various process streams, to optimize the transport and recovery of the poly(vinyl acetal) resin particles. Systems and processes described herein facilitate increased production of the final resin product by minimizing product loss and maximizing on-line operation time and production flexibility.

Abstract: Polymers, and systems and methods for making and using the same are described herein. A polymer includes ethylene and at least one alpha olefin having from 4 to 20 carbon atoms. The polymer is formed by a trimmed catalyst system including a supported catalyst including bis(n-propylcyclopentadienyl) hafnium (R1)(R2) and a trim catalyst comprising meso-O(SiMe2Ind)2Zr(R1)(R2), wherein R1 and R2 are each, independently, methyl, chloro, fluoro, or a hydrocarbyl group.

Abstract: Polymerization reactor systems providing integrated liquid-solid sampling systems are disclosed. Methods for operating such polymerization reactor systems and for measuring a property of the liquid portion of liquid-solid mixture are described.

Abstract: Polymers, and systems and methods for making and using the same are described herein. A polymer includes ethylene and at least one alpha olefin having from 4 to 20 carbon atoms. The polymer has a melt index ratio (MIR) greater than about 40. The polymer also has a value for Mw1/Mw2 of at least about 2.0, wherein Mw1/Mw2 is a ratio of a weight average molecular weight (Mw) for a first half of a temperature rising elution (TREF) curve from a cross-fractionation (CFC) analysis to an Mw for a second half of the TREF curve. The polymer also has a value for Tw1?Tw2 of less than about ?15° C., wherein Tw1?Tw2 is a difference of a weight average elution temperature (Tw) for the first half of the TREF curve to a Tw for the second half of the TREF curve.

Abstract: Catalyst systems and methods for making and using the same. A method of polymerizing olefins to produce a polyolefin polymer with a multimodal composition distribution, includes contacting ethylene and a comonomer with a catalyst system. The catalyst system includes a first catalyst compound and a second catalyst compound that are co-supported to form a commonly supported catalyst system. The first catalyst compound includes a compound with the general formula (C5HaR1b)(C5HcR2d)HfX2. The second catalyst compound includes at least one of the following general formulas: In both catalyst systems, the R groups can be independently selected from any number of substituents, including, for example, H, a hydrocarbyl group, a substituted hydrocarbyl group, or a heteroatom group, among others.

Abstract: Catalyst systems and methods for making and using the same. A method of polymerizing olefins to produce a polyolefm polymer with a multimodal composition distribution, includes contacting ethylene and a comonomer with a catalyst system. The catalyst system includes a first catalyst compound and a second catalyst compound that are co-supported to form a commonly supported catalyst system. The first catalyst compound includes a compound with the general formula (C5HaR1b) (C5HcR24)HfX2. The second catalyst compound comprises the following formula: (A), wherein each R3 or R4 is independently H, a hydrocarbyl group, a substituted hydrocarbyl group, or a heteroatom group, wherein each R3 or R4 may be the same or different, and each X is independently a leaving group selected from a labile hydrocarbyl, a substituted hydrocarbyl, a heteroatom group, or a divalent radical that links to an R3 group.

Abstract: Ethylene/1-butene copolymers made with a single site catalyst system have high melt strength and good processability.

Abstract: Catalyst and solid component of catalyst for the (co)polymerization of ethylene, comprising titanium, magnesium, chlorine, a protic organo-oxygenated compound Dp and a neutral aprotic electron-donor compound D, in the following molar ranges: Mg/Ti=1.0-50; D/Ti=1.0-15; Cl/Ti=6.0-100; Dp/D=0.05-3; and a process for obtaining said component.

Abstract: Provided is an ethylene copolymer having 40 wt. % to 70 wt. % of units derived from ethylene and at least 30 wt. % of units derived from at least one ?-olefin having 3 to 20 carbon atoms and has the following properties: (a) a weight-average molecular weight (Mw), as measured by GPC, in the range of about 50,000 to about 200,000 g/mol; (b) a melting point (Tm) in ° C., as measured by DSC, that satisfies the relation: Tm>3.4×E?180 where E is the weight % of units derived from ethylene in the copolymer; (c) a ratio of Mw/Mn of about 1.8 to about 2.5; (d) a content of Group 4 metals of no more than 5 ppm; and (e) a ratio of wt ppm Group 4 metals/wt ppm Group 5 metals of at least 3. Also provided are methods for making an ethylene copolymer and compositions comprising an ethylene copolymer.

Abstract: The purpose of the present invention is to obtain an ethylene•?-olefin•non-conjugated polyene copolymer that has a low permanent compression set at low temperatures, is flexible, and has an excellent balance of rubber elasticity at low temperatures and tensile strength at normal temperatures. This ethylene-based polymer is an ethylene•?-olefin•non-conjugated polyene copolymer that includes units derived from ethylene (A), units derived from an ?-olefin (B) containing 4-20 carbon atoms, and units derived from a non-conjugated polyene (C) and satisfies (1)-(4). (1) The molar ratio of (A) to (B) is 40/60-90/10, (2) the contained amount of the units derived from (C) is 0.1-6.0 mol %, (3) ML(1+4)125° C. is 5-100, and (4) the B value is 1.20 or more.

Abstract: An aqueous perfluoroelastomer dispersion and method for producing a perfluoroelastomer using a specific fluorosurfactant and capable of achieving a sufficient number of particles and a sufficient polymerization rate. The method includes providing an aqueous dispersion containing perfluoroelastomer particles by emulsion-polymerizing a perfluoromonomer in an aqueous medium in the presence of a specific fluorosurfactant in an amount of 2 parts by mass or more for 100 parts by mass of the aqueous medium.

Abstract: The present invention provides a resist or a compound for use as a resist, which is highly sensitive and well-balanced without losing the fundamental physical properties required as a chemically amplified resist (e.g., resolution, line edge roughness (LER)). The present invention is directed to a (meth)acrylate compound represented by general formula (1) and a process for preparation thereof, as well as a (meth)acrylic copolymer obtainable by polymerization of the (meth)acrylate compound of general formula (1) and a photosensitive resin composition thereof: (wherein R1 represents a hydrogen atom or a methyl group, R2 represents a linear or branched alkyl group containing 2 to 4 carbon atoms, and each R3 may be the same or different and represents a group represented by the following formula (2) or (3), etc.) (provided that formulae (2) and (3) are as defined in the specification of the present application).

Abstract: The actinic ray-sensitive or radiation-sensitive resin composition of the present invention contains a resin (P) including a repeating unit (i) having a group which decomposes by the action of an acid represented by the following General Formula (1), a pattern forming method using the composition, a method for manufacturing an electronic device, and an electronic device.

Abstract: Processes and systems for making a poly(vinyl acetal) resin particles are provided. The processes and systems described herein utilize one or more methods, including, for example, slurry dilution and/or filtration of various process streams, to optimize the transport and recovery of the poly(vinyl acetal) resin particles. Systems and processes described herein facilitate increased production of the final resin product by minimizing product loss and maximizing on-line operation time and production flexibility.

Abstract: Processes and systems for making a poly(vinyl acetal) resin particles are provided. The processes and systems described herein utilize one or more methods, including, for example, slurry dilution and/or filtration of various process streams, to optimize the transport and recovery of the poly(vinyl acetal) resin particles. Systems and processes described herein facilitate increased production of the final resin product by minimizing product loss and maximizing on-line operation time and production flexibility.

Abstract: In one or more embodiments, the present invention provides a novel approach to the addition of plasticizers for softening TPUs, i.e., lowering the durometer and the melt viscosity. This approach involves incorporating bonded sulfonate groups with quaternary ammonium counterions into the TPU. In one or more embodiments of the present invention, the softening of TPU is achieved by incorporating an ionic diol, such as N,N-bis (2-hydoxyethyl)-2-aminoethane-sulfonic acid (BES), coupled with various bulky alkyl ammonium cations, during the chain extension step of the TPU synthesis. It is believed that that steric hindrance of the bulky quaternary ammonium groups weakens the dipole-dipole interactions of the sulfonate groups and/or lowers the crystallinity of the hard block, thereby creating additional free volume that softens the polymer and lowers the melt viscosity.

Abstract: Tertiary amine catalysts having isocyanate reactive groups that are capable of forming thermally stable covalent bonds able to withstand temperatures up to 120° C. are disclosed. These catalyst can be used to produce polyurethane foam having the following desirable characteristics: a) very low chemical emissions over a wide range of environmental conditions and isocyanate indexes (e.g. indexes as low as 65 but higher than 60) while meeting all physical property requirements; b) sufficient hydrolytic stability to maintain the catalyst covalently bound to foam without leaching of tertiary amine catalyst when foam is exposed to water or aqueous solutions even at temperatures higher than ambient (temperature range 25° C. to 90° C.

Abstract: The invention relates to a chemically degradable cured epoxy resin system containing one or more epoxide resins and one or more curing agents, characterized in that the curing agent contains at least one cyanate, with which the epoxy resin reacts to form an epoxy resin polymer containing cyanurates.

Abstract: A two-component curable epoxy resin system having an epoxy component containing a unique combination of two or more epoxy resins with at least one of the epoxy resins being an epoxy novolac type resin. The composite made from such resin system exhibits high glass transition temperature.

Abstract: The present invention relates to polyester polyols obtainable or obtained by esterification of 10 to 70 mol % of at least one compound from the group consisting of terephthalic acid (TPA), dimethyl terephthalate (DMT), polyethylene terephthalate (PET), phthalic anhydride (PA), phthalic acid and isophthalic acid, 0.1 to 30 mol % of one or more fatty acids and/or fatty acid derivatives, 10 to 70 mol % of one or more aliphatic or cycloaliphatic diols having 2 to 18 carbon atoms or alkoxylates thereof, 5 to 70 mol % of a polyether polyol prepared by alkoxylating an aromatic starter molecule having a functionality of not less than 2, and of 0 to 70 mol % of a tri- or polyol other than the polyether polyol, all based on the total amount of the components used, wherein the amounts used of the components add up to 100 mol %.

Abstract: The present invention relates to a method for producing a carbonate compound and methacrylic acid or an ester thereof, containing a step (a1) of obtaining hexachloroacetone and hydrogen chloride from acetone and chlorine molecule, a step (a2) of obtaining a dialkyl carbonate and chloroform from hexachloroacetone and an alkyl alcohol, a step (b1) of obtaining 1,1,1-trichloro-2-methyl-2-propanol from chloroform and acetone, a step (b2+b3 or b4) of obtaining methacrylic acid or an ester thereof and hydrogen chloride from 1,1,1-trichloro-2-methyl-2-propanol and water or an alcohol, and a step (c1 or c2) of obtaining chlorine molecule by reacting hydrogen chloride with oxygen molecule.

Abstract: The present invention provides novel catalysts of formula (I), where M1 and M2 are different and are independently selected from Mg, Zn, Fe, Co, Al and Cr, and catalyst systems comprising these catalysts. The invention also relates to the use of the inventive catalysts and catalyst systems to catalyse the reaction between i) carbon dioxide and an epoxide, ii) an epoxide and an anhydride, or iii) a lactide and/or a lactone. The invention also relates to a method for producing a catalyst of formula (I).

Abstract: The invention is directed to a fluorescent dye according to the general formula I: with C is a core moiety comprising 20 to 200 atoms; S same or different ether residues comprising 1 to 10 carbon atoms; n is an integer ranging from 2 to 500; m is an integer ranging from 0 to 500; x is an integer ranging from 2 to 50; y is an integer ranging from 1 to 50; R same or different residue comprising a reactive group capable of forming a covalent bond with a biomolecule; F same or different fluorophores covalently bound to (S)n. The fluorescent dyes can be conjugated to a biomolecule and used for flow cytometry and/or by fluorescence microscopy.

Abstract: The present invention relates to a process for producing nylon-6,6 by a) providing a muconic acid starting material selected from muconic acid, esters of muconic acid, lactones of muconic acid and mixtures thereof, b) subjecting the muconic acid starting material provided in step a) at least to some extent to a reaction with hydrogen in the presence of at least one hydrogenation catalyst Hb) to give adipic acid, c1) subjecting the muconic acid starting material provided in step a) to some extent to a reaction with hydrogen in the presence of at least one hydrogenation catalyst Hc1) to give 1,6-hexanediol, or c2) subjecting the adipic acid obtained in step b) to some extent to a reaction with hydrogen in the presence of at least one hydrogenation catalyst Hc2) to give 1,6-hexanediol, d) subjecting the 1,6-hexanediol obtained in step c1) or c2) to amination in the presence of an amination catalyst to obtain hexamethylenediamine, e) subjecting the hexamethylenediamine obtained in step d) and at least a portion o

Abstract: Flame retardant polyesters obtainable by reacting an aromatic or aliphatic dicarboxylic acid and/or ester of anhydride thereof, with an aliphatic polyol or mixtures thereof and with melamine, are provided. Methods of making said polyesters are also provided.

Abstract: Compositions and methods for the production of siloxane materials using an azaphosphatrane as a catalyst. In one embodiment, there is provided a process for the ring opening polymerization of a cyclosiloxane in the presence of an azaphosphatrane. In another embodiment, there is provided a composition and method for condensation curing of a moisture curable composition using an azaphosphatrane.

Abstract: A curable silicone composition comprising: (A) an organopolysiloxane represented by the average unit formula: (R13SiO1/2)x(R22SiO2/2)y(R3SiO3/2)z (R1 are alkyl groups, alkenyl groups, aryl groups, or aralkyl groups; R2 are alkyl groups or alkenyl groups; R3 is an alkyl group, aryl group, or an aralkyl group, provided that, in a molecule, at least 0.5 mol % of R1 to R3 are the alkenyl groups, at least one of R3 is the aryl group or the aralkyl group; and x, y and z are numbers satisfying: 0.01?x?0.5, 0.01?y?0.4, 0.1?z?0.9, and x+y+z=1); (B) a straight-chain organopolysiloxane having at least two alkenyl groups in a molecule; (C) an organopolysiloxane having at least two silicon atom-bonded hydrogen atoms in a molecule; and (D) a hydrosilylation reaction catalyst. A cured product exhibiting excellent dispersibility of phosphor and having crack resistance is formed.

Abstract: A coalescent consisting essentially of a residue from a process for forming propyleneglycol phenyl ether, the coalescent consisting essentially of 65%-75% by weight, based on the weight of the residue, dipropyleneglycol phenyl ether, 8%-10% by weight, based on the weight of the coalescent, monopropyleneglycol phenyl ether, 4%-6% by weight, based on the weight of the coalescent, tripropyleneglycol phenyl ether, and 0.1%-10% by weight, based on the weight of the coalescent, alkalinity(reported as NaOH) is provided. Also provided is a method for forming certain low-VOC, low cost, coalesced aqueous polymeric dispersions including, as copolymerized units, from 70% to 100% by weight, based on the solids weight of the aqueous polymeric dispersion, vinyl acetate monomer and an aqueous coating composition including the coalesced aqueous polymeric dispersion.

Abstract: The invention relates to a method to reduce or prevent agglomeration of rubber particles in aqueous media by LCST compounds and elastomers obtained thereby. The invention further relates to elastomer products comprising the same or derived therefrom.

Abstract: Methods and compositions are provided for preparation of thermoplastic gels. The compositions have a base composition including a thermoplastic gel and a softener oil and the gel has a hardness between 15 Shore 000 and 65 Shore 000. The gel may also include an additive, such as a mineral filler, an anti-tack agent, and a mixture of a mineral filler and an anti-tack agent. The softener oil may be a high molecular weight oil having a molecular weight greater than about 250 g/mol.

Abstract: The present invention provides a method for granulating a polyamide or a polyamide composition, whereby it becomes possible to granulate even a polyamide that has such a melt viscosity that the polyamide cannot be pelletized into a strand-like shape easily. In the present invention, a polyamide, whose melt viscosity at glass transition temperature+160° C. and a shear rate of 100 s?1 is 3 Pa·s to 200 Pa·s and whose terminal amino group concentration is 5 ?eq/g to 70 ?eq/g, is melted by heating to a range of glass transition temperature+160° C. to glass transition temperature+180° C. of the polyamide, and then is solidified by dropping the molten polyamide in the form of granules onto a metallic belt, thereby producing granules.

Abstract: The present disclosure provides a core-shell nanocomposite material comprising an intrinsically conductive polymer (ICP) and surface-modified cellulose nanocrystals (CNCs) as well as synthesis for preparing same and its use thereof in various applications.

Abstract: Provided is a method of producing a masterbatch, in which a reduction in the viscosity of a polyester resin is inhibited and thereby a metal salt compound can be incorporated in a large amount. This method is a method of producing a masterbatch that comprises 0.4 to 10 parts by mass of at least one metal salt compound selected from the group consisting of metal benzoates, metal aliphatic carboxylates, metal aromatic phosphates, metal salts of sulfonamide compounds and metal salts of sulfonimide compounds with respect to 100 parts by mass of a polyester resin, wherein when the polyester resin and the metal salt compound are fed to an extruder and kneaded, the cylinder temperature of the extruder is controlled in a range of (the melting point of the polyester resin—60° C.) to (the melting point of the polyester resin—10° C.).

Abstract: Carbon fiber reinforced plastic (“CFRP”) composite layups and processes for manufacturing CFRP composite layups that integrate z-conductivity features directly into CFRP composite layups during the manufacturing processes for lightning protection, more particularly, inherent edge glow protection from lightning direct effects, and electrical current flow path control. CFRP composite layups are configured during the manufacturing processes to provide inter-ply electrical connections between composite plies of the CFRP composite layups, therefore avoiding the need for add-on protection features that result in significant cost and weight penalties.

Abstract: A multi-layered nanocomposite film for use in packaging is provided. More particularly, the film contains at least one core layer positioned adjacent to at least one outer layer. For example, in one embodiment, the film contains a core layer that is positioned between two outer layers. The core layer(s) and/or outer layer(s) may be formed from a polymer composition that contains an ethylene polymer, nanoclay having an organic surface treatment, and a compatibilizer that includes an olefin component and a polar component.

Abstract: A heat-shrinkable polyester film comprising ethylene terephthalate as a main component, containing not less than 0 mol % and not more than 5 mol % of a monomer component capable of serving as an amorphous component relative to the total of a polyester resin component, and having a main shrinkage direction in a lengthwise direction, wherein the heat-shrinkable polyester film satisfies heat shrinkage characteristics of the width direction and the lengthwise direction and the molecular orientation angle difference which is a difference between a molecular orientation angle of an edge of one end in the width direction and a molecular orientation angle of an edge of the other end.

Abstract: There is provided herein a method of making hydroxymethylphosphonate comprising reacting paraformaldehyde, at least one dialkyl phosphite and at least one trialkyl phosphite, in the presence of at least one amine catalyst

Abstract: A composition for and method of making extruded polystyrene (XPS) foam is provided. The composition includes enhanced concentrations of graphite as an infrared attenuation agent to achieve an XPS foam having an improved thermal insulation performance, while still maintaining a low content of open cells in the XPS foam.

Abstract: Molecularly imprinted polymers (MIPs) are materials exhibiting molecular recognition of a target molecule. MIPs are synthesized in the presence of an aflatoxin template, a mimic to the targeted molecule, used as an imprint that is further washed away with suitable solvent after completion of the polymerization process, leaving a cavity in the polymer of the same stereochemistry, functionality and morphology to the template. When the MIP encounters an aflatoxin, the molecule is bound in the cavity with a receptor-like affinity.

Abstract: The present invention relates to an open-cell foam composition, a hydrophobic open-cell foam prepared using the composition, and a method for preparing the hydrophobic open-cell foam. Specifically, the present invention provides an open-cell foam composition and a method for preparing a hydrophobic open-cell foam having hydrophobicity/oleophobicity and improved heat resistance as a result of partially or completely coating the surface of the inner framework structure of an open-cell foam, prepared using the composition, with silica gel, in which the method comprises continuously and efficiently preparing a melamine foam from a resin.

Abstract: The present invention relates to a process for recovering individual polymers, such as nylon and polyolefin, from a nylon-containing source such as a carpet. The process includes the steps of shredding a nylon fiber source such as a carpet wherein the shredding is conducted in the presence of a liquid that wets the carpet, granulating the wet shredded carpet slurry, further diluting the granulated slurry by adding additional water, subsequently refining the fibers and removing substantial amounts of polypropylene fibers from the slurry, preferably using a lamella clarifier, and recovering the nylon fibers by hydrocloning the slurry.

Abstract: A method is provided for preparing a reprocessed rubber from thermoset rubber particles. The method comprises the steps of: providing a plurality of thermoset rubber particles; inducing dynamic swelling and dynamic compatibilization of the plurality of rubber particles; admixing at least one de-linking agent with the swelled and wetted rubber particles; and wherein the method is further characterized in that the step of admixing the at least one de-linking agent is carried out under thermo-mechanical mixing.

Abstract: A process to enhance the chemical recycling of polyurethane foam comprises improving the process of grinding (which is a necessary precursor to chemolysis reactions), by employing a wetting process, concurrent with grinding, which reduces the loss of foam during grinding process.

Abstract: A novel rubber composition is provided, which contains an EPDM, a peroxide crosslinking. agent and amorphous silica in combination, and can be imparted with a light color such as white or a non-black color and formed into a sheet conveying roller excellent in mechanical properties because the crosslinking of the EPDM is not inhibited. A sheet conveying roller formed from the rubber composition is also provided. The rubber composition contains a rubber component including an EPDM, a peroxide crosslinking agent, not less than 10 parts by mass of amorphous silica based on 100 parts by mass of the rubber component, and calcium carbonate. The sheet conveying roller (1) is formed from the rubber composition.

Abstract: Plasticized compositions comprising polyamide or polyamide/ionomer blend and poly(trimethylene ether) glycol are provided. Also articles prepared from these compositions are provided.

Abstract: A resin composition comprising 100 parts by mass of a polymer (A) and 0.5 parts to 60 parts by mass of a high dielectric material (B), the high dielectric material (B) having a relative dielectric constant at 20° C. of 10 or more, a melting point of 45° C. or lower, and a boiling point of 150° C. or higher.

Abstract: This invention relates to the use of a composition of aliphatic esters having the following general formula: R1—O—C(O)—R4—C(O)—[—O—R2—O—C(O)—R5—C(O)—]m—O—R3 in which: R1 is selected from one or more of the groups consisting of H, linear and branched saturated and unsaturated alkyl residues of the C1-C24 type, and polyol residues esterified with C1-C24 monocarboxylic acids; R2 comprises —CH2—C(CH3)2—CH2— and C2-C8 alkylene groups, and comprises at least 50% in moles of the said —CH2—C(CH3)2—CH2— groups; R3 is selected from one or more of the groups consisting of H, linear and branched saturated and unsaturated alkyl residues of the C1-C24 type, and polyol residues esterified with C1-C24 monocarboxylic acids; R4 and R5 comprise one or more C2-C22 alkylenes and comprise at least 50% in moles of C7 alkylenes; m lies between 1 and 20, as plasticizers for polymer compositions.

Abstract: Provided is a vinyl chloride resin composition for powder molding that can provide a molded product having superior flexibility at low temperatures. The vinyl chloride resin composition for powder molding includes (a) vinyl chloride resin particles, (b) a plasticizer, and (c) vinyl chloride resin fine particles having an average degree of polymerization of at least 1,000 and no greater than 5,000.

Abstract: The present disclosure is directed to a base film having a thickness from 8 to 152 microns, a 60 degree gloss value from 2 to 35, an optical density greater than or equal to 2 and a dielectric strength greater than 1400 V/mil. The base film comprises a chemically converted (partially or wholly aromatic) polyimide in an amount from 63 to 96 weight percent of the base film. The base film further comprises a pigment and a matting agent. The matting agent is present in an amount from 1.6 to 10 weight percent of the base film, has a median particle size from 1.3 to 10 microns, and has a density from 2 to 4.5 g/cc. The pigment is present in an amount from 2 to 35 weight percent of the base film. The present disclosure is also directed to coverlay films comprising the base film in combination with an adhesive layer.