Abstract: The present disclosure provides antibodies that specifically bind to botulinum neurotoxins (e.g., BoNT/A, BoNT/B, BoNT/C, BoNT/D, BoNT/E, BoNT/F, BoNT/G, etc.) and the epitopes bound by those antibodies. The antibodies and derivatives thereof that specifically bind to the neutralizing epitopes provided herein can be used to neutralize botulinum neurotoxin and are therefore also useful in the treatment of botulism.

Abstract: Embodiments herein report compositions of alpha-1 antitrypsin fusion polypeptides or peptide derivatives thereof. In certain embodiments, compositions and methods relate to generating a construct of use in pharmaceutically acceptable compositions to treat a subject in need of alpha-1 antitrypsin therapy or treatment. In other embodiments, compositions and methods disclosed herein concern linking alpha-1 antitrypsin or derivative thereof to an immune fragment.

Abstract: The present invention relates to a process for extraction of cassava starch. Particularly, the present invention relates to a process for extraction of cassava starch with a device. More particularly, the present invention relates to a process for extraction starch with a device and one or more enzymes.

Abstract: A process for preparing sugammadex sodium comprising: reacting a ?-cyclodextrin of formula I with a halogenating agent in the presence of N-methyl-2-pyrrolidone to provide a compound of formula II; and reacting the compound of formula II with 3-mercapto propionic acid in the presence of a sodium base and an organic solvent to provide sugammadex sodium formula III:

Abstract: An method for preparing an anion polymerization initiator, a device for preparing the same and an anion polymerization initiator prepared therefrom are provided. And the method for preparing an anion polymerization initiator according to present invention is characterized in that an amine compound of Formula 1 and/or Formula 2; an organometallic compound; and/or a conjugated diene compound are introduced in the form of a solution and reacted.

Abstract: A supported molded catalyst having increased hardness, the supported molded catalyst being capable of improving the long-term stability of a reaction for producing a conjugated diolefin by catalytic oxidative dehydrogenation from a mixed gas including a monoolefin having 4 or more carbon atoms and molecular oxygen; and a method for producing the catalyst is provided. A molded catalyst for conjugated diolefin production, the molded catalyst being a catalyst for producing a conjugated diolefin by a catalytic oxidative dehydrogenation reaction from a mixed gas including a monoolefin having 4 or more carbon atoms and molecular oxygen, and being produced by molding a composite metal oxide and a glass fiber-like inorganic auxiliary agent.

Abstract: Copolymerization of elemental sulfur with functional comonomers afford sulfur copolymers having a high molecular weight and high sulfur content. Nucleophilic activators initiate sulfur polymerizations at relative lower temperatures and in solutions, which enable the use of a wider range of comonomers, such as vinylics, styrenics, and non-homopolymerizing comonomers. Nucleophilic activators promote ring-opening reactions to generate linear polysulfide intermediates that copolymerize with comonomers. Dynamic sulfur-sulfur bonds enable re-processing or melt processing of the sulfur polymer. Chalcogenide-based copolymers have a refractive index of about 1.7-2.6 at a wavelength in a range of about 5000 nm-8????. The sulfur copolymer can be a thermoplastic or a thermoset for use in elastomers, resins, lubricants, coatings, antioxidants, cathode materials for electrochemical cells, dental adhesives/restorations, and polymeric articles such as polymeric films and free-standing substrates.

Abstract: Provided are a rubber composition for pneumatic tires with excellent fluidity and excellent degradation resistance, and a pneumatic tire formed from the rubber composition. The present invention relates to a rubber composition for pneumatic tires containing a rubber component including a halogenated butyl rubber, and an organic peroxide.

Abstract: A method for surface modification of nanoparticles includes the separate steps of removing ligands from the surface of the nanoparticles to form ligand-free nanoparticles, and mixing new ligands with the ligand-free nanoparticles to form modified nanoparticles.

Abstract: To provide a photopolymerizable composition which can be quickly cured by light of from 300 nm to 500 nm, and a cured product of which is less colored. A photopolymerizable composition comprising a compound having an anthracene skeleton represented by the following formula (1), a compound having a benzophenone skeleton and a radical polymerizable compound: wherein each of R1 and R2 which may be the same or different, is a C1-20 alkyl group, a C6-20 aryl group, an alkylcarbonyl group having a C1-20 alkyl group, an arylcarbonyl group having a C6-20 aryl group, an alkyloxycarbonyl group having a C1-20 alkyl group, or an aryloxycarbonyl group having a C6-20 aryl group, and each of X and Y which may be the same or different, is a hydrogen atom or a C1-8 alkyl group.

Abstract: The present invention is a curable composition characterized by including a 2-cyanoacrylate and a particle containing titanium oxide and silicon oxide. The preferable content of the particle is in a range from 0.1 to 10.0 parts by mass based on 100 parts by mass of the 2-cyanoacrylate.

Abstract: Disclosed herein is a process for producing polymers of an N-vinyl carboxamide, including the steps of flowing a reaction mixture containing an aqueous liquid containing at least one polymerisation initiator, N-vinyl carboxamide monomer or a monomer mixture containing N-vinyl carboxamide into a reactor system, and polymerising the monomer or monomer mixture to produce the polymer of a N-vinyl carboxamide. The polymers resulting therefrom may be hydrolysed to provide polymers containing vinyl amine units. Also disclosed herein is an apparatus suitable for producing the polymers.

Abstract: A method is provided to control the short chain branching (SCB) distribution of an ethylene-butene (EB) polyethylene resin that is prepared in a gas phase polymerization process using a specific type of magnesium-titanium Ziegler Natta catalyst. The method allows the level of short chain branching to be increased in the low molecular weight fraction of the resin by increasing the polymerization residence time. The polymers that are produced in accordance with this invention may be useful for the preparation of cast films and blown films, especially for stretch film applications.

Abstract: The present invention relates to ethylene-1-hexene-1-butene terpolymer and a film including the same. The ethylene-1-hexene-1-butene terpolymer according to the present invention has an optimized range of density and melt index and includes 1-hexene and 1-butene as comonomers, and can provide a polymer showing excellent properties by regulating the content ratio of the comonomers in a certain range. Therefore, the film prepared by using the same can be usefully used because it has excellent stickiness, processibility, and falling dart impact strength which are especially suitable for stretch films.

Abstract: The present invention provides a methacrylic resin composition for non-contact hot plate welding comprising a methacrylic resin comprising 80 to 99.9% by mass of a methacrylic acid ester monomer unit and 0.1 to 20% by mass of a unit of at least one additional vinyl monomer copolymerizable with the methacrylic acid ester monomer, wherein the methacrylic resin composition has a melt flow rate (MFR) of 2.5 g/10 min or lower at 230° C. at a load of 3.8 kg.

Abstract: UV-absorbing polymers are provided that have at least one anhydride repeating unit that is covalently attached to at least one UV-absorbing moiety selected from the group consisting of functionalized dibenzoylmethanes, benzophenone sulfonamides, triphenyl triazines, and combinations thereof. Also provided are formulations comprising the UV-absorbing polymers.

Abstract: The present invention relates to star polymer having a core made up of a crosslinked network of polymers derived from a mixture of one or more multi-functional monomers and one or more mono-functional monomers and where the star polymer has arms made of polymers derived from a mixture of one or more mono-functional monomers, where the star contains at least three arms bonded to the core. The invention further relates to lubricating compositions containing an oil of lubricating viscosity and the described star polymers as well as methods of lubricating a mechanical device with the described lubricating compositions.

Abstract: The present invention relates to a rapid assembled small-sized block polymer material with low quenching temperature and the preparation and application thereof. In particular, the present invention discloses a block copolymer, and glass transition temperature of the block copolymer is less than 120° C. The present invention also discloses the preparation and application of the block copolymer. The block copolymer can achieve excellent phase separation and rapid patterning at a lower annealing temperature (e.g. 80° C.) and a shorter annealing time (e.g. 30 s), and a photolithographic pattern with a very high resolution (e.g. 5 nm half-pitch) can be further obtained by etching, which provides a new photolithographic mean for further extension of Moore's Law to achieve semiconductor photolithography with a resolution of less than 10 nm, or even 5 nm (half-pitch).

Abstract: An elastomeric polymer, comprising (1) a hard segment in the amount of 10% to 60% by weight of the elastomeric polymer, wherein the hard segment includes a urethane, urea, or urethaneurea; and (2) a soft segment in the amount of 40% to 90% by weight of the elastomeric polymer, wherein the soft segment includes a polyisobutylene macrodiol and/or diamine. Additionally disclosed is a method of forming a polyisobutylene-based thermoplastic urethane, comprising the steps of (a) reacting a polyisobutylene macrodiol and/or diamine with a diisocyanate to form a first reaction mixture; (b) combining a metal catalyst and a chain extender with the first reaction mixture to create a second reaction mixture, a molar ratio of the metal catalyst to the diisocyanate being greater than 0.0:1 and less than or equal to 0.4:1; and (c) reacting the second reaction mixture for a period of time sufficient to form the polyisobutylene-based thermoplastic urethane.

Abstract: The present invention provides polymers and methods of preparing the same. In certain embodiments, the polymers comprise acrylate repeating units that have been derivatized (e.g., reduced and/or substituted) to form new polymeric structures. In certain embodiments, the polymers described herein self-assemble to form well-defined nanostructures. In some instances, the nanostructures exhibit relatively small d-spacing (e.g., a d-spacing value of 10 nm or less). Due to their properties, the polymers described herein are useful in a variety of applications including functional materials and biomedical applications.

Abstract: The invention provides a (meth)acrylic block copolymer that exhibits a high curing rate when irradiated with active energy rays and also has a low viscosity. The (meth)acrylic block copolymer includes a methacrylic polymer block (a1) and a methacrylic polymer block (a2) that each have an active energy ray curable group including a partial structure (1) of the following general formula (1), and further includes an acrylic polymer block (B) that has no active energy ray curable groups and is present between the methacrylic polymer block (a1) and the methacrylic polymer block (a2). The content of monomer units derived from methyl methacrylate relative to all monomer units in the methacrylic polymer block (a1) and the methacrylic polymer block (a2) is not less than 30 mass %. The content of monomer units derived from an alkyl acrylate ester having an alkyl group with 6 or more carbon atoms relative to all monomer units in the acrylic polymer block (B) is not less than 40 mass %.

Abstract: This invention relates to compositions and a process for stabilizing or solubilize a phenolic resin containing a mixture of linear phenolic resins and calixarenes. The process comprises contacting the phenolic resin with an epoxide, to at least partially alkoxylate the phenolic hydroxyl groups of the calixarenes. This process forms a stabilized or solubilized phenolic resin with an increased solubility in a hydrocarbon solvent.

Abstract: This invention relates to an alkoxylated calixarene resin comprising one or more modified calixarene alkoxylate compounds. The invention also relates to a process for preparing a solubilized alkoxylated calixarene resin comprising reacting a phenolic resin mixture, comprising linear phenolic resins and calixarene compounds having phenolic hydroxyl groups, with one or more epoxide-containing compounds to alkoxylate one or more of the phenolic hydroxyl groups of the calixarene compounds to form a solubilized phenolic resin mixture, and reacting the solubilized phenolic resin mixture with one or more alkylene oxides.

Abstract: A compound or a resin represented by the following formula (1).

Abstract: The invention relates to compositions and methods for solid freeform fabrication of medical devices, components and medical applications, in which the composition includes a thermoplastic polyurethane which is particularly suited for such processing. The useful thermoplastic polyurethanes are derived from (a) an aromatic diisocyanate component, (b) a polyol component, and (c) a chain extender component where the molar ratio of (c) to (b) is from 2.4 to 4.7.

Abstract: The invention relates to a process for producing a ring-opening polymerization product by reacting at least one polyisocyanate and 2-oxo-1,3-dioxolane-4-carboxylic acid and subjecting the reaction product to a temperature within the range of from about 40 to about 150° C. in the presence of a catalytic amount of at least one non-nucleophilic base. The obtained polymerization product may be present as a foam and is suitable as binder, insulation material, sealant or coating and in the production of mattresses or wound pads.

Abstract: The invention relates to compositions and methods for solid freeform fabrication of medical devices, components and applications in which the composition includes a thermoplastic polyurethane which is particularly suited for such processing. The useful thermoplastic polyurethanes are derived from (a) an aromatic diisocyanate component, (b) a polyol component, and (c) a chain extender component where the molar ratio of (c) to (b) is at least 4.25.

Abstract: The invention relates to an additive suitable for increasing compressive strength during the production of polyurethane soft foam, which contains at least one compound (V) containing, (i) more than three hydrogen atoms which are reactive with respect to isocyanates, (ii) an average hydroxyl number, determined according to DIN 53240-1: 2013-06, from 110-280 mg KOH/g, preferably 120-250 mg KOH/g, and (iv) >50 wt.-% ethylene oxide bound in the molecule, wt.-% with respect to the total alkylene oxide, and to a method for producing polyurethane foams and to a polyurethane foam and to the use thereof as described.

Abstract: A rigid polyurethane resin composition contains a polyisocyanate component containing polyphenylmethane polyisocyanate and alicyclic polyisocyanate, and a polyol component. In the polyisocyanate component, the ratio of an isocyanate group derived from the alicyclic polyisocyanate with respect to the total amount of an isocyanate group derived from the polyphenylmethane polyisocyanate and the isocyanate group derived from the alicyclic polyisocyanate is 10 to 70 mol %.

Abstract: The present invention relates to a polyisocyanate composition comprising a formation component having isocyanate groups, the isocyanate groups having been reacted to an extent of ?98% with at least one CH-acidic compound, characterized in that the formation component consists to an extent of ?51% by weight of at least one polyisocyanate based on pentamethylene 1,5-diisocyanate having a content of isocyanurate trimer of ?60 area %, based on the total weight of the polyisocyanates based on pentamethylene 1,5-diisocyanate, and the remaining proportion up to 100% by weight of the total amount of polyisocyanates present in the formation component consists of at least one aliphatic or cycloaliphatic polyisocyanate. The present invention further provides a one-component system comprising the polyisocyanate composition, a process for producing a coating on a substrate, and the coatings obtainable from the one-component system.

Abstract: This invention provides a new dicyclopentadiene phenol and 2,6-dimethyl phenol copolymer epoxy resin with excellent heat resistance, low dielectric constant Dk, low dissipation factor Df having the formula 1. Preparation of dicyclopentadiene phenol and 2,6-dimethyl phenol copolymer epoxy resin in two steps: Step 1, reacting (a1) dicyclopentadiene phenol resin represented by formula 2 with (a2) 2,6-dimethyl phenol in the presence of acid catalyst by (a3) aldehyde compounds to synthesize dicyclopentadiene phenol-2,6-dimethyl phenol copolymer, and Step 2, reacting dicyclopentadiene phenol and 2,6-dimethyl phenol copolymer with excess epichlorhydrin under NaOH condition to prepare dicyclopentadiene phenol and 2,6-dimethyl phenol copolymer epoxy resin.

Abstract: Methods for preparing pre-dynamic cross-linked polymer compositions are described. Methods of preparing dynamic cross-linked polymer compositions using pre-dynamic cross-linked polymer compositions are also described.

Abstract: Methods, compositions, reagents, and systems that allow for the preparation and utilization of sulfonamide salt polymer electrolytes are disclosed herein. Methods and reagents to prepare sulfonamide salt monomers are also disclosed herein. The sulfonamide salt polymer electrolytes can be used as components in energy storage devices, conductive materials, electrochemical cells, gels, adhesives, and drug delivery vehicles.

Abstract: The present invention relates to a process for producing a liquid composition comprising a functionalized ?-conjugated polythiophenes, comprising the process steps of i) providing a liquid phase comprising a) thiophene monomers of the general formula (I) wherein X,Y are identical or different and are O, S, or NR1, wherein R1 is hydrogen or an aliphatic or aromatic residue having 1 to 18 carbon atoms; A is organic residue carrying an anionic functional group; b) an oxidizing agent; and c) a solvent; ii) oxidatively polymerizing the thiophene monomers of the general formula (I) to obtain a liquid composition comprising functionalized ?-conjugated polythiophenes; wherein (?1) the pH of the liquid phase provided in process step i) is adjusted to a value below 7.0, wherein the pH is determined at a temperature of 20° C.; and (?2) the chloride content of the liquid phase provided in process step i) is less than 10000 ppm, based on the total weight of the liquid phase.

Abstract: A low chromatic aberration polyester different-shrinkage composite yarn is made of polyester POY yarn and polyester FDY composite yarn. The polyester POY yarn and polyester FDY yarn is obtained by spinning the polyester solution, the rupture strength of the low color polyester different-shrinkage composite yarn is ?1.9 cN/dtex, the elongation at break is 30.0±5.0%, the crimp shrinkage is 2.50±3.0%, the network degree is 20±5/m, the color difference ?E is less than 0.200. In the invention, the magnesium ethylene glycol is relatively mild, the thermal degradation coefficient is small, the oligomers in the polymerization process is reduced, and the oligomers in the dissolution process are further reduced, so that the appearance of stains and streaks reduces during the dyeing and post-processing heat setting of the polyester fiber, which ensures the fiber's leveling and rubbing fastness.

Abstract: An ultra-high IV polyester suitable for high melt strength end-uses, such as injection blow molding, pipe extrusion, profile extrusion, and extrusion blow molding, is provided, having IV of greater than 0.9; and a process for its production having high IV lift rate during SSP processing.

Abstract: The present disclosure relates to a dimer that includes a first hydroxyl-functionalized naphthalene group and a second hydroxyl-functionalized naphthalene group, where the first hydroxyl-functionalized naphthalene group and the second hydroxyl-functionalized naphthalene group are connected by a bridging group. The present disclosure also relates to a polymer synthesized using the dimer, as well as methods for synthesizing both the dimer and the polymer.

Abstract: To provide a polyarylene sulfide (hereinafter, PAS) manufacturing method and PAS manufacturing device that further eliminates processing costs in manufacturing PAS, by recovering from solid content containing an unreacted sulfur source and alkali metal halide produced as a byproduct the sulfur source and the solid content with a reduced amount of the sulfur source, and then conveniently and easily reusing the unreacted sulfur source without performing a large-scale process.

Abstract: Composition of comprising nano metal oxide/hydroxide particles and a polyorganosiloxane having increased refractive index, processes to cure these compositions for making transparent coats, shaped articles by an extrusion or molding process having a refractive index above the refractive index of the polyorganosiloxane. Use of the cured polyorganosiloxane compositions as optical devices, coats, lenses or light guides.

Abstract: A silicone gel composition comprising: (A) branched organopolysiloxane having, on average, at least two alkenyl groups bonded to silicon atoms in a molecule, and a viscosity ranging from 10 to 10,000 mPa·s at 25° C.; (B) organohydrogenpolysiloxane; (C) platinum-based addition reaction catalyst; and (D) a reaction product of (d1) alkali metal silanolate with (d2) at least one ceric salt selected from cerium chloride and a carboxylic acid salt of cerium.

Abstract: In a polyurethane gel 1 including a gel layer 2 and a coat layer 3 covering the gel layer 2, the gel layer 2 is produced by allowing at least aliphatic polyisocyanate having an average functionality of more than 2.0 to react with polyol having an average functionality of 3.0 or less, and the coat layer 3 is produced by allowing at least aliphatic diisocyanate and/or alicyclic diisocyanate to react with bifunctional active hydrogen compound.

Abstract: Polyester-based resin particles including a polyester-based resin as a base resin, in which the base resin exhibits a plurality of endothermic peaks corresponding to crystal melting temperatures by DSC measurement, at least one of the endothermic peaks exists in each region of a low temperature side region and a high temperature side region, a maximum endothermic peak of the low temperature side region and a maximum endothermic peak of the high temperature side region exhibit a crystal melting heat amount ratio (low temperature side crystal melting heat amount/high temperature side crystal melting heat amount) in a range of 0.1 to 1.5, and the polyester-based resin particles have a volume average particle diameter of 1 to 50 ?m.

Abstract: A method for producing a coagulated article includes coagulating an aqueous urethane resin composition with a coagulant containing a metal salt and water and being heated to 40° C. or higher. A coagulated article having excellent texture can be obtained without using an organic solvent. Further, an organic solvent is not used for a coagulating bath, and therefore there is no fear of exposure to a harmful volatile substance or diffusion of the substance into the environment, and further the treatment of waste liquid of such a coagulating bath is easy, which contributes to suppression of the cost of production. Therefore, a coagulated article obtained by the method can be advantageously used in producing gloves, a coating material, a simulated leather sheet, and the like.

Abstract: A thermoplastic elastomer composition for crosslinked foam and the manufacturing method thereof are provided. The thermoplastic elastomer composition comprising (A) an ethylene-based copolymer; (B) a first copolymer; (C) a second copolymer, wherein the component (B) and (C) are copolymers comprising a vinyl aromatic monomer and a conjugated diene monomer, the first copolymer having a conjugated diene hydrogenation rate of at least 80% and the second copolymer having a conjugated diene hydrogenation rate of no more than 10%; (D) an organic peroxide; and (E) a foaming agent, wherein a mass ratio (A/(B+C)) of the component (A) to a combination of the component (B) and the component (C) is 95/5 to 5/95; and a mass ratio (B/C) of the component (B) to the component (C) is 9/1 to 1/9. A crosslinked foam made from the composition and the manufacturing method thereof are also provided.

Abstract: The present invention provides a method of preparing a reinforced composite fabric. The method includes steps of: forming a high-hardness thermoplastic elastomeric yarn and a low-hardness thermoplastic elastomeric yarn with a melting point from 50° C. to 150° C. into a fabric; and hot-pressing the fabric under a hot-pressing temperature to form the reinforced composite fabric. The hot-pressing temperature is higher than or equal to the melting point of the low-hardness thermoplastic elastomeric yarn but lower than the melting point of the high-hardness thermoplastic elastomeric yarn. The present invention also provides a reinforced composite fabric made by the method. The reinforced composite fabric can be made by a simple and an eco-friendly process, and has the advantages of high tensile strength and high impact strength.

Abstract: The present disclosure relates to polyolefin compositions containing high concentrations of reinforcing fibers. The present disclosure also relates to methods of preparing such compositions from water based polyolefin dispersions. The present disclosure also relates to the preparation of compositions containing a desired level of reinforcing fibers.

Abstract: The invention relates to a method for welding a polyamide plastic and a poly(meth)acrylate—particularly a polymethyl methacrylate—plastic using a primer, said primer containing at least one copolymer synthesised from at least one styrene or styrene derivative and at least one maleic anhydride or maleic anhydride derivative. The invention also relates to correspondingly welded products.

Abstract: Provided is a water soluble film, and detergent packets comprising the film as an encasing material. The film contains a (meth)acrylic polymer that is a blend of a hard polymer and a soft polymer, and a plasticizer.

Abstract: The invention includes methods of reversibly tuning the effective pore size and/or solute rejection selectivity of a nanoporous lyotropic liquid crystal (LLC) polymer membrane. The membranes of the invention have high levels of pore size uniformity, allowing for size discrimination separation, and may be used for separation processes such as liquid-phase separations.

Abstract: A prepreg includes conductive fibers impregnated with a matrix resin, the prepreg having a conductive region where a conductive material is dispersed in the resin. In the present invention, a resin layer composed of at least the matrix resin preferably is present on one or both surfaces of a conductive fiber layer composed of at least the conductive fibers, and the conductive region is present at least in the resin layer. In addition, the above-described conductive region preferably is present continuously in the thickness direction. The conductive region preferably is a conductive region where the conductive material is dispersed in the matrix resin, and the resin in the conductive region preferably forms a continuous phase with the matrix resin in other regions. A volume resistivity of the conductive region preferably is 1/1,000 or less of that of other regions of the matrix resin.