Abstract: This invention describes a method of conjugating a cell binding agent such as an antibody with an effector group (e.g., a cytotoxic agent) or a reporter group (e.g., a radionuclide), whereby the reporter or effector group is first reacted with a bifunctional linker and the mixture is then used without purification for the conjugation reaction with the cell binding agent. The method described in this invention is advantageous for preparation of stably-linked conjugates of cell binding agents, such as antibodies with effector or reporter groups. This conjugation method provides in high yields conjugates of high purity and homogeneity that are without inter-chain cross-linking and inactivated linker residues.

Abstract: The present disclosure provides bispecific proteins that bind to two antigens, as well as their compositions, uses, and methods of making.

Abstract: Provided are hypromellose acetate succinate (HPMCAS) which exhibits high solubility and can suppress generation of undissolved materials when dissolved in a solvent; an HPMCAS-containing composition; and a method for producing the HPMCAS. More specifically, provided are HPMCAS having a ratio of 2-position MS to 3-position MS of 1.2 or less, wherein the 2-position MS means a molar substitution of hydroxypropyl group by which a hydrogen atom of a hydroxyl group on 2-position carbon of each glucose unit of the HPMCAS has been directly replaced, and the 3-position MS means a molar substitution of hydroxypropyl group by which a hydrogen atom of a hydroxyl group on 3-position carbon of each glucose unit of the HPMCAS has been directly replaced; a composition comprising the HPMCAS and a solvent; and the method for producing the HPMCAS.

Abstract: A functionalization is performed with a dissolved oligo- or polysaccharide derivative which contains at least one free functional group, especially an amino group, linked through a polar carbamate linkage and a spacer (X), according to the general formula I:

Abstract: A method of making natural polymer (nano)particles, comprises two immiscible phases and a surface active agent, wherein one phase includes a natural polymer source and ionic liquid; stirring the combined phases with surfactant to form a microemulsion; adjusting the ratios of ionic liquid, surfactant, and immiscible phase to determine a particular size of natural polymer nanoparticles; stirring antisolvent into the emulsion; diluting the emulsion; and washing and drying precipitated polymer (nano)particles from the emulsion. The immiscible phase comprises at least one of immiscible solvent, oil, or immiscible ionic liquid. The ionic liquid phase includes natural polymer dissolved in ionic solvent. The antisolvent is water, other protic solvent or additive. The emulsion is diluted with, more immiscible phase, 1-butanol, or a mutually miscible solvent, or oil. The emulsion is diluted with an excess of the volume of the emulsion.

Abstract: The present invention concerns methods of derivatizing sialic acids which may be present on glycan moieties. This can be of use in determining the glycosylation profiles of, for example, glycoproteins and glycolipids and the use of such methods in clinical analysis as well as biological development and control.

Abstract: The present invention provides a method for improved preparation of Sugammadex sodium.

Abstract: A process for preparing (1?6)-?-D-glucan. A large amount of (1?6)-?-D-glucan can be prepared from banana by using this process. The chemical structure of (1?6)-?-D-glucan is shown as Scheme 1. The yield of (1?6)-?-D-glucan is 3-16 g/kg (with a purity of 85%-95%). This process provides a feasible technique for extensive utilization of banana, and can improve the additional value of banana products. This process is helpful for the sustainable development of banana processing industry.

Abstract: Disclosed are a modified conjugated diene polymer and a method for preparing the same. The modified conjugated diene polymer and the method for preparing the same advantageously provide superior compatibility with an inorganic filler, heat generation, tensile strength and abrasion resistance, low fuel consumption and excellent resistance on wet roads.

Abstract: A rubber compound containing silicon dioxide for the production of tires and comprising a polymer base with a cross-linkable unsaturated chain, a filler comprising silicon dioxide, a silane bonding agent and a vulcanization system. The filler further comprises a composite mineral consisting of a mineral of the zeolite family, onto which a layer of silicon dioxide has been deposited.

Abstract: The present invention relates to a method for preparing an acrylonitrile-butadiene-styrene graft copolymer having improved impact strength, which comprises: a step of preparing diene-based rubber latex by adding an acrylate-based cross-linking agent (Step 1); and a step of inserting the same cross-linking agent with the acrylate-based cross-linking agent, an aromatic vinyl-based compound and a vinyl cyan-based compound to the diene-based rubber latex and then subjecting thereof to graft copolymerization (Step 2), an acrylonitrile-butadiene-styrene graft copolymer prepared by the method, and an acrylonitrile-butadiene-styrene thermoplastic resin comprising the same.

Abstract: The invention covers a supported catalyst system prepared according to a process comprising the following step: i). impregnating a silica-containing catalyst support having a specific surface area of from 150 m2/g to 800 m2/g, preferably 280 m2/g to 600 m2/g, with one or more titanium compounds of the general formula selected from RnTi(OR?)m and (RO)nTi(OR?)m, wherein R and R? are the same or different and are selected from hydrocarbyl groups containing from 1 to 12 carbon and halogens, and wherein n is 0 to 4, m is 0 to 4 and m+n equals 4, to form a titanated silica-containing catalyst support having a Ti content of at least 0.1 wt % based on the weight of the Ti-impregnated catalyst support wherein the supported catalyst system further comprises an alumoxane and a metallocene.

Abstract: A compound containing a structural unit derived from a novel vinyl ether compound. This compound contains a structural unit represented by formula (1), in which the rings (Z1, Z2, Y1, Y2) are aromatic hydrocarbon rings; X1 and X2 represent a single bond or —S—; R represents a single bond or a specific divalent group; R1a and R1b represent a single bond or a C1-4 alkylene group; R2a and R2b represent a specific substituent group such as a monovalent hydrocarbon group; R3a and R3b represent a cyano group, a halogen atom, or a monovalent hydrocarbon; m1 and m2 are integers of 0 or greater; n1 and n2 are integers of 0-4; V1 is a group represented by formulas (a1)-(a3); and V2 is a group represented by formulas (a1)-(a4). In formulas (a1)-(a4), * represents a bonding hand, while ** and *** represent a bonding hand with an oxygen atom.

Abstract: Catalyst systems and methods for making and using the same. A method for making a catalyst support includes forming a mixture of a support material and a fluoride donor. The mixture is added to a fluidized bed reactor. The mixture is fluidized to form a fluidized bed while maintaining a flow rate of a fluidizing gas of about 0.1 ft./sec at less than about 370° C. and greater than about 0.35 ft./sec at temperatures greater than about 370° C. The mixture is calcined to decompose the fluoride donor, forming a fluorinated support.

Abstract: The present invention relates to a process for producing polypropylene polymer composition by polymerizing propylene with a C4 to C8 a-olefin comonomer and with ethylene in a sequential polymerization process with at least two reactors connected in series in the presence of a solid Ziegler-Natta catalyst component being free of external carrier material and any phthalic compounds, and wherein the C4 to C8 a-olefin comonomer content in the propylene polymer composition is at least 4.5 wt-%.

Abstract: A process for preparing water-soluble homo- or copolymers comprising (meth)acrylamide by free-radical polymerization of an aqueous solution of monoethylenically unsaturated monomers comprising at least (meth)acrylamide in the presence of at least one stabilizer for prevention of polymer degradation by molecular oxygen. The stabilizer is preferably one selected from the group of sulfur compounds, sterically hindered amines, N-oxides, nitroso compounds, aromatic hydroxyl compounds and ketones, more preferably 2-mercaptobenzothiazole or a salt thereof.

Abstract: Disclosed herein are graphene quantum dot tagged paraffin suppressants such as graphene tagged paraffin inhibitors and paraffin dispersants and methods of making and using thereof. The graphene quantum dots are covalently bound to residues of paraffin inhibitors or dispersed with paraffin dispersants to form tagged paraffin suppressants active in inhibiting paraffin crystallization or dispersing crystalized paraffin wax in crude oils and compositions comprising crude oils. The dots can be tailored to fluoresce at wavelengths with minimized correspondence to the natural fluorescence of crude oils, enabling the measurement of the concentration of the paraffin suppressants in crude oils or compositions comprising crude oils.

Abstract: A curable composition contains a polymerizable compound and a polymerization initiator. The polymerization initiator initiates polymerization to cure the polymerizable compound. The curable composition further contains compounds having the following general formulae (1) and (2): wherein X1 is selected from a hydroxy group, a carboxy group, a sulfo group, an amino group, and an alkoxy group, l1 denotes an integer in the range of 0 to 7, m1 denotes an integer in the range of 1 to 5, and n1 denotes an integer in the range of 1 to 16, and X2 is selected from a hydroxy group, a carboxy group, a sulfo group, an amino group, and an alkoxy group, l2 denotes an integer in the range of 0 to 7, m2 denotes an integer in the range of 1 to 5, and n2 denotes an integer in the range of 1 to 16.

Abstract: A first composition (A) contains (i) at least one compound (I) selected from the group consisting of triallyl isocyanurate, and triallyl cyanurate, wherein the compound (I) is preferably triallyl isocyanurate, and (ii) at least one bis(alkenylamide) compound. A second composition (B) contains the first composition (A) and at least one polyolefin copolymer. The composition (B) is used for the production of a film for encapsulation of an electronic device, especially a solar cell.

Abstract: The invention provides polymers comprising repeating units derived from (a) from 16% by weight to about 35% by weight of said polymer of at least one N-vinyl lactam monomer; (b) at least one monomer selected from the group consisting of functionalized and unfunctionalized C1-C6 alkyl (meth)acrylates, C1-C6 alkyl (meth)acrylamides and combinations thereof; and (c) at least one monomer selected from the group consisting of functionalized and unfunctionalized C8-C30 branched alkyl (meth)acrylates, C8-C30 branched alkyl (meth)acrylamides, and combinations thereof; wherein the polymer has a glass transition temperature of greater than about 45° C. The invention further provides various compositions, such as, personal care, sun care, coatings, and pharmaceutical compositions comprising the polymers described herein. The invention furthermore provides water-resistant sun care compositions comprising the polymers described herein. Subscripts x, y and z are described herein.

Abstract: Synthesis and characterization of starch based pH-responsive nanoparticles for controlled drug delivery are described. Polymethacrylic acid grafted starch (PMAA-g-St) nanoparticles with various molar ratio of starch to MAA were synthesized by a new one-pot method that enabled simultaneous grafting of PMAA and nanoparticle formation in an aqueous medium. NMR data showed that polysorbate 80 was polymerized into the graft polymer. Nanoparticles were relatively spherical with narrow size distribution and porous surface morphology and exhibited pH-dependent swelling in physiological pH range. The particle size and magnitude of volume phase transition were dependent on PMAA content and formulation parameters such as surfactant levels, cross-linker amount, and total monomer concentration. The results showed that the new pH-responsive nanoparticles possessed useful properties for controlled drug delivery.

Abstract: A method of making flexible polyurethane foams mixes a polyol (a hydroxyl group containing compound) with a cesium and/or rubidium fluoride catalyst, and reacts such mixture with at least one isocyanate. The cesium and/or rubidium fluoride may be used as the sole catalyst, replacing the blowing and gelling catalysts, such as amines, and metallic catalysts, such as a tin catalyst. Or, the cesium and/or rubidium fluoride may be used as a catalyst promoter in combination with traditional amine blowing and gelling catalysts and tin catalysts. The resulting flexible polyurethane foams exhibit increased thermal conductivity and lower levels of volatile organic compound emissions.

Abstract: The present invention relates to novel aqueous polyurethane dispersions produced using at least two poly(tetramethylene glycol) polyether polyols with different average molar masses and at least two different polyisocyanate components.

Abstract: Epoxy curatives and two-part compositions comprising epoxy curative and epoxy resin parts are provided as well as methods of their use in liquid shim applications. Epoxy curatives comprise at least one cycloaliphatic polyamine curative and at least one second curative selected from a) an aliphatic polyamidoamine and b) an adduct of an excess of an unbranched polyetherdiamine with an epoxy resin.

Abstract: Disclosed are methods for preparing and collecting a polyaromatic compound. Also disclosed are products comprising a polyaromatic compound.

Abstract: A process for making oligomers of polybutylene terephthalate (PBT) with desirable intrinsic viscosity and carboxylic end group concentrations includes combining 1.4-butane diol (BDO). terephthalic acid and a catalyst to from a mixture and heating the mixture until the clearing point is reached based on visual inspection. The PBT oligomers are used in a continuous process for making polybutylene terephthalate (PBT) resin.

Abstract: A polycarbonate resin includes a repeat unit represented by Formula 1; a repeat unit represented by Formula 2; and a repeat unit represented by Formula 3, wherein the polycarbonate resin has a weight average molecular weight of about 15,000 g/mol to about 60,000 g/mol and a melt index of about 3 g/10 min to about 40 g/10 min.: wherein R1, R2, R3, R4, a, b, c, and d are the same as defined in the specification. The polycarbonate resin for film can exhibit excellent scratch resistance, elongation, chemical resistance and heat resistance, and can be used to prepare a film in roll form without any protective film.

Abstract: Alkylene oxide polymerizations are performed in the presence of a double metal cyanide polymerization catalyst and certain magnesium, Group 3-Group 15 metal or lanthanide series metal compounds. The presence of the magnesium, Group 3-Group 15 metal or lanthanide series metal compound provides several benefits including more rapid catalyst activation, faster polymerization rates and the reduction in the amount of ultra high molecular weight polymers that are formed. The catalyst mixture is unexpectedly useful in making polyethers having low equivalent weights.

Abstract: Fluorinated silane compounds, compositions containing the fluorinated silane compounds, and articles prepared using the fluorinated silane compounds and compositions are described. The fluorinated silane compounds can be soluble or dispersible in aqueous media, such as water, and can be used to coat articles, such as glass articles.

Abstract: The present invention relates to methods for producing polyaspartic acids with a weight-average molecular weight (Mw) of from 6,000 to 15,000 g/mol. The invention also relates to polyaspartic acids which can be obtained by the method according to the invention, to a composition containing the polyaspartic acids, and to the use thereof as scale inhibitors, dispersants and as an additive in dishwashing agents, detergents or cleaning agents.

Abstract: The invention relates to a process for preparing a salt from diamine and dicarboxylic acid, the process comprising contacting a diamine gas, having a gas temperature T-gas, with a dicarboxylic acid, thereby forming a reaction mixture comprising diamine/dicarboxylic acid salt, wherein the dicarboxylic acid and the reaction mixture are kept at a temperature T-mixture of at least 10° C. below the lowest of the melting temperature of the dicarboxylic acid (Tm-acid) and the melting temperature of the resulting diamine/dicarboxylic acid salt (Tm-salt). The invention also relates to a process for preparing a polyamide comprising preparing a salt from diamine and dicarboxylic acid.

Abstract: Provided are a novel polyamide polymer obtained by polymerizing monomers including aromatic diamine substituted with a nitrile group and an amide group and an aromatic dibasic acid compound, a spinning dope comprising the same, and a polyamide molded article. A fiber obtained using the novel polyamide polymer according to the present invention, particularly, a fiber obtained by spinning the polymer according to the present invention may have high strength and high elasticity, such that the fiber may be applied to various industrial fields.

Abstract: A process includes utilizing biorenewable resveratrol or a resveratrol-derived material as a bio-derived crosslinker to form a crosslinked polymeric material.

Abstract: A process includes utilizing biorenewable cis-3-hexenol to form a bio-derived cross-linker and utilizing the bio-derived cross-linker to form a cross-linked polymeric material.

Abstract: The present invention relates to ligands, nanocrystal complexed with the ligands and their use for bio-imaging.

Abstract: The present invention provides novel and improved processes for treating a lignocellulosic biomass or technical lignin using ionic liquids to obtain lignin breakdown products.

Abstract: A process includes forming a bio-derived crosslinking material from biorenewable aconitic acid. The process includes initiating a chemical reaction to form a bio-derived crosslinking material that includes multiple functional groups. The chemical reaction includes converting each carboxylic acid group of a biorenewable aconitic acid molecule to one of the multiple functional groups.

Abstract: Treated liquid crystal polymer powders have been subjected to surface treatment with plasma or ultra violet rays, a paste including the treated liquid crystal polymer powders and a dispersion medium, a liquid crystal polymer sheet comprising the treated liquid crystal polymer powders or the paste including the treated liquid crystal polymer powders and a dispersion medium into a sheet, a stack including the liquid crystal polymer sheet as a resin layer, and a method of manufacturing the treated liquid crystal polymer powders are provided by the present disclosure.

Abstract: A fiber-reinforced composite material of the present invention is a fiber-reinforced composite material comprising: an epoxy resin cured product obtained by curing an epoxy resin composition and a reinforcing fiber, wherein the epoxy resin composition comprises an epoxy resin (A) and a curing agent (B); 10 to 80% by mass of the curing agent (B) is 1,2,4-cyclohexanetricarboxylic acid-1,2-anhydride; and the reinforcing fiber comprises one or more selected from the group consisting of a carbon fiber, an aramid fiber, and a boron fiber.

Abstract: A method is presented for forming a collapsed foam film-like structure, the method including positioning a composition applicator adjacent to a hot non-permeable dryer surface, producing a first frothed dispersion or frothed solution from a first dispersion or solution, applying the first frothed dispersion or frothed solution to the dryer surface, allowing the first frothed dispersion or frothed solution to convert to a collapsed foam film-like structure, and scraping the collapsed foam film-like structure from the dryer surface. The method can further include producing a second dispersion or solution, blending the first dispersion or solution and the second dispersion or solution, frothing the blended dispersion or solution, applying the blended frothed dispersion or frothed solution to the dryer surface, and allowing the frothed dispersion or frothed solution to convert to a collapsed foam film-like structure.

Abstract: This invention relates to a a one-step process for making a polymer composite suspension for coating plastic films characterized in that a first polymer is synthesized in-situ optionally in the presence of other polymers and in the presence of clay. Preferably the polymer composite suspension comprises a) 1.0 to 11.0 wt % of clay or silane modified clay, b) 0.1 to 10.0 wt % of poly (acrylic acid), which is a copolymer of acrylic acid (AA) with at least one other monomer selected from 2-ethylhexyl acrylate (EHA), ?-carboxyethyl acrylate (?-CEA), methacrylamidoethyl ethylene urea (WAM II) and ethoxylated behenyl methacrylate (?-EM), c) 1.0 to 15.0 wt % of other polymers, preferably poly (vinyl alcohol) and d) 70 to 97 wt % of water or mixture of water with 2-propanol. The coating films made from the suspensions show good barrier capabilities against water vapor and oxygen can be used to make barrier layers on or within plastic films for packaging applications.

Abstract: The present invention concerns a method for producing polyurethane foams by reacting an isocyanate component with a component that is reactive to isocyanates and that comprises at least one polyether carbonate polyol, the reaction taking place in the presence of a non-amine antioxidant and an amine antioxidant. The invention also concerns polyurethane foams produced using the claimed method and the use of said foams.

Abstract: A foam material having one glass transition temperature (Tg) and made from an immiscible composition having at least two glass transition temperatures (Tg) by an extrusion process wherein said composition (C) comprises at least one polyarylene (P1) polymer, wherein more than 50% by moles (moles %) of the recurring units of said (P1) polymer are recurring units (R1) consisting of an arylene group, wherein said arylene group is a hydrocarbon divalent group consisting of one core composed of one benzene ring or of a plurality of benzene rings fused together by sharing two or more neighboring ring carbon atoms, said benzene ring being optionally substituted, wherein each of said arylene group is bound to two other arylene groups of neighboring recurring units (R1) through a first C—C bond (E1) and a second C—C bond (E2), wherein at least 20 moles % of recurring units (R1) are kink-forming arylene units (R1-b), the remainder being rigid rod-forming arylene units (R1-a) different from aryleneR1_b units, wherein in

Abstract: Foamable aqueous compositions can be foamed and applied to porous substrates to make light-blocking dry opacifying elements. Such compositions have 0.05-15 weight % of porous particles; at least 20 weight % of a binder; at least 0.0001 weight % of additives (including a surfactant); water; and at least 0.001 weight % of an opacifying colorant. Each porous particle includes a continuous polymeric phase and discrete pores; a mode particle size of 2-50 ?m; and a porosity of 20-70 volume %. The continuous polymeric phase Tg is >80° C. and has a polymer viscosity of 80-500 centipoises at an ethyl acetate shear rate of 100 sec?1 at a concentration of 20 weight % at 25° C. The dry opacifying element light blocking value is at least 4 and has a luminous reflectance >40% as measured by the color space Y tristimulus value. The foamed aqueous composition has a foam density of 0.1-0.5 g/cm3.

Abstract: The present invention is a polymer composition comprising a hydrogenated crystalline cycloolefin ring-opening polymer (A) that comprises a repeating unit derived from a polycyclic norbornene-based monomer that includes three or more rings, 5 to 100 parts by weight of a glass filler (B) based on 100 parts by weight of the hydrogenated crystalline cycloolefin ring-opening polymer (A), and 5 to 20 parts of a metal oxide (C) based on 100 parts by weight of the hydrogenated crystalline cycloolefin ring-opening polymer (A), and a formed article. The polymer composition according to the present invention exhibits excellent electrical properties (low dielectric loss tangent), excellent adhesion to plating, and excellent reflow heat resistance, and can maintain strength even when subjected to high-temperature/high-humidity conditions.

Abstract: The present disclosure provides an aerogel composition which is durable and easy to handle, which has favorable performance in aqueous environments, and which also has favorable combustion and self-heating properties. Also provided is a method of preparing an aerogel composition which is durable and easy to handle, which has favorable performance in aqueous environments, and which has favorable combustion and self-heating properties. Further provided is a method of improving the hydrophobicity, the liquid water uptake, the heat of combustion, or the onset of thermal decomposition temperature of an aerogel composition.

Abstract: The present disclosure provides an aerogel composition which is durable and easy to handle, which has favorable performance in aqueous environments, and which also has favorable combustion and self-heating properties. Also provided is a method of preparing an aerogel composition which is durable and easy to handle, which has favorable performance in aqueous environments, and which has favorable combustion and self-heating properties. Further provided is a method of improving the hydrophobicity, the liquid water uptake, the heat of combustion, or the onset of thermal decomposition temperature of an aerogel composition.

Abstract: A boron-containing nucleating agent is provided for use with a polyarylene sulfide. The boron-containing nucleating agent can have low crystallinity, a small particle size, and a large specific surface area. By selectively controlling certain aspects of the nucleating agent, the crystallization properties of a thermoplastic composition including the nucleating agent and a polyarylene sulfide can be significantly improved. For instance, the recrystallization temperature can be increased, which can allow the “cooling time” during a molding cycle to be substantially reduced. Through use of the boron-containing nucleating agent the recrystallization temperature can be greater than about 231° C.

Abstract: [Problem] To provide a magnesium hydroxide-based solid solution which has smaller primary particles and secondary particles and improved reactivity with an acid as compared with conventional magnesium hydroxide (Mg(OH)2), improves the flame retardancy and mechanical strength of a resin, and also forms a non-sedimenting slurry, providing the same handleability as a liquid. [Structure] A magnesium hydroxide-based solid solution represented by the following formula (1): Mg(OH)2-xRx (Formula 1), wherein R represents a monovalent organic acid, and x represents 0<x<1. The magnesium hydroxide-based solid solution is a magnesium oxide (MgO) precursor. A flame retardant for a synthetic resin, including the magnesium hydroxide-based solid solution as an active ingredient. A synthetic resin composition characterized by including 0.1 to 50 parts by weight of the magnesium hydroxide-based solid solution (b) per 100 parts by weight of a synthetic resin (a); and a molded article thereof.

Abstract: An oxygen-absorbing resin composition containing a base resin having a thermoplastic resin; and an oxygen-absorbing component having at least the one selected from the group consisting of an ester, an amide, an imide or a dicarboxylic acid derived from an acid anhydride represented by the following formula (1), wherein, a ring X is an aliphatic ring having an unsaturated bond, n is a number of the substituents Y bonded to the ring X and is an integer of 0 or 1, and Y is an alkyl group, and a polymer having a constituent unit stemming from the acid anhydride. An oxygen-absorbing polyester resin composition exhibits excellent oxygen-absorbing property even in the absence of transition metal catalyst without accompanied by the deterioration of the polyester resin used as a the base resin, the oxygen-absorbing property being strong enough for maintaining gas-barrier properties.