Abstract: A 1,2,4-triazine of formula (I): and its process of manufacture and use.

Abstract: A rubber composition for the manufacture of tires, based on one or more diene elastomers, on one or more reinforcing fillers and on a vulcanization system, characterized in that the said vulcanization system comprises one or more 1,2,4-triazine compounds of formula:

Abstract: Composition (C) for coating ingestible solid forms, comprising, per 100% of its mass—from 10% to 90% of a graft copolymer of polyvinyl alcohol and of polyethers (Pi), and—from 10% to 90% by mass of an auxiliary coating agent, characterized in that a non-zero mass proportion of said auxiliary agent is polydextrose. Processes for the preparation and use thereof.

Abstract: The present invention provides a method for manufacturing a cellulose nanofiber, characterized by comprising the step of fibrillating cellulose in a polyester based resin, preferably in a polyester based resin having an ester group concentration of 6.0 mmol/g or more and a cellulose nanofiber produced by the manufacturing method concerned. In addition, the present invention provides a masterbatch composition containing the cellulose nanofibers and the polyester based resin. Furthermore, the present invention provides a resin composition containing the masterbatch composition and a diluent resin and a processed product thereof.

Abstract: A biodegradable resin composition containing a biodegradable resin and a cellulose having a crystallinity of less than 50%; and a biodegradable resin molded article wherein the biodegradable resin composition as defined above is molded. The biodegradable resin composition can be suitably used for various industrial applications, such as daily sundries, household electric appliance parts, and automobile parts.

Abstract: A biodegradable resin composition containing a biodegradable resin and a cellulose having a crystallinity of X (%), wherein the cellulose is obtained by a step including subjecting a cellulose-containing raw material to a pulverization treatment (A), wherein the cellulose-containing raw material contains a cellulose having a crystallinity of Y (%), and has a bulk density of from 100 to 500 kg/m3, and an average particle size of from 0.01 to 1.0 mm, and contains a cellulose in an amount of 20% by weight or more of a residue component obtained by removing water from the raw material, wherein X and Y satisfy the following formulas: 50?X?Y?5 (1) and 55?Y?99 (2). The biodegradable resin composition can be suitably used for various industrial applications, such as daily sundries, household electric appliance parts, and automobile parts.

Abstract: A mixture includes a polymer solution, especially a cellulose solution, a first additive in the form of an inorganic lubricant and/or stabilizer, for example graphite, and a second additive as an adsorbent, for example activated carbon. The inorganic lubricants and/or stabilizers do not weaken the positive properties of the adsorbent but can even improve them. The mixture can be used to produce fibers (7) or moldings.

Abstract: A method of making a biodegradable composite is carried out by: (a) providing an aqueous mixture comprising partially hydrolyzed cellulose in a dissolution media; (b) providing a solution comprising a aliphatic polyester in a polar organic solvent; (c) combining the mixture with the solution to form a precipitate; (d) washing the precipitate with water to remove solvent and dissolution media and form a wet biodegradable composite; and then (e) drying the wet biodegradable composite to form a dry biodegradable composite. Composites made from the method are also described.

Abstract: A method for preparing pimaric acid type resin acids includes the following steps: step (1) adding refined resin acid, turpentine, or rosin along with maleic anhydride at a mass ratio of 1:0.3-1.5 into a reaction bottle, dissolving the ingredients into a C1-C10 lower fatty acid solvent, the mass ratio of the C1-C10 low fatty acid to refined resin acid is 0.05-30:1, then carrying out additional reaction by heating directly or with assistance of a microwave, subsequently cooling, crystallizing, filtering, and washing; and step (2) combining the filtrates collected in step (1), stripping the solvent by vacuum distillation to obtain pimaric acid type resin acid coarse product, dissolving the resulting coarse product in NaOH aqueous solution to prepare aqueous solution of pimaric acid type resin acid salt, adjusting the pH level to 6-14 with a mineral acid or an organic acid while stirring, and either directly purifying or acidifying followed by purifying, the resulting precipitation to obtain the final product.

Abstract: An arthroplasty device is provided having an interpenetrating polymer network (IPN) hydrogel that is strain-hardened by swelling and adapted to be held in place in a joint by conforming to a bone geometry. The strain-hardened IPN hydrogel is based on two different networks: (1) a non-silicone network of preformed hydrophilic non-ionic telechelic macromonomers chemically cross-linked by polymerization of its end-groups, and (2) a non-silicone network of ionizable monomers. The second network was polymerized and chemically cross-linked in the presence of the first network and has formed physical cross-links with the first network. Within the IPN, the degree of chemical cross-linking in the second network is less than in the first network. An aqueous salt solution (neutral pH) is used to ionize and swell the second network. The swelling of the second network is constrained by the first network resulting in an increase in effective physical cross-links within the IPN.

Abstract: The present invention relates to an alternating or statistical conjugated copolymer comprising: at least one benzotriazole unit B having general formula (Ia) or (Ib): wherein the group R is selected from alkyl, aryl, acyl or thioacyl groups, possibly substituted; at least one conjugated structural unit A, wherein each unit B is connected with at least one unit A in any of the positions 4, 5, 6 or 7, preferably in positions 4 or 7.

Abstract: The invention pertains to the field of membrane protein immobilization onto supports. It relates to a product comprising a support and at least one membrane protein attached to the surface thereof, characterized in that said membrane protein is attached to said support using an amphiphilic molecule with which said membrane protein is complexed. It also relates to a process for preparing such product, as well as to various applications in the fields of diagnosis, drug design and biotechnologies. It further relates to a kit, together with a functionalized amphiphilic molecule, for preparing a product according to the invention comprising a support and an amphiphilic molecule, wherein the amphiphilic molecule and the support interact through a hydrophobic bond, an ionic bond, a specific bond or a covalent bond.

Abstract: The present invention is directed to polymeric article comprising a blend of (a) a first polymeric component; (b) a second polymeric component, the second polymeric component including a propylene elastomer or a substantially linear or linear ethylene polymer; and (c) at least one reinforcement material. The polymeric articles desirably have one or more of the following characteristics: a soft touch feel, low gloss appearance, or a high surface durability.

Abstract: Sulfonated graft copolymer obtained by radical graft copolymerization of one or more synthetic monomers in the presence of hydroxyl-containing naturally derived materials. The graft copolymer includes 0.1 to 100 wt %, based on weight of the total synthetic monomers, of at least one monoethylenically unsaturated monomer having a sulfonic acid group, monoethylenically unsaturated sulfuric acid ester or salt thereof, with the monomer and hydroxyl-containing naturally derived materials present in a weight ratio of 5:95 to 95:5.

Abstract: The invention relates to compositions and articles containing a cross-linked polymer matrix and an immobilized active liquid, as well as methods of making and using the same.

Abstract: The invention relates to a method for the preparation of a polymer hydrogel, comprising cross-linking a precursor comprising a hydrophilic polymer optionally in combination with a second hydrophilic polymer, using a polycarboxylic acid as the cross-linking agent. The invention further concerns the polymer hydrogel obtainable by the method of the invention and the use thereof in a number of different applications.

Abstract: The graft copolymer comprises a polymerizable monomer (A1) represented by general formula (III) and a polymerizable monomer (B1) containing a pyridyl group, and a ligand can be bonded via the functional group at the terminus of R3a. In the formula, R1a represents a polymerizable group, R2a represents an alkylene group having a carbon number of 2-5, R3a represents an organic group having at a terminus a functional group selected from among an azide group, a phenyl azide group, a carboxyl group, a primary to quaternary amino group, an acetal group, an aldehyde group, a thiol group, a disulfide group, an active ester group, a trialkoxysilyl group, and a polymerizable group, and n represents any integer from 5 to 20,000.

Abstract: A method of curing a coating composition and a method of forming a cured coating on an automobile component are provided. The coating composition comprises a radical polymerizable compound and an organoborane-amine complex having an organoborane initiator, an amine blocking agent, and water. The method of curing the coating composition comprises the steps of combining the organoborane-amine complex, the radical polymerizable compound, and water to form the coating composition. Carbon dioxide is introduced into the coating composition or into a composition including at least one of the organoborane-amine complex, the radical polymerizable compound, and water prior to forming the coating composition. Carbonic acid is formed in situ within the coating composition through reaction of the water and carbon dioxide. The organoborane-amine complex is decomplexed with the carbonic acid thereby separating the organoborane initiator and the amine blocking agent.

Abstract: An inorganic board is formed of an aluminosilicate setting material, a wooden reinforcing material and an aggregating agent. The wooden reinforcing material is covered by the aggregating agent, and this agent is covered by the aluminosilicate setting material. A method of manufacturing the inorganic board has the steps of covering a wooden reinforcing material with an aggregating agent; producing a starting material mixture by mixing the thus-obtained wooden reinforcing material with an aluminosilicate powder, an alkali metal hydroxide and water glass; and molding and curing the thus-obtained starting material mixture.

Abstract: The purpose of the present invention is to improve the water absorption of a water-absorbent resin without sacrificing the productivity, production cost, safety, and so on. Provided is a sustainable and renewable water-absorbent resin with excellent whiteness, which is suitable for mass consumption as disposal diapers or the like, and which can dispense with excessive purification of raw material acrylic acid. Also provided is a process for the production of a water-absorbent resin, which comprises: a step of preparing acrylic monomers; a step of polymerizing the monomers; and a step of drying the obtained aqueous gel, wherein the monomers at the time of polymerization contain at least 400 ppm of propionic acid.