An isocyanate composition according to the present invention contains: a difunctional or more-functional isocyanate compound; and 1.0 ppm by mass to 1.0×10.sup.4 ppm by mass, based on the isocyanate compound, of a compound having at least one unsaturated bond excluding unsaturated bonds constituting an aromatic ring, the compound being different from the isocyanate.

The present invention relates to a curable resin composition, etc., having excellent in applicability and workability. Specifically, the present invention relates to a resin composition, etc., including: one or more base polymers selected from the group consisting of (A) a polymer having two or more alkenyl groups and (B) a polyorganosiloxane having a hydroxyl group bound to a silicon atom; (C) a silica powder surface-treated with an alkyl silane; and (D) a compound including one or more elements selected from the group consisting of boron, phosphorus, sulfur, and nitrogen.

Disclosed herein are polysaccharide-elastomer masterbatch compositions and processes for preparing the masterbatch compositions. One method comprises a step of a) mixing i) an aqueous polysaccharide dispersion, or ii) a basic aqueous polysaccharide solution, with a rubber latex solution containing a rubber component to form a mixture. The method further comprises the steps of: b) coagulating the mixture obtained in step a) to produce a coagulated mass; and c) drying the coagulated mass obtained in step b). The masterbatch compositions are useful in preparing rubber-containing articles.

An isocyanate composition according to the present invention contains: a difunctional or more-functional isocyanate compound; and 1.0 ppm by mass to 1.0 × 10.sup.4 ppm by mass, based on the isocyanate compound, of a compound having at least one unsaturated bond excluding unsaturated bonds constituting an aromatic ring, the compound being different from the isocyanate.

Disclosed is a method for precipitating a polymer by adding a precipitation agent into a first suspension to form a second suspension; wherein the first suspension comprises a polymer and an aqueous solvent; and wherein the polymer comprises a copolymer comprising a structural unit derived from an acid group-containing monomer and a structural unit derived from a hydrophobic group-containing monomer. The method for precipitation of a polymer disclosed herein is developed to initiate the bond disruption and/or breakage between the polymer and the aqueous solvent within the second suspension. This is accompanied with the structural transformation of the polymer driven by the intermolecular and intramolecular interactions of the polymer chains which brings about the precipitation of the polymer. The method circumvents both complex separation process and contamination of the polymer, enables excellent materials recovery and allows the precipitation of the polymer to be achieved within a short time frame. An application of the method for precipitating a polymeric binder in a battery electrode is disclosed herein.

Provided are methods of producing sulfur- and phosphorus-containing polymers from beta-lactones. The sulfur- and phosphorus-containing polymers include bio-based sulfur- and phosphorus-containing polymers that may be obtained from renewable sources.

The present invention belongs to the technical field of functional film materials; disclosed are a wavelength-controllable cellulose iridescent film and a method for preparation thereof. The method is: (1) mixing well a cellulose nanocrystal (CNC) suspension with lactic acid solution and glucose solution to obtain a CNC/lactic acid/glucose mixed solution; said CNC suspension being a cellulose nanocrystal suspension; (2) drying the CNC/lactic acid/glucose mixed solution to form a film to obtain a cellulose iridescent film. The method of the present invention is simple and low in cost. In the present invention, by means of the addition of lactic acid and glucose, the prepared film has iridescent film characteristics; the wavelength of the iridescent film is within the range of visible light, and the wavelengths of different colors of iridescent film are controllable.

Disclosed are compositions comprising polyesters containing a chain of residue of: diols and diesters along the chain, wherein at least a portion of the diesters are 1, 1-diester-1-alkenes, and the chains have alkene groups incorporated into the chains; the composition comprising one or more of the following: i ether groups derived from alcohols, diols, polyols, or a combination thereof obtained via Michael addition to the alkene groups and a residue of the alkene groups remaining after Michael addition; ii the formed polyesters contain one percent or less of residual 1, 1-diester-1-alkene which are unreacted; iii one or more free radical inhibitors; and iv a stabilizer comprising one or more of: oxo acids phosphorous or esters thereof, aluminum sulfate, stannous pyrophosphate, stannous sulfate, aluminum dihydrogenphosphate or decomposition products thereof. The stabilizer is present in an amount sufficient to enhance stability of the polyester without lowering reactivity of the polyester.

The present disclosure is directed to a curable precursor of a pressure sensitive adhesive comprising a) a (co)polymeric material comprising a rubber-based elastomeric material; b) a polyfunctional aziridine curing agent; and c) an acid generating agent. The present disclosure is also directed to a method of manufacturing such pressure sensitive adhesives and uses thereof.

The present invention provides antimicrobial and/or antiviral properties for polymers and synthetic fibers that have stain resistant properties. The synthetic fiber comprises a polymer, such as a copolymer comprising from 85 to 99.5 percent by weight of a polyamide based on the total weight of the fiber and an aromatic sulfonate or a salt thereof present in a range from 0.5 to 10 percent by weight based on the total weight of the fiber, one or more metal compounds or ions thereof dispersed within the copolymer, and a phosphorus compound.