Abstract: The present invention provides a polyaspartic composition comprising a reaction product of a polyamine and a Michael addition receptor reacted in the presence of a catalyst comprising a phenolic compound, with the proviso that the phenolic compound is not a phenol which is substituted with tert-butyl groups in both ortho positions to the oxygen. Suitable phenolic compounds include phenols, phenolic aldehydes, alkylphenols, benzenediols, cashew nut oil, and combinations thereof. Coatings, adhesives, sealants, composites, castings, and films comprising a polyurea composition may be made by reacting a polyisocyanate with the inventive polyaspartic composition. In particular, floor coatings made with the inventive polyaspartic composition have an elongated work time and a short walk-on time compared to current floor coatings.

Abstract: Among other things, the present disclosure provides compositions and methods for an elastomeric cross-linked polyester material. Such an elastomeric cross-linked polyester material, in some embodiments, comprises a plurality of polymeric units of the general formula (-A-B-)p, wherein p is an integer greater than 1; and a plurality of urethane cross-links each of which covalently links two polymeric units to one another, which two linked polymeric unit each had at least one free hydroxyl or amino group prior to formation of the crosslink.

Abstract: A composition is provided including a compound (A) represented by Formula (1) and a compound (B) represented by Formula (2), wherein the compound (B) is contained in an amount of 0.00002 to 0.2 parts by mass with respect to 100 parts by mass of the compound (A): (R1—COO)n—R2—(NCO)m . . . (1) (in Formula (1), R1 is an ethylenically unsaturated group having 2 to 7 carbon atoms; R2 is an (m+n)-valent hydrocarbon group having 1 to 7 carbon atoms; and n and m are each an integer of 1 or 2) (in Formula (2), R is (—R2—(OCO—R1), and R1 and R2 are the same as those in Formula (1)).

Abstract: The present invention provides an ionizing radiation curable paint composition which is capable of forming a cured film that has excellent elongation (for example, 30% or more) under heating and has excellent solvent resistance and chemical resistance and which can contain an alcohol as a diluent solvent. The ionizing radiation curable paint composition contains a urethane (meth)acrylate oligomer (A1) having 6 or more (meth)acryloyl groups and having a weight average molecular weight of 3,000 to 50,000, wherein the urethane (meth)acrylate oligomer (A1) is a silicone-modified oligomer having a constituent unit (a) derived from a multifunctional (meth)acrylate monomer having a hydroxy group and 3 or more (meth)acryloyl groups, a constituent unit (b) derived from an alcohol having 2 or more hydroxy groups and having a molecular weight of 100 or lower, a constituent unit (c) derived from isophorone diisocyanate, and a constituent unit (d) derived from a carbinol-modified polysiloxane.

Abstract: The disclosed adhesive compositions comprise (A) an isocyanate component comprising an isocyanate-terminated prepolymer that is the reaction product of a polyisocyanate and an isocyanate-reactive mixture comprising a phosphate ester polyol. The disclosed adhesive compositions further comprise (B) an isocyanate-reactive component polyol component comprising a polyol. In some embodiments, methods for preparing two-component adhesives formulations are disclosed comprising preparing an isocyanate component comprising an isocyanate-terminated prepolymer by reacting a polyisocyanate with an isocyanate-reactive mixture comprising a phosphate ester polyol and preparing an isocyanate-reactive component comprising a polyol. The methods further comprise mixing the isocyanate component and the isocyanate-reactive component at a stoichiometric ratio (NCO/OH) of from about 1.0 to about 5.0. Methods for forming laminate structures, and the laminate structures themselves, are also disclosed.

Abstract: A thermosetting coating composition includes a hydroxyl group-containing resin (A), a blocked polyisocyanate curing agent (B), and an amine compound (C) represented by the formula (1). In the formula (1), R1 to R5 each independently represents a hydrogen atom or an organic group having one or more carbon atoms. The organic group may contain one or more atoms selected from the group consisting of oxygen atoms, nitrogen atoms, sulfur atoms, and halogen atoms.

Abstract: A water-based polyurethane resin and a method for manufacturing the same are provided. The method for manufacturing the water-based polyurethane includes: a preparation step of a prepolymer, a dilution step of the prepolymer, a water dispersion and chain extension step, and an acrylic synthesis step. The method further includes mixing polyol and polyisocyanate to obtain a prepolymer, and diluting the prepolymer by adding acrylic monomer in the prepolymer. In the water-based polyurethane resin, at least one of the polyhydric alcohol, polyisocyanate, and the acrylic monomer includes a compound with a cyclic structure.

Abstract: A process for preparing a polyurethane polymer comprises the step of: I) mixing a first component (100) comprising a polyisocyanate with a second reactant component (200) comprising a compound having Zerewitinoff-active hydrogen atoms in a mixing vessel (300) to obtain a reaction mixture (400), wherein the first reactant component (100) and/or the second reactant component (200) are contacted with a catalyst bed (500) before they are mixed in the mixing vessel (300) and/or the reaction mixture (400) is contacted with a catalyst bed (500), wherein the catalyst bed (500) contains a catalyst reversibly sorbed on a substrate, the catalyst catalyses the reaction of isocyanate groups with themselves or with Zerewitinoff-active compounds and the catalyst is released into the first component (100), second component (200) or reaction mixture (400) that is in contact with the catalyst bed (500), such that a reaction mixture (410) containing the catalyst is obtained.

Abstract: Provided is a polycarbonate polyol used as a raw material of a polyurethane that has an excellent balance of flexibility, mechanical strength and solvent resistance. The polycarbonate polyol includes structural units derived from a polyhydric alcohol and has a hydroxyl value of 20 to 450 mg KOH/g. The polyhydric alcohol includes: a diol (A) containing not less than 70% by weight of a specific oxyalkylene glycol (A1); and a trihydric to hexahydric branched alcohol (B) having 3 to 12 carbon atoms. In the polycarbonate polyol, structural units derived from the branched alcohol (B) is contained in an amount of 0.005 to 5.0% by mole in the structural units derived from the polyhydric alcohol. A ratio of a structural unit (X1) represented by the following Formula (X1) in the structural units derived from the branched alcohol (B) is not higher than 50% by mole.

Abstract: The present invention relates to the use of tertiary amines as catalysts for the cross-linking of isocyanate groups which are aliphatically and/or cyclo-aliphatically bonded. The catalysts according to the invention have the particular advantage that they are thermally latent.

Abstract: Articles are provided including at least one polyurethane prepared from: (a) about 1 equivalent of at least one polyisocyanate; (b) about 0.005 to about 0.35 equivalent of at least one polycaprolactone polyol; (c) about 0.01 to about 1.0 equivalent of at least one polyol selected from the group consisting of ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, 1,2-ethanediol, propanediol, butanediol, pentanediol, hexanediol, heptanediol, octanediol, nonanediol, decanediol, dodecane diol, octadecanediol, cyclopentanediol, 1,4-cyclohexanediol, cyclohexanedimethanol, 1,4-benzenedimethanol, xylene glycol, hydroxybenzyl alcohol, dihydroxytoluene, bis(2-hydroxyethyl) terephthalate, 1,4-bis(hydroxyethyl)piperazine, N,N?,bis(2-hydroxyethyl)oxamide and mixtures thereof; and (d) about 0.01 to about 0.

Abstract: Provided is a polycarbonate polyol used as a raw material of a polyurethane that yields a polyurethane solution having good storage stability and exhibits excellent flexibility and solvent resistance. This polycarbonate polyol is a polycarbonate diol that includes structural units represented by the following Formulae (A) and (B), wherein, R1 and R2 each independently represent an alkyl group having 1 to 4 carbon atoms and, in this range of the number of carbon atoms, optionally have an oxygen atom, a sulfur atom, a nitrogen atom, a halogen atom, or a substituent containing these atoms; and R3 represents a linear aliphatic hydrocarbon having 3 or 4 carbon atoms. This polycarbonate diol has a molecular weight of 500 to 5,000, and the value of the following Formula (I) is 0.3 to 20.0: (Content ratio of branched-chain moiety in polymer)/(Content ratio of carbonate group in polymer)×100(%) (I).

Abstract: A polyisocyanurate raw material composition containing a polyfunctional isocyanate, a compound (I) represented by general formula (I) shown below, and an epoxy compound. In general formula (I), each of R1 to R5 represents a hydrogen atom, an alkoxy group of 1 to 10 carbon atoms, an alkyl group of 2 to 10 carbon atoms (or an alkyl group of 1 to 10 carbon atoms in the case of R3 to R5), an aryl group of 6 to 12 carbon atoms, an amino group, a monoalkylamino group of 1 to 10 carbon atoms, a dialkylamino group of 2 to 20 carbon atoms, a carboxy group, a cyano group, a fluoroalkyl group of 1 to 10 carbon atoms, or a halogen atom (provide that R1 and R2 are not both hydrogen atoms).

Abstract: A composition including at least one compound having a perfluoropolyether group and a curable site, wherein in a molecular weight distribution curve in gel permeation chromatography measurement, the following formula is satisfied: M2/M1?3.5, wherein M1 is a molecular weight at a main peak, and M2 is a molecular weight at 25% intensity of an intensity of the main peak on a higher molecular weight side than M1. Also disclosed is a curable composition containing the composition and a method for producing the curable composition.

Abstract: Embodiments relate to a polythiourethane-based plastic lens. When a polythiourethane-based plastic lens is polymerized according to the embodiment, the types, contents, and the like of the polythiol compounds and the isocyanate compounds are adjusted to control the storage moduli at room temperature and high temperatures, their variations, the energy attenuation (KEL) obtained therefrom, and the glass transition temperature, whereby the polythiourethane-based plastic lens thus obtained is enhanced in impact resistance and thermal resistance.

Abstract: A method of treating, reducing or preventing bacterial infection in a wound, the method comprising: applying a film on the wound, the film including a biodegradable polymer with bacteriophages dispersed therein, wherein the polymer is a poly (ester amide urea).

Abstract: The elastomeric yarn for safety applications discloses an elastomeric yarn that reliably breaks at 200% stretch and is therefore appropriate for use with a sacrificial textile. The elastomeric yarn for safety applications discloses the polyurethane segments, the copolymer segments, the necessary plurality of cross-links required to form a structure of a polyurethane based elastomeric yarn that reliably breaks at 200% stretch.

Abstract: An object of the present invention is to provide a novel rotaxane and a polyurethane using the same. The present invention provides a rotaxane having a crown ether and a chain molecule piercing through the cyclic structure of the crown ether, wherein a hydroxyl group exists at one terminal of the chain molecule, and a hydroxyl group bonds to the cyclic structure of the crown ether. The present invention further provides a polyurethane using the rotaxane as a polyol component.

Abstract: The invention relates to a process for the preparation of polyisocyanates with dimer, trimer and/or allophanate and optionally urethane structure.

Abstract: An isocyanate composition according to the present invention contains: a difunctional or more-functional isocyanate compound; and 1.0 ppm by mass to 1.0×104 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.