Provided is a material having an excellent sound-absorbing performance which can be easily applied to the desired area at the operation site and which can effectively prevent sound leakage. The material includes an open-cell soft polyurethane foam prepared from a 2-part reactive urethane resin composition prepared from a polyisocyanate component and a polyol-containing component, wherein the polyol-containing component comprises a polyol component, catalysts, a foam stabilizer, an amine compound having primary or secondary amino groups, and carbon dioxide; wherein an average sound absorption coefficient of said polyurethane foam is 30% or more, measured in accordance with JIS A 1405-2:2007 for 63 hertz to 5000 hertz; and the length of liquid-dripping is within 300 mm.

In a polyurethane dispersion obtained by water-dispersing a polyurethane resin, the polyurethane resin is a reaction product obtained by reacting at least a polyisocyanate component with an active hydrogen group-containing component containing an active hydrogen compound having an anionic group, a ratio of the total moles of a urethane group and a urea group is 1.5 mol or more with respect to 1 kg of the polyurethane dispersion, and the carbonate ion concentration is 700 ppm or less with respect to the polyurethane dispersion.

A cleaning wiper blade comprises a hand grip part and an elastic part. The elastic part comprises a polyurethane. The polyurethane comprises a reactant of a composition including an isocyanate compound which includes diisocyanate and polyfunctional isocyanate, and an alcohol which includes polyfunctional alcohol. The diisocyanate has an aromatic ring in a molecule. When a molecule of the polyurethane is ionized with a mass spectrometer of a direct sample injection system, then obtained M1, M2 and M3 satisfy the is 0.013 to 0.300, and a concentration of the polyfunctional alcohol in the polyurethane is 0.12 mmol/g to 0.65 mmol/g.

The present invention relates to a polyurethane, which is particularly suitable as binder for a printing ink, which is obtainable by reacting: a) a polyol component including: i) at least one polytetramethylene glycol, ii) at least one diol having a molecular weight of not more than 200 g/mol being different from polytetramethylene glycol, iii) at least one trivalent or higher-valent alcohol having a molecular weight of not more than 6000 g/mol, b) an isocyanate component including at least one organic diisocyanate compound and c) at least one di-functional amine compound and at least one mono-functional amine compound.

The present invention relates to processes for the manufacture of aqueous polyurethane dispersions that can be used as adhesives or coatings, are solvent free and have low VOC emissions, and are environmentally friendly. Also encompassed are the dispersions as such, compositions containing them and their use as coatings and adhesives.

Silicone polyurea block copolymers are prepared by copolymerizing: (a) a diamine composition that includes a polyethylene glycol diamine, and optionally, a dipiperidyl alkane; (b) a monofunctional silicone isocyanate; and (c) a diisocyanate. Compositions useful as passivating coatings comprising the block copolymer are also provided, and substrates coated with the compositions. Methods of preparing and using the compositions are also described.

The present invention relates to polymers having dynamic urea bonds and more specifically to polymers having hindered urea bonds (HUBs). The present invention also relates to: (a) malleable, repairable, and reprogrammable shape memory polymers having HUBs, (b) reversible or degradable (e.g., via hydrolysis or aminolysis) linear, branched or network polymers having HUBs, and (c) to precursors for incorporation of HUBs into these polymers. The HUB technology can be applied to and integrated into a variety of polymers, such as polyureas, polyurethanes, polyesters, polyamides, polycarbonates, polyamines, and polysaccharides to make linear, branched, and cross-linked polymers. Polymers incorporating the HUBs can be used in a wide variety of applications including plastics, coatings, adhesives, biomedical applications, such as drug delivery systems and tissue engineering, environmentally compatible packaging materials, and 4D printing applications.

An aqueous dispersion containing at least one copolymer, the copolymer being preparable by initially charging an aqueous dispersion of at least one polyurethane, and then polymerizing a mixture of olefinically unsaturated monomers in the presence of the polyurethane, where a water-soluble initiator is used, the metered addition of the olefinically unsaturated monomers is effected in such a way that a concentration of 6.0% by weight, based on the total amount of olefinically unsaturated monomers, in the reaction solution is not exceeded over the entire duration of the reaction, and the mixture of the olefinically unsaturated monomers contains at least one polyolefinically unsaturated monomer.

A method for preparing a high-temperature self-crosslinking aqueous polyurethane dispersion. By using isocyanate (NCO) blocking agent to block part of the NCO, and using the hydroxyalkyl ethylenediamine chain extender in the post-chain extension stage to introduce hydroxyl groups, the polymer macromolecular structure containing both blocked NCO groups and hydroxyl groups can be prepared. The aqueous polyurethane dispersion does not need to mix with other waterborne resins and crosslinkers when applied. A sufficient cross-linking reaction is performed between the NCO released and hydroxyl groups on the polymer macromolecular chain to form a high-density cross-linked structure when curing at 100-150° C. for 20-30 min, thus obtaining a high-performance waterborne coating that can be used in the form of one-pack.

A method for preparing a high-temperature self-crosslinking aqueous polyurethane dispersion. By using isocyanate (NCO) blocking agent to block part of the NCO, and using the hydroxyalkyl ethylenediamine chain extender in the post-chain extension stage to introduce hydroxyl groups, the polymer macromolecular structure containing both blocked NCO groups and hydroxyl groups can be prepared. The aqueous polyurethane dispersion does not need to mix with other waterborne resins and crosslinkers when applied. A sufficient cross-linking reaction is performed between the NCO released and hydroxyl groups on the polymer macromolecular chain to form a high-density cross-linked structure when curing at 100-150° C. for 20-30 min, thus obtaining a high-performance waterborne coating that can be used in the form of one-pack.