The invention relates to a composition and to a process for preparing moisture-crosslinking polymers under catalysis by at least one metal-siloxane-silanol(ate) compound, and to the use of the composition in the CASE sector (coatings, adhesives, sealants and elastomers), especially in the field of adhesives and sealants.

Disclosed is a moisture reactive polyurethane hot melt adhesive composition that can be applied to substrates at a low coating weight even at application temperatures as low as 60 to 95° C. while retaining the advantageous high tack, green strength, cured bond strength and toughness of conventional high melting point polyurethane hot melt adhesives.

Disclosed is an adhesive system and method of use thereof wherein the adhesive composition comprises a moisture curable adhesive comprised of an isocyanate terminated prepolymer and a cure accelerator having two curatives components having different cure kinetics. The cure accelerator is comprised of an isocyanate reactive compound comprising a primary, secondary or tertiary amino group, or a primary thiol group having faster curing kinetics resulting an increase in bead stability within the first minutes and a polyol selected from a diol and/or triol with slower curing kinetics allowing for sufficient open time and yet a fast strength build up. The preferred method of application of the adhesive system is via a 1K application gun.

The present disclosure provides a liquid-state reactive polyurethane adhesive, which includes a polyurethane prepolymer. The polyurethane prepolymer is blocked by an isocyanate group, and the polyurethane prepolymer is obtained by a polymerization reaction, a reactive monomer of the polymerization reaction includes a polyisocyanate, a polyol, a stabilizer, a catalyst and a hydrophobic filler. A functionality of the polyisocyanate is 2.4 to 3. A molecular weight of the polyol is 1000 to 8000, and the polyol has hydrolysis resistance. The stabilizer has a structure represented by formula (I). The catalyst has a structure represented by formula (II). Formula (I) and formula (II) are as defined in the specification.

Embodiments of the present disclosure are directed towards formulated polyol compositions that include a first polyether polyol having an average hydroxyl number from 112 to 280 mg KOH/g, a second polyether polyol having an average hydroxyl number from 18.5 to 51 mg KOH/g, a third polyether polyol having an average hydroxyl number from 20 to 70 mg KOH/g, and at least one of: fourth polyether polyol having an average hydroxyl number from 112 to 280 mg KOH/g; and a methoxypolyethylene glycol having an average hydroxyl number from 56 to 190 mg KOH/g.

A flexible polyurethane foam material with strong support and high elasticity is made by foaming the following raw materials by weight: 80-120 parts of lignin-based block copolymer molecular-level combined polyether; 45-65 parts of isocyanate; 0.5-5 parts of foaming catalyst; 1-10 parts of water; and 1-3 parts of foam stabilizer; the lignin-based block copolymer molecular-level combined polyether is based on lignosulfonate, molecular chain of lignosulfonate is cut and embedded by using solvation effect of polyether polyol to form a molecular-level combined polyether that is polymerized and formed by aromatic polymer fragments of lignosulfonate and aliphatic polymer fragments of polyether polyol. The foaming catalyst can be a foaming catalyst commonly used in the technical field.

A process for producing an isocyanate-group terminated polyoxazolidinone comprising the copolymerization of a polyisocyanate compound (A) with two or more isocyanate groups with a polyepoxide compound (B) with two or more epoxy groups in the presence of a specific catalyst (C), wherein the molar ratio of the isocyanate groups of the polyisocyanate compound (B) to the epoxy groups of the polyepoxide compound (A) is larger than 2:1 and less than 25:1. The resulting isocyanate-group terminated polyoxazolidinones is also provided.

In an adhesive selection method, test data is acquired by subjecting an adhesion complex, obtained by integrally bonding one material and an other material that are heterogeneous using an adhesive, to a shear test, in which a tensile shear load is applied to the adhesion complex in a direction that causes shear deformation in the adhesive, until adhesive failure takes place. Based on the test data, a plurality of two- or three-dimensional FEM analysis models of the adhesion complex with varied adhesives are constructed. On each of the analysis models, a simulation is performed in which a tensile shear load is applied. Based on the stresses and locations of the stresses generated in each of the analysis models in the course of the, the adhesive for binding one member made of the one material and the other member made of the other material is selected from among the adhesives.

The present invention relates to a selective process for the preparation of NCO-functionalized polyols, to their use in the preparation of silylated polyurethanes, to processes for preparing silylated polyurethanes and to silylated polyurethanes obtainable by a reaction of NCO-functionalized polyol with amino silane and to their use in CASE applications (coatings, adhesives, sealants and elastomers).

The present invention provides a blocked polyisocyanate composition comprising a blocked polyisocyanate formed through blocking at least a part of isocyanate groups possessed by a polyisocyanate derived from one or two or more diisocyanates selected from the group consisting of an aliphatic diisocyanate and an alicyclic diisocyanate with an active methylene-based compound comprising a malonic acid diester, wherein a specific molar ratio calculated from contents (mol %) of isocyanurate groups, iminooxadiazinedione groups, uretdione groups, and allophanate groups is 0.05 or more and 0.60 or less.