The present invention relates to a moisture-crosslinkable sealant composition comprising: at least one polyurethane P comprising at least two NCO end functions; at least one polyimine A obtained via a process comprising a step of reaction between at least: a) a (poly)urethane-aldehyde comprising at least 2 aldehyde functions; b) a primary diamine; c) optionally in the presence of a primary monoamine or a monoaldehyde if the —CHO/NH.sub.2 molar ratio is other than 1.

A linear polymer containing isocyanate groups and having an NCO content in the range from 0.3% to 1.5% by weight and a monomeric diisocyanate content of not more than 0.5% by weight, wherein it is obtained from the reaction of at least one monomeric aromatic diisocyanate and a polyether diol having an OH number in the range from 5 to 21 mg KOH/g in an NCO/OH ratio of at least 5/1 and subsequent removal of a majority of the monomeric aromatic diisocyanate by means of a suitable separation method, and to moisture-curing polyurethane compositions having a monomeric diisocyanate content of less than 0.1% by weight, comprising said polymer. The polymer of the invention enables elastic adhesives having high elongation, surprisingly high strength and surprisingly good adhesion to plastic substrates.

The present invention relates to compounds having one of the following formulae (I) and (II):

##STR(I)##

##STR(II)##

and also to the uses thereof.

The present invention relates to isocyanate-terminated prepolymers based on polyoxymethylene-polyoxyalkylene block copolymers, to a process for their preparation, and to the use of these isocyanate-terminated prepolymers as isocyanate components in 1- and 2-component systems for coatings, adhesives and sealants.

The present invention relates to an aqueous polyurethane dispersion, a method for the preparation thereof, a product comprising the same, and use thereof for a coating composition, an impregnating composition, an adhesive or a sealant. The aqueous polyurethane dispersion comprises a polyurethane obtained by reacting a system comprising the following components: A1) at least one polyisocyanate having an isocyanate functionality of not less than 2; A2) at least two different polytetramethylene ether glycols A2a) and A2b), the A2a) having a number average molecular weight of not more than 1500 g/mol, the A2b) having a number average molecular weight of more than 1500 g/mol; and A3) at least one anionic or potentially anionic hydrophilic agent having a number average molecular weight of 32 g/mol to 400 g/mol and containing hydroxyl and carboxyl functions; B) at least one amino-functional anionic or potentially anionic hydrophilic agent; and C) at least one amino-functional compound having a number average molecular weight of 32 g/mol to 400 g/mol and containing no hydrophilic group; wherein the ratio of the number average molecular weight of the A2a) to the number average molecular weight of the A2b) is 1:9 to less than 1:1, and the weight of the A3) amounts to 20% to 70% of the weight of the hydrophilic agents of the system, wherein the hydrophilic agents of the system are components A3 and B.

Described herein is a moisture-curing polyurethane hot-melt adhesive including at least 80% by weight, based on a total weight of the moisture-curing polyurethane hot-melt adhesive, of isocyanate-terminated prepolymer obtainable by mixing diisocyanate (a) with compounds having at least two isocyanate-reactive groups (b) and reacting the mixture to form the isocyanate-terminated prepolymer, where the compounds having at least two isocyanate-reactive groups (b) include at least one polylactide (b1) obtainable by reacting lactide with a linear difunctional starter molecule having 2 to 20 carbon atoms and the isocyanate content of the isocyanate-terminated prepolymer is 1 to 5% by weight. Also described herein is a process for producing such a moisture-curing polyurethane hot-melt adhesive and a method of using the moisture-curing polyurethane hot-melt adhesive in bonding of substrates.

A binder has at least one isocyanate and at least one biopolymer mixed with water. The biopolymer may be a biopolymer nanoparticle or cooked and chemically modified starch. Optionally, the binder may also include urea. The biopolymer and water are mixed, and the isocyanate is added to the mixture. The binder may have a viscosity that is suitable for being sprayed on a substrate to make a composite material, for example a viscosity of 700 cP or less or 500 cP or less at 40° C. The substrate may be wood, another lignocellulosic material, or synthetic or natural fibers. In particular examples, the binder is used to make no added formaldehyde wood composites including particle board and fiberboard. Alternatively, the binder may have a higher viscosity and be used to make plywood.

A poly(meth)acrylate urethane polymer, obtained from the reaction of at least one monomeric diisocyanate and a poly(meth)acrylate polyol having an OH number in the range from 50 to 200 mg KOH/g in an NCO/OH ratio of at least 3/1, followed by removal of a majority of the monomeric diisocyanate by means of a suitable separation method, wherein it has an NCO content in the range from 2.5% to 8% by weight, based on the poly(meth)acrylate urethane polymer, and a residual content of unconverted monomeric diisocyanates of not more than 0.5% by weight, and to the use thereof as additive and to moisture-curing polyurethane compositions.

A modified polycarbodiimide compound which is obtained by modifying at least some of carbodiimide groups in a polycarbodiimide derived from a diisocyanate compound, said polycarbodiimide having a terminal blocked with a hydrophilic compound, with an aromatic heterocyclic compound such as 3,5-dimethylpyrazole having endocyclic secondary amine nitrogen has a potential for a cuing agent, and exhibits the activity of the carbodiimide groups by being unblocked at relatively low temperatures.

A moisture-curable composition, including: a) at least one polyurethane polymer P having isocyanate groups; b) at least one blocked polyamine BA having blocked, hydrolytically activatable amino groups; and c) at least one monoamine MA of formula (V),

##STR00001##

where R.sup.a represents a linear, cyclic, or branched alkyl or alkenyl radical or optionally substituted aryl radical with 1 to 12 C atoms and optionally including ether oxygen atoms; R.sup.b and R.sup.c either independently represent a rest R.sup.a or a hydrogen atom, where at least one of R.sup.b and R.sup.c is a hydrogen atom, or R.sup.b and R.sup.c together with the N atom of monoamine MA form an aldimine group that under influence of water hydrolyzes to a aldehyde and an amine R.sup.a—NH.sub.2; wherein polymer P is the reaction product of 2,4- and/or 2,6-toluylene diisocyanate (TDI) and at least one polyol, wherein the polyol has an average functionality of >2.