A structural polyurethane adhesive includes a polyisocyanate component containing a urethane prepolymer having an isocyanate group at its terminal and a derivative of xylylene diisocyanate; and a polyol component containing a macropolyol having a number average molecular weight of 500 or more and 10000 or less, and an average number of hydroxyl groups of 1.9 or more and 4.0 or less.

A coating composition can include an aliphatic polyisocyanate and a polyaspartate combined at an equivalent ratio of from 0.9 to 1.8, the aliphatic polyisocyanate having an NCO % of from 6 wt % to 25 wt % based on ISO 11909:2007. The coating composition can also include a pigment at a pigment to binder ratio of from 0.05 to 1.3, a drying agent in an amount of from 0.5 wt % to 5 wt % based on a total weight of the coating composition, and a bismuth compound. The coating composition can have a total solvent content of less than or equal to 250 g/L.

Provided is a photo-curable composition capable of creating a three-dimensional object excellent in both of: stiffness and strength; and toughness. Specifically, provided is a photo-curable composition including: a blocked isocyanate represented by the general formula (1); a chain extender; and a photo-radical generator: ##STR00001##
wherein, in the general formula (1), A.sub.1 to A.sub.4 each independently represent a structure represented by the following general formula (2), and B represents a structure represented by the following general formula (3) ##STR00002##

A coating method in which a first coating composition is applied to the surface of an object to be coated to obtain a first uncured coating film, a second coating composition is applied to the first uncured coating film to obtain a second uncured coating film, and the first uncured coating film and the second uncured coating film are then cured simultaneously by heating, wherein the first coating composition contains a hydroxyl group-containing resin component and the second coating composition contains an isocyanate component containing a triisocyanate represented by general formula (I) (in the formula, the multiple Y.sup.1 each independently are a single bond or a C1-20 divalent hydrocarbon group which optionally contains one or more selected from the group consisting of an ester group and an ether group, and R.sup.1 is a hydrogen atom or a C1-12 monovalent hydrocarbon group) and the above-mentioned hydroxyl group-containing resin component, is provided. ##STR00001##

The invention relates to a process for preparing a derivatized polysaccharide and stable isocyanate-based dispersions comprising derivatized polysaccharide.

A polyaspartic coating composition that contains: an aspartic acid ester compound of formula (I):

##STR00001##

where X is an n-valent organic group, R.sub.1 and R.sub.2 are identical or different organic groups inactive against an isocyanate group under reaction conditions, and n is an integer of 2 or more; and a polyisocyanate composition comprising a polyisocyanate obtained from at least one trisocyanate compound of formula (VIII):

##STR00002##

where each Y.sup.1 independently represents a single bond, or a divalent hydrocarbon group which may have at least one selected from the group consisting of an ester structure and an ether structure, the Y.sup.1 groups are identical to or different from each other, and R.sup.3 is a hydrogen atom or a monovalent hydrocarbon group.

A curable composition including: a component (a): a polycarbonate polyol having a hydroxyl value of 40 to 75 mgKOH/g; a component (b): a polycarbonate polyol having a hydroxyl value of 100 to 280 mgKOH/g; and a component (c): a polyisocyanate having an average number of functional groups per molecule, of 2 to 6.

The present invention relates to alkoxysilane-functionalized and allophanate-functionalized urethanes, methods for the preparation thereof, coating compositions comprising these and to the use thereof.

An alkoxysilane-functionalized and allophanate-functionalized coating material including a) a binder component of 10-99 wt % of at least one reaction product of I. and II. wherein I includes A) at least one alkoxysilane-containing monourethane A) of the formula 1 R.sub.n(OR.sub.1).sub.3-nSi—R.sup.2—NH—(C═O)—OR.sup.3 wherein R, R.sup.1, R.sup.2 and R.sup.3 represent hydrocarbon radicals having 1-8 carbon atoms, and n represents 0-2, and B) at least one diisocyanate B), and II includes the subsequent reaction of C) with at least one diol and/or polyol C), in a ratio of NCO groups of reaction product I to OH groups of the diol and/or polyol II. C) of 1.0:1.5 to 1.0:0.6; b) 1-90 wt % of at least one further binder component distinct from a) a hydroxyl-containing or amino-containing binder component, c) 0-50 wt % of at least one polyisocyanate having an NCO functionality of at least 2, d) 0-5 wt % of at least one catalyst, wherein components a)-d) add up to 100 wt %.

The present invention relates to alkoxysilane-functionalized allophanates, to methods for production thereof, and to the use thereof. In particular, the alkoxysilane-functionalized allophanate includes the reaction product of A) at least one alkoxysilane group-containing monourethane A) of the formula 1

R.sub.n(OR.sup.1).sub.3-nSi—R.sup.2—NH—(C═O)—OR.sup.3   formula 1,

where R, R.sup.1, R.sup.2 and R.sup.3 are each independently hydrocarbyl radicals having 1-8 carbon atoms, which may be linear, branched or cyclic, or else may be integrated together to form a cyclic system, and n is 0-2, and B) at least one diisocyanate B), in a molar ratio of A) to B) of 3:1 to 1.5:1.