A continuous process for producing a polyurea concentrate or powder. The process includes combing at least one amine and an isocayante in the presence of a liquid diluent or a base oil in a rotor stator mixer. The concentrate comprises a polyurea in a base oil wherein the concentration of from about 20 weight percent to about 50, or 40 or 35 or 30 weight percent of polyurea based on total weight of grease thickener. The powder has particle size of 2 to 400 microns. This concentrate or powder can then be formulated by grease manufacturers to the desired final properties without the need for handling of the isocyanate and amine raw materials.

A particulate polyurea compound a2) for reducing gloss of coatings, a resin composition and a crosslinkable composition comprising the particulate polyurea compound is provided, wherein the volume percentage of particles of the particulate polyurea compound having a diameter of smaller than 10 μm is equal or less than 40%, and the volume percentage of the polyurea product having a diameter larger than 20 μm is equal or more than 11%.

An aqueous dispersion of a capsule composed of a polymeric shell surrounding a core, the core containing an amine blocked isocyanate, the amine blocked isocyanate comprises at least two isocyanate groups blocked by a blocking group, the blocking groups are independently from each other represented by a secondary amine The aqueous dispersion is suitable as reactive binder chemistry in coatings and inks.

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.

There is provided a compatibilizer for polyester resin which can produce better compatibility than conventional counterparts, and a polyester resin composition using the compatibilizer. The compatibilizer comprises a polycarbodiimide compound represented by the formula (1) describe below wherein the carbodiimide equivalent of the polycarbodiimide compound is 280 or higher; and in the formula (1), R.sup.1 and R.sup.2 are residues formed by eliminating a functional group from an organic compound having the one functional group reactive with an isocyanate group; R.sup.3 is a divalent residue formed by eliminating two isocyanate groups from a diisocyanate compound; R.sup.4 is a divalent residue formed by eliminating two hydroxyl groups from a diol compound; X.sup.1 and X.sup.2 are bonds formed by reaction of the functional group of the organic compound with one of the two isocyanate groups of the diisocyanate compound; and m and n=1 to 20, m+n≤25, and p=0 to 39, provided that the number of carbodiimide groups in one molecule is 2 to 40.

##STR00001##

This invention generally provides blocked isocyanate compositions and more specially blocked isocyanate compositions useful in aminoplastic resins, phenoplastic resins or latex resins for composite wood products, wherein the blocked isocyanate composition is obtained by adding alkylene carbonate to a blocked isocyanate (A), wherein the blocked isocyanate (A) is obtained by reacting a secondary amine (a1) with a reaction product (a2) of a polyfunctional isocyanate and a monofunctional hydroxyl containing compound, wherein the monofunctional hydroxyl containing compound is a polyethylene oxide polymer with terminal hydroxyl group, polyoxyethylene-polyoxypropylene monols or a mixture thereof, wherein the portion of blocked isocyanate (A) by weight percentage of the blocked isocyanate composition is between 50 and 90, preferably between 60 and 80. The compositions are stable at room temperature when mixed with active hydrogen containing compounds. The composition has low visicosity and after de-block has the potential to reduce free formaldehyde levels in formaldehyde containing resins.

This invention generally provides blocked isocyanate compositions and more specially blocked isocyanate compositions useful in aminoplastic resins, phenoplastic resins or latex resins for composite wood products, wherein the blocked isocyanate composition is obtained by adding alkylene carbonate to a blocked isocyanate (A), wherein the blocked isocyanate (A) is obtained by reacting a secondary amine (a1) with a reaction product (a2) of a polyfunctional isocyanate and a monofunctional hydroxyl containing compound, wherein the monofunctional hydroxyl containing compound is a polyethylene oxide polymer with terminal hydroxyl group, polyoxyethylene-polyoxypropylene monols or a mixture thereof, wherein the portion of blocked isocyanate (A) by weight percentage of the blocked isocyanate composition is between 50 and 90, preferably between 60 and 80. The compositions are stable at room temperature when mixed with active hydrogen containing compounds. The composition has low visicosity and after de-block has the potential to reduce free formaldehyde levels in formaldehyde containing resins.

Provided herein according to embodiments is a prepolymer compound of formula I: ##STR00001##
and a prepolymer compound of formula II: ##STR00002##
A polymerizable liquid composition comprising the prepolymer compound, methods of use in forming a three-dimensional object, and objects produced are also provided.

Provided herein according to embodiments is a prepolymer compound of formula I: ##STR00001##
and a prepolymer compound of formula II: ##STR00002##
A polymerizable liquid composition comprising the prepolymer compound, methods of use in forming a three-dimensional object, and objects produced are also provided.

The present invention relates to a multi-aziridine compound having: a) at least 2 of the following structural units (A) whereby R.sub.1 is H; R.sub.2 and R.sub.4 are independently chosen from H, a linear group containing from 1 to 8 carbon atoms and optionally containing one or more heteroatoms, a branched or cyclic group containing from 3 to 8 carbon atoms and optionally containing one or more heteroatoms, phenyl, benzyl, or pyridinyl; R.sub.3 is chosen from a linear group containing from 1 to 8 carbon atoms and optionally containing one or more heteroatoms, a branched or cyclic group containing from 3 to 8 carbon atoms and optionally containing one or more heteroatoms, phenyl, benzyl, or pyridinyl; or R.sub.2 and R.sub.3 (in case R.sub.2 is different than H) may be part of the same cyclic group containing from 3 to 8 carbon atoms; R′ and R″ are independently H or an aliphatic hydrocarbon group containing from 1 to 12 carbon atoms; and b) a molecular weight of at least 600 Daltons, wherein the molecular weight is determined using MALDI-TOF mass spectrometry according to the description.