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.

A preparation method for a corrosion-resistant coating of a reinforcing steel for marine concrete, comprising the steps: (1) pretreating the surface of a reinforcing steel; (2) preparing self-repairing corrosion microcapsules; (3) preparing a cathodic electrophoresis coating; (4) carrying out cathodic electrophoresis; and (5) curing. The electrophoresis coating of the present invention contains the self-repairing corrosion microcapsules, metal powder, and graphene oxide powder. The corrosion resistance of the coating is improved under the co-action of the self-repairing properties of the self-repairing microcapsules and cathodic protection. The corrosion-resistant coating has excellent adhesion and corrosion resistance, prolonging the service life of reinforcing steel. It is widely used for the protection of reinforcing steels for marine concrete, and also for the protection of metal structures in general environment.

Embodiments relate to a porous polyurethane polishing pad for use in a chemical mechanical planarization (CMP) process of semiconductors and a process for producing the same. In the porous polyurethane polishing pad, it is possible to control the size and distribution of pores, whereby the polishing performance (i.e., polishing rate) of the polishing pad can be adjusted, by way of employing thermally expanded microcapsules as a solid phase foaming agent and an inert gas as a gas phase foaming agent.

Provided are a method of preparing a polyurethane prepolymer with high functionality and the polyurethane prepolymer with high functionality prepared therefrom and a curing agent comprising the same. The method includes the steps of: Step (A): providing an alcohol composition comprising a first polyol having 2 or 3 OH groups and a second polyol having 4 or more OH groups; Step (B): reacting the alcohol composition with a polyisocyanate to undergo a first polymerization, so as to obtain an intermediate; wherein a molar ratio of a total number of the OH groups of the alcohol composition to a total number of NCO groups of the polyisocyanate is from 1:2 to 1:6; and Step (C): adding a catalyst to carry out a second polymerization of the intermediate to obtain the polyurethane prepolymer with high functionality, which has four or more NCO groups.

The present invention relates to a modified polyisocyanate and use thereof, in particular as a crosslinking component of water-soluble or water-dispersible coatings. The modified polyisocyanate is obtained by a reaction of a system comprising the following components: at least an aminosulfonic acid; at least a polyisocyanate; at least a tertiary amine; and optionally a polyether alcohol containing an ethylene oxide group. The modified polyisocyanate comprises at least an iminooxadiazinedione structure and at least an isocyanurate structure, the weight ratio of the iminooxadiazinedione structure to the isocyanurate structure being 1:300 to 1:5. The amount of sulfonate group of the modified polyisocyanate is 0.75% by weight to 1.1% by weight, based on the amount of the modified polyisocyanate as 100% by weight. The viscosity thereof is 500 mPa.Math.s to 10000 mPa.Math.s, as determined according to DIN EN ISO 3219:1994-10 at a temperature of 23° C. and a shear rate of 10 s.sup.−1. The coating comprising the modified polyisocyanate of the present invention can be manually stirred well, and the resulting coating layer has high gloss and good transparency.

An alternative polyurethane composition is provided comprising a reaction product of an azidated polyol and a poly(alkynyl carbamate) allophanate prepolymer, wherein the poly(alkynyl carbamate) allophanate prepolymer comprises a reaction product of a first alkynol and a poly(alkynyl carbamate) prepolymer, in the presence of a metallo-organic compound of the formula: M(acac).sub.n, wherein, M=a metal, acac=an acetylacetonate residue, and n=2 or 3, wherein the poly(alkynyl carbamate) prepolymer comprises a reaction product of a polyisocyanate and a stoichiometric equivalent of a second alkynol, and wherein the polyisocyanate comprises isocyanate groups and uretdione groups. The inventive alternative polyurethane compositions may be used to provide solventborne or waterborne coatings, adhesives, sealants, films, elastomers, castings, foams, and composites.

Provided is a waterborne resin crosslinking agent and the like capable of inhibiting lowering of gloss (relative specular glossiness) of cured films (waterborne resin coating films) after heating. The waterborne resin crosslinking agent includes a polycarbodiimide compound (A) and a polycarbodiimide compound (B); the polycarbodiimide compound (A) has a structure in which isocyanate groups at both terminals are each capped with a hydrophilic organic compound, and at least one of the hydrophilic organic compounds has a molecular weight of 340 or more; the polycarbodiimide compound (B) has a structure in which isocyanate groups at both terminals are each capped with a monool compound having 3 to 18 carbon atoms; when the monool compound has 3 to 17 carbon atoms, the polycarbodiimide compound (A) is in an amount of 5 to 95 parts by mass per 100 parts by mass in total of the polycarbodiimide compound (A) and the polycarbodiimide compound (B); and when the monool compound has 18 carbon atoms, the polycarbodiimide compound (A) is in an amount of 30 to 70 parts by mass per 100 parts by mass in total of the polycarbodiimide compound (A) and the polycarbodiimide compound (B).

Disclosed herein is a coating composition obtained by mixing a resin and/or hardener; a sagging control agent (SCA) reactive to resin and/or hardener; and a catalyst. Further disclosed herein are methods of preparing 1K and 2K coating compositions and using the coating compositions in an automotive to form a clearcoat.

The disclosure relates to a thermoset omniphobic composition, which includes a thermoset polymer with first, second, and third backbone segments, urethane groups linking the first and third backbone segments, and urea groups linking the first and second backbone segments. The first, second, and third backbone segments generally correspond to urethane or urea reaction products of polyisocyanate(s), amine-functional hydrophobic polymer(s), and polyol(s), respectively. The thermoset omniphobic composition has favorable omniphobic properties, for example as characterized by water and/or oil contact and/or sliding angles. The thermoset omniphobic composition can be used as a coating on any of a variety of substrates to provide omniphobic properties to a surface of the substrate. Such omniphobic coatings can be scratch resistant, ink/paint resistant, dirt-repellent, and optically clear. The thermoset omniphobic composition can be applied by different coating methods including cast, spin, roll, spray and dip coating methods.

Disclosed is an aliphatic polyisocyanate composition, wherein the molar ratio of an iminooxadiazinedione structure to an isocyanurate structure is 0.01-0.8:1, and the molar ratio of an iminooxadiazinedione structure in a polymer larger than three molecules to the iminooxadiazinedione structure in the composition is 0.2-0.8:1. Provided are a method for preparing the aliphatic polyisocyanate composition, and a coating composition. The aliphatic polyisocyanate composition has both a lower viscosity and a better crosslinking property. The composition can significantly reduce the usage amount of a solvent when used in a coating composition, is more environmentally friendly and also has a better paint film property. The preparation method has a simple process and mild conditions, is easy to operate and control, and is suitable for industrial scale production.