A process for manufacturing an object involves the steps of: I) depositing a radically cross-linked resin on a carrier so that a layer of a structuring material joined to the carrier is obtained, said layer corresponding to a first selected cross-section of the object; II) depositing a radically cross-linked resin on a previously applied layer of the structuring material so that an additional layer of the structuring material is obtained which corresponds to a further selected cross-section of the object and which is joined to the previously applied layer; III) repeating step II) until the object is formed, wherein the deposition of a radically cross-linked resin in steps I) and II) includes the application of a radically cross-linkable resin to the carrier or the previously applied layer and is performed at least in step II) by applying energy to a selected region of a radically cross-linkable resin, corresponding to the selected cross-section of the object, the radically cross-linkable resin having a viscosity (23 C., DIN EN ISO 2884-1) of 5 mPas to 100,000 mPas. The invention further relates to the use of such a resin in an additive manufacturing process. The radically cross-linkable resin comprises a curable component which is obtained by reacting a polyisocyanate or a polyisocyanate descendant containing at least one oxadiazine trione group (formula I) with a compound that contains acrylate, methacrylate or vinyl ether double bonds and 25 Zerewitinoff active H atoms.

Disclosed is an imine-type quaternary ammonium salt catalyst, wherein the catalyst has a general structure formula shown by formula I below; in the formula, R1 and R2, respectively, are independently selected from a C1-C20 linear alkyl or a branched C3-C20 alkyl, and a C1-C20 hydroxylalkyl, a C3-C8 cycloalkyl, and arylated alkyl; R3 is a linear or branched alkyl, cycloalkyl or aryl; and R4 is hydrogen, aryl, a linear C1-C15 alkyl or branched C3-C15 alkyl. Also disclosed are a method for preparing the catalyst and a polyisocyanate composition prepared therefrom. The catalyst, by introducing an imine structure, on the basis of ensuring high catalytic activity thereof, is allowed to have properties of high temperature decomposition and inactivation, and when applied to the synthesis of polyisocyanate, can effectively prevent the risk of explosive polymerization caused by an uncontrolled reaction.

Disclosed is an imine-type quaternary ammonium salt catalyst, wherein the catalyst has a general structure formula shown by formula I below; in the formula, R1 and R2, respectively, are independently selected from a C1-C20 linear alkyl or a branched C3-C20 alkyl, and a C1-C20 hydroxylalkyl, a C3-C8 cycloalkyl, and arylated alkyl; R3 is a linear or branched alkyl, cycloalkyl or aryl; and R4 is hydrogen, aryl, a linear C1-C15 alkyl or branched C3-C15 alkyl. Also disclosed are a method for preparing the catalyst and a polyisocyanate composition prepared therefrom. The catalyst, by introducing an imine structure, on the basis of ensuring high catalytic activity thereof, is allowed to have properties of high temperature decomposition and inactivation, and when applied to the synthesis of polyisocyanate, can effectively prevent the risk of explosive polymerization caused by an uncontrolled reaction.

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.

The present invention relates to curable compositions, in particular, thiol-ene-curing compositions, a method of coating using said curable compositions, cured compositions obtained by curing said curable compositions, cured articles, comprising said cured compositions, a certain compound comprising olefinically unsaturated functional groups and a silyl functional group for use in said curable compositions and a method of manufacturing the curable compositions.

A coating composition can be made by providing an aminoalkoxysilane and, in the substantial absence of water, reacting at least a portion of the aminoalkoxysilane with at least one epoxide-containing compound including an aliphatic group to yield at least one alkoxysilylamine, and then reacting the alkoxysilylamine with at least one isocyanate reagent containing at least two isocyanate groups to yield a monomer having plural alkoxysilane groups and, in many embodiments, at least two branched aliphatic groups having at least six carbon atoms. A coating composition thus formed exhibits high durability and good flexibility. Also disclosed is a method of applying a coating composition to a substrate and allowing the coating composition to cure, and the cured coating resulting from such application.

The present disclosure provides a pressure sensor composition that includes a crosslinked polymer, a conductive carbon material and an elastomeric rubber, pressure sensors including the same, and methods of preparation and use thereof.

A photopolymerizable composition including: a polymer matrix or a precursor thereof containing a reaction product of an acrylate-based polyol and a compound containing at least one isocyanate group; a photoreactive monomer; and a non-reactive fluoro compound and a photoinitiator; a hologram recording medium produced from the composition; an optical element including the hologram recording medium; and a method of recording a hologram using the photopolymerizable composition.

The present invention relates to a new process for preparing polyisocyanates containing isocyanurate groups and being flocculation-stable in solvents from (cyclo)aliphatic diisocyanates.

A polyurethane elastomer, which can be a foam, generated from (a) an organic diisocyanate, (b) a polyester resin, (c) a chain extender comprised of a polyhydric alcohol, (d) a crosslinker, (e) a plasticizer, (f) a surfactant, (g) a bio-additive, (h) a blowing agent, and (i) an optional dye; and optionally where the elastomer has, for example, a hardness value of, for example, from about 15 Asker C to about 60 Asker C, a tensile strength of from about 1 MPa to about 10 MPa, a resilience of from about 30 percent to about 60 percent, an elongation at break of from about 150 percent to about 700 percent, and a tear strength from about 2 Newtons/millimeters to about 4 Newtons/millimeters, and which elastomers can be selected for footwear.