Patent classifications
C08G18/7887
Polyurethane polymers cured via azido-alkyne cycloaddition at ambient or mild curing conditions
An alternative polyurethane composition is provided which comprises a reaction product of an azidated polyol and a poly(alkynyl carbamate) prepolymer reacted at a temperature of from 20° C. to 120° C., wherein the poly(alkynyl carbamate) prepolymer comprises a reaction product of a polyisocyanate and a stoichiometric equivalent of an alkynol of the formula (I),
HC≡C—R.sup.1R.sup.2—OH (I),
and wherein R.sup.1 is an electron-withdrawing group selected from the group consisting of carbonyl, ester, amide, and urethane and R.sup.2 is a linear or branched alkyl chain having from 1 to 15 carbon atoms. The inventive alternative polyurethane composition position may be used to provide adhesives, sealants, films, elastomers, castings, foams, and composites.
UV curable coating compositions containing aliphatic urethane acrylate resins
Described in preferred embodiments are UV curable coating compositions including a unique blend of aliphatic urethane acrylate resins. Also described are coated articles and methods for their production involving the use of the coating compositions.
MODIFIED POLYISOCYANATE
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.
Thiol-ene-curing compositions
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.
Modified polyisocyanate
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.
Non-reactive fluoro compound and photopolymer composition comprising the same
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.
POLYURETHANE ELASTOMERS, BIO-ADDITIVE COMPOSITIONS
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.
UV curable coating compositions containing aliphatic urethane acrylate resins
Described in preferred embodiments are UV curable coating compositions including a unique blend of aliphatic urethane acrylate resins. Also described are coated articles and methods for their production involving the use of the coating compositions.
POLYURETHANE POLYMERS CURED VIA AZIDO-ALKYNE CYCLOADDITION AT AMBIENT OR MILD CURING CONDITIONS
An alternative polyurethane composition is provided which comprises a reaction product of an azidated polyol and a poly(alkynyl carbamate) prepolymer reacted at a temperature of from 20° C. to 120° C., wherein the poly(alkynyl carbamate) prepolymer comprises a reaction product of a polyisocyanate and a stoichiometric equivalent of an alkynol of the formula (I),
HC≡C—R.sup.1R.sup.2—OH (I),
and wherein R.sup.1 is an electron-withdrawing group selected from the group consisting of carbonyl, ester, amide, and urethane and R.sup.2 is a linear or branched alkyl chain having from 1 to 15 carbon atoms. The inventive alternative polyurethane composition position may be used to provide adhesives, sealants, films, elastomers, castings, foams, and composites.
Process for manufacturing an object, and use of a radically cross-linkable resin in an additive manufacturing process
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.