Curable composition for use in a high temperature lithography-based photopolymerization process and method of producing crosslinked polymers therefrom
US-2024325117-A1 · Oct 3, 2024 · US
US10465034B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10465034-B2 |
| Application number | US-201615544037-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 15, 2016 |
| Priority date | Jan 20, 2015 |
| Publication date | Nov 5, 2019 |
| Grant date | Nov 5, 2019 |
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The invention relates to a crystallization stable polyester prepolymers for producing HDI- and PDI-based, solvent free two component (2K)-polyurethane- and/or polyurea coating agents.
Opening claim text (preview).
The invention claimed is: 1. A process for preparing prepolymers having isocyanate groups and having an NCO content of 2.8% to 18.0% by weight, a mean isocyanate functionality of 1.9 to 3.0 and a viscosity, measured to DIN EN ISO 3219, of max. 3000 mPas at 23° C., comprising reacting 1,5-diisocyanatopentane and/or 1,6-diisocyanatohexane with: A) at least one polyester polyol of mean functionality from 1.9 to 2.3 and of number-average molecular weight from 300 to 3000 g/mol, prepared from aliphatic dicarboxylic acids and/or anhydrides thereof with excess amounts of polyfunctional alcohols, wherein the polyfunctional alcohols are branched aliphatic diols to an extent of at least 30% by weight, based on the total amount of polyfunctional alcohols, and B) at least one polycaprolactone polyester of mean functionality from 2.0 to 3.0 and number-average molecular weight from 176 to 2000 g/mol, at temperatures of 20 to 200° C., observing an equivalents ratio of isocyanate groups to hydroxyl groups of 4:1 to 200:1, wherein the proportion of the polyester component A) in the total amount of the polyester components A) and B) converted is from 15% to 70% by weight. 2. The process according to claim 1 , wherein the polyol components A) and B) are reacted with the diisocyanate(s) as a mixture or successively in any sequence. 3. A process for preparing prepolymers having isocyanate groups and having an NCO content of 2.8% to 18.0% by weight, a mean isocyanate functionality of 1.9 to 3.0 and a viscosity, measured to DIN EN ISO 3219, of max. 3000 mPas at 23° C., comprising reacting in separate reactions 1,5-diisocyanatopentane and/or 1,6-diisocyanatohexane with A) at least one polyester polyol of mean functionality from 1.9 to 2.3 and of number-average molecular weight from 300 to 3000 g/mol, prepared from aliphatic dicarboxylic acids and/or anhydrides thereof with excess amounts of polyfunctional alcohols, where the polyfunctional alcohols are branched aliphatic diols to an extent of at least 30% by weight, based on the total amount of polyfunctional alcohols, and B) at least one polycaprolactone polyester of mean functionality from 2.0 to 3.0 and number-average molecular weight from 176 to 2000 g/mol, at temperatures of 20 to 200° C., observing an equivalents ratio of isocyanate groups to hydroxyl groups of 4:1 to 200:1, and the prepolymers thus obtained are blended with one another in such a way that the proportion of the polyester component A) in the total amount of the polyester components A) and B) converted is from 15% to 70% by weight. 4. A process for preparing prepolymers having isocyanate groups and having an NCO content of 2.8% to 18.0% by weight, a mean isocyanate functionality of 1.9 to 3.0 and a viscosity, measured to DIN EN ISO 3219, of max. 3000 mPas at 23° C., comprising reacting in multiple individual reactions 1,5-diisocyanatopentane and/or 1,6-diisocyanatohexane with mixtures of A) at least one polyester polyol of mean functionality from 1.9 to 2.3 and of number-average molecular weight from 300 to 3000 g/mol, prepared from aliphatic dicarboxylic acids and/or anhydrides thereof with excess amounts of polyfunctional alcohols, where the polyfunctional alcohols are branched aliphatic diols to an extent of at least 30% by weight, based on the total amount of polyfunctional alcohols, with B) at least one polycaprolactone polyester of mean functionality from 2.0 to 3.0 and number-average molecular weight from 176 to 2000 g/mol, at temperatures of 20 to 200° C., observing an equivalents ratio of isocyanate groups to hydroxyl groups of 4:1 to 200:1, and the prepolymers thus obtained are blended with one another in such a way that the proportion of the polyester component A) in the total amount of the polyester components A) and B) converted is from 15% to 70% by weight. 5. A process for preparing prepolymers having isocyanate groups and having an NCO content of 2.8% to 18.0% by weight, a mean isocyanate functionality of 1.9 to 3.0 and a viscosity, measured to DIN EN ISO 3219, of max. 3000 mPas at 23° C., comprising reacting 1,5-diisocyanatopentane and/or 1,6-diisocyanatohexane in separate reactions with i) a mixture/mixtures of A) at least one polyester polyol of mean functionality from 1.9 to 2.3 and of number-average molecular weight from 300 to 3000 g/mol, prepared from aliphatic dicarboxylic acids and/or anhydrides thereof with excess amounts of polyfunctional alcohols, where the polyfunctional alcohols are branched aliphatic diols to an extent of at least 30% by weight, based on the total amount of polyfunctional alcohols, with B) at least one polycaprolactone polyester of mean functionality from 2.0 to 3.0 and number-average molecular weight from 176 to 2000 g/mol, and ii) at least one polyester polyol according to A, and/or iii) at least one polyester polymer according to B, at temperatures of 20 to 200° C., observing an equivalents ratio of isocyanate groups to hydroxyl groups of 4:1 to 200:1, and the prepolymers thus obtained are blended with one another such that the proportion of the polyester component A) in the total amount of the polyester components A) and B) converted is from 15% to 70% by weight. 6. The process for preparing prepolymers having isocyanate groups according to claim 1 , wherein the proportion of the polyester component A), based on the total amount of the polyester components A) and B) used, is 20% to 65% by weight. 7. The process for preparing prepolymers having isocyanate groups according to claim 1 , wherein the branched aliphatic diols used for preparation of component A) are those of the general formula HO—X—OH in which X is a branched alkyl or alkenyl radical having 3 to 36 carbon atoms. 8. The process for preparing prepolymers having isocyanate groups according to claim 1 , wherein component A) comprises polyester polyols based on succinic acid and/or adipic acid, ethane-1,2-diol, butane-1,4-diol, hexane-1,6-diol, glycerol and/or 1,1,1-trimethylolpropane, and the branched aliphatic diols butane-1,3-diol, neopentyl glycol, 2-butyl-2-ethylpropane-1,3-diol, 2,2,4-trimethylpentane-1,5-diol and 2,2,4- and/or 2,4,4-trimethylhexanediol. 9. The process for preparing prepolymers having isocyanate groups according to claim 1 , wherein component B) comprises polyester polyols which have been prepared by ring opening polymerization from ε-caprolactone using butane-1,4-diol, diethylene glycol, neopentyl glycol, hexane-1,6-diol, glycerol and/or 1,1,1-trimethylolpropane as starter molecule. 10. A process for preparing prepolymers having isocyanate groups according to claim 1 , wherein, after the reaction or blending, excess unconverted monomeric diisocyanates are removed by thin-film distillation of the prepolymers having isocyanate groups. 11. Prepolymers having isocyanate groups and having an NCO content of 2.8% to 18.0% by weight, a mean isocyanate functionality of 1.9 to 3.0 and a viscosity, measured to DIN EN ISO 3219, of max. 3000 mPas at 23° C., obtained by the process according to claim 1 . 12. In a process for production of polyurethane polymers, the improvement comprising including the prepolymers according to claim 11 as starting components. 13. A coating composition comprising the prepolymers having isocyanate groups according to claim 11 . 14. A substrate coated with the coating composition according to claim 13 . 15. A molding comprising the prepolymers having isocyanate groups according to claim 11 .
derived from dicarboxylic acids and dialcohols · CPC title
Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step · CPC title
Caprolactone and/or substituted caprolactone · CPC title
Two or more polyesters of different physical or chemical nature (C08G18/44 takes precedence) · CPC title
formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates · CPC title
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