Aqueous stone-chip-resistant polyurethane dispersion body and preparation method thereof
A technology of polyurethane dispersion and anti-stone impact, applied in the direction of polyurea/polyurethane coatings, coatings, etc., can solve the problems of no correlation and different technical fields, achieve simple lines, low VOC content, and realize large-scale industrial production Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Example Embodiment
[0046] 3. Resin Example 1:
[0047] In the reactor, 92g of polycarbonate diol (Mn=3000) compound was dewatered at 105°C for 2 hours under negative pressure of -0.09MPa, and the water content was confirmed to be 0.02%; then 28g of isophorone diisocyanate Add, pre-react at 70℃ for 30min, then add 0.08g of catalyst, and react for 2 hours to reach the set NCO value of 7.94~7.74%; then add 7.2g of dimethylolpropionic acid and continue the reaction at 80℃ After 4 hours, reach the set NCO value of 5.83~5.53%; then add 20g of hexanediol and continue to react at 85℃ for 0.5 hours to reach the set NCO value of 1.80~1.55%; then dissolve 7.2g of trimethylamine in N -40g of methylpyrrolidone, then add it to the reactor, neutralize at 50℃ for 1 hour; then add 176.72g of deionized water of formula, and carry out reverse emulsification under high-speed dispersion conditions; finally add chain extender to the emulsion 4.8 g of butanediamine, continued emulsification and chain extension for 0.5 h...
Example Embodiment
[0049] 4. Resin Example 2:
[0050] In the reactor, 60g of the polycarbonate diol (Mn=1000) compound was dewatered at 100°C for 3 hours under negative pressure of -0.07MPa to confirm that the water content was 0.025%; then hydrogenated diphenylmethane diisocyanate Add 40g, pre-react at 90℃ for 30min, then add 0.12g of catalyst, and react for 0.5 hours to reach the set NCO value of 11.01~10.91%; then add 14g of dimethylolbutyric acid and continue the reaction at 95℃ After 2 hours, reach the set NCO value of 6.39~6.09%; then add 12g of propylene glycol and continue the reaction at 80℃ for 1 hour to reach the set NCO value of 1.92~1.72%; then dissolve 13.6g of triethylamine in N- 24g of methylpyrrolidone, then added to the reactor, neutralized at 60°C for 45min; then added the formula amount of deionized water 214.28g, reversed emulsification under high-speed dispersion conditions; finally added chain extender hexamethylene in the emulsion 6g of amine, continued emulsification and ...
Example Embodiment
[0052] 5. Resin Example 3:
[0053] In the reaction kettle, 76g of polycaprolactone diol (Mn=2000) compound was dewatered at 103℃ for 2 hours under negative pressure of -0.07MPa, and the water content was 0.03%; then hydrogenated diphenylmethane diisocyanate Add 56g, pre-react at 80℃ for 30min, then add 0.2g of catalyst, and react for 1 hour to reach the set NCO value of 12.11-11.81%; then add 11.6g of dimethylolbutyric acid and continue at 90℃ React for 3 hours to reach the set NCO value of 6.59~6.29%; then add 4g of butanediol and continue the reaction at 95°C for 0.5 hours to reach the set NCO value of 2.27~2.07%; then add 11.6g of triethylenediamine Dissolve in 32g of N-methylpyrrolidone, then add to the reactor, and neutralize at 65°C for 0.5 hours; then add 185.4g of deionized water of the formula, and perform reverse emulsification under high-speed dispersion; finally add to the emulsion 3.2 g of chain extender butanediamine, continued emulsification and chain extension f...
PUM
Property | Measurement | Unit |
---|---|---|
Acid value | aaaaa | aaaaa |
Viscosity | aaaaa | aaaaa |
Acid value | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap