Synthetic method of phosphate modified urethane acrylate
A technology of polyurethane acrylate and synthesis method, which is applied in the direction of polyurea/polyurethane adhesive, adhesive type, adhesive, etc., can solve the problems of unseen synthesis method and application, etc., and achieve high functionality and good flexibility , the effect of reducing the dosage
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0028] Add 400g of polyether diol (Mn=400, 1.00mol) into a 1000ml four-neck flask, vacuum dehydrate at 90-100°C for 1 hour, cool down to 30°C, add 101g (1.00mol) of triethylamine, 50g of toluene , Slowly add 51.2g (0.33mol) POCl dropwise at this temperature 3 After the dropwise addition, react at 40° C. for 3 hours, wash the product with water until neutral, separate layers, and distill under reduced pressure to obtain 398 g of hydroxyl-terminated polymer (hydroxyl value 135.3 mgKOH / g). Add the product dropwise to 213g (0.96mol) IPDI, keep the temperature at 70°C, and add 113.2g (0.98mol) hydroxyethyl acrylate and 2 drops of dibutyltin dilaurate to the vicinity of the theoretical isocyanate value. React at 75°C until the NCO characteristic peak cannot be detected by infrared, and then the phosphate-modified polyurethane acrylate is obtained.
Embodiment 2
[0030] Add 450g of polyester diol (Mn=600, 0.75mol) into a 1000ml four-necked bottle, vacuum dehydrate at 90-100°C for 1 hour, cool down to 30°C, add 75.8g (0.75mol) of triethylamine, 50g Toluene, slowly drop 38.4g (0.25mol) POCl at this temperature 3 After the dropwise addition, react at 50° C. for 2.5 hours, wash the product with water until neutral, separate layers, and distill under reduced pressure to obtain 391 g of a hydroxyl-terminated polymer (hydroxyl value: 91.3 mgKOH / g). Add this product dropwise to 111.4g (0.64mol) 80 / 20TDI, keep the temperature at 70°C, and add 75.1g (0.65mol) of hydroxyethyl acrylate and 2 drops of dibutyltin dilaurate to near the theoretical isocyanate value The catalyst is reacted at 75°C until the NCO characteristic peak is not detected by infrared, and the product is obtained.
Embodiment 3
[0032]Add 500g of polyether diol (Mn=1000, 0.5mol) into a 1000ml four-necked bottle, vacuum dehydrate at 90-100°C for 1 hour, cool down to 30°C, add 50.5g (0.5mol) of triethylamine, 50g Toluene, slowly drop 26.1g (0.17mol) POCl at this temperature 3 In a four-neck flask, react at 35° C. for 4 hours after the dropwise addition, wash the product with water until neutral, separate layers, and distill under reduced pressure to obtain 475 g of a hydroxyl-terminated polymer (hydroxyl value 55 mgKOH / g). Take 200g of this product and add dropwise to 33.6g (0.2mol) HDI, keep the temperature at 60°C, and add 27.3g (0.21mol) of hydroxyethyl methacrylate and 1 drop of dilauric acid dilaurate to the vicinity of the theoretical isocyanate value. Butyl tin catalyst, react at 70°C until the NCO characteristic peak is not detected by infrared, and the product is obtained.
PUM
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, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com