Radiation curable compositions
A radiation curing, composition technology, applied in coatings, polyurea/polyurethane coatings, etc., can solve problems such as increased processing and expenditure
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Embodiment 1
[0079] Preparation of Acrylated Allophanate
[0080] To a three liter round bottom flask equipped with a stirrer, heater, dropping funnel and oxygen inlet tube was charged 1275.0 g (15.18 eq) of hexamethylene diisocyanate, 468.6 g (1.36 eq) of poly(ε- caprolactone) ester (PCHEA) and 0.85 g of butylated hydroxytoluene stabilizer. The mixture was stirred under air until homogeneous and heated to 80°C when 1.49 g of zinc octoate (22% Zn) catalyst was added. The reaction mixture was then heated to 100° C. and maintained at this temperature for three and a half hours when the isocyanate was determined to be 29.55% NCO by potentiometric titration. 0.7 g of benzoyl chloride was added to deactivate the zinc catalyst. The viscosity is less than 20mPa·sec at 25°C.
Embodiment 2
[0082] Preparation of HPA / PCHEA Adduct of Acrylated Allophanate
[0083] To a 500 ml round bottom flask equipped with a stirrer, heater, dropping funnel and oxygen inlet tube was added 94.1 g (0.66 eq) of acrylated ureidoacrylate from Example 1, 43.5 g (0.33 eq) of hydroxypropyl acrylate Ester (HPA), 113.9g (0.33eq) PCHEA and 1.25g butylated hydroxytoluene stabilizer. The mixture was stirred until homogeneous when 0.06 g of dibutyltin dilaurate catalyst was added. The reaction mixture was then heated to 60°C and held at this temperature for six hours when no isocyanate was visible in the IR spectrum. The viscosity at 25°C was 2,600 mPa·sec and the density was 9.3 lbs / gal.
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Abstract
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