US 12,234,316 B2
Acrylate oligomer and preparation method and application method thereof
Tao Xie, Hangzhou (CN); Jingjun Wu, Hangzhou (CN); Qian Zhao, Hangzhou (CN); and Jiada Chen, Hangzhou (CN)
Assigned to Zhejiang University, Hangzhou (CN)
Filed by ZHEJIANG UNIVERSITY, Hangzhou (CN)
Filed on Apr. 17, 2022, as Appl. No. 17/722,371.
Claims priority of application No. 202110608425.0 (CN), filed on Jun. 1, 2021.
Prior Publication US 2022/0403095 A1, Dec. 22, 2022
Int. Cl. C08F 2/46 (2006.01); C08F 2/50 (2006.01); C08G 18/10 (2006.01); C08G 18/67 (2006.01); C08G 61/04 (2006.01)
CPC C08G 18/673 (2013.01) [C08G 18/10 (2013.01)] 6 Claims
 
1. A method of preparing light-cured polyacrylate from an acrylate oligomer, wherein, the acrylate oligomer is obtained by a reaction of isocyanate group-terminated oligomer and formate-terminated ethylene glycol methacrylate:

OG Complex Work Unit Chemistry
wherein R is methyl;
the isocyanate group-terminated oligomer is obtained by reacting an isocyanate-containing compound with an active hydrogen-containing compound, and the molar ratio of isocyanate to active hydrogen is greater than 1;
the active hydrogen-containing compound can be selected from one or more of polyols or polyamines;
the polyol is selected from one or more of polyester polyol, polyether polyol, polycarbonate polyol, polybutadiene polyol, polyolefin polyol or polyacrylate polyol; the polyamine is selected from one or more of polyetheramine, dichlorodiaminodiphenylmethane, and diethyltoluenediamine;
the isocyanate-containing compound is selected from one or more of toluene diisocyanate, diphenylmethane diisocyanate, hexamethylene diisocyanate, isophorone diisocyanate, xylylene diisocyanate, and dicyclohexylmethane diisocyanate;
wherein, the method comprises the following steps:
1) mixing the acrylate oligomer with a reactive diluent and adding an initiator to obtain a mixture;
2) using a light source matching the initiator to cure the mixture in step 1) to obtain a light-cured sample; and
3) if the acrylate oligomer does not contain urea bonds, placing the light-cured sample obtained in step 2) at a temperature of 60-100° C. and a humidity of 60-90% for 1-48 hours; if the acrylate oligomer contains urea bonds, treating the light-cured sample obtained in step 2) at a temperature of 60-100° C. for 1-48 hours.