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Effect of (meth)acrylates on in situ visible light polymerization of dimethacrylamide

机译:(甲基)丙烯酸酯对二甲基丙烯酰胺原位可见光聚合的影响

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This study reports in situ visible light copolymerization of a synthesized dimethacrylamide with the selected (meth)acrylates. The effects of these selected comonomers with different functional groups on the polymerization rate, degree of conversion, gel time and compressive strength were investigated. The results showed that in situ copolymerization of the dimethacrylamide with the comonomers having an electron-withdrawing and/or acrylate group could significantly increase the polymerization rate, degree of conversion and compressive strength. Contrarily, an electron-donating group on either carbon-carbon double bond or ester linkage could slow down the polymerization. In comparison, its methacrylate counterpart, triethylene glycol dimethacrylate-based system did not show a clear pattern. The formed H-bonds between (meth)acrylamide and organic acid groups may be responsible for higher compressive strengths. Within the limitation of this study, it is concluded that in situ polymerization of dimethacrylamide under visible light can be accelerated by copolymerization with monomers having electron-withdrawing and/or acrylate groups and vice versa.
机译:本研究报告原位可见光共聚的合成二甲基丙烯酰胺与选定的(甲基)丙烯酸酯。研究了这些所选共聚单体对不同官能团的影响,对聚合速率,转化程度,凝胶时间和抗压强度进行了研究。结果表明,与具有释放电子和/或丙烯酸酯基团的共聚单体的二甲基丙烯酰胺的原位共聚可以显着提高聚合速率,转化程度和抗压强度。相反,碳 - 碳双键或酯键上的电子提供的基团可以减缓聚合。相比之下,其甲基丙烯酸酯对应物,三甘醇二甲基丙烯酸酯基体系没有显示出清晰的图案。 (甲基)丙烯酰胺和有机酸基团之间的形成的H键可以负责更高的抗压强度。在该研究的局限质内,得出结论,在可见光下,通过与具有电子抽出的单体和/或丙烯酸酯基团的单体来加速二甲基丙烯酰胺的原位聚合,反之亦然。

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