Mechanisms, polymerization rate scaling, and oxygen inhibition with an ultra-rapid monovinyl urethane acrylate

被引:28
作者
Cramer, Neil B. [1 ]
O'Brien, Casey P. [1 ]
Bowman, Christopher N. [1 ,2 ]
机构
[1] Univ Colorado, Dept Chem Engn, Boulder, CO 80309 USA
[2] Univ Colorado, Hlth Sci Ctr, Dept Restorat Dent, Denver, CO 80045 USA
关键词
Photopolymerization; Oxygen inhibition; Monomers;
D O I
10.1016/j.polymer.2008.08.051
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Certain monovinyl (meth)acrylate monomers with secondary functionalities such as urethanes have been shown to exhibit extremely rapid curing rates. In this work, the polymerization mechanism, polymerization rate scaling, and relative oxygen inhibition are evaluated for an ultra-rapid butyl urethane acrylate and an analogous aliphatic urethane diacrylate. The aliphatic urethane diacrylate was found to have increased polymerization rates at higher initiation rates relative to the butyl urethane acrylate, primarily due to different termination mechanisms. Additionally, due to higher viscosity and crosslinking density, the aliphatic urethane diacrylate was found to exhibit a greater resistance to oxygen inhibition. The flux of oxygen into the aliphatic urethane diacrylate was 1/3 that of butyl urethane acrylate. Suppressed termination likely contributes to the rapid polymerization kinetics of butyl urethane acrylate. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4756 / 4761
页数:6
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