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Synthesis and photopolymerization kinetics of linear alicyclic urethane acrylate macromonomer in presence of reactive diluents

机译:活性稀释剂存在下线性脂环族氨基甲酸酯丙烯酸酯大分子单体的合成及光聚合动力学

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This study deals with the photopolymerization of a macromonomer in the presence of reactive diluents using Photo Differential Scanning Calorimetry or Photo DSC. The kinetic profiles of these systems showed that the rate of photopolymerization rapidly increases at very early stages of the reaction. The rate of reaction was further found to increase with the addition of crosslinking agents. The addition of trifunctional crosslinking agent to the macromonomeric formulation resulted in a higher polymerization rate and conversion than that of a difunctional crosslinking agent. From the heat flow profiles, the kinetic parameters such as induction time, time to attain peak maximum, rate of maximum polymerization, and final conversion were noted for all the formulations. The initiation of photopolymerization was found to depend on the functionality while the in situ viscosity controlled the time scale for reaction diffusion which resulted in varying levels of conversions. Other parameters such as effect of temperature and concentration of photoinitiator on photocuring kinetics are also discussed.
机译:这项研究使用光差示扫描量热法或Photo DSC研究了在存在反应性稀释剂的情况下大分子单体的光聚合。这些系统的动力学曲线表明,在反应的非常早期,光聚合速率迅速增加。还发现反应速度随着交联剂的添加而增加。在大分子单体配方中添加三官能交联剂比双官能交联剂具有更高的聚合速率和转化率。从热流曲线中,注意到所有制剂的动力学参数,例如诱导时间,达到峰最大值的时间,最大聚合速率和最终转化率。发现光聚合的引发取决于功能性,而原位粘度控制反应扩散的时间尺度,这导致变化的转化水平。还讨论了其他参数,例如温度和光引发剂浓度对光固化动力学的影响。

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