首页> 外文期刊>Journal of Photochemistry and Photobiology, A. Chemistry >Kinetic studies of cationic photopolymerizations of phenyl glycidyl ether: termination/trapping rate constants for iodonium photoinitiators
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Kinetic studies of cationic photopolymerizations of phenyl glycidyl ether: termination/trapping rate constants for iodonium photoinitiators

机译:苯基缩水甘油醚阳离子光聚合的动力学研究:碘鎓光引发剂的终止/捕获速率常数

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In this contribution, we have performed a comprehensive investigation of cationic photopolymerizations of phenyl glycidyl ether using two iodonium photoinitiators: diaryliodonium hexafluoroantimonate (IHA), and (tolycumyl) iodonium tetrakis (pentafluorophenyl) borate (IPB). We characterized these reactions using dark-cure experiments in which the polymerization was monitored in the dark after illuminating it for a pre-determined period of time, and obtained profiles of the rate constant for termination/trapping as a function of time. Our studies reveal that though these photoinitiators result in similar reaction kinetics (reaction rate and conversion profiles that are nearly identical) for constant illumination with a Hg(Xe) arc lamp, they lead to very different results in the dark-cure experiments with the iodonium borate salt exhibiting a higher polymerization rater at a given time, and a higher limiting conversion (76%) than observed for the iodonium antimonate salt (62%). These dark-cure trends were explained by the fact that the rate constant for termination/trapping was approximately 50% higher for the iodonium antimonate photoinitiator (0.04 and 0.027 min~(-1) for the IHA and IBP photoinitiators at 50°C, respectively). The active center concentrations and propagation rate constants were also characterized. Relative to the IPB, it was found that the IHA initiator leads to a higher active center concentration (due to the higher molar absorptivity of this initiator at the prominent emission wavelengths of the light source) but a lower propagation rate constant. Therefore, these two photoinitiators yield nearly identical kinetic profiles under constant illumination due to the fact that the IPB photoinitiator leads to a lower active center concentration, which is offset by a higher value of the propagation rate constant, and a lower value of the rate constant for termination/trapping.
机译:在这项贡献中,我们使用两种碘鎓光引发剂进行了全面的苯基缩水甘油醚的阳离子光聚合研究:六氟锑酸二芳基碘鎓(IHA)和四甲苯基(甲苯基)碘鎓(五氟苯基)硼酸盐(IPB)。我们使用暗固化实验对这些反应进行了表征,在该实验中,在预定的时间段内照亮聚合后在黑暗中监控聚合,并获得了终止/捕获的速率常数随时间变化的曲线。我们的研究表明,尽管使用Hg(Xe)弧光灯持续照射,这些光引发剂会产生相似的反应动力学(反应速率和转化曲线几乎相同),但它们在碘鎓的暗固化实验中却产生了截然不同的结果硼酸盐在给定的时间内显示出更高的聚合速率,并且极限转化率(76%)比碘鎓碘酸盐(62%)更高。这些暗固化趋势是由以下事实解释的:锑酸碘鎓光引发剂的终止/俘获速率常数大约高50%(IHA和IBP光引发剂在50°C分别为0.04和0.027 min〜(-1)。 )。还对活性中心浓度和传播速率常数进行了表征。相对于IPB,发现IHA引发剂导致较高的活性中心浓度(由于该引发剂在光源的突出发射波长处的较高的摩尔吸收率)但具有较低的传播速率常数。因此,由于IPB光引发剂导致较低的活性中心浓度(被较高的传播速率常数值和较低的速率常数值所抵消),因此这两种光引发剂在恒定照明下产生的动力学曲线几乎相同。用于终止/陷阱。

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