首页> 外文期刊>Journal of Photochemistry and Photobiology, A. Chemistry >Inhibition effect of N,N-diglycidyl-4-glycidyloxy aniline on photosensitized cationic polymerization of formulations involving resorcinol diglycidyl ether and poly(propylene glycol)diglycidyl ether
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Inhibition effect of N,N-diglycidyl-4-glycidyloxy aniline on photosensitized cationic polymerization of formulations involving resorcinol diglycidyl ether and poly(propylene glycol)diglycidyl ether

机译:N,N-二缩水甘油基-4-缩水甘油基氧基苯胺对间苯二酚二缩水甘油基醚和聚(丙二醇)二缩水甘油基醚的制剂的光敏阳离子聚合的抑制作用

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Cationic photopolymerization studies of poly(propylene glycol)diglycidyl ether with and without 25 wt% of resorcinol diglycidyl ether were carried out in presence of bis(4-methylphenyl)iodonium hexafluorophosphate as photoinitiator. Analyses were carried out using polychromatic radiation at different temperatures in a photo differential scanning calorimeter. The formulations showed an enhancement in the rate of polymerization on addition of resorcinol diglycidyl ether. The same formulations when subjected to photosensitized polymerization in presence of 1-chloro-4-propoxy-9H-thioxanthen-9-one, showed a reverse behavior in rate due to partial absorption of radiation by resorcinol diglycidyl ether. Studies carried out on by the addition of N,N-diglycidy1-4-glycidyloxy aniline as inhibitor on the photosensitized formulations showed higher scavenging activity by inhibitor. The addition of nitrogen containing epoxy monomer as inhibitor can lead to its possible crosslinking within the matrix on polymerization along with a decrease in rate of polymerization without compromising on the final observed conversion. This effect can occur readily for non vitrifying systems. Thus, this observation provides an insight into its possible usage in a rate controlled photopolymerizable epoxy formulations. The photopolymerization kinetics were found to depend on the nature of generation, propagation and scavenging of active centers which are heavily dependent on diffusional restrictions imparted by in situ viscosity of the system. The kinetic estimations as well as evaluation of autocatalytic kinetic model are investigated. (C) 2015 Elsevier B.V. All rights reserved.
机译:在双(4-甲基苯基)碘化六氟磷酸盐作为光引发剂的情况下,对有和没有25%(重量)间苯二酚二缩水甘油醚的聚(丙二醇)二缩水甘油醚进行阳离子光聚合研究。在光差示扫描量热仪中使用多色辐射在不同温度下进行分析。当加入间苯二酚二缩水甘油醚时,该制剂显示出聚合速率的提高。当在1-氯-4-丙氧基-9H-噻吨酮-9-一的存在下进行光敏聚合时,相同的制剂由于间苯二酚二缩水甘油醚对辐射的部分吸收而在速率上表现出相反的行为。通过在光敏制剂上加入N,N-二缩水甘油1-4-缩水甘油氧基苯胺作为抑制剂进行的研究表明,该抑制剂具有更高的清除活性。加入含氮的环氧单体作为抑制剂可导致其在聚合时在基质内可能发生交联,同时聚合速率降低而不会影响最终观察到的转化率。对于非玻璃化系统,这种效果很容易发生。因此,该观察提供了其在速率控制的可光聚合环氧制剂中可能使用的见解。发现光聚合动力学取决于活性中心的产生,传播和清除的性质,活性中心严重依赖于体系原位粘度赋予的扩散限制。研究了动力学估计以及自动催化动力学模型的评估。 (C)2015 Elsevier B.V.保留所有权利。

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