首页> 外文期刊>Progress in Organic Coatings: An International Review Journal >Simultaneous initiation of radical and cationic polymerization reactions using the 'G1' copper complex as photoredox catalyst: Applications of free radical/cationic hybrid photopolymerization in the composites and 3D printing fields
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Simultaneous initiation of radical and cationic polymerization reactions using the 'G1' copper complex as photoredox catalyst: Applications of free radical/cationic hybrid photopolymerization in the composites and 3D printing fields

机译:使用“G1”铜络合物同时引发自由基和阳离子聚合反应,作为光致毒剂催化剂:自由基/阳离子杂化光聚合在复合材料和3D印刷领域的应用

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摘要

This investigation presents the use of a photoredox catalyst "G1" as a photoinitiating system for free radical/cationic hybrid polymerization under mild irradiation conditions. The G1 system (G1/iodonium salt/N-vinylcarbazole), can simultaneously initiate the free radical and cationic polymerization reactions upon exposure to a visible (405 nm) light from a Light Emitting Diode (LED) source. The multicomponent G1 system is able to simultaneously generate radical and cationic species through a catalytic photoredox process. The curing of thin samples (25 mu m), thick samples (1.4 mm) as well as the manufacture of hybrid system/glass fibers composites ( 2 to 4 mm thickness) was realized and the influence of the ratio of cationic/radical monomer blends on the polymerization kinetics was studied. The use of G1 in visible light photoinitiating system for the access to composites and 3D printing experiments was particularly outlined. G1 was also shown to have low levels of migration from the cured materials. When compared to reference materials ("F1", a similar copper complex and an anthracene derivative, dibutoxy anthracene), G1 showed better polymerization efficiency. The initiation efficiency was investigated through the real-time Fourier transform infrared (RT-FTIR) spectroscopy and optical pyrometry. Dynamical Mechanical Analysis has been used to determine the glass temperature transition of the cured hybrid system as a complementary technique.
机译:该研究表明,在温和照射条件下,使用光致毒剂催化剂“G1”作为光引发系统,用于自由基/阳离子杂化聚合。 G1系统(G1 /碘鎓盐/ N-乙烯基咔唑)可以在暴露于来自发光二极管(LED)源的可见(405nm)光时同时引发自由基和阳离子聚合反应。多组分G1系统能够通过催化的光毒毒剂方法同时产生自由基和阳离子。薄样品(25μm),厚样品(1.4mm)的固化以及混合系统/玻璃纤维复合材料(2至4mm厚)的制造,并对阳离子/自由基单体混合物的比例的影响研究了聚合动力学。特别概述了在可见光光引发系统中使用G1以获得复合材料和3D打印实验。还显示G1从固化材料具有低水平的迁移。与参考材料(“F1”相比(“F1”,类似的铜络合物和蒽衍生物,二丁氧基蒽),G1显示出更好的聚合效率。通过实时傅里叶变换红外(RT-FTIR)光谱和光学热测定来研究启动效率。用于确定固化混合系统的玻璃温度转变作为互补技术的动力学力学分析。

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