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Photopolymerization Kinetics of a Thiol-Enol Composition Determined via Recording/Playback of a Transmission Holographic Diffraction Grating

机译:硫醇-烯醇组合物的光聚合动力学,通过透射/全息衍射光栅的记录/回放确定。

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摘要

The kinetics of thiol-enol photopolymerization of a hybrid composition based on a tetraacrylate monomer and a thiol-siloxane oligomer was studied with the use of a holographic recording of elementary transmission phase gratings. The degrees of conversion of double bonds in the tetraacrylate monomer after the polymerization in air and in an inert atmosphere of SF6 were measured via IR spectroscopy. It is shown that the use of the thiol-siloxane oligomer efficiently suppresses oxygen inhibition of the photopolymerization. When the photoinitiator concentration is increased to more than 10(-2) mol/L, the photopolymerization rate levels off. An increase in the thiol-siloxane oligomer concentration leads to an extremal dependence of the photopolymerization rate on the oligomer concentration; the maximum rate is reached at an oligomer concentration of about 0.07 mol/L. The kinetic scheme of photopolymerization in the hybrid photopolymer composition was analyzed, and an analytical expression for the photopolymerization rate was obtained. The correlation between the kinetic constants of the thiol-enol photopolymerization was evaluated on the basis of the obtained parameters of the kinetic model.
机译:基于全息图记录了基本透射相光栅,研究了基于四丙烯酸酯单体和硫醇基硅氧烷低聚物的杂化组合物的硫醇-烯醇光聚合动力学。在空气中和在SF 6的惰性气氛中聚合之后,四丙烯酸酯单体中双键的转化程度通过IR光谱法测量。结果表明,使用硫醇-硅氧烷低聚物可有效地抑制光聚合的氧抑制。当光引发剂浓度增加到大于10(-2)mol / L时,光聚合速率趋于稳定。硫醇-硅氧烷低聚物浓度的增加导致光聚合速率对低聚物浓度的极端依赖性;因此,低聚物浓度会导致光致聚合速率的增加。在约0.07 mol / L的低聚物浓度下达到最大速率。分析了杂化光聚合物组合物中光聚合的动力学方案,并获得了光聚合速率的解析表达式。基于所获得的动力学模型参数,评估硫醇-烯醇光聚合的动力学常数之间的相关性。

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