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Synthesis, characterization, and non-isothermal curing kinetics of two silicon-containing arylacetylenic monomers

机译:两种含硅的芳基炔属单体的合成,表征和非等温固化动力学

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Vinyltri(phenylethynyl)silane ((ph-Ca parts per thousand C)(3)-Si-C=CH(2); VTPES) and phenyltri(phenylethynyl)silane ((ph-Ca parts per thousand C)(3)-Si-ph; PTPES) were synthesized by Grignard reaction. Their molecular structures were characterized by means of (1)H NMR, ~(13)C NMR, ~(29)Si NMR, and FT-IR spectroscopy. Their nonisothermal thermal curing processes were characterized by DSC, and the corresponding kinetic data, for example activation energy (E), pre-exponential factor (A), and the order of the reaction (n), were obtained by the Kissinger method. The results showed that the melting points of VTPES and PTPES were 84 and 116 A degrees C, respectively. Their curing reaction rates were consistent with first-order kinetic equations. VTPES monomer had a lower activation energy and curing temperature as a result of coordination between reactive groups.
机译:乙烯基三(苯基乙炔基)硅烷((ph-Ca千分之一碳)(3)-Si-C = CH(2); VTPES)和苯基三(苯基乙炔基)硅烷((ph-Ca千分之一碳)(3)- Si-ph; PTPES)是通过Grignard反应合成的。它们的分子结构通过(1)H NMR,〜(13)C NMR,〜(29)Si NMR和FT-IR光谱表征。通过DSC对它们的非等温热固化过程进行了表征,并通过基辛格方法获得了相应的动力学数据,例如活化能(E),预指数因子(A)和反应顺序(n)。结果表明,VTPES和PTPES的熔点分别为84和116 A摄氏度。它们的固化反应速率与一阶动力学方程一致。由于反应性基团之间的配位,VTPES单体的活化能和固化温度较低。

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