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Synthesis and cure kinetics of diphenyl(diphenylethynyl)silane monomer

机译:二苯基(二苯基乙炔基)硅烷单体的合成与固化动力学

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摘要

Diphenyl(diphenylethynyl)silane ((ph-C≡C)_2-Si-ph_2) (DPDPES) was synthesized by the Grignard reaction. The corresponding isothermal and non-isothermal cure kinetics of DPDPES were analyzed by using differential scanning calorimetry (DSC), and the molecular structure was characterized by H-NMR. The results showed that all the cure curves were typically sigmoid shape and cure reactions could be described by an autocatalytic kinetic model by isothermal DSC. The kinetic data, for example, activation energy (E) and frequency factor (A), were 119.22 kJ/mol and 4.67 × 10~7 (s~(-1)), respectively. The non-isothermal DSC analyses showed that E and A were 162.12 kJ/mol and 1.32 × 10~9 (s~(-1)), respectively, and the reaction order was 0.94. Based on the research work of this paper, it can be said that the cure reaction of DPDPES monomer was of autocatalytic and diffusion-controlled characteristics, and the effect of the diffusion was more evident at low temperature. The cure reaction of DPDPES was a first-order kinetic reaction.
机译:通过格氏反应合成了二苯基(二苯基乙炔基)硅烷((ph-C≡C)_2-Si-ph_2)(DPDPES)。用差示扫描量热法(DSC)分析了DPDPES的相应的等温和非等温固化动力学,并用1 H-NMR表征了分子结构。结果表明,所有固化曲线均为典型的S形,固化反应可通过等温DSC自动催化动力学模型描述。动力学数据例如活化能(E)和频率因子(A)分别为119.22 kJ / mol和4.67×10〜7(s〜(-1))。非等温DSC分析表明,E和A分别为162.12 kJ / mol和1.32×10〜9(s〜(-1)),反应级数为0.94。根据本文的研究工作,可以说DPDPES单体的固化反应具有自催化和扩散控制的特性,在低温下扩散的影响更为明显。 DPDPES的固化反应是一级动力学反应。

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