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Non-isothermal kinetics of thermal degradation of DGEBA/ TU-DETA epoxy system

机译:DGEBA / TU-DETA环氧体系热降解的非等温动力学

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摘要

A curing agent Thiourea-diethylenetriamine (TU-DETA) was successfully prepared with its structure characterized by Fourier transform infrared spectrum and nuclear magnetic resonance (~(13)C-NMR spectrum). The curing agent TU-DETA contained incompletely reacted material diethylenetriamine (DETA) and the polymerization degree (n) of TU-DETA was equaled to either 1 or 3 according to liquid chromatog-raphy-mass spectrometry (LC-MS) analysis. Kinetics of thermal degradation of DGEBA (diglycidyl ether of bisphenol A)/TU-DETA epoxy system was investigated with thermogravimetric analysis (TGA) under non-isothermal conditions with heating rates of 5, 10, 12.5, 15, and 20°C/min. The derivative thermogravimetry curves of DGEBA/TU-DETA epoxy system revealed that the thermal degradation process was only a single weight-loss step. The apparent average activation energy calculated with the Flynn-Wall-Ozawa method was 140.4 kJ/mol. With a combination of the Coats-Redfern and Phadnis-Deshpande methods, it was showed that the most probable mechanism of degradation process of the cured epoxy resin was Fl deceleration type.
机译:以傅里叶变换红外光谱和核磁共振(〜(13)C-NMR光谱)为特征,成功制备了硫脲-二亚乙基三胺固化剂(TU-DETA)。固化剂TU-DETA包含不完全反应的物质二亚乙基三胺(DETA),根据液相色谱-质谱(LC-MS)分析,TU-DETA的聚合度(n)等于1或3。在非等温条件下以5、10、12.5、15和20°C / min的升温速率通过热重分析(TGA)研究了DGEBA(双酚A的二缩水甘油醚)/ TU-DETA环氧体系的热降解动力学。 DGEBA / TU-DETA环氧体系的导数热重曲线表明,热降解过程只是一个失重步骤。用Flynn-Wall-Ozawa方法计算的表观平均活化能为140.4 kJ / mol。结合Coats-Redfern和Phadnis-Deshpande方法,结果表明,固化的环氧树脂降解过程最可能的机理是Fl减速类型。

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