天然橡胶/丁基橡胶热降解动力学研究

M. Sholeh, I. N. Indrajati, A. Yuniari
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引用次数: 2

摘要

了解橡胶在氧化环境中加热时如何分解在材料的加工和使用中非常重要。在本工作中,我们进行了热重分析,并利用三个等转化动力学模型来获得天然橡胶/丁基橡胶热降解的表观活化能。RSS/丁基和添加剂的共混使用实验室双辊轧机进行。混合化合物的固化时间通过移动模流变仪测定。使用实验室热压机在160°C、150 kg/cm2的压力下对该化合物进行模压。热重分析是在30°C至800°C、200 ml/min的空气流量和5、10、15和20°C/min的加热速率下进行的。动力学参数由三个等转化模型(Kissinger、Doyle和Flynn–Wall–Ozawa模型)确定。结果表明,共混物的热分解分为两个阶段,DTG峰倾向于向更高的温度移动,并且DTG峰的值随着加热速率的增加而增加,并且三个等转化模型给出了相似的表观活化能。所获得的活化能可用于预测材料的热寿命。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kinetic studies on thermal degradation of natural rubber/butyl rubber
The knowledge of how rubber breakdown on heating in oxidative environment is important in processing and using the material. In the present work, we performed thermogravimetric analysis and utilized three iso-conversional kinetic models to get apparent activation energies of thermal degradation of natural rubber/butyl rubber. Blending of RSS/butyl and additives was done using a laboratory two-roll mill. Cure time of the blended compound was determined by a moving die rheometer. The compound was compression moulded at 160°C with a pressure of 150 kg/cm 2 using a laboratory hot press. Thermogravimetric analysis was carried out from 30°C to 800°C in air flow of 200 ml/min with heating rates of 5, 10, 15, and 20°C/min. The kinetic parameters were determined by three isoconversional models (Kissinger, Doyle, and Flynn–Wall–Ozawa model).  The result revealed that the thermal decomposition of the blend occurs in two stages, DTG peaks tends to shift to a higher temperature and the values of DTG peaks increase with the increase of heating rate, and the three isoconversional models gave similar apparent activation energies. The activation energy obtained can be used to predict thermal lifetime of the material.
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