差示扫描量热法
放热反应
共聚物
热失控
量热法
材料科学
甲基丙烯酸甲酯
苯乙烯
高分子化学
聚合
化学工程
热力学
化学
聚合物
有机化学
复合材料
物理
工程类
功率(物理)
电池(电)
作者
Jihe Zhao,Xuefeng Gui,Wenhai Zhang,Shudong Lin,Yuanyuan Tu,Jiwen Hu,Daguang He,Xiaohua Huang
标识
DOI:10.1016/j.tca.2021.179052
摘要
Thermal runaway primarily occurs during the course of copolymerization due to the release of large amounts of heat. In this paper, the thermal risk associated with styrene-methyl methacrylate bulk copolymerization was firstly investigated by differential scanning calorimetry (DSC) and accelerating rate calorimetry (ARC). The result found that the exothermic behavior was greatly affected by the initiator concentration, in contrast the exothermic enthalpy was not. This exothermic behavior was firstly illustrated via polymerization mechanism. The temperature and pressure have changed dramatically during the adiabatic runaway copolymerization, which demonstrated a great potential risk of thermal runaway. Kinetic parameters, such as TNR, TSADT was calculated accordingly, which provided guidance for the safety of storage and transportation. This study will provide a helpful safety assessment for the styrene-methyl methacrylate bulk copolymerization, which is widely used in industry.
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