锌
二甲基亚砜
热分解
差示扫描量热法
诱导期
分解
化学
等温过程
无机化学
氧化物
化学分解
X射线光电子能谱
亚砜
分析化学(期刊)
有机化学
化学工程
催化作用
物理
工程类
热力学
作者
Wenqian Wu,Zichao Guo,Liping Chen,Wanghua Chen,Shichun Weng,Huabo Li
标识
DOI:10.1021/acs.oprd.1c00275
摘要
Dimethyl sulfoxide (DMSO) is widely used in the chemical industry. However, it has a non-neglectful thermal runaway risk due to the nature of self-accelerating decomposition near the boiling point. Under the background that zinc oxide (ZnO) may extend the isothermal induction period of thermal decomposition of DMSO, this article conducts an in-depth study for the phenomenon with the techniques such as differential scanning calorimetry (DSC), accelerating rate calorimetry (ARC), gas chromatography–mass spectrometry (GC–MS), X-ray photoelectron spectroscopy (XPS), and X-ray diffractometry (XRD). After being mixed with ZnO, the maximum decomposition rate of DMSO was significantly reduced and the adiabatic induction period of DMSO decomposition was extended by 3.27 times, indicating that the thermal decomposition intensity of DMSO was obviously reduced. It was experimentally demonstrated that ZnO did not change the decomposition pathways of DMSO, but it could promote the decomposition of methanethiol, which was a decomposition intermediate of DMSO and could potentially serve as a promoter on the decomposition of DMSO.
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