自燃
电子顺磁共振
燃烧
化学
煤
激进的
傅里叶变换红外光谱
热重分析
氧气
差示扫描量热法
极限氧浓度
光化学
有机化学
化学工程
热力学
核磁共振
工程类
物理
作者
Yutao Zhang,Jing Zhang,Yaqing Li,Sheng Gao,Chaoping Yang,Xueqiang Shi
出处
期刊:ACS omega
[American Chemical Society]
日期:2021-03-12
卷期号:6 (11): 7669-7679
被引量:37
标识
DOI:10.1021/acsomega.0c06322
摘要
To investigate and better understand the mechanism of coal spontaneous combustion, the distributions, evolution, and oxidation characteristics of functional groups in different coal samples were characterized using in situ Fourier transform infrared (FTIR) and electron paramagnetic resonance (EPR) experiments. The macroscopic characteristics of coal spontaneous combustion in relation to functional groups were also analyzed using the thermogravimetric/differential scanning calorimetry–FTIR coupling technique. The experimental results indicated that −OH was the most active groups of coal spontaneous combustion. It not only could react with the absorbed oxygen spontaneously but also found to be the main product of the chemisorption. Consequently, −OH was believed to contribute most both for the loss and increase of coal mass during the process of spontaneous combustion. Aliphatic hydrocarbons were the main components to form −C–O–O• and could be further oxidized into C═O. However, reactions between aliphatic hydrocarbons and oxygen were nonspontaneous. EPR experiments suggested that the tendency of coal spontaneous combustion acutely depended on the stability and survival time of free radicals. The more the stable and longer survival time of free radicals are, the lower the tendency of coal spontaneous combustion is.
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