Abstract
Coal spontaneous combustion (CSC) remains a significant threat to regional ecological environments. As coal mining operations extend deeper into the earth, the increasingly complex mechanical force conditions in deep-seated mines escalate the potential risk of CSC. Mechanical forces such as ground stress and mechanical cutting are traditionally believed to be linked to CSC through the following pathway: mechanical forces act → mechanical energy is input → mechanical crushing and pulverization occur → coal–oxygen contact area increases → CSC accelerates. Noteworthily, these forces do more than just physically break coal; they also trigger a mechanochemical effect (MCE) that alters coal's microscopic chemistry. However, an independent evaluation of its influence on CSC was lacking. This study characterized coal's microscopic chemical group responses to the MCE. It was found that the MCE led to the degradation of aliphatic side chains while enhancing the polycondensation of aromatic ring structures, indicating a synergistic effect. Additionally, an increase in oxygen-containing functional groups, such as alkyl/aryl ethers, suggested enhanced interactions of the coal microscopic groups with oxygen due to mechanical forces. Based on these findings, an MCE-modified coal macromolecular model was developed and molecular quantum mechanical calculations were conducted. The results indicated that the MCE boosted coal macromolecule reactivity, thus facilitating easier activation. These conclusions were validated through modern thermal analysis tests. Finally, this study proposed a new pathway of mechanical forces acting on CSC: mechanical forces act → mechanical energy is input → the MCE occurs → evolutions of the microscopic groups within coal are induced → Activity of coal molecules is enhanced → CSC accelerates.
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