水基黏液抑制含气煤吸附解吸特性的实验研究与分子动力学模拟探索

IF 4.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
ACS Omega Pub Date : 2025-10-08 DOI:10.1021/acsomega.5c02732
Wenbin Jin, , , Yanpeng Xu*, , , Zhi Li, , and , Xin Zhang, 
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引用次数: 0

摘要

针对采煤工作面作业中瓦斯排放超标和瓦斯事故风险增加的严重问题,我们的团队开发了一种新型、高效的煤矿瓦斯封堵抑制剂─含水胶浆。本研究结合13C核磁共振、傅里叶变换红外(FTIR)、低温氮吸附微物理实验和分子动力学模拟,探讨煤的吸附和解吸性能的抑制机理。结果表明,含水浆液处理后,煤样对甲烷分子的吸附和解吸能力明显降低。水基黏液阻塞或覆盖煤的孔隙结构,导致煤的总比表面积和总孔隙体积显著减小。这反过来又影响了甲烷的吸附和解吸通道,从而削弱了煤对甲烷的吸附和解吸能力。处理后,煤表面脂肪族碳含量增加,羧基减少,羰基增加,从而抑制了甲烷分子的吸附和解吸过程。同时,含水黏液对煤的羟基、芳烃环和芳烃结构的影响很小。基于这些发现,鉴定了煤大分子的分子结构为C123H60N2O5。分子动力学模拟结果进一步表明,含水黏液的加入显著增强了煤的亲水性,增加了水分子在煤表面的扩散系数,进一步强化了“锁水效应”,从而阻碍了甲烷分子的吸附和解吸过程。此外,水基黏液的引入增加了甲烷分子之间以及煤结构与甲烷分子之间的相互作用和配位数,从而降低了甲烷的扩散系数。这导致煤对甲烷分子的解吸能力进一步减弱。同时,水基胶浆的加入显著降低了体系总能量和煤与甲烷的相互作用能,增加了煤解吸甲烷所需的能量。因此,解吸过程变得更加困难,进一步削弱了煤解吸甲烷分子的能力。本研究揭示了含水黏液通过物理和化学相互作用抑制甲烷在煤中的吸附和解吸的微观机理,为煤矿瓦斯控制提供了重要的理论见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploration of Experimental Research and Molecular Dynamics Simulation on the Adsorption and Desorption Characteristics of Gas-Bearing Coal with Water-Based Mucilage Suppression

In response to the severe issue of excessive gas emissions and the increased risk of gas accidents during mining face operations, our team has developed a novel, efficient gas-blocking suppressant for coal mines─aqueous mucilage. This study combines 13C NMR, Fourier-transform infrared (FTIR), low-temperature nitrogen adsorption microphysical experiments with molecular dynamics simulations to explore the inhibitory mechanisms on the adsorption and desorption properties of coal. The results indicate that, after treatment with aqueous mucilage, the coal sample’s ability to adsorb and desorb methane molecules is significantly reduced. Water-based mucilage blocks or covers the pore structure of coal, leading to a significant reduction in the total specific surface area and total pore volume of the coal. This, in turn, affects the channels for methane adsorption and desorption, thereby weakening the coal’s ability to adsorb and desorb methane. Post-treatment, the coal surface shows an increase in aliphatic carbon content, a decrease in carboxyl groups, and an increase in carbonyl groups, thereby inhibiting the adsorption and desorption processes of methane molecules. Meanwhile, the effect of aqueous mucilage on the coal’s hydroxyl, aromatic ring, and aromatic hydrocarbon structures is minimal. Based on these findings, the molecular structure of the coal macromolecule is identified as C123H60N2O5. Molecular dynamics simulation results further indicate that the addition of aqueous mucilage significantly enhances the hydrophilicity of coal, increases the diffusion coefficient of water molecules on the coal surface, and further strengthens the “water lock effect,” thereby hindering the adsorption and desorption processes of methane molecules. Furthermore, the introduction of the water-based Mucilage increases the interactions and coordination number between methane molecules as well as between the coal structure and methane molecules, which in turn reduces the diffusion coefficient of methane. This results in a further weakening of the coal’s desorption capacity for methane molecules. At the same time, the addition of the water-based Mucilage significantly decreases the total energy of the system and the interaction energy between coal and methane, which increases the energy required for methane desorption from the coal. Consequently, the desorption process becomes more difficult, further impairing the coal’s ability to desorb methane molecules. This study reveals the microscopic mechanism by which aqueous mucilage inhibits methane adsorption and desorption in coal through both physical and chemical interactions, providing important theoretical insights for gas control in coal mines.

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来源期刊
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
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