不同含水率煤层瓦斯解吸-扩散碳同位素演化规律及影响机理

    Carbon isotope evolution law and influencing mechanism of gas desorption-diffusion in coal seams with different water contents

    • 摘要: 瓦斯抽采是煤矿瓦斯灾害防治的主要技术手段,含水率差异显著影响瓦斯解吸-扩散行为及碳同位素分馏过程,现有研究对不同含水率条件下瓦斯碳同位素演化规律与内在影响机理尚缺乏系统认识。基于气体地球化学与同位素分馏理论,以云南平庆煤矿C7+8煤层为研究对象,系统探究了常压解吸与粉碎释放条件下瓦斯碳同位素(δ13C)的演化规律及影响机理。研究结果表明:常压解吸过程中,瓦斯解吸气量比值呈现“快速增长-稳定增长”的两阶段特征;CH4、CO2、C2H6δ13C值均随解吸时间呈负指数变大,随解吸气量比值呈线性递增,其中,CH4的碳同位素分馏效应最显著,C2H6最弱。粉碎释放条件下,不同含水率煤样的瓦斯解吸气量比值稳定增长;CH4δ13C值随解吸时间呈负指数变大,且含水率越高同位素值越重,与解吸气量比值保持线性递增关系。碳同位素分馏效应的核心机理为:12C—H键极性弱于13C—H键导致12CH4优先解吸,解吸动力、分子作用力及甲烷水溶作用共同加剧分馏过程。研究成果为揭示含水率控制下煤层瓦斯抽采微观机制、优化抽采效果评价方法提供了理论依据与技术支撑。

       

      Abstract: Gas extraction is the primary technical measure for coal mine gas disaster prevention. Water content difference significantly affects gas desorption-diffusion behavior and carbon isotope fractionation process, while existing studies lack a systematic understanding of the carbon isotope evolution law and internal mechanism of gas under different water content conditions. Based on gas geochemistry and isotope fractionation theory, this study takes the C7+8 coal seam of Pingqing Coal Mine in Yunnan as the research object, and systematically explores the evolution law and influencing mechanism of gas carbon isotope (δ13C) under normal pressure desorption and crushing release conditions. The results show that, during normal pressure desorption, the gas desorption volume ratio presents a two-stage feature of “rapid growth followed by stable growth”; the δ13C values of CH4, CO2, and C2H6 all become heavier in a negative exponential trend with desorption time and increase linearly with the desorption volume ratio, with CH4 showing the most significant fractionation effect and C2H6 the weakest. Under crushing release conditions, the desorption volume ratio of coal samples with different water contents increases steadily; the δ13C value of CH4 becomes heavier exponentially with desorption time (higher water content leads to heavier isotope value) and maintains a linear positive correlation with the desorption volume ratio. The core mechanism of carbon isotope fractionation is that the weaker polarity of 12C—H bonds than 13C—H bonds causes the preferential desorption of 12CH4, while desorption dynamics, molecular forces, and methane water solubility jointly intensify this process. The research provides a theoretical basis and technical support for revealing the micro-mechanism of gas extraction controlled by water content and optimizing evaluation methods of gas extraction effect.

       

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