基于巨正则蒙特卡罗和分子动力学方法的多元气体在气肥煤中的竞争吸附研究

    Study on competitive adsorption of multicomponent gas in gas-fat coal based on GCMC and molecular dynamics

    • 摘要: 为探究CH4、CO2、H2S 3种气体在气肥煤中的赋存特性,揭示不同温度下3种气体在气肥煤中的吸附动力学过程及不同体积分数下3种气体的竞争吸附微观机理,基于巨正则蒙特卡罗(GCMC)和分子动力学(MD)方法,研究温度为273.15~313.15 K、压力为0~3 MPa条件下,CH4、CO2和H2S在煤层中的二元混合组分(CH4/H2S和CO2/H2S)的竞争吸附,以及不同体积分数对气体吸附量、等量吸附热、能量分布、选择性系数和概率密度分布的影响。结果表明:煤对气体的吸附量由大到小依次为H2S、CO2、CH4;CH4、CO2和H2S的吸附动力学特性与准二级动力学模型吻合良好,拟合度均值分别为0.993 0、0.999 7、0.999 8;吸附平衡时,吸附量随温度的升高而逐渐降低,二级吸附速率常数随温度升高而先增大后减小;当CH4的体积分数由10%增至90%时,CH4的饱和吸附量由1.86 cm3/g增至7.89 cm3/g,H2S的饱和吸附量由41.54 cm3/g降至28.71 cm3/g;CO2的体积分数由10%增至90%时,CO2的饱和吸附量由6.64 cm3/g增至26.66 cm3/g,H2S的饱和吸附量由36.17 cm3/g降至10.86 cm3/g;CH4/H2S和CO2/H2S二元组分的吸附选择性系数均随平衡压力的增大呈指数形式衰减,即先快速减小后缓慢减小,最终趋于平缓。

       

      Abstract: To investigate the occurrence characteristics of CH4, CO2, and H2S in gas-fat coal, reveal their adsorption kinetic processes in gas-fat coal at different temperatures and the microscopic mechanism of competitive adsorption among the three gases under different volume fractions, the competitive adsorption of binary mixtures (CH4/H2S and CO2/H2S) in coal seams was studied using Grand Canonical Monte Carlo (GCMC) and molecular dynamics (MD) methods under conditions of 273.15-313.15 K and 0-3 MPa. The influences of volume fractions on gas adsorption capacity, isosteric heat of adsorption, energy distribution, selectivity coefficient, and probability density distribution were analyzed. The results show that the order of gas adsorption capacity in coal from high to low is H2S > CO2 > CH4. The adsorption kinetics of CH4, CO2, and H2S agree well with the pseudo-second-order kinetic model, with average fitting degrees of 0.993 0, 0.999 7, and 0.999 8, respectively. At adsorption equilibrium, the adsorption capacity gradually decreases with increasing temperature, while the second-order adsorption rate constant k2 first decreases and then increases with rising temperature. When the volume fraction of CH4 increases from 10% to 90%, the saturated adsorption capacity of CH4 rises from 1.86 cm3/g to 7.89 cm3/g, while that of H2S decreases from 41.54 cm3/g to 28.71 cm3/g. As the volume fraction of CO2 increases from 10% to 90%, the saturated adsorption capacity of CO2 increases from 6.64 cm3/g to 26.66 cm3/g, whereas that of H2S decreases from 36.17 cm3/g to 10.86 cm3/g. The adsorption selectivity coefficients of the CH4/H2S and CO2/H2S binary systems decay exponentially with increasing equilibrium pressure: they decrease rapidly at first, then slowly, and finally tend to be stable.

       

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