Influencing Factors and Adsorption Process of N2/CH4/CO2 Competitive Adsorption in Coal

吸附 过程(计算) 化学 化学工程 材料科学 环境科学 物理化学 计算机科学 有机化学 工程类 操作系统
作者
Hongyu Pan,Mingrui Han,Tianjun Zhang,Bingnan Ji,Mingyue Pan,Zefan Li,Shipeng Zhu
出处
期刊:Energy & Fuels [American Chemical Society]
卷期号:38 (22): 22182-22191 被引量:3
标识
DOI:10.1021/acs.energyfuels.4c04363
摘要

To investigate the influence of key factors (temperature, pressure, and particle size) on the competitive adsorption of N2/CH4/CO2 on coal, a self-built multicomponent gas adsorption apparatus was used based on the breakthrough curve method to conduct competitive adsorption experiments under different conditions. The adsorption process was dynamically analyzed by combining adsorption kinetics models with the pore structure characteristics of the samples. The results showed that increasing the temperature promotes competitive adsorption and enhances the preferential adsorption of CO2, while increasing the pressure and particle size mesh number inhibits competitive adsorption and weakens the preferential adsorption of CO2. The experimental data fitted well with the Yoon-Nelson, Thomas, and Clark kinetic models, with R2 values all above 0.9. The mass transfer rate constants followed the order k(N2) > k(CH4) > k(CO2). As temperature and pressure increased or particle size mesh number increased, the k values for each component increased, enhancing the gas mass transfer rate. The adsorption capacities (qT) and Clark constants (A) for each component showed the order CO2 > CH4 > N2, indicating that the coal samples had the highest adsorption capacity and strength for CO2, followed by CH4 and then N2. Lowering the temperature, increasing the pressure, or increasing the particle size mesh number all led to increases in qT and A for each component. The samples exhibited good pore connectivity, with the most developed micropores having a diameter of 2.05 nm, and relatively large specific surface area and pore volume. During competitive adsorption, N2 was initially adsorbed and then displaced by CH4 and CO2, with CH4 subsequently displaced by CO2. These conclusions provide some guidance for the study of competitive adsorption of multicomponent gases in coal, further improving the related theory of coal competitive adsorption.
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