Sorption Hysteresis Characterization of CH4 and CO2 on Anthracite, Bituminous Coal, and Lignite at Low Pressure

Abstract

Sorption hysteresis characterization of CH4 and CO2 on lignite, bituminous coal, and anthracite were studied to improve the understanding of the interaction between gas molecules and different ranks of coal and further improve the precision of the adsorption methods in characterizing pore structure at low pressure. Pore structure of three ranks of coal was investigated with scanning electron microscopy (SEM) and nitrogen (N2) adsorption. Then, CH4 and CO2 sorption isotherms were measured using the gravimetric method under 288, 308, and 328 K. The N2 sorption isotherms show that a wide distribution of pore size existed in three coal samples, and with the process of coalification, the specific surface area (SSA) decreased and then increased, while the pore size of coal monotonically decreased. This is confirmed by SEM observation. The measured sorption isotherms were then decomposed into simultaneously running adsorption and absorption branches based on the assumption that the former is totally reversible and the latter completely irreversible. The reconstructed adsorption branches can be well described by both Langmuir model and Dubinin–Radushkevich (D–R) equation. The absorption, which represents the sorption hysteresis portion, increased with pressure, but decreased with temperature. The absorbed amount of gas increased with pressure, but the absorption of CO2 increased concavely with gas pressure while CH4 followed an upward exponential function. Also, the absorption varied with coal rank, following a U-shaped function. This study can provide new insights to CH4 and CO2 sorption hysteresis on coal and other organic geomaterials.