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Study on Ultrasonic Modification of CH4/CO2 Competitive Adsorption Behavior in Coal: A Pore Wall Molecular Structure
Chenhao Tian1,2,3, Liang Wang1,2,3, Wei Yang4
1Key Laboratory of Theory and Technology on Coal and Rock Dynamic Disaster Prevention and Control, National Mine Safety Administration, China University of Mining and Technology, Xuzhou 221116, China.
None:
Ultrasonic excitation can increase the coal seam permeability to improve the CO2 injection efficiency during the CO2-ECBM process, but it may also cause changes in the coal molecules. To investigate the effect of chemical change caused by ultrasonics on CH4 and CO2 competitive adsorption behavior, this paper constructs the pore wall molecular structure model based on the coal chemical structure test results. The molecular simulation results show that the CH4 adsorption heat and adsorption density decreased with an increased pore size in single-component gas adsorption. The oxygen-containing structure slightly increased CH4 adsorption heat by reducing the effective pore size. Compared with CH4, CO2 had more significant adsorption characteristics. The CH4 and CO2 adsorption densities were more obviously affected by the effective pore size and dominant adsorption sites, respectively. In the gas competitive adsorption behavior, the energy probability density distribution curves showed that with increased CO2 injection, part of CH4 transferred from the low-energy to the high-energy region. During the CO2 injection, the gas density in the pores gradually increased, making the interaction energy between CH4 and CO2 more significant, especially for small pores. The injection of CO2 into large pores more effectively weakened the interaction energy between coal and CH4, weakening the CH4 adsorption capacity. The oxygen-containing structure may inhibit the competitive adsorption behavior in small pores, and this effect gradually weakened or even reversed with the increase of pore size. Ultrasonic excitation reduced the oxygen-containing structure, which improved the competitive adsorption behavior in small pores.
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