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Influence of injection pressure on gas adsorption and desorption of anthracite.
- Source :
-
Energy . Feb2024, Vol. 288, pN.PAG-N.PAG. 1p. - Publication Year :
- 2024
-
Abstract
- In this paper, THM model and coal molecular model are established to study the gas adsorption and desorption behavior in coal seam at different injection pressures. The results show that, the total energy decreases during the adsorption process and increases in the desorption process. CO 2 has a stronger adsorption capacity which is in a dominant position in the competition adsorption process, while N 2 is in a weak position. The order of the diffusion coefficient is N 2 >CH 4 (CH 4 –N 2) > CH 4 (CH 4 –CO 2) > CO 2. The diffusion coefficient does not necessarily increase with the increase of injection pressure. At the same injection pressure, the relative concentration of CH 4 in the CH 4 –CO 2 system is greater than that in the CH 4 –N 2 system, and injection of CO 2 to promote CH 4 desorption is significantly better than the injection of N 2. With the increase of injection pressure, the average relative concentration of CH 4 /CO 2 /N 2 in the vacuum layer increased. The optimal injection pressure for N 2 injection to promote CH 4 desorption is 2 MPa, and the reasonable injection pressure for CO 2 injection is 1–3 MPa. • THM model and coal molecular model are established to study the gas adsorption and desorption at different injection pressures. • The total energy of the system decreases during the adsorption process and increases in the desorption process. • The diffusion coefficient does not necessarily increase with the increase of gas injection pressure. • Relative concentration of CO 2 in the vacuum layer is lower than N 2 , the adsorption performance of CO 2 is greater than N 2. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 03605442
- Volume :
- 288
- Database :
- Academic Search Index
- Journal :
- Energy
- Publication Type :
- Academic Journal
- Accession number :
- 174641920
- Full Text :
- https://doi.org/10.1016/j.energy.2023.129828