Molecular Dynamics Insights Into the Phase Equilibria and Thermophysical Properties of CO2–H2S–Brine System During Acid Gas Sequestration in Saline Aquifers

This work represents an extensive molecular dynamics (MDs) simulation study with the microstructural insight at the interface to simultaneously predict the phase equilibria, transport, and interfacial properties of the CO2–H2S–brine system within the range of temperatures 323.15–393.15 K, pressures up to 30 MPa, H2S contents of 0–70 mol%, and salt molalities of 1–4 mol/kg, aiming to address the insufficiency of data under typical conditions of acid gas sequestration. The validation results demonstrate that the average absolute deviations (AAD%) for the predicted solubility of CO2 and H2S in water and in 2 mol/kg NaCl solution were found to be 5.45%, 6.34%, 5.78%, and 5.41%, respectively. Moreover, the AAD% for interfacial tension (IFT) and density were 6.74% and 3.70%, respectively, verifying the validity and performance of the applied force field parameters and computational methods. The simulation results indicated that H2S solubility in brine is more sensitive to changes in the acid gas composition and temperature compared to CO2 solubility. The presence of H2S remarkably reduces the CO2–H2S–brine IFT, with the reduction degree depending on the H2S content. Increasing the H2S mole fraction in acid gas mixtures delays convective mixing by reducing the brine density. At about 64 mol% H2S, the aqueous solution's density equals that of fresh brine, which is the highest H2S content that can maintain the benefit of convective mixing in the dissolution trapping. The maximum acid gas column height that can be safely stored is most significant at lower temperature and H2S content. On the basis of the results, pressure, temperature, and salt molality have a higher influence on the viscosity than density in the studied ranges. The new data generated by the current study can be utilized to develop predictive models of acid gas long‐term behavior, which will reduce the uncertainty of real storage schemes.