The formation of gas hydrate is a serious threat to the safe and effective completion of deepwater drilling and transportation operations, although it is considered as a potential energy resource. The inorganic salts are generally used as thermodynamic inhibitors; CaCl2 as a common additive in drilling fluids exhibits unique properties. In this study, we explored the dissociation mechanism of CH4 hydrate in CaCl2 solutions at the macroscopic and microscopic scale using experiment and molecular dynamics (MD) simulation. The experimental results showed that CaCl2 accelerated the dissociation rate of CH4 hydrate. The dissociation rate of CH4 hydrate increased with the increase of CaCl2 concentration at large depressurization pressure and was mainly affected by pressure when the depressurization pressure was lower. MD simulations were used to give an atomic scale interpretation of the macroscopic results obtained from the experiment. The results showed that the addition of CaCl2 destroyed the resistance liquid film formed during CH4 hydrate dissociation, thus accelerating the dissociation process, in good agreement with experimental results. HIGHLIGHTS: • The amount of CaCl2 affects CH4 hydrate dissociation at large depressurization pressure. • The dissociation of CH4 hydrate at low depressurization pressure is dependent on pressure. • Ca2+ destroys effectively the resistance liquid film produced during hydrate dissociation. • MD simulation results are in agreement with those of the experiment.
Keywords: CaCl2; Dissociation; Experiment; Methane hydrate; Molecular dynamics simulation.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.