Promoting Effect of Common Marine Cations on Hydrate Dissociation and Structural Evolution under a Static Electric Field

Natural gas hydrate, a potential energy resource, is attracting worldwide attention. In this study, we propose a new method of hydrate dissociation which uses seawater and electrostatic fields (SE method) cooperatively. The hydrate molecular dissocia-tion mechanism of gas hydrate is a key issue in studying the kinetic properties of gas hydrate using the SE method. Therefore, molecular dynamics simulations were used to investigate the thermodynamic properties and structural changes of methane hydrate (MH) in multiple kinds of salt solutions under an electrostatic field. The results show that the electric field can drive cations into the MH phase to form a series of random semiopen cages, which are essentially temporary and metastable. The variation in free energy indicates that it is more difficult for divalent cations to enter the hydrate phase than monovalent cations, meaning that the hydrate structures formed with divalent cations are more unstable. Then, the ion current occurred in the hydrate phase (called ion migration in this study), which greatly accelerated hydrate dissociation. In contrast, the promotion effect of cations with the same charge on MH dissociation is as follows: Sr2+ > K+ Na+ > Ca2+ Mg2+. In general, the presence of common marine cations enhanced the promotion effect of the electric field on gas hydrate dissociation.

Automated summary

In this study, a new method of hydrate dissociation using seawater and electrostatic fields cooperatively (SE method) was proposed. Molecular dynamics simulations were used to investigate the thermodynamic properties and structural changes of methane hydrate in multiple salt solutions under an electrostatic field. The results showed that the electric field can drive cations into the hydrate phase, accelerating hydrate dissociation.