4.7 Article

Facilitating gas hydrate dissociation kinetics and gas migration in clay interlayer by surface cations shielding effects

Journal

FUEL
Volume 318, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2022.123576

Keywords

Methane hydrate; Illite mineral; Molecular dynamics simulation; Dissociation behaviors; Cation shielding effect; Nanobubbles

Funding

  1. National Key Research and Development Project [2018YFE0126400]
  2. Key Program of Marine Economy Development (Six Marine Industries) Special Foun-dation of Department of Natural Resources of Guangdong Province [GDNRC [2020] 047]
  3. Fundamental Research Funds for National Universities, China University of Geosciences (Wuhan) [CUGGC09]
  4. National Natural Science Foundation of China [41976203]
  5. International Postdoctoral Exchange Fellowship Program [PC2021073]

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This study investigated the dissociation of methane hydrate in clay sediments using molecular dynamics simulations. It was found that methane nanobubbles form at the liquid water/hydrate interface for the cations in the system, while forming on the mineral surface for the cations outside the system. Additionally, the release of methane diffuses faster in the system with cations compared to the system without cations and sandy pores.
Knowledge of the kinetics of the gas hydrate dissociation in microporous sediments is a critical and fundamental issue for improving the gas recovery from fine-grained natural gas hydrate (NGH) reservoirs. Herein, molecular dynamics (MD) simulations were performed to investigate methane hydrate dissociation in clay sediments. Two initial configurations which comprised liquid bulk and clay mineral phases were adopted, and the later phase comprised two illite sheets and occupied by a hydrate phase with clay cations in and out of the interlayer. The results show that methane nanobubbles form at liquid water/hydrate interface for the cations in system, not like forming spherical cap-shaped nanobubbles on the mineral surface for the cations out system. This phenomenon can be attributed to the cations stably adsorbing on the clay surface, the cation film and ion hydration effect shielding the dissociated methane close to the solid surface. An increasing amount of released methane (approximately three times) diffuses from the pore phase to the bulk phase as driven by the Brownian motion in the cations in the system, as compared with the dissociation in cations out system and sandy pores; however, the diffusion of the released water is the opposite. Additionally, the injection speeds of heat flow against porosity were estimated to maintain a constant dissociation rate in the illite mineral hydrate reservoir. This study provides guidance for the scientific optimization of hydrate reservoirs, and for subsequent gas production from sediments with low permeabilities.

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