Molecular dynamics study on roles of surface mixed hydrate in the CH4/CO2 replacement mechanisms

Abstract

The CH4/CO2 replacement method is a promising approach for the exploitation of natural gas hydrates, offering dual benefits of extracting CH4 and sequestering CO2. This technique not only facilitates the extraction process but also mitigates the greenhouse effect and maintains geological stability, thereby contributing to sustainable energy utilization and environmental preservation. Currently, there are multiple viewpoints about the replacement mechanism. Furthermore, mixed hydrates can form on the surface during the replacement process. The unclear mechanism of CH4/CO2 replacement and the obstruction of mass transfer caused by the mixed hydrate impede its practical applicability. Clarifying the effects of surface mixed hydrate in replacement mechanisms can offer valuable insights for identifying optimal operating conditions in practical exploitation applications. Therefore, the present study aims to reveal the significant roles of surface mixed hydrates in the replacement mechanism by employing the molecular dynamics simulation methodology. The results showed that under the mechanism of cage complete rupture, the surface mixed hydrate decomposes rapidly to form a thickening water zone. Additionally, each layer of the hydrate cage structure undergoes a process from deformation or partial rupture to sudden complete disintegration, which is concomitant with an abrupt change of potential energy. Under the mechanism of cage incomplete rupture, the surface mixed hydrates hinder mass transfer and decelerate the reaction rate. A similar situation arises when the number of the surface mixed hydrate layers is increased. Therefore, the key to distinguishing the replacement mechanism lies in whether the environmental conditions are sufficient to break the potential energy barrier of the surface mixed hydrate and disrupt its cage structure.