LAUSR

Abstract Recent but limited studies have shown that multistep slow depressurization based on mixed CH4/CO2 hydrate dissociation can enhance CH4 recovery and increases CO2 storage after CO2 injection into CH4 hydrate [1,2]. For the first time, the resistivity variation and gas recovery and storage variation was investigated to study the change in hydrate saturation and production/storage yield. Lab-scale CH4 and CO2 rich mixed hydrates were synthesized to mimic the production and injection well scenario. The mixed hydrates were synthesized in sandstone with moderate to high water saturation using two different CH4/CO2 gas mixtures. Furthermore, mixed CH4/CO2 hydrates were dissociated three to six steps based on cyclic depressurization. Pressure, resistivity and gas chromatography data were collected. The presence of two thermodynamic stability zones provided an opportunity for additional CH4 recovery and CO2 storage during mixed hydrate dissociation. Gas and water migration between the injection and production well caused CO2 hydrate reformation, improvement in CO2 sweep area and movement of the CO2 hydrate front toward the production well. Multiple peaks in CH4 recovery and CO2 storage suggest major dissociation and reformation. Peak values were independent of mixed hydrate type. Peaks values of CH4 rich hydrates occurred at high pressure than peak values of CO2 rich hydrates. The slight change in resistance during depressurization below pure CH4 hydrate stability pressure confirms the loss of CH4 hydrate mass recovered by the formation of CO2 hydrate mass. This study discusses the correlation between the change in resistivity and type of guest molecule and its concentration and initial water saturation. The results of this study will be useful to explore the application of slow depressurization for the dissociation of CH4/CO2 mixed hydrates to improve CH4 recovery and CO2 storage.