A Pore-Level Study of Dense-Phase CO2 Foam Stability in the Presence of Oil

The ability of foam to reduce CO2 mobility in CO2 sequestration and CO2 enhanced oil recovery processes relies on maintaining foam stability in the reservoir. Foams can destabilize in the presence of oil due to mechanisms impacting individual lamellae. Few attempts have been made to measure the stability of CO2 foams in the presence of oil in a realistic pore network at reservoir pressure. Utilizing lab-on-a-chip technology, the pore-level stability of dense-phase CO2 foam in the presence of a miscible and an immiscible oil was investigated. A secondary objective was to determine the impact of increasing surfactant concentration and nanoparticles on foam stability.<br /> In the absence of oil, all surfactant-based foaming solutions generated fine-textured and strong foam that was less stable both when increasing surfactant concentrations and when adding nanoparticles. Ostwald ripening was the primary destabilization mechanism both in the absence of oil and in the presence of immiscible oil. Moreover, foam was less stable in the presence of miscible oil, compared to immiscible oil, where the primary destabilization mechanism was lamellae rupture. Overall, direct pore-scale observations of dense-phase CO2 foam in realistic pore network revealed foam destabilization mechanisms at high-pressure conditions. Highlights<br /> Pore-scale observations of dense-phase CO2 foam in realistic pore network revealed foam destabilization mechanisms at high-pressure conditions. A comprehensive laboratory investigation of CO2 foam stability in the presence of oil at high pressure.