Pore-scale supercritical CO2 dissolution and mass transfer under imbibition conditions. (June 2016)

• Record Type: Journal Article
• Authors: Chang, Chun; Zhou, Quanlin; Kneafsey, Timothy J.; Oostrom, Mart; Wietsma, Thomas W.; Yu, Qingchun
• Is Part Of: Advances in water resources. Volume 92(2016)
• Page Start: 142
• Page End: 158
• Publication Date: 2016-06
• Subjects: Geological carbon storage -- Micromodel -- Imbibition -- CO2 dissolution -- Mass transfer -- Relative permeability; Hydrology -- Periodicals; Hydrodynamics -- Periodicals; Hydraulic engineering -- Periodicals; 551.48
• DOI: 10.1016/j.advwatres.2016.03.015
• Languages: English
• ISSNs: 0309-1708

Abstract

Highlight: Pore-scale imbibition and scCO2 dissolution experiments were conducted in a sandstone-analog pore network. Periodic and non-equilibrium scCO2 dissolution was observed in the millimeter-scale pore network. Coupled water flow and scCO2 dissolution was investigated at pore-network scale and pore scale. Non-monotonic relative permeability of water was measured and analyzed. Abstract: In modeling of geological carbon storage, dissolution of supercritical CO2 (scCO2 ) is often assumed to be instantaneous with equilibrium phase partitioning. In contrast, recent core-scale imbibition experiments have shown a prolonged depletion of residual scCO2 by dissolution, implying a non-equilibrium mechanism. In this study, eight pore-scale scCO2 dissolution experiments in a 2D heterogeneous, sandstone-analog micromodel were conducted at supercritical conditions (9 MPa and 40 °C). The micromodel was first saturated with deionized (DI) water and drained by injecting scCO2 to establish a stable scCO2 saturation. DI water was then injected at constant flow rates after scCO2 drainage was completed. High resolution time-lapse images of scCO2 and water distributions were obtained during imbibition and dissolution, aided by a scCO2 -soluble fluorescent dye introduced with scCO2 during drainage. These images were used to estimate scCO2 saturations and scCO2 depletion rates. Experimental results show that (1) a time-independent, varying number of water-flow channels are created during imbibition and later dominant dissolution by the random nature of water flow at the micromodel inlet, and (2) a time-dependent number of water-flow channels are created by coupled imbibition and dissolution following completion of dominant imbibition. The number of water-flow paths, constant or transient in nature, greatly affects the overall depletion rate of scCO2 by dissolution. The average mass fraction of dissolved CO2 (dsCO2 ) in water effluent varies from 0.38% to 2.72% of CO2 solubility, indicating non-equilibrium scCO2 dissolution in the millimeter-scale pore network. In general, the transient depletion rate decreases as trapped, discontinuous scCO2 bubbles and clusters within water-flow paths dissolve, then remains low with dissolution of large bypassed scCO2 clusters at their interfaces with longitudinal water flow, and finally increases with coupled transverse water flow and enhanced dissolution of large scCO2 clusters. The three stages of scCO2 depletion, common to experiments with time-independent water-flow paths, are revealed by zoom-in image analysis of individual scCO2 bubbles and clusters. The measured relative permeability of water, affected by scCO2 dissolution and bi-modal permeability, shows a non-monotonic dependence on saturation. The results for experiments with different injection rates imply that the non-equilibrium nature of scCO2 dissolution becomes less important when water flow is relatively low and the time scale for dissolution is large, and more pronounced when heterogeneity is strong.