Carbon capture, storage, and utilization technologies target a reduction in net CO emissions to mitigate greenhouse gas effects. The largest such projects worldwide involve storing CO through enhanced oil recovery-a technologically and economically feasible approach that combines both storage and oil recovery. Successful implementation relies on detailed measurements of CO-oil properties at relevant reservoir conditions (P = 2.0-13.0 MPa and T = 23 and 50 °C). In this paper, we demonstrate a microfluidic method to quantify the comprehensive suite of mutual properties of a CO and crude oil mixture including solubility, diffusivity, extraction pressure, minimum miscibility pressure (MMP), and contact angle. The time-lapse oil swelling/extraction in response to CO exposure under stepwise increasing pressure was quantified via fluorescence microscopy, using the inherent fluorescence property of the oil. The CO solubilities and diffusion coefficients were determined from the swelling process with measurements in strong agreement with previous results. The CO-oil MMP was determined from the subsequent oil extraction process with measurements within 5% of previous values. In addition, the oil-CO-silicon contact angle was measured throughout the process, with contact angle increasing with pressure. In contrast with conventional methods, which require days and ∼500 mL of fluid sample, the approach here provides a comprehensive suite of measurements, 100-fold faster with less than 1 μL of sample, and an opportunity to better inform large-scale CO projects.

Solvent bitumen extraction processes are alternatives to thermal processes with potential for improved economic and environmental performance. However, solvent interaction with bitumen commonly results in in situ asphaltene precipitation and deposition, which can hinder flow and reduce the process efficiency. Successful implementation requires one to select a solvent that improves recovery with minimal flow assurance problems. The majority of candidate industrial solvents are in the form of mixtures containing a wide range of hydrocarbon fractions, further complicating the selection process. In this study, we quantify the pore-scale asphaltene deposition using two commonly available solvent mixtures, natural gas condensate and naphtha, using a microfluidic platform. The results are also compared with those of two typical pure solvents, n-pentane and n-heptane, with all cases evaluated with both 50 and 100 μm pore-throat spacing. The condensate produced more asphaltenes and pore-space damage than the naphtha and exhibited deposition dynamics similar to that of pentane and heptane. This similarity is due to the presence of a large amount of light hydrocarbon fractions in condensate (∼85 wt % of C5s–C7s) dictating the overall deposition dynamics. Naphtha, which contains heavier fractions (∼70 wt % of C8s–C11s) and aromatic/naphthenic components, generated less asphaltenes and exhibited a slower deposition rate, resulting in less pore damage and overall better performance.

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