4.7 Article

Microfluidic mass transfer of CO2 at elevated pressures: implications for carbon storage in deep saline aquifers

Journal

LAB ON A CHIP
Volume 21, Issue 20, Pages 3942-3951

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1lc00106j

Keywords

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Funding

  1. Canada First Research Excellence Fund (CFREF), Future Energy System (FES) at the University of Alberta [T02-P05]
  2. Canada Foundation for Innovation [CFI 34546]
  3. Natural Sciences and Engineering Research Council of Canada (NSERC)
  4. Alberta Innovates (AI)
  5. NSERC Canada Research Chairs Program [CRC 233147, RGPIN-2020-05511]

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This study conducted high-pressure microfluidic experiments to investigate the mass transfer process of CO2 into water under various states. Results showed that bubbles/droplets under high pressure conditions reach a steady state faster and the volumetric mass transfer coefficient increases with the Reynolds number and high pressure at the supercritical state. Additionally, the microfluidic results demonstrated a significant increase in the volumetric mass transfer of CO2 into water by two to three orders of magnitude compared to chemical engineering applications using millimeter-sized capillaries.
Carbon capture and sequestration (CCS) in a deep saline aquifer is one of the most promising technologies to mitigate anthropologically emitted carbon dioxide. Accurately quantifying the mass transport of CO2 at pore-scales is crucial but challenging for successful CCS deployment. Here, we conduct high-pressure microfluidic experiments, mimicking reservoir conditions up to 9.5 MPa and 35 degrees C, to elucidate the microfluidic mass transfer process of CO2 at three different states (i.e., gas, liquid, and supercritical phase) into water. We measure the size change of CO2 micro-bubbles/droplets generated using a microfluidic T-junction to estimate the volumetric mass transfer coefficient (k(L)a), quantifying the rate change of CO2 concentration under the driving force of concentration gradient. The results show that bubbles/droplets under high-pressure conditions reach a steady state faster than low pressure. The measured volumetric mass transfer coefficient increases with the Reynolds number (based on the liquid slug) and is nearly independent of the injection pressure for both the gas and liquid phases. In addition, k(L)a significantly enlarges with increasing high pressure at the supercritical state. Compared with various chemical engineering applications using millimeter-sized capillaries (with typical k(L)a measured ranging from approximate to 0.005 to 0.8 s(-1)), the microfluidic results show a significant increase in the volumetric mass transfer of CO2 into water by two to three orders of magnitude, O (10(2)-10(3)), with decreasing hydrodynamic diameter (of approximate to 50 mu m).

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