Sammendrag
The dissolution of carbon-dioxide (CO2) in deep saline aquifers is an important trapping mechanism in carbon
storage. This process is triggered by unstable high-density CO2 front, which later promotes density-driven
mixing, hydrodynamic dispersion of CO2 and favors the long-term sequestration. In many former studies,
the effects of hydrodynamic dispersion and multispecies geochemical reactions have been ignored.
This work elaborates the impacts of these simplifications on the dynamics of convective mixing by numerical
simulations. Geochemical effects were studied by the implementation of rock-fluid and fluid-fluid interactions
for typical sandstone and carbonate aquifers. Results show that accounting for the hydrodynamic dispersion
decreases the convection onset time and increases the CO2 dissolution flux, which is more significant in
larger dispersivities and Rayleigh numbers. Results indicate that carbonate geochemical reactions intense
the long-term overall efficiency of the process, while decrease the total amount of sequestered carbon in
the diffusion-dominated period. Conversely the sandstone geochemical interactions were shown to have a
different impact on the process compared to carbonate interactions. Results also reinforce the importance of
realistic geochemical representation and the importance of spatial and temporal dependence of the reactions
pathway, subsequent to the finger development for more detailed simulation of the CO2 storage process.
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