Dissolution trapping
is one of the primary mechanisms of carbon
dioxide (CO2) storage in deep saline aquifers. The determination
of the realized rates of CO2 dissolution requires an understanding
of the mixing process that takes place following the emplacement of
CO2 into the formation. Owing to the difficulty of reproducing
the time-dependent convective process in porous media, experiments
so far have largely focused on 2D systems (e.g., Hele-Shaw cells)
and used analogue fluid pairs with properties that differ from the
subsurface CO2/brine system. Here, we present a novel experimental
approach to investigate the evolution of the convective mixing process
in 3D porous media (homogeneous packings of glass beads) using X-ray
computed tomography (CT). We explore a range of Rayleigh numbers (Ra = 3000–55000) and observe directly the mixing
structures that arise upon dissolution. We compute from the images
the temporal evolution of the spatial moments of the concentration
distribution, including the cumulative dissolved mass, the location
of the center of mass, and the standard deviation of the concentration
field. The scalings of the spatial moments suggest an impact of hydrodynamic
dispersion on the longitudinal mixing. We propose a simplified representation
of the mixing process by analogy with the 1D advection–dispersion
model. This enables the estimation of the bulk advective velocity
and the effective longitudinal dispersion coefficient for each bead
packing. These estimates suggest that the presence of the finger pattern
and the counter-current flow structure enhance the longitudinal spreading
of the solute by roughly 1 order of magnitude compared to unidirectional
dispersion of a single-solute plume.