Published online by Cambridge University Press: 06 November 2013
The geologic sequestration of carbon dioxide ( CO2) in structural and stratigraphic traps is a viable option to reduce anthropogenic emissions. While dissolution of theCO2 stored in these traps reduces the long-term leakage risk, the dissolution process remains poorly understood in systems that reflect the appropriate subsurface geometry. Here, we study dissolution in a porous layer that exhibits a feature relevant forCO2 storage in structural and stratigraphic traps: a finiteCO2 source along the top boundary that extends only part way into the layer. This feature represents the finite extent of the interface between free-phaseCO2 pooled in a trap and the underlying brine. Using theory and simulations, we describe the dissolution mechanisms in this system for a wide range of times and Rayleigh numbers, and classify the behaviour into seven regimes. For each regime, we quantify the dissolution flux numerically and model it analytically, with the goal of providing simple expressions to estimate the dissolution rate in real systems. We find that, at late times, the dissolution flux decreases relative to early times as the flow of unsaturated water to theCO2 source becomes constrained by a lateral exchange flow though the reservoir. Application of the models to several representative reservoirs indicates that dissolution is strongly affected by the reservoir properties; however, we find that reservoirs with high permeabilities (  $k\geq 1$  Darcy) that are tens of metres thick and several kilometres wide could potentially dissolve hundreds of megatons ofCO2 in tens of years.
 $k\geq 1$  Darcy) that are tens of metres thick and several kilometres wide could potentially dissolve hundreds of megatons ofCO2 in tens of years.
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