Dissolution-driven convection in a Hele-Shaw cell

Motivated by convection in the context of geological carbon-dioxide (CO2) storage, we present an experimental study of dissolution-driven convection in a Hele-Shaw cell for Rayleigh numbers R in the range 100 < R < 1700. We use potassium permanganate (KMnO4) in water as an analog for CO2 in brine and infer concentration profiles at high spatial and temporal resolution and accuracy from transmitted light intensity. We describe behavior from first contact up to 65% average saturation and measure several global quantities including dissolution flux, average concentration, amplitude of perturbations away from pure one-dimensional diffusion, and horizontally averaged concentration profiles. We show that the flow evolves successively through distinct regimes starting with a simple one-dimensional diffusional profile. This is followed by linear growth in which fingers are initiated and grow quasi-exponentially, independently of one-another. Once the fingers are well-established, a flux-growth regime begins as fresh fluid is brought to the interface and contaminated fluid removed, with the flux growing to a local maximum. During this regime, fingers still propagate independently. However, beyond the flux maximum, fingers begin to interact and zip together from the root down in a merging regime. Several generations of merging occur before only persistent primary fingers remain. Beyond this, the reinitiation regime begins with new fingers created between primary existing ones before merging into them. Through appropriate scaling, we show that the regimes are universal and independent of layer thickness (equivalently R) until the fingers hit the bottom. At this time, progression through these regimes is interrupted and the flow transitions to a saturating regime. In this final regime, the flux gradually decays in a manner well described by a Howard-style phenomenological model. (C) 2013 American Institute of Physics. [http://dx.doi.org/10.1063/1.4790511]