Dissolution rate variability at carbonate surfaces: 4D X-ray micro-tomography and stochastic modeling investigations

Abstract

We provide a detailed 3D characterization of the geometry evolution and dissolution rate mapping at the surface of four carbonate samples, namely a calcite spar crystal, two limestone rock fragments, and an aragonite ooid, using time-lapse X-ray micro-tomography during dissolution experiments at pH 4.0. Evaluation of the retreat and mapping of the reaction rates at the whole surface of the samples reveals a large spatial variability in the dissolution rates, reflecting the composition and the specific contributions of the different regions of the samples. While crystal edges and convex topographies record the highest dissolution rates, the retreat is slower for flat surfaces and in topographic lows (i.e., concave areas), suggesting surface-energy related and/or diffusion-limited reactions. Microcrystalline aragonite has the highest rate of dissolution compared to calcite. Surprisingly, rough microcrystalline calcite surface dissolves globally more slowly than the {101̄4} faces of the calcite spar crystal. The presence of mineral impurities in rocks, through the development of a rough interface that may affect the transport of species across the surface, may explain the slight decrease in reactivity with time. Finally, a macroscopic stochastic model using the set of detachment probabilities at corner, edge, and face (terrace) sites obtained from kinetic Monte Carlo simulations is applied at the spar crystal scale to account for the effect of site coordination onto reactivity. Application of the model to the three other carbonate samples is discussed regarding their geometry and composition. The results suggest that the global dissolution process of carbonate rocks does not reflect only the individual behavior of their forming minerals, but also the geometry of the crystals and the shape of the fluid-mineral interface.