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Rock dissolution patterns and geochemical shutdown of $\text{CO}_{2}$–brine–carbonate reactions during convective mixing in porous media

Published online by Cambridge University Press:  05 January 2015

X. Fu
Affiliation:
Department of Civil & Environmental Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA
L. Cueto-Felgueroso
Affiliation:
Department of Civil & Environmental Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA Civil Engineering School, Technical University of Madrid, Madrid, Spain
D. Bolster
Affiliation:
Department of Civil and Environmental Engineering and Earth Sciences, University of Notre Dame, Notre Dame, IN 46556, USA
R. Juanes*
Affiliation:
Department of Civil & Environmental Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA
*
Email address for correspondence: [email protected]

Abstract

Motivated by the process of $\text{CO}_{2}$ convective mixing in porous media, here we study the formation of rock-dissolution patterns that arise from geochemical reactions during Rayleigh–Bénard–Darcy convection. Under the assumption of instantaneous chemical equilibrium, we adopt a formulation of the local reaction rate as a function of scalar dissipation rate, a measure that depends solely on flow and transport, and chemical speciation, which is a measure that depends only on the equilibrium thermodynamics of the chemical system. We use high-resolution simulations to examine the interplay between the density-driven hydrodynamic instability and the rock dissolution reactions, and analyse the impact of geochemical reactions on the macroscopic mass exchange rate. We find that dissolution of carbonate rock initiates in regions of locally high mixing, but that the geochemical reaction shuts down significantly earlier than shutdown of convective mixing. This early shutdown feature reflects the important role that chemical speciation plays in this hydrodynamics–reaction coupled process. Finally, we extend our analysis to three dimensions and explore the morphology of dissolution patterns in three dimensions.

Type
Papers
Copyright
© 2015 Cambridge University Press 

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