Mineral sequestration of carbon dioxide in basalt: A pre-injection overview of the CarbFix project

Abstract

In this paper we describe the thermodynamic and kinetic basis for mineral storage of carbon dioxide in basaltic rock, and how this storage can be optimized. Mineral storage is facilitated by the dissolution of CO 2 into the aqueous phase. The amount of water required for this dissolution decreases with decreased temperature, decreased salinity, and increased pressure. Experimental and field evidence suggest that the factor limiting the rate of mineral fixation of carbon in silicate rocks is the release rate of divalent cations from silicate minerals and glasses. Ultramafic rocks and basalts, in glassy state, are the most promising rock types for the mineral sequestration of CO 2 because of their relatively fast dissolution rate, high concentration of divalent cations, and abundance at the Earth's surface. Admixture of flue gases, such as SO 2 and HF, will enhance the dissolution rates of silicate minerals and glasses. Elevated temperature increases dissolution rates but porosity of reactive rock formations decreases rapidly with increasing temperature. Reduced conditions enhance mineral carbonation as reduced iron can precipitate in carbonate minerals. Elevated CO 2 partial pressure increases the relative amount of carbonate minerals over other secondary minerals formed. The feasibility to fix CO 2 by carbonation in basaltic rocks will be tested in the CarbFix project by: (1) injection of CO 2 charged waters into basaltic rocks in SW Iceland, (2) laboratory experiments, (3) studies of natural analogues, and (4) geochemical modelling.