Evidence for passive mineral carbonation from carbon isotope geochemistry of interstitial air in mine wastes from the Dumont Nickel Project (Abitibi, Quebec).
Abstract:
A decrease of CO2 concentration in the mining waste cell, from atmospheric concentrations (~390 ppmv) near the surface of the cell to ~100 ppmv near the bottom, reflects active CO2 consumption by the residues. This cell contains mining waste with a large grain size distribution ranging from blocks (<40cm) to silt-size grains. Magnesium-rich minerals such as lizardite, chrysotile and brucite are the major minerals in the residues. Mineralogical analyses (XRD, SEM and EPMA) reveal precipitation of brugnatellite and hydromagnesite, with a lamellar texture on the surface of serpentine grains. In order to better identify the different processes involved in carbonation, the carbon isotopic composition of the interstitial gases was analysed in-situ with a WS-CRDS instrument. An increase of d13C(air) from -8‰ to ~2 ‰ is correlated with the decrease in CO2 concentration within the cell, and can be explained by dissolution of atmospheric CO2 in interstitial water (Dco2-DIC 11‰) in the DNP mining residues. As gas advection is slow, CO2 supply driven by diffusion is the limiting step in the experimental cell. CO2 dissolution in interstitial water under this limited CO2 supply condition enriches 13C in residual CO2 in interstitial air. Optimized mineral carbonation reactions in DNP mining waste will require an unconstrained CO2 supply.
