The two-phase flow characterization (CO 2 /water) of a Triassic sandstone core from the Paris Basin, France, is reported in this paper. Absolute properties (porosity and water permeability), capillary pressure, relative permeability with hysteresis between drainage and imbibition, and residual trapping capacities have been assessed at 9 MPa pore pressure and 28 C (CO 2 in liquid state) using a single core-flooding apparatus associated with magnetic resonance imaging. Different methodologies have been followed to obtain a data set of flow properties to be upscaled and used in large-scale CO 2 geological storage evolution modeling tools. The measurements are consistent with the properties of well-sorted water-wet porous systems. As the mineralogical investigations showed a nonnegligible proportion of carbonates in the core, the experimental protocol was designed to observe potential impacts on flow properties of mineralogical changes. The magnetic resonance scanning and mineralogical observations indicate mineral dissolution during the experimental campaign, and the core-flooding results show an increase in porosity and water absolute permeability. The changes in two-phase flow properties appear coherent with the pore structure modifications induced by the carbonates dissolution but the changes in relative permeability could also be explained by a potential increase of the water-wet character of the core. Further investigations on the impacts of mineral changes are required with other reactive formation rocks, especially carbonate-rich ones, because the implications can be significant both for the validity of laboratory measurements and for the outcomes of in situ operations modeling.
International audienceThis article presents the main outputs from the multidisciplinary Carmex project (2009-2012), which was concerned with the possibility of applying ex situ mineral carbonation concepts to mafic/ultramafic mining wastes. Focus points of the project included (i) matching significant and accessible mining wastes to large CO2 emitters through a dedicated geographical information system (GIS), (ii) analysis of aqueous carbonation mechanisms of mining waste and process development and (iii) environmental assessment of ex situ mining waste carbonation through life cycle assessment (LCA) methodology. With a number of materials associated with the mining sector, the project took a close look at the aqueous carbonation mechanisms for these materials and obtained unexpected carbonation levels (up to 80%) by coupling mechanical exfoliation and reactive carbonation. Results from this work support the possibility of processing serpentine-rich peridotites without applying the classical first step of heat activation. Perspectives are also given for the carbonation of Ni-pyrometallurgical slag available closed to ultramafic mining residues. LCA of the mining waste carbonation system as a whole made it clear that the viability of this CO2 storage option lies with the carbonation process itself and optimisation of its operating conditions. By combining the body of knowledge acquired by this project, it is concluded that New Caledonia, with its insularity and local abundance of 'carbonable' rocks and industrial wastes coupled with significant greenhouse gas (GHG) emissions from world-class nickel pyro and hydrometallurgical industries stands out as a strong potential candidate for application of ex situ mineral carbonation
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