One of the major concerns of carbon capture and storage (CCS) projects is the prediction of the long-term storage security of injected CO2. When injected underground in saline aquifers or depleted oil and gas fields, CO2 mixes with the resident brine to form carbonic acid. The carbonic acid can react with the host carbonate rock, and alter the rock structure and flow properties. In this study, we have used X-ray micro-tomography and focused ion beam scanning electron microscopy (FIB-SEM) techniques to investigate the dissolution behavior in wettability-altered carbonate rocks at the nm- to µm-scale, to investigate CO2 storage in depleted oil fields that have oil-wet or mixed-wet conditions. Our novel procedure of injecting oil after reactive transport has revealed previously unidentified (ghost) regions of partially-dissolved rock grains that were difficult to identify in X-ray tomographic images after dissolution from single fluid phase experiments. We show that these ghost regions have a significantly higher porosity and pore sizes that are an order of magnitude larger than that of unreacted grains. The average thickness of the ghost regions as well as the overall rock dissolution decreases with increasing distance from the injection point. During dissolution micro-porous rock retains much of its original fabric. This suggests that considering the solid part of these ghost regions as macro (bulk) pore space can result in the overestimation of porosity and permeability predicted from segmented X-ray tomographic images, or indeed from reactive transport models that assume a uniform, sharp reaction front at the grain surface.
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- School of Energy, Geoscience, Infrastructure and Society, Institute for GeoEnergy Engineering - Associate Professor
- School of Energy, Geoscience, Infrastructure and Society - Associate Professor
Person: Academic (Research & Teaching)