Quantification of sub-resolution porosity in carbonate rocks by applying high-salinity contrast brine using X-ray microtomography differential imaging

Characterisation of the pore space in carbonate reservoirs and aquifers is of utmost importance in a number of applications such as enhanced oil recovery, geological carbon storage and contaminant transport. We present a new experimental methodology that uses high-salinity contrast brine and differential imaging acquired by X-ray tomography to non-invasively obtain three-dimensional spatially resolved information on porosity and connectivity of two rock samples, Portland and Estaillades limestones, including sub-resolution micro-porosity. We demonstrate that by injecting 30 wt% KI brine solution, a sufficiently high phase contrast can be achieved allowing accurate three-phase segmentation based on differential imaging. This results in spatially resolved maps of the solid grain phase, sub-resolution micro-pores within the grains, and macro-pores. The total porosity values from the three-phase segmentation for two carbonate rock samples are shown to be in good agreement with Helium porosity measurements. Furthermore, our flow-based method allows for an accurate estimate of pore connectivity and a distribution of porosity within the sub-resolution pores

Pore-scale dissolution by CO₂ saturated brine in a multimineral carbonate at reservoir conditions: impact of physical and chemical heterogeneity

We study the impact of physical and chemical heterogeneity on reaction rates in multimineral porous media. We selected two pairs of carbonate samples of different physical heterogeneity in accordance with their initial computed velocity distributions and then injected CO 2 saturated brine at reservoir conditions at two flow rates. We periodically imaged the samples using X-ray microtomography. The mineralogical composition was similar (a ratio of dolomite to calcite of 8:1), but the intrinsic reaction rates and mineral spatial distribution were profoundly different. Visualizations of velocity fields and reacted mineral distributions revealed that a dominant flow channel formed in all cases. The more physically homogeneous samples had a narrower velocity distribution and more preexisting fast channels, which promoted dominant channel formation in their proximity. In contrast, the heterogeneous samples exhibit a broader distribution of velocities and fewer fast channels, which accentuated nonuniform calcite distribution and favored calcite dissolution away from the initially fast pathways. We quantify the impact of physical and chemical heterogeneity by computing the proximity of reacted minerals to the fast flow pathways. The average reaction rates were an order of magnitude lower than the intrinsic ones due to mass transfer limitations. The effective reaction rate of calcite decreased by an order of magnitude, in both fast channels and slow regions. After channel formation calcite was shielded by dolomite whose effective rate in slow regions could even increase. Overall, the preferential channeling effect, as opposed to uniform dissolution, was promoted by a higher degree of physical and/or chemical heterogeneity

Erratum to: 36th International Symposium on Intensive Care and Emergency Medicine

[This corrects the article DOI: 10.1186/s13054-016-1208-6.]

Reaction Rates in Chemically Heterogeneous Rock: Coupled Impact of Structure and Flow Properties Studied by X-ray Microtomography

We study dissolution in a chemically heterogeneous medium consisting of two minerals with contrasting initial structure and transport properties. We perform a reactive transport experiment using CO2-saturated brine at reservoir conditions in a millimeter-scale composite core composed of Silurian dolomite and Ketton limestone (calcite) arranged in series. We repeatedly image the composite core using X-ray microtomography (XMT) and collect effluent to assess the individual mineral dissolution. The mineral dissolution from image analysis was comparable to that measured from effluent analysis using inductively coupled plasma mass spectrometry (ICP-MS). We find that the ratio of the effective reaction rate of calcite to that of dolomite decreases with time, indicating the influence of dynamic transport effects originating from changes in pore structure coupled with differences in intrinsic reaction rates. Moreover, evolving flow and transport heterogeneity in the initially heterogeneous dolomite is a key determinant in producing a two-stage dissolution in the calcite. The first stage is characterized by a uniform dissolution of the pore space, while the second stage follows a single-channel growth regime. This implies that spatial memory effects in the medium with a heterogeneous flow characteristic (dolomite) can change the dissolution patterns in the medium with a homogeneous flow characteristic (calcite)

4D in situ synchrotron X-ray tomographic microscopy and laser-based heating study of oil shale pyrolysis

The comprehensive characterization and analysis of the evolution of micro-fracture networks in oil shales during pyrolysis is important to understand the complex petrophysical changes during hydrocarbon recovery. We used time-resolved X-ray microtomography to perform pore-scale dynamic imaging with a synchrotron light source to capture in 4-D (three-dimensional image + real time) the evolution of fracture initiation, growth, coalescence and closure. A laser-based heating system was used to pyrolyze a sample of Eocene Green River (Mahogany Zone) up to 600 °C with tomograms acquired every 30 s at 1.63 µm computed voxel size and analyzed using Digital Volume Correlation (DVC) for full 3-D strain and deformation maps. At 354 °C the first isolated micro-fractures were observed and by 378 °C, a connected fracture network was formed as the solid organic matter was transformed into volatile hydrocarbon components. With increasing temperature, we observed simultaneous pore space growth and coalescence as well as temporary closure of minor fractures caused by local compressive stresses. This indicates that the evolution of individual fractures not only depends on organic matter composition but also on the dynamic development of neighboring fractures. Our results demonstrate that combining synchrotron X-ray tomography, laser-based heating and DVC provides a powerful methodology for characterizing dynamics of multi-scale physical changes during oil shale pyrolysis to help optimize hydrocarbon recovery

Reservoir-condition pore-scale imaging of dolomite reaction with supercritical CO<inf>2</inf>acidified brine: Effect of pore-structure on reaction rate using velocity distribution analysis

To investigate the impact of rock heterogeneity and flowrate on reaction rates and dissolution dynamics, four millimetre-scale Silurian dolomite samples were pre-screened based on their physical heterogeneity, defined by the simulated velocity distributions characterising each flow field. Two pairs of cores with similar heterogeneity were flooded with supercritical carbon-dioxide (scCO 2 ) saturated brine under reservoir conditions, 50 °C and 10 MPa, at a high (0.5 ml/min) and low (0.1 ml/min) flowrate. Changes to the pore structure brought about by dissolution were captured in situ using X-ray microtomography (micro-CT) imaging. Mass balance from effluent analysis sh owed a good agreement with calculations from imaging. Image calculated reaction rates (r eff ) were 5-38 times lower than the corresponding batch reaction rate under the same conditions of temperature and pressure but without mass transfer limitations. For both high (Péclet number = 2600-1200) and low (Péclet number = 420-300) flow rates, an impact of the initial rock heterogeneity was observed on both reaction rates and permeability-porosity relationships