336 research outputs found

    Dynamic reservoir-condition microtomography of reactive transport in complex carbonates: effect of initial pore structure and initial brine pH

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    We study the impact of brine acidity and initial pore structure on the dynamics of fluid/solid reaction at high Péclet numbers and low Damköhler numbers. A laboratory μ-CT scanner was used to image the dissolution of Ketton, Estaillades, and Portland limestones in the presence of CO2-acidified brine at reservoir conditions (10 MPa and 50°C) at two injected acid strengths for a period of 4 hours. Each sample was scanned between 6 and 10 times at ∼4 μm resolution and multiple effluent samples were extracted. The images were used as inputs into flow simulations, and analysed for dynamic changes in porosity, permeability, and reaction rate. Additionally, the effluent samples were used to verify the image-measured porosity changes. We find that initial brine acidity and pore structure determine the type of dissolution. Dissolution is either uniform where the porosity increases evenly both spatially and temporally, or occurs as channelling where the porosity increase is concentrated in preferential flow paths. Ketton, which has a relatively homogeneous pore structure, dissolved uniformly at pH = 3.6 but showed more channelized flow at pH = 3.1. In Estaillades and Portland, increasingly complex carbonates, channelized flow was observed at both acidities with the channel forming faster at lower pH. It was found that the effluent pH, which is higher than that injected, is a reasonably good indicator of effective reaction rate during uniform dissolution, but a poor indicator during channelling. The overall effective reaction rate was up to 18 times lower than the batch reaction rate measured on a flat surface at the effluent pH, with the lowest reaction rates in the samples with the most channelized flow, confirming that transport limitations are the dominant mechanism in determining reaction dynamics at the fluid/solid boundary

    Pore-scale dynamics and the multiphase Darcy law

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    Synchrotron x-ray microtomography combined with sensitive pressure differential measurements were used to study flow during steady-state injection of equal volume fractions of two immiscible fluids of similar viscosity through a 57-mm-long porous sandstone sample for a wide range of flow rates. We found three flow regimes. (1) At low capillary numbers, Ca, representing the balance of viscous to capillary forces, the pressure gradient, ∇ P , across the sample was stable and proportional to the flow rate (total Darcy flux) q t (and hence capillary number), confirming the traditional conceptual picture of fixed multiphase flow pathways in porous media. (2) Beyond Ca ∗ ≈ 10 − 6 , pressure fluctuations were observed, while retaining a linear dependence between flow rate and pressure gradient for the same fractional flow. (3) Above a critical value Ca > Ca i ≈ 10 − 5 we observed a power-law dependence with ∇ P ∼ q a t with a ≈ 0.6 associated with rapid fluctuations of the pressure differential of a magnitude equal to the capillary pressure. At the pore scale a transient or intermittent occupancy of portions of the pore space was captured, where locally flow paths were opened to increase the conductivity of the phases. We quantify the amount of this intermittent flow and identify the onset of rapid pore-space rearrangements as the point when the Darcy law becomes nonlinear. We suggest an empirical form of the multiphase Darcy law applicable for all flow rates, consistent with the experimental results

    The impact of porous media heterogeneity on non-Darcy flow behaviour from pore-scale simulation

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    The effect of pore-scale heterogeneity on non-Darcy flow behaviour is investigated by means of direct flow simulations on 3-D images of a beadpack, Bentheimer sandstone and Estaillades carbonate. The critical Reynolds number indicating the cessation of the creeping Darcy flow regime in Estaillades carbonate is two orders of magnitude smaller than in Bentheimer sandstone, and is three orders of magnitude smaller than in the beadpack. It is inferred from the examination of flow field features that the emergence of steady eddies in pore space of Estaillades at elevated fluid velocities accounts for the early transition away from the Darcy flow regime. The non-Darcy coefficient β, the onset of non-Darcy flow, and the Darcy permeability for all samples are obtained and compared to available experimental data demonstrating the predictive capability of our approach. X-ray imaging along with direct pore-scale simulation of flow provides a viable alternative to experiments and empirical correlations for predicting non-Darcy flow parameters such as the β factor, and the onset of non-Darcy flow

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

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    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
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