A flow‐through experiment was performed to investigate evolution of a fractured carbonate caprock during flow of CO2‐acidified brine. A core was taken from the Amherstburg limestone, a caprock formation overlying the Bois Blanc and Bass Islands formations, which have been used to demonstrate CO2 storage in the Michigan basin. The inlet brine was representative of deep saline brines saturated with CO2, resulting in a starting pH of 4.4. Experimental conditions were 27 °C and 10 MPa. X‐ray computed tomography and scanning electron microscopy were used to observe evolution of fracture geometry and to investigate mineralogical changes along the fracture surface. The initial brine flow corresponded to an average fluid velocity of 110 cm hr−1. After one week, substantial mineral dissolution caused the average cross‐sectional area of the fracture to increase from 0.09 cm2 to 0.24 cm2. This demonstrates that carbonate caprocks, if fractured, can erode quickly and may jeopardize sealing integrity when hydrodynamic conditions promote flow of CO2‐acidified brine. However, changes to fracture permeability due to mineral dissolution may be offset by unaltered constrictions along the flow path and by increases in surface roughness. In this experiment, preferential dissolution of calcite over dolomite led to uneven erosion of the fracture surface and an increase in roughness. In areas with clay minerals, calcite dissolution left behind a silicate mineral‐rich microporous coating along the fracture wall. Thus, the evolution of fracture permeability will depend in a complex way on the carbonate content, as well as the heterogeneity of the minerals and their spatial patterning. © 2011 Society of Chemical Industry and John Wiley & Sons, Ltd
Geochemical reactions may alter the permeability of leakage pathways in caprocks, which serve a critical role in confining CO 2 in geologic carbon sequestration. A caprock specimen from a carbonate formation in the Michigan sedimentary Basin was fractured and studied in a high-pressure core flow experiment. Inflowing brine was saturated with CO 2 at 40°C and 10 MPa, resulting in an initial pH of 4.6, and had a calcite saturation index of -0.8. Fracture permeability decreased during the experiment, but subsequent analyses did not reveal calcite precipitation. Instead, experimental observations indicate that calcite dissolution along the fracture pathway led to mobilization of less soluble mineral particles that clogged the flow path. Analyses of core sections via electron microscopy, synchrotron-based X-ray diffraction imaging, and the first application of microbeam Ca K-edge X-ray absorption near edge structure, provided evidence that these occlusions were fragments from the host rock rather than secondary precipitates. X-ray computed tomography showed a significant loss of rock mass within preferential flow paths, suggesting that dissolution also removed critical asperities and caused mechanical closure of the fracture. The decrease in fracture permeability despite a net removal of material along the fracture pathway demonstrates a nonintuitive, inverse relationship between dissolution and permeability evolution in a fractured carbonate caprock.
Fractures in geological formations may enable migration of environmentally relevant fluids, as in leakage of CO2 through caprocks in geologic carbon sequestration. We investigated geochemically induced alterations of fracture geometry in Indiana Limestone specimens. Experiments were the first of their kind, with periodic high-resolution imaging using X-ray computed tomography (xCT) scanning while maintaining high pore pressure (100 bar). We studied two CO2-acidified brines having the same pH (3.3) and comparable thermodynamic disequilibrium but different equilibrated pressures of CO2 (PCO2 values of 12 and 77 bar). High-PCO2 brine has a faster calcite dissolution kinetic rate because of the accelerating effect of carbonic acid. Contrary to expectations, dissolution extents were comparable in the two experiments. However, progressive xCT images revealed extensive channelization for high PCO2, explained by strong positive feedback between ongoing flow and reaction. The pronounced channel increasingly directed flow to a small region of the fracture, which explains why the overall dissolution was lower than expected. Despite this, flow simulations revealed large increases in permeability in the high-PCO2 experiment. This study shows that the permeability evolution of dissolving fractures will be larger for faster-reacting fluids. The overall mechanism is not because more rock dissolves, as would be commonly assumed, but because of accelerated fracture channelization.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.