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3D Mapping of calcite and a demonstration of its relevance to permeability evolution in reactive fractures
Institution:1. Department of Civil and Environmental Engineering, University of Michigan, Ann Arbor, MI, United States;2. Department of Civil and Environmental Engineering, Princeton University, Princeton, NJ, United States;1. CEMSE, King Abdullah University of Science and Technology, Thuwal, Saudi Arabia;2. DISAT, Politecnico di Torino, Torino, Italy;3. ICES, The University of Texas at Austin, USA;4. Mathematics Institute, University of Warwick, UK;1. Graduate Institute of Hydrological and Oceanic Science, National Central University, No. 300, Jhongda Rd., Jhongli City, Taoyuan County 320, Taiwan (ROC);2. Environmental Health Sciences, Johns Hopkins University, 615 N. Wolfe Street, Baltimore, MD 21205, US;1. Korea Institute of Geoscience and Mineral Resources, 124, Gwahak-ro, Yuseong-gu, Daejeon 34132, Republic of Korea;2. Disaster Prevention Research Institute, Kyoto University, Gokasho, Uji, Kyoto 611-0011, Japan;1. School of Petroleum Engineering, UNSW, Sydney, Australia;2. Department of Petroleum Engineering, Shahid Bahonar University of Kerman, Kerman, Iran;1. Mechanical and Aerospace Engineering, University of California San Diego, San Diego, CA, USA;2. Mechanical Engineering, San Diego State University, San Diego, CA, USA;3. Pacific Northwest National Laboratory, Richland, WA, USA;4. Energy Resources Engineering, Stanford University, Stanford, CA, USA
Abstract:There is a need to better understand reaction-induced changes in fluid transport in fractured shales, caprocks and reservoirs, especially in the context of emerging energy technologies, including geologic carbon sequestration, unconventional natural gas, and enhanced geothermal systems. We developed a method for 3D calcite mapping in rock specimens. Such information is critical in reactive transport modeling, which relies on information about the locations and accessible surface area of reactive minerals. We focused on calcite because it is a mineral whose dissolution could lead to substantial pathway alteration because of its high solubility, fast reactivity, and abundance in sedimentary rocks. Our approach combines X-ray computed tomography (XCT) and scanning electron microscopy. The method was developed and demonstrated for a fractured limestone core containing about 50% calcite, which was 2.5 cm in diameter and 3.5 cm in length and had been scanned using XCT. The core was subsequently sectioned and energy dispersive X-ray spectroscopy was used to determine elemental signatures for mineral identification and mapping. Back-scattered electron microscopy was used to identify features for co-location. Finally, image analysis resulted in characteristic grayscale intensities of X-ray attenuation that identify calcite. This attenuation mapping ultimately produced a binary segmented 3D image of the spatial distribution of calcite in the entire core. To demonstrate the value of this information, permeability changes were investigated for hypothetical fractures created by eroding calcite from 2D rock surfaces. Fluid flow was simulated using a 2D steady state model. The resulting increases in permeability were profoundly influenced by the degree to which calcite is contiguous along the flow path. If there are bands of less reactive minerals perpendicular to the direction of flow, fracture permeability may be an order of magnitude smaller than when calcite is contiguous. These results emphasize the importance of characterizing spatial distribution of calcite in heterogeneous rocks that also contain a similar abundance of less reactive minerals.
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