Dynamic Development of Geochemical Reaction Fronts During Hydraulic Stimulation of Shale

dc.contributor.author Noel, Vincent
dc.contributor.author Druhan, Jennifer L.
dc.contributor.author Gündoğar, Aslı
dc.contributor.author Kovscek, Anthony R.
dc.contributor.author Brown Jr, Gordon E.
dc.contributor.author Bargar, John R.
dc.date.accessioned 2023-07-27T19:49:52Z
dc.date.available 2023-07-27T19:49:52Z
dc.date.issued 2023
dc.description.abstract Injection of acidic hydraulic fracture fluid (HFF) into shale formations for unconventional oil/gas production results in chemical reactions in the shale matrix that can alter fluid transport. Here, we report the results of set of experiments designed to evaluate the impact of calcite dissolution as a function of carbonate mineral content on matrix chemical reactivity and pore-space modification concomitant with imbibition. We tracked acidic HFF transport in four samples of Wolfcamp shale with calcite contents varying from 4% to 59% by monitoring the rate and spatial extent of bromide tracer transport using synchrotron-based X-ray fluorescence microprobe (XFM) imaging. Concurrently, we also carried out XFM imaging of the spatial distribution of Ca in the Wolfcamp shale cores (as a proxy of calcite distribution). Our approach thus yields a direct record of time-resolved selective ion transport resulting from the penetration of acidic HFF and the associated mineral transformations in the shale cores. We show that the variability in calcite content of Wolfcamp shale samples can directly affect the rate and spatial extent of imbibition. Although reaction of the acidic HFF with carbonates in shales enhances calcite dissolution and increases porosity, the spatial extent of calcite dissolution in the shale matrix is limited due to a rapid neutralization of pH. The relative abundance and spatial distribution of calcite control the chemical saturation state of the HFF progressing into the matrix. As a result, calcite has a major impact on the spatial extent and rate of matrix alteration and thus on HFF transport during subsurface reservoir stimulation. Consequently, increased calcite content in the shale matrix inhibits the spatial extent of the pore-volume increase and, by extension, the spatial extent and rate of imbibition. Our results thus show that the overall rates of calcite dissolution approach the rates of acidic HFF transport (i. e., Damko spacing diaeresis hler number similar to 1), which could contribute to the efficiency of subsurface reservoir stimulation. A better understanding of HFF-calcite reaction rates is crucial for improving the prediction and optimization of fluid transport across HFF-shale interfaces during hydraulic fracturing. en_US
dc.description.sponsorship Center for Mechanistic Control of Water -Hydrocarbon -Rock Interactions in Unconventional and Tight Oil Formations - U.S. Department of Energy (DOE) , Office of Science under BES Award [DE-SC0019165]; U.S. DOE; National Institutes of Health, National Institute of General Medical Sciences [P41GM103393] en_US
dc.description.sponsorship This research was funded by the Center for Mechanistic Control of Water -Hydrocarbon -Rock Interactions in Unconventional and Tight Oil Formations (CMC-UF) , an Energy Frontier Research Center funded by the U.S. Department of Energy (DOE) , Office of Science under BES Award DE-SC0019165. The Stanford Synchrotron Radiation Lightsource (SSRL) and SLAC National Accelerator Laboratory are supported by the U.S. DOE and by the National Institutes of Health, National Institute of General Medical Sciences (including P41GM103393) . We thank Dr. Adam Jew for his assistance in conducting the experiments. We grate- fully acknowledge Dr. Sam Webb, Dr. Sharon Bone, and the technical staff at SSRL for their technical support during the X-ray fluorescence mapping measurements. We also acknowledge Dr. Johanna Nelson, Dr. Yechuan Chen, and the technical staff at SSRL for their technical support during the Synchrotron -based transmission micro -tomography. The authors further thank Dr. Guangchao Li (Stanford University) for his help in the ICP analyses. en_US
dc.identifier.doi 10.1016/j.apgeochem.2022.105542
dc.identifier.issn 0883-2927
dc.identifier.issn 1872-9134
dc.identifier.scopus 2-s2.0-85144601474
dc.identifier.uri https://doi.org/10.1016/j.apgeochem.2022.105542
dc.identifier.uri https://hdl.handle.net/11147/13572
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.relation.ispartof Applied Geochemistry en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Geochemical reaction front en_US
dc.subject Mineral dissolution en_US
dc.subject Matrix alteration en_US
dc.subject Reactive transport en_US
dc.subject Hydraulic stimulation en_US
dc.subject Unconventional shale en_US
dc.title Dynamic Development of Geochemical Reaction Fronts During Hydraulic Stimulation of Shale en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.institutional Gündoğar, Aslı
gdc.author.wosid Noel, Vincent/D-9826-2018
gdc.bip.impulseclass C4
gdc.bip.influenceclass C5
gdc.bip.popularityclass C4
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.collaboration.industrial false
gdc.description.department İzmir Institute of Technology. Energy Systems Engineering en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q2
gdc.description.volume 148 en_US
gdc.description.wosquality Q1
gdc.identifier.openalex W4313400367
gdc.identifier.wos WOS:000913925600001
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gdc.oaire.isgreen false
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gdc.oaire.sciencefields 01 natural sciences
gdc.oaire.sciencefields 0105 earth and related environmental sciences
gdc.openalex.collaboration International
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gdc.opencitations.count 4
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gdc.scopus.citedcount 7
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relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4003-8abe-a4dfe192da5e

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