Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/13572
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dc.contributor.authorNoel, Vincent-
dc.contributor.authorDruhan, Jennifer L.-
dc.contributor.authorGündoğar, Aslı-
dc.contributor.authorKovscek, Anthony R.-
dc.contributor.authorBrown Jr, Gordon E.-
dc.contributor.authorBargar, John R.-
dc.date.accessioned2023-07-27T19:49:52Z-
dc.date.available2023-07-27T19:49:52Z-
dc.date.issued2023-
dc.identifier.issn0883-2927-
dc.identifier.issn1872-9134-
dc.identifier.urihttps://doi.org/10.1016/j.apgeochem.2022.105542-
dc.identifier.urihttps://hdl.handle.net/11147/13572-
dc.description.abstractInjection 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.sponsorshipCenter 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.sponsorshipThis 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.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofApplied Geochemistryen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectGeochemical reaction fronten_US
dc.subjectMineral dissolutionen_US
dc.subjectMatrix alterationen_US
dc.subjectReactive transporten_US
dc.subjectHydraulic stimulationen_US
dc.subjectUnconventional shaleen_US
dc.titleDynamic development of geochemical reaction fronts during hydraulic stimulation of shaleen_US
dc.typeArticleen_US
dc.institutionauthorGündoğar, Aslı-
dc.departmentİzmir Institute of Technology. Energy Systems Engineeringen_US
dc.identifier.volume148en_US
dc.identifier.wosWOS:000913925600001en_US
dc.identifier.scopus2-s2.0-85144601474en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1016/j.apgeochem.2022.105542-
dc.authorwosidNoel, Vincent/D-9826-2018-
dc.identifier.scopusqualityQ2-
item.grantfulltextopen-
item.openairetypeArticle-
item.fulltextWith Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
Appears in Collections:Energy Systems Engineering / Enerji Sistemleri Mühendisliği
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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