X-ray microtomography characterization of porosity, permeability and reactive surface changes during dissolution

Numerical programs for simulating flow and reactive transport in porous media are essential tools for predicting reservoir properties changes triggered by CO 2 underground injection. At reservoir scale, meshed models in which equations are solved assuming that constant macroscopic properties can be...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of contaminant hydrology 2011-03, Vol.120, p.45-55
Hauptverfasser: Gouze, Philippe, Luquot, Linda
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 55
container_issue
container_start_page 45
container_title Journal of contaminant hydrology
container_volume 120
creator Gouze, Philippe
Luquot, Linda
description Numerical programs for simulating flow and reactive transport in porous media are essential tools for predicting reservoir properties changes triggered by CO 2 underground injection. At reservoir scale, meshed models in which equations are solved assuming that constant macroscopic properties can be defined in each cells, are widely used. However, the parameterization of the dissolution–precipitation problem and of the feedback effects of these processes on the flow field is still challenging. The problem arises from the mismatch between the scales at which averaged parameters are defined in the meshed model and the scale at which chemical reactions occur and modify the pore network geometry. In this paper we investigate the links between the dissolution mechanisms that control the porosity changes and the related changes of the reactive surface area and of the permeability. First, the reactive surface area is computed from X-ray microtomography data obtained before and after a set of dissolution experiments of pure calcite rock samples using distinctly different brine–CO 2 mixtures characterizing homogeneous to heterogeneous dissolution regimes. The results are used to validate the power law empirical model relating the reactive surface area to porosity proposed by Luquot and Gouze (2009). Second, we investigate the spatial distribution of the effective hydraulic radius and of the tortuosity, two structural parameters that control permeability, in order to explain the different porosity–permeability relationships observed for heterogeneous and homogeneous dissolution regimes. It is shown that the increase of permeability is due to the decrease of the tortuosity for homogeneous dissolution, whereas it is due to the combination of tortuosity decrease and hydraulic radius increase for heterogeneous dissolution. For the intermediate dissolution regime, identified to be the optimal regime for increasing permeability with small changes in porosity, the increase of permeability results from a large increase in the mean effective hydraulic radius of the sample.
doi_str_mv 10.1016/j.jconhyd.2010.07.004
format Article
fullrecord <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_00617671v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0169772210000835</els_id><sourcerecordid>845393071</sourcerecordid><originalsourceid>FETCH-LOGICAL-a477t-b0b3e71e8beec1ccac2234d595d41f36acc4d188e0374b322dfebc5373f1a6323</originalsourceid><addsrcrecordid>eNqFkdGL1DAQxoMo3nr6J6h5E8Guk6TbtE_HcagnLPigB76FNJnuZmmbmrQL9a83peu93lMmw2---ZiPkLcMtgxY8fm0PRnfH2e75ZB6ILcA-TOyYaUUWQFQPSebxFWZlJxfkVcxngBAllC-JFccZJXKYkOG31nQM-2cCX70nT8EPRxnao46aDNicH_16HxPfUMHH3x04_yJDhg61LVr04_q3tKACXZnpHEKjTa4zPcHjNROwfUHal2Mvp0WpdfkRaPbiG8u7zV5-Prl1919tv_x7fvd7T7TuZRjVkMtUDIsa0TDjNGGc5HbXbWzOWtEoY3JLStLBCHzWnBuG6zNTkjRMF0ILq7Jx1X3qFs1BNfpMCuvnbq_3aulB1AwWUh2Zon9sLJD8H8mjKPqXDTYtrpHP0VVFmlLCVI8TeY7UQmQi-ZuJdNhYwzYPJpgoJYE1UldElRLggpkspSnuXeXDVPdoX2c-h9ZAt6vQKO90ofgonr4mRQEsIqXkEMiblYC033PDoOKxmFv0LqAZlTWuydM_APRnrqq</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>845393071</pqid></control><display><type>article</type><title>X-ray microtomography characterization of porosity, permeability and reactive surface changes during dissolution</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Gouze, Philippe ; Luquot, Linda</creator><creatorcontrib>Gouze, Philippe ; Luquot, Linda</creatorcontrib><description>Numerical programs for simulating flow and reactive transport in porous media are essential tools for predicting reservoir properties changes triggered by CO 2 underground injection. At reservoir scale, meshed models in which equations are solved assuming that constant macroscopic properties can be defined in each cells, are widely used. However, the parameterization of the dissolution–precipitation problem and of the feedback effects of these processes on the flow field is still challenging. The problem arises from the mismatch between the scales at which averaged parameters are defined in the meshed model and the scale at which chemical reactions occur and modify the pore network geometry. In this paper we investigate the links between the dissolution mechanisms that control the porosity changes and the related changes of the reactive surface area and of the permeability. First, the reactive surface area is computed from X-ray microtomography data obtained before and after a set of dissolution experiments of pure calcite rock samples using distinctly different brine–CO 2 mixtures characterizing homogeneous to heterogeneous dissolution regimes. The results are used to validate the power law empirical model relating the reactive surface area to porosity proposed by Luquot and Gouze (2009). Second, we investigate the spatial distribution of the effective hydraulic radius and of the tortuosity, two structural parameters that control permeability, in order to explain the different porosity–permeability relationships observed for heterogeneous and homogeneous dissolution regimes. It is shown that the increase of permeability is due to the decrease of the tortuosity for homogeneous dissolution, whereas it is due to the combination of tortuosity decrease and hydraulic radius increase for heterogeneous dissolution. For the intermediate dissolution regime, identified to be the optimal regime for increasing permeability with small changes in porosity, the increase of permeability results from a large increase in the mean effective hydraulic radius of the sample.</description><identifier>ISSN: 0169-7722</identifier><identifier>EISSN: 1873-6009</identifier><identifier>DOI: 10.1016/j.jconhyd.2010.07.004</identifier><identifier>PMID: 20797806</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Carbon Dioxide - analysis ; Carbon storage ; Computational fluid dynamics ; Dissolution ; Earth Sciences ; Environmental Monitoring ; Environmental Pollutants - analysis ; Environmental Sciences ; Fluid flow ; Geophysics ; Global Changes ; Hydraulics ; Mathematical models ; Models, Theoretical ; Permeability ; Physics ; Porosity ; Reactive transport ; Salts - analysis ; Sciences of the Universe ; Soil Pollutants - analysis ; Tortuosity ; Water Movements ; Water Pollutants - analysis ; X-Ray Microtomography</subject><ispartof>Journal of contaminant hydrology, 2011-03, Vol.120, p.45-55</ispartof><rights>2010 Elsevier B.V.</rights><rights>Copyright © 2010 Elsevier B.V. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a477t-b0b3e71e8beec1ccac2234d595d41f36acc4d188e0374b322dfebc5373f1a6323</citedby><cites>FETCH-LOGICAL-a477t-b0b3e71e8beec1ccac2234d595d41f36acc4d188e0374b322dfebc5373f1a6323</cites><orcidid>0000-0002-4389-3019</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jconhyd.2010.07.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,315,781,785,886,3551,27926,27927,45997</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20797806$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00617671$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Gouze, Philippe</creatorcontrib><creatorcontrib>Luquot, Linda</creatorcontrib><title>X-ray microtomography characterization of porosity, permeability and reactive surface changes during dissolution</title><title>Journal of contaminant hydrology</title><addtitle>J Contam Hydrol</addtitle><description>Numerical programs for simulating flow and reactive transport in porous media are essential tools for predicting reservoir properties changes triggered by CO 2 underground injection. At reservoir scale, meshed models in which equations are solved assuming that constant macroscopic properties can be defined in each cells, are widely used. However, the parameterization of the dissolution–precipitation problem and of the feedback effects of these processes on the flow field is still challenging. The problem arises from the mismatch between the scales at which averaged parameters are defined in the meshed model and the scale at which chemical reactions occur and modify the pore network geometry. In this paper we investigate the links between the dissolution mechanisms that control the porosity changes and the related changes of the reactive surface area and of the permeability. First, the reactive surface area is computed from X-ray microtomography data obtained before and after a set of dissolution experiments of pure calcite rock samples using distinctly different brine–CO 2 mixtures characterizing homogeneous to heterogeneous dissolution regimes. The results are used to validate the power law empirical model relating the reactive surface area to porosity proposed by Luquot and Gouze (2009). Second, we investigate the spatial distribution of the effective hydraulic radius and of the tortuosity, two structural parameters that control permeability, in order to explain the different porosity–permeability relationships observed for heterogeneous and homogeneous dissolution regimes. It is shown that the increase of permeability is due to the decrease of the tortuosity for homogeneous dissolution, whereas it is due to the combination of tortuosity decrease and hydraulic radius increase for heterogeneous dissolution. For the intermediate dissolution regime, identified to be the optimal regime for increasing permeability with small changes in porosity, the increase of permeability results from a large increase in the mean effective hydraulic radius of the sample.</description><subject>Carbon Dioxide - analysis</subject><subject>Carbon storage</subject><subject>Computational fluid dynamics</subject><subject>Dissolution</subject><subject>Earth Sciences</subject><subject>Environmental Monitoring</subject><subject>Environmental Pollutants - analysis</subject><subject>Environmental Sciences</subject><subject>Fluid flow</subject><subject>Geophysics</subject><subject>Global Changes</subject><subject>Hydraulics</subject><subject>Mathematical models</subject><subject>Models, Theoretical</subject><subject>Permeability</subject><subject>Physics</subject><subject>Porosity</subject><subject>Reactive transport</subject><subject>Salts - analysis</subject><subject>Sciences of the Universe</subject><subject>Soil Pollutants - analysis</subject><subject>Tortuosity</subject><subject>Water Movements</subject><subject>Water Pollutants - analysis</subject><subject>X-Ray Microtomography</subject><issn>0169-7722</issn><issn>1873-6009</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkdGL1DAQxoMo3nr6J6h5E8Guk6TbtE_HcagnLPigB76FNJnuZmmbmrQL9a83peu93lMmw2---ZiPkLcMtgxY8fm0PRnfH2e75ZB6ILcA-TOyYaUUWQFQPSebxFWZlJxfkVcxngBAllC-JFccZJXKYkOG31nQM-2cCX70nT8EPRxnao46aDNicH_16HxPfUMHH3x04_yJDhg61LVr04_q3tKACXZnpHEKjTa4zPcHjNROwfUHal2Mvp0WpdfkRaPbiG8u7zV5-Prl1919tv_x7fvd7T7TuZRjVkMtUDIsa0TDjNGGc5HbXbWzOWtEoY3JLStLBCHzWnBuG6zNTkjRMF0ILq7Jx1X3qFs1BNfpMCuvnbq_3aulB1AwWUh2Zon9sLJD8H8mjKPqXDTYtrpHP0VVFmlLCVI8TeY7UQmQi-ZuJdNhYwzYPJpgoJYE1UldElRLggpkspSnuXeXDVPdoX2c-h9ZAt6vQKO90ofgonr4mRQEsIqXkEMiblYC033PDoOKxmFv0LqAZlTWuydM_APRnrqq</recordid><startdate>20110301</startdate><enddate>20110301</enddate><creator>Gouze, Philippe</creator><creator>Luquot, Linda</creator><general>Elsevier B.V</general><general>[Amsterdam]: Elsevier Science B.V</general><general>Elsevier</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>KR7</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-4389-3019</orcidid></search><sort><creationdate>20110301</creationdate><title>X-ray microtomography characterization of porosity, permeability and reactive surface changes during dissolution</title><author>Gouze, Philippe ; Luquot, Linda</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a477t-b0b3e71e8beec1ccac2234d595d41f36acc4d188e0374b322dfebc5373f1a6323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Carbon Dioxide - analysis</topic><topic>Carbon storage</topic><topic>Computational fluid dynamics</topic><topic>Dissolution</topic><topic>Earth Sciences</topic><topic>Environmental Monitoring</topic><topic>Environmental Pollutants - analysis</topic><topic>Environmental Sciences</topic><topic>Fluid flow</topic><topic>Geophysics</topic><topic>Global Changes</topic><topic>Hydraulics</topic><topic>Mathematical models</topic><topic>Models, Theoretical</topic><topic>Permeability</topic><topic>Physics</topic><topic>Porosity</topic><topic>Reactive transport</topic><topic>Salts - analysis</topic><topic>Sciences of the Universe</topic><topic>Soil Pollutants - analysis</topic><topic>Tortuosity</topic><topic>Water Movements</topic><topic>Water Pollutants - analysis</topic><topic>X-Ray Microtomography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gouze, Philippe</creatorcontrib><creatorcontrib>Luquot, Linda</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Civil Engineering Abstracts</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of contaminant hydrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gouze, Philippe</au><au>Luquot, Linda</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>X-ray microtomography characterization of porosity, permeability and reactive surface changes during dissolution</atitle><jtitle>Journal of contaminant hydrology</jtitle><addtitle>J Contam Hydrol</addtitle><date>2011-03-01</date><risdate>2011</risdate><volume>120</volume><spage>45</spage><epage>55</epage><pages>45-55</pages><issn>0169-7722</issn><eissn>1873-6009</eissn><abstract>Numerical programs for simulating flow and reactive transport in porous media are essential tools for predicting reservoir properties changes triggered by CO 2 underground injection. At reservoir scale, meshed models in which equations are solved assuming that constant macroscopic properties can be defined in each cells, are widely used. However, the parameterization of the dissolution–precipitation problem and of the feedback effects of these processes on the flow field is still challenging. The problem arises from the mismatch between the scales at which averaged parameters are defined in the meshed model and the scale at which chemical reactions occur and modify the pore network geometry. In this paper we investigate the links between the dissolution mechanisms that control the porosity changes and the related changes of the reactive surface area and of the permeability. First, the reactive surface area is computed from X-ray microtomography data obtained before and after a set of dissolution experiments of pure calcite rock samples using distinctly different brine–CO 2 mixtures characterizing homogeneous to heterogeneous dissolution regimes. The results are used to validate the power law empirical model relating the reactive surface area to porosity proposed by Luquot and Gouze (2009). Second, we investigate the spatial distribution of the effective hydraulic radius and of the tortuosity, two structural parameters that control permeability, in order to explain the different porosity–permeability relationships observed for heterogeneous and homogeneous dissolution regimes. It is shown that the increase of permeability is due to the decrease of the tortuosity for homogeneous dissolution, whereas it is due to the combination of tortuosity decrease and hydraulic radius increase for heterogeneous dissolution. For the intermediate dissolution regime, identified to be the optimal regime for increasing permeability with small changes in porosity, the increase of permeability results from a large increase in the mean effective hydraulic radius of the sample.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>20797806</pmid><doi>10.1016/j.jconhyd.2010.07.004</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-4389-3019</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0169-7722
ispartof Journal of contaminant hydrology, 2011-03, Vol.120, p.45-55
issn 0169-7722
1873-6009
language eng
recordid cdi_hal_primary_oai_HAL_hal_00617671v1
source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Carbon Dioxide - analysis
Carbon storage
Computational fluid dynamics
Dissolution
Earth Sciences
Environmental Monitoring
Environmental Pollutants - analysis
Environmental Sciences
Fluid flow
Geophysics
Global Changes
Hydraulics
Mathematical models
Models, Theoretical
Permeability
Physics
Porosity
Reactive transport
Salts - analysis
Sciences of the Universe
Soil Pollutants - analysis
Tortuosity
Water Movements
Water Pollutants - analysis
X-Ray Microtomography
title X-ray microtomography characterization of porosity, permeability and reactive surface changes during dissolution
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-17T23%3A39%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=X-ray%20microtomography%20characterization%20of%20porosity,%20permeability%20and%20reactive%20surface%20changes%20during%20dissolution&rft.jtitle=Journal%20of%20contaminant%20hydrology&rft.au=Gouze,%20Philippe&rft.date=2011-03-01&rft.volume=120&rft.spage=45&rft.epage=55&rft.pages=45-55&rft.issn=0169-7722&rft.eissn=1873-6009&rft_id=info:doi/10.1016/j.jconhyd.2010.07.004&rft_dat=%3Cproquest_hal_p%3E845393071%3C/proquest_hal_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=845393071&rft_id=info:pmid/20797806&rft_els_id=S0169772210000835&rfr_iscdi=true