Hydrogen wettability and capillary pressure in Clashach sandstone for underground hydrogen storage

Hydrogen (H2) can support the transition to net-zero carbon (C) emissions by facilitating increased renewable energy use by acting as an energy store to balance supply and demand. Underground H2 storage in porous media is investigated due to its high capacity and economical price. An important unknown in underground porous media H2 storage is the volume of recoverable H2 which is partly controlled by the H2 wettability. Current H2 contact angle data in sandstone systems span large ranges and fall short of clarifying if H2 wettability changes with pressure. We computed novel in-situ receding and advancing contact angles for the H2-brine-Clashach sandstone system at pore fluid pressures of 2–7 MPa and for nitrogen (N2)-brine-Clashach sandstone at 5 MPa, based on X-ray microtomography images of gas displacement and trapping in Clashach sandstone. A centrifuge analysis of the capillary pressure (Pc) at varying water saturations was conducted for N2. The H2 Pc curve was derived from the N2 Pc, the N2 wettability measurements, and existing information on the density differential between brine and H2 and N2, and the interfacial tensions of these gases. The results show no change of the H2-brine-Clashach sandstone contact angles within the examined pressure range, with mean receding (drainage) and advancing (imbibition) contact angles of 61° ± 24–26° and 58° ± 20–22°, respectively, at all pore fluid pressures, indicating a water-wet rock and implying that based on the wettability alone, no decrease in H2 recovery with increasing pressure (i.e. reservoir depth) is expected. While residual trapping was consistent with trapping in water-wet systems, the observed increase in residual trapping at 7 MPa requires further investigation. Alignment with other wettability studies in sandstone systems indicates that for contact angles around 60–70°, wettability may not always be the main control for the H2 saturation in the pore space but that H2 dissolution and channeling events may significantly affect those parameters. Further, contact angle measurements in artificial systems significantly underestimate in-situ contact angles as provided by this study, highlighting the need for microtomography-based wettability investigations. We found relatively low irreducible water saturations of 12.6–14.0 % at H2 Pc of 0.43 MPa, suggesting a favorable H2 relative permeability in Clashach and high H2 storage capacity. Our results provide detailed insights into the controls on H2 displacement and capillary trapping as well as crucial input parameters for the modelling and design of H2 storage operations in porous media.

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Bibliographic Details
Main Authors: Thaysen, Eike M., Jangda, Zaid, Hassanpouryouzband, Aliakbar, Menke, Hannah, Singh, Kamaljit, Butler, Ian B., Heinemann, Niklas, Edlmann, Katriona
Other Authors: European Commission
Format: artículo biblioteca
Language:English
Published: Elsevier 2024-09-10
Subjects:μCT, Capillary pressure, Flow experiments, Hydrogen, Nitrogen, Underground storage, Wetting state, Ensure access to affordable, reliable, sustainable and modern energy for all,
Online Access:http://hdl.handle.net/10261/364339
http://dx.doi.org/10.13039/501100000780
https://api.elsevier.com/content/abstract/scopus_id/85198522004
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id dig-idaea-es-10261-364339
record_format koha
institution IDAEA ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-idaea-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del IDAEA España
language English
topic μCT
Capillary pressure
Flow experiments
Hydrogen
Nitrogen
Underground storage
Wetting state
Ensure access to affordable, reliable, sustainable and modern energy for all
μCT
Capillary pressure
Flow experiments
Hydrogen
Nitrogen
Underground storage
Wetting state
Ensure access to affordable, reliable, sustainable and modern energy for all
spellingShingle μCT
Capillary pressure
Flow experiments
Hydrogen
Nitrogen
Underground storage
Wetting state
Ensure access to affordable, reliable, sustainable and modern energy for all
μCT
Capillary pressure
Flow experiments
Hydrogen
Nitrogen
Underground storage
Wetting state
Ensure access to affordable, reliable, sustainable and modern energy for all
Thaysen, Eike M.
Jangda, Zaid
Hassanpouryouzband, Aliakbar
Menke, Hannah
Singh, Kamaljit
Butler, Ian B.
Heinemann, Niklas
Edlmann, Katriona
Hydrogen wettability and capillary pressure in Clashach sandstone for underground hydrogen storage
description Hydrogen (H2) can support the transition to net-zero carbon (C) emissions by facilitating increased renewable energy use by acting as an energy store to balance supply and demand. Underground H2 storage in porous media is investigated due to its high capacity and economical price. An important unknown in underground porous media H2 storage is the volume of recoverable H2 which is partly controlled by the H2 wettability. Current H2 contact angle data in sandstone systems span large ranges and fall short of clarifying if H2 wettability changes with pressure. We computed novel in-situ receding and advancing contact angles for the H2-brine-Clashach sandstone system at pore fluid pressures of 2–7 MPa and for nitrogen (N2)-brine-Clashach sandstone at 5 MPa, based on X-ray microtomography images of gas displacement and trapping in Clashach sandstone. A centrifuge analysis of the capillary pressure (Pc) at varying water saturations was conducted for N2. The H2 Pc curve was derived from the N2 Pc, the N2 wettability measurements, and existing information on the density differential between brine and H2 and N2, and the interfacial tensions of these gases. The results show no change of the H2-brine-Clashach sandstone contact angles within the examined pressure range, with mean receding (drainage) and advancing (imbibition) contact angles of 61° ± 24–26° and 58° ± 20–22°, respectively, at all pore fluid pressures, indicating a water-wet rock and implying that based on the wettability alone, no decrease in H2 recovery with increasing pressure (i.e. reservoir depth) is expected. While residual trapping was consistent with trapping in water-wet systems, the observed increase in residual trapping at 7 MPa requires further investigation. Alignment with other wettability studies in sandstone systems indicates that for contact angles around 60–70°, wettability may not always be the main control for the H2 saturation in the pore space but that H2 dissolution and channeling events may significantly affect those parameters. Further, contact angle measurements in artificial systems significantly underestimate in-situ contact angles as provided by this study, highlighting the need for microtomography-based wettability investigations. We found relatively low irreducible water saturations of 12.6–14.0 % at H2 Pc of 0.43 MPa, suggesting a favorable H2 relative permeability in Clashach and high H2 storage capacity. Our results provide detailed insights into the controls on H2 displacement and capillary trapping as well as crucial input parameters for the modelling and design of H2 storage operations in porous media.
author2 European Commission
author_facet European Commission
Thaysen, Eike M.
Jangda, Zaid
Hassanpouryouzband, Aliakbar
Menke, Hannah
Singh, Kamaljit
Butler, Ian B.
Heinemann, Niklas
Edlmann, Katriona
format artículo
topic_facet μCT
Capillary pressure
Flow experiments
Hydrogen
Nitrogen
Underground storage
Wetting state
Ensure access to affordable, reliable, sustainable and modern energy for all
author Thaysen, Eike M.
Jangda, Zaid
Hassanpouryouzband, Aliakbar
Menke, Hannah
Singh, Kamaljit
Butler, Ian B.
Heinemann, Niklas
Edlmann, Katriona
author_sort Thaysen, Eike M.
title Hydrogen wettability and capillary pressure in Clashach sandstone for underground hydrogen storage
title_short Hydrogen wettability and capillary pressure in Clashach sandstone for underground hydrogen storage
title_full Hydrogen wettability and capillary pressure in Clashach sandstone for underground hydrogen storage
title_fullStr Hydrogen wettability and capillary pressure in Clashach sandstone for underground hydrogen storage
title_full_unstemmed Hydrogen wettability and capillary pressure in Clashach sandstone for underground hydrogen storage
title_sort hydrogen wettability and capillary pressure in clashach sandstone for underground hydrogen storage
publisher Elsevier
publishDate 2024-09-10
url http://hdl.handle.net/10261/364339
http://dx.doi.org/10.13039/501100000780
https://api.elsevier.com/content/abstract/scopus_id/85198522004
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spelling dig-idaea-es-10261-3643392024-10-27T21:53:14Z Hydrogen wettability and capillary pressure in Clashach sandstone for underground hydrogen storage Thaysen, Eike M. Jangda, Zaid Hassanpouryouzband, Aliakbar Menke, Hannah Singh, Kamaljit Butler, Ian B. Heinemann, Niklas Edlmann, Katriona European Commission Consejo Superior de Investigaciones Científicas [https://ror.org/02gfc7t72] μCT Capillary pressure Flow experiments Hydrogen Nitrogen Underground storage Wetting state Ensure access to affordable, reliable, sustainable and modern energy for all Hydrogen (H2) can support the transition to net-zero carbon (C) emissions by facilitating increased renewable energy use by acting as an energy store to balance supply and demand. Underground H2 storage in porous media is investigated due to its high capacity and economical price. An important unknown in underground porous media H2 storage is the volume of recoverable H2 which is partly controlled by the H2 wettability. Current H2 contact angle data in sandstone systems span large ranges and fall short of clarifying if H2 wettability changes with pressure. We computed novel in-situ receding and advancing contact angles for the H2-brine-Clashach sandstone system at pore fluid pressures of 2–7 MPa and for nitrogen (N2)-brine-Clashach sandstone at 5 MPa, based on X-ray microtomography images of gas displacement and trapping in Clashach sandstone. A centrifuge analysis of the capillary pressure (Pc) at varying water saturations was conducted for N2. The H2 Pc curve was derived from the N2 Pc, the N2 wettability measurements, and existing information on the density differential between brine and H2 and N2, and the interfacial tensions of these gases. The results show no change of the H2-brine-Clashach sandstone contact angles within the examined pressure range, with mean receding (drainage) and advancing (imbibition) contact angles of 61° ± 24–26° and 58° ± 20–22°, respectively, at all pore fluid pressures, indicating a water-wet rock and implying that based on the wettability alone, no decrease in H2 recovery with increasing pressure (i.e. reservoir depth) is expected. While residual trapping was consistent with trapping in water-wet systems, the observed increase in residual trapping at 7 MPa requires further investigation. Alignment with other wettability studies in sandstone systems indicates that for contact angles around 60–70°, wettability may not always be the main control for the H2 saturation in the pore space but that H2 dissolution and channeling events may significantly affect those parameters. Further, contact angle measurements in artificial systems significantly underestimate in-situ contact angles as provided by this study, highlighting the need for microtomography-based wettability investigations. We found relatively low irreducible water saturations of 12.6–14.0 % at H2 Pc of 0.43 MPa, suggesting a favorable H2 relative permeability in Clashach and high H2 storage capacity. Our results provide detailed insights into the controls on H2 displacement and capillary trapping as well as crucial input parameters for the modelling and design of H2 storage operations in porous media. Thaysen, Butler, Heinemann, Hassanpouryouzband and Edlmann gratefully acknowledge the funding support from the Engineering and Physical Science Research Council (EPSRC) HyStorPor project [grant number EP/S027815/1] and from the Fuel Cells and Hydrogen 2 Joint Undertaking (JU) under grant agreement No 101006632. The JU receives support from the European Union's Horizon 2020 research and innovation program and Hydrogen Europe and Hydrogen Europe Research. Peer reviewed 2024-07-24T06:23:02Z 2024-07-24T06:23:02Z 2024-09-10 artículo http://purl.org/coar/resource_type/c_6501 Journal of Energy Storage 97, Part B, 112916 (2024) http://hdl.handle.net/10261/364339 10.1016/j.est.2024.112916 http://dx.doi.org/10.13039/501100000780 2-s2.0-85198522004 https://api.elsevier.com/content/abstract/scopus_id/85198522004 en #PLACEHOLDER_PARENT_METADATA_VALUE# info:eu-repo/grantAgreement/EC/H2020/101006632 Journal of Energy Storage Publisher's version https://doi.org/10.1016/j.est.2024.112916 Sí open Elsevier