Please use this identifier to cite or link to this item: http://hdl.handle.net/10174/39413

Title: Preliminary assessment of CO2 storage potential of deep saline aquifers in the Lusitanian Basin, (Portugal): mineralogical andchemical constrains
Authors: Pedro, Jorge
Moita, Patricia
Ribeiro, Carlos
Kilpatrick, Andrew
Edlmann, Katriona
Wilkinson, Mark
Afonso, Paula
Barradas, João
Carneiro, Júlio
Issue Date: 2025
Publisher: EGU General Assembly 2025
Citation: Pedro et al, 2025. Preliminary assessment of CO2 storage potential of deep saline aquifers in the Lusitanian Basin, (Portugal): mineralogical andchemical constrains. EGU General Assembly 2025
Abstract: The reduction of atmospheric CO2 through its safe geological storage, as CCUS techniques is one of the goals to achieve the 2050 commitment. Within the scope of thePILOTSTRATEGY project, two sedimentary sequences Triassic (on-shore) and Cretaceous (off shore) were object of a detailed study in order to evaluate their potential as CO2storage complexes in the Lusitanian basin (west Portuguese margin). A multi-disciplinary, multi-analytical approach was applied to the potential reservoirs and caprock samples to their characterization. The obtained results (XRD, TGA,petrography) refl ect the predominance of siliciclastic composition of the reservoirs (mainly quartz and K-feldspar) whereas the caprock exhibit a carbonate (mainly calcite)(Cretaceous) or gypsum (Triassic) composition. Several batch reaction experiments were carried out at Edinburgh University (UEDIN). Samples from the Cretaceous storage complex reacted with a NaCl brine injected withCO2 at controlled P=100bar, T=40°C conditions for 30days during which the chemical composition of the brine was regularly analysed. The elemental variations of thebrine reacting with the reservoir samples refl ect the dissolution of the present mineralogical phases, namely the K-feldspar, pyrite and clay minerals, and in some cases theprecipitation of new phases, such as opaline silica. The composition of the brine reacting with the caprock, registered an increase in Ca content at the fi rst 2 days, interpreted as being the result of the limestone dissolution,without further variation throughout the experiment with a constant pH (6.36-6.57). The identifi cation of newly formed phases and evidence of dissolution as future and ongoing work are fundamental in understanding the entire process and predictability ofthe reservoir and sealant.
URI: http://hdl.handle.net/10174/39413
Type: lecture
Appears in Collections:ICT - Comunicações - Em Congressos Científicos Internacionais

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