Geochemical modelling of the weathering zone of the “Mina Fe” U deposit (Spain): A natural analogue for nuclear spent fuel alteration and stability processes in radwaste disposal

• Published in: Applied geochemistry 2008-04, Vol.23 (4), p.807-821
• Main Authors: Arcos, D., del Villar, L. Pérez, Bruno, J., Domènech, C.
• Format: Article
• Language: English
• Subjects: Earth sciences; Earth, ocean, space; Engineering and environment geology. Geothermics; Exact sciences and technology; Geochemistry; Pollution, environment geology
• ISSN: 0883-2927; 1872-9134
• DOI: 10.1016/j.apgeochem.2007.07.010

The “Mina Fe” U deposit (Salamanca, Spain) has been studied in the context of Enresa’s programme for U-mine sites restoration and also as a natural analogue for processes in high-level nuclear waste (HLNW) geological disposal. The investigations encompassed an array of geoscience disciplines, such as structural geology, mineralogy, hydrogeology and elemental and isotopic geochemistry and hydrogeochemistry of the site. Based on the obtained results, a conceptual mineralogical and geochemical model was performed integrating the main geochemical processes occurring at the site: the interaction between oxidised and slightly acidic water with pyrite, pitchblende, calcite and dolomite, as essential minerals of the U fracture-filling mineralisation, and hydroxyapatite from the host rock, as the main source of P. This conceptual model has been tested in a systematic numerical model, which includes the main kinetic (pyrite and pitchblende dissolution) and equilibrium processes (carbonate mineral dissolution, and goethite, schoepite and autunite secondary precipitation). The results obtained from the reactive-transport model satisfactorily agree with the conceptual model previously established. The assumption of the precipitation of coffinite as a secondary mineral in the system cannot be correctly evaluated due to the lack of hydrochemical data from the reducing zone of the site and valid thermodynamic and kinetic data for this hydrated U(IV)-silicate. This precipitation can also be hampered by the probable existence of dissolved U(IV)-organic matter and/or uranyl carbonate complexes, which are thermodynamically stable under the alkaline and reducing conditions that prevail in the reducing zone of the system. Finally, the intense downwards oxic and acidic alteration in the upper part of the system is of no relevance for the performance assessment of a HLNW disposal. However, the acidic and oxidised conditions are quickly buffered to neutral–alkaline and reducing at very shallow depths, of relevance for the performance assessment of a HLNW repository, even in a natural or artificially perturbed geological environment as “Mina Fe”.