Mobility of daughter elements of 238U decay chain during leaching by In Situ Recovery (ISR): New insights from digital autoradiography. (September 2020)

• Record Type: Journal Article
• Authors: Angileri, A.; Sardini, P.; Beaufort, D.; Amiard, G.; Beaufort, M.F.; Nicolai, J.; Siitari-Kauppi, M.; Descostes, M.
• Is Part Of: Journal of environmental radioactivity. Volume 220/221(2020)
• Publication Date: 2020-09
• Subjects: Uranium mining -- Autoradiograph -- In-situ leaching -- Radium mobility; Radioactivity -- Periodicals; Radiation, Background -- Periodicals; Radioecology -- Periodicals; Radioactive pollution -- Periodicals; Environmental Pollutants -- Periodicals; Radioactive Pollutants -- Periodicals; Radioactivity -- Periodicals; Radioécologie -- Périodiques; Pollution radioactive -- Périodiques; Fond de rayonnement -- Périodiques; 539.752
• DOI: 10.1016/j.jenvrad.2020.106274
• Languages: English
• ISSNs: 0265-931X

Abstract

Abstract: In highly permeable sedimentary rock formations, U extraction by in-situ leaching techniques (ISR − In-Situ Recovery) is generally considered to have a limited environmental impact at ground level. Significantly, this method of extraction produces neither mill tailings nor waste rocks. Underground, however, the outcome for 238 U daughter elements in aquifers is not well known because of their trace concentrations in the host rocks. Thus, understanding the in-situ mobility of these elements remains a challenge. Two samples collected before and after six months of ISR experiments (Dulaan Uul, Mongolia) were studied with the help of a digital autoradiography technique (DA) of alpha particles, bulk alpha spectrometry, and complementary petrographic observation methods. These techniques demonstrate that before and after leaching, the radioactivity is concentrated in altered and microporous Fe–Ti oxides. Most of the daughter elements of U remain trapped in the rock after the leaching process. DA confirms that the alpha activity of the Fe–Ti oxides remains high after uranium leaching, and the initial secular equilibrium of the 238 U series for 230 Th to 210 Po daughter elements (including 226 Ra) of the fresh rocks is maintained after leaching. While these findings should be confirmed by more systematic studies, they already identify potential mechanisms explaining why the U-daughter concentrations in leaching water are low. Highlights: We evaluate the mobility of 238U daughter elements during In Situ Recovery. Digital Autoradiography is used to locate and quantify rock's alpha emissions. Fe–Ti oxides aggregates control the mobility of 226Ra in permeable sandstones. Radioactivity of 238U series elements remains stable in Fe–Ti aggregates.