Mobility and retention mechanisms of 238U, 230Th, 226Ra, and 210Pb in soils from the waste dump of an abandoned Cu mine
Year: 2025
Type: article
Abstract: The interactions of uranium-series radionuclides with soils allow for the assessment of their mobility and retention in the environment. However, waste dumps from abandoned mines, such as the one studied in this work, present complex conditions due to the presence of high concentrations of heavy metals. The studied waste dump contains high concentrations of Fe, Cu, and As, mainly due to the presence of chalcopyrite (CuFeS 2 ), arsenopyrite (FeAsS), malachite (Cu 2 CO 3 (OH) 2 ), azurite (Cu 3 (CO 3 ) 2 (OH) 2 ), and pyrite (FeS 2 ), together with the presence of torbernite (Cu 2 (UO 2 ) 2 (PO 4 ) 2 ·8H 2 O) and zeunerite (Cu 2 (UO 2 ) 2 (AsO 4 ) 2 ·10H 2 O) of hydrothermal geological origin. Samples were collected from three profiles in three zones selected according to the radioactive content of the study area. The correlations obtained between Fe and organic matter, both in the principal component analysis and in the parameter weights of the multiple regression analysis, revealed that the main retention mechanism was the formation of inner-sphere complexes. On the other hand, the sequential analysis of 235 U, 234 Th, 226 Ra, and 210 Pb using the Schultz method allowed for the evaluation of the evolution of the site, as the associations of these radionuclides evolved towards a significant increase in the carbonate fraction. • Inner-sphere complexes with organic matter and Fe/Mn oxides drive U-series retention. • Waste-dump (MTA-1) soils show elevated OM, Fe, Cu, and S from ore accumulation. • Radionuclide activity peaks vary by profile and depth, correlating with OM content. • PCA and regression confirm OM and Fe as main factors in U-series immobilization.
Source: Journal of Hazardous Materials
Language: English
Subfield: Radiological and Ultrasound Technology
Field: Health Professions
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $4,340
Award: G611649908
OpenAlex ID: W4416730478
