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Distribution, characterization, and geochemical controls of elements of concern in uranium mine tailings, Key Lake, Saskatchewan, Canada
Authors:Sean A Shaw  M Jim Hendry  Joseph Essilfie-Dughan  Tom Kotzer  Dirk Wallschläger
Institution:aDepartment of Geological Sciences, University of Saskatchewan, Saskatoon, Saskatchewan, Canada S7N 5E2;bCameco Corporation, Saskatoon, Saskatchewan, Canada S7M 1J3;cEnvironmental & Resource Sciences Program and Department of Chemistry, Trent University, Peterborough, Ontario, Canada K9J 7B8
Abstract:The distribution of As, Mo, Ni and Se in the aqueous and solid phases of U mine tailings in the Deilmann Tailings Management Facility (DTMF), located at the Key Lake mine in northern Saskatchewan, Canada, was defined using as-discharged tailings samples collected monthly starting in 1996 and core samples collected from the DTMF from 3 locations on 3 occasions between 2004 and 2009. These data indicated that the DTMF can be divided into two geochemical zones; tailings generated from the Deilmann ore body between 1996 and 2000 and tailings from the McArthur River ore body, mined after July 2000. The Deilmann tailings solids are generally characterized by greater elemental concentrations than those in the McArthur River tailings, particularly for As, Co and Ni. These elevated concentrations are attributed to the abundance of Ni–Co–As–S minerals in this ore. The mean aqueous concentrations of As, Mo, Ni, and Se are 3.7, 23.2, 0.14, and 0.02 mg L−1, respectively, in the Deilmann porewaters and 0.20, 4.16, 0.06, and 0.03 mg L−1, respectively, in the McArthur River porewaters. Similarly, the mean As, Mo, Ni, and Se solid phase concentrations are 5.89 × 103, 69.9, 3.20 × 103, and 17.4 μg g−1, respectively, for the Deilmann tailings and 440, 13.6, 551, and 3.03 μg g−1 in the McArthur River tailings. Statistically, pH remained unchanged from the time of discharge while Eh values have remained oxic with no significant change between the two tailings types over 15 a of residence time. Results from sequential extractions, thermodynamic modeling, and results of complimentary research indicated that ferrihydrite solubility is the dominant control on aqueous As concentrations and also plays a role in controlling dissolved Mo, Ni and Se.
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