posted on 2015-05-19, 00:00authored byAnirban Basu, Shaun
T. Brown, John N. Christensen, Donald J. DePaolo, Paul W. Reimus, Jeffrey
M. Heikoop, Giday Woldegabriel, Ardyth M. Simmons, Brian M. House, Matt Hartmann, Kate Maher
In
situ recovery (ISR) uranium (U) mining mobilizes U in its oxidized
hexavalent form (U(VI)) by oxidative dissolution of U from the roll-front
U deposits. Postmining natural attenuation of residual U(VI) at ISR
mines is a potential remediation strategy. Detection and monitoring
of naturally occurring reducing subsurface environments are important
for successful implementation of this remediation scheme. We used
the isotopic tracers 238U/235U (δ238U), 234U/238U activity ratio, and 34S/32S (δ34S), and geochemical
measurements of U ore and groundwater collected from 32 wells located
within, upgradient, and downgradient of a roll-front U deposit to
detect U(VI) reduction and U mobility at an ISR mining site at Rosita,
TX, USA. The δ238U in Rosita groundwater varies from
+0.61‰ to −2.49‰, with a trend toward lower δ238U in downgradient wells. The concurrent decrease in U(VI)
concentration and δ238U with an ε of 0.48‰
± 0.08‰ is indicative of naturally occurring reducing
environments conducive to U(VI) reduction. Additionally, characteristic 234U/238U activity ratio and δ34S values may also be used to trace the mobility of the ore zone groundwater
after mining has ended. These results support the use of U isotope-based
detection of natural attenuation of U(VI) at Rosita and other similar
ISR mining sites.