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Paper No. 5
Presentation Time: 9:25 AM

APPLICATIONS OF URANIUM ISOTOPES TO URANIUM IN-SITU RECOVERY SITES


PLACZEK, Christa J., Clean Chemistry Team 
Nuclear and Radiochemistry, C-NR, 
Los Alamos National Laboratory, MS-J514, Los Alamos, NM 87545, LINHOFF, Benjamin, Department of Marine Chemistry and Geochemistry, Woods Hole Oceanographic Institution, Mail Stop 25, Woods Hole, MA 02543, HEIKOOP, Jeff, Earth and Environmental Sciences Division, Los Alamos National Lab, Los Alamos, NM 87545 and RICIPUTI, Lee R., Clean Chemistry Team 
Nuclear and Radiochemistry, C-NR, MS-J514, Los Alamos, NM 87545, cplaczek@lanl.gov

Chemical transformations near the earth’s surface cause significant variability in 234U/238U and, only recently measurable, smaller differences in 238U/235U. Variability in both these ratios is observed in U ore concentrates from deposits precipitated by low temperature reduction processes. Such deposits, particularly sandstone “roll fronts”, are commonly mined using in situ recovery (ISR). U isotopes can be useful tools in both understanding the formation of roll fronts and in monitoring remediation efforts during and after ISR.

To explore these potential applications, we present 234U/238U and 238U/235U ratios of water obtained from monitoring wells associated with uranium ore deposits in southwestern Texas. Samples were obtained from: 1) the oxidizing zone located up the hydrologic gradient from the ore body; 2) within the ore zone; and 3) in the reducing zone down the hydrologic gradient from the ore body. Isotopic data is available from both natural and mined ore bodies, and from sites that have been subjected to variable degrees of remediation.

Aqueous weathering of minerals containing U results in preferential leaching of 234U from a-damaged crystal lattice sites; the result is that low 234U/238U is indicative of significant U loss. Conversely, high 234U/238U is indicative of U addition from water. Low 234U/238U characterizes the zone subjected to ISR and likely reflects intense chemical leaching that occurs during the ISR process. This contrasts with higher, but variable ratios in the reducing zone. The differing ratios in these two zones suggest that 234U/238U can be used to trace U subjected to ISR. 234U/238U in the oxidizing zone is variable. Here, 234U/238U is negatively correlated with U concentration, a situation that suggests that sandstone roll front deposits have high and quantifiable natural U mobility.

Variations in 238U/235U have only been recently measured and are generally attributed to reduction and oxidation processes (redox). Data from an unmined roll front deposit strongly support the assertion that this fractionation is linked to redox conditions; 238U/235U is highest in the oxidizing zone and lowest in the reducing zone. Low 238U/235U, indicative of a strongly reducing environment, is present in all wells down-gradient of the ISR sites.

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