INVESTIGATION OF URANIUM SPECIATION AND MINERALOGY ASSOCIATED WITH URANIUM IN-SITU RECOVERY OPERATIONS
Very few examples of geochemical modeling of the groundwater restoration process exist in the open literature. However, the existing models focus on the water quality of the confined aquifer and neglect mineralogy. In this study, the one-dimensional transport functionality of PHREEQC was used to monitor uranium, selenium, and radium speciation and mineralogy across all phases (i.e., baseline, mining, and restoration) of an ISR operation. The model takes into consideration redox, dissolution, precipitation, and sorption reactions; results are compared to published water quality data from the Highland Uranium Project and model limitations are discussed.
Under reducing baseline conditions, the dominant mineralogy includes coffinite, pyrite, hematite, magnetite, and ferroselite. Greater than 99% of the uranium and selenium is present as coffinite and ferroselite, respectively. Conversely, 94% of radium remains in the aqueous phase. As expected under the oxidizing conditions created by the active mining process, uranium oxidizes to U(VI) and a significant fraction precipitates as soddyite. Selenium is oxidized to Se(IV), which remains in the aqueous phase. Restoration of the confined aquifer via groundwater sweep and H2S injection result in the reduction and precipitation of uranium as uraninite; selenium precipitates as native selenium metal. Therefore, within the constructs of this conceptual model, while the groundwater quality of the ISR site post-remediation may resemble baseline water quality, the mineralogy of the system is different.