Fe-solid phase transformations under highly basic conditions

Hyperalkaline and saline radioactive waste fluids with elevated temperatures from S-SX high-level waste tank farm at Hanford, WA, USA accidentally leaked into sediments beneath the tanks, initiating a series of geochemical processes and reactions whose significance and extent was unknown. Among the most important processes was the dissolution of soil minerals and precipitation of stable secondary phases. The objective of this investigation was to study the release of Fe into the aqueous phase upon dissolution of Fe-bearing soil minerals, and the subsequent formation of Fe-rich precipitates. Batch reactors were used to conduct experiments at 50 degrees C using solutions similar in composition to the waste fluids. Results clearly showed that, similarly to Si and Al, Fe was released from the dissolution of soil minerals (most likely phyllosilicates such as biotite, smectite and chlorite). The extent of Fe release increased with base concentration and decreased with A1 concentration in the contacting solution. The maximum apparent rate of Fe release (0.566 x 10(-13) mol m(-2) s(-1)) was measured in the treatment with no A1 and a concentration of 4.32 mol L-1 NaOH in the contact solution. Results from electron microscopy indicated that while Si and A1 precipitated together to form feldspathoids in the groups of cancrinite and/or socialite, Fe precipitation followed a different pathway leading to the formation of hematite and goethite. The newly formed Fe oxy-hydroxides may increase the sorption capacity of the sediments, promote surface mediated reactions such as precipitation and heterogeneous redox reactions, and affect the phase distribution of contaminants and radionuclides. (C) 2007 Elsevier Ltd. All rights reserved.