Perrhenate sorption kinetics in zerovalent iron in high pH and nitrate media

Abstract

Technetium(Tc)-99 is one of major risk drivers in low level radioactive liquid waste at the U.S. Department of Energy sites. Cementitious waste technology (CWT) has been considered immobilizing pertechnetate, Tc(VII)O4−, in brine and alkaline waste solutions, as Tc(IV) oxides and/or sulfides with the use of reducing agents like slag. In this study, zero valent iron (ZVI) was evaluated as a potential reducing agent in CWT as a function of pH and [nitrate] (0–0.1M) using perrhenate, Re(VII)O4−, as an analogue for Tc(VII)O4−. Batch Re(VII)O4− sorption experiments in conjunction with X-ray absorption spectroscopic analysis showed that the Re(VII) sorption occurred via the reductive precipitation of Re(IV)O2(s) and the extent of sorption decreased with increasing pH from 8 to 10. Interestingly, pseudo 2nd order kinetic rates increased with increasing [nitrate] which was attributed to co-adsorption of NH4+ (i.e., a reaction product of reduced nitrate by ZVI), facilitating electrostatic attraction towards ReO4− under alkaline conditions. Considering the thermodynamically favorable reduction of Tc(VII) over Re(VII), ZVI might have potential for improving the reduction capacity of the current CWT.