The radionuclide technetium is a common surface and groundwater contaminant
at many nuclear fuels processing facilities. This research investigated a
new method for removing pertechnetate from contaminated waters based on the
low aqueous solubility of reduced technetium species. The removal method i
nvolved electrostatic adsorption of pertechnetate at an anodically polarize
d magnetite electrode, followed by reduction of the adsorbed Tc(VII). This
method was capable of reducing technetium associated beta activity below th
e 900 pCi/L drinking water maximum contaminant level set by the US EPA for
manmade beta activity. Upon termination of the applied polarization, the re
duced technetium species remained adhered to the magnetite electrode under
anaerobic conditions. Under aerobic conditions, the technetium was slowly r
eleased back into solution, indicating that the reduced technetium is affor
ded a degree of cathodic protection due to preferential oxidation of the ma
gnetite. The advantages of this electrosorption/reduction technique over di
rect cathodic reduction are an increase in the stability of the reduced tec
hnetium, removal to lower aqueous concentrations, and greatly increased rem
oval kinetics.