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This study presents an experimental investigation on Zr separation from Zr-2.5Nb by anode potentiostatic electrorefining in LiCl-KCl-ZrCl4 0.5 wt. % at 773 K for irradiated CANDU pressure tube decontamination. By the ORIGEN-2 code calculation, radioactive characteristics were investigated to show that Nb-94 was the most significant radionuclide with an aspect of waste level reduction by electrorefining. Three electrorefining tests were performed by fixing the applied potential as −0.9 V (vs. Ag/AgCl 1 wt. %) at the anode to dissolve only Zr. A cathode basket was installed to collect detached deposits from the cathode. Electrorefining results showed Zr was deposited on the cathode with a small amount of Nb and other alloying elements. The chemical form of the cathode deposits was shown to be only Zr metal or a mixture of Zr metal and ZrCl, depending on the experimental conditions related to the surface area ratio of the cathode to the anode. It was determined that the Zr metal reduction at the cathode was attributed to the two-step reduction reaction of Zr4+/ZrCl and ZrCl/Zr.

The corrosion of nuclear-grade steels in lead–bismuth eutectic (LBE) complicates the realization of high coolant temperatures. Corrosion tests of T91, HT9, and SS316L were performed in static cells at 600 °C for 2000 h at an oxygen level of 10−6 wt.%. The obtained corrosion surfaces of post-processed samples were characterized by several microscopy methods. Up to 1000 h, all the alloys exhibited an evolution of duplex oxide layers, which were spalled until 2000 h due to their increased thickness and decreased integrity. Following the spallation, a thin internal Cr-rich oxide layer was formed above the Cr-depleted zone for T91 and HT9. SS316L was penetrated by LBE down to 300 μm in severe cases. A comparison on the corrosion depths of the materials with regard to the parabolic oxidation law with abundant literature data suggests that it may lose its validity once the duplex layer is destroyed as it allows LBE to penetrate the metal substrate.