Most nuclear safety agencies around the world agree that deep geological repositories (DGRs) constructed hundreds of meters below ground in stable host rock formations are viable solutions to safely isolate used nuclear fuel. In Canada, the DGR design involves storing used nuclear fuel in sealed copper coated used fuel containers (UFC) surrounded by highly compacted bentonite blocks (HCB) ~500 m underground. Shortly after emplacement, heat generated by radioactive decay of the used fuel will warm the UFC and its surroundings, desiccating the HCB and decreasing moisture on the container surface. As water vapour is driven from the UFC surface, the presence of minor amounts of dissolved salts may cause droplet formation prior to complete evaporation, during which deposits of salts may be left behind on the UFC. Later, as conditions evolve and the relative humidity increases and the temperature decreases, condensation of liquid water on the UFC surfaces will produce droplets again, due to the deliquescence of minor salt deposits. In either the wetting or the drying scenario, secondary spreading and spatial separation of anodic and cathodic reactions and consequent non-uniform corrosion could be possible, due to the droplet geometry.

To investigate this scenario, the quartz crystal microbalance (QCM) technique is being used. The QCM initially consists of a quartz plate, covered by gold electrodes on both sides where a layer of copper is deposited on the crystal by using magnetron sputtering. In this technique, the change in the resonance frequency of a vibrating quartz crystal is correlated to its mass change due to the corrosion process. To investigate the effect of salts and their deliquescence behaviours, different salts (NaCl, CaCl₂, and MgCl₂) and CR10-E simulated groundwater were loaded on the copper surface using an inkjet printer, and then corrosion tests were performed at different temperatures and relative humidity (RH) values. In parallel, a set of long-term vapour-phase corrosion tests was performed on wrought and cold-sprayed copper coupons at 75 °C and different RH values. As part of the post-experiment analysis, the corrosion products were analyzed using a suite of surface analysis techniques, including optical microscopy, Raman spectroscopy, and scanning electron microscopy (SEM).

The results from QCM experiments at RH values below salts deliquescence point showed a low mass change that could correlate with less corrosion in comparison to the experiments at RH values above salts deliquescence point. It’s worth noting that even at RH values below the deliquescence point of the salts, a trace of corrosion was observed which could be indicative of the presence of monolayers of water on the surface. The results obtained from NaCl and CR10-E exposure conditions showed higher mass change and therefore higher corrosion in comparison to CaCl₂ and MgCl₂ salts. As for the long-term vapour-phase corrosion tests, Raman spectroscopy confirmed the presence of CuO and Cu₂O on the surface as corrosion products. Further surface characterizations and mass loss measurements are underway to determine the extent of corrosion on the copper coupons.