The potential 14C (carbon-14, radiocarbon) flux from disposal of 14C containing waste into air is compared with the natural 14C emanation rate from soil in order to put the 14C hazard potential from disposal of this waste in perspective with the 14C exposure from cosmogenic origin. Chemical corrosion of neutron irradiated metals, steel and Zircaloy, is bounded by diffusion of water through a thermodynamically stable metal-oxide layer and dissolution of this metal-oxide in a nuclear plant. Many countries process radioactive waste for disposal using cementitious materials, an acknowledged end-point management technique for this waste. The metal-oxides are also stable when these waste forms are embedded in cementitious materials. The 14C release rate from this Zircaloy at these alkaline and reducing conditions is comparable to the natural 14C emanation rate from soil into air. Neutron irradiated graphite and spent ion exchange resins are chemically inert and therefore other release mechanisms need to be assumed. Radiolytic corrosion is used to determine the 14C release rate from this graphite. Moreover, ion exchange—with ingressing anionic species that have a higher affinity than contained anionic 14C—is proposed as a release mechanism for these resins.

The gas release and speciation of carbon species from irradiated and unirradiated Zircaloy-4 samples, representative for the fuel cladding as used in Belgian nuclear power plants, were studied in a saturated Ca(OH)2 solution in anaerobic conditions. This environment is relevant for the Belgian Supercontainer design, as perceived for the geological disposal of high-level nuclear waste. To achieve this, we performed simple immersion and potentiostatic corrosion tests. Potentiodynamic polarization curves, recorded prior to the potentiostatic tests, revealed that irradiation seems to induce changes on the Zircaloy-4 corrosion behavior, such as a shift of the corrosion potential. Potentiostatic corrosion tests on unirradiated Zircaloy-4 provided a corrosion rate of ~54 nm/yr over a 7 day-experiment, whilst a corrosion rate of only ~4 nm/yr was calculated for the irradiated sample. Gas chromatography revealed that during simple immersion tests, which lasted 195 days, hydrogen, methane, ethane, and CO2 were produced, with methane being the major compound. Assuming that all carbon released from the metal was transformed into gaseous compounds, this yields to a corrosion rate ranging from 57 to 84 nm/yr for the irradiated sample. However, caution has to be taken on these corrosion rate and more tests should be performed to confirm these results.