The dual effect of Mg on the long-term alteration rate of AVM nuclear waste glasses

Inactive Mg-containing nuclear waste glasses simulating actual HLW glasses produced at the AVM facility since 1995 (Marcoule, France), were leached in aqueous solution in order to assess their long term behaviour. The focus was on the effect of Mg. Our findings show that the distribution of Mg between the gel and the secondary crystalline phases strongly influences the glass dissolution rate. asses were leached in initially pure water (T = 50 °C, surface/volume ratio (S/V) = 55 cm−1) with and without addition of Mg2+ in the solution. “Mg-free” AVM glasses were also leached in initially pure water (50 °C, 200 cm−1) with and without addition of Mg2+ in the solution. Accurate identification of Mg-smectite secondary phases and gel composition calculations enable us to explain the different observed behaviours. AVM 10 was the less altered glass in pure water. Its gel is more protective than the other probably because it is mainly balanced by Mg2+. The addition of Mg2+ in the solution triggers the precipitation of smectite (not observed in pure water experiments), which consumes silicon from the gel, leading finally to a significant increase of the glass alteration. o focused on the AVM 6 glass which was the most altered glass in pure water of available AVM glasses. Contrary to AVM 10, the gel of AVM 6 is mainly balanced by Na+. The addition of Mg2+ in the solution allows the replacement of Na by Mg within the gel. This reaction clearly improves the gel properties and allows the rate to decrease more rapidly, in spite of the precipitation of smectite (also observed in pure water experiments). y, the two glasses were altered in synthetic groundwater (SGW) with a high Mg–Ca content. As expected from the previous observations, AVM 10 was insensitive to the presence of alkaline earths in the leaching solution whereas AVM 6 glass exhibited a lower rate than in pure water thanks to the incorporation of Mg and Ca within the gel.