Abstract

AbstractKnowledge of the structural organization of nuclear waste glasses at the atomic scale is the basis for further studies of macroscopic properties (e.g., fracture toughness, chemical durability, and leaching rate). Recent studies have focused on the iodine dissolution mechanism in oxide‐based glasses synthesized under high‐pressure conditions, but there is still a lack of key information on the extent of the modifications caused by iodine entering the glass network. We therefore decided to conduct an in‐depth study by nuclear magnetic resonance on two series of aluminoborosilicate glasses synthetized under high pressure conditions and doped with either I2 or I2O5. The obtained 11B, 23Na, and 27Al nuclear magnetic resonance (NMR) spectra were fitted and correlated with the iodine content in order to find possible relationships with the local environment change for the probed cations. These data showed that iodine has no effect on the coordination of aluminum and very little effects on that of boron. In contrast, we found an expected relationship of the I content with the 23Na NMR parameters. In comparison with previous studies on the non‐bridging oxygen (NBO) distribution in aluminoborosilicate, we suggest that Na+ is mainly scavenged from silica tetrahedra with one or two NBO ( or ) as no boron planar triangles with one NBO are expected for such compositions. From those information, we establish a model for iodine dissolution in nuclear waste glass that is consistent with previous studies.

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