Titanate-based ceramics for separated long-lived radionuclides

Abstract

Studies have been conducted in France to minimize the potential long-term impact of nuclear waste by enhanced chemical separation of the minor actinides (Np, Am, Cm) and some long-lived fission products (I, Cs, Tc). Two options may be considered following this work: ( i) the initial reference option is transmutation by neutron bombardment in nuclear facilities, ( ii) the second option would be to incorporate the separated elements into an inorganic matrix ensuring long-term stability. In the case of specific conditioning, zirconolite and hollandite are the potential host phases for the minor actinides and caesium, respectively. Both of these matrices have shown strong potential: ( i) for incorporating the respective radioelement in the crystalline structure, ( ii) for fabricating the ceramic by natural sintering in air, ( iii) for chemical durability with a very low initial alteration rate (about 10 –2 g m –2 d –1 at 100 °C), then very rapidly reach alteration rates more than four orders of magnitude lower. In the case of zirconolite ceramics, the high chemical durability is conserved even after amorphization of the crystalline structure by external irradiation with heavy ions or by self-irradiation in natural zirconolites 550 million years old. To cite this article: C. Fillet et al., C. R. Chimie 7 (2004).