Résumé
Due to a natural occurrence, a good resistance to radiation damage and a low solubility in neutral and basic conditions, Nd-britholite of formula Ca9Nd(PO4)5(SiO4)F2 was already considered as a potential host matrix for the specific immobilization of trivalent actinides. The incorporation of tetravalent actinides like Th, U or Ce in the structure was examined through the elaboration of Ca9Nd1−x
AnIV
x
(PO4)5−x
(SiO4)1+x
F2 samples. This study was the early beginning of the incorporation of 239Pu and/or 238Pu in order to evaluate the effects of α-decay on the britholite structure. The preparation of the samples was realized through dry chemistry methods using mechanical grinding in order to optimize the conditions of synthesis. The results showed that the incorporation of thorium in britholite structure was successful up to 20 wt.% leading to the formation of solid solutions. For U(IV), the incorporation was incomplete: only 5–8 wt.% of uranium was incorporated instead of 10 wt.% expected. The secondary phase, which was uranium enriched, was identified as the calcium uranate CaU2O5+y
. The incorporation of Pu(IV) was studied using Ce(IV) as a surrogate. The results were quite good: major part of cerium was introduced in the structure but was partly reduced in Ce(III) during the heating treatment.