Author/Authors :
Numakura، نويسنده , , Masahiko and Okamoto، نويسنده , , Yoshihiro and Yaita، نويسنده , , Tsuyoshi and Shiwaku، نويسنده , , Hideaki and Akatsuka، نويسنده , , Hiroshi and Nezu، نويسنده , , Atsushi and Tajima، نويسنده , , Keisuke and Shimohara، نويسنده , , Yasuaki and Bessada، نويسنده , , Catherine and Pauvert، نويسنده , , Olivier and Zanghi، نويسنده , , Didier and Chamelot، نويسنده , , Pierre and Matsuura، نويسنده , , Haruaki، نويسنده ,
Abstract :
X-ray absorption fine structure (XAFS) measurements on terbium fluoride in molten lithium fluoride and in molten lithium–calcium fluoride mixtures, (e.g. 0.20TbF3–0.80LiF, 0.20TbF3–0.62LiF–0.18CaF2, 0.20TbF3–0.48LiF–0.32CaF2, 0.50TbF3–0.50LiF, and 0.50TbF3–0.38LiF–0.12CaF2), have been carried out. In the solid state, coordination number of terbium (Ni) and inter ionic distances between terbium and fluorine in the first neighbor (ri) are nearly constant in all mixtures. In 0.20TbF3–0.80LiF, 0.20TbF3–0.62LiF–0.18CaF2 and 0.50TbF3–0.50LiF mixtures, Niʹs decrease from ca. 8 to 6 and riʹs also decrease from ca. 2.29 to 2.26 Å on melting. On the other hands, in molten 0.20TbF3–0.48LiF–0.32CaF2 and 0.50TbF3–0.38LiF–0.12CaF2 mixtures, Niʹs are slightly larger than 6 and riʹs do not change. These facts correspond to the amount of F− supplied by solvent melts, i.e. the effect of CaF2 becomes predominant at bCaF2 > 0.32 in ternary 0.20TbF3–aLiF–bCaF2 mixtures and at bCaF2 > 0.12 in ternary 0.50TbF3–aLiF–bCaF2 mixtures.
Keywords :
Lithium fluoride , Calcium fluoride , Molten salt , X-ray absorption fine structure (XAFS) , Terbium fluoride