Abstract
The coordination of U 4+ and Th 4+ in concentrated CaCl 2 solutions is studied by U and Th L III edge extended X-ray absorption fine structure (EXAFS) spectroscopy. With the decrease of concentration of CaCl 2 from 6.9 to 4 M, the Cl − ion coordination number N Cl in the U 4+ coordination sphere decreases from 3.4 to 1.3, while the hydration number N O increases from 4.5 to 6.7. The combined coordination number N O +N Cl of U 4+ in concentrated Cl − solution (8.0), is lower than that in 1.5 M perchloric acid aqueous solution (9.0). For Th 4+ , the decrease of concentration from 6.9 to 4 M CaCl 2 , the coordination number N Cl in the Th 4+ coordination sphere decreased slightly from 1.9 to 1.5, while coordination number N O increased from 7.6 to 8.8. The N O +N Cl of Th 4+ in concentrated Cl − solution (9.0), is similar to that in 1.5 M perchloric acid. The bond distance of U–Cl (2.67 Å), is shorter than that of Th–Cl (2.76 Å), because of low coordination number N O to U 4+ . By adding HCl into the system, the U 4+ and Th 4+ coordination sphere is unchanged. The coordination structures of U 4+ and Th 4+ in concentrated LiCl is also discussed.
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CITATION STYLE
Uehara, A., Fujii, T., Matsuura, H., Sato, N., Nagai, T., Minato, K., … Okamoto, Y. (2011). EXAFS analysis of uranium(IV) and thorium(IV) complexes in concentrated CaCl 2 solutions. Proceedings in Radiochemistry, 1(1), 161–165. https://doi.org/10.1524/rcpr.2011.0030
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