Investigation of Aquo and Chloro Complexes of UO₂²⁺, NpO₂⁺, Np⁴⁺, and Pu³⁺ by X-ray Absorption Fine Structure Spectroscopy

U, Np, and Pu L(II,III)-edge X-ray absorption fine structure (XAFS) spectra were collected for the UO(2)(2+), NpO(2)(+), Np(4+), and Pu(3+) ions as a function of chloride concentration in aqueous solution. At low chloride concentration, the hydration numbers and corresponding bond lengths for the different ions are as follows: UO(2)(2+), N= 5.3, R = 2.41 Å; NpO(2)(+), N = 5.0, R = 2.50 Å; Np(4+), N = 11.2, R = 2.40 Å; Pu(3+), N = 10.2, R = 2.51 Å. As the Cl(-) concentration increases, inner-sphere Cl(-) complexation occurs, resulting in a decrease in the hydration numbers and an expansion of the actinide-oxygen (water) bond lengths. The Pu(3+) ion shows only a decrease in hydration number (40%) and no inner-sphere Cl(-) complexation for [Cl(-)] < 14 M. For concentrations up to 10-14 M Cl(-), the average Cl(-) coordination numbers and bond lengths are as follows: UO(2)(2+), N = 2.6, R = 2.73 Å; NpO(2)(+), N = 1.0, R = 2.84 Å; Np(4+), N = 2.0, R = 2.61 Å. Structural changes are observed in the near-edge spectral region as shown by significant changes in the white line intensities upon Cl(-) complexation. For ions with similar structures, i.e. Pu(3+) and Np(4+) or the actinyl ions NpO(2)(+) and UO(2)(2+), positive energy shifts are observed with increasing oxidation state. The ability to use XAFS speciation results to calculate equilibrium constants and the relationship of these results to previous studies are discussed.

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