Retention mechanisms and microstructure of Eu(III) on manganese dioxide studied by batch and high resolution EXAFS technique

Author:

Sheng G. D.,Yang S. T.1,Li Y. M.2,Gao X.3,Huang Y. Y.3,Hu J.1,Wang X. K.

Affiliation:

1. Key Laboratory of Novel Thin Film Solar Cells, Institute of Plasma Physics, Chinese Academy of Sciences, P.O. Box 1126, Hefei, 230031, P.R. China

2. School of Chemistry and Chemical Engineering, Shaoxing University, Huancheng West Road 508, Shaoxing, Zhejiang 312000, P.R. China

3. Shanghai Synchrotron Radiation Facility (SSRF), Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201204, P.R. China

Abstract

Abstract The batch experiment and high resolution EXAFS technique with bent crystal analyzer were combined to study Eu(III) retention mechanisms on β-MnO2 as a function of various environmental factors. The results indicated that the sorption of Eu(III) onto β-MnO2 was obviously dependent on pH but independent of ionic strength, suggesting the formation of inner-sphere surface complexes. Results of high resolution EXAFS analysis showed that Eu was surrounded by 8 ± 1 O atoms in the first shell at R Eu−O ≈ 2.40 Å for all sorption samples. A second shell of Mn atoms at R Eu−Mn ≈ 3.78 Å was observed for all sorption samples, which was associated with the formation of a bidendate inner-sphere complex with chemical bonding via edge sharing to MnO6-octahedron. This study shows the utility of high resolution EXAFS technique with bent crystal analyzer to discriminate the fluorescence peak of Eu(III) from that of manganese hydroxides, whose fluorescence peaks are too close in energy to be discriminated by the conventional EXAFS technique with a low resolving solid-state detector. Both the macroscopic interaction data and the molecular level evidence of Eu(III) surface speciation at the oxide-water interface should be factored into better evaluation of Eu(III) and related radionuclide mobility in the natural environment.

Publisher

Walter de Gruyter GmbH

Subject

Physical and Theoretical Chemistry

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