20–22 May 2014
Schloss Böttstein
Europe/Zurich timezone
AnXAS 2014

Plutonium oxidation state speciation in aqueous solution studied by Pu L and M edge high energy resolution XANES technique

20 May 2014, 17:30
4h 30m
Swiss Light Source (Paul Scherrer Institut)

Swiss Light Source

Paul Scherrer Institut

5232 Villigen Switzerland
Board: 8
Poster Solution and Coordination Chemistry of the Actinides Poster

Speaker

Mr Ivan Pidchenko (Institute for Nuclear Waste Disposal)

Description

In this work four electrochemically aqueous plutonium (Pu) species prepared in perchloric acid solution at different oxidation states (III, IV, V, VI) as well as Pu(IV) colloids are characterized for the first time by Pu L3 and M5 edge high energy resolution X-ray absorption near-edge structure spectroscopy (HR-XANES). A Johann type five-analyzer crystal spectrometer recently installed and commissioned at the INE-Beamline for actinide research at the ANKA synchrotron radiation facility, Karlsruhe, Germany was applied Different to conventional XANES several spectral features could be identified. The most intense absorption resonances (White Line, WL) have higher intensities for all Pu L3 HR-XANES spectra compared to the conventional XANES. Additionally, the Pu(V) and Pu(VI) L3 HR-XANES spectra exhibit better resolved post-edge features. The energy distance between the WL and this resonance is sensitive to the bond distance between the Pu and axial O atoms in Pu(V) and Pu(VI). Extended X-ray absorption fine structure (EXAFS) investigation is performed to correlate oxidation states with average Pu-O bonding distances. For the Pu(VI) M5 edge HR-XANES a feature at higher energy is well resolved, which might be sensitive to changes in Pu-O bond length and to the level of hybridization of metal and axial oxygen valence orbitals. A pre-edge ‘shoulder’ is detected in the Pu(III) spectrum. The origin of hitherto unresolved features is elucidated by quantum chemical calculations using the FEFF9.5 code. The HR-XANES experimental technique provides new insights into the actinides electronic structure and allows detection of minor contributions of Pu oxidation states in oxidation state mixtures.

Primary author

Mr Ivan Pidchenko (Institute for Nuclear Waste Disposal)

Co-authors

Dr Bernd Schimmelpfennig (Institute for Nuclear Waste Disposal) Dr David Fellhauer (Institute for Nuclear Waste Disposal) Dr Joerg Rothe (Karlsruhe Institute of Technology - Institute for Nuclear Waste Dispoasal) Dr Kathy DARDENNE (Institut für Nukleare Entsorgung (INE), Karlsruhe Institute of Technologie (KIT)) Mr Tim Pruessmann (Karlruhe Institute of Technology) Dr Tonya Vitova (Institute for Nuclear Waste Disposal)

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