4.7 Article

Sorption of americium/europium onto magnetite under saline conditions: Batch experiments, surface complexation modelling and X-ray absorption spectroscopy study

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 561, 期 -, 页码 708-718

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2019.11.047

关键词

Trivalent radionuclides; Sorption; Magnetite; XAS; Molecular mechanism; Complexation constants; Saline systems; CD-MUSIC model; Titration

资金

  1. German Federal Ministry of Economic Affairs and Energy (BMWi) [02 E 11496 B]

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Hypothesis: This study investigates the adsorption of americium and its chemical analogue europium on magnetite, which is expected to form as a major long-term steel canister corrosion product under anoxic and highly saline conditions. Experiments: The sorption of europium on magnetite (solid/liquid ratio = 0.5 g/L) was investigated batch wise in NaCl brines with ionic strength I = 1 m, 3.5 m, and 6.67 m, as a function of pH(m) for two europium concentrations (6 x 10(-10) m, 1.2 x 10(-5) m). Information on the chemical nature of the surface species was obtained by X-ray absorption spectroscopy (XAS) at the americium L-3-edge. Findings: Retention of europium by magnetite of >99.5% was found above pH(m) 6.4 for all ionic strengths for europium concentration of 6 x 10(-10) m. No ionic strength effect was observed in this pH(m) range. At 1.2 x 10(-5) m europium concentration, 95 +/- 4% sorption was found above pH(m) 7.5 for I = 1 m and above pH(m) 8.0 for I = 3.5 m and 6.67 m. A small ionic strength effect was observed in this case. X-ray absorption spectroscopy (XAS) results are consistent with the batch sorption experiment outcomes, showing an insignificant effect of ionic strength on the pH(m) dependent sorption. Results from potentiometric titrations of the solid phase, batch sorption experiments and spectroscopy were interpreted consistently with a charge distribution multi-site (CD-MUSIC) triple layer surface complexation model assuming surface coordination of the metal ion via a tridentate binding mode. (C) 2019 Elsevier Inc. All rights reserved.

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