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Characterization of homoionic Fe-type montmorillonite: Potential chemical species of iron contaminant
Authors:Naofumi Kozai  Sachi Kawamura  Tamotsu Kozaki  Toshihiko Ohnuki  Takahiro Sato  Fumitaka Esaka
Institution:a Advanced Science Research Center, Japan Atomic Energy Agency (JAEA), Tokai, Ibaraki 319-1195, Japan
b Division of Energy & Environmental Systems, Graduate School of Engineering, Hokkaido University, Sapporo 060-8628, Japan
c Department of Advanced Radiation Technology, JAEA, Takasaki, Gunma 370-1292, Japan
d Division of Environment and Radiation Sciences, JAEA, Tokai, Ibaraki 319-1195, Japan
Abstract:Fe2+-montmorillonite with Fe2+ ions occupying cation exchange sites is an ideal transformation product in bentonite buffer material. In our previous study on preparation and characterization of Fe2+-montmorillonite, the montmorillonite sample that adsorbed Fe2+ ions on almost all of the cation exchange sites was prepared using a FeCl2 solution under an inert gas condition N. Kozai, Y. Adachi, S. Kawamura, K. Inada, T. Kozaki, S. Sato, H. Ohashi, T. Ohnuki, T. Banba, J. Nucl. Sci. Technol. 38 (2001) 1141]. In view of the unstable nature of iron(II) chemical species, this study attempted to determine the potential contaminant iron chemical species in the sample. Nondestructive elemental analysis revealed that a small amount of chloride ions remained dispersed throughout the clay particles. The chloride ion retention may be due to the adsorption of FeCl+ ion pairs in the initial FeCl2 solution and the subsequent containment of the Cl ions that are dissociated from the FeCl+ ion pairs during excess salt removal treatment. Two explanations are advanced for the second process: the slow release of the remaining Cl ions from the collapsed interlayer of the montmorillonite, and the transformation of a minor fraction of the remaining FeCl+ ion pairs to iron(III) hydroxide chloride complexes having low solubility.
Keywords:Montmorillonite  Iron  Chloride  Corrosion product  High-level radioactive waste
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