Summary
Surface chemical states of 57Co2+ and 119Sb5+ ions adsorbed on γ-Fe2O3 and NiFe2O4 were studied in the presence of the aqueous phase using the magnetic interaction between the substrates and 57Fe2+ or 119Sn4+ arising from the adsorbed species. Two chemical forms were observed for the 57Co2+ adsorbed on γ-Fe2O3; one giving a peak in the high-field region and another giving a broad distribution in the lower fields, which were attributed to 57Co2+ at surface B sites of the spinel structure of γ-Fe2O3 and 57Co2+ species weakly bonded to the substrate, respectively. In case of the NiFe2O4 substrate, the latter species was dominant and was converted to the former by heating. Most of the 119Sb5+ ions adsorbed on the γ-Fe2O3 and NiFe2O4 particles were found to have a certain magnetic interaction with the magnetically ordered ions of the substrates.
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References
Okada T., Ambe S., Ambe F. and Sekizawa H., J. Phys. Chem., 86 (1982) 4726.
Ambe F., Okada T., Ambe S. and Seklizawa H., J. Phys. Chem., 88 (1984) 3015.
Ambe F., Ambe S., Okada T. and Sekizawa H., in Geochemical Processes at Mineral Surfaces, edited by A. Davis and K. F. Hayes (American Chemical Society, Washington, D.C.) 1986, p. 403.
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Ambe, S., Okada, T. & Ambe, F. Emission Mössbauer studies of 57Co2+ and 119Sb5+ adsorbed on γ-Fe2O3 and NiFe2O4 surfaces. Il Nuovo Cimento D 18, 313–317 (1996). https://doi.org/10.1007/BF02458910
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DOI: https://doi.org/10.1007/BF02458910