Cation and cation vacancy distribution equilibria in the cubic phase of jacobsite-hausmannite solid solution system have been calculated by a defect-chemical approach as a function of some equilibrium constants, partial pressure of oxygen Po
2 and compositional ratio x in Mn
xFe
3−xO
4 (x=1 to 3). The concentration of metal vacancy was zero and a considerable amount of Fe
2+ in the octahedral site, which was equal to Fe
3+ in the tetrahedral site, appeared in case of appropriate values of equilibrium constants and small values of Po
2. The distribution results in a fairly good agreement with the reported Mössbauer spectroscopic data. In spite of constant metal ratio, the concentraion of Fe
2+ is lessened with increasing Po
2 and metal vacancy in the tetrahedral site appeared considerably. These results suggest that the estimation of temperature and Po
2 for formation of natural specimen is possible from the observed values of cation distribution, if some thermodynamic values are known.
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