Phase equilibrium in the system Ln-Mn-O VI: Ln=Ho and Tb at 1100°C |
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Authors: | Kenzo Kitayama Minehito Kobayashi Hisataka Takano Naomi Nambu Hideyuki Hirasawa |
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Affiliation: | Department of Applied Chemistry and Biotechnology, Faculty of Engineering, Niigata Institute of Technology, Kashiwazaki, Niigata 945-1195, Fujihashi, Japan |
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Abstract: | Phase equilibria were established in Ho-Mn-O and Tb-Mn-O systems at 1100°C by varying the oxygen partial pressure from −log(PO2/atm)=0-13.00, and phase diagrams for the corresponding Ln2O3-MnO-MnO2 systems at 1100°C were presented. Stable Ln2O3, MnO, Mn3O4, LnMnO3, and LnMn2O5 phases were found at 1100°C, whereas Ln2Mn2O7, Ln2MnO4, Mn2O3, and MnO2 were not found to be stable. Small nonstoichiometric ranges were found in the LnMnO3 phase, with the composition of LnMnO3 represented as functions of log(PO2/atm), and . Activities of the components in the solid solution were calculated from these equations. The composition of LnMnO3 may range from Ln2O3 rich to Ln2O3 poor, while MnO is slightly nonstoichiometric, being oxygen rich and LnMn2O5 seems to be nonstoichiometric. Lattice constants of LnMnO3 quenched at different oxygen partial pressures and of LnMn2O5 quenched in air were determined. The standard Gibbs energy changes of the reactions appearing in the phase diagrams were also calculated. The relationship between the tolerance factor of LnMnO3 and ΔG0of reaction, (1/2)Ln2O3+MnO+(1/4)O2=LnMnO3, is shown graphically. |
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Keywords: | Phase equilibrium Thermogravimetry Holmium-manganese oxide Terbium manganese oxide Gibbs energy |
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