An experimental study of the Fe-Mn exchange between garnet and ilmenite |
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| Authors: | Anne Feenstra Martin Engi |
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| Institution: | (1) Mineralogisch-petrographisches Institut, University of Berne, Baltzerstrasse 1, CH-3012 Berne, Switzerland, CH |
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| Abstract: | The exchange equilibrium
was studied by reversal experiments as a function of temperature (650 ≤ T ≤ 1000 °C), pressure (10 ≤ P ≤ 20 kbar), and chemical composition. Experiments were performed in a piston-cylinder apparatus using starting mixtures consisting
of 95% garnet and 5% ilmenite. At the lower temperatures, 3–5% PbO flux was added to the reactants. The PbO was reduced to
metallic lead by the graphite of the capsules. The EMP analysis shows that ilmenite is essentially a solid solution of FeTiO3 and MnTiO3 with up to 4.5 mol% Fe2O3 (for Fe-rich compositions). Garnet is compositionally close to (Fe,Mn)3 Al2Si3O12 but apparently contains up to 1.0 wt% TiO2. As garnet was usually analyzed within 5–15 μm distance from ilmenite grains, the Ti measured in garnet appears to be largely
an analytical artifact (due to secondary fluorescence). This was confirmed by analyzing profiles across a couple constructed
from ilmenite and Ti-free garnet. The more than 100 exchange runs indicate that the distribution coefficient KD =(X
Mn
gnt·X
Fe
ilm)/(X
Fe
gnt·X
Mn
ilm)] is essentially independent of P and decreases with T. With a few exceptions at Mn-rich compositions, the present results are consistent with previous studies on the Fe-Mn partitioning
between garnet and ilmenite. Contrary to previous studies, however, the narrow experimental brackets obtained during the present
calibration constrain that, at constant T, KD is larger for Mn-rich compositions than for Fe-rich ones. This compositional dependence of KD will complicate garnet-ilmenite geothermometry. Mutually consistent activity models for Fe-Mn garnet and ilmenite, based
on a thermodynamic analysis of the present results and other phase equilibria studies in the system Fe-MnO-Al2O3-TiO2-SiO2-O2, will be presented in a following contribution (M. Engi and A. Feenstra, in preparation).
Received: 12 September 1996 / Accepted: 11 December 1997 |
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