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American Mineralogist; November 2000; v. 85; no. 11-12; p. 1686-1693
© 2000 Mineralogical Society of America
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The heat capacity of MgCr2O4, FeCr2O4, and Cr2O3 at low temperatures and derived thermodynamic properties

Stephan Klemme1,2,*, Hugh St.C. O’Neill1, Walter Schnelle3,4 and Eberhard Gmelin4

1 Research School of Earth Sciences, The Australian National University, Canberra, ACT 0200, Australia
2 Department of Earth Sciences, University of Bristol, Wills Memorial Building, Queen’s Road, Bristol BS8 1RJ, U.K.
3 Max-Planck-Institut für Chemische Physik fester Stoffe, Pirnaer Landstrasse 176, 01257 Dresden, Germany
4 Max-Planck-Institut für Festkörperforschung, Heisenbergstrasse 1, 70569 Stuttgart, Germany

Correspondence: * E-mail: stephan.klemme{at}bristol.ac.uk

The heat capacity of synthetic eskolaite, Cr2O3, and of the synthetic spinels magnesiochromite, MgCr2O4, and chromite, FeCr2O4 were measured from 1.5 K to 340 K. For MgCr2O4, a substantial magnetic contribution to the entropy is revealed by a sharp peak in the heat capacity curve at 12.55 ± 0.05 K, which indicates the transition to antiferromagnetic long-range order. Integration of the heat capacity curve yields a value of 118.3 ± 1.2 J/(mol·K) for the standard entropy at 298.15 K, which is in excellent agreement with that calculated from phase equilibria studies on the reaction MgCr2O4 + SiO2 = Cr2O3 + MgSiO3. The new calorimetric results for Cr2O3 indicate a standard entropy at 298.15 K of 82.8 ± 0.8 J/(mol·K). The measurements for FeCr2O4 show three distinct heat capacity anomalies, one of which (peaking at 36.5 ± 0.2 K) was missed by previous low temperature heat capacity measurements, which only extend down to 53 K. Integration of the heat capacity curve yields a value for the standard entropy at 298.15 K of 152.2 ± 3.0 J/(mol·K) for FeCr2O4, some 6 J/(mol·K) greater than the previous calorimetric value.

These low-temperature heat capacity data were combined with high-temperature heat content measurements from the literature to derive heat capacity equations for all three phases to 1800 K. The resulting heat capacity equations were then used to extract revised recommended values of the standard enthalpies of formation and entropies of MgCr2O4 and Cr2O3 from phase equilibrium data. For FeCr2O4, the phase equilibrium data are of dubious accuracy, the enthalpy of formation is only approximate.




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