The heat capacity of three synthetic polycrystalline almandine garnets (ideal formula Fe3Al2Si3O12) and one natural almandine-rich single crystal was measured. The samples were characterized by optical microscopy, electron microprobe analysis, X-ray powder diffraction, and Mössbauer spectroscopy. Measurements were performed in the temperature range 3 to 300 K using relaxation calorimetry and between 282 and 764 K using DSC methods. All garnets show a prominent λ-type heat-capacity anomaly at low temperatures resulting from a paramagnetic-antiferromagnetic phase transition. For two Fe3+-free or nearly Fe3+-free synthetic almandines, the phase transition is sharp and occurs at 9.2 K. Almandine samples that have ~3% Fe3+ show a λ-type peak that is less sharp and that occurs at 8.0 ± 0.2 K. The low-T CP data were adjusted slightly using the DSC results to improve the experimental accuracy. Integration of the low-T CP data yields calorimetric standard entropy, S∘, values between 336.7 ± 0.8 and 337.8 ± 0.8 J/(mol·K). The smaller value is recommended as the best S∘ for end-member stoichiometric almandine, because it derives from the “best” Fe3+-free synthetic sample.
The lattice (vibrational) heat capacity of almandine was calculated using the single-parameter phonon dispersion model of Komada and Westrum (1997), which allows the non-lattice heat capacity (Cex) behavior to be modeled. An analysis shows the presence of an electronic heat-capacity contribution (Cel, Schottky anomaly) superimposed on a larger magnetic heat-capacity effect (Cmag) around 17 K. The calculated lattice entropy at 298.15 K is Svib = 303.3 J/(mol·K) and it contributes about 90% to the total standard entropy at 298 K. The non-lattice entropy is Sex = 33.4 J/(mol·K) and consists of Smag = 32.1 J/(mol·K) and Sel = 1.3 J/(mol·K) contributions. The CP behavior for almandine above 298 K is given by the polynomial [in J/(mol·K)]:
which is calculated using the measured DSC data together with one published heat-content datum determined by transposed-drop calorimetry along with a new determination in this work that gives H1181K − H302K = 415.0 ± 3.2 kJ/mol.
Using our S∘ value and the CP polynomial for almandine, we derived the enthalpy of formation, ΔH°f, from an analysis of experimental phase equilibrium results on the reactions almandine + 3rutile = 3ilmenite + sillimanite + 2quartz and 2ilmenite = 2Fe + 2rutile + O2. A ΔH°f = −5269.63 kJ/mol was obtained.