The phase relations at high pressure and high temperature for the FeTiO3-Mg
TiO3 join were determined using several different experimental methods. Thr
ough a series of multi-anvil experiments, a phase boundary with a negative
slope was observed between MgTiO3 I (ilmenite structure) and a high pressur
e phase with the MgTiO3 II (lithium niobate structure) after quenching. The
enthalpy of transformation of MgTiO3 I to MgTiO3 II was determined through
transposed-temperature-drop calorimetry to be 28.78 +/- 1.45 kJ/mol. The e
nthalpy of transformation from ilmenite to lithium niobate structure was al
so determined for three intermediate compositions on the FeTiO3-MgTiO3 join
, Fe0.2Mg0.8TiO3, Fe0.5Mg0.5TiO3 and Fe0.8Mg0.2TiO3, and confirmed for FeTi
O3, and was found to be a linear function of composition. These experiments
represent one of the first successful calorimetric measurements on small s
amples (1 to 3 mg) synthesized at high pressures (15 to 21 GPa). X-ray anal
ysis during compression of Fe0.5Mg0.5TiO3 II in a diamond cell confirmed a
room temperature transition at 28 GPa to Fe0.5Mg0.5TiO3 III (a GdFeO3-type
perovskite structure), similar to the transitions previously observed in Fe
TiO3 and MnTiO3. The Fe0.5Mg0.5TiO3 sample was heated to 802 degrees C at 2
1 GPa, and it was observed that the stable high temperature, high pressure
phase is perovskite, Fe0.5Mg0.5TiO3 III. The above data combined confirm th
e stability of a continuous perovskite solid solution at high pressure and
temperature for the FeTiO3-MgTiO3 join.