Controlled time-temperature oxidation reaction in a synthetic Mg-hercynite

摘要

The oxidation of a synthetic hercynite with composition Fe0.6992+Mg0.301Al1.941Fe0.0593+O4 was investigated by X-ray single-crystal diffraction. Heating runs at 500 degrees C up to 212 h did not produce detectable oxidation, but only a small variation in oxygen coordinate u, consistent with very limited reordering of Mg and Al in tetrahedral (T) and octahedral (M) sites, respectively. Oxidation began after the first run at 600 degrees C, producing progressive decreases in u, cell parameter a and the mean atomic number in T site. After 1,842 h at 600 degrees C, the transformation was close to equilibrium, with about 70% of ferrous iron transformed into ferric. This produced about 0.17 vacancies per formula unit, and caused a great increase in the displacement parameters of oxygen and M sites. Vacancies were strongly ordered in M sites, and the oxygen displacement parameter becames anisotropic, unlike stoichiometric spinels-because some of the oxygen coordination polyhedra have a vacancy instead of a cation in one vertex. The behaviour of displacement parameters in this case supports the calculated point defect distribution.