Oxidation of the hexagonal Zr(Cr0.4Fe0.6)2 Laves phase

Abstract The hexagonal (C14-type) Laves phase Zr(Cr0.40Fe0.60)2 when oxidized in an open furnace was studied by X-ray diffraction and Mossbauer spectroscopy techniques. Oxidation modified part of the original Laves phase and Zr oxides, Cr oxides, α-Cr, (Fe, Cr) oxides, α-Fe and α-Fe2O3 appeared. The behaviour of these phases, particularly the Fe-bearing phases, is described in detail through a two stage process (stage I from 0 to ∼7 wt% O2 and stage II up to 22 wt% O2). A very small amount of O2 (stage I) is enough to induce the formation of α-Fe upon oxidation, sustaining a model previously suggested for the oxidation of the Laves phases. This α-Fe is highly Cr-substituted. Oxidation proceeds through the increasing presence of α-Fe2O3 and through the structural evolution of Zr oxides (formation of monoclinic, tetragonal and cubic ZrO2).