Because of the excellent oxidation resistance and superior mechanical properties at high-temperature environment, Ni-based alloy, 718 (Ni-19Fe-19Cr-5Nb-0.6Al-1Ti-3Mo) is one of the most used materials for gas turbines and related aerospace applications. Regarding to the oxidation performance of Alloy718, even though the chromium content 19 mass% is not sufficient to form a protective Cr2O3 scale on Ni-Fe-Cr alloys, the Alloy718 has excellent oxidation resistance by formation of an exclusive Cr2O3 scale. Based on our previous studies, the Nb addition to a Ni–19Fe–19Cr alloy could develop a continuous CrNbO4 layer at the metal-oxide interface, which acts as a diffusion barrier for inward oxygen and outward Fe and Ni diffusion and is favorable for rapid establishment of an external Cr2O3 scale. However, the interpretation in theprevious works is limited to insufficient information of defect chemistry in CrNbO4 oxides. To our knowledge, and the motivation for this study is that the defect chemistry of rutile CrNbO4 oxides has barely been studied to describe the composition versus oxygen partial pressure phase diagrams in this system. Therefore, the dependence of lattice constants and oxygen deficiency of CrNbO4 on oxygen partial pressure were investigated in the current study.The CrNbO4 compounds used in this study were prepared by a solid-state reaction method. The initial materials of Cr2O3 and Nb2O5 had at least a purity of 99.9%. Oxygen partial pressure was varied during the heat treatment at 1000oC, the following buffers: Ni/NiO (P O2 ≒10-11 atm), Co/CoO (P O2 ≒10-12 atm), Fe/FeO (P O2 ≒10-15 atm), H2/H2O (P O2 ≒10-17 atm), Mn/MnO (P O2 ≒10-24 atm) were used for yielding different levels of oxygen deficiency in the CrNbO4. At relatively higher oxygen partial pressure, a small quantity of oxygen vacancies (≒0.01) created under Ni/NiO (P O2 ≒10-11 atm) at 1000oC. Based on the results, maximum 0.05 per formula unit of vacancies could be created. However, a partial formation of Cr2O3 was found when reduced CrNbO4 samples were tried to be obtained below the partial pressure of Fe/FeO (P O2 ≒10-15 atm) at 1000oC (Fig. 2). This could be attributed to the valence states from Nb5+ to Nb4+, forming a solid-solution of NbO2-CrNbO4 under relatively lower partial pressure at 1000oC. Based on experimental data, an increase NbO2 dissolution in NbO2-CrNbO4 solid-solution, that is, (Nb,Cr)O2, leading to the Cr2O3 precipitation under Mn/MnO (P O2 ≒10-24 atm) at 1000oC. The present results show that CrNbO4 may initially formed and changed into (Nb,Cr)O2 solid-solution with increasing oxidation time. (Nb,Cr)O2 could coexist with Cr2O3 under low oxygen partial pressure at 1000oC.
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