摘要
The thermal oxidation of ZrAl2 in the temperature range of 550–750℃ in pure oxygen has been investigated by a combinational experimental approach using X-ray diffraction, scanning electron microscopy/energy dispersive spectrometer, Auger electron spectroscopy and cross-sectional transmission electron microscopy. The thermal oxidation leads to the growth of anomalously thick(up to 4.5 μm)amorphous(Zr0.33 Al0.67)O1.66 surficial layers at temperatures as high as 750℃. The oxidation kinetics obeys a parabolic law with an activation energy of 143 kJ/mol. The underlying mechanism for the formation of such micrometer-thick amorphous oxide surficial layers has been discussed on the basis of interface thermodynamics and the occurrence of high interface stability associated with a synchronous oxidation of Al and Zr elements.
The thermal oxidation of ZrAl2 in the temperature range of 550–750℃ in pure oxygen has been investigated by a combinational experimental approach using X-ray diffraction, scanning electron microscopy/energy dispersive spectrometer, Auger electron spectroscopy and cross-sectional transmission electron microscopy. The thermal oxidation leads to the growth of anomalously thick（up to 4.5 μm）amorphous(Zr0.33 Al0.67)O1.66 surficial layers at temperatures as high as 750℃. The oxidation kinetics obeys a parabolic law with an activation energy of 143 kJ/mol. The underlying mechanism for the formation of such micrometer-thick amorphous oxide surficial layers has been discussed on the basis of interface thermodynamics and the occurrence of high interface stability associated with a synchronous oxidation of Al and Zr elements.
基金
financially supported by the National Natural Science Foundation of China (No. 51571148)
the National Key Research and Development Program of China (No. 2017YFE0302600 and No. 2017YFB0701801)
the Thousand Talents Program for Distinguished Young Scholars of China
