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The oxidation behavior of a nickel-based superalloy at 1000°C in air was investigated through X-ray diffraction, scanning electron microscopy, and energy-dispersive spectroscopy analysis. A series of oxides, including external oxide scales(Cr_2O_3,(TiO_2 + Mn Cr_2O_4)) and internal oxides(Al_2O_3,Ti N), were formed on the surface or sub-surface of the substrate at 1000°C in experimental still air. The oxidation resistance of the alloy was dependent on the stability of the surface oxide layer. The continuity and density of the protective Cr_2O_3 scale were affected by minor alloying elements such as Ti and Mn. The outermost oxide scale was composed of TiO_2 rutile and Mn Cr_2O_4 spinel, and the growth of TiO_2 particles was controlled by the outer diffusion of Ti ions through the pre-existing oxide layer. Severe internal oxidation occurred beneath the external oxide scale, consuming Al and Ti of the strength phase γ′(Ni_3(Al,Ti)) and thereby severely deteriorating the surface mechanical properties. The depth of the internal oxidation region was approximately 35 μm after exposure to experimental air at 1000°C for 80 h.
The oxidation behavior of a nickel-based superalloy at 1000 ° C in air was investigated by X-ray diffraction, scanning electron microscopy, and energy-dispersive spectroscopy analysis. A series of oxides, including external oxide scales (Cr 2 O 3, (TiO 2 + Mn Cr 2 O 4) and internal oxides (Al 2 O 3, Ti N), were formed on the surface or sub-surface of the substrate at 1000 ° C in experimental still air. The oxidation resistance of the alloy was dependent on the stability of the surface oxide layer . The continuity and density of the protective Cr 2 O 3 scale were affected by minor alloying elements such as Ti and Mn. The outermost oxide scale was composed of TiO 2 rutile and Mn Cr 2 O 4 spinel, and the growth of TiO 2 particles was controlled by the outer diffusion of Ti ions through the pre-existing oxide layer. Severe internal oxidation occurred beneath the external oxide scale, consuming Al and Ti of the strength phase γ ’(Ni_3 (Al, Ti)) and thereby severely deteriorating the surface mecha The depth of the internal oxidation region was approximately 35 μm after exposure to experimental air at 1000 ° C for 80 h.