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Cyclic Oxidation Behavior of IN 718 Superalloy in Air at High Temperatures

机译:IN 718高温合金在空气中高温下的循环氧化行为

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Ni-base superalloy IN 718 was cyclically oxidized in laboratory air at temperatures ranging from 750 to 950 °C for up to 12 cycles (14 h/cycle). The kinetic behaviour as well as the surface morphology, and the oxide phases of the scales were characterized by means of weight gain measurements, cyclic oxidation kinetics, scanning electron microscopy equipped with energy dispersive spectroscopy (SEM-EDS), and X-ray diffraction (XRD) analysis techniques. The results showed that as the oxidation temperature increased, the oxidation rate, the external scale thickness, and internal oxidation zone increased. It was suggested that the oxidation rate was controlled by the diffusion of substrate elements in the alloy and the inward diffusion of oxygen through the oxide scale. The oxidation kinetics followed a sub-parabolic rate law and, the activation energy of oxidation was 249 ± 20 kJ mol−1. The scaling process was controlled mainly by the diffusion of chromium, titanium, manganese, and oxygen ions through the chromia scale. IN 718 showed low weight gain and very slow reaction rates of substrate elements at 750 °C. At 850 °C, a continuous and very thin oxide scale was formed. At 950 °C, XRD and EDS-elemental mapping analysis revealed that a complex oxide scale had formed. It consisted of an outermost layer of TiO2–MnCr2O4 spinels, inner layer of Cr2O3, and the inner most layer composed of Ni3Nb enriched with Nb, Ti and Al oxides underneath the chromia layer. The oxide scale at this temperature seemed to be thicker layer, significant spallation and volatilization had apparently occurred, and greater internal corrosion was identified. The doping effect of titanium was observed, where it was found to be diffused through the chromia scale to form TiO2 at the oxide-gas interface as well as internally and at the oxide alloy interface. The amount of rutile (TiO2) at the oxide surface increased with temperature. In view of Mn contents in the alloy, the manganese–chromium spinel oxide was inferred to have played an important role in cyclic oxidation behaviour of IN 718, where the change in oxidation kinetic was noted. The Al contents would cause internal Al-rich oxide formation at grain boundaries.
机译:镍基高温合金IN 718在实验室空气中在750至950°C的温度下循环氧化多达12个循环(14 h /循环)。通过重量增加测量,循环氧化动力学,配有能量色散谱仪(SEM-EDS)的扫描电子显微镜和X射线衍射()来表征氧化皮的动力学行为,表面形态和氧化相。 XRD)分析技术。结果表明,随着氧化温度的升高,氧化速率,外部氧化皮厚度和内部氧化区增加。有人认为,氧化速率是由合金中基体元素的扩散和氧在氧化皮中的向内扩散控制的。氧化动力学遵循抛物线速率律,氧化的活化能为249±20 kJ mol -1 。结垢过程主要由铬,钛,锰和氧离子通过氧化铬的扩散控制。 IN 718在750°C下显示出低的增重和非常慢的底物元素反应速率。在850℃下,形成连续且非常薄的氧化皮。在950°C时,XRD和EDS元素图谱分析表明已形成复杂的氧化皮。它由TiO 2 –MnCr 2 O 4 尖晶石的最外层和Cr 2 O的最内层组成 3 ,最内层由氧化铬层下面的富含Nb,Ti和Al氧化物的Ni 3 Nb组成。在该温度下的氧化物垢似乎更厚,明显地发生了剥落和挥发,并且发现了更大的内部腐蚀。观察到钛的掺杂作用,发现钛在氧化铬尺度上扩散通过氧化铬,在氧化物-气体界面以及内部和氧化物合金界面形成TiO 2 。氧化物表面的金红石(TiO 2 )的含量随温度的升高而增加。考虑到合金中的Mn含量,可以推断锰-铬尖晶石氧化物在IN 718的循环氧化行为中起了重要作用,并注意到氧化动力学的变化。 Al含量将在晶界处引起内部富Al氧化物的形成。

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