钇对铸造Ni-30Cr合金氧化行为的影响

Yifan Zhang, Dongming Zhu, David A. Shores
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引用次数: 18

摘要

铸态Ni-30Cr和Ni-30Cr-0.5 y合金在1000℃纯O2中进行不同时间的氧化,然后在炉内冷却至室温,或在1000℃和不同温度之间热循环。在Ni-30Cr合金的等温氧化过程中,加入0.5% y可使Ni-30Cr合金的等温氧化速率降低约3.6倍,并收集了等温氧化过程、连续炉冷却过程和热循环过程中尺度断裂事件产生的声发射信号。这些数据表明,正如其他人所表明的那样,Ni-30Cr-0.5 y上形成的水垢比Ni-30Cr上形成的水垢具有更强的抗断裂能力。在氧化时间相等的情况下,更重要的是,在厚度相等的情况下,含y合金的这种优势是显而易见的。SEM和EDAX分析表明,在短时间氧化(2 h)后,含y和无y合金表面均形成连续的Cr2O3氧化层,但经过较长时间的氧化和热循环后,外层均形成NiO或NiCr2O4氧化层。由于Cr2O3与NiO或NiCr2O4之间的热膨胀差异,在冷却过程中会产生热应力。在内尺度/外尺度界面以及金属/尺度界面处观察到剥落现象。等尺度厚度下尺度应变的x射线测量结果表明,含y合金在等温氧化期结束时的生长应变较大,且该合金冷却至室温后的残余应变也较大。使用基于弹性应变能的模型,在相同的尺度厚度下,含y合金的尺度断裂(一种衡量尺度粘附力的方法)的表面能估计值明显更高。声发射和应变测量结果都与Y提高金属/尺度界面固有强度的建议一致。对于含y合金来说,较小的氧化皮开裂速率和较慢的氧化皮生长速率可以进一步延缓NiO或NiCr2O4过生长层的形成,而过生长层本身可能会降低氧化皮的完整性。
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Effect of yttrium on the oxidation behavior of cast Ni-30Cr alloy

Cast Ni-30Cr and Ni-30Cr-0.5Y alloys were oxidized at 1000°C in pure O2 for various times, then were either furnace cooled to room temperature, or thermally cycled between 1000°C and different lower temperatures. The isothermal oxidation rate of the Ni-30Cr alloy was reduced by about a factor of 3.6 by the addition of 0.5% Y. Acoustic emission signals, which are generated by scale fracture events, were collected during isothermal oxidation, during continuous furnace cooling and during thermal cycling. These data showed, as others have shown, that the scale formed on Ni-30Cr-0.5Y was significantly more resistant to fracture than that on Ni-30Cr. This advantage of the Y-containing alloy was evident for comparisons based on equal oxidation times, and more importantly, at equal scale thicknesses. SEM and EDAX analyses show that continuous Cr2O3 scales were formed on both Y-bearing and Y-free alloys after a short time of oxidation (2 h), but after a longer period of oxidation and thermal cycling, a NiO or NiCr2O4 outer layer was found. This outer scale created a new interface with the Cr2O3 scale where thermal stresses will be generated during cooling due to the thermal expansion difference between Cr2O3 and NiO or NiCr2O4. Spallation at the inner scale/outer scale interface, as well as at the metal/scale interface, was observed. X-ray measurements of scale strains at equal scale thicknesses showed that the growth strains (at the end of the isothermal oxidation period) were larger on the Y-containing alloy, and that this alloy also sustained larger residual strains upon cooling to room temperature. Using a model based on elastic strain energy, estimates of the surface energy for scale fracture (a measure of scale adhesion) were significantly higher for the Y-containing alloy at equal scale thicknesses. Both the AE and the strain measurements are consistent with the proposal that Y improves the inherent strength of the metal/scale interface. The smaller rate of scale cracking for Y-containing alloys, combined with their slower scale growth rate, offers the further benefit of delaying the onset of NiO or NiCr2O4 overgrowth layers, which themselves may degrade the integrity of the scale.

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