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HYDROGEN DEPTH-PROFILING AND DESORPTION KINETICS IN RAPIDLY SOLIDIFIED Al-Fe ALLOYS

机译:快速固化的Al-Fe合金中的氢气深度分析和解吸动力学

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Hydrogen surface segregation and trapping in rapidly solidified Al-0.2; 0.5 at% Fe alloys has been studied through elastic recoil detection technique, Rutherford backscattering spectroscopy and thermal desorption spectroscopy. It was detected that most hydrogen was localized in the subsurface regions (400 nm) and estimated to be 3.6 at% in Al-0.2 Fe alloy. Strong hydrogen segregation on air-side surface in alloy showed increase in its content up to 9.6 at% after heat treatment at 500°C. Our results indicated that solute-vacancy interactions and microstructural features affect hydrogen behaviour in Al-Fe alloys. The hydrogen trapping at iron atoms in the substitutional sites was concluded to be predominant.
机译:氢表面偏析和捕获在快速凝固的Al-0.2中;已经通过弹性反冲检测技术,Rutherford反向散射光谱和热解吸光谱研究了0.5%的0.5个AT%Fe合金。检测到,大多数氢在地下区域(400nm)中局部地定位,估计在Al-0.2 Fe合金中为3.6at%。在500℃下热处理后,合金中的空气侧表面上的强氢偏析在热处理后,其含量高达9.6at%。我们的研究结果表明,溶质空位相互作用和微观结构特征影响Al-Fe合金中的氢行为。结论是主要位点的铁原子的氢气俘获占主导地位。

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