Phase Evolution in Two-Phase Alloys During Severe Plastic Deformation

N. Pant, N. Verma, Y. Ashkenazy, P. Bellon, R. Averback
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引用次数: 8

Abstract

Abstract Phase evolution in FCC metals with strongly interacting alloy components during severe plastic deformation is investigated using molecular dynamics simulations. Specifically, we study the alloy microstructure in steady state, nucleation and growth of precipitates in supersaturated alloys, and the dissolution of precipitates in undersaturated alloys. The results are compared to a modified effective temperature model, providing a physical understanding for the atomic processes underlying the model and a perspective on its strengths and weaknesses. Key observations in this work are nucleation and growth of precipitates during SPD at a temperature of 100 K; Gibbs-Thomson-like behavior relating steady-state solubility to precipitate size under sustained shearing; a direct relationship between the effective temperature and the shear modulus; and the importance of cluster agglomeration during precipitate growth. The study also reveals that the mechanism of forced chemical mixing depends on precipitate size, adding complications for effective temperature models describing inhomogeneous systems. The simulations are shown to provide good semi-quantitative agreement with experimental findings reported in the literature.
两相合金在剧烈塑性变形过程中的相演化
采用分子动力学方法研究了含强相互作用合金成分的FCC金属在剧烈塑性变形过程中的相演化。具体来说,我们研究了合金在稳态下的显微组织,过饱和合金中析出相的形核和生长,以及欠饱和合金中析出相的溶解。将结果与改进的有效温度模型进行比较,为模型背后的原子过程提供了物理理解,并对其优缺点进行了展望。本工作的主要观察结果是在100k温度下SPD过程中析出相的成核和生长;在持续剪切作用下,稳态溶解度与析出物大小之间的gibbs - thomson样行为;有效温度与剪切模量有直接关系;以及在析出相生长过程中团簇聚集的重要性。该研究还揭示了强迫化学混合的机制取决于沉淀的大小,这增加了描述非均匀系统的有效温度模型的复杂性。模拟结果与文献中报道的实验结果半定量一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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