On diffusion behaviors in face centered cubic phase of Al-Co-Cr-Fe-Ni-Ti high-entropy superalloys

被引:57
作者
Chen, Shiyao [1 ]
Li, Qin [1 ]
Zhong, Jing [1 ]
Xing, Fangzhou [1 ]
Zhang, Lijun [1 ]
机构
[1] Cent S Univ, State Key Lab Powder Met, Changsha 410083, Hunan, Peoples R China
关键词
High-entropy superalloys; Al-Co-Cr-Fe-Ni-Ti; Diffusion; Diffusion multiple; HitDIC; Interdiffusivity; HIGH-THROUGHPUT DETERMINATION; COMPOSITION-DEPENDENT INTERDIFFUSIVITIES; SELF-DIFFUSION; THERMODYNAMIC DESCRIPTION; SLUGGISH DIFFUSION; SOLID-SOLUTION; X X; NICKEL; ALLOYS; COEFFICIENTS;
D O I
10.1016/j.jallcom.2019.03.286
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Owning the excellent high temperature properties, low cost and density, Al-Co-Cr-Fe-Ni-Ti high-entropy superalloys (HESAs) represent a potential substitute for Ni-based superalloys. In this paper, the composition-dependent interdiffusivity matrices of face centered cubic (fcc) Al-Co-Cr-Fe-Ni-Ti HESAs at 1473 K were first determined via a combination of diffusion multiple technique and HitDIC software based on the numerical inverse method. The correlations between the main interdiffusivities and the components suggest that alloying elements play great impact on diffusion in HESAs. After that, comprehensive comparisons of the interdiffusivities and tracer diffusivities in present fcc HESAs with the literature data in fcc-based pure elements, lower-order alloys and traditional high-entropy alloys were conducted. The results indicate that the sluggish diffusion effect exists for only some of the components in the present HESAs. Moreover, comparisons of the diffusion coefficients between the HESAs and traditional Ni-based superalloys with refractory elements show that the interdiffusivities in the present HESAs are lower than the Ni-based superalloys with most refractory elements, but higher than those with Ir, Re and Os. Furthermore, it is also found that refractory elements need to be added in order to further improve the creep resistance of the HESAs. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:255 / 264
页数:10
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