Strategy for pinpointing the formation of B2 CuZr in metastable CuZr-based shape memory alloys

被引:144
作者
Song, K. K. [1 ,2 ]
Pauly, S. [1 ]
Zhang, Y. [1 ]
Gargarella, P. [1 ]
Li, R. [3 ]
Barekar, N. S. [1 ]
Kuehn, U. [1 ]
Stoica, M. [1 ]
Eckert, J. [1 ,2 ]
机构
[1] IFW Dresden, Inst Komplexe Mat, D-01069 Dresden, Germany
[2] Tech Univ Dresden, Inst Werkstoffwissensch, D-01062 Dresden, Germany
[3] Beihang Univ, Dept Mat Sci & Engn, Beijing 100083, Peoples R China
基金
中国国家自然科学基金;
关键词
Differential thermal analysis; Glass matrix composites; Intermetallics; Martensitic transformation; Solid state phase transformation; BULK METALLIC-GLASS; DEFORMATION-INDUCED NANOCRYSTALLIZATION; MECHANICAL-PROPERTIES; MARTENSITIC-TRANSFORMATION; FORMING ABILITY; THERMAL-STABILITY; MATRIX COMPOSITES; AL; MICROSTRUCTURE; PHASE;
D O I
10.1016/j.actamat.2011.07.017
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In the present work we systematically investigated the formation of high-temperature B2 CuZr intermetallics in 36 metastable CuZr-based alloys. The results demonstrate that a B2 CuZr solid-phase transformation exists at high temperature. Based on continuous heating transformation diagrams the CuZr-based alloys can be classified into three different types, related to the precipitation and stability of the B2 phase. A new prediction strategy for the formation of different sized CuZr-based shape memory bulk metallic glass composites (BMGC) is proposed by considering the competition between vitrification, the precipitation of metastable B2 CuZr and room-temperature equilibrium phases. These insights are condensed into a new parameter, K = T-f/T-L, where T-f and T-L, are the final temperature of the B2 CuZr phase transformation during heating and the liquidus temperature of the alloy, respectively, which is suggested to predict and select a compositional region of different sized BMGC. This new approach could be of great significance for the development of metastable CuZr-based shape memory alloys with enhanced deformability. (C) 2011 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:6620 / 6630
页数:11
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