Origin of abnormal multi-stage martensitic transformation behavior in aged Ni-rich Ti-Ni shape memory alloys

被引:244
作者
Fan, GL
Chen, W
Yang, S
Zhu, JH
Ren, XB [1 ]
Otsuka, K
机构
[1] Xi An Jiao Tong Univ, Multidisciplinary Mat Res Ctr, Xian 710049, Peoples R China
[2] Xi An Jiao Tong Univ, State Key Lab Mech Behav Mat, Xian 710049, Peoples R China
[3] Xi An Jiao Tong Univ, State Key Lab Elect Insulat Power Equipment, Xian 710049, Peoples R China
[4] Xi An Jiao Tong Univ, Dept Phys, Xian 710049, Peoples R China
[5] Natl Inst Mat Sci, Mat Phys Grp, Tsukuba, Ibaraki 3050047, Japan
基金
日本科学技术振兴机构; 中国国家自然科学基金;
关键词
shape memory alloy; Ti-Ni; single crystal; martensitic transformation; aging; precipitation;
D O I
10.1016/j.actamat.2004.06.002
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
After aging Ni-rich Ti-Ni alloys exhibit finely dispersed Ti3Ni4 particles embedded in B2 matrix. Under such condition the B2 matrix normally undergoes two-stage martensitic transformation B2-R-B19'. However, there is also evidence of three-stage transformation. The origin of such abnormal three-stage transformation remains controversial. In the present study, we made a comparative study between single crystals and corresponding polycrystals and found that all single crystals exhibit normal two-stage transformation, being independent of Ni content. By comparison, polycrystals with low Ni content (50.6Ni) show three-stage transformation, but those with high Ni content (51.5Ni) again exhibit normal two-stage transformation. These new findings are consistent with a simple scenario that different transformation behaviors are a result of competition between preferential grain-boundary precipitation of Ti3Ni4 particles and a tendency for homogeneous precipitation when supersaturation of Ni is large. This is a natural consequence of the nucleation kinetics of supersaturated solid solutions in polycrystalline state. The above scenario not only explains the abnormal three-stage transformation but also the normal two-stage transformation. (C) 2004 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:4351 / 4362
页数:12
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