Room-temperature mechanically induced solid-state devitrifications of glassy Zr65Al7.5Ni10Cu12.5Pd5 alloy powders

被引:31
|
作者
El-Eskandarany, MS
Saida, J
Inoue, A
机构
[1] Japan Sci & Technol Corp, Inoue SuperLiquid Glass Project, Exploratory Res Adv Technol, Sendai, Miyagi 9820807, Japan
[2] Tohoku Univ, Interdisciplinary Res Ctr, Aoba Ku, Sendai, Miyagi 9808578, Japan
[3] Tohoku Univ, Mat Res Inst, Sendai, Miyagi 9800807, Japan
关键词
glassy alloys; Zr-based alloys; metastable phase; nanocrystalline materials; devitrifications;
D O I
10.1016/S1359-6454(03)00287-8
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The high-energy ball milling technique was employed for synthesizing a single phase of glassy Zr65Al7.5Ni10Cu12.5Pd5 alloy powder, using a room-temperature mechanical alloying method. Whereas the glass transition temperature of the obtained glassy alloy is 683 K, the crystallization temperature is 783 K. The mechanically alloyed Zr65Al7.5Ni10Cu12.5Pd5 Glassy powders maintain their unique disordered structure through a large supercooled liquid region (100 K). The possibility of devitrification of the synthetic glassy phase upon increasing the ball milling time was investigated. The results have shown that the glassy powder that is obtained after 173 ks of milling is subjected to numerous lattice imperfections and tends to transform into a metastable big-cube phase after further ball milling (259-432 ks). After 540 ks of milling, a complete glassy-metastable phase transformation is achieved and the end-product of this stage of milling is nanocrystalline big-cube powder that has a lattice constant of 1.2293 nm. As the milling time increases (720 ks), the obtained big-cube phase can no longer withstand the shear and impact stresses that are generated by the milling media and is transformed into a new metastable phase of nanocrystalline fcc-Zr65Al7.5Ni10Cu12.5Pd5. The fec-metastable phase transforms into a mixture of Zr2Cu and Zr6NiAl2 crystalline phases at rather high temperature, as high as 993 K. (C) 2003 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:4519 / 4532
页数:14
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