Amorphization and devitrification reactions in metallic glass alloys

被引:17
|
作者
Perepezko, J. H.
Hamann, J.
Hebert, R. J.
Roesner, H.
Wilde, G.
机构
[1] Univ Wisconsin, Dept Mat Sci & Engn, Madison, WI 53706 USA
[2] Res Ctr Karlsruhe, Inst Nanotechnol, D-76021 Karlsruhe, Germany
关键词
amorphous materials; nanostructure; nucleation; crystallization; deformation induced transitions; devitrification;
D O I
10.1016/j.msea.2005.11.074
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The devitrification of amorphous phases can be controlled to yield a high nucleation density and a nanoscale microstructure based upon either nanocrystals dispersed in an amorphous matrix or a completely nanocrystalline solid. For both rapidly solidified marginal glass forming alloys and slowly cooled bulk glass forming alloys, the high nucleation densities are related to heterogeneous nucleation reactions that are sensitive to the initial as-prepared state of the amorphous phase. Selective doping of Al based glasses, for example, can enhance the nucleation densities from 10(21) to 10(23) m(-3). The heterogeneous nature of the local structure is reflected also in the response of amorphous alloys to deformation-induced synthesis of nanocrystals. Moreover, kinetics studies have revealed that the governing devitrification reactions often proceed under transient conditions that can lead to relatively stable and robust nanoscale microstructures. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:84 / 89
页数:6
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