Polytypic transformations of the HfCr2 Laves phase - Part II: Kinetics of the polymorphic C14 → C15 transformation

被引:5
|
作者
Aufrecht, J. [1 ]
Leineweber, A. [1 ]
Mittemeijer, E. J. [1 ,2 ]
机构
[1] Max Planck Inst Intelligent Syst, D-70569 Stuttgart, Germany
[2] Univ Stuttgart, Inst Mat Sci, D-70569 Stuttgart, Germany
关键词
Laves phases; Phase transformation (crystallographic aspects kinetics and mechanisms); Defects: planar faults; Diffraction; (electron; neutron and X-ray); MODELS;
D O I
10.1016/j.intermet.2011.05.010
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
The progress of the polymorphic phase transformation C14 -> C15 of the HfCr2 Laves phase has been traced using two different parameters: (i) the normalized intensity of the 100 reflection of the C14 phase and, (ii) the ratio of certain lattice spacings common to all Laves phases. These tracing parameters allow determination of the degree of transformation. The effective activation energy of the phase transformation has been determined using the equivalent-time method on the basis of the isothermal annealing experiments for three alloys of different composition within the homogeneity range of the HfCr2 phase. For the stoichiometric alloy a value of 235-240 kJ/mol for the effective activation energy of the C14 -> C15 transformation has been obtained. The corresponding values for the non-stoichiometric alloys vary from 180 kJ/mol to 300 kJ/mol: the activation energy increases with decreasing Hf content, adopting the kinetic data determined from the lattice spacings. The magnitude of the values obtained for the effective activation energy indicates that jumps of individual atoms at kinks of gliding synchro-Shockley partial dislocation determine the kinetics of the polytypic shear transformation C14 -> C15 of the HfCr2 Laves phase. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1442 / 1447
页数:6
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