Kinetics of diffusional phase transformation in multicomponent elastic-plastic materials

被引:21
作者
Fischer, FD
Simha, NK
Svoboda, J
机构
[1] Montan Univ Leoben, Inst Mech, A-8700 Leoben, Austria
[2] Austrian Acad Sci, Erich Schmid Inst Mat Sci, A-8700 Leoben, Austria
[3] Univ Miami, Dept Mech Engn, Coral Gables, FL 33124 USA
[4] Acad Sci Czech Republ, Inst Phys Mat, CZ-61662 Brno, Czech Republic
来源
JOURNAL OF ENGINEERING MATERIALS AND TECHNOLOGY-TRANSACTIONS OF THE ASME | 2003年 / 125卷 / 03期
关键词
D O I
10.1115/1.1586939
中图分类号
TH [机械、仪表工业];
学科分类号
0802 ;
摘要
The goal of this paper is to derive a micromechanics framework to study the kinetics of transformation due to interface migration in elastic-plastic materials. Both coherent and incoherent interfaces as well as interstitial and substitutional atomic diffusion are considered, and diffusional transformations are contrasted with martensitic ones. Assuming the same dissipation for the rearrangement of all substitutional components and no dissipation due to diffusion in an interface in the case of a multicomponent diffusional transformation, we show that the chemical driving force of the interface motion is represented by the jump in the chemical potential of the lattice forming constituent. Next, the mechanical driving force is shown to have the same,form for both coherent and friction-less (sliding) interfaces in an elastic-plastic material. Using micromechanics arguments we show that the dissipation and consequently the average mechanical driving force at the interface due to transformation in a microregion can be estimated in terms of the bulk fields. By combining the chemical and mechanical parts, we obtain the kinetic equation,for the volume fraction of the transformed phase due to a multicomponent diffusional transformation. Finally, the communication between individual microregions and the macroscale is expressed by proper parameters and initial as well as boundary conditions. This concept can be implemented into standard frameworks of computational mechanics.
引用
收藏
页码:266 / 276
页数:11
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