Mathematical Modeling of Solid-State Diffusion during Mechanical Alloying

2006 ◽  
Vol 249 ◽  
pp. 105-110 ◽  
Author(s):  
Boris B. Khina ◽  
Boleslaw Formanek

It is known experimentally that solid-state interdiffusion is substantially enhanced during plastic deformation. This is especially noticeable in Mechanical Alloying (MA) which is used for producing a wide range of metastable materials (supersaturated solid solutions, amorphous phases, nanostructures) with unique properties. However, a physical mechanism of enhanced diffusion during MA is not clearly understood yet, and a comprehensive model of this complex phenomenon has not been developed so far. Moreover, the role of the diffusion process in MA is hotly debated in literature. In this work a new, self-consistent mathematical model of solid-state interdiffusion in a binary substitutional system A-B during periodic plastic deformation is developed. The model includes basic physical factors that affect diffusion, such as generation of non-equilibrium point defects by gliding screw dislocations during deformation and their relaxation in periods between impacts. The cross-link terms are considered, and interaction of point defects with edge dislocations and incoherent phase boundary A/B is taken into account. Computer simulation is performed using realistic data (e.g., quasi-equilibrium self-diffusion coefficients known in literature) and the process parameters typical of MA in a vibratory mill. A repeated “deformation-rest” cycle is considered. The results of modeling reveal the physical mechanism of the enhancement of solid-state diffusion by periodic plastic deformation during MA and demonstrate that within the frame of this approach supersaturated solid solutions can form within a reasonably short processing time.

1995 ◽  
Vol 66 (15) ◽  
pp. 1903-1905 ◽  
Author(s):  
J. Schilz ◽  
K. Pixius ◽  
W. Wunderlich ◽  
W. A. Kaysser

2002 ◽  
Vol 17 (1) ◽  
pp. 52-59 ◽  
Author(s):  
N.F. Gao ◽  
Y. Miyamoto

The joining of a Ti3SiC2 ceramic with a Ti–6Al–4V alloy was carried out at the temperature range of 1200–1400 °C for 15 min to 4 h in a vacuum. The total diffusion path of joining was determined to be Ti3SiC2/Ti5Si3Cx/Ti5Si3Cx + TiCx/TiCx/Ti. The reaction was rate controlled by the solid-state diffusion below 1350 °C and turned to the liquid-state diffusion controlled with a dramatic increase of parabolic rate constant Kp when the temperature exceeded 1350 °C. The TiCx tended to grow at the boundarywith the Ti–6Al–4V alloy at a higher temperature and longer holding time. TheTi3SiC2/Ti–6Al–4V joint is expected to be applied to implant materials.


2016 ◽  
Vol 686 ◽  
pp. 794-802 ◽  
Author(s):  
Yuan Yuan ◽  
Dajian Li ◽  
Yuanyuan Guan ◽  
Hans J. Seifert ◽  
Nele Moelans

Sign in / Sign up

Export Citation Format

Share Document