Forschungsbericht 1999-2000 | |
Institut für Materialphysik (ehemals Institut für Metallforschung) Wilhelm-Klemm-Str. 10 48149 Münster Tel. (0251) 83-3 35 71 Fax: (0251) 83-3 83 46 e-mail: mehrer@nwz.uni-muenster.de WWW: http://www.uni-muenster.de/Physik/MF Geschäftsführender Direktor: Prof. Dr. H. Mehrer | |
Forschungsschwerpunkte 1999 - 2000
Fachbereich 11 - Physik Institut für Materialphysik Diffusion in Metals, Intermetallics, and Silicides | ||||
Diffusion in intermetallic phases of the system Al-Fe
Self-diffusion of Fe and solute diffusion of In and Zn was studied as a function of temperature
in three alloys of the Fe-Al system with the nominal compositions Fe3Al,
Fe2Al and FeAl employing the radiotracer technique. Most of the measurements
were performed in the B2-structure regions of the phase diagram, some in the A2-region, and
few in the D03-structure region. Diffusion of In and Zn is slightly faster than Fe
diffusion in all three alloys. For Fe3Al the ordering transitions between A2 and
B2 and between B2 and D03 lead to slightly higher activation enthalpies in the
phases with the higher degree of order. Within the B2 phase-field increasing Al content also
leads to slight increases of activation enthalpies. This increase is correlated with an increase in
long-range order. Possible diffusion mechanisms are briefly discussed in the light of
experimental information on the defect structure in Fe-Al and in context with ab-initio
calculations of defect properties.
Interdiffusion studies were performed in the Fe-Al system using diffusion couples.
Concentration depth profiles were measured by electron microprobe analysis. Interdiffusion
coefficients deduced thereof show linear Arrhenius behaviour over the investigated
temperature range. From the interdiffusion coefficients Al diffusion coefficients were deduced
via Darken-Manning's equation using Fe tracer diffusion coefficients and theoretical results for
the thermodynamic factor. Al diffusion is in the same range as Fe diffusion.
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Hans-Joachim Peter