Abstract
Solid-to-solid diffusion couples were assembled and annealed to examine the diffusion between pure Mg (99.96 pct) and Al (99.999 pct). Diffusion anneals were carried out at 573 K, 623 K and 673 K (300 °C, 350 °C and 400 °C) for 720, 360, and 240 hours, respectively. Optical and scanning electron microscopes were used to identify the formation of the intermetallic phases, γ-Mg17Al12, and β-Mg2Al3, as well as the absence of the ε-Mg23Al30 in the diffusion couples. The thicknesses of the γ-Mg17Al12 and β-Mg2Al3 phases were measured and the parabolic growth constants were calculated to determine the activation energies for growth. Concentration profiles were determined with electron microprobe analysis using pure elemental standards. Composition-dependent interdiffusion coefficients in Mg-solid solution, γ-Mg17Al12, β-Mg2Al3, and Al-solid solutions were calculated based on the Boltzmann-Matano analysis. Integrated and average effective interdiffusion coefficients for each phase were also calculated, and the magnitude was the highest for the β-Mg2Al3 phase, followed by γ-Mg17Al12, Al-solid solution, and Mg-solid solution. Intrinsic diffusion coefficients based on Huemann’s analysis (e.g., marker plane) were determined for the ~ Mg-62 at. pct Al in the β-Mg2Al3 phase. Activation energies and the pre-exponential factors for the interdiffusion and intrinsic diffusion coefficients were calculated for the temperature range examined. The β-Mg2Al3 phase was found to have the lowest activation energies for growth and interdiffusion among all four phases studied. At the marker location in the β-Mg2Al3 phase, the intrinsic diffusion of Al was found to be faster than that of Mg. Extrapolations of the impurity diffusion coefficients in the terminal solid solutions were made and compared with the available self-diffusion and impurity diffusion data from the literature. Thermodynamic factor, tracer diffusion coefficients, and atomic mobilities at the marker plane composition were approximated using the available literature values of Mg activity in the β-Mg2Al3 phase.
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Acknowledgments
This research was sponsored by the U.S. Department of Energy, Assistant Secretary for Energy Efficiency and Renewable Energy, Office of Vehicle Technologies, as part of the Lightweight Materials Program. The authors would also like to acknowledge the assistance of Dr. Emmanuel Perez and the staff engineers at the Materials Characterization Facility at the University of Central Florida.
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Manuscript submitted May 24, 2011.
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Brennan, S., Bermudez, K., Kulkarni, N.S. et al. Interdiffusion in the Mg-Al System and Intrinsic Diffusion in β-Mg2Al3 . Metall Mater Trans A 43, 4043–4052 (2012). https://doi.org/10.1007/s11661-012-1248-8
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DOI: https://doi.org/10.1007/s11661-012-1248-8