Metastable intermetallic phases in the Al-Sm system

Date
2019-12-01
Authors
Zhou, S. H.
Meng, F. Q.
Kramer, Matthew
Ott, Ryan
Zhang, Feng
Ye, Zhuo
Jain, Shubhra
Napolitano, Ralph
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Ames Laboratory
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Abstract

The thermodynamic landscape involving several metastable phases in the glass-forming Al-Sm system is assessed, integrating experimental measurements and first principles calculations into a comprehensive CALPHAD description. The phases examined here include Al41Sm5-η, Al60Sm11-ε, Al5Sm-θ, Al5Sm-π and Al4Sm-γ, having basis stoichiometries from 9 to 20 at% Sm, a range over which the Al-fcc and Al3Sm phases are stable. Amongst the metastable phases examined, our findings indicate that the Al41Sm5-η and Al60Sm11-ε phases comprise the convex hull of minimum formation energies at absolute zero. Competitive crystallization processes were investigated through situ X-ray diffraction and differential scanning calorimetry and used to assess relative stability within the overall landscape. Asserting thermodynamic scenarios consistent with our measurements, temperature-dependent Gibbs free energies for the metastable phases are proposed along with the corresponding constrained phase diagrams, comprehensively showing metastable phases and associated invariant reactions. Assumptions and limitations of the proposed thermodynamic model are discussed with reference to available transport data.

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This is a manuscript of an article published as Zhou, S. H., F. Q. Meng, M. J. Kramer, R. T. Ott, F. Zhang, Z. Ye, S. Jain, and R. E. Napolitano. "Metastable intermetallic phases in the Al-Sm system." Materials Today Communications 21 (2019): 100673. DOI: 10.1016/j.mtcomm.2019.100673. Posted with permission.

Keywords
intermetallic, metastability, X-ray diffraction, CALPHAD, devitrification
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