Metallothermic reduction of Sc2O3 using Al–Ca alloys equilibrated with CaO–CaCl2 flux

Through a fundamental study, the mechanism of metallothermic reduction of Sc2O3 in a CaO–CaCl2 flux system was determined via a thermochemical equilibrium method, aiming to produce an Al–Sc–Ca alloy (Sc: ∼0.5–3.6 wt%; Ca: ∼0.8–1.8 wt%) at 1273–1623 K. The effect of the oxygen potential on Sc reducti...

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Veröffentlicht in:Journal of materials research and technology 2024-01, Vol.28, p.327-334
Hauptverfasser: Lee, Byong Pil, Choi, Joon Sung, Ko, Jae Woong, Park, Jin Gyun, Min, Dong Joon, Sohn, Il
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Sprache:eng
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Zusammenfassung:Through a fundamental study, the mechanism of metallothermic reduction of Sc2O3 in a CaO–CaCl2 flux system was determined via a thermochemical equilibrium method, aiming to produce an Al–Sc–Ca alloy (Sc: ∼0.5–3.6 wt%; Ca: ∼0.8–1.8 wt%) at 1273–1623 K. The effect of the oxygen potential on Sc reduction was investigated to establish a general mechanism of Sc reduction. The effect of the CaO activity on the flux and content of Ca in the alloy was evaluated to confirm the role of Ca in the mechanism of metallothermic CaScO2.5 reduction. Under CaO-saturated flux, the Sc recovery increased significantly. The oxygen potential established by the Ca–CaO equilibrium was the driving force for enhanced Sc recovery. The Sc recovery was positively correlated with the excess Ca (amount of Ca oxidized directly to CaO) in the alloy. The enthalpy and entropy of the metallothermic reduction were calculated from the temperature-dependence of the equilibrium constant using the van't Hoff equation. The equilibrium constant decreased with increasing temperature, indicating that the reaction is exothermic. An Al–Sc alloy with a maximum Sc content of 3.98 % was obtained via metallothermic reduction. The formation of the desired Al3Sc compound was verified using X-ray diffraction. The uniform distribution of Sc in the alloy and faceted morphology of Al3Sc were confirmed by scanning electron microscopy (SEM) and electron probe micro-analysis (EPMA).
ISSN:2238-7854
DOI:10.1016/j.jmrt.2023.11.283