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Fabrication of Mg–Pr and Mg–Li–Pr alloys by electrochemical co-reduction from their molten chlorides

•Mg–Pr bulk alloys were first fabricated by potentiostatic electrolysis in LiCl–KCl eutectic melts.•The electrochemical co-reduction mechanism of Mg, Pr and Li ions was determined by different electrochemical techniques.•The proportion of Pr element in Mg–Pr alloys was controlled by changing the con...

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Published in:Electrochimica acta 2013-09, Vol.107, p.209-215
Main Authors: Tang, Hao, Yan, Yong-De, Zhang, Mi-Lin, Li, Xing, Han, Wei, Xue, Yun, Zhang, Zhi-Jian, He, Hui
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container_title Electrochimica acta
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Yan, Yong-De
Zhang, Mi-Lin
Li, Xing
Han, Wei
Xue, Yun
Zhang, Zhi-Jian
He, Hui
description •Mg–Pr bulk alloys were first fabricated by potentiostatic electrolysis in LiCl–KCl eutectic melts.•The electrochemical co-reduction mechanism of Mg, Pr and Li ions was determined by different electrochemical techniques.•The proportion of Pr element in Mg–Pr alloys was controlled by changing the concentration of PrCl3 in the melts during electrolysis process.•The ratio of Li element in Mg–Li–Pr alloys was regulated by changing the concentration of MgCl2 in the melts during electrolysis course. This work presents the electrochemical deposition of Mg–Pr and Mg–Li–Pr alloys on tungsten electrodes in molten LiCl–KCl–MgCl2–PrCl3 system. The electrochemical behavior of Mg(II), Pr(III), and Li(I) ions and alloy formation process in the melts were investigated by cyclic voltammetry (CV) and open circuit chronopotentiometry (OCP). Spherical bulk alloys were obtained by potentiostatic and galvanostatic electrolysis at −1.85V for 3h and −6.00Acm−2 for 2h, respectively. Pr and Li contents in the alloys were regulated by changing the concentration of PrCl3 and MgCl2 in the melts. The proportion of Pr was controlled from 9.73 to 19.93wt.% in Mg–Pr alloys and the ratio of Li changed from 0.10 to 37.27wt.% in Mg–Li–Pr alloys. X-ray diffraction (XRD) indicated that Mg–Pr alloys were solely comprised of α-Mg and Mg12Pr phases. However, in Mg–Li–Pr alloys, the phases were transformed from Mg12Pr to Mg3Pr, accompanied by the transition of matrix (from α-Mg to β-Li). The microstructure and micro-zone chemical analysis of Mg–Pr and Mg–Li–Pr alloys were characterized by scanning electron microscopy (SEM) with energy dispersive spectrometry (EDS).
doi_str_mv 10.1016/j.electacta.2013.05.129
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This work presents the electrochemical deposition of Mg–Pr and Mg–Li–Pr alloys on tungsten electrodes in molten LiCl–KCl–MgCl2–PrCl3 system. The electrochemical behavior of Mg(II), Pr(III), and Li(I) ions and alloy formation process in the melts were investigated by cyclic voltammetry (CV) and open circuit chronopotentiometry (OCP). Spherical bulk alloys were obtained by potentiostatic and galvanostatic electrolysis at −1.85V for 3h and −6.00Acm−2 for 2h, respectively. Pr and Li contents in the alloys were regulated by changing the concentration of PrCl3 and MgCl2 in the melts. The proportion of Pr was controlled from 9.73 to 19.93wt.% in Mg–Pr alloys and the ratio of Li changed from 0.10 to 37.27wt.% in Mg–Li–Pr alloys. X-ray diffraction (XRD) indicated that Mg–Pr alloys were solely comprised of α-Mg and Mg12Pr phases. However, in Mg–Li–Pr alloys, the phases were transformed from Mg12Pr to Mg3Pr, accompanied by the transition of matrix (from α-Mg to β-Li). 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This work presents the electrochemical deposition of Mg–Pr and Mg–Li–Pr alloys on tungsten electrodes in molten LiCl–KCl–MgCl2–PrCl3 system. The electrochemical behavior of Mg(II), Pr(III), and Li(I) ions and alloy formation process in the melts were investigated by cyclic voltammetry (CV) and open circuit chronopotentiometry (OCP). Spherical bulk alloys were obtained by potentiostatic and galvanostatic electrolysis at −1.85V for 3h and −6.00Acm−2 for 2h, respectively. Pr and Li contents in the alloys were regulated by changing the concentration of PrCl3 and MgCl2 in the melts. The proportion of Pr was controlled from 9.73 to 19.93wt.% in Mg–Pr alloys and the ratio of Li changed from 0.10 to 37.27wt.% in Mg–Li–Pr alloys. X-ray diffraction (XRD) indicated that Mg–Pr alloys were solely comprised of α-Mg and Mg12Pr phases. However, in Mg–Li–Pr alloys, the phases were transformed from Mg12Pr to Mg3Pr, accompanied by the transition of matrix (from α-Mg to β-Li). 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This work presents the electrochemical deposition of Mg–Pr and Mg–Li–Pr alloys on tungsten electrodes in molten LiCl–KCl–MgCl2–PrCl3 system. The electrochemical behavior of Mg(II), Pr(III), and Li(I) ions and alloy formation process in the melts were investigated by cyclic voltammetry (CV) and open circuit chronopotentiometry (OCP). Spherical bulk alloys were obtained by potentiostatic and galvanostatic electrolysis at −1.85V for 3h and −6.00Acm−2 for 2h, respectively. Pr and Li contents in the alloys were regulated by changing the concentration of PrCl3 and MgCl2 in the melts. The proportion of Pr was controlled from 9.73 to 19.93wt.% in Mg–Pr alloys and the ratio of Li changed from 0.10 to 37.27wt.% in Mg–Li–Pr alloys. X-ray diffraction (XRD) indicated that Mg–Pr alloys were solely comprised of α-Mg and Mg12Pr phases. However, in Mg–Li–Pr alloys, the phases were transformed from Mg12Pr to Mg3Pr, accompanied by the transition of matrix (from α-Mg to β-Li). 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subjects Alloys
Chlorides
Electrochemical co-reduction
Electrodes
Extraction of praseodymium
Magnesium base alloys
Melts
Mg–Li–Pr alloys
Mg–Pr alloys
Molten chlorides
Phases
Scanning electron microscopy
Tungsten base alloys
title Fabrication of Mg–Pr and Mg–Li–Pr alloys by electrochemical co-reduction from their molten chlorides
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