2007
DOI: 10.1016/j.jallcom.2006.09.056
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An electrochemical method for the preparation of Mg–Li alloys at low temperature molten salt system

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Cited by 44 publications
(23 citation statements)
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“…Therefore, electrochemical methods for the preparation of magnesium base alloys are drawing increased attention. In our previous study, we have successfully prepared Mg-Li alloys on a magnesium cathode from the LiCl-KCl melts and investigated the electrochemical formation process and phase control of Mg-Li alloys at 693-783 K [6,7]. However, in these methods, remaining some shortcomings include a long process time and high energy consumption.…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, electrochemical methods for the preparation of magnesium base alloys are drawing increased attention. In our previous study, we have successfully prepared Mg-Li alloys on a magnesium cathode from the LiCl-KCl melts and investigated the electrochemical formation process and phase control of Mg-Li alloys at 693-783 K [6,7]. However, in these methods, remaining some shortcomings include a long process time and high energy consumption.…”
Section: Introductionmentioning
confidence: 99%
“…[6] Our group has exploited successfully a relatively simpler electrochemical method in which the codeposition of the Mg-Li binary alloys is achieved on a molybdenum at KCl-LiCl (50:50 wt pct) melts containing different MgCl 2 concentrations at 943 K (670°C). [7] Nowadays, the electrochemical codeposition has been used widely to prepare alloys. Iida et al [8][9][10] investigated the electrochemical codeposition of Sm-Co alloys from LiCl-KCl-SmCl 3 -CoCl 2 melts, and they studied electrochemical formation of Yb-Ni and Sm-Ni alloy films by Li codeposition method from chloride melts.…”
Section: Introductionmentioning
confidence: 99%
“…Because the amount of CaO-B 2 O 3 sintered sample used in the experiment was 10 g, the theoretical output of CaB 6 was calculated to be 3.96 g. According to the actual output of CaB 6 (1.03 g) collected during the experiment, the product formation rate only reached 25%. Based on the experimental fact that the CaO-B 2 O 3 sintered samples were deposited at the bottom of the crucible after completion of the electrolytic run, we can further infer that the lower product formation rate is attributed to the slow diffusion of the CaO-B 2 O 3 sintered samples in the molten salt [10,11]. In the high temperature CaCl 2 -NaCl molten salt, CaO has better solubility and diffuses more easily in the molten salt through molecular heat-proliferation movement.…”
Section: Resultsmentioning
confidence: 85%