2005
DOI: 10.1016/j.jpcs.2004.06.055
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Modeling of anodic dissolution of U–Pu–Zr ternary alloy in the molten LiCl–KCl electrolyte

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Cited by 44 publications
(24 citation statements)
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“…The amount of U-Zr loaded into the anode basket (typically 2-3 g) was always in excess compared to the amount of U dissolved by anodic oxidation, in order to prevent Zr oxidation (U is selectively dissolved since it is less noble than Zr [12] During electrodeposition, cathodic, anodic and cell potentials were monitored and samples (about 100 mg) were taken from the salt phase before and after each electrolysis.…”
Section: Methodsmentioning
confidence: 99%
“…The amount of U-Zr loaded into the anode basket (typically 2-3 g) was always in excess compared to the amount of U dissolved by anodic oxidation, in order to prevent Zr oxidation (U is selectively dissolved since it is less noble than Zr [12] During electrodeposition, cathodic, anodic and cell potentials were monitored and samples (about 100 mg) were taken from the salt phase before and after each electrolysis.…”
Section: Methodsmentioning
confidence: 99%
“…The cathodic cut-off potential was set to a value of −1.25 V which ensures conditions for a selective grouped separation of An from Ln [10,11]. A potential of −1.00 V was used as the anode cut-off potential to avoid oxidation of Zr from the U-Pu-Zr alloy [20]. For all runs under potentiostatic conditions, a cathode potential of −1.25 V was applied.…”
Section: Electrorefining Of U-pu-zr Alloymentioning
confidence: 99%
“…After 1600 C the anode potential suddenly increased and the electrolysis was stopped. According to the weight and composition of the UZr alloy, at this point the anode was depleted in U and the positive jump in anodic potential indicated the start of Zr dissolution (above À1.0 V) [17]. The anode was then replaced by the UPuZr alloy.…”
Section: Potential Evolution During Electrorefiningmentioning
confidence: 99%