Published September 1, 2013
| Version v1
Journal article
Electrochemical formation of Dy–Ni alloys in molten NaCl–KCl–DyCl3
- 1. Environment, Safety and Health Organization, Kyoto University, Yoshida-honmachi, Sakyo-ku, Kyoto 606-8501 (Japan)
- 2. Graduate School of Energy Science, Kyoto University, Yoshida-honmachi, Sakyo-ku, Kyoto 606-8501 (Japan)
Description
The electrochemical formation of Dy–Ni alloys was investigated in a molten NaCl–KCl–DyCl3 (0.50 mol%) system at 973 K. Cyclic voltammetry and open-circuit potentiometry at a Ni electrode indicated the formation of several Dy–Ni alloy phases. Alloy samples were prepared by one- or two-step potentiostatic electrolysis of a Ni plate electrode at various potentials. Scanning electron microscopy observations and X-ray diffraction measurements confirmed the formation of DyNi2, DyNi3, Dy2Ni7, and DyNi5. The formation reactions of the Dy–Ni alloys and the corresponding potentials were determined, and the optimum electrolysis conditions for the separation of Nd and Dy from molten salts containing both Nd(III) and Dy(III) ions are discussed
Availability note (English)
Available from http://dx.doi.org/10.1016/j.electacta.2013.05.095Additional details
Identifiers
- DOI
- 10.1016/j.electacta.2013.05.095;
- PII
- S0013-4686(13)01018-9;
Publishing Information
- Journal Title
- Electrochimica Acta
- Journal Volume
- 106
- Journal Page Range
- p. 293-300
- ISSN
- 0013-4686
- CODEN
- ELCAAV
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45053029
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ALLOYS; DYSPROSIUM; ELECTROLYSIS; MOLTEN SALTS; POTENTIOMETRY; SCANNING ELECTRON MICROSCOPY; VOLTAMETRY; X-RAY DIFFRACTION
- Descriptors DEC
- CHEMICAL ANALYSIS; COHERENT SCATTERING; DIFFRACTION; ELECTRON MICROSCOPY; ELEMENTS; LYSIS; METALS; MICROSCOPY; QUANTITATIVE CHEMICAL ANALYSIS; RARE EARTHS; SALTS; SCATTERING; TITRATION; VOLUMETRIC ANALYSIS
Optional Information
- Copyright
- Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.