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Effect of cathode material on the electrorefining of U in LiCl-KCl molten salts

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dc.contributor.authorLee, Chang Hwa-
dc.contributor.authorKim, Tack-Jin-
dc.contributor.authorPark, Sungbin-
dc.contributor.authorLee, Sung-Jai-
dc.contributor.authorPaek, Seung-Woo-
dc.contributor.authorAhn, Do-Hee-
dc.contributor.authorCho, Sung-Ki-
dc.date.accessioned2024-02-27T13:00:36Z-
dc.date.available2024-02-27T13:00:36Z-
dc.date.issued2017-05-
dc.identifier.issn0022-3115-
dc.identifier.issn1873-4820-
dc.identifier.urihttps://scholarworks.bwise.kr/kumoh/handle/2020.sw.kumoh/26990-
dc.description.abstractThe influence of cathode materials on the U electrorefining process is examined using electrochemical measurements and SEM-EDX observations. Stainless steel (STS), Mo, and W electrodes exhibit similar U reduction/oxidation behavior in 500 degrees C LiCl-KCl-UC13 molten salts, as revealed by the cyclic voltammo-grams. However, slight shifts are observed in the cathodic and anodic peak potentials at the STS electrode, which are related to the fast reduction/oxidation kinetics associated with this electrode. The U deposits on the Mo and W electrodes consist of uniform dendritic chains of U in rhomboidal-shaped crystals, whereas several U dendrites protruding from the surface are observed for the STS electrode. EDX mapping of the electrode surfaces reveals that simple scraping of the U dendrites from W electrodes pretreated in dilute HCI-l solutions to dissolve the residual salt, results in clear removal of the U deposits, whereas a thick U deposit layer strongly adheres to the STS electrode surface even after treatment. This result is expected to contribute to the development of an effective and continuous U recovery process using electrorefining. (C) 2017 Elsevier B.V. All rights reserved.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER SCIENCE BV-
dc.titleEffect of cathode material on the electrorefining of U in LiCl-KCl molten salts-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.jnucmat.2017.03.023-
dc.identifier.wosid000400218100023-
dc.identifier.bibliographicCitationJOURNAL OF NUCLEAR MATERIALS, v.488, pp 210 - 214-
dc.citation.titleJOURNAL OF NUCLEAR MATERIALS-
dc.citation.volume488-
dc.citation.startPage210-
dc.citation.endPage214-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaNuclear Science & Technology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryNuclear Science & Technology-
dc.subject.keywordPlusURANIUM-
dc.subject.keywordPlusREDUCTION-
dc.subject.keywordPlusGRAPHITE-
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