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Cited 24 time in webofscience Cited 24 time in scopus
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dc.contributor.authorLee, JY-
dc.contributor.authorKim, JW-
dc.contributor.authorChang, BY-
dc.contributor.authorKim, HT-
dc.contributor.authorPark, SM-
dc.date.accessioned2015-06-25T02:31:52Z-
dc.date.available2015-06-25T02:31:52Z-
dc.date.created2009-03-16-
dc.date.issued2004-01-
dc.identifier.issn0013-4651-
dc.identifier.other2015-OAK-0000004245en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/11140-
dc.description.abstractEffects of ethoxylated alpha-naphtholsulfonic acid (ENSA) on the initial stages of tin plating have been studied on iron electrodes in an acidic stannous sulfate solution containing phenolsulfonic acid as a supporting electrolyte using potentiodynamic polarization, electrochemical quartz crystal microbalance (EQCM), scanning probe microscopy (SPM), and electrochemical impedance spectroscopy techniques. The smallest exchange current density and a larger transfer coefficient are observed at a typical ENSA concentration used in industrial plating baths, i.e., 0.013 M. The SPM imaging and EQCM measurements show that ENSA molecules form a compact structure by interacting with neighboring molecules at the iron surface, which controls the mass transport for Sn(II) reduction. The EQCM studies indicate that the ENSA molecules remain stably adsorbed on the electrode surface at considerably high overpotentials. The ENSA molecules present in both the tin layers and the solution are found to slow the hydrogen evolution reaction at, as well as the corrosion process of, the tin-plated electrode, acting as an anticorrosion agent in commercial tin plating baths. (C) 2004 The Electrochemical Society.-
dc.description.statementofresponsibilityopenen_US
dc.languageEnglish-
dc.publisherELECTROCHEMICAL SOC INC-
dc.relation.isPartOfJOURNAL OF THE ELECTROCHEMICAL SOCIETY-
dc.rightsBY_NC_NDen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kren_US
dc.titleEffects of ethoxylated alpha-naphtholsulfonic acid on tin electroplating at iron electrodes-
dc.typeArticle-
dc.contributor.college화학과en_US
dc.identifier.doi10.1149/1.1690289-
dc.author.googleLee, JYen_US
dc.author.googleKim, JWen_US
dc.author.googlePark, SMen_US
dc.author.googleKim, HTen_US
dc.author.googleChang, BYen_US
dc.relation.volume151en_US
dc.relation.issue5en_US
dc.contributor.id10200281en_US
dc.relation.journalJOURNAL OF THE ELECTROCHEMICAL SOCIETYen_US
dc.relation.indexSCI급, SCOPUS 등재논문en_US
dc.relation.sciSCIen_US
dc.collections.nameJournal Papersen_US
dc.type.rimsART-
dc.identifier.bibliographicCitationJOURNAL OF THE ELECTROCHEMICAL SOCIETY, v.151, no.5, pp.C333 - C341-
dc.identifier.wosid000221436900033-
dc.date.tcdate2019-01-01-
dc.citation.endPageC341-
dc.citation.number5-
dc.citation.startPageC333-
dc.citation.titleJOURNAL OF THE ELECTROCHEMICAL SOCIETY-
dc.citation.volume151-
dc.contributor.affiliatedAuthorPark, SM-
dc.identifier.scopusid2-s2.0-2942558549-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc18-
dc.description.scptc18*
dc.date.scptcdate2018-10-274*
dc.type.docTypeArticle-
dc.subject.keywordPlusCRITICAL MICELLE CONCENTRATION-
dc.subject.keywordPlusSULFATE-SOLUTIONS-
dc.subject.keywordPlusELECTROCHEMICAL PROBE-
dc.subject.keywordPlusPARTITION-COEFFICIENT-
dc.subject.keywordPlusORGANIC ADDITIVES-
dc.subject.keywordPlusBRIGHT TIN-
dc.subject.keywordPlusTHIOUREA-
dc.subject.keywordPlusNUCLEATION-
dc.subject.keywordPlusDEPOSITION-
dc.subject.keywordPlusELECTROCRYSTALLIZATION-
dc.relation.journalWebOfScienceCategoryElectrochemistry-
dc.relation.journalWebOfScienceCategoryMaterials Science, Coatings & Films-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaElectrochemistry-
dc.relation.journalResearchAreaMaterials Science-

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