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Utilize este identificador para citar ou criar um link para este item: http://acervodigital.unesp.br/handle/11449/39352
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dc.contributor.authorPereira, Francisco C.-
dc.contributor.authorMoretto, Ligia M.-
dc.contributor.authorDe Leo, Manuela-
dc.contributor.authorZanoni, Maria Valnice Boldrin-
dc.contributor.authorUgo, Paolo-
dc.date.accessioned2014-05-20T15:29:52Z-
dc.date.accessioned2016-10-25T18:05:11Z-
dc.date.available2014-05-20T15:29:52Z-
dc.date.available2016-10-25T18:05:11Z-
dc.date.issued2006-08-04-
dc.identifierhttp://dx.doi.org/10.1016/j.aca.2006.05.056-
dc.identifier.citationAnalytica Chimica Acta. Amsterdam: Elsevier B.V., v. 575, n. 1, p. 16-24, 2006.-
dc.identifier.issn0003-2670-
dc.identifier.urihttp://hdl.handle.net/11449/39352-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/39352-
dc.description.abstractA procedure for the standardization of ensembles of gold nanodisk electrodes (NEE) of 30 nm diameter is presented, which is based on the analytical comparison between experimental cyclic voltammograms (CV) obtained at the NEEs in diluted solutions of redox probes and CV patterns obtained by digital simulation. Possible origins of defects sometimes found in NEEs are discussed. Selected NEEs are then employed for the study of the electrochemical oxidation of iodide in acidic solutions. CV patterns display typical quasi-reversible behavior which involves associated chemical reactions between adsorbed and solution species. The main CV characteristics at the NEE compare with those observed at millimeter sized gold disk electrodes (Au-macro), apart a slight shift in E1/2 values and slightly higher peak to peak separation at the NEE. The detection limit (DC) at NEEs is 0.3 mu M, which is more than one order of magnitude lower than DL at the Au-macro (4 RM). The mechanism of the electrochemical oxidation of iodide at NEEs is discussed. Finally, NEEs are applied to the direct determination of iodide at micromolar concentration levels in real samples, namely in some ophthalmic drugs and iodized table salt. (c) 2006 Elsevier B.V. All rights reserved.en
dc.format.extent16-24-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectnanoelectrode ensemblespt
dc.subjectiodidept
dc.subjectvoltammetrypt
dc.subjectedible saltpt
dc.subjectophthalmic drugspt
dc.titleGold nanoelectrode ensembles for direct trace electroanalysis of iodideen
dc.typeoutro-
dc.contributor.institutionUniv Venice-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Federal do Rio Grande do Norte (UFRN)-
dc.description.affiliationUniv Venice, Dipartimento Chim Fis, I-30123 Venice, Italy-
dc.description.affiliationUNESP, Inst Chem, Dept Analyt Chem, BR-14800900 Araraquara, SP, Brazil-
dc.description.affiliationUniv Fed Rio Grande Norte, Dept Chem, BR-59072970 Natal, RN, Brazil-
dc.description.affiliationUnespUNESP, Inst Chem, Dept Analyt Chem, BR-14800900 Araraquara, SP, Brazil-
dc.identifier.doi10.1016/j.aca.2006.05.056-
dc.identifier.wosWOS:000239674600003-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofAnalytica Chimica Acta-
dc.identifier.orcid0000-0002-2296-1393-
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