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dc.contributor.authorSantos, D. P.-
dc.contributor.authorBergamini, M. F.-
dc.contributor.authorFogg, A. G.-
dc.contributor.authorZanoni, Maria Valnice Boldrin-
dc.date.accessioned2014-05-20T15:24:59Z-
dc.date.accessioned2016-10-25T17:59:19Z-
dc.date.available2014-05-20T15:24:59Z-
dc.date.available2016-10-25T17:59:19Z-
dc.date.issued2005-09-01-
dc.identifierhttp://dx.doi.org/10.1007/s00604-005-0374-z-
dc.identifier.citationMicrochimica Acta. Vienna: Springer Wien, v. 151, n. 1-2, p. 127-134, 2005.-
dc.identifier.issn1436-5073-
dc.identifier.urihttp://hdl.handle.net/11449/35476-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/35476-
dc.description.abstractGlassy carbon electrodes were coated with films of poly( glutamic acid) ( PG), and the modified electrode proved to be very effective in the oxidation of caffeic acid. The performance of the film was also tested with ascorbic acid, coumaric acid, ferulic acid, sinapic acid and chlorogenic acid. At pH 5.6, all the hydroxycinnamic acids yield a higher peak current intensity when oxidized after incorporation in the PG-modified electrode, and only the oxidation of ascorbic acid exhibits overpotential reduction. At pH 3.5 only caffeic and chlorogenic acid are incorporated in the modified electrode and exhibit a well-defined oxidation wave at +0.51 V and +0.48 V, which is the base for their determination. Linear calibration graphs were obtained from 9 x 10(-6) mol L-1 to 4 x 10(-5) mol L-1 caffeic acid by linear voltammetric scan and from 4 x 10(-6) mol L-1 to 3 x 10(-5) mol L-1 by square wave voltammetric scan. The method was successfully applied to the determination of caffeic acid in red wine samples without interference from other hydroxycinnamic acids or ascorbic acid.en
dc.format.extent127-134-
dc.language.isoeng-
dc.publisherSpringer-
dc.sourceWeb of Science-
dc.subjecthydroxycinnamatespt
dc.subjectcaffeic acidpt
dc.subjectpoly(glutamic acid)pt
dc.subjectmodified electrodept
dc.titleApplication of a glassy carbon electrode modified with poly(glutamic acid) in caffeic acid determinationen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniv Luton-
dc.contributor.institutionLoughborough Univ Technol-
dc.description.affiliationUniv Estadual Paulista, Inst Quim, Dept Quim Analit, BR-14800900 Araraquara, SP, Brazil-
dc.description.affiliationUniv Luton, Luton Inst, Luton LU1 5DU, Beds, England-
dc.description.affiliationLoughborough Univ Technol, Loughborough LE11 3TU, Leics, England-
dc.description.affiliationUnespUniv Estadual Paulista, Inst Quim, Dept Quim Analit, BR-14800900 Araraquara, SP, Brazil-
dc.identifier.doi10.1007/s00604-005-0374-z-
dc.identifier.wosWOS:000231797900017-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofMicrochimica Acta-
dc.identifier.orcid0000-0002-2296-1393-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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