dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorUniv Luton
dc.contributorLoughborough Univ Technol
dc.date.accessioned2014-05-20T15:21:38Z
dc.date.accessioned2022-10-05T16:12:23Z
dc.date.available2014-05-20T15:21:38Z
dc.date.available2022-10-05T16:12:23Z
dc.date.created2014-05-20T15:21:38Z
dc.date.issued2006-01-01
dc.identifierDyes and Pigments. Oxford: Elsevier B.V., v. 68, n. 1, p. 19-25, 2006.
dc.identifier0143-7208
dc.identifierhttp://hdl.handle.net/11449/32758
dc.identifier10.1016/j.dyepig.2004.12.008
dc.identifierWOS:000232169400003
dc.identifier0000-0002-2296-1393
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3905248
dc.description.abstractThe Indanthrene Olive Green B (C.I. Vat Green 3; C.I. 69500), VG3 dye, a vat dye bearing an anthraquinonoid group and a ketonic group, can be detected by differential pulse voltammetry in alkaline solution using glassy carbon electrode. on the adsorbed form the dyes are reduced into three cathodic steps at -0.54 V, -0.65 V and -0.93 V vs Ag/AgCl. The leuco form generated after previous electrolysis at controlled potential of -1 V can be detected by voltammetry due to its reoxidation peak at -0.08 V. An analytical method is proposed for determining the vat dye using modified glassy carbon electrode by electrochemical activation in alkaline medium. Linear relationship was observed between l(Pu) vs concentration from I X 10(-5) mol L-1 to 6.0 X 10(-4) mol L-1. The detection limit was calculated to be 9.3 X 10(-6) mol L-1. (c) 2005 Elsevier Ltd. All rights reserved.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationDyes and Pigments
dc.relation3.767
dc.relation0,819
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectindanthrene dyes
dc.subjectvoltammetric reduction
dc.subjectdye determination
dc.subjectvat dyes
dc.titleApplication of voltammetric technique to the analysis of indanthrene dye in alkaline solution
dc.typeArtigo


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