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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/31393
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dc.contributor.authorCorreia, PRM-
dc.contributor.authorOliveira, P. V.-
dc.contributor.authorNeto, JAG-
dc.contributor.authorNobrega, J. A.-
dc.date.accessioned2014-05-20T15:20:02Z-
dc.date.accessioned2016-10-25T17:53:02Z-
dc.date.available2014-05-20T15:20:02Z-
dc.date.available2016-10-25T17:53:02Z-
dc.date.issued2004-01-01-
dc.identifierhttp://dx.doi.org/10.1039/b400519h-
dc.identifier.citationJournal of Analytical Atomic Spectrometry. Cambridge: Royal Soc Chemistry, v. 19, n. 7, p. 917-922, 2004.-
dc.identifier.issn0267-9477-
dc.identifier.urihttp://hdl.handle.net/11449/31393-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/31393-
dc.description.abstractThe use of internal standardization for simultaneous atomic absorption spectrometry (SIMAAS) was investigated for Cd and Pb determination in whole blood. The comparison of thermochemical and physicochemical parameters allowed the selection of Ag, Bi, and Tl as internal standard candidates. Correlation graphs, plotted from the normalized absorbance signals (n = 20) of internal standard (axis y) versus analyte ( axis x), precision and accuracy were used to select Ag as the most appropriate internal standard. Blood samples were diluted (1 + 9) with 0.11% (m/v) Triton X-100 + 1.1% (v/v) HNO3 + 0.28% (m/v) NH4H2PO4 + 10 mug L-1 Ag+. Pyrolysis and atomization temperatures for the optimized heating program were 550 and 1700 degreesC, respectively. Characteristic masses based on integrated absorbance were 1.68 +/- 0.01 pg for Cd and 30.3 +/- 0.1 pg for Pb. The detection limits (DL) were 0.095 +/- 0.001 mug L-1 and 0.86 +/- 0.01 mug L-1 for Cd and Pb, respectively. The mean RSD for all determinations was the same for Cd (13 +/- 9%) with or without Ag as internal standard ( IS). on the other hand, the use of Ag as IS improved the RSD for Pb from 3.6 +/- 4.0% to 2.2 +/- 2.0%. An effective contribution of the internal standard Ag was verified in the recoveries of spiked samples (0.5 mug L-1 Cd2+ and 5.0 mug L-1 Pb2+). The mean recoveries were 81 +/- 8% and 91 +/- 4% for Cd, and 80 +/- 11% and 93 +/- 6% for Pb without and with IS correction, respectively. This is the first application of IS for a simultaneous determination by SIMAAS.en
dc.format.extent917-922-
dc.language.isoeng-
dc.publisherRoyal Soc Chemistry-
dc.sourceWeb of Science-
dc.titleSilver as internal standard for simultaneous determination of Cd and Pb in whole blood by electrothermal atomic absorption spectrometryen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)-
dc.description.affiliationUniv São Paulo, Inst Quim, BR-05513970 São Paulo, Brazil-
dc.description.affiliationUniv Estadual Paulista, Dept Quim Analit, BR-14801970 Araraquara, SP, Brazil-
dc.description.affiliationUniv Fed Sao Carlos, Dept Quim, BR-13560970 Sao Carlos, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, Dept Quim Analit, BR-14801970 Araraquara, SP, Brazil-
dc.identifier.doi10.1039/b400519h-
dc.identifier.wosWOS:000222472700016-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Analytical Atomic Spectrometry-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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