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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/36309
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dc.contributor.authorFernandes, Kelly G.-
dc.contributor.authorNogueira, Ana Rita A.-
dc.contributor.authorGomes Neto, José Anchieta-
dc.contributor.authorNobrega, Joaquim A.-
dc.date.accessioned2014-05-20T15:26:04Z-
dc.date.accessioned2016-10-25T18:00:38Z-
dc.date.available2014-05-20T15:26:04Z-
dc.date.available2016-10-25T18:00:38Z-
dc.date.issued2007-02-28-
dc.identifierhttp://dx.doi.org/10.1016/j.talanta.2006.06.008-
dc.identifier.citationTalanta. Amsterdam: Elsevier B.V., v. 71, n. 3, p. 1118-1123, 2007.-
dc.identifier.issn0039-9140-
dc.identifier.urihttp://hdl.handle.net/11449/36309-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/36309-
dc.description.abstractThis work describes an analytical procedure for vanadium determination in human hair slurries by electrothermal AAS using longitudinal heating (LHGA) and transversal heating (THGA) graphite furnace atomizers. The samples were powdered using cryogenic grinding and the hair slurries containing 0.2% (m/v) were prepared in three different media for determination of vanadium: 0.14 mol L-1 HNO3, 0.1% (v/v) Triton X-100 and 0.1% (v/v) water soluble tertiary amines (CFA-C, pH 8). The limits of detection (LOD), limits of quantification (LOQ), and characteristic masses obtained were 0.28, 0.95 mu g L-1 and 35 pg (LHGA) and 0.34, 1.13 mu g L-1 and 78 pg (THGA), respectively. The accuracy of the analytical results obtained by the proposed procedure in both equipments was confirmed by a paired t-test at the 95% confidence level and compared with a conventional procedure based on acid digestion. (c) 2006 Elsevier B.V. All rights reserved.en
dc.format.extent1118-1123-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectvanadiumpt
dc.subjecthuman hairpt
dc.subjectslurry samplingpt
dc.subjectgraphite furnace AASpt
dc.subjectLHGApt
dc.subjectTHGApt
dc.titleDetermination of vanadium in human hair slurries by electrothermal atomic absorption spectrometryen
dc.typeoutro-
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)-
dc.contributor.institutionEmpresa Brasileira de Pesquisa Agropecuária (EMBRAPA)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniv Fed Sao Carlos, Grp Anal Instrumental Aplicada, Dept Quim, BR-13560970 Sao Carlos, Brazil-
dc.description.affiliationEmbrapa Pecuaria Sudeste, Sao Carlos, SP, Brazil-
dc.description.affiliationUniv Estadual Paulista, Dept Quim Analit, Araraquara, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, Dept Quim Analit, Araraquara, SP, Brazil-
dc.identifier.doi10.1016/j.talanta.2006.06.008-
dc.identifier.wosWOS:000244536800018-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofTalanta-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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