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dc.contributor.authorWelz, Bernhard-
dc.contributor.authorSantos, Lisia Maria Gobbo dos-
dc.contributor.authorAraujo, Rennan Geovanny Oliveira-
dc.contributor.authorJacob, Silvana do C.-
dc.contributor.authorVale, Maria Goreti R.-
dc.contributor.authorOkruss, Michael-
dc.contributor.authorRoss, Helmut Becker-
dc.creatorWelz, Bernhard-
dc.creatorSantos, Lisia Maria Gobbo dos-
dc.creatorAraujo, Rennan Geovanny Oliveira-
dc.creatorJacob, Silvana do C.-
dc.creatorVale, Maria Goreti R.-
dc.creatorOkruss, Michael-
dc.creatorRoss, Helmut Becker-
dc.date.accessioned2012-05-29T13:57:17Z-
dc.date.issued2010-
dc.identifier.issn0584-8547-
dc.identifier.urihttp://www.repositorio.ufba.br/ri/handle/ri/5980-
dc.descriptionTrabalho completo: acesso restrito, p. 258–262pt_BR
dc.description.abstractThe simultaneous determination of cadmium and iron in plant and soil samples has been investigated using high-resolution continuum source graphite furnace atomic absorption spectrometry. The primary cadmium resonance line at 228.802 nm and an adjacent secondary iron line at 228.726 nm, which is within the spectral interval covered by the charge-coupled device (CCD) array detector, have been used for the investigations. Due to the very high iron content in most of the soil samples the possibility has been investigated to reduce the sensitivity and extend the working range by using side pixels for measurement at the line wings instead of the line core. It has been found that the calibration curves measured at all the analytically useful pixels of this line consisted of two linear parts with distinctly different slopes. This effect has been independent of the positioning of the wavelength, i.e., if the Cd line or the Fe line was in the center of the CCD array. The most likely explanation for this unusual behavior is a significant difference between the instrument width ΔλInstr and the absorption line width ΔλAbs, which is quite pronounced in the case of Fe. Using both parts of the calibration curves and simultaneous measurement at the line center and at the wings made it possible to extend the working range for the iron determination to more than three orders of magnitude.pt_BR
dc.language.isoenpt_BR
dc.publisherElsevierpt_BR
dc.sourcehttp://dx.doi.org/10.1016/j.sab.2010.01.007pt_BR
dc.subjectHigh-resolution continuum source AASpt_BR
dc.subjectElectrothermal atomizationpt_BR
dc.subjectIron determinationpt_BR
dc.subjectCalibration graphspt_BR
dc.subjectLine wingspt_BR
dc.titleUnusual calibration curves observed for iron using high-resolution continuum source graphite furnace atomic absorption spectrometrypt_BR
dc.title.alternativeSpectrochimica Acta Part B: Atomic Spectroscopypt_BR
dc.typeArtigo de Periódicopt_BR
dc.identifier.numberv. 65, n. 3pt_BR
dc.embargo.liftdate10000-01-01-
Aparece nas coleções:Artigo Publicado em Periódico (Química)

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