Publicação:
Simultaneous determination of As, Cu, Mn, Sb, and Se in drinking water by GFAAS with transversely heated graphite atomizer and longitudinal zeeman-effect background correction

dc.contributor.authorFilho, Volnei Resta A. [UNESP]
dc.contributor.authorFernandes, Kelly G. [UNESP]
dc.contributor.authorDe Moraes, Mercedes [UNESP]
dc.contributor.authorGomes Neto, José A. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:20:24Z
dc.date.available2014-05-27T11:20:24Z
dc.date.issued2002-01-01
dc.description.abstractA method has been developed for the direct and simultaneous determination of As, Cu, Mn, Sb, and Se in drinking water by electrothermal atomic absorption spectrometry (ETAAS) using a transversely heated graphite tube atomizer (THGA) with longitudinal Zeeman-effect background correction. The thermal behavior of analytes during the pyrolysis and atomization stages was investigated in 0.028 mol L-1 HNO3, 0.14 mol L-1 HNO3 and 1 + 1 (v/v) diluted water using mixtures of Pd(NO3)2 + Mg(NO3)2 as the chemical modifier. With 5 μg Pd + 3 μg Mg as the modifier, the pyrolysis and atomization temperatures of the heating program of the atomizer were fixed at 1400°C and 2100°C, respectively, and 20 μL of the water sample (sample + 0.28 mol L-1 HNO3, 1 + 1, v/v), dispensed into the graphite tube, analytical curves were established ranging from 5.00 -50.0 μg L-1 for As, Sb, Se; 10.0 - 100 μg L-1 for Cu; and 20.0 - 200 μg L-1 for Mn. The characteristic masses were around 39 pg As, 17 pg Cu, 60 pg Mn, 43 pg Sb, and 45 pg Se, and the lifetime of the tube was around 500 firings. The limits of detection (LOD) based on integrated absorbance (0.7 μg L-1 As, 0.2 μg L-1 Cu, 0.6 μg L-1 Mn, 0.3 μg L-1 Sb, 0.9 μg L-1 Se) exceeded the requirements of the Brazilian Food Regulations (decree # 310-ANVS from the Health Department), which established the maximum permissible level for As, Cu, Mn, Sb, and Se at 50 μg L-1, 1000 μg L-1, 2000 μg L-1, 5 μg L-1, and 50 μg L-1, respectively. The relative standard deviations (n = 12) were typically < 5.3% for As, < 0.5% for Cu, < 2.1% for Mn, < 11.7% for Sb, and < 9.2% for Se. The recoveries of As, Cu, Mn, Sb, and Se added to the mineral water samples varied from 102-111%, 91-107%, 92-109%, 89-97%, and 101-109%, respectively. Accuracy for the determination of As, Cu, Mn, Sb, and Se was checked using standard reference materials NIST SRM 1640 - Trace Elements in Natural Water, NIST SRM 1643d - Trace Elements in Water, and 10 mineral water samples. A paired t-test showed that the results were in agreement with the certified values of the standard reference materials at the 95% confidence level.en
dc.description.affiliationInstituto de Química Universidade Estadual Paulista, P.O. Box 355, 14801-970 Araraquara-SP
dc.description.affiliationUnespInstituto de Química Universidade Estadual Paulista, P.O. Box 355, 14801-970 Araraquara-SP
dc.format.extent7-11
dc.identifier.citationAtomic Spectroscopy, v. 23, n. 1, p. 7-11, 2002.
dc.identifier.issn0195-5373
dc.identifier.scopus2-s2.0-0036126948
dc.identifier.urihttp://hdl.handle.net/11449/66806
dc.language.isoeng
dc.relation.ispartofAtomic Spectroscopy
dc.relation.ispartofjcr1.123
dc.relation.ispartofsjr0,327
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectantimony
dc.subjectarsenic
dc.subjectcopper
dc.subjectdrinking water
dc.subjectgraphite
dc.subjectmagnesium derivative
dc.subjectmanganese
dc.subjectnitric oxide
dc.subjectpalladium complex
dc.subjectselenium
dc.subjecttrace element
dc.subjectatomic absorption spectrometry
dc.subjectchemical analysis
dc.subjectinstrumentation
dc.subjectmaterials
dc.subjectmolecular weight
dc.subjectpyrolysis
dc.subjectreference value
dc.subjectwater analysis
dc.subjectwater contamination
dc.subjectwater sampling
dc.titleSimultaneous determination of As, Cu, Mn, Sb, and Se in drinking water by GFAAS with transversely heated graphite atomizer and longitudinal zeeman-effect background correctionen
dc.typeArtigo
dspace.entity.typePublication

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