You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/39475
Full metadata record
DC FieldValueLanguage
dc.contributor.authorNeto, JAG-
dc.contributor.authorMontes, R.-
dc.contributor.authorCardoso, Arnaldo Alves-
dc.date.accessioned2014-05-20T15:30:01Z-
dc.date.accessioned2016-10-25T18:05:24Z-
dc.date.available2014-05-20T15:30:01Z-
dc.date.available2016-10-25T18:05:24Z-
dc.date.issued1999-12-06-
dc.identifierhttp://dx.doi.org/10.1016/S0039-9140(99)00184-8-
dc.identifier.citationTalanta. Amsterdam: Elsevier B.V., v. 50, n. 5, p. 959-966, 1999.-
dc.identifier.issn0039-9140-
dc.identifier.urihttp://hdl.handle.net/11449/39475-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/39475-
dc.description.abstractAn automated system with a C-18 bonded silica gel packed minicolumn is proposed for spectrophotometric detection of arsenic using flow-injection hydride generation following sorbent extraction preconcentration. Complexes formed between arsenic(III) and ammonium diethyl dithiophosphate (ADDP) are retained on a C-18 sorbent. The eluted As-DDP complexes are merged with a 1.5% (w/v) NaBH4 and the resulting solution is thereafter injected into the hydride generator/gas-liquid separator. The arsine generated is carried out by a stream of N-2 and trapped in an alkaline iodine solution in which the analyte is determined by the arsenomolybdenum blue method. With preconcentration time of 120 s, calibration in the 5.00-50.0 mu g As l(-1) range and sampling rate of about 20 samples h(-1) are achieved, corresponding to 36 mg ADDP plus 36 mg ammonium heptamolybdate plus 7 mg hydrazine sulfate plus 0.7 mg stannous chloride and about 7 mi sample consumed per determination. The detection limit is 0.06 mu g l(-1) and the relative standard deviation (n = 12) for a typical 17.0 mu g As l(-1) sample is ca. 6%. The accuracy was checked for arsenic determination in plant materials from the NIST (1572 citrus leaves; 1573 tomato leaves) and the results were in agreement with the certified values at 95% confidence level. Good recoveries (94-104%) of spiked tap waters, sugars and synthetic mixtures of trivalent and pentavalent arsenic were also found. (C) 1999 Elsevier B.V. B.V. All rights reserved.en
dc.format.extent959-966-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectspectrophotometrypt
dc.subjecthydride generationpt
dc.subjectflow-injection analysispt
dc.subjectammonium diethyl dithiophosphatept
dc.subjectarsenicpt
dc.titleSpectrophotometric detection of arsenic using flow-injection hydride generation following sorbent extraction preconcentrationen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniv Estadual Paulista, Dept Quim Analit, Inst Quim, BR-14801970 Araraquara, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, Dept Quim Analit, Inst Quim, BR-14801970 Araraquara, SP, Brazil-
dc.identifier.doi10.1016/S0039-9140(99)00184-8-
dc.identifier.wosWOS:000083990300006-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofTalanta-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.