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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/68389
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dc.contributor.authorRissato, Sandra Regina-
dc.contributor.authorGalhiane, Mario Sergio-
dc.contributor.authorDe Souza, Antonio G.-
dc.contributor.authorApon, Bernhard M.-
dc.date.accessioned2014-05-27T11:21:36Z-
dc.date.accessioned2016-10-25T18:21:05Z-
dc.date.available2014-05-27T11:21:36Z-
dc.date.available2016-10-25T18:21:05Z-
dc.date.issued2005-09-01-
dc.identifierhttp://dx.doi.org/10.1590/S0103-50532005000600022-
dc.identifier.citationJournal of the Brazilian Chemical Society, v. 16, n. 5, p. 1038-1047, 2005.-
dc.identifier.issn0103-5053-
dc.identifier.urihttp://hdl.handle.net/11449/68389-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/68389-
dc.description.abstractThe aim of this paper was to apply a multiresidue method using Supercritical Fluid Extraction (SFE) and capillary gas chromatography with electron capture and mass spectrometry detections in the analysis of the levels of pesticide residues in fruits and vegetables. Single laboratory validation of both solid-liquid and supercritical fluid extraction methods was carried out for 32 compounds selected from four pesticide classes (organochlorine, organonitrogen, organophosphorus and pyretroid) in blank and fortified samples of fresh lettuce, potato, apple and tomato. Recoveries for the majority of pesticides from fortified samples at fortification level of 0.04-0.10 mg kg -1 ranged 74-96% for both methods and confirmation of pesticide identity was performed by gas-chromatography-mass spectrometry in a selected-ion monitoring mode. Both methods showed good limits of detection (less 0.01 mg kg-1, depending on the pesticide and matrix) and the SFE method minimized environmental concerns, time, and laboratory work. ©2005 Sociedade Brasileira de Química.en
dc.format.extent1038-1047-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectFruits, vegetables-
dc.subjectPesticides multiresidue analysis-
dc.subjectSupercritical fluid extraction-
dc.titleDevelopment of a supercritical fluid extraction method for simultaneous determination of organophosphorus, organohalogen, organonitrogen and pyretroids pesticides in fruit and vegetables and its comparison with a conventional method by GC-ECD and GC-MSen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Federal da Paraíba (UFPB)-
dc.contributor.institutionChromapon Inc.-
dc.description.affiliationDepartamento de Química Universidade Estadual Paulista, Av. Luiz Edmundo Carrijo Coube s/n, 17033-360 Bauru - SP-
dc.description.affiliationDepartamento de Química Universidade Federal da Paraíba, 58059-900 João Pessoa -PB-
dc.description.affiliationChromapon Inc., 9815 Carmenite Road, Whittier, CA 90605-
dc.description.affiliationUnespDepartamento de Química Universidade Estadual Paulista, Av. Luiz Edmundo Carrijo Coube s/n, 17033-360 Bauru - SP-
dc.identifier.doi10.1590/S0103-50532005000600022-
dc.identifier.scieloS0103-50532005000600022-
dc.identifier.wosWOS:000233012700022-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-30744467420.pdf-
dc.relation.ispartofJournal of the Brazilian Chemical Society-
dc.identifier.scopus2-s2.0-30744467420-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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