Speciation of Fe(II) and Fe(III) by using dispersive liquid-liquid microextraction and flame atomic absorption spectrometry

Detalhes bibliográficos
Autor(a) principal: Bahar,Soleiman
Data de Publicação: 2012
Outros Autores: Zakerian,Razieh
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000500021
Resumo: An extraction method for Fe(III) from water sample before spectrometric determination was developed. Dispersive liquid-liquid microextraction (DLLME) technique was successfully used as sample preparation method for flame atomic absorption spectrometry (FAAS). In the proposed approach, 8-hydroxy quinoline (oxine) was used as chelating agent, chloroform and methanol were selected as extraction and dispersive solvents, respectively. Some factors influencing the extraction efficiency of Fe(III) and its subsequent determination were studied and optimized, including: type and volume of extraction and dispersive solvents, pH of sample solution, concentration of the chelating agent and extraction time. Under the optimized conditions, the enrichment factor of this method for Fe(III) was 462. The limit of detection for Fe(III) was 4.5 ng mL-1, and the relative standard deviation (RSD) 1.4% (n = 5, c = 400 ng mL-1).
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spelling Speciation of Fe(II) and Fe(III) by using dispersive liquid-liquid microextraction and flame atomic absorption spectrometrydispersive liquid-liquid microextractionFe(II)Fe(III)flame atomic absorption spectrometrywater samplesAn extraction method for Fe(III) from water sample before spectrometric determination was developed. Dispersive liquid-liquid microextraction (DLLME) technique was successfully used as sample preparation method for flame atomic absorption spectrometry (FAAS). In the proposed approach, 8-hydroxy quinoline (oxine) was used as chelating agent, chloroform and methanol were selected as extraction and dispersive solvents, respectively. Some factors influencing the extraction efficiency of Fe(III) and its subsequent determination were studied and optimized, including: type and volume of extraction and dispersive solvents, pH of sample solution, concentration of the chelating agent and extraction time. Under the optimized conditions, the enrichment factor of this method for Fe(III) was 462. The limit of detection for Fe(III) was 4.5 ng mL-1, and the relative standard deviation (RSD) 1.4% (n = 5, c = 400 ng mL-1).Sociedade Brasileira de Química2012-05-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000500021Journal of the Brazilian Chemical Society v.23 n.5 2012reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532012000500021info:eu-repo/semantics/openAccessBahar,SoleimanZakerian,Razieheng2012-06-01T00:00:00Zoai:scielo:S0103-50532012000500021Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2012-06-01T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Speciation of Fe(II) and Fe(III) by using dispersive liquid-liquid microextraction and flame atomic absorption spectrometry
title Speciation of Fe(II) and Fe(III) by using dispersive liquid-liquid microextraction and flame atomic absorption spectrometry
spellingShingle Speciation of Fe(II) and Fe(III) by using dispersive liquid-liquid microextraction and flame atomic absorption spectrometry
Bahar,Soleiman
dispersive liquid-liquid microextraction
Fe(II)
Fe(III)
flame atomic absorption spectrometry
water samples
title_short Speciation of Fe(II) and Fe(III) by using dispersive liquid-liquid microextraction and flame atomic absorption spectrometry
title_full Speciation of Fe(II) and Fe(III) by using dispersive liquid-liquid microextraction and flame atomic absorption spectrometry
title_fullStr Speciation of Fe(II) and Fe(III) by using dispersive liquid-liquid microextraction and flame atomic absorption spectrometry
title_full_unstemmed Speciation of Fe(II) and Fe(III) by using dispersive liquid-liquid microextraction and flame atomic absorption spectrometry
title_sort Speciation of Fe(II) and Fe(III) by using dispersive liquid-liquid microextraction and flame atomic absorption spectrometry
author Bahar,Soleiman
author_facet Bahar,Soleiman
Zakerian,Razieh
author_role author
author2 Zakerian,Razieh
author2_role author
dc.contributor.author.fl_str_mv Bahar,Soleiman
Zakerian,Razieh
dc.subject.por.fl_str_mv dispersive liquid-liquid microextraction
Fe(II)
Fe(III)
flame atomic absorption spectrometry
water samples
topic dispersive liquid-liquid microextraction
Fe(II)
Fe(III)
flame atomic absorption spectrometry
water samples
description An extraction method for Fe(III) from water sample before spectrometric determination was developed. Dispersive liquid-liquid microextraction (DLLME) technique was successfully used as sample preparation method for flame atomic absorption spectrometry (FAAS). In the proposed approach, 8-hydroxy quinoline (oxine) was used as chelating agent, chloroform and methanol were selected as extraction and dispersive solvents, respectively. Some factors influencing the extraction efficiency of Fe(III) and its subsequent determination were studied and optimized, including: type and volume of extraction and dispersive solvents, pH of sample solution, concentration of the chelating agent and extraction time. Under the optimized conditions, the enrichment factor of this method for Fe(III) was 462. The limit of detection for Fe(III) was 4.5 ng mL-1, and the relative standard deviation (RSD) 1.4% (n = 5, c = 400 ng mL-1).
publishDate 2012
dc.date.none.fl_str_mv 2012-05-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000500021
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000500021
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532012000500021
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.23 n.5 2012
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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