Determination of copper in human hair and tea samples after dispersive liquid-liquid microextraction based on solidification of floating organic drop (DLLME-SFO)

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=S0103-50532012000600023
Resumo: A simple method of dispersive liquid-liquid microextraction-solidified floating organic drop (DLLME-SFO) prior to flame atomic absorption spectrometry was successfully used for separating and preconcentrating copper in human hair and tea samples. The proposed method was simple, cheap, and has high precision. In this study, optimization of experimental parameters influencing the extraction, such as type and volume of extraction and disperser solvents, pH, the amount of chelating agent and extraction time was normally carried out using a step-by-step approach, in which each factor was varied sequentially. The effect of the interfering ions on the analytes recovery was also investigated. The calibration graph was linear in the range of 5-200 ng mL-1 with limit of detection of 3.4 ng mL-1. The relative standard deviation (RSD) was 0.7% (n = 10, C = 2 ng mL-1) and the enhancement factor was 28.
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spelling Determination of copper in human hair and tea samples after dispersive liquid-liquid microextraction based on solidification of floating organic drop (DLLME-SFO)dispersive liquid-liquid microextractionsolidificationcopper determinationtea and human hair analysisA simple method of dispersive liquid-liquid microextraction-solidified floating organic drop (DLLME-SFO) prior to flame atomic absorption spectrometry was successfully used for separating and preconcentrating copper in human hair and tea samples. The proposed method was simple, cheap, and has high precision. In this study, optimization of experimental parameters influencing the extraction, such as type and volume of extraction and disperser solvents, pH, the amount of chelating agent and extraction time was normally carried out using a step-by-step approach, in which each factor was varied sequentially. The effect of the interfering ions on the analytes recovery was also investigated. The calibration graph was linear in the range of 5-200 ng mL-1 with limit of detection of 3.4 ng mL-1. The relative standard deviation (RSD) was 0.7% (n = 10, C = 2 ng mL-1) and the enhancement factor was 28.Sociedade Brasileira de Química2012-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000600023Journal of the Brazilian Chemical Society v.23 n.6 2012reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532012000600023info:eu-repo/semantics/openAccessBahar,SoleimanZakerian,Razieheng2012-07-13T00:00:00Zoai:scielo:S0103-50532012000600023Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2012-07-13T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Determination of copper in human hair and tea samples after dispersive liquid-liquid microextraction based on solidification of floating organic drop (DLLME-SFO)
title Determination of copper in human hair and tea samples after dispersive liquid-liquid microextraction based on solidification of floating organic drop (DLLME-SFO)
spellingShingle Determination of copper in human hair and tea samples after dispersive liquid-liquid microextraction based on solidification of floating organic drop (DLLME-SFO)
Bahar,Soleiman
dispersive liquid-liquid microextraction
solidification
copper determination
tea and human hair analysis
title_short Determination of copper in human hair and tea samples after dispersive liquid-liquid microextraction based on solidification of floating organic drop (DLLME-SFO)
title_full Determination of copper in human hair and tea samples after dispersive liquid-liquid microextraction based on solidification of floating organic drop (DLLME-SFO)
title_fullStr Determination of copper in human hair and tea samples after dispersive liquid-liquid microextraction based on solidification of floating organic drop (DLLME-SFO)
title_full_unstemmed Determination of copper in human hair and tea samples after dispersive liquid-liquid microextraction based on solidification of floating organic drop (DLLME-SFO)
title_sort Determination of copper in human hair and tea samples after dispersive liquid-liquid microextraction based on solidification of floating organic drop (DLLME-SFO)
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
solidification
copper determination
tea and human hair analysis
topic dispersive liquid-liquid microextraction
solidification
copper determination
tea and human hair analysis
description A simple method of dispersive liquid-liquid microextraction-solidified floating organic drop (DLLME-SFO) prior to flame atomic absorption spectrometry was successfully used for separating and preconcentrating copper in human hair and tea samples. The proposed method was simple, cheap, and has high precision. In this study, optimization of experimental parameters influencing the extraction, such as type and volume of extraction and disperser solvents, pH, the amount of chelating agent and extraction time was normally carried out using a step-by-step approach, in which each factor was varied sequentially. The effect of the interfering ions on the analytes recovery was also investigated. The calibration graph was linear in the range of 5-200 ng mL-1 with limit of detection of 3.4 ng mL-1. The relative standard deviation (RSD) was 0.7% (n = 10, C = 2 ng mL-1) and the enhancement factor was 28.
publishDate 2012
dc.date.none.fl_str_mv 2012-06-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000600023
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000600023
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532012000600023
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.6 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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