Determination of acidic herbicides in water samples by in situ derivatization, single drop microextraction and gas chromatography-mass spectrometry
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , , |
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=S0103-50532011001200016 |
Resumo: | A method for the determination of trace amounts of acidic herbicides in water samples was developed. The analytical procedure involves in situ derivatization of analytes to their methyl esters with dimethyl sulfate, sampling using single drop microextraction (SDME) and gas chromatography-mass spectrometry (GC-MS). The effects of pH, ionic strength, extraction time, solvent of extraction as well as derivatization conditions were studied. Methyl esters were extracted using 2 µL of n-heptane. The response was linearly dependent on the concentration in the range 0.05-10.0 ng mL-1. Limits of detection were achieved at the level of 1.8-3.0 ng L-1. Derivatization-SDME/GC-MS analysis yielded good precision (RSD between 7.0 and 15.2%). The method was validated by analysis of spiked matrix samples. |
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Journal of the Brazilian Chemical Society (Online) |
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Determination of acidic herbicides in water samples by in situ derivatization, single drop microextraction and gas chromatography-mass spectrometryacidic herbicides residuesdirect derivatization-SDMEGC-MSA method for the determination of trace amounts of acidic herbicides in water samples was developed. The analytical procedure involves in situ derivatization of analytes to their methyl esters with dimethyl sulfate, sampling using single drop microextraction (SDME) and gas chromatography-mass spectrometry (GC-MS). The effects of pH, ionic strength, extraction time, solvent of extraction as well as derivatization conditions were studied. Methyl esters were extracted using 2 µL of n-heptane. The response was linearly dependent on the concentration in the range 0.05-10.0 ng mL-1. Limits of detection were achieved at the level of 1.8-3.0 ng L-1. Derivatization-SDME/GC-MS analysis yielded good precision (RSD between 7.0 and 15.2%). The method was validated by analysis of spiked matrix samples.Sociedade Brasileira de Química2011-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011001200016Journal of the Brazilian Chemical Society v.22 n.12 2011reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532011001200016info:eu-repo/semantics/openAccessAraujo,LiliaPrieto,AvismelsiTroconis,MaríaUrribarri,GrilenaSandrea,WilliamsMercado,Jaireng2012-01-05T00:00:00Zoai:scielo:S0103-50532011001200016Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2012-01-05T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Determination of acidic herbicides in water samples by in situ derivatization, single drop microextraction and gas chromatography-mass spectrometry |
title |
Determination of acidic herbicides in water samples by in situ derivatization, single drop microextraction and gas chromatography-mass spectrometry |
spellingShingle |
Determination of acidic herbicides in water samples by in situ derivatization, single drop microextraction and gas chromatography-mass spectrometry Araujo,Lilia acidic herbicides residues direct derivatization-SDME GC-MS |
title_short |
Determination of acidic herbicides in water samples by in situ derivatization, single drop microextraction and gas chromatography-mass spectrometry |
title_full |
Determination of acidic herbicides in water samples by in situ derivatization, single drop microextraction and gas chromatography-mass spectrometry |
title_fullStr |
Determination of acidic herbicides in water samples by in situ derivatization, single drop microextraction and gas chromatography-mass spectrometry |
title_full_unstemmed |
Determination of acidic herbicides in water samples by in situ derivatization, single drop microextraction and gas chromatography-mass spectrometry |
title_sort |
Determination of acidic herbicides in water samples by in situ derivatization, single drop microextraction and gas chromatography-mass spectrometry |
author |
Araujo,Lilia |
author_facet |
Araujo,Lilia Prieto,Avismelsi Troconis,María Urribarri,Grilena Sandrea,Williams Mercado,Jair |
author_role |
author |
author2 |
Prieto,Avismelsi Troconis,María Urribarri,Grilena Sandrea,Williams Mercado,Jair |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Araujo,Lilia Prieto,Avismelsi Troconis,María Urribarri,Grilena Sandrea,Williams Mercado,Jair |
dc.subject.por.fl_str_mv |
acidic herbicides residues direct derivatization-SDME GC-MS |
topic |
acidic herbicides residues direct derivatization-SDME GC-MS |
description |
A method for the determination of trace amounts of acidic herbicides in water samples was developed. The analytical procedure involves in situ derivatization of analytes to their methyl esters with dimethyl sulfate, sampling using single drop microextraction (SDME) and gas chromatography-mass spectrometry (GC-MS). The effects of pH, ionic strength, extraction time, solvent of extraction as well as derivatization conditions were studied. Methyl esters were extracted using 2 µL of n-heptane. The response was linearly dependent on the concentration in the range 0.05-10.0 ng mL-1. Limits of detection were achieved at the level of 1.8-3.0 ng L-1. Derivatization-SDME/GC-MS analysis yielded good precision (RSD between 7.0 and 15.2%). The method was validated by analysis of spiked matrix samples. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-12-01 |
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=S0103-50532011001200016 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011001200016 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-50532011001200016 |
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.22 n.12 2011 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 |
_version_ |
1750318172779577344 |