Evaluation of a nafion coated glassy carbon electrode for determination of paraquat by differential pulse voltammetry
Autor(a) principal: | |
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Data de Publicação: | 2004 |
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=S0103-50532004000500020 |
Resumo: | This paper presents an evaluation of a Nafion coated glassy carbon electrode for determination of paraquat in river water and urine by differential pulse voltammetry. The film was formed applying 4 µL of a 1% (m/v) Nafion solution, which was evaporated under an infrared light. The maximum signal to noise ratio was obtained using a 40 mmol L-1 Britton-Robinson buffer at pH 12 as supporting electrolyte. For an accumulation time of 5.0 min in open circuit, the limit of detection was 0.7 µg L-1, while the quantification limit was 1.0 µg L-1, with a linear dynamic range up to 12 µg L-1. In these conditions, a sequence of ten experiments lead to a relative standard deviation of peak current of 2.2% for a 10 µg L-1 paraquat solution. Ion pair formation in solution was the major factor of error in analysis. Despite the film to avoid adsorption of anionic species at the electrode surface, paraquat suffers strong association in solution with humic substances, proteins, clays, anionic surfactants, etc. These interactions decrease the accumulation of paraquat in the Nafion film and, as a consequence, the magnitude of the reduction peak, requiring that quantifications have to be made by standard addition. Recoveries between 87 and 106% were obtained for river waters and urine samples spiked with 1.0 and 3.0 µg L-1 paraquat. |
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Evaluation of a nafion coated glassy carbon electrode for determination of paraquat by differential pulse voltammetryparaquat determinationriver waterurinemodified electrodevoltammetryion exchangeThis paper presents an evaluation of a Nafion coated glassy carbon electrode for determination of paraquat in river water and urine by differential pulse voltammetry. The film was formed applying 4 µL of a 1% (m/v) Nafion solution, which was evaporated under an infrared light. The maximum signal to noise ratio was obtained using a 40 mmol L-1 Britton-Robinson buffer at pH 12 as supporting electrolyte. For an accumulation time of 5.0 min in open circuit, the limit of detection was 0.7 µg L-1, while the quantification limit was 1.0 µg L-1, with a linear dynamic range up to 12 µg L-1. In these conditions, a sequence of ten experiments lead to a relative standard deviation of peak current of 2.2% for a 10 µg L-1 paraquat solution. Ion pair formation in solution was the major factor of error in analysis. Despite the film to avoid adsorption of anionic species at the electrode surface, paraquat suffers strong association in solution with humic substances, proteins, clays, anionic surfactants, etc. These interactions decrease the accumulation of paraquat in the Nafion film and, as a consequence, the magnitude of the reduction peak, requiring that quantifications have to be made by standard addition. Recoveries between 87 and 106% were obtained for river waters and urine samples spiked with 1.0 and 3.0 µg L-1 paraquat.Sociedade Brasileira de Química2004-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532004000500020Journal of the Brazilian Chemical Society v.15 n.5 2004reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532004000500020info:eu-repo/semantics/openAccessOliveira,Ulisses M. F. deLichtig,JaimMasini,Jorge C.eng2004-11-10T00:00:00Zoai:scielo:S0103-50532004000500020Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2004-11-10T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Evaluation of a nafion coated glassy carbon electrode for determination of paraquat by differential pulse voltammetry |
title |
Evaluation of a nafion coated glassy carbon electrode for determination of paraquat by differential pulse voltammetry |
spellingShingle |
Evaluation of a nafion coated glassy carbon electrode for determination of paraquat by differential pulse voltammetry Oliveira,Ulisses M. F. de paraquat determination river water urine modified electrode voltammetry ion exchange |
title_short |
Evaluation of a nafion coated glassy carbon electrode for determination of paraquat by differential pulse voltammetry |
title_full |
Evaluation of a nafion coated glassy carbon electrode for determination of paraquat by differential pulse voltammetry |
title_fullStr |
Evaluation of a nafion coated glassy carbon electrode for determination of paraquat by differential pulse voltammetry |
title_full_unstemmed |
Evaluation of a nafion coated glassy carbon electrode for determination of paraquat by differential pulse voltammetry |
title_sort |
Evaluation of a nafion coated glassy carbon electrode for determination of paraquat by differential pulse voltammetry |
author |
Oliveira,Ulisses M. F. de |
author_facet |
Oliveira,Ulisses M. F. de Lichtig,Jaim Masini,Jorge C. |
author_role |
author |
author2 |
Lichtig,Jaim Masini,Jorge C. |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Oliveira,Ulisses M. F. de Lichtig,Jaim Masini,Jorge C. |
dc.subject.por.fl_str_mv |
paraquat determination river water urine modified electrode voltammetry ion exchange |
topic |
paraquat determination river water urine modified electrode voltammetry ion exchange |
description |
This paper presents an evaluation of a Nafion coated glassy carbon electrode for determination of paraquat in river water and urine by differential pulse voltammetry. The film was formed applying 4 µL of a 1% (m/v) Nafion solution, which was evaporated under an infrared light. The maximum signal to noise ratio was obtained using a 40 mmol L-1 Britton-Robinson buffer at pH 12 as supporting electrolyte. For an accumulation time of 5.0 min in open circuit, the limit of detection was 0.7 µg L-1, while the quantification limit was 1.0 µg L-1, with a linear dynamic range up to 12 µg L-1. In these conditions, a sequence of ten experiments lead to a relative standard deviation of peak current of 2.2% for a 10 µg L-1 paraquat solution. Ion pair formation in solution was the major factor of error in analysis. Despite the film to avoid adsorption of anionic species at the electrode surface, paraquat suffers strong association in solution with humic substances, proteins, clays, anionic surfactants, etc. These interactions decrease the accumulation of paraquat in the Nafion film and, as a consequence, the magnitude of the reduction peak, requiring that quantifications have to be made by standard addition. Recoveries between 87 and 106% were obtained for river waters and urine samples spiked with 1.0 and 3.0 µg L-1 paraquat. |
publishDate |
2004 |
dc.date.none.fl_str_mv |
2004-10-01 |
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=S0103-50532004000500020 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532004000500020 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-50532004000500020 |
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.15 n.5 2004 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_ |
1750318165806546944 |