A catalytic kinetic spectrophotometric determination of organophosphorus pesticides in vegetable samples
Autor(a) principal: | |
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Data de Publicação: | 2012 |
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=S0103-50532012000200019 |
Resumo: | A simple selective and sensitive catalytic kinetic spectrophotometric method for the determination of trace amount of organophosphorus pesticides has been proposed. The method is based on the catalytic effect of organophosphorus pesticides (malathion, dimethoate and phorate) on the oxidation of LCV (leuco crystal violet) by potassium iodate in hydrochloric acid medium to give a violet colored dye. The dye shows maximum absorption at 592 nm. The fixed-time method was used for 15 min. The system obeys Beers law in the range of 0.02-0.2, 0.032-0.32 and 0.03-0.3 µg mL-1, for malathion, dimethoate, and phorate, respectively. Important analytical parameters such as time, temperature, reagent concentration, acidity etc, have been optimized for complete color reaction. Sandells sensitivity and molar absorptivity for the system were found to be 0.0002, 0.0004, 0.0004 µg cm-2 and 1.2 × 10(6), 5.21 × 10(5), 6.3 × 10(5) L mol-1cm-1, respectively. The proposed method was satisfactorily applied to micro-level determination of organophosphorus pesticides in vegetable samples. |
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A catalytic kinetic spectrophotometric determination of organophosphorus pesticides in vegetable samplesorganophosphorus pesticidespotassium iodateleuco crystal violetspectrophotometryvegetablesA simple selective and sensitive catalytic kinetic spectrophotometric method for the determination of trace amount of organophosphorus pesticides has been proposed. The method is based on the catalytic effect of organophosphorus pesticides (malathion, dimethoate and phorate) on the oxidation of LCV (leuco crystal violet) by potassium iodate in hydrochloric acid medium to give a violet colored dye. The dye shows maximum absorption at 592 nm. The fixed-time method was used for 15 min. The system obeys Beers law in the range of 0.02-0.2, 0.032-0.32 and 0.03-0.3 µg mL-1, for malathion, dimethoate, and phorate, respectively. Important analytical parameters such as time, temperature, reagent concentration, acidity etc, have been optimized for complete color reaction. Sandells sensitivity and molar absorptivity for the system were found to be 0.0002, 0.0004, 0.0004 µg cm-2 and 1.2 × 10(6), 5.21 × 10(5), 6.3 × 10(5) L mol-1cm-1, respectively. The proposed method was satisfactorily applied to micro-level determination of organophosphorus pesticides in vegetable samples.Sociedade Brasileira de Química2012-02-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000200019Journal of the Brazilian Chemical Society v.23 n.2 2012reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532012000200019info:eu-repo/semantics/openAccessTiwari,NeetuAsthana,Anupamaeng2012-03-02T00:00:00Zoai:scielo:S0103-50532012000200019Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2012-03-02T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
A catalytic kinetic spectrophotometric determination of organophosphorus pesticides in vegetable samples |
title |
A catalytic kinetic spectrophotometric determination of organophosphorus pesticides in vegetable samples |
spellingShingle |
A catalytic kinetic spectrophotometric determination of organophosphorus pesticides in vegetable samples Tiwari,Neetu organophosphorus pesticides potassium iodate leuco crystal violet spectrophotometry vegetables |
title_short |
A catalytic kinetic spectrophotometric determination of organophosphorus pesticides in vegetable samples |
title_full |
A catalytic kinetic spectrophotometric determination of organophosphorus pesticides in vegetable samples |
title_fullStr |
A catalytic kinetic spectrophotometric determination of organophosphorus pesticides in vegetable samples |
title_full_unstemmed |
A catalytic kinetic spectrophotometric determination of organophosphorus pesticides in vegetable samples |
title_sort |
A catalytic kinetic spectrophotometric determination of organophosphorus pesticides in vegetable samples |
author |
Tiwari,Neetu |
author_facet |
Tiwari,Neetu Asthana,Anupama |
author_role |
author |
author2 |
Asthana,Anupama |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Tiwari,Neetu Asthana,Anupama |
dc.subject.por.fl_str_mv |
organophosphorus pesticides potassium iodate leuco crystal violet spectrophotometry vegetables |
topic |
organophosphorus pesticides potassium iodate leuco crystal violet spectrophotometry vegetables |
description |
A simple selective and sensitive catalytic kinetic spectrophotometric method for the determination of trace amount of organophosphorus pesticides has been proposed. The method is based on the catalytic effect of organophosphorus pesticides (malathion, dimethoate and phorate) on the oxidation of LCV (leuco crystal violet) by potassium iodate in hydrochloric acid medium to give a violet colored dye. The dye shows maximum absorption at 592 nm. The fixed-time method was used for 15 min. The system obeys Beers law in the range of 0.02-0.2, 0.032-0.32 and 0.03-0.3 µg mL-1, for malathion, dimethoate, and phorate, respectively. Important analytical parameters such as time, temperature, reagent concentration, acidity etc, have been optimized for complete color reaction. Sandells sensitivity and molar absorptivity for the system were found to be 0.0002, 0.0004, 0.0004 µg cm-2 and 1.2 × 10(6), 5.21 × 10(5), 6.3 × 10(5) L mol-1cm-1, respectively. The proposed method was satisfactorily applied to micro-level determination of organophosphorus pesticides in vegetable samples. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-02-01 |
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=S0103-50532012000200019 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000200019 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-50532012000200019 |
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.2 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 |
_version_ |
1750318173099393024 |