Electrochemical oxidation, adsorption and quantification of 1,2-benzopyrone employing a glassy carbon electrode
Autor(a) principal: | |
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Data de Publicação: | 2014 |
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=S0103-50532014000300009 |
Resumo: | The electrooxidation of 1,2-benzopyrone (BP) was assessed via linear voltammetry and electrochemical impedance spectroscopy on a glassy carbon electrode in dibasic potassium phosphate buffer. The oxidation process for BP requires one electron and forms a ketone. This oxidation product was adsorbed by the electrode surface to form a film that blocks active sites and increases in thickness over consecutive measurements. The oxidation conditions were optimized using factorial design and Doehlert matrices. This electrochemical method was compared to high performance liquid chromatography (HPLC), which has a detection limit of 26.4 µmol L-1 for BP. The voltammetric results were statistically similar to those from HPLC; however, the method was faster, simpler, more easily acquired, more sensitive, and required less organic solvent. |
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Electrochemical oxidation, adsorption and quantification of 1,2-benzopyrone employing a glassy carbon electrode1,2-benzopyroneguacoadsorption processmultivariate optimizationThe electrooxidation of 1,2-benzopyrone (BP) was assessed via linear voltammetry and electrochemical impedance spectroscopy on a glassy carbon electrode in dibasic potassium phosphate buffer. The oxidation process for BP requires one electron and forms a ketone. This oxidation product was adsorbed by the electrode surface to form a film that blocks active sites and increases in thickness over consecutive measurements. The oxidation conditions were optimized using factorial design and Doehlert matrices. This electrochemical method was compared to high performance liquid chromatography (HPLC), which has a detection limit of 26.4 µmol L-1 for BP. The voltammetric results were statistically similar to those from HPLC; however, the method was faster, simpler, more easily acquired, more sensitive, and required less organic solvent.Sociedade Brasileira de Química2014-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014000300009Journal of the Brazilian Chemical Society v.25 n.3 2014reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0103-5053.20140004info:eu-repo/semantics/openAccessAzevedo,Luiz Fernando M. deTrevisan,Marcello G.Garcia,Jerusa S.Lucho,Alzira M. S.eng2014-03-19T00:00:00Zoai:scielo:S0103-50532014000300009Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2014-03-19T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Electrochemical oxidation, adsorption and quantification of 1,2-benzopyrone employing a glassy carbon electrode |
title |
Electrochemical oxidation, adsorption and quantification of 1,2-benzopyrone employing a glassy carbon electrode |
spellingShingle |
Electrochemical oxidation, adsorption and quantification of 1,2-benzopyrone employing a glassy carbon electrode Azevedo,Luiz Fernando M. de 1,2-benzopyrone guaco adsorption process multivariate optimization |
title_short |
Electrochemical oxidation, adsorption and quantification of 1,2-benzopyrone employing a glassy carbon electrode |
title_full |
Electrochemical oxidation, adsorption and quantification of 1,2-benzopyrone employing a glassy carbon electrode |
title_fullStr |
Electrochemical oxidation, adsorption and quantification of 1,2-benzopyrone employing a glassy carbon electrode |
title_full_unstemmed |
Electrochemical oxidation, adsorption and quantification of 1,2-benzopyrone employing a glassy carbon electrode |
title_sort |
Electrochemical oxidation, adsorption and quantification of 1,2-benzopyrone employing a glassy carbon electrode |
author |
Azevedo,Luiz Fernando M. de |
author_facet |
Azevedo,Luiz Fernando M. de Trevisan,Marcello G. Garcia,Jerusa S. Lucho,Alzira M. S. |
author_role |
author |
author2 |
Trevisan,Marcello G. Garcia,Jerusa S. Lucho,Alzira M. S. |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Azevedo,Luiz Fernando M. de Trevisan,Marcello G. Garcia,Jerusa S. Lucho,Alzira M. S. |
dc.subject.por.fl_str_mv |
1,2-benzopyrone guaco adsorption process multivariate optimization |
topic |
1,2-benzopyrone guaco adsorption process multivariate optimization |
description |
The electrooxidation of 1,2-benzopyrone (BP) was assessed via linear voltammetry and electrochemical impedance spectroscopy on a glassy carbon electrode in dibasic potassium phosphate buffer. The oxidation process for BP requires one electron and forms a ketone. This oxidation product was adsorbed by the electrode surface to form a film that blocks active sites and increases in thickness over consecutive measurements. The oxidation conditions were optimized using factorial design and Doehlert matrices. This electrochemical method was compared to high performance liquid chromatography (HPLC), which has a detection limit of 26.4 µmol L-1 for BP. The voltammetric results were statistically similar to those from HPLC; however, the method was faster, simpler, more easily acquired, more sensitive, and required less organic solvent. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-03-01 |
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=S0103-50532014000300009 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014000300009 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.5935/0103-5053.20140004 |
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.25 n.3 2014 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_ |
1750318175742853120 |