Potentiometric study of cetylpyridinium chloride cooperative binding to anionic azo-dyes
Autor(a) principal: | |
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Data de Publicação: | 2007 |
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=S0103-50532007000200017 |
Resumo: | The binding of cetylpyridinium chloride (CPC) with some azo dyes (X6G, 3-BL, DY-42) has been extensively studied at various concentration of dyes, using cetylpyridinium-selective membrane electrode as a fast and accurate method. Klotz logarithmic plots have been constructed from EMF measurements. These plots indicated cooperativity in all of interactions. The accurate binding isotherms have been obtained and analyzed using Hill equation. The values of Hill equation parameters have been estimated and determined by considering this fact that saturation parameter of binding in the Hill equation (y) can be determined from the ratio of electromotive force (EMF) measurements in the presence and absence of dye. In all of the interactions Hill coefficients indicate cooperative binding in CPC-dye interactions due to the combination of both electrostatic and hydrophobic interactions. Intrinsic Gibbs energies of binding processes have been also calculated and interpreted on basis of interaction mechanism. |
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Potentiometric study of cetylpyridinium chloride cooperative binding to anionic azo-dyescetylpyridinium chloridecooperative bindingbinding isothermHill equationdye-surfactantThe binding of cetylpyridinium chloride (CPC) with some azo dyes (X6G, 3-BL, DY-42) has been extensively studied at various concentration of dyes, using cetylpyridinium-selective membrane electrode as a fast and accurate method. Klotz logarithmic plots have been constructed from EMF measurements. These plots indicated cooperativity in all of interactions. The accurate binding isotherms have been obtained and analyzed using Hill equation. The values of Hill equation parameters have been estimated and determined by considering this fact that saturation parameter of binding in the Hill equation (y) can be determined from the ratio of electromotive force (EMF) measurements in the presence and absence of dye. In all of the interactions Hill coefficients indicate cooperative binding in CPC-dye interactions due to the combination of both electrostatic and hydrophobic interactions. Intrinsic Gibbs energies of binding processes have been also calculated and interpreted on basis of interaction mechanism.Sociedade Brasileira de Química2007-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532007000200017Journal of the Brazilian Chemical Society v.18 n.2 2007reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532007000200017info:eu-repo/semantics/openAccessHosseinzadeh,RezaBordbar,Abdol-KhaleghMatin,Amir AbbasMaleki,Ramineng2007-06-13T00:00:00Zoai:scielo:S0103-50532007000200017Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2007-06-13T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Potentiometric study of cetylpyridinium chloride cooperative binding to anionic azo-dyes |
title |
Potentiometric study of cetylpyridinium chloride cooperative binding to anionic azo-dyes |
spellingShingle |
Potentiometric study of cetylpyridinium chloride cooperative binding to anionic azo-dyes Hosseinzadeh,Reza cetylpyridinium chloride cooperative binding binding isotherm Hill equation dye-surfactant |
title_short |
Potentiometric study of cetylpyridinium chloride cooperative binding to anionic azo-dyes |
title_full |
Potentiometric study of cetylpyridinium chloride cooperative binding to anionic azo-dyes |
title_fullStr |
Potentiometric study of cetylpyridinium chloride cooperative binding to anionic azo-dyes |
title_full_unstemmed |
Potentiometric study of cetylpyridinium chloride cooperative binding to anionic azo-dyes |
title_sort |
Potentiometric study of cetylpyridinium chloride cooperative binding to anionic azo-dyes |
author |
Hosseinzadeh,Reza |
author_facet |
Hosseinzadeh,Reza Bordbar,Abdol-Khalegh Matin,Amir Abbas Maleki,Ramin |
author_role |
author |
author2 |
Bordbar,Abdol-Khalegh Matin,Amir Abbas Maleki,Ramin |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Hosseinzadeh,Reza Bordbar,Abdol-Khalegh Matin,Amir Abbas Maleki,Ramin |
dc.subject.por.fl_str_mv |
cetylpyridinium chloride cooperative binding binding isotherm Hill equation dye-surfactant |
topic |
cetylpyridinium chloride cooperative binding binding isotherm Hill equation dye-surfactant |
description |
The binding of cetylpyridinium chloride (CPC) with some azo dyes (X6G, 3-BL, DY-42) has been extensively studied at various concentration of dyes, using cetylpyridinium-selective membrane electrode as a fast and accurate method. Klotz logarithmic plots have been constructed from EMF measurements. These plots indicated cooperativity in all of interactions. The accurate binding isotherms have been obtained and analyzed using Hill equation. The values of Hill equation parameters have been estimated and determined by considering this fact that saturation parameter of binding in the Hill equation (y) can be determined from the ratio of electromotive force (EMF) measurements in the presence and absence of dye. In all of the interactions Hill coefficients indicate cooperative binding in CPC-dye interactions due to the combination of both electrostatic and hydrophobic interactions. Intrinsic Gibbs energies of binding processes have been also calculated and interpreted on basis of interaction mechanism. |
publishDate |
2007 |
dc.date.none.fl_str_mv |
2007-04-01 |
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=S0103-50532007000200017 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532007000200017 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-50532007000200017 |
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.18 n.2 2007 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_ |
1750318167816667136 |