Synthesis and characterization of poly-o-toluidine: kinetic and structural aspects

Detalhes bibliográficos
Autor(a) principal: Cordeiro,Maria Angela de Moraes
Data de Publicação: 2005
Outros Autores: Gonçalves,Débora, Bulhões,Luis Otavio de Sousa, Cordeiro,João Manuel Marques
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Materials research (São Carlos. Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392005000100003
Resumo: Poly(o-methylaniline) (poly-o-toluidine, PTOL) was synthesized by chemical oxidation of o-toluidine with ammonium peroxydisulfate in an aqueous 1.0 mol L-1 HCl solution. The progress of polymerization was followed by measuring the open-circuit potential (OCP) of a Pt electrode immersed in the reaction medium with the polymerization time. The chemical synthesis of PTOL was carried out at different monomer:oxidant (M:O) molar ratios (4:1, 2:1, 1.5:1, 1:1, and 0.66:1), and the products obtained were characterized by infrared spectroscopy, gel permeation chromatography, and X-ray diffraction. The molecular weight and percentage of crystallinity of PTOL are higher for samples synthesized in an excess of the monomer, i.e. at higher M:O ratios. However, the yield of PTOL prepared at higher M:O ratios is considerably low, in particular at a 4:1 M:O ratio, which is the M:O ratio most commonly used in the literature to synthesize polyaniline and its derivatives.
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spelling Synthesis and characterization of poly-o-toluidine: kinetic and structural aspectspoly-o-toluidinepolymerization mechanismopen-circuit potentialpolyaniline derivativesPoly(o-methylaniline) (poly-o-toluidine, PTOL) was synthesized by chemical oxidation of o-toluidine with ammonium peroxydisulfate in an aqueous 1.0 mol L-1 HCl solution. The progress of polymerization was followed by measuring the open-circuit potential (OCP) of a Pt electrode immersed in the reaction medium with the polymerization time. The chemical synthesis of PTOL was carried out at different monomer:oxidant (M:O) molar ratios (4:1, 2:1, 1.5:1, 1:1, and 0.66:1), and the products obtained were characterized by infrared spectroscopy, gel permeation chromatography, and X-ray diffraction. The molecular weight and percentage of crystallinity of PTOL are higher for samples synthesized in an excess of the monomer, i.e. at higher M:O ratios. However, the yield of PTOL prepared at higher M:O ratios is considerably low, in particular at a 4:1 M:O ratio, which is the M:O ratio most commonly used in the literature to synthesize polyaniline and its derivatives.ABM, ABC, ABPol2005-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392005000100003Materials Research v.8 n.1 2005reponame:Materials research (São Carlos. Online)instname:Universidade Federal de São Carlos (UFSCAR)instacron:ABM ABC ABPOL10.1590/S1516-14392005000100003info:eu-repo/semantics/openAccessCordeiro,Maria Angela de MoraesGonçalves,DéboraBulhões,Luis Otavio de SousaCordeiro,João Manuel Marqueseng2005-03-24T00:00:00Zoai:scielo:S1516-14392005000100003Revistahttp://www.scielo.br/mrPUBhttps://old.scielo.br/oai/scielo-oai.phpdedz@power.ufscar.br1980-53731516-1439opendoar:2005-03-24T00:00Materials research (São Carlos. Online) - Universidade Federal de São Carlos (UFSCAR)false
dc.title.none.fl_str_mv Synthesis and characterization of poly-o-toluidine: kinetic and structural aspects
title Synthesis and characterization of poly-o-toluidine: kinetic and structural aspects
spellingShingle Synthesis and characterization of poly-o-toluidine: kinetic and structural aspects
Cordeiro,Maria Angela de Moraes
poly-o-toluidine
polymerization mechanism
open-circuit potential
polyaniline derivatives
title_short Synthesis and characterization of poly-o-toluidine: kinetic and structural aspects
title_full Synthesis and characterization of poly-o-toluidine: kinetic and structural aspects
title_fullStr Synthesis and characterization of poly-o-toluidine: kinetic and structural aspects
title_full_unstemmed Synthesis and characterization of poly-o-toluidine: kinetic and structural aspects
title_sort Synthesis and characterization of poly-o-toluidine: kinetic and structural aspects
author Cordeiro,Maria Angela de Moraes
author_facet Cordeiro,Maria Angela de Moraes
Gonçalves,Débora
Bulhões,Luis Otavio de Sousa
Cordeiro,João Manuel Marques
author_role author
author2 Gonçalves,Débora
Bulhões,Luis Otavio de Sousa
Cordeiro,João Manuel Marques
author2_role author
author
author
dc.contributor.author.fl_str_mv Cordeiro,Maria Angela de Moraes
Gonçalves,Débora
Bulhões,Luis Otavio de Sousa
Cordeiro,João Manuel Marques
dc.subject.por.fl_str_mv poly-o-toluidine
polymerization mechanism
open-circuit potential
polyaniline derivatives
topic poly-o-toluidine
polymerization mechanism
open-circuit potential
polyaniline derivatives
description Poly(o-methylaniline) (poly-o-toluidine, PTOL) was synthesized by chemical oxidation of o-toluidine with ammonium peroxydisulfate in an aqueous 1.0 mol L-1 HCl solution. The progress of polymerization was followed by measuring the open-circuit potential (OCP) of a Pt electrode immersed in the reaction medium with the polymerization time. The chemical synthesis of PTOL was carried out at different monomer:oxidant (M:O) molar ratios (4:1, 2:1, 1.5:1, 1:1, and 0.66:1), and the products obtained were characterized by infrared spectroscopy, gel permeation chromatography, and X-ray diffraction. The molecular weight and percentage of crystallinity of PTOL are higher for samples synthesized in an excess of the monomer, i.e. at higher M:O ratios. However, the yield of PTOL prepared at higher M:O ratios is considerably low, in particular at a 4:1 M:O ratio, which is the M:O ratio most commonly used in the literature to synthesize polyaniline and its derivatives.
publishDate 2005
dc.date.none.fl_str_mv 2005-03-01
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=S1516-14392005000100003
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392005000100003
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S1516-14392005000100003
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 ABM, ABC, ABPol
publisher.none.fl_str_mv ABM, ABC, ABPol
dc.source.none.fl_str_mv Materials Research v.8 n.1 2005
reponame:Materials research (São Carlos. Online)
instname:Universidade Federal de São Carlos (UFSCAR)
instacron:ABM ABC ABPOL
instname_str Universidade Federal de São Carlos (UFSCAR)
instacron_str ABM ABC ABPOL
institution ABM ABC ABPOL
reponame_str Materials research (São Carlos. Online)
collection Materials research (São Carlos. Online)
repository.name.fl_str_mv Materials research (São Carlos. Online) - Universidade Federal de São Carlos (UFSCAR)
repository.mail.fl_str_mv dedz@power.ufscar.br
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