Synthesis and characterization of poly-o-toluidine: kinetic and structural aspects
Autor(a) principal: | |
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Data de Publicação: | 2005 |
Outros Autores: | , , |
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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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 |
_version_ |
1754212657787830272 |