Atividade eletrocatalítica de nanopartículas de hexacianoferrato de rutênio para eletro-oxidação de glicerol
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Tipo de documento: | Tese |
Idioma: | por |
Título da fonte: | Biblioteca Digital de Teses e Dissertações da UFMA |
Texto Completo: | https://tedebc.ufma.br/jspui/handle/tede/tede/2864 |
Resumo: | In the present work, the ruthenium (III) hexacyanoferrate complex was tested for glycerol oxidation using two distinct forms of modification of the vitreous carbon electrode. In the first one, the vitreous carbon electrode was modified by electrodeposition through cyclic voltammetry at determined potential and already described in the literature, and in the second, the carbon glass electrode was modified by nanoparticles supported on Vulcan XC-72 carbon, which were synthesized by the alcohol reduction method. Subsequently, the electrocatalysts were characterized by chemical-chemical techniques and tested by electrochemical techniques. The physico-chemical characterization of ruthenium hexacyanoferrate (III) was carried out by Electron Spectrophotometry in the UV-Vis region (UV-Vis), Infrared Vibrational Spectroscopy (FTIR), Electron Transmission Electron Microscopy (TEM), Dispersive Energy X-rays (EDX) and X-ray Diffraction (XRD). Electrochemical characterization occurred by cyclic voltammetry, rotational disk electrode, chronoamperometry and electrochemical impedance spectroscopy (EIS). EDX analysis for the nanoparticles showed that the theoretical starting composition is approximately the same experimentally proven. XRD and TEM analyzes provided the size of the synthesized particles on the order of 3.8 nm, as well as the distribution and dispersion in the carbon carrier. The electrochemical results on the glycerol oxidation reaction showed that the synthesis performed by the alcohol reduction method showed an increase in electrocatalytic current when compared to the unmodified electrode. Through a study with a rotating disk electrode it was possible to verify the involvement of 3.8 electrons in the oxidation reaction of glycerol. Electrochemical impedance spectroscopy has shown that the charge transfer resistance of glycerol electro-oxidation decreases as the potential and concentration of glycerol increase. The carbon-supported ruthenium hexacyanoferrate nanoparticle-modified electrode showed an efficiency in the glycerol oxidation reaction being a viable option for use as a catalyst in direct alcohol fuel cells. |
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MARQUES, Aldaléa Lopes Brandes076486263-49http://lattes.cnpq.br/0121030502015990MARQUES, Aldaléa Lopes Brandes076486263-49http://lattes.cnpq.br/0121030502015990BRITO, Natilene Mesquitahttp://lattes.cnpq.br/5662692111796966RODRIGUES, Isaide de Araújohttp://lattes.cnpq.br/3696115712661158LUZ, Rita de Cassia Silvahttp://lattes.cnpq.br/1282444701404832LIMA, Roberto Batista dehttp://lattes.cnpq.br/4982744838486744013991003-43http://lattes.cnpq.br/5345949888760079VIÉGAS, Deracilde Santana da Silva2019-10-01T13:46:54Z2019-04-05VIÉGAS, Deracilde Santana da Silva. Atividade eletrocatalítica de nanopartículas de hexacianoferrato de rutênio para eletro-oxidação de glicerol. 2019. 100 f. Tese (Programa de Pós-Graduação em Rede - Rede de Biodiversidade e Biotecnologia da Amazônia Legal/CCBS) - Universidade Federal do Maranhão, São Luís, 2019.https://tedebc.ufma.br/jspui/handle/tede/tede/2864In the present work, the ruthenium (III) hexacyanoferrate complex was tested for glycerol oxidation using two distinct forms of modification of the vitreous carbon electrode. In the first one, the vitreous carbon electrode was modified by electrodeposition through cyclic voltammetry at determined potential and already described in the literature, and in the second, the carbon glass electrode was modified by nanoparticles supported on Vulcan XC-72 carbon, which were synthesized by the alcohol reduction method. Subsequently, the electrocatalysts were characterized by chemical-chemical techniques and tested by electrochemical techniques. The physico-chemical characterization of ruthenium hexacyanoferrate (III) was carried out by Electron Spectrophotometry in the UV-Vis region (UV-Vis), Infrared Vibrational Spectroscopy (FTIR), Electron Transmission Electron Microscopy (TEM), Dispersive Energy X-rays (EDX) and X-ray Diffraction (XRD). Electrochemical characterization occurred by cyclic voltammetry, rotational disk electrode, chronoamperometry and electrochemical impedance spectroscopy (EIS). EDX analysis for the nanoparticles showed that the theoretical starting composition is approximately the same experimentally proven. XRD and TEM analyzes provided the size of the synthesized particles on the order of 3.8 nm, as well as the distribution and dispersion in the carbon carrier. The electrochemical results on the glycerol oxidation reaction showed that the synthesis performed by the alcohol reduction method showed an increase in electrocatalytic current when compared to the unmodified electrode. Through a study with a rotating disk electrode it was possible to verify the involvement of 3.8 electrons in the oxidation reaction of glycerol. Electrochemical impedance spectroscopy has shown that the charge transfer resistance of glycerol electro-oxidation decreases as the potential and concentration of glycerol increase. The carbon-supported ruthenium hexacyanoferrate nanoparticle-modified electrode showed an efficiency in the glycerol oxidation reaction being a viable option for use as a catalyst in direct alcohol fuel cells.No presente trabalho, o complexo de hexacianoferrato de rutênio (III) foi testado para oxidação de glicerol empregando-se duas formas distintas de modificação do eletrodo de carbono vítreo. Na primeira, o eletrodo de carbono vítreo foi modificado por eletrodeposição, através de voltametria cíclica em potencial determinado e já descrito na literatura, e na segunda modificou-se o eletrodo de carbono vítreo por nanopartículas suportadas em carbono Vulcan XC-72, que foram sintetizadas pelo método de redução por álcool. Posteriormente, os eletrocatalisadores foram caracterizados por técnicas fisco-quimicas e testados por técnicas eletroquímicas. A caracterização físico-química de hexacianoferrato de rutênio (III) se deu por Espectrofotometria Eletrônica na região do UV-Vis (UV-Vis), Espectroscopia Vibracional na região do Infravermelho (FTIR), Microscopia Eletrônica de Transmissão (MET), Energia dispersiva de raios-X (EDX) e Difração de Raios-X (DRX). As caracterizações eletroquímicas ocorreram por voltametria cíclica, eletrodo de disco rotatório, cronoamperometria e Espectroscopia de impedância eletroquímica (EIE). A análise de EDX para as nanoparticulas mostrou que a composição teórica de partida é aproximadamente a mesma comprovada experimentalmente. As análises de DRX e MET forneceram o tamanho das partículas sintetizadas na ordem de 3,8 nm, bem como a distribuição e dispersão no suporte de carbono. Os resultados eletroquímicos frente a reação de oxidação de glicerol mostraram que a síntese realizada pelo método de redução por alcool mostrou aumento de corrente eletrocatalítica quando comparado ao eletrodo não modificado. Através de estudo com eletrodo de disco rotátorio foi possível verificar o envolvimento de 3,8 elétrons na reação de oxidação de glicerol. A espectroscopia de impedância eletroquímica mostrou que a resistência de transferência de carga da eletro-oxidação de glicerol diminui à medida que o potencial e a concentração de glicerol aumentam. O eletrodo modificado com nanopartícula de hexacianoferrato de rutênio suportado em carbono apresentou uma eficiência na reação de oxidação de glicerol sendo uma opção viável para uso como catalisador em células a combustível de álcool direto.Submitted by Daniella Santos (daniella.santos@ufma.br) on 2019-10-01T13:46:54Z No. of bitstreams: 1 DeracildeViégas.pdf: 1822029 bytes, checksum: 2b4546db1bd0f9bbc987977648cfc7da (MD5)Made available in DSpace on 2019-10-01T13:46:54Z (GMT). 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dc.title.por.fl_str_mv |
Atividade eletrocatalítica de nanopartículas de hexacianoferrato de rutênio para eletro-oxidação de glicerol |
dc.title.alternative.eng.fl_str_mv |
Electrocatalytic activity of ruthenium hexacyanoferrate nanoparticles for glycerol electrooxidation |
title |
Atividade eletrocatalítica de nanopartículas de hexacianoferrato de rutênio para eletro-oxidação de glicerol |
spellingShingle |
Atividade eletrocatalítica de nanopartículas de hexacianoferrato de rutênio para eletro-oxidação de glicerol VIÉGAS, Deracilde Santana da Silva Eletro-oxidação Glicerol Hexacianoferrato de Rutênio Nanopartículas Electrooxidation Glycerol Ruthenium-Hexacyanoferrate Nanoparticles Eletroquímica |
title_short |
Atividade eletrocatalítica de nanopartículas de hexacianoferrato de rutênio para eletro-oxidação de glicerol |
title_full |
Atividade eletrocatalítica de nanopartículas de hexacianoferrato de rutênio para eletro-oxidação de glicerol |
title_fullStr |
Atividade eletrocatalítica de nanopartículas de hexacianoferrato de rutênio para eletro-oxidação de glicerol |
title_full_unstemmed |
Atividade eletrocatalítica de nanopartículas de hexacianoferrato de rutênio para eletro-oxidação de glicerol |
title_sort |
Atividade eletrocatalítica de nanopartículas de hexacianoferrato de rutênio para eletro-oxidação de glicerol |
author |
VIÉGAS, Deracilde Santana da Silva |
author_facet |
VIÉGAS, Deracilde Santana da Silva |
author_role |
author |
dc.contributor.advisor1.fl_str_mv |
MARQUES, Aldaléa Lopes Brandes |
dc.contributor.advisor1ID.fl_str_mv |
076486263-49 |
dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/0121030502015990 |
dc.contributor.referee1.fl_str_mv |
MARQUES, Aldaléa Lopes Brandes |
dc.contributor.referee1ID.fl_str_mv |
076486263-49 |
dc.contributor.referee1Lattes.fl_str_mv |
http://lattes.cnpq.br/0121030502015990 |
dc.contributor.referee2.fl_str_mv |
BRITO, Natilene Mesquita |
dc.contributor.referee2Lattes.fl_str_mv |
http://lattes.cnpq.br/5662692111796966 |
dc.contributor.referee3.fl_str_mv |
RODRIGUES, Isaide de Araújo |
dc.contributor.referee3Lattes.fl_str_mv |
http://lattes.cnpq.br/3696115712661158 |
dc.contributor.referee4.fl_str_mv |
LUZ, Rita de Cassia Silva |
dc.contributor.referee4Lattes.fl_str_mv |
http://lattes.cnpq.br/1282444701404832 |
dc.contributor.referee5.fl_str_mv |
LIMA, Roberto Batista de |
dc.contributor.referee5Lattes.fl_str_mv |
http://lattes.cnpq.br/4982744838486744 |
dc.contributor.authorID.fl_str_mv |
013991003-43 |
dc.contributor.authorLattes.fl_str_mv |
http://lattes.cnpq.br/5345949888760079 |
dc.contributor.author.fl_str_mv |
VIÉGAS, Deracilde Santana da Silva |
contributor_str_mv |
MARQUES, Aldaléa Lopes Brandes MARQUES, Aldaléa Lopes Brandes BRITO, Natilene Mesquita RODRIGUES, Isaide de Araújo LUZ, Rita de Cassia Silva LIMA, Roberto Batista de |
dc.subject.por.fl_str_mv |
Eletro-oxidação Glicerol Hexacianoferrato de Rutênio Nanopartículas |
topic |
Eletro-oxidação Glicerol Hexacianoferrato de Rutênio Nanopartículas Electrooxidation Glycerol Ruthenium-Hexacyanoferrate Nanoparticles Eletroquímica |
dc.subject.eng.fl_str_mv |
Electrooxidation Glycerol Ruthenium-Hexacyanoferrate Nanoparticles |
dc.subject.cnpq.fl_str_mv |
Eletroquímica |
description |
In the present work, the ruthenium (III) hexacyanoferrate complex was tested for glycerol oxidation using two distinct forms of modification of the vitreous carbon electrode. In the first one, the vitreous carbon electrode was modified by electrodeposition through cyclic voltammetry at determined potential and already described in the literature, and in the second, the carbon glass electrode was modified by nanoparticles supported on Vulcan XC-72 carbon, which were synthesized by the alcohol reduction method. Subsequently, the electrocatalysts were characterized by chemical-chemical techniques and tested by electrochemical techniques. The physico-chemical characterization of ruthenium hexacyanoferrate (III) was carried out by Electron Spectrophotometry in the UV-Vis region (UV-Vis), Infrared Vibrational Spectroscopy (FTIR), Electron Transmission Electron Microscopy (TEM), Dispersive Energy X-rays (EDX) and X-ray Diffraction (XRD). Electrochemical characterization occurred by cyclic voltammetry, rotational disk electrode, chronoamperometry and electrochemical impedance spectroscopy (EIS). EDX analysis for the nanoparticles showed that the theoretical starting composition is approximately the same experimentally proven. XRD and TEM analyzes provided the size of the synthesized particles on the order of 3.8 nm, as well as the distribution and dispersion in the carbon carrier. The electrochemical results on the glycerol oxidation reaction showed that the synthesis performed by the alcohol reduction method showed an increase in electrocatalytic current when compared to the unmodified electrode. Through a study with a rotating disk electrode it was possible to verify the involvement of 3.8 electrons in the oxidation reaction of glycerol. Electrochemical impedance spectroscopy has shown that the charge transfer resistance of glycerol electro-oxidation decreases as the potential and concentration of glycerol increase. The carbon-supported ruthenium hexacyanoferrate nanoparticle-modified electrode showed an efficiency in the glycerol oxidation reaction being a viable option for use as a catalyst in direct alcohol fuel cells. |
publishDate |
2019 |
dc.date.accessioned.fl_str_mv |
2019-10-01T13:46:54Z |
dc.date.issued.fl_str_mv |
2019-04-05 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/doctoralThesis |
format |
doctoralThesis |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
VIÉGAS, Deracilde Santana da Silva. Atividade eletrocatalítica de nanopartículas de hexacianoferrato de rutênio para eletro-oxidação de glicerol. 2019. 100 f. Tese (Programa de Pós-Graduação em Rede - Rede de Biodiversidade e Biotecnologia da Amazônia Legal/CCBS) - Universidade Federal do Maranhão, São Luís, 2019. |
dc.identifier.uri.fl_str_mv |
https://tedebc.ufma.br/jspui/handle/tede/tede/2864 |
identifier_str_mv |
VIÉGAS, Deracilde Santana da Silva. Atividade eletrocatalítica de nanopartículas de hexacianoferrato de rutênio para eletro-oxidação de glicerol. 2019. 100 f. Tese (Programa de Pós-Graduação em Rede - Rede de Biodiversidade e Biotecnologia da Amazônia Legal/CCBS) - Universidade Federal do Maranhão, São Luís, 2019. |
url |
https://tedebc.ufma.br/jspui/handle/tede/tede/2864 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Federal do Maranhão |
dc.publisher.program.fl_str_mv |
PROGRAMA DE PÓS-GRADUAÇÃO EM REDE - REDE DE BIODIVERSIDADE E BIOTECNOLOGIA DA AMAZÔNIA LEGAL/CCBS |
dc.publisher.initials.fl_str_mv |
UFMA |
dc.publisher.country.fl_str_mv |
Brasil |
dc.publisher.department.fl_str_mv |
DEPARTAMENTO DE TECNOLOGIA QUÍMICA/CCET |
publisher.none.fl_str_mv |
Universidade Federal do Maranhão |
dc.source.none.fl_str_mv |
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Biblioteca Digital de Teses e Dissertações da UFMA |
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