Comparative cyclic voltammetry and SEM analysis of tin electrodes in citrate buffer solutions

Autores
Gervasi, Claudio; Alvarez, Patricia Eugenia; Fiori Bimbi, María Victoria del Valle; Folquer, Maria Eugenia
Año de publicación
2007
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The anodic oxidation of tin in citrate buffer solutions has been studied by cyclic voltammetry and scanning electron microscopy. In order to identify each individual process, a numerical method was used to resolve into single processes the electrochemical behaviour.The results indicate that primary passivation is due to the formation of a Sn(II)-containing surface film. This film is not further oxidized at higher anodic potentials. There is evidence that during secondary passivation direct oxidation of Sn to Sn(IV) takes place, either as soluble ions or as a hydroxide layer. The results of this work improve, as well as, confirm theories previously advanced.
Fil: Gervasi, Claudio. Universidad Nacional de La Plata. Facultad de Ingenierí­a. Departamento de Ingeniería Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina
Fil: Alvarez, Patricia Eugenia. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Física; Argentina
Fil: Fiori Bimbi, María Victoria del Valle. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Física; Argentina
Fil: Folquer, Maria Eugenia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; Argentina. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química Física; Argentina
Materia
Tin
citrate buffer
passive films
voltammetry
SEM
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/102901
Acceder
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oai_identifier_str oai:ri.conicet.gov.ar:11336/102901
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Comparative cyclic voltammetry and SEM analysis of tin electrodes in citrate buffer solutionsGervasi, ClaudioAlvarez, Patricia EugeniaFiori Bimbi, María Victoria del ValleFolquer, Maria EugeniaTincitrate bufferpassive filmsvoltammetrySEMhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The anodic oxidation of tin in citrate buffer solutions has been studied by cyclic voltammetry and scanning electron microscopy. In order to identify each individual process, a numerical method was used to resolve into single processes the electrochemical behaviour.The results indicate that primary passivation is due to the formation of a Sn(II)-containing surface film. This film is not further oxidized at higher anodic potentials. There is evidence that during secondary passivation direct oxidation of Sn to Sn(IV) takes place, either as soluble ions or as a hydroxide layer. The results of this work improve, as well as, confirm theories previously advanced.Fil: Gervasi, Claudio. Universidad Nacional de La Plata. Facultad de Ingenierí­a. Departamento de Ingeniería Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; ArgentinaFil: Alvarez, Patricia Eugenia. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Física; ArgentinaFil: Fiori Bimbi, María Victoria del Valle. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Física; ArgentinaFil: Folquer, Maria Eugenia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; Argentina. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química Física; ArgentinaElsevier Science Sa2007-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/102901Gervasi, Claudio; Alvarez, Patricia Eugenia; Fiori Bimbi, María Victoria del Valle; Folquer, Maria Eugenia; Comparative cyclic voltammetry and SEM analysis of tin electrodes in citrate buffer solutions; Elsevier Science Sa; Journal of Electroanalytical Chemistry; 601; 1-2; 3-2007; 194-2040022-07281572-6657CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0022072806006541info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jelechem.2006.11.019info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:24:41Zoai:ri.conicet.gov.ar:11336/102901instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:24:41.461CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Comparative cyclic voltammetry and SEM analysis of tin electrodes in citrate buffer solutions
title Comparative cyclic voltammetry and SEM analysis of tin electrodes in citrate buffer solutions
spellingShingle Comparative cyclic voltammetry and SEM analysis of tin electrodes in citrate buffer solutions
Gervasi, Claudio
Tin
citrate buffer
passive films
voltammetry
SEM
title_short Comparative cyclic voltammetry and SEM analysis of tin electrodes in citrate buffer solutions
title_full Comparative cyclic voltammetry and SEM analysis of tin electrodes in citrate buffer solutions
title_fullStr Comparative cyclic voltammetry and SEM analysis of tin electrodes in citrate buffer solutions
title_full_unstemmed Comparative cyclic voltammetry and SEM analysis of tin electrodes in citrate buffer solutions
title_sort Comparative cyclic voltammetry and SEM analysis of tin electrodes in citrate buffer solutions
dc.creator.none.fl_str_mv Gervasi, Claudio
Alvarez, Patricia Eugenia
Fiori Bimbi, María Victoria del Valle
Folquer, Maria Eugenia
author Gervasi, Claudio
author_facet Gervasi, Claudio
Alvarez, Patricia Eugenia
Fiori Bimbi, María Victoria del Valle
Folquer, Maria Eugenia
author_role author
author2 Alvarez, Patricia Eugenia
Fiori Bimbi, María Victoria del Valle
Folquer, Maria Eugenia
author2_role author
author
author
dc.subject.none.fl_str_mv Tin
citrate buffer
passive films
voltammetry
SEM
topic Tin
citrate buffer
passive films
voltammetry
SEM
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The anodic oxidation of tin in citrate buffer solutions has been studied by cyclic voltammetry and scanning electron microscopy. In order to identify each individual process, a numerical method was used to resolve into single processes the electrochemical behaviour.The results indicate that primary passivation is due to the formation of a Sn(II)-containing surface film. This film is not further oxidized at higher anodic potentials. There is evidence that during secondary passivation direct oxidation of Sn to Sn(IV) takes place, either as soluble ions or as a hydroxide layer. The results of this work improve, as well as, confirm theories previously advanced.
Fil: Gervasi, Claudio. Universidad Nacional de La Plata. Facultad de Ingenierí­a. Departamento de Ingeniería Química; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina
Fil: Alvarez, Patricia Eugenia. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Física; Argentina
Fil: Fiori Bimbi, María Victoria del Valle. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Física; Argentina
Fil: Folquer, Maria Eugenia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; Argentina. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química Física; Argentina
description The anodic oxidation of tin in citrate buffer solutions has been studied by cyclic voltammetry and scanning electron microscopy. In order to identify each individual process, a numerical method was used to resolve into single processes the electrochemical behaviour.The results indicate that primary passivation is due to the formation of a Sn(II)-containing surface film. This film is not further oxidized at higher anodic potentials. There is evidence that during secondary passivation direct oxidation of Sn to Sn(IV) takes place, either as soluble ions or as a hydroxide layer. The results of this work improve, as well as, confirm theories previously advanced.
publishDate 2007
dc.date.none.fl_str_mv 2007-03
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/102901
Gervasi, Claudio; Alvarez, Patricia Eugenia; Fiori Bimbi, María Victoria del Valle; Folquer, Maria Eugenia; Comparative cyclic voltammetry and SEM analysis of tin electrodes in citrate buffer solutions; Elsevier Science Sa; Journal of Electroanalytical Chemistry; 601; 1-2; 3-2007; 194-204
0022-0728
1572-6657
CONICET Digital
CONICET
url http://hdl.handle.net/11336/102901
identifier_str_mv Gervasi, Claudio; Alvarez, Patricia Eugenia; Fiori Bimbi, María Victoria del Valle; Folquer, Maria Eugenia; Comparative cyclic voltammetry and SEM analysis of tin electrodes in citrate buffer solutions; Elsevier Science Sa; Journal of Electroanalytical Chemistry; 601; 1-2; 3-2007; 194-204
0022-0728
1572-6657
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0022072806006541
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jelechem.2006.11.019
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier Science Sa
publisher.none.fl_str_mv Elsevier Science Sa
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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score 13.070432

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