Electrochemistry of solvated proton in dimethylsulphoxide : II. Kinetics and mechanism of the electrolytic evolution of hydrogen on iron
- Autores
- Posadas, Dionisio; Podestá, José J.; Arvia, Alejandro Jorge
- Año de publicación
- 1970
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The kinetics of the electrolytic evolution of hydrogen on iron electrodes using solutions of HCl in DMSO has been investigated. The electrode reaction was studied within the temperature range from 20 to 45°C at various HCl concentrations, in the presence of an excess of potassium perchlorate. The mechanism interpreting the electrode reaction comprises as first step the simple solvated-hydrogen-ion discharge as rate-controlling followed probably by a hydrogen adatom combination process. The theoretical parameters derived from this mechanism coincide with the results obtained from steady as well as from non-steady measurements.
Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas - Materia
-
Ciencias Exactas
Química
Dimethylsulphoxide
Iron - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by/4.0/
- Repositorio
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/119942
Ver los metadatos del registro completo
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Electrochemistry of solvated proton in dimethylsulphoxide : II. Kinetics and mechanism of the electrolytic evolution of hydrogen on ironPosadas, DionisioPodestá, José J.Arvia, Alejandro JorgeCiencias ExactasQuímicaDimethylsulphoxideIronThe kinetics of the electrolytic evolution of hydrogen on iron electrodes using solutions of HCl in DMSO has been investigated. The electrode reaction was studied within the temperature range from 20 to 45°C at various HCl concentrations, in the presence of an excess of potassium perchlorate. The mechanism interpreting the electrode reaction comprises as first step the simple solvated-hydrogen-ion discharge as rate-controlling followed probably by a hydrogen adatom combination process. The theoretical parameters derived from this mechanism coincide with the results obtained from steady as well as from non-steady measurements.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas1970info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf1225-1232http://sedici.unlp.edu.ar/handle/10915/119942enginfo:eu-repo/semantics/altIdentifier/issn/0013-4686info:eu-repo/semantics/altIdentifier/doi/10.1016/0013-4686(70)85016-2info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:28:20Zoai:sedici.unlp.edu.ar:10915/119942Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:28:20.734SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
Electrochemistry of solvated proton in dimethylsulphoxide : II. Kinetics and mechanism of the electrolytic evolution of hydrogen on iron |
title |
Electrochemistry of solvated proton in dimethylsulphoxide : II. Kinetics and mechanism of the electrolytic evolution of hydrogen on iron |
spellingShingle |
Electrochemistry of solvated proton in dimethylsulphoxide : II. Kinetics and mechanism of the electrolytic evolution of hydrogen on iron Posadas, Dionisio Ciencias Exactas Química Dimethylsulphoxide Iron |
title_short |
Electrochemistry of solvated proton in dimethylsulphoxide : II. Kinetics and mechanism of the electrolytic evolution of hydrogen on iron |
title_full |
Electrochemistry of solvated proton in dimethylsulphoxide : II. Kinetics and mechanism of the electrolytic evolution of hydrogen on iron |
title_fullStr |
Electrochemistry of solvated proton in dimethylsulphoxide : II. Kinetics and mechanism of the electrolytic evolution of hydrogen on iron |
title_full_unstemmed |
Electrochemistry of solvated proton in dimethylsulphoxide : II. Kinetics and mechanism of the electrolytic evolution of hydrogen on iron |
title_sort |
Electrochemistry of solvated proton in dimethylsulphoxide : II. Kinetics and mechanism of the electrolytic evolution of hydrogen on iron |
dc.creator.none.fl_str_mv |
Posadas, Dionisio Podestá, José J. Arvia, Alejandro Jorge |
author |
Posadas, Dionisio |
author_facet |
Posadas, Dionisio Podestá, José J. Arvia, Alejandro Jorge |
author_role |
author |
author2 |
Podestá, José J. Arvia, Alejandro Jorge |
author2_role |
author author |
dc.subject.none.fl_str_mv |
Ciencias Exactas Química Dimethylsulphoxide Iron |
topic |
Ciencias Exactas Química Dimethylsulphoxide Iron |
dc.description.none.fl_txt_mv |
The kinetics of the electrolytic evolution of hydrogen on iron electrodes using solutions of HCl in DMSO has been investigated. The electrode reaction was studied within the temperature range from 20 to 45°C at various HCl concentrations, in the presence of an excess of potassium perchlorate. The mechanism interpreting the electrode reaction comprises as first step the simple solvated-hydrogen-ion discharge as rate-controlling followed probably by a hydrogen adatom combination process. The theoretical parameters derived from this mechanism coincide with the results obtained from steady as well as from non-steady measurements. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas |
description |
The kinetics of the electrolytic evolution of hydrogen on iron electrodes using solutions of HCl in DMSO has been investigated. The electrode reaction was studied within the temperature range from 20 to 45°C at various HCl concentrations, in the presence of an excess of potassium perchlorate. The mechanism interpreting the electrode reaction comprises as first step the simple solvated-hydrogen-ion discharge as rate-controlling followed probably by a hydrogen adatom combination process. The theoretical parameters derived from this mechanism coincide with the results obtained from steady as well as from non-steady measurements. |
publishDate |
1970 |
dc.date.none.fl_str_mv |
1970 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Articulo 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://sedici.unlp.edu.ar/handle/10915/119942 |
url |
http://sedici.unlp.edu.ar/handle/10915/119942 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/issn/0013-4686 info:eu-repo/semantics/altIdentifier/doi/10.1016/0013-4686(70)85016-2 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International (CC BY 4.0) |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International (CC BY 4.0) |
dc.format.none.fl_str_mv |
application/pdf 1225-1232 |
dc.source.none.fl_str_mv |
reponame:SEDICI (UNLP) instname:Universidad Nacional de La Plata instacron:UNLP |
reponame_str |
SEDICI (UNLP) |
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SEDICI (UNLP) |
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Universidad Nacional de La Plata |
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UNLP |
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UNLP |
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SEDICI (UNLP) - Universidad Nacional de La Plata |
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alira@sedici.unlp.edu.ar |
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score |
13.070432 |