Kinetics and mechanism of the electrochemical oxidation of graphite in bisulphate melts
- Autores
- Arvia, Alejandro Jorge; Triaca, Walter Enrique; Videla, Héctor A.
- Año de publicación
- 1970
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The kinetics of the electrochemical oxidation of graphite to volatile compounds by electrolysing molten bisulphates in the temperature range from 180 to 320°C has been studied by conventional steady-state and non-steady-state measurements. CO2, CO and traces of SO2 are formed during the electrochemical reaction. Assuming 4 Faraday/mol of CO2, the anodic efficiency is about 90%. The CO2/CO ratio is about 2 and is independent of the cd in the range considered. The electrochemical reaction is compared to the thermal oxidation of graphite. The reaction is interpreted through a scheme involving consecutive reactions, where the rate-determining step, under Temkin conditions, is a thermal process involving a desorption of intermediates following either a first-order or second-order process depending on the type of adsorption obeyed. The activation energy derived from the rate constant at the rest potential is about 42·5 Kcal/mol.
Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas - Materia
-
Ciencias Exactas
Química
Electrochemical oxidation
Kinetics
Graphite - 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:10915/121692
Ver los metadatos del registro completo
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Kinetics and mechanism of the electrochemical oxidation of graphite in bisulphate meltsArvia, Alejandro JorgeTriaca, Walter EnriqueVidela, Héctor A.Ciencias ExactasQuímicaElectrochemical oxidationKineticsGraphiteThe kinetics of the electrochemical oxidation of graphite to volatile compounds by electrolysing molten bisulphates in the temperature range from 180 to 320°C has been studied by conventional steady-state and non-steady-state measurements. CO<sub>2</sub>, CO and traces of SO<sub>2</sub> are formed during the electrochemical reaction. Assuming 4 Faraday/mol of CO<sub>2</sub>, the anodic efficiency is about 90%. The CO<sub>2</sub>/CO ratio is about 2 and is independent of the cd in the range considered. The electrochemical reaction is compared to the thermal oxidation of graphite. The reaction is interpreted through a scheme involving consecutive reactions, where the rate-determining step, under Temkin conditions, is a thermal process involving a desorption of intermediates following either a first-order or second-order process depending on the type of adsorption obeyed. The activation energy derived from the rate constant at the rest potential is about 42·5 Kcal/mol.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/pdf9-24http://sedici.unlp.edu.ar/handle/10915/121692enginfo:eu-repo/semantics/altIdentifier/issn/0013-4686info:eu-repo/semantics/altIdentifier/doi/10.1016/0013-4686(70)90002-2info: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:UNLP2025-09-29T11:28:54Zoai:sedici.unlp.edu.ar:10915/121692Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:28:54.515SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
Kinetics and mechanism of the electrochemical oxidation of graphite in bisulphate melts |
title |
Kinetics and mechanism of the electrochemical oxidation of graphite in bisulphate melts |
spellingShingle |
Kinetics and mechanism of the electrochemical oxidation of graphite in bisulphate melts Arvia, Alejandro Jorge Ciencias Exactas Química Electrochemical oxidation Kinetics Graphite |
title_short |
Kinetics and mechanism of the electrochemical oxidation of graphite in bisulphate melts |
title_full |
Kinetics and mechanism of the electrochemical oxidation of graphite in bisulphate melts |
title_fullStr |
Kinetics and mechanism of the electrochemical oxidation of graphite in bisulphate melts |
title_full_unstemmed |
Kinetics and mechanism of the electrochemical oxidation of graphite in bisulphate melts |
title_sort |
Kinetics and mechanism of the electrochemical oxidation of graphite in bisulphate melts |
dc.creator.none.fl_str_mv |
Arvia, Alejandro Jorge Triaca, Walter Enrique Videla, Héctor A. |
author |
Arvia, Alejandro Jorge |
author_facet |
Arvia, Alejandro Jorge Triaca, Walter Enrique Videla, Héctor A. |
author_role |
author |
author2 |
Triaca, Walter Enrique Videla, Héctor A. |
author2_role |
author author |
dc.subject.none.fl_str_mv |
Ciencias Exactas Química Electrochemical oxidation Kinetics Graphite |
topic |
Ciencias Exactas Química Electrochemical oxidation Kinetics Graphite |
dc.description.none.fl_txt_mv |
The kinetics of the electrochemical oxidation of graphite to volatile compounds by electrolysing molten bisulphates in the temperature range from 180 to 320°C has been studied by conventional steady-state and non-steady-state measurements. CO<sub>2</sub>, CO and traces of SO<sub>2</sub> are formed during the electrochemical reaction. Assuming 4 Faraday/mol of CO<sub>2</sub>, the anodic efficiency is about 90%. The CO<sub>2</sub>/CO ratio is about 2 and is independent of the cd in the range considered. The electrochemical reaction is compared to the thermal oxidation of graphite. The reaction is interpreted through a scheme involving consecutive reactions, where the rate-determining step, under Temkin conditions, is a thermal process involving a desorption of intermediates following either a first-order or second-order process depending on the type of adsorption obeyed. The activation energy derived from the rate constant at the rest potential is about 42·5 Kcal/mol. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas |
description |
The kinetics of the electrochemical oxidation of graphite to volatile compounds by electrolysing molten bisulphates in the temperature range from 180 to 320°C has been studied by conventional steady-state and non-steady-state measurements. CO<sub>2</sub>, CO and traces of SO<sub>2</sub> are formed during the electrochemical reaction. Assuming 4 Faraday/mol of CO<sub>2</sub>, the anodic efficiency is about 90%. The CO<sub>2</sub>/CO ratio is about 2 and is independent of the cd in the range considered. The electrochemical reaction is compared to the thermal oxidation of graphite. The reaction is interpreted through a scheme involving consecutive reactions, where the rate-determining step, under Temkin conditions, is a thermal process involving a desorption of intermediates following either a first-order or second-order process depending on the type of adsorption obeyed. The activation energy derived from the rate constant at the rest potential is about 42·5 Kcal/mol. |
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/10915/121692 |
url |
http://sedici.unlp.edu.ar/handle/10915/121692 |
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)90002-2 |
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) |
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application/pdf 9-24 |
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SEDICI (UNLP) - Universidad Nacional de La Plata |
repository.mail.fl_str_mv |
alira@sedici.unlp.edu.ar |
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