Kinetics and mechanism of the electrochemical oxidation of the NO−<sub>2</sub> ion on platinum in AgNO<sub>2</sub>-acetonitrile solution
- Autores
- Castellano, Carlos E.; Calandra, Alfredo J.; Arvia, Alejandro Jorge
- Año de publicación
- 1974
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The anodic oxidation of NO−2 ion dissolved as AgNO2 in ACN, in the range − 12° to 68°C, is investigated using platinum electrodes. Single and multiple linear potential sweep and rotating disc electrode techniques are used. The electrochemical reaction is interpreted with the following sequence of reactions: rds (1) NO2 = NO2 + e (2) [2 NO2 ⇋ N2O4] (3) NO2 + NO2 = NO + NO3 (4) NO = NO- + e (5) NO+ + NO2 = N2O3 (6) [N2O3 ⇋ NO + NO2] Step (1) behaves as an irreversible step which at high potentials is diffusion controlled, while step (4) corresponds to a reversible charge transfer step. The chemical reactions are fast processes. The postulated reaction mechanism for the anodic discharge of the NO−2 ion implies the preferential reaction of the initial product with a NO−2 ion instead of a solvent molecule as it occurred with solutions employing other aprotic solvents.
Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas - Materia
-
Ciencias Exactas
Química
Electrochemical oxidation
NO−2 ion - 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:10915/121709
Ver los metadatos del registro completo
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Kinetics and mechanism of the electrochemical oxidation of the NO−<sub>2</sub> ion on platinum in AgNO<sub>2</sub>-acetonitrile solutionCastellano, Carlos E.Calandra, Alfredo J.Arvia, Alejandro JorgeCiencias ExactasQuímicaElectrochemical oxidationNO−2 ionThe anodic oxidation of NO−2 ion dissolved as AgNO2 in ACN, in the range − 12° to 68°C, is investigated using platinum electrodes. Single and multiple linear potential sweep and rotating disc electrode techniques are used. The electrochemical reaction is interpreted with the following sequence of reactions: rds (1) NO<sub>2</sub> = NO<sub>2</sub> + e (2) [2 NO<sub>2</sub> ⇋ N<sub>2</sub>O<sub>4</sub>] (3) NO<sub>2</sub> + NO<sub>2</sub> = NO + NO<sub>3</sub> (4) NO = NO- + e (5) NO+ + NO<sub>2</sub> = N<sub>2</sub>O<sub>3</sub> (6) [N<sub>2</sub>O<sub>3</sub> ⇋ NO + NO<sub>2</sub>] Step (1) behaves as an irreversible step which at high potentials is diffusion controlled, while step (4) corresponds to a reversible charge transfer step. The chemical reactions are fast processes. The postulated reaction mechanism for the anodic discharge of the NO−<sub>2</sub> ion implies the preferential reaction of the initial product with a NO−<sub>2</sub> ion instead of a solvent molecule as it occurred with solutions employing other aprotic solvents.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas1974info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf701-712http://sedici.unlp.edu.ar/handle/10915/121709enginfo:eu-repo/semantics/altIdentifier/issn/0013-4686info:eu-repo/semantics/altIdentifier/doi/10.1016/0013-4686(74)80013-7info: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:10915/121709Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:28:55.197SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
Kinetics and mechanism of the electrochemical oxidation of the NO−<sub>2</sub> ion on platinum in AgNO<sub>2</sub>-acetonitrile solution |
title |
Kinetics and mechanism of the electrochemical oxidation of the NO−<sub>2</sub> ion on platinum in AgNO<sub>2</sub>-acetonitrile solution |
spellingShingle |
Kinetics and mechanism of the electrochemical oxidation of the NO−<sub>2</sub> ion on platinum in AgNO<sub>2</sub>-acetonitrile solution Castellano, Carlos E. Ciencias Exactas Química Electrochemical oxidation NO−2 ion |
title_short |
Kinetics and mechanism of the electrochemical oxidation of the NO−<sub>2</sub> ion on platinum in AgNO<sub>2</sub>-acetonitrile solution |
title_full |
Kinetics and mechanism of the electrochemical oxidation of the NO−<sub>2</sub> ion on platinum in AgNO<sub>2</sub>-acetonitrile solution |
title_fullStr |
Kinetics and mechanism of the electrochemical oxidation of the NO−<sub>2</sub> ion on platinum in AgNO<sub>2</sub>-acetonitrile solution |
title_full_unstemmed |
Kinetics and mechanism of the electrochemical oxidation of the NO−<sub>2</sub> ion on platinum in AgNO<sub>2</sub>-acetonitrile solution |
title_sort |
Kinetics and mechanism of the electrochemical oxidation of the NO−<sub>2</sub> ion on platinum in AgNO<sub>2</sub>-acetonitrile solution |
dc.creator.none.fl_str_mv |
Castellano, Carlos E. Calandra, Alfredo J. Arvia, Alejandro Jorge |
author |
Castellano, Carlos E. |
author_facet |
Castellano, Carlos E. Calandra, Alfredo J. Arvia, Alejandro Jorge |
author_role |
author |
author2 |
Calandra, Alfredo J. Arvia, Alejandro Jorge |
author2_role |
author author |
dc.subject.none.fl_str_mv |
Ciencias Exactas Química Electrochemical oxidation NO−2 ion |
topic |
Ciencias Exactas Química Electrochemical oxidation NO−2 ion |
dc.description.none.fl_txt_mv |
The anodic oxidation of NO−2 ion dissolved as AgNO2 in ACN, in the range − 12° to 68°C, is investigated using platinum electrodes. Single and multiple linear potential sweep and rotating disc electrode techniques are used. The electrochemical reaction is interpreted with the following sequence of reactions: rds (1) NO<sub>2</sub> = NO<sub>2</sub> + e (2) [2 NO<sub>2</sub> ⇋ N<sub>2</sub>O<sub>4</sub>] (3) NO<sub>2</sub> + NO<sub>2</sub> = NO + NO<sub>3</sub> (4) NO = NO- + e (5) NO+ + NO<sub>2</sub> = N<sub>2</sub>O<sub>3</sub> (6) [N<sub>2</sub>O<sub>3</sub> ⇋ NO + NO<sub>2</sub>] Step (1) behaves as an irreversible step which at high potentials is diffusion controlled, while step (4) corresponds to a reversible charge transfer step. The chemical reactions are fast processes. The postulated reaction mechanism for the anodic discharge of the NO−<sub>2</sub> ion implies the preferential reaction of the initial product with a NO−<sub>2</sub> ion instead of a solvent molecule as it occurred with solutions employing other aprotic solvents. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas |
description |
The anodic oxidation of NO−2 ion dissolved as AgNO2 in ACN, in the range − 12° to 68°C, is investigated using platinum electrodes. Single and multiple linear potential sweep and rotating disc electrode techniques are used. The electrochemical reaction is interpreted with the following sequence of reactions: rds (1) NO<sub>2</sub> = NO<sub>2</sub> + e (2) [2 NO<sub>2</sub> ⇋ N<sub>2</sub>O<sub>4</sub>] (3) NO<sub>2</sub> + NO<sub>2</sub> = NO + NO<sub>3</sub> (4) NO = NO- + e (5) NO+ + NO<sub>2</sub> = N<sub>2</sub>O<sub>3</sub> (6) [N<sub>2</sub>O<sub>3</sub> ⇋ NO + NO<sub>2</sub>] Step (1) behaves as an irreversible step which at high potentials is diffusion controlled, while step (4) corresponds to a reversible charge transfer step. The chemical reactions are fast processes. The postulated reaction mechanism for the anodic discharge of the NO−<sub>2</sub> ion implies the preferential reaction of the initial product with a NO−<sub>2</sub> ion instead of a solvent molecule as it occurred with solutions employing other aprotic solvents. |
publishDate |
1974 |
dc.date.none.fl_str_mv |
1974 |
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/10915/121709 |
url |
http://sedici.unlp.edu.ar/handle/10915/121709 |
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(74)80013-7 |
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 701-712 |
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SEDICI (UNLP) - Universidad Nacional de La Plata |
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