Electrocatalytic hydrogenation of acetophenone and benzophenone using palladium electrodes

Autores
Villalba, Matias Ariel; del Pozo, Maria; Calvo, Ernesto Julio
Año de publicación
2015
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
We have studied the electrocatalytic hydrogenation of acetophenone and benzophenone using a) potentiometric titration of adsorbed hydrogen by the organic reactant in excess, b) electrochemical impedance spectroscopy at a potential at the onset of hydrogen evolution and c) electrolysis at constant potential at high adsorbed hydrogen coverage. The rate of reactions between adsorbed hydrogen and adsorbed ketones and the respective alcohols intermediates of hydrogenation have been obtained from the titration curves at different organic reagent concentrations. Both the reaction rate and the charge transfer resistance, Rct, for the H+/Hads reaction follow a concentration dependence that can be interpreted by a Langmuir adsorption isotherm for the organic molecules and also a blockage of the palladium surface for the hydrogen adsorption. From the results of electrolysis at controlled potential under high hydrogen coverage, the faradaic yield and the product distribution, namely 1-phenylethanol, ethylbenzene, diphenylmethanol, diphenylmethane have been obtained.
Fil: Villalba, Matias Ariel. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: del Pozo, Maria. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Calvo, Ernesto Julio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Materia
Acetophenone
Benzophenone
Electrocatalysis
Hydrogenation
Palladium
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/50073
Acceder
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repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Electrocatalytic hydrogenation of acetophenone and benzophenone using palladium electrodesVillalba, Matias Arieldel Pozo, MariaCalvo, Ernesto JulioAcetophenoneBenzophenoneElectrocatalysisHydrogenationPalladiumhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1We have studied the electrocatalytic hydrogenation of acetophenone and benzophenone using a) potentiometric titration of adsorbed hydrogen by the organic reactant in excess, b) electrochemical impedance spectroscopy at a potential at the onset of hydrogen evolution and c) electrolysis at constant potential at high adsorbed hydrogen coverage. The rate of reactions between adsorbed hydrogen and adsorbed ketones and the respective alcohols intermediates of hydrogenation have been obtained from the titration curves at different organic reagent concentrations. Both the reaction rate and the charge transfer resistance, Rct, for the H+/Hads reaction follow a concentration dependence that can be interpreted by a Langmuir adsorption isotherm for the organic molecules and also a blockage of the palladium surface for the hydrogen adsorption. From the results of electrolysis at controlled potential under high hydrogen coverage, the faradaic yield and the product distribution, namely 1-phenylethanol, ethylbenzene, diphenylmethanol, diphenylmethane have been obtained.Fil: Villalba, Matias Ariel. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaFil: del Pozo, Maria. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaFil: Calvo, Ernesto Julio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaPergamon-Elsevier Science Ltd2015-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/50073Villalba, Matias Ariel; del Pozo, Maria; Calvo, Ernesto Julio; Electrocatalytic hydrogenation of acetophenone and benzophenone using palladium electrodes; Pergamon-Elsevier Science Ltd; Electrochimica Acta; 164; 5-2015; 53-570013-4686CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.electacta.2015.02.113info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0013468615003990info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:33:28Zoai:ri.conicet.gov.ar:11336/50073instacron: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 09:33:28.951CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Electrocatalytic hydrogenation of acetophenone and benzophenone using palladium electrodes
title Electrocatalytic hydrogenation of acetophenone and benzophenone using palladium electrodes
spellingShingle Electrocatalytic hydrogenation of acetophenone and benzophenone using palladium electrodes
Villalba, Matias Ariel
Acetophenone
Benzophenone
Electrocatalysis
Hydrogenation
Palladium
title_short Electrocatalytic hydrogenation of acetophenone and benzophenone using palladium electrodes
title_full Electrocatalytic hydrogenation of acetophenone and benzophenone using palladium electrodes
title_fullStr Electrocatalytic hydrogenation of acetophenone and benzophenone using palladium electrodes
title_full_unstemmed Electrocatalytic hydrogenation of acetophenone and benzophenone using palladium electrodes
title_sort Electrocatalytic hydrogenation of acetophenone and benzophenone using palladium electrodes
dc.creator.none.fl_str_mv Villalba, Matias Ariel
del Pozo, Maria
Calvo, Ernesto Julio
author Villalba, Matias Ariel
author_facet Villalba, Matias Ariel
del Pozo, Maria
Calvo, Ernesto Julio
author_role author
author2 del Pozo, Maria
Calvo, Ernesto Julio
author2_role author
author
dc.subject.none.fl_str_mv Acetophenone
Benzophenone
Electrocatalysis
Hydrogenation
Palladium
topic Acetophenone
Benzophenone
Electrocatalysis
Hydrogenation
Palladium
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv We have studied the electrocatalytic hydrogenation of acetophenone and benzophenone using a) potentiometric titration of adsorbed hydrogen by the organic reactant in excess, b) electrochemical impedance spectroscopy at a potential at the onset of hydrogen evolution and c) electrolysis at constant potential at high adsorbed hydrogen coverage. The rate of reactions between adsorbed hydrogen and adsorbed ketones and the respective alcohols intermediates of hydrogenation have been obtained from the titration curves at different organic reagent concentrations. Both the reaction rate and the charge transfer resistance, Rct, for the H+/Hads reaction follow a concentration dependence that can be interpreted by a Langmuir adsorption isotherm for the organic molecules and also a blockage of the palladium surface for the hydrogen adsorption. From the results of electrolysis at controlled potential under high hydrogen coverage, the faradaic yield and the product distribution, namely 1-phenylethanol, ethylbenzene, diphenylmethanol, diphenylmethane have been obtained.
Fil: Villalba, Matias Ariel. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: del Pozo, Maria. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Calvo, Ernesto Julio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
description We have studied the electrocatalytic hydrogenation of acetophenone and benzophenone using a) potentiometric titration of adsorbed hydrogen by the organic reactant in excess, b) electrochemical impedance spectroscopy at a potential at the onset of hydrogen evolution and c) electrolysis at constant potential at high adsorbed hydrogen coverage. The rate of reactions between adsorbed hydrogen and adsorbed ketones and the respective alcohols intermediates of hydrogenation have been obtained from the titration curves at different organic reagent concentrations. Both the reaction rate and the charge transfer resistance, Rct, for the H+/Hads reaction follow a concentration dependence that can be interpreted by a Langmuir adsorption isotherm for the organic molecules and also a blockage of the palladium surface for the hydrogen adsorption. From the results of electrolysis at controlled potential under high hydrogen coverage, the faradaic yield and the product distribution, namely 1-phenylethanol, ethylbenzene, diphenylmethanol, diphenylmethane have been obtained.
publishDate 2015
dc.date.none.fl_str_mv 2015-05
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/11336/50073
Villalba, Matias Ariel; del Pozo, Maria; Calvo, Ernesto Julio; Electrocatalytic hydrogenation of acetophenone and benzophenone using palladium electrodes; Pergamon-Elsevier Science Ltd; Electrochimica Acta; 164; 5-2015; 53-57
0013-4686
CONICET Digital
CONICET
url http://hdl.handle.net/11336/50073
identifier_str_mv Villalba, Matias Ariel; del Pozo, Maria; Calvo, Ernesto Julio; Electrocatalytic hydrogenation of acetophenone and benzophenone using palladium electrodes; Pergamon-Elsevier Science Ltd; Electrochimica Acta; 164; 5-2015; 53-57
0013-4686
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1016/j.electacta.2015.02.113
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0013468615003990
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Pergamon-Elsevier Science Ltd
publisher.none.fl_str_mv Pergamon-Elsevier Science Ltd
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
_version_ 1844613028635475968
score 13.069144

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