Electrocatalytic hydrogenation of acetophenone and benzophenone using palladium electrodes

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 po...

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Autores principales: Villalba, Matias Ariel, Calvo, Ernesto Julio
Publicado: 2015
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00134686_v164_n_p125_Villalba
http://hdl.handle.net/20.500.12110/paper_00134686_v164_n_p125_Villalba
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spelling paper:paper_00134686_v164_n_p125_Villalba2023-06-08T14:35:47Z Electrocatalytic hydrogenation of acetophenone and benzophenone using palladium electrodes Villalba, Matias Ariel Calvo, Ernesto Julio Acetophenone Benzophenone Electrocatalysis Hydrogenation Palladium Charge transfer Electrocatalysis Electrochemical impedance spectroscopy Electrodes Electrolysis Hydrogen Hydrogenation Ketones Palladium Reaction intermediates Titration Voltammetry Acetophenones Benzophenone Charge transfer resistance Concentration dependence Electrocatalytic hydrogenation Langmuir adsorption isotherms Potentiometric titrations Product distributions Gas adsorption 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. © 2015 Elsevier Ltd. Fil:Villalba, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Calvo, E.J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2015 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00134686_v164_n_p125_Villalba http://hdl.handle.net/20.500.12110/paper_00134686_v164_n_p125_Villalba
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Acetophenone
Benzophenone
Electrocatalysis
Hydrogenation
Palladium
Charge transfer
Electrocatalysis
Electrochemical impedance spectroscopy
Electrodes
Electrolysis
Hydrogen
Hydrogenation
Ketones
Palladium
Reaction intermediates
Titration
Voltammetry
Acetophenones
Benzophenone
Charge transfer resistance
Concentration dependence
Electrocatalytic hydrogenation
Langmuir adsorption isotherms
Potentiometric titrations
Product distributions
Gas adsorption
spellingShingle Acetophenone
Benzophenone
Electrocatalysis
Hydrogenation
Palladium
Charge transfer
Electrocatalysis
Electrochemical impedance spectroscopy
Electrodes
Electrolysis
Hydrogen
Hydrogenation
Ketones
Palladium
Reaction intermediates
Titration
Voltammetry
Acetophenones
Benzophenone
Charge transfer resistance
Concentration dependence
Electrocatalytic hydrogenation
Langmuir adsorption isotherms
Potentiometric titrations
Product distributions
Gas adsorption
Villalba, Matias Ariel
Calvo, Ernesto Julio
Electrocatalytic hydrogenation of acetophenone and benzophenone using palladium electrodes
topic_facet Acetophenone
Benzophenone
Electrocatalysis
Hydrogenation
Palladium
Charge transfer
Electrocatalysis
Electrochemical impedance spectroscopy
Electrodes
Electrolysis
Hydrogen
Hydrogenation
Ketones
Palladium
Reaction intermediates
Titration
Voltammetry
Acetophenones
Benzophenone
Charge transfer resistance
Concentration dependence
Electrocatalytic hydrogenation
Langmuir adsorption isotherms
Potentiometric titrations
Product distributions
Gas adsorption
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. © 2015 Elsevier Ltd.
author Villalba, Matias Ariel
Calvo, Ernesto Julio
author_facet Villalba, Matias Ariel
Calvo, Ernesto Julio
author_sort Villalba, Matias Ariel
title Electrocatalytic hydrogenation of acetophenone and benzophenone using palladium electrodes
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
publishDate 2015
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00134686_v164_n_p125_Villalba
http://hdl.handle.net/20.500.12110/paper_00134686_v164_n_p125_Villalba
work_keys_str_mv AT villalbamatiasariel electrocatalytichydrogenationofacetophenoneandbenzophenoneusingpalladiumelectrodes
AT calvoernestojulio electrocatalytichydrogenationofacetophenoneandbenzophenoneusingpalladiumelectrodes
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