An acrolein production route from ethanol ...
Document type :
Article dans une revue scientifique: Article original
DOI :
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Title :
An acrolein production route from ethanol and methanol mixtures over FeMo-based catalysts
Author(s) :
Borowiec, Anita [Auteur]
Devaux, Jean-François [Auteur]
Dubois, Jean-Luc [Auteur]
Jouenne, L. [Auteur]
Bigan, Muriel [Auteur]
BioEcoAgro - UMR-T 1158
Institut Charles Viollette (ICV) - ULR 7394
Institut Charles Viollette (ICV) - EA 7394 [ICV]
Simon, Pardis [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Trentesaux, Martine [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Faye, Jérémy [Auteur]
Capron, Mickael [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Dumeignil, Franck [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Devaux, Jean-François [Auteur]
Dubois, Jean-Luc [Auteur]
Jouenne, L. [Auteur]
Bigan, Muriel [Auteur]

BioEcoAgro - UMR-T 1158
Institut Charles Viollette (ICV) - ULR 7394
Institut Charles Viollette (ICV) - EA 7394 [ICV]
Simon, Pardis [Auteur]

Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Trentesaux, Martine [Auteur]

Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Faye, Jérémy [Auteur]
Capron, Mickael [Auteur]

Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Dumeignil, Franck [Auteur]

Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Journal title :
Green Chemistry
Abbreviated title :
Green Chem.
Volume number :
19
Pages :
2666-2674
Publication date :
2017
HAL domain(s) :
Chimie/Catalyse
English abstract : [en]
Acrolein is the simplest unsaturated aldehyde, which – due to its high reactivity – has found application as an intermediate in the chemical industry. Nowadays, this chemical is commercially obtained by propylene oxidation, ...
Show more >Acrolein is the simplest unsaturated aldehyde, which – due to its high reactivity – has found application as an intermediate in the chemical industry. Nowadays, this chemical is commercially obtained by propylene oxidation, which is based on fossil resources. Herein, an alternative production method starting from methanol and ethanol mixtures is presented. The reaction was performed over FeMo-based catalysts synthesized at different Mo/Fe ratios (i.e., 1.5, 2.0 and 2.5) and calcined at different temperatures (i.e., 350, 400 and 450 °C). The operational conditions were found by a Design of Experiments method, which showed that the most important factor influencing the acrolein yield was the reaction temperature. During these studies the best catalytic performance was observed for FeMo2.5 calcined at 400 °C (i.e., 39%). Catalysts were characterised by different methods (e.g., TGA-DSC, XRD, etc.). Advanced quasi in situ XPS studies have shown that the molybdenum present on the catalyst surface performs the redox cycle during the reaction.Show less >
Show more >Acrolein is the simplest unsaturated aldehyde, which – due to its high reactivity – has found application as an intermediate in the chemical industry. Nowadays, this chemical is commercially obtained by propylene oxidation, which is based on fossil resources. Herein, an alternative production method starting from methanol and ethanol mixtures is presented. The reaction was performed over FeMo-based catalysts synthesized at different Mo/Fe ratios (i.e., 1.5, 2.0 and 2.5) and calcined at different temperatures (i.e., 350, 400 and 450 °C). The operational conditions were found by a Design of Experiments method, which showed that the most important factor influencing the acrolein yield was the reaction temperature. During these studies the best catalytic performance was observed for FeMo2.5 calcined at 400 °C (i.e., 39%). Catalysts were characterised by different methods (e.g., TGA-DSC, XRD, etc.). Advanced quasi in situ XPS studies have shown that the molybdenum present on the catalyst surface performs the redox cycle during the reaction.Show less >
Language :
Anglais
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
ENSCL
Université de Lille
CNRS
Centrale Lille
Univ. Artois
Université de Lille
CNRS
Centrale Lille
Univ. Artois
Collections :
Research team(s) :
Valorisation des alcanes et de la biomasse (VAALBIO)
Submission date :
2019-09-25T14:05:30Z
2020-09-15T08:36:04Z
2020-09-15T08:36:04Z
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