New insights on the catalytic reductive ...
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Autre communication scientifique (congrès sans actes - poster - séminaire...): Communication dans un congrès sans actes
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Title :
New insights on the catalytic reductive amination of hydroxyacetone amination over RUWXC/AC Catalyst
Author(s) :
Boulos, Joseph [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Goc, Firat [Auteur]
Institut de recherches sur la catalyse et l'environnement de Lyon [IRCELYON]
Perret, Noémie [Auteur]
Institut de recherches sur la catalyse et l'environnement de Lyon [IRCELYON]
Rataboul, Franck [Auteur]
Institut de recherches sur la catalyse et l'environnement de Lyon [IRCELYON]
Marceau, Eric [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Dhainaut, Jeremy [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
royer, sebastien [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Goc, Firat [Auteur]
Institut de recherches sur la catalyse et l'environnement de Lyon [IRCELYON]
Perret, Noémie [Auteur]
Institut de recherches sur la catalyse et l'environnement de Lyon [IRCELYON]
Rataboul, Franck [Auteur]
Institut de recherches sur la catalyse et l'environnement de Lyon [IRCELYON]
Marceau, Eric [Auteur]

Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Dhainaut, Jeremy [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
royer, sebastien [Auteur]

Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Conference title :
SCF'23
City :
Nantes
Country :
France
Start date of the conference :
2023-06-26
English keyword(s) :
Reductive amination
carbides
biomass conversion
bimetallic catalysts
carbides
biomass conversion
bimetallic catalysts
HAL domain(s) :
Chimie/Catalyse
English abstract : [en]
The production of chemicals and liquid fuels from renewable and non-edible lignocellulosic biomass has been considered as a promising way to reduce our dependance to fossil resources as well as to reduce CO2 release. ...
Show more >The production of chemicals and liquid fuels from renewable and non-edible lignocellulosic biomass has been considered as a promising way to reduce our dependance to fossil resources as well as to reduce CO2 release. Especially, nitrogen-containing molecules, particularly primary amines, are broadly used for the synthesis of pharmaceuticals, polymers, surfactants, agrochemicals, and dyes[1]. Owing to the high O/C ratio (~1/1) in biomass feedstocks[2], the production of oxygenates from biomass is rather straightforward and has been largely studied. However, the further production of valuable nitrogen-containing products is far less evident due to the deficit of efficient amination strategies of oxygenates. One way is the amination of aldehydes and ketones to primary amines, employing ammonia as the nitrogen source[3]. Due to the development of biorefining, renewable aldehydes and ketones including glycolaldehyde, glyceraldehyde, hydroxyacetone, and aromatic compounds are nowadays available at large scales, opening new opportunities to produce nitrogen-containing compounds[4]. For example, Liang et al. reported the use of partly reduced Ru/ZrO2 for the reductive amination of different biomass-based aldehydes/ketones in aqueous ammonia[5]. Despite this encouraging development, effective heterogeneous catalytic systems that allow the amination reaction to take place under milder conditions (T < 100 °C, P < 50 bar, aqueous phase, and without additives) with high amines’ yields are still lacking. In particular, the production of large-market amino alcohols from hydroxyacetone hasn’t been reported so far. Herein, we report the preparation of a highly efficient and robust catalyst, RuWxC/AC, for the reductive amination of hydroxyacetone (Figure 1). By varying several process parameters including time, temperature, the nature of nitrogen source, and pressure, up to 60 mol.% amines’ yield has been obtained. The promoting effect of tungsten carbide nanoparticles has been particularly investigated. Finally, a kinetic study has been conducted and will be discussed.Show less >
Show more >The production of chemicals and liquid fuels from renewable and non-edible lignocellulosic biomass has been considered as a promising way to reduce our dependance to fossil resources as well as to reduce CO2 release. Especially, nitrogen-containing molecules, particularly primary amines, are broadly used for the synthesis of pharmaceuticals, polymers, surfactants, agrochemicals, and dyes[1]. Owing to the high O/C ratio (~1/1) in biomass feedstocks[2], the production of oxygenates from biomass is rather straightforward and has been largely studied. However, the further production of valuable nitrogen-containing products is far less evident due to the deficit of efficient amination strategies of oxygenates. One way is the amination of aldehydes and ketones to primary amines, employing ammonia as the nitrogen source[3]. Due to the development of biorefining, renewable aldehydes and ketones including glycolaldehyde, glyceraldehyde, hydroxyacetone, and aromatic compounds are nowadays available at large scales, opening new opportunities to produce nitrogen-containing compounds[4]. For example, Liang et al. reported the use of partly reduced Ru/ZrO2 for the reductive amination of different biomass-based aldehydes/ketones in aqueous ammonia[5]. Despite this encouraging development, effective heterogeneous catalytic systems that allow the amination reaction to take place under milder conditions (T < 100 °C, P < 50 bar, aqueous phase, and without additives) with high amines’ yields are still lacking. In particular, the production of large-market amino alcohols from hydroxyacetone hasn’t been reported so far. Herein, we report the preparation of a highly efficient and robust catalyst, RuWxC/AC, for the reductive amination of hydroxyacetone (Figure 1). By varying several process parameters including time, temperature, the nature of nitrogen source, and pressure, up to 60 mol.% amines’ yield has been obtained. The promoting effect of tungsten carbide nanoparticles has been particularly investigated. Finally, a kinetic study has been conducted and will be discussed.Show less >
Language :
Anglais
Peer reviewed article :
Non
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
Université de Lille
CNRS
Centrale Lille
ENSCL
Univ. Artois
CNRS
Centrale Lille
ENSCL
Univ. Artois
Collections :
Research team(s) :
Matériaux pour la catalyse (MATCAT)
Submission date :
2023-11-17T14:54:03Z
2023-11-23T15:22:50Z
2023-11-23T15:22:50Z
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