Cyclodextrin-assisted low-metal Ni-Pd/Al2O3 ...
Type de document :
Article dans une revue scientifique
URL permanente :
Titre :
Cyclodextrin-assisted low-metal Ni-Pd/Al2O3 bimetallic catalysts for the direct amination of aliphatic alcohols
Auteur(s) :
Tomer, Ajay [Auteur]
Kusema, Bright T. [Auteur]
Paul, Jean-Francois [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Przybylski, Cédric [Auteur]
Monflier, Eric [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
UCCS Équipe Catalyse Supramoléculaire
Pera-Titus, Marc [Auteur]
Ponchel, Anne [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
UCCS Équipe Catalyse Supramoléculaire
Kusema, Bright T. [Auteur]
Paul, Jean-Francois [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Przybylski, Cédric [Auteur]
Monflier, Eric [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
UCCS Équipe Catalyse Supramoléculaire
Pera-Titus, Marc [Auteur]
Ponchel, Anne [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
UCCS Équipe Catalyse Supramoléculaire
Titre de la revue :
Journal of Catalysis
Numéro :
368
Pagination :
172-189
Éditeur :
Elsevier
Date de publication :
2018-12
Discipline(s) HAL :
Chimie/Catalyse
Chimie/Chimie théorique et/ou physique
Chimie/Chimie théorique et/ou physique
Résumé en anglais : [en]
This paper reports the use of β-cyclodextrin as a pre-shaping agent for the preparation of low-metal xNi-yPd/Al2O3 catalysts (x = 2, 5 wt% and y = 0.2, 0.5, 1.0 wt%) targeting the direct amination of 1-octanol with ammonia. ...
Lire la suite >This paper reports the use of β-cyclodextrin as a pre-shaping agent for the preparation of low-metal xNi-yPd/Al2O3 catalysts (x = 2, 5 wt% and y = 0.2, 0.5, 1.0 wt%) targeting the direct amination of 1-octanol with ammonia. Six different preparation methods were used aiming at tuning the Ni-Pd interaction. The catalysts were finely characterized by XRD, H2-TPR, CO pulse chemisorption, STEM-EELS/EDS-SDD and XPS, while the elementary interaction between Ni-Pd-cyclodextrin was assessed by marrying ESI-MS experiments with DFT calculations. Among the different methods studied, the most outstanding effect was obtained when β-cyclodextrin was pre-adsorbed on γ-Al2O3 before impregnating the Ni and Pd nitrate precursors. At such conditions, the best formulation (5Ni-0.5Pd/Al-CD_M4) afforded 90% conversion and 71% yield to 1-octylamine (TON = 93) in the amination of 1-octanol with ammonia at 160 °C for 4 h, which places it among the most active and selective Ni catalysts reported in the literature.Lire moins >
Lire la suite >This paper reports the use of β-cyclodextrin as a pre-shaping agent for the preparation of low-metal xNi-yPd/Al2O3 catalysts (x = 2, 5 wt% and y = 0.2, 0.5, 1.0 wt%) targeting the direct amination of 1-octanol with ammonia. Six different preparation methods were used aiming at tuning the Ni-Pd interaction. The catalysts were finely characterized by XRD, H2-TPR, CO pulse chemisorption, STEM-EELS/EDS-SDD and XPS, while the elementary interaction between Ni-Pd-cyclodextrin was assessed by marrying ESI-MS experiments with DFT calculations. Among the different methods studied, the most outstanding effect was obtained when β-cyclodextrin was pre-adsorbed on γ-Al2O3 before impregnating the Ni and Pd nitrate precursors. At such conditions, the best formulation (5Ni-0.5Pd/Al-CD_M4) afforded 90% conversion and 71% yield to 1-octylamine (TON = 93) in the amination of 1-octanol with ammonia at 160 °C for 4 h, which places it among the most active and selective Ni catalysts reported in the literature.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
ENSCL
CNRS
Centrale Lille
Univ. Artois
Université de Lille
CNRS
Centrale Lille
Univ. Artois
Université de Lille
Collections :
Équipe(s) de recherche :
Catalyse et chimie supramoléculaire (CASU)
Modélisation et spectroscopies (MODSPEC)
Modélisation et spectroscopies (MODSPEC)
Date de dépôt :
2019-09-25T15:06:55Z
2021-03-04T13:37:00Z
2021-03-04T13:37:00Z