Tailoring the product selectivity of co/sio2 ...
Type de document :
Article dans une revue scientifique: Article original
URL permanente :
Titre :
Tailoring the product selectivity of co/sio2 fischer-tropsch synthesis catalysts by lanthanide doping
Auteur(s) :
Ribeiro, Mauro Celso [Auteur]
Gnanamani, Muthu K. [Auteur]
Garcia, Richard [Auteur]
Jacobs, Gary [Auteur]
Rabelo-Neto, Raimundo Crisostomo [Auteur]
Bellot Noronha, Fabio [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Gomes, Igor F. [Auteur]
Davis, Burtron H. [Auteur]
Gnanamani, Muthu K. [Auteur]
Garcia, Richard [Auteur]
Jacobs, Gary [Auteur]
Rabelo-Neto, Raimundo Crisostomo [Auteur]
Bellot Noronha, Fabio [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Gomes, Igor F. [Auteur]
Davis, Burtron H. [Auteur]
Titre de la revue :
Catalysis Today
Nom court de la revue :
Catal. Today
Numéro :
343
Pagination :
80-90
Date de publication :
2020-03-01
ISSN :
0920-5861
Mot(s)-clé(s) en anglais :
Higher oxygenate synthesis
Fischer-Tropsch synthesis
Cobalt
Ceria
Lanthanides
Fischer-Tropsch synthesis
Cobalt
Ceria
Lanthanides
Discipline(s) HAL :
Chimie/Catalyse
Résumé en anglais : [en]
The effect of the nature of the lanthanide (Ln = La, Ce, Pr, Sm, Gd) on the structure and reactivity of Co/SiO2 catalysts for CO hydrogenation (i.e., Fischer Trospch synthesis) was investigated. In-situ temperature programmed ...
Lire la suite >The effect of the nature of the lanthanide (Ln = La, Ce, Pr, Sm, Gd) on the structure and reactivity of Co/SiO2 catalysts for CO hydrogenation (i.e., Fischer Trospch synthesis) was investigated. In-situ temperature programmed reduction with extended x-ray absorption fine structure and x-ray absorption near edge spectroscopy (TPR-EXAFS/XANES) of the structure of both Co and Ln containing phases under activation and CO hydrogenation conditions were performed. Concerning catalyst selectivity (made at comparable conversion levels), while methane selectivity was higher for the Gd-doped catalyst (∼100%, relative) compared to the unpromoted catalyst, the selectivity to olefins plus alcohols and C2-C4 products was higher (∼35%, relative), compared to the unpromoted catalyst. The Ce-promoted Co/SiO2 catalyst presented the highest oxygenate/olefin selectivity (∼40%), among the promoted catalysts tested at a similar conversion level of ∼20%. Under reactive conditions (both following H2 activation and during CO+H2 flow), a mixture containing small LnOX/CoO/Co° nanocrystallites likely constitute the active sites during reaction. These results imply that the presence of the lanthanide likely introduces surface defects in the oxides (LnOX and/or CoO) located at the metallic cobalt nanoparticle rim which may serve as active sites for active O-containing species (e.g., mobile Type II OH groups) that may either serve as chain termination species, or generate chain terminating species such as formates (i.e., essentially molecularly adsorbed CO) upon CO adsorption.Lire moins >
Lire la suite >The effect of the nature of the lanthanide (Ln = La, Ce, Pr, Sm, Gd) on the structure and reactivity of Co/SiO2 catalysts for CO hydrogenation (i.e., Fischer Trospch synthesis) was investigated. In-situ temperature programmed reduction with extended x-ray absorption fine structure and x-ray absorption near edge spectroscopy (TPR-EXAFS/XANES) of the structure of both Co and Ln containing phases under activation and CO hydrogenation conditions were performed. Concerning catalyst selectivity (made at comparable conversion levels), while methane selectivity was higher for the Gd-doped catalyst (∼100%, relative) compared to the unpromoted catalyst, the selectivity to olefins plus alcohols and C2-C4 products was higher (∼35%, relative), compared to the unpromoted catalyst. The Ce-promoted Co/SiO2 catalyst presented the highest oxygenate/olefin selectivity (∼40%), among the promoted catalysts tested at a similar conversion level of ∼20%. Under reactive conditions (both following H2 activation and during CO+H2 flow), a mixture containing small LnOX/CoO/Co° nanocrystallites likely constitute the active sites during reaction. These results imply that the presence of the lanthanide likely introduces surface defects in the oxides (LnOX and/or CoO) located at the metallic cobalt nanoparticle rim which may serve as active sites for active O-containing species (e.g., mobile Type II OH groups) that may either serve as chain termination species, or generate chain terminating species such as formates (i.e., essentially molecularly adsorbed CO) upon CO adsorption.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
CNRS
Centrale Lille
ENSCL
Univ. Artois
Université de Lille
Centrale Lille
ENSCL
Univ. Artois
Université de Lille
Collections :
Date de dépôt :
2022-03-02T07:14:28Z