Catalysts based on nickel salt ...
Type de document :
Article dans une revue scientifique: Article original
DOI :
URL permanente :
Titre :
Catalysts based on nickel salt heteropolytungstates for selective oxidation of diphenyl sulfide
Auteur(s) :
Munoz, M. [Auteur]
Greber, M. [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Ben Tayeb Meziane, Karima [Auteur]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement (LASIRE) - UMR 8516
Lamonier, Carole [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Cabello, C. I. [Auteur]
Romanelli, G. P. [Auteur]
Greber, M. [Auteur]
Greber, M. [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Ben Tayeb Meziane, Karima [Auteur]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement (LASIRE) - UMR 8516
Lamonier, Carole [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Cabello, C. I. [Auteur]
Romanelli, G. P. [Auteur]
Greber, M. [Auteur]
Titre de la revue :
Green Process. Synth.
Numéro :
12
Pagination :
-
Date de publication :
2023-07-26
ISSN :
2191-9542
Mot(s)-clé(s) en anglais :
phosphoro/silicoheteropolyanions
Ni( II ) Keggin heteropolytungstates
modified clays
clean oxidation
diphenyl sulfide
Ni( II ) Keggin heteropolytungstates
modified clays
clean oxidation
diphenyl sulfide
Discipline(s) HAL :
Chimie/Catalyse
Résumé en anglais : [en]
Nickel salts of Keggin heteropolytungstates with the general formula Ni x A y W12−y O39or40 (A = Si/P) were synthesized and studied as bulk catalytic materials or supported ones by deposition on modified and functionalized ...
Lire la suite >Nickel salts of Keggin heteropolytungstates with the general formula Ni x A y W12−y O39or40 (A = Si/P) were synthesized and studied as bulk catalytic materials or supported ones by deposition on modified and functionalized clay minerals (pillared layered clay and porous clay heterostructure). Characterizations by Raman, 31P and 29Si-NMR, and ESEM-EDS techniques showed that pure and supported systems preserved the Ni/W ratio and the expected structural properties of heteropolyanions. These materials were evaluated as catalysts in the selective oxidation of sulfides to sulfoxides or sulfones, using aqueous hydrogen peroxide and mild reaction conditions. The bulk materials, with a higher content of Ni, displayed a remarkable catalytic behavior in the oxidation of diphenyl sulfide (Ni3PW11NiO40H, 90% conversion in 15 min at 75°C, 100% sulfone selectivity in 3 h). Supported catalysts, particularly the non-functionalized PCH (Ni2SW12O40/PCH), showed excellent activity, with also being selective in the oxidation of sulfide to sulfoxide (87% conversion, 88.9% sulfoxide selectivity). The reuse of these materials was studied in the optimum reaction conditions, resulting in similar activity and selectivity.Lire moins >
Lire la suite >Nickel salts of Keggin heteropolytungstates with the general formula Ni x A y W12−y O39or40 (A = Si/P) were synthesized and studied as bulk catalytic materials or supported ones by deposition on modified and functionalized clay minerals (pillared layered clay and porous clay heterostructure). Characterizations by Raman, 31P and 29Si-NMR, and ESEM-EDS techniques showed that pure and supported systems preserved the Ni/W ratio and the expected structural properties of heteropolyanions. These materials were evaluated as catalysts in the selective oxidation of sulfides to sulfoxides or sulfones, using aqueous hydrogen peroxide and mild reaction conditions. The bulk materials, with a higher content of Ni, displayed a remarkable catalytic behavior in the oxidation of diphenyl sulfide (Ni3PW11NiO40H, 90% conversion in 15 min at 75°C, 100% sulfone selectivity in 3 h). Supported catalysts, particularly the non-functionalized PCH (Ni2SW12O40/PCH), showed excellent activity, with also being selective in the oxidation of sulfide to sulfoxide (87% conversion, 88.9% sulfoxide selectivity). The reuse of these materials was studied in the optimum reaction conditions, resulting in similar activity and selectivity.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Université de Lille
CNRS
Centrale Lille
ENSCL
Univ. Artois
CNRS
Centrale Lille
ENSCL
Univ. Artois
Collections :
Équipe(s) de recherche :
Catalyse pour l’énergie et la synthèse de molécules plateforme (CEMOP)
Date de dépôt :
2023-10-20T06:57:28Z
2023-11-03T12:05:59Z
2023-11-03T12:05:59Z
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