Calcium Hydroxyapatite: A Highly Stable ...
Type de document :
Article dans une revue scientifique: Article original
DOI :
URL permanente :
Titre :
Calcium Hydroxyapatite: A Highly Stable and Selective Solid Catalyst for Glycerol Polymerization
Auteur(s) :
Ebadipour, Negisa [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Paul, Sébastien [Auteur]
Centrale Lille
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Katryniok, Benjamin [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Dumeignil, Franck [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Paul, Sébastien [Auteur]

Centrale Lille
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Katryniok, Benjamin [Auteur]

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

Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Titre de la revue :
Catalysts
Nom court de la revue :
Catalysts
Numéro :
11
Pagination :
1247
Date de publication :
2021-10-17
ISSN :
2073-4344
Discipline(s) HAL :
Chimie/Catalyse
Résumé en anglais : [en]
Calcium-based catalysts are of high interest for glycerol polymerization due to their high catalytic activity and large availability. However, their poor stability under reaction conditions is an issue. In the present ...
Lire la suite >Calcium-based catalysts are of high interest for glycerol polymerization due to their high catalytic activity and large availability. However, their poor stability under reaction conditions is an issue. In the present study, we investigated the stability and catalytic activity of Ca-hydroxyapatites (HAps) as one of the most abundant Ca-source in nature. A stochiometric, Ca-deficient and Ca-rich HAps were synthesized and tested as catalysts in the glycerol polymerization reaction. Deficient and stochiometric HAps exhibited a remarkable 100% selectivity to triglycerol at 15% of glycerol conversion at 245 °C after 8 h of reaction in the presence of 0.5 mol.% of catalyst. Moreover, under the same reaction conditions, Ca-rich HAp showed a high selectivity (88%) to di- and triglycerol at a glycerol conversion of 27%. Most importantly, these catalysts were unexpectedly stable towards leaching under the reaction conditions based on the ICP-OES results. However, based on the catalytic tests and characterization analysis performed by XRD, XPS, IR, TGA-DSC and ICP-OES, we found that HAps can be deactivated by the presence of the reaction products themselves, i.e., water and polymers.Lire moins >
Lire la suite >Calcium-based catalysts are of high interest for glycerol polymerization due to their high catalytic activity and large availability. However, their poor stability under reaction conditions is an issue. In the present study, we investigated the stability and catalytic activity of Ca-hydroxyapatites (HAps) as one of the most abundant Ca-source in nature. A stochiometric, Ca-deficient and Ca-rich HAps were synthesized and tested as catalysts in the glycerol polymerization reaction. Deficient and stochiometric HAps exhibited a remarkable 100% selectivity to triglycerol at 15% of glycerol conversion at 245 °C after 8 h of reaction in the presence of 0.5 mol.% of catalyst. Moreover, under the same reaction conditions, Ca-rich HAp showed a high selectivity (88%) to di- and triglycerol at a glycerol conversion of 27%. Most importantly, these catalysts were unexpectedly stable towards leaching under the reaction conditions based on the ICP-OES results. However, based on the catalytic tests and characterization analysis performed by XRD, XPS, IR, TGA-DSC and ICP-OES, we found that HAps can be deactivated by the presence of the reaction products themselves, i.e., water and polymers.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 :
Équipe(s) de recherche :
Valorisation des alcanes et de la biomasse (VAALBIO)
Date de dépôt :
2022-03-24T09:02:49Z
2023-01-11T10:52:59Z
2023-01-11T10:52:59Z
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