Les Inscriptions à la Bibliothèque sont ouvertes en
ligne via le site: https://biblio.enp.edu.dz
Les Réinscriptions se font à :
• La Bibliothèque Annexe pour les étudiants en
2ème Année CPST
• La Bibliothèque Centrale pour les étudiants en Spécialités
A partir de cette page vous pouvez :
Retourner au premier écran avec les recherches... |
Détail de l'auteur
Auteur Daniel F. Shantz
Documents disponibles écrits par cet auteur
Affiner la rechercheAmine-functionalized ordered mesoporous silica transesterification catalysts / Victor Varela Guerrero in Industrial & engineering chemistry research, Vol. 48 N° 23 (Décembre 2009)
[article]
in Industrial & engineering chemistry research > Vol. 48 N° 23 (Décembre 2009) . - pp. 10375–10380
Titre : Amine-functionalized ordered mesoporous silica transesterification catalysts Type de document : texte imprimé Auteurs : Victor Varela Guerrero, Auteur ; Daniel F. Shantz, Auteur Année de publication : 2010 Article en page(s) : pp. 10375–10380 Note générale : Industrial chemistry Langues : Anglais (eng) Mots-clés : Amine-Functionalized--Ordered--Mesoporous--Silica--Transesterification--Catalysts Résumé : The synthesis, characterization, and catalytic behavior of several amine-functionalized ordered mesoporous silica (OMS) materials are reported. All samples show catalytic activity for the conversion of glyceryl tributyrate with methanol to methyl esters in high yield (>60%). The reactivity of the amines approximately correlates with the pK values of the free amines. The effect of the amine identity, loading, and substrate pore size is also reported. To determine if leached amine was responsible for the observed reactivity, the hot filtrate method was employed. Those experiments show that upon removal of the OMS material the reaction conversion does not increase, indicating surface-tethered amines are primarily responsible for the observed reactivity. The stability of the most promising catalyst, 3-(anilinopropyl)-MCM-41 was analyzed via recycle studies. Leaching of the amine is observed via a decrease in conversion with multiple recycles and a concomitant change in sample color. Capping the residual silanols groups with hexamethyldisilazane leads to an increase in the catalyst stability with a decrease in activity. The work indicates that these solids are interesting alternatives to conventional homogeneous catalysts for this class of chemistry. ISSN : 0888-5885 En ligne : http://pubs.acs.org/doi/abs/10.1021/ie9003915 [article] Amine-functionalized ordered mesoporous silica transesterification catalysts [texte imprimé] / Victor Varela Guerrero, Auteur ; Daniel F. Shantz, Auteur . - 2010 . - pp. 10375–10380.
Industrial chemistry
Langues : Anglais (eng)
in Industrial & engineering chemistry research > Vol. 48 N° 23 (Décembre 2009) . - pp. 10375–10380
Mots-clés : Amine-Functionalized--Ordered--Mesoporous--Silica--Transesterification--Catalysts Résumé : The synthesis, characterization, and catalytic behavior of several amine-functionalized ordered mesoporous silica (OMS) materials are reported. All samples show catalytic activity for the conversion of glyceryl tributyrate with methanol to methyl esters in high yield (>60%). The reactivity of the amines approximately correlates with the pK values of the free amines. The effect of the amine identity, loading, and substrate pore size is also reported. To determine if leached amine was responsible for the observed reactivity, the hot filtrate method was employed. Those experiments show that upon removal of the OMS material the reaction conversion does not increase, indicating surface-tethered amines are primarily responsible for the observed reactivity. The stability of the most promising catalyst, 3-(anilinopropyl)-MCM-41 was analyzed via recycle studies. Leaching of the amine is observed via a decrease in conversion with multiple recycles and a concomitant change in sample color. Capping the residual silanols groups with hexamethyldisilazane leads to an increase in the catalyst stability with a decrease in activity. The work indicates that these solids are interesting alternatives to conventional homogeneous catalysts for this class of chemistry. ISSN : 0888-5885 En ligne : http://pubs.acs.org/doi/abs/10.1021/ie9003915