Nature of the active sites in Al-MCM-41 nano-structured catalysts for the selective rearrangement of cyclohexanone oxime toward ɛ-caprolactam

Al-MCM-41 type nano-structured catalysts with different Al contents were prepared by direct hydrothermal synthesis. All the materials were characterized by XRD, N2 adsorption, TEM, SEM, ICP-OES, FT-IR and adsorption of pyridine coupled to FT-IR spectroscopy. The relationship between the Al contents...

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Detalhes bibliográficos
Autores: Vaschetto, Eliana Gabriela, Pecchi Sanchez, Gina Angela, Casuscelli, Sandra Graciela, Eimer, Griselda Alejandra
Tipo de documento: artigo
Estado:Versão publicada
Data de publicação:2014
País:Argentina
Recursos:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositório:CONICET Digital (CONICET)
Idioma:inglês
OAI Identifier:oai:ri.conicet.gov.ar:11336/32027
Acesso em linha:http://hdl.handle.net/11336/32027
Access Level:Acceso aberto
Palavra-chave:Al Contents
Al-Mcm-41
Silanol Nests
Acidic Strength
Ɛ-Caprolactam
https://purl.org/becyt/ford/2.4
https://purl.org/becyt/ford/2
Descrição
Resumo:Al-MCM-41 type nano-structured catalysts with different Al contents were prepared by direct hydrothermal synthesis. All the materials were characterized by XRD, N2 adsorption, TEM, SEM, ICP-OES, FT-IR and adsorption of pyridine coupled to FT-IR spectroscopy. The relationship between the Al contents in the synthesis gel and final solid, the degree of Al introduction in tetrahedral coordination into the framework, the formation of nest silanols and the relative density of the acidic hydroxyl sites has been exhaustively analyzed. We could corroborate that hydroxyl groups present in silanol nests are the direct responsible of the weakly acid character of our materials. Moreover, a critical concentration of framework Al seems to be necessary to generate such nests, after which the acid sites density is strongly increased, according the framework Al amount increasing. The enhancement in the density of acidic nest silanols (active sites for the selective rearrangement of cyclohexanone oxime toward ɛ-caprolactam) reached by increasing the Al content, permitted to us achieve a cyclohexanone oxime conversion about 66%. The ɛ-caprolactam selectivity was 100% for all the evaluated catalysts, indicating that the acidic strength was kept sufficiently weak to not catalyze the formation of by-products.