Hydrophobic-hydrophilic balance of ZSM-5 zeolites on the two-phase ketalization of glycerol with acetone

Herein, ZSM-5 zeolites of several Si/Al mole ratios, and varying hydrophobicity were used as catalysts in the ketalization of glycerol. The water formed in the reaction adsorbs on acidic sites, hampering the catalytic conversion of glycerol. The conversion drops even more by adding water in the reac...

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Detalles Bibliográficos
Autores: Catuzo, Gabriel L. [UNESP], Santilli, Celso V. [UNESP], Martins, Leandro [UNESP]
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2020
País:Brasil
Institución:Universidade Estadual Paulista (UNESP)
Repositorio:Repositório Institucional da UNESP
Idioma:inglés
OAI Identifier:oai:repositorio.unesp.br:11449/201989
Acceso en línea:http://dx.doi.org/10.1016/j.cattod.2020.07.008
http://hdl.handle.net/11449/201989
Access Level:acceso abierto
Palabra clave:Contact angle
Hydrophobicity of zeolites
Solketal
Two-phase reaction
Descripción
Sumario:Herein, ZSM-5 zeolites of several Si/Al mole ratios, and varying hydrophobicity were used as catalysts in the ketalization of glycerol. The water formed in the reaction adsorbs on acidic sites, hampering the catalytic conversion of glycerol. The conversion drops even more by adding water in the reaction mixture, intensifying the adsorption in hydrophilic zeolites. However, the samples with the higher Si/Al ratio and abundant hydrophobic ≡Si-O-Si≡ linkages had the uppermost turnover frequency. The reaction proceeds at the interface of the glycerol and acetone phases. Since the catalyst preferentially stays in the glycerol phase due to gravity action, the full catalytic action of the catalyst is hindered. Contact angle measurements with the glycerol/zeolite systems confirmed that the hydrophobic zeolite had the lowest affinity with glycerol, thus improving the interfacial solubilization of glycerol/acetone in the vicinity of active sites turning it much more efficient. The catalytic action was further enhanced by partially ion-exchanging external acid sites with minor quantities of bulky n-hexylammonium cations, turning the zeolite more hydrophobic and a strong candidate for other acid-catalyzed interfacial liquid-phase reactions.