Porous Nanostructured Catalysts Based on Silicates and Their Surface Functionality: Effects of Silica Source and Metal Added in Glycerol Valorization

Author:

Carmo José Vitor C.1ORCID,Nogueira Joabson1ORCID,Bertoldo Gabriela M.1,Clemente Francisco E.1,Oliveira Alcineia C.1ORCID,Campos Adriana F.2,Duarte Gian C. S.2,Tehuacanero-Cuapa Samuel3ORCID,Jiménez-Jiménez José4,Rodríguez-Castellón Enrique4ORCID

Affiliation:

1. Departamento de Química Analítica e Físico-Química, Universidade Federal do Ceará, Campus do Pici, Bloco 940, Fortaleza 60455-760, Ceará, Brazil

2. CETENE, Cidade Universitária, Recife 50740-545, Pernambuco, Brazil

3. Instituto de Física, Universidad Nacional Autonoma de México, Circuito de la Investigación s/n, Ciudad Universitaria, México City 04510, Mexico

4. Departamento de Química Inorgánica, Facultad de Ciencias, Instituto Interuniversitario de Investigación en Biorrefinerías I3B, Universidad de Málaga, 29071 Málaga, Spain

Abstract

A series of nanospherical-shaped silicates containing heteroatoms (Al, Zr or Ti) were successfully synthesized using tetraethylorthosilicate (TEOS) or silica colloids as a silicon source. These metallosilicate nanospheres were used as silicon nutrients to obtain silicalite zeolites with micro-mesoporosity and improved textural properties. The results demonstrated that TEOS acted as a suitable silicon source to produce amorphous silicates and a spherical-type zeolite architecture with Zr and Ti heteroatoms included in their framework, with preferable particle size and crystallinity. The surface functionality of the mesostructured nanospheres and zeolite silicates provide active centers for the esterification of glycerol with acetic acid (EG) reaction. The dispersion of Cu entities on the surface of the zeolites achieved high glycerol conversions selectively producing triacetin in comparison with Fe counterparts.

Funder

Ministerio de Ciencia e Innovación, Spain

“ERDF A way of making Europe” by the European Union NextGenerationEU/PRTR

FUNCAP

Publisher

MDPI AG

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