Publication:
Preparation of Al/Fe-pillared clays: effect of the starting mineral

Consultable a partir de

Date

2017

Authors

Muñoz Alvear, Helir Joseph
Blanco, Carolina
Vicente, Miguel Ángel
Galeano, Luis Alejandro

Director

Publisher

MDPI
Acceso abierto / Sarbide irekia
Artículo / Artikulua
Versión publicada / Argitaratu den bertsioa

Project identifier

MINECO//MAT2013-47811-C2-1-R/ES/
ES/1PE/MAT2016-78863

Abstract

Four natural clays were modified with mixed polyoxocations of Al/Fe for evaluating the effect of the physicochemical properties of the starting materials (chemical composition, abundance of expandable clay phases, cationic exchange capacity and textural properties) on final physicochemical and catalytic properties of Al/Fe-PILCs. The aluminosilicate denoted C2 exhibited the highest potential as starting material in the preparation of Al/Fe-PILC catalysts, mainly due to its starting cationic exchange capacity (192 meq/100 g) and the dioctahedral nature of the smectite phase. These characteristics favored the intercalation of the mixed (Al13􀀀x/Fex)7+ Keggin-type polyoxocations, stabilizing a basal spacing of 17.4 Å and high increase of the BET surface (194 m2/g), mainly represented in microporous content. According to H2-TPR analyses, catalytic performance of the incorporated Fe in the CatalyticWet Peroxide Oxidation (CWPO) reaction strongly depends on the level of location in mixed Al/Fe pillars. Altogether, such physicochemical characteristics promoted high performance in CWPO catalytic degradation of methyl orange in aqueous medium at very mild reaction temperatures (25.0 1.0 C) and pressure (76 kPa), achieving TOC removal of 52% and 70% of azo-dye decolourization in only 75 min of reaction under very low concentration of clay catalyst (0.05 g/L).

Keywords

Smectite, Pillared clay, Keggin-like mixed Al/Fe polyoxocation, Mineralogical composition, Catalytic wet peroxide oxidation

Department

Química Aplicada / Kimika Aplikatua

Faculty/School

Degree

Doctorate program

Editor version

Funding entities

The financial support from Proyecto Agua Potable Nariño (BPIN 2014000100020), CT&I Fund of the SGR—Colombia is kindly acknowledged. HJM also gratefully thanks the MSc scholarship granted by Departamento de Nariño (BPIN 2013000100092) and managed by CEIBA Foundation, Colombia. M.A.V. and A.G. thank the support from the Spanish Ministry of Economy and Competitiveness (MINECO) and the European Regional Development Fund (FEDER) (projects MAT2013-47811-C2-R and MAT2016-78863-C2-R). A.G. is also grateful for financial support from Santander Bank through the Research Intensification Program.

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