Development of a Novel 3D Highly Porous Structure for TiO2 Immobilization and Application in As(III) Oxidation
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Published:2023-10-11
Issue:20
Volume:15
Page:14760
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ISSN:2071-1050
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Container-title:Sustainability
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language:en
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Short-container-title:Sustainability
Author:
Scherer Filho Julio A.1, Marinho Belisa A.12ORCID, Vignola Fabiola1, Mazur Luciana P.1, González Sergio Y. G.1, da Silva Adriano1, Ulson de Souza Antônio Augusto1ORCID, Guelli Ulson de Souza Selene M. A.1ORCID
Affiliation:
1. Laboratory of Mass Transfer (LABMASSA), Department of Chemical Engineering (EQA), Federal University of Santa Catarina (UFSC), Florianópolis 88040-900, Brazil 2. Department for Nanostructured Materials, Jožef Stefan Institute, Jamova 39, 1000 Ljubljana, Slovenia
Abstract
One of the main drawbacks of the application of photocatalysis for wastewater treatment is the use of dispersed photocatalysts, which are difficult to remove from effluent after the treatment process and may pose additional toxicity to the receiving bodies. As an alternative, immobilized catalysts can be applied; however, this strategy can increase the difficulties in mass and photo transfer. This work presents the development of an inert and highly porous support for TiO2 immobilization. The produced materials have a high surface area and contribute to diminishing the difficulties in mass and phototransfer during photocatalysis. Different types of polymeric materials were tested as support, and a Taguchi experimental design with an L9 arrangement was used to optimize the immobilization process and evaluate the effect of TiO2 content and the use of bidding agents, ultrasound, and thermic treatment. The grey automotive polyurethane foam proved to be the best support, using 5.0% of TiO2 (wt.%) in the immobilization suspension with Triton X as the binding agent and heat treatment during immobilization. At the optimal conditions, it was possible to achieve total As(III) oxidation (below the analytical detection limit) in 240 min, with nearly 100% As(V) present in solution at the end of the reaction (almost no As adsorption on the catalyst surface). In addition, the catalytic bed was able to promote the As(III) complete oxidation in up to five consecutive cycles without significant leaching or deactivation of the immobilized TiO2.
Subject
Management, Monitoring, Policy and Law,Renewable Energy, Sustainability and the Environment,Geography, Planning and Development,Building and Construction
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