Palladium@mesoporous titania core@shell nanoparticles with uniform and narrow particle size distribution were synthesised using a four component “water in oil” microemulsion system. The prepared materials were well characterised using N2 adsorption–desorption measurements, temperature program oxidation, X-ray diffraction, ICP-OES, DRS UV-Vis, PL, TGA and transmission electron microscopy techniques. The core@shell nanoparticles showed very good absorption in both the UV and visible regions and a low bandgap, indicating that the prepared materials are visiblelight-active, unlike the pristine TiO2 P25. The activity of the prepared materials was evaluated in the photodegradation of phenol using both UV and visible light, in batch and continuous flow trickle-bed and Taylor flow photoreactors. The prepared 2%Pd@mTiO2 core@shell nanoparticles showed better photocatalytic performance for phenol degradation in visible light in comparison to pristine TiO2 P25 and conventional 0.5%Pd/TiO2 P25 catalysts. The TiO2 P25 and conventional 0.5%Pd/TiO2 P25 catalysts showed gradual catalyst deactivation due to photocorrosion, the deposition of intermediates and Pd metal leaching. In comparison, the 2%Pd@mTiO2 catalyst showed higher catalyst stability and reusability. The 2%Pd@mTiO2 catalysts showed very high and stable phenol degradation (97% conversion) in continuous flow over 52 h. The results showed the feasibility of utilising the developed continuous Taylor flow photoreactor for phenol degradation or as a wastewater treatment plant.

Continuous Flow Photocatalytic Degradation of Phenol Using Palladium@Mesoporous TiO2 Core@Shell Nanoparticles

Artioli N.;
2023-01-01

Abstract

Palladium@mesoporous titania core@shell nanoparticles with uniform and narrow particle size distribution were synthesised using a four component “water in oil” microemulsion system. The prepared materials were well characterised using N2 adsorption–desorption measurements, temperature program oxidation, X-ray diffraction, ICP-OES, DRS UV-Vis, PL, TGA and transmission electron microscopy techniques. The core@shell nanoparticles showed very good absorption in both the UV and visible regions and a low bandgap, indicating that the prepared materials are visiblelight-active, unlike the pristine TiO2 P25. The activity of the prepared materials was evaluated in the photodegradation of phenol using both UV and visible light, in batch and continuous flow trickle-bed and Taylor flow photoreactors. The prepared 2%Pd@mTiO2 core@shell nanoparticles showed better photocatalytic performance for phenol degradation in visible light in comparison to pristine TiO2 P25 and conventional 0.5%Pd/TiO2 P25 catalysts. The TiO2 P25 and conventional 0.5%Pd/TiO2 P25 catalysts showed gradual catalyst deactivation due to photocorrosion, the deposition of intermediates and Pd metal leaching. In comparison, the 2%Pd@mTiO2 catalyst showed higher catalyst stability and reusability. The 2%Pd@mTiO2 catalysts showed very high and stable phenol degradation (97% conversion) in continuous flow over 52 h. The results showed the feasibility of utilising the developed continuous Taylor flow photoreactor for phenol degradation or as a wastewater treatment plant.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11379/583585
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