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Continuous Flow Photocatalytic Degradation of Phenol Using Palladium@Mesoporous TiO2 Core@Shell Nanoparticles
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 visible-light-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
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 visible-light-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
Moses T. Yilleng (Autor:in) / Nancy Artioli (Autor:in) / David Rooney (Autor:in) / Haresh Manyar (Autor:in)
2023
Aufsatz (Zeitschrift)
Elektronische Ressource
Unbekannt
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| British Library Online Contents | 2016
| British Library Online Contents | 2016
| British Library Online Contents | 2016
| British Library Online Contents | 2016
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