Insight into the enhanced catalytic activity of a red mud based Fe2O3/Zn–Al layered double hydroxide in the photo-Fenton reaction
In this work, the catalytic activity of an Fe2O3/Zn–Al layered double hydroxide (F/ZA-LDH) in the photo-Fenton reaction has been studied in detail. The F/ZA-LDH composite exhibited significantly enhanced catalytic activity in a photo-Fenton system. The apparent rate constant of F/ZA-LDH in the photo...
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Veröffentlicht in: | Catalysis science & technology 2020-11, Vol.10 (21), p.7365-7377 |
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Sprache: | eng |
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Zusammenfassung: | In this work, the catalytic activity of an Fe2O3/Zn–Al layered double hydroxide (F/ZA-LDH) in the photo-Fenton reaction has been studied in detail. The F/ZA-LDH composite exhibited significantly enhanced catalytic activity in a photo-Fenton system. The apparent rate constant of F/ZA-LDH in the photo-Fenton reaction was about 4 times higher than that of the pure Zn–Al LDH, and was about 10 times higher than that of the red mud, which was the main material for synthesized F/ZA-LDH. It was found that besides the increased surface area (45.64 m3 g−1) and enhanced pore volume of the F/ZA-LDH composite, the suitable concentration of oxygen vacancies could account for the significantly enhanced catalytic activity of F/ZA-LDH. The oxygen vacancies favor the visible light absorption and the efficient charge separation and transfer of F/ZA-LDH. Moreover, density functional theory (DFT) calculations were used to explore the electronic structures of the as-prepared samples, and the photocatalytic activity of F/ZA-LDH was also analyzed based on the results of electronic structures. The F/ZA-LDH composite exhibited excellent settleability, good reusability and stability in use. Finally, the possible mechanisms involved in the photo-Fenton system catalyzed by F/ZA-LDH have been proposed. This work would provide a systematic understanding of the high catalytic activity of the Fe2O3/Zn–Al layered double hydroxide which has been prepared using bulk waste red mud as the main material via mechanochemical synthesis. |
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ISSN: | 2044-4753 2044-4761 |
DOI: | 10.1039/d0cy01539c |