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Direct sunlight-driven degradation of 2-chlorophenol catalyzed by kaolinite-supported ZnO

Commercial and laboratory-prepared ZnO nanoparticles are assessed here as a photocatalyst in photodegradation of aqueous 2-chlorophenol under direct sunlight. Kaolinite is used as a support for ZnO to enable its recovery after reuse. The composite ZnO/kaolinite is prepared by growing ZnO nanoparticl...

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Bibliographic Details
Published in:International journal of environmental science and technology (Tehran) 2019-10, Vol.16 (10), p.6267-6276
Main Authors: Zyoud, A. H., Zorba, T., Helal, M., Zyoud, S., Qamhiya, N., Hajamohideen, A-R., Zyoud, Sh, Hilal, H. S.
Format: Article
Language:English
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Summary:Commercial and laboratory-prepared ZnO nanoparticles are assessed here as a photocatalyst in photodegradation of aqueous 2-chlorophenol under direct sunlight. Kaolinite is used as a support for ZnO to enable its recovery after reuse. The composite ZnO/kaolinite is prepared by growing ZnO nanoparticles directly on kaolinite surface and is characterized by a number of methods such as electronic absorption spectra, photoluminescence spectra, X-ray diffraction and scanning electron microscopy. All ZnO systems (commercial, synthetic and supported) exhibit the wurtzite phase. The composite ZnO/kaolinite shows higher photocatalysis efficiency in 2-chlorophenol degradation over both commercial and synthetic ZnO powders. The composite ZnO/kaolinite is also easier to recover and reuse, showing no observable loss in its catalyst efficiency even after five cycles. These features highlight the merit of using composite ZnO/kaolinite as photocatalyst in water purification with direct sunlight for the first time. All catalyst systems are more efficient in basic media (pH ~ 8.5) than in neutral and acidic media, as rationalized by the point of zero charge concepts here. Moreover, the composite ZnO/kaolinite shows enhanced catalytic efficiency in 2-chlorophenol photodegradation in a wider pH range, compared to other counterparts, which shows another added value.
ISSN:1735-1472
1735-2630
DOI:10.1007/s13762-019-02272-z