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In relation to this article, we declare that there is no conflict of interest.
Publication history
Received July 9, 2020
Accepted November 22, 2020
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Degradation mechanism, reaction pathways and kinetics for the mineralization of Bisphenol A using hybrid ZnO/graphene oxide nano-catalysts

Department of Chemical Engineering, Dr B R Ambedkar National Institute of Technology, Jalandhar, Punjab-144011, India
bansala@nitj.ac.in
Korean Journal of Chemical Engineering, March 2021, 38(3), 485-497(13), 10.1007/s11814-020-0718-8
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Abstract

Removal of Bisphenol A (BPA) from surface waters is necessary before consumption. A study, therefore, was conducted to degrade BPA using graphene oxide, ZnO and ZnO decorated on graphene oxide. Hydrothermal method was used to synthesize the hybrid nano-catalysts. 99.5% photocatalytic degradation of BPA was achieved by using ZG0.6 nano-catalyst in comparison to bare ZnO and GO nano-catalysts at natural pH of 7.5 in 60 min of UV irradiation. The higher photocatalytic activity of ZG0.6 nano-catalyst could be ascribed to an improved surface area, efficient charge separation as well as the decreased recombination rate of electron-hole charge carriers, leading to the generation of highly reactive hydroxyl radicals for the degradation of BPA. Photocatalytic degradation followed Langmuir-Hinshelwood model with pseudo-first-order kinetics. The degradation mechanism is also detailed with identification of reaction intermediates. Degradation pathways, based on LCMS analysis, have been proposed. The pathways revealed the formation of smaller by-products such as phenol, hydroquinol and (Z)-3-hydroxyacrylaldehyde. The developed ZG0.6 nano-catalyst were found to be reusable for consecutive five runs without much loss in the activity and have the advantage of effective charge separation.

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