Please use this identifier to cite or link to this item:
https://idr.l3.nitk.ac.in/jspui/handle/123456789/16535
Title: | Photocatalytic degradation of diclofenac using TiO2-CdS heterojunction catalysts under visible light irradiation |
Authors: | Elangovan M. Bharathaiyengar S.M. PonnanEttiyappan J. |
Issue Date: | 2021 |
Citation: | Environmental Science and Pollution Research Vol. 28 , 14 , p. 18186 - 18200 |
Abstract: | The present study reports the photocatalytic degradation of analgesic drug diclofenac using the hydrothermally prepared TiO2-CdS heterojunction catalyst. The results suggest that the prepared catalysts exhibited excellent photocatalytic activity under visible light irradiation. The photodegradation kinetics were well fitted to the pseudo-first-order reaction. The apparent reaction rate constant for TC5 catalyst in the diclofenac degradation was 0.02316 min−1. Mineralisation of diclofenac using TC5 photocatalyst was around 86% within 4 h of irradiation time. The operating parameters such as optimal catalyst dosage, apparent solution pH and the effect of initial diclofenac concentration were also studied using the TC5 catalyst. The role of active species in the degradation mechanism was elucidated and it was found that the hydroxyl radical is the main active species in the diclofenac degradation mechanism. The charge transfer between heterojunction catalysts is facilitated by direct Z-scheme heterojunction structure. The coupled photocatalysts also showed good photochemical stability and reusability over five successive reaction cycles. The tentative degradation pathway has been devised based on LC-MS peaks, and it is found that only m/z 224, m/z 178 and m/z 124 were persisted at the end of the reaction. © 2021, Springer-Verlag GmbH Germany, part of Springer Nature. |
URI: | https://doi.org/10.1007/s11356-020-11538-w http://idr.nitk.ac.in/jspui/handle/123456789/16535 |
Appears in Collections: | 1. Journal Articles |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.