Mousavi-Kamazani, M., Shirani, M., Beshkar, F. et al. (1 more author) (2020) One-step ultrasonic production of novel worm-like Bi₇(PO₄)O₉ photocatalyst for efficient degradation of ciprofloxacin antibiotic under simulated solar light. Journal of Materials Science: Materials in Electronics, 31 (22). pp. 19657-19671. ISSN 0957-4522
Abstract
For the first time, novel worm-like Bi₇(PO₄)O₉ photocatalysts have been fabricated via a versatile sonochemical route using new capping agent. The impacts of ultrasonic power, time of sonication, and capping agent on the morphology of Bi₇(PO₄)O₉ products were also studied. In addition, the photocatalytic performance of the Bi₇(PO₄)O₉ nanostructures was studied by the degradation of ciprofloxacin as antibiotic contaminant under simulated solar light illumination. The results indicated that the hierarchical Bi₇(PO₄)O₉ photocatalyst with energy gap of 2.92 eV has superior photodegradation efficiency about 91% after 2 h of simulated solar light irradiation, even after five recycles. Moreover, the effects of antibiotic concentration, photocatalyst dosage, and morphology of the products on the photocatalytic activity were investigated. The dependable photodegradation mechanism was expressed based on the active oxidative species trapping, which disclosed the photogenerated superoxide (•O₂−) and hydroxyl (•OH) radicals were the chief species in the degradation of ciprofloxacin by Bi₇(PO₄)O₉ nanostructures.
Metadata
Item Type: | Article |
---|---|
Authors/Creators: |
|
Keywords: | Chemical Engineering; Engineering |
Dates: |
|
Institution: | The University of Leeds |
Academic Units: | The University of Leeds > Faculty of Engineering & Physical Sciences (Leeds) > School of Chemistry (Leeds) > Inorganic Chemistry (Leeds) |
Depositing User: | Symplectic Publications |
Date Deposited: | 22 Jul 2024 14:47 |
Last Modified: | 22 Jul 2024 14:47 |
Published Version: | https://link.springer.com/article/10.1007/s10854-0... |
Status: | Published |
Publisher: | Springer |
Identification Number: | 10.1007/s10854-020-04492-3 |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:214129 |