4.7 Article

A comparative study of bismuth-based photocatalysts with titanium dioxide for perfluorooctanoic acid degradation

Journal

CHINESE CHEMICAL LETTERS
Volume 30, Issue 12, Pages 2225-2230

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cclet.2019.07.058

Keywords

Photocatalysis; Perfluorooctanoic acid; Bismuth-based catalysts; TiO2; 254 nm UV light; Persistent organic pollutants

Funding

  1. Ministry of Science and Technology of the People's Republic of China [2016YFE0112200, 2016YFC0202700]
  2. National Natural Science Foundation of China [21507011, 21677037, 21607027]
  3. Natural Science Foundation of Shanghai [19ZR1471200, 17ZR1440200]

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Bismuth-based material has been broadly studied due to their potential applications in various areas, especially used as promising photocatalysts for the removal of persistent organic pollutants (POPs) and several approaches have been adopted to tailor their features. Herein, the bismuth-based photocatalysts (BiOCl, BiPO4, BiOPO4/BiOCl) were synthesized by hydrothermal method and advanced characterization techniques (XRD, SEM, EDS elemental mapping, Raman and UV-vis DRS) were employed to analyze their morphology, crystal structure, and purity of the prepared photocatalysts. These synthesized photocatalysts offered a praiseworthy activity as compared to commercial TiO2 (P25) for the degradation of model pollutant perfluorooctanoic acid (PFOA) under 254 nm UV light. It was interesting to observe that all synthesized photocatalysts show significant degradation of PFOA and their photocatalytic activity follows the order: bismuth-based catalysts > TiO2 (P25) > without catalyst. Bismuth-based catalysts degraded the PFOA by almost 99.99% within 45 min while this degradation efficiency was 66.05% with TiO2 under the same reaction condition. Our work shows that the bismuth-based photocatalysts are promising in PFOA treatment. (C) 2019 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.

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