posted on 2023-02-22, 09:10authored byLin Yanyan, Tonni Agustiono Kurniawan, Z Ying, Ahmad B. Albadarin, Gavin WalkerGavin Walker
This study investigates the photocatalytic degradation of acetaminophen (Ace) from synthetic
wastewater by individual TiO2, TiO2/SiO2 and/or WO3/TiO2/SiO2 composite under UV-VIS
illumination. To characterize changes in their morphology and crystal structures before and after
treatment, Χ-ray diffraction (ΧRD), Fourier transform infrared spectroscopy (FTIR) , DRS
UV-VIS absorption spectra, Brunaer-Emmer-Teller (BET) and scanning electron microscopy
(SEM) techniques were used. The effects of varying loading ratios of the WO3 on the TiO2/SiO2
composite for Ace degradation were studied. Operating parameters such as initial concentration,
reaction time, dose of photocatalyst and pH were tested. Degradation by-products were also
presented. It is found that the photodegradation performance of the WO3/TiO2/SiO2 composite as
a photocatalyst in this study could be enhanced by optimizing the loading ratio of the WO3.
About 3% (w/w) of WO3/TiO2/SiO2 was found to improve the degradation of Ace from 33% to
95% at the same initial concentration of 5 mg/L. The resulting oxidation by-products included
hydroquinone and 1,4-benzoquinone. Under the same conditions, the result of photocatalytic
degradation by the 3% (w/w) of WO3/TiO2/SiO2 composite was significantly higher (95%) than
that by the individual TiO2/SiO2 (42%) and/or by the TiO2 alone (33%). Under optimized
conditions (1.5 g/L; 3% (w/w) of WO3/TiO2/SiO2 composite; pH 9; 4 h of reaction time), 95% of
Ace removal with an initial concentration of 5 mg/L could be attained. However, the treated
effluents still could not meet the discharge standard of less than 0.2 mg/L set by China’s and US
legislation. This indicates that further subsequent treatment like biological processes is still
necessary for completing the removal of target pollutant from the wastewater samples.
Funding
Xiamen University's Foundation of Technology
20720150070
History
Publication
Journal of Molecular Liquids;243, pp. 761-770
Publisher
Elsevier
Note
peer-reviewed
The full text of this article will not be available in ULIR until the embargo expires on the 26/8/2019
Other Funding information
Xiamen University's Foundation of Technology
Rights
This is the author’s version of a work that was accepted for publication in Journal of Molecular Liquids. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Journal of Molecular Liquids, 2017, 343, pp. 761-770, https://doi.org/10.1016/j.molliq.2017.08.092