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Abstract

In this study, we evaluated the feasibility of treating water contaminated with ketoprofen (KET) by ultrasound (US) and sono-activated persulfate (US/PS) systems. The effects of different reaction parameters, such as the initial pharmaceutical compound concentration (C0), persulfate concentration, ultrasonic power, and initial pH of the solution (pHi) on the KET removal and reaction kinetics were investigated. Tert-butyl alcohol (TBA) was used as a chemical probe to identify the predominant radicals in the US and US/PS systems. The results demonstrated that the persulfate oxidant can be activated by US under neutral and alkaline conditions. Moreover, KET was predominantly degraded by hydroxyl radicals (HO.) generated by the activation of persulfate. Under alkaline conditions, the removal efficiency of KET improved with increasing amount of persulfate added. HO. was the dominant radical at a more alkaline pH in both US and US/PS systems, which was verified by the tert-butyl alcohol probe. These results provide insights into the treatment of water contaminated with pharmaceutical compounds.

Details

Title
Removal of Ketoprofen from Water by Sono-Activated Persulfate Oxidation
Author
Yu-Jung, Liu 1 ; He Boyu 1 ; Ching-Yao, Hu 2 ; Shang-Lien, Lo 3 

 National Taiwan University, Graduate Institute of Environmental Engineering, Taipei, Taiwan (GRID:grid.19188.39) (ISNI:0000 0004 0546 0241) 
 Taipei Medical University, School of Public Health, Taipei, Taiwan (GRID:grid.412896.0) (ISNI:0000 0000 9337 0481) 
 National Taiwan University, Graduate Institute of Environmental Engineering, Taipei, Taiwan (GRID:grid.19188.39) (ISNI:0000 0004 0546 0241); National Taiwan University, NTU Research Center for Future Earth, Taipei, Taiwan (GRID:grid.19188.39) (ISNI:0000 0004 0546 0241) 
Publication year
2020
Publication date
Jul 2020
Publisher
Springer Nature B.V.
ISSN
0049-6979
e-ISSN
1573-2932
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2419779509
Copyright
© Springer Nature Switzerland AG 2020.