Electro-catazone treatment of ozone-resistant drug ibuprofen: Interfacial reaction kinetics, influencing mechanisms, and degradation sites
- Authors
- Xinyang Li; Hao Zhang; Fujun Ma; Shuang Cheng; Zhen Shen; Jiahe Zhang; Jiacheng Min; Yutian Wang; Guicheng Liu; Hong Yao
- Issue Date
- Dec-2021
- Publisher
- Elsevier science
- Keywords
- Electro-catazone; Interfacial reaction; Elementary reactions library; Degradation pathway; Wastewater treatment
- Citation
- Journal of Hazardous Materials Advances, v.4, pp 1 - 11
- Pages
- 11
- Indexed
- SCOPUS
ESCI
- Journal Title
- Journal of Hazardous Materials Advances
- Volume
- 4
- Start Page
- 1
- End Page
- 11
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/3950
- DOI
- 10.1016/j.hazadv.2021.100023
- ISSN
- 2772-4166
2772-4166
- Abstract
- Electro-heterogeneous catalytic ozonation (E-catazone) is a promising advanced oxidation process using a unique TiO2 nanoflower (TiO2-NF)-coated porous Ti anode. This study investigated interfacial reaction kinetics and the influencing mechanism of E-catazone degrading ozone-resistant drug ibuprofen. An elementary reactions library of the E-catazone process was established. The kinetic rate of key interfacial reactions under different operation parameters was quantitatively resolved. It was found that parameters such as current, initial pH, O 3 concentration, and flowrate mainly affect & BULL;OH formation and ibuprofen removal via influencing three key interfacial reactions including anodic TiO2-NF surface hydroxylation, subsequent TiO2-NF -OH/O3 heterogeneous catalysis, and cathodic generation of H2O2. In addition, the degradation pathways and sites of ibuprofen were also predicted via theoretical chemistry calculation, showing that & BULL;OH attacked C(12), C(11), or C(6) atom of the benzene ring in the ibuprofen via a radical adduct formation pathway. The results of this study will guide the application of the E-catazone process in the efficient removal of ozone-resistant drugs.
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Collections - College of Natural Science > Division of Physics & Semiconductor Science > 1. Journal Articles

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