The Degradation of Aqueous Oxytetracycline by an O3/CaO2 System in the Presence of HCO3−: Performance, Mechanism, Degradation Pathways, and Toxicity Evaluation

Author:

Li Zedian1,Xiang Liangrui2,Pan Shijia2,Zhu Dahai1,Li Shen3,Guo He2

Affiliation:

1. School of Energy and Materials, Shanghai Polytechnic University, Shanghai 201209, China

2. College of Biology and the Environment, Nanjing Forestry University, Nanjing 210037, China

3. Anhui Jiuwu Tianhong Environmental Protection Technology Co., Ltd., Hefei 230011, China

Abstract

This research constructed a novel O3/CaO2/HCO3− system to degrade antibiotic oxytetracycline (OTC) in water. The results indicated that CaO2 and HCO3− addition could promote OTC degradation in an O3 system. There is an optimal dosage of CaO2 (0.05 g/L) and HCO3− (2.25 mmol/L) that promotes OTC degradation. After 30 min of treatment, approximately 91.5% of the OTC molecules were eliminated in the O3/CaO2/HCO3− system. A higher O3 concentration, alkaline condition, and lower OTC concentration were conducive to OTC decomposition. Active substances including ·OH, 1O2, ·O2−, and ·HCO3− play certain roles in OTC degradation. The production of ·OH followed the order: O3/CaO2/HCO3− > O3/CaO2 > O3. Compared to the sole O3 system, TOC and COD were easier to remove in the O3/CaO2/HCO3− system. Based on DFT and LC-MS, active species dominant in the degradation pathways of OTC were proposed. Then, an evaluation of the toxic changes in intermediates during OTC degradation was carried out. The feasibility of O3/CaO2/HCO3− for the treatment of other substances, such as bisphenol A, tetracycline, and actual wastewater, was investigated. Finally, the energy efficiency of the O3/CaO2/HCO3− system was calculated and compared with other mainstream processes of OTC degradation. The O3/CaO2/HCO3− system may be considered as an efficient and economical approach for antibiotic destruction.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jiangsu Province in China

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

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