Simultaneous electrochemical degradation of tetracycline and metronidazole through a high-efficiency and low-energy-consumption advanced oxidation process

With the increasing complexity of water environment pollution, it is becoming ever more practical to study the simultaneous removal of multiple pollutants in water. Electrochemical advanced oxidation technology is considered to be one of the most promising green approaches for the degradation of organic pollutants. Herein, Ti3+ and oxygen vacancies (VO) self-doped TiO2-x nanotube array electrodes are employed to investigate the simultaneous degradation and an energy consumption assessment for the effective removal of the antibiotics tetracycline (TC) and metronidazole (MNZ). The electrocatalytic performance of the nanotube arrays prepared at different reduction times is significantly different. The electrochemical reduction of TiO2 nanotube arrays for 10 min presents the best degradation performance for TC and MNZ. When a mixed solution of TC and MNZ is simultaneously degraded, the removal rate of TC (50 mg L-1) and MNZ (50 mg L-1) within 3 h reaches 100%, while the chemical oxygen demand (COD) removal rate is 79.1%. The energy consumption is significantly reduced compared to the degradation of a single substance. Simultaneously, the current utilization rate of the electrochemical degradation system is also significantly improved, with a specific energy consumption of only 85.78 kWh kg- 1 and an average current efficiency that can reach 20.2%.

Automated summary

In this study, Ti3+ and oxygen vacancies self-doped TiO2-x nanotube array electrodes were used to investigate the simultaneous degradation of antibiotics tetracycline and metronidazole in water. The results showed that the nanotube arrays prepared with a reduction time of 10 minutes exhibited the best degradation performance. When a mixed solution of tetracycline and metronidazole was simultaneously degraded, the removal rate reached 100% within 3 hours, with a chemical oxygen demand removal rate of 79.1%. The energy consumption was significantly reduced compared to the degradation of a single substance, and the current utilization rate of the electrochemical degradation system was also significantly improved, with a specific energy consumption of 85.78 kWh kg-1 and an average current efficiency of 20.2%.