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Published on: December 5, 2019
Anode-Cathode Synergistic Filter Activating Peroxymonosulfate at Multiple Active Sites for Highly Efficient and
Jiana Jing1,2,3, Huizhong Wu1,2,3, Xuechun Wang1,2,3
1Key Laboratory of Pollution Process and Environmental Criteria, Ministry of Education, College of Environmental Science and Engineering, Nankai University, Tianjin 300350, China.
This study developed an efficient dual-electrode system using modified LaCoO3-Ti4O7 anodes and nanocarbon-modified carbon felt cathodes to activate peroxymonosulfate (PMS) for rapid wastewater treatment, significantly reducing energy consumption and achieving complete pollutant removal.
Area of Science:
- Environmental Science
- Electrochemistry
- Materials Science
Background:
- Developing efficient peroxymonosulfate (PMS) activation systems is crucial for effective wastewater treatment, addressing limitations like low capacity, poor mineralization, and high energy use.
- Existing methods often struggle with efficiency and broad applicability across different water types.
Purpose of the Study:
- To design and evaluate a novel dual-electrode system for enhanced PMS activation.
- To investigate the co-activation mechanism of PMS by modified LaCoO3-Ti4O7 anodes and nanocarbon-modified carbon felt cathodes.
- To assess the system's efficiency in pollutant removal, mineralization, and energy consumption for diverse wastewater types.
Main Methods:
- Fabrication of an oxygen vacancy-mediated LaCoO3-modified Ti4O7 (LCVTO) anode and in situ grown nanocarbon-modified carbon felt (C/CF) cathode.
- Utilizing the dual-electrode system for PMS activation to degrade sulfamethoxazole (SMX).
- Employing in situ electrochemical infrared spectroscopy and density functional theory (DFT) calculations to elucidate the reaction mechanism and active sites.
Main Results:
- Achieved 100% sulfamethoxazole (SMX) elimination in 37.3 seconds with a significantly enhanced rate constant (15.84 min⁻¹).
- Demonstrated a substantial reduction in energy consumption (7.9% and 4.6% of individual electrode processes) and high pollutant removal flux (1061 L/m²·h).
- Identified multiple active sites (Co, Vo, and nanocarbon) contributing to the generation of reactive oxygen species (ROS) like •OH, SO4•-, and ¹O2, with nanocarbon enhancing ¹O2 production.
Conclusions:
- The LCVTO/C-CF dual-electrode system effectively co-activates PMS for rapid and efficient pollutant degradation.
- The system exhibits excellent pH adaptability (4-14), reusability, and continuous operation capabilities, making it resilient to wastewater matrix interference.
- This advanced oxidation process offers a promising, energy-efficient, and economical solution for treating various industrial and municipal wastewaters.
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