Affiliations 

  • 1 College of Environmental Science and Engineering, Guilin University of Technology, Guilin, 541004, China; Guangxi Key Laboratory of Theory and Technology for Environmental Pollution Control, Guilin University of Technology, Guilin, 541004, China; Collaborative Innovation Center for Water Pollution Control and Water Safety in Karst area, Guilin University of Technology, Guilin, 541004, China; Department of Environmental Engineering, Faculty of Engineering and Green Technology, Universiti Tunku Abdul Rahman, 31900, Kampar, Perak, Malaysia. Electronic address: lamsm@utar.edu.my
  • 2 College of Environmental Science and Engineering, Guilin University of Technology, Guilin, 541004, China; Guangxi Key Laboratory of Theory and Technology for Environmental Pollution Control, Guilin University of Technology, Guilin, 541004, China; Collaborative Innovation Center for Water Pollution Control and Water Safety in Karst area, Guilin University of Technology, Guilin, 541004, China; Department of Petrochemical Engineering, Faculty of Engineering and Green Technology, Universiti Tunku Abdul Rahman, 31900, Kampar, Perak, Malaysia
  • 3 College of Environmental Science and Engineering, Guilin University of Technology, Guilin, 541004, China; Guangxi Key Laboratory of Theory and Technology for Environmental Pollution Control, Guilin University of Technology, Guilin, 541004, China; Collaborative Innovation Center for Water Pollution Control and Water Safety in Karst area, Guilin University of Technology, Guilin, 541004, China
  • 4 College of Environmental Science and Engineering, Guilin University of Technology, Guilin, 541004, China; Guangxi Key Laboratory of Theory and Technology for Environmental Pollution Control, Guilin University of Technology, Guilin, 541004, China; Collaborative Innovation Center for Water Pollution Control and Water Safety in Karst area, Guilin University of Technology, Guilin, 541004, China. Electronic address: zenghonghu@glut.edu.cn
Chemosphere, 2020 Apr;245:125565.
PMID: 31855765 DOI: 10.1016/j.chemosphere.2019.125565

Abstract

An approach that can recuperate of energy from wastewater treatment process is highly necessitate and would help to surmount the both environmental pollution and energy crisis issues. A photocatalytic fuel cell (PFC) employing an anodic TiO2/ZnO/Zn and a cathodic CuO/Cu has been applied to degrade the raw greywater, which realized advanced organics destruction, bacteria disinfection, and synchronously electricity production. The improved photocatalytic performance has been observed when the cell was incorporated with anodic TiO2/ZnO/Zn under UV and sunlight irradiation due to the enhanced electric field conductivity of the catalysts and heterojunction interface of TiO2. In the constructed UV-activated PFC system, the electricity production capability was observed with the measured voltage and power density of 868 mV and 0.0172 mW cm-2, respectively. Advanced chemical oxygen demand (COD) removal efficiency of greywater achieved a 100% completion within 60 min of light irradiation. The Escherichia coli (E. coli) colonies decreased significantly and accounted ∼99% disinfection efficiency. Moreover, the photoelectrochemical and photoluminescence (PL) experiments elucidated that the charge carrier separation efficiency were higher when TiO2 was coupled to ZnO. The organic matter elimination principle was assessed by radical trapping experiment, and the findings indicated that the hydroxyl (OH) radical and hole (h+) appeared as major functions in the reaction. The stable cycle operation of the cell has been also obtained owing to the stable and film-type materials of anodic material. This performance was among the highest documented for PFC using real wastewater effluent as the fuel source.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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