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A novel photoelectric integration process (MPEC) was developed to degrade Amaranth. In the MPEC, the output voltage of the microbial fuel cells (MFCs) was used to assist the dual slant-placed electrodes thin-film photocatalytic (PC). With two MFCs connected in series, the MPEC process realized the highest decolorization efficiency. It is close to that of the external bias photoelectrocatalytic (PEC), and 7% higher than that of the self-generated electric field-assisted photoelectrocatalytic (SPEC). The feasibility of MPEC pre-treatment and MFC post-treatment of Amaranth was investigated. The results demonstrated that MPEC pre-treatment of Amaranth could improve its biodegradability. The higher MPEC decolorization efficiency indicated the stronger biodegradability of the obtained intermediates and the higher MFC output voltage. When the MPEC decolorization efficiency was gradually increased to 50%, the removal efficiencies of total Chemical Oxygen Demand (COD) by the MPEC and MFC increased; when the decolorization efficiency was increased above 50%, the removal efficiencies became stable. MPEC enhanced the biodegradability efficiently and was applicable to pre-treat textile wastewater. [ABSTRACT FROM AUTHOR]

A dual slant-placed electrodes thin-film photocatalytic (PC) reactor was proposed and successfully applied to degrade Amaranth. In this PC reactor, both the TiO2/Ti photoanode and the Cu cathode are slant-placed in the reaction chamber, and aqueous thin-film formed on the surface of both electrodes as wastewater flowed over them. The degradation efficiency was significantly improved as a result of additional degradation at the cathode. When the TiO2photocatalyst was irradiated with UV light, photogenerated electrons were spontaneously transferred from the anode to the cathode, driven by the electric field self-generated between the TiO2/Ti anode and the Cu cathode, based on the principle of establishing a Schottky barrier. On the Cu cathode surface, the transferred photoelectrons either reacted with dissolved oxygen to form H2O2,which then oxidized the dye, resulting in indirect oxidation decolourization, or reacted with the dye, resulting in direct reduction decolourization. The colour removal efficiency of the cathode was about half that of the photoanode. These processes together with direct oxidation of the photogenerated holes on the photoanode gave dual electrode degradation of the dye, and the degradation efficiency was significantly improved. [ABSTRACT FROM AUTHOR]