Photoelectrocatalysis (PEC) has been already proposed as a polishing treatment for wastewater treatment plants (WWTPs) effluents. In this work, the impact of polarization reversal during PEC process has been studied and evaluated on the basis of the removal of organic substance and color, biodegradability of the matrix, and inactivation of the catalyst. Effluents were sampled from a full-scale WWTP and alternatively treated by electrochemical oxidation (EC), photolysis (PL), photocatalysis (PC), photoelectrocatalysis, and photoelectrocatalysis with reverse polarization (PECr). The efficiency and the kinetics of the process, in terms of removal of organic substance and color, were not affected by reverse polarization and very similar results were obtained by PEC and PECr. The biodegradability of the effluents strongly increased both by PECr (RSBR: 0.84 ± 0.07), and by PEC and PL (0.89 ± 0.11, and 0.78 ± 0.02, respectively). In the selected polarization reversal mode (100 s at −0.1 V every 500 s at 4 V, cell voltage), a similar photocurrent loss after PEC and PECr was observed, suggesting no effect on the activity of the TiO2 mesh. This study can serve as a base for future research on polarization reversal to optimize operation parameters and exploit the procedure to preventing fouling and inactivation of the catalyst.

Impact of Polarization Reversal during Photoelectrocatalytic Treatment of WWTP Effluents

Collivignarelli M. C.;Carnevale Miino M.;Caccamo F. M.;Abba A.
;
2023-01-01

Abstract

Photoelectrocatalysis (PEC) has been already proposed as a polishing treatment for wastewater treatment plants (WWTPs) effluents. In this work, the impact of polarization reversal during PEC process has been studied and evaluated on the basis of the removal of organic substance and color, biodegradability of the matrix, and inactivation of the catalyst. Effluents were sampled from a full-scale WWTP and alternatively treated by electrochemical oxidation (EC), photolysis (PL), photocatalysis (PC), photoelectrocatalysis, and photoelectrocatalysis with reverse polarization (PECr). The efficiency and the kinetics of the process, in terms of removal of organic substance and color, were not affected by reverse polarization and very similar results were obtained by PEC and PECr. The biodegradability of the effluents strongly increased both by PECr (RSBR: 0.84 ± 0.07), and by PEC and PL (0.89 ± 0.11, and 0.78 ± 0.02, respectively). In the selected polarization reversal mode (100 s at −0.1 V every 500 s at 4 V, cell voltage), a similar photocurrent loss after PEC and PECr was observed, suggesting no effect on the activity of the TiO2 mesh. This study can serve as a base for future research on polarization reversal to optimize operation parameters and exploit the procedure to preventing fouling and inactivation of the catalyst.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1500038
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