Photoelectrochemical cell for simultaneous electricity generation and heavy metals recovery from wastewater

J Hazard Mater. 2017 Feb 5;323(Pt B):681-689. doi: 10.1016/j.jhazmat.2016.10.037. Epub 2016 Oct 18.

Abstract

The feasibility of simultaneous recovery of heavy metals from wastewater (e.g., acid mining and electroplating) and production of electricity is demonstrated in a novel photoelectrochemical cell (PEC). The photoanode of the cell bears a nanoparticulate titania (TiO2) film capped with the block copolymer [poly(ethylene glycol)-b-poly(propylene glycol)-b-poly(ethylene glycol)] hole scavenger, which consumed photogenerated holes, while the photogenerated electrons transferred to a copper cathode reducing dissolved metal ions and produced electricity. Dissolved silver Ag+, copper Cu2+, hexavalent chromium as dichromate Cr2O72- and lead Pb2+ ions in a mixture (0.2mM each) were removed at different rates, according to their reduction potentials. Reduced Ag+, Cu2+ and Pb2+ ions produced metal deposits on the cathode electrode which were mechanically recovered, while Cr2O72- reduced to the less toxic Cr3+ in solution. The cell produced a current density Jsc of 0.23mA/cm2, an open circuit voltage Voc of 0.63V and a maximum power density of 0.084mW/cm2. A satisfactory performance of this PEC for the treatment of lead-acid battery wastewater was observed. The cathodic reduction of heavy metals was limited by the rate of electron-hole generation at the photoanode. The PEC performance decreased by 30% after 9 consecutive runs, caused by the photoanode progressive degradation.

Keywords: Electricity generation; Heavy metals reduction; Photoelectrochemical cell; Wastewater treatment.