| Literature DB >> 27817875 |
Dawei Wang1, Yi Li2, Gianluca Li Puma3, Panagiotis Lianos4, Chao Wang1, Peifang Wang1.
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. Copyright ÂEntities:
Keywords: Electricity generation; Heavy metals reduction; Photoelectrochemical cell; Wastewater treatment
Year: 2016 PMID: 27817875 DOI: 10.1016/j.jhazmat.2016.10.037
Source DB: PubMed Journal: J Hazard Mater ISSN: 0304-3894 Impact factor: 10.588