Photoelectrocatalytic oxidation of Cu(II)-EDTA at the TiO2 electrode and simultaneous recovery of Cu(II) by electrodeposition.

The simultaneous decomplexation of Cu-EDTA and electrodeposition recovery of Cu(2+) ions was attempted in a photoelectrocatalytic (PEC) system using TiO2/Ti as the anode and stainless steel as the cathode. At a current density of 0.5 mA/cm(2), removal efficiencies of 0.05 mM Cu-EDTA by photocatalysis, electrooxidation, and PEC processes were determined to be 15, 43, and 72% at 3 h, respectively. Recovery percentages of Cu(2+) ions were determined to be 10, 33, and 67%, respectively. These results indicated that a synergetic effect in the decomplexation of Cu-EDTA and recovery of Cu(2+) ions occurred in the PEC process, which favored acid conditions and increased with the current densities. The removal of Cu-EDTA and Cu(2+) ions can be described by a pseudo-first-order kinetics model. Ca(2+) ions significantly increase the removal of Cu-EDTA and recovery of Cu(2+) ions. Intermediates, including Cu-NTA, Cu-EDDA, acetic acid, formic acid, and oxalic acid, were identified, and a decomplexation pathway of Cu-EDTA was proposed. The Cu-EDTA decomplexation at the anode via oxidation of hydroxyl radicals was revealed. On the basis of X-ray photoelectron spectra analysis, a reduction pathway of Cu(2+) ions at the cathode was discussed. The present study may provide a promising alternative for destruction of the metal complex and recovery of metal ions.