The photocatalytic oxidation (PCO) of Cu(II)-ethylene diamine tetra-acetic acid (EDTA), employing immobilized TiO2, under natural sunlight rather than artificial UV light conditions, was investigated at a latitude 38 degrees. The immobilized TiO2 film was prepared using a sol gel process, the crystalline structure of which was identified, by X-ray diffraction analysis, as a mixture of the rutile and anatase forms. The PCO of Cu(II)-EDTA was examined in a circulating reactor with 20 L of 10(-4) M Cu(II)-EDTA and synthetic and real wastewaters at pH 4 and 6.5, respectively. The removals of both Cu(II) and DOC were initially relatively rapid, but slowed as the reaction proceeded and generally followed first-order kinetics. The rate constants for the removal of Cu(II) and DOC were 1.1 x 10(-3) and 1.6 x 10(-3) min-1, respectively. The efficiency of the PCO in the decomplexation of Cu(II)-EDTA increased with increasing H2O2 dose using both the synthetic and real wastewaters. Therefore, we suggest the PCO process using the solar/immobilized TiO2 system, with addition of H2O2 as well as filtration for the removal of suspended solids, can be effectively applied to the treatment of Cu(II)-EDTA containing real wastewater.