Degradation of phenol by synergistic chlorine-enhanced photo-assisted electrochemical oxidation

Hybridization of a UV-C photoreactor with an electrochemical cell led to the discovery of a distinctive synergistic mechanism for the degradation and mineralization of phenol when free chlorine-producing anodes were utilized in the presence of chloride. After 6 h, photochemical (UV) treatment resulted in 29% phenol mineralization and electrochemical (EL) treatment resulted in 35% and 52% mineralization using boron-doped diamond (BDD) and ruthenium oxide on titanium (DSA-Cl-2) anodes, respectively. However, the photo-assisted electrochemical (UVEL) process removed 88% and 96% of total organic carbon (TOC) after 6 h with BDD and DSA-Cl-2 anodes, respectively. The hybrid UVEL process generated highly reactive hydroxyl and chlorine radicals by the photolysis of in situ electrogenerated free chlorine. As a result, the UVEL treatment produced fewer chlorinated by-products compared to EL alone. UVEL with DSA-Cl2 had the highest TOC removal after 6 h (96%), one of the highest mineralization rates (0.38h(-1)), and the lowest energy demand per order TOC removed (E-EO = 104 kW h m(-3) order(-1)) without any residual toxicity after dechlorination. Generally, conventional advanced oxidation processes (UV/O-3 and UV/H2O2) were most effective at mineralization up to 50%, but UVEL appeared more cost effective for mineralization beyond 75%. (C) 2013 Elsevier B.V. All rights reserved.