Abstract
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 6h, 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-Cl2) anodes, respectively. However, the photo-assisted electrochemical (UVEL) process removed 88% and 96% of total organic carbon (TOC) after 6h with BDD and DSA-Cl2 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 6h (96%), one of the highest mineralization rates (0.38h−1), and the lowest energy demand per order TOC removed (EEO=104kWhm−3order−1) without any residual toxicity after dechlorination. Generally, conventional advanced oxidation processes (UV/O3 and UV/H2O2) were most effective at mineralization up to 50%, but UVEL appeared more cost effective for mineralization beyond 75%.
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