Photochemical treatment of tyrosol, a model phenolic compound present in olive mill wastewater, by hydroxyl and sulfate radical-based advanced oxidation processes (AOPs).

The photochemical degradation and mineralization of tyrosol (TSL), a model phenolic compound present in olive mill wastewater, were studied by UV-254 nm irradiated peroxymonosulfate (PMS), hydrogen peroxide (HO) and persulfate (PS). Effects of initial TSL concentration, UV fluence, pH, phosphate buffer and presence of inorganic anions (i.e., Cl, SO and NO) were also investigated. Sulfate and hydroxyl radicals were demonstrated to be responsible for TSL degradation and mineralization. Regardless of the treatment conditions, pseudo-first-order kinetics could be obtained, with the efficiencies following UV/PS > UV/HO > UV/PMS. The better removal of TSL by UV/PS correlated with the quantum yield and concentration of sulfate radical in the system. Albeit acidic condition slightly enhanced the performance of the AOPs, complete oxidation of TSL was achieved at pH 6.8 by both UV/PS and UV/HO. Though, inorganic anions or different concentrations of phosphate buffer did not affect TSL degradation kinetics, presence of inorganic ions decreased significantly the TOC removal for both UV/PMS and UV/HO processes. Meanwhile, UV/PS process was the least influenced by inorganic ions and showed the highest TOC removal of ∼35%. Overall, UV/PS process was the most effective for TSL degradation and mineralization in the presence or absence of common water constituents.