Abstract
Natural organic matter (NOM) is known to be present in all natural water systems. Due to the different characteristics of surface and ground waters, the photocatalytic degradation efficiency of NOMdepends on several inhibiting and enhancing factors. The presence of hardness causing divalent cations (Ca2+, Mg2+, Fe2+/Fe3+) as well as the accompanying common anions (e.g. Cl-, NO3- ,SO42- and HCO3-/CO32-) have considerable effects on the degradation kinetics as expressed by DOC (dissolved organic carbon) and UV254 (UV absorbance at 254 nm). Ternary systems formed through cation bridging of NOM displayed different adsorptive properties onto TiO2 revealing an enhancement in removal rates. Presence of common anions as Cl-, NO3- and SO42- exerted significant effects compared to the inhibitory effects due to the presence of pH dependent HCO3-/CO32- system. Carbonate species strictly altered the degradation efficiency possibly through the direct and competitive reactions with hydroxyl radicals. Comparative evaluations of the respective outcomes of the source dependent water quality parameters are discussed.
© 2016 by Walter de Gruyter Berlin/Boston
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- Design of CeyCoxTi (1-x) O3+δ Perovskite for Photocatalysis: A Statistical Study
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- Depletion of Several Antibiotics Used in Industrial Process Using Immobilized TiO2
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- Application of Photocatalysis for the Removal of Natural Organic Matter in Simulated Surface and Ground Waters
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- Degradation of 4-n-nonylphenol in Water by 20 kHz Ultrasound
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