Schumacher, J.Salhi, E.Jekel, M.von Gunten, U.Buffle, M.O.2011-07-012011-07-012011-07-01200610.1016/j.watres.2006.02.026https://infoscience.epfl.ch/handle/20.500.14299/69212WOS:000238014600017Due to a lack of adequate experimental techniques, the kinetics of the first 20 s of ozone decomposition in natural water and wastewater is still poorly understood. Introducing a continuous quench-flow system (CQFS), measurements starting 350 ms after ozone addition are presented for the first time. Very high HO. to O-3 exposures ratios (R-ct = integral HO(.)dt/integral O(3)dt) reveal that the first 20s of ozonation present oxidation conditions that are similar to ozone-based advanced oxidation processes (AOP). The oxidation of carbamazepine could be accurately modeled using O-3 and HO. exposures measured with CQFS during wastewater ozonation. These results demonstrate the applicability of bench scale determined second-order rate constants for wastewater ozonation. Important degrees of pharmaceutical oxidation and microbial inactivation are predicted, indicating that a significant oxidation potential is available during wastewater ozonation, even when ozone is entirely decomposed in the first 20 s. (c) 2006 Elsevier Ltd. All rights reserved.ozonehydroxyl radicalsAopozone demandquench-flow systemkineticsdisinfectionpharmaceuticalswastewaterdrinking waterOzonation ProcessesDrinking-WaterQuality CriteriaResistanceEstrogensProductsKineticsEffluentChlorineRemovaltext::journal::journal article::research article