Oxidation of pharmaceuticals during ozonation and advanced oxidation processes

This study investigates the oxidation of pharmaceuticals during conventional ozonation and advanced oxidation processes (AOPs) applied in drinking water treatment. In a first step, second-order rate constants for the reactions of selected pharmaceuticals with ozone (k(O3)) and OH radicals (k(OH)) were determined in bench-scale experiments (in brackets apparent k(O3) at pH 7 and T = 20 degreesC): bezafibrate (590 +/- 50 M-1 s(-1)), carbamazepine (similar to3 x 10(5) M-1 s(-1)), diazepam (0.75 +/- 0.15 M-1 s(-1)), diclofenac (similar to1 X 10(6) M-1 s(-1)), 17alpha-ethinylestradiol (similar to3 x 10(6) M-1 s(-1)), ibuprofen (9.6 +/- 1.0 M-1 s(-1)), iopromide (<0.8 M-1 s(-1)), sulfamethoxazole (similar to2.5 x 10(6) M-1 s(-1)), and roxithromycin (similar to7 x 10(4) M-1 s(-1)). For five of the pharmaceuticals the apparent k(O3) at pH 7 was >5 x 10(4) M-1 s(-1), indicating that these compounds are completely transformed during ozonation processes. Values for kOH ranged from 3.3 to 9.8 x 10(9) M-1 s(-1). Compared to other important micropollutants such as MTBE and atrazine, the selected pharmaceuticals reacted about two to three times faster with OH radicals. In the second part of the study, oxidation kinetics of the selected pharmaceuticals were investigated in ozonation experiments performed in different natural waters. It could be shown that the second-order rate constants determined in pure aqueous solution could be applied to predict the behavior of pharmaceuticals dissolved in natural waters. Overall it can be concluded that ozonation and AOPs are promising processes for an efficient removal of pharmaceuticals in drinking waters.