RESUMO
This study compares the effects of ozonation (0.4-3.0 mg O(3)/mg DOC) and TiO(2)-catalyzed ozonation - TiO(2)-O(3) (0.4-3.0 mgO(3)/mg DOC; 1.0 mgTiO(2)/L) at pH 6 on the content and structure of natural organic matter (NOM) and trihalometane (THM) and haloacetonitrile (HAN) precursors in groundwater. The investigated groundwater from Northern Serbia is rich in NOM (9.85 mg/L DOC) which is mostly of hydrophobic character (65% fulvic acid and 14% humic acid fraction). It was found that the TiO(2)-catalyzed process, by favoring the radical mechanism of NOM oxidation, resulted in a more effective reduction in the content of total NOM (up to 18% DOC) compared to ozonation alone (up to 6% DOC). The use of TiO(2) also resulted in an improvement of ozonation in terms of THM precursor content removal (up to 80%). On the other hand, the application of both oxidation treatments resulted in an increase in the HANFP compared to the raw water. NOM oxidation during ozonation and TiO(2)-O(3) caused changes in their structure in the direction of an increased proportion of the hydrophilic fraction (up to 70%), which has the most reactive THM and HAN precursors, as well as the fraction with the highest content of their brominated species.
