Natural organic matter (NOM) is a complex mixture of heterogeneous compounds with varying functional groups and molecular sizes. Understanding the impact of NOM on the generation of photochemically produced reactive intermediates (PPRIs) and their potential inhibitory effects on photolysis has remained challenging due to the variations in the reactivities and concentrations of these functional groups. To address this gap, tannic acid (TA), gallic acid (GA), catechin (CAT), and tryptophan (Trp), were chosen as potential substitutes for NOM. Their effects on the photochemical transformation process were evaluated and compared with the widely used Suwannee River NOM (SRNOM). Atrazine (ATZ) was selected as a probe organic micropollutant (OMP). In this investigation, a significantly higher concentration of HO• was observed compared to O21, and the triplet excited state ( NOM*3). The findings suggest that the substituted phenols, particularly those with carboxylate-substitutions, played a substantial role in HO• formation, while electron-rich moieties acted as antioxidants, consuming NOM*3. Hydroxyl, carboxylic, and amino acid were the active groups for O21 formation. However, the inhibitory effects induced by the NOM surrogates were significant and mainly attributed to the direct photolysis inhibition caused by the inner filter effect. The scope of this work was further extended to include SRNOM, where similar trends with less pronounced formation of PPRIs and inner filter effects were observed. Therefore, this study sheds some light on the role of the functional groups in NOM during photochemical transformations of OMPs, thereby deepening our understanding of their fate in aqueous systems.
Keywords: Amines; Carboxylic groups; Natural organic matter; Phenolic groups; Photochemically produced reactive intermediates.
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