Abstract

This paper focuses on the study of the photochemical activity of dissolved organic matter present in rainwater. Formation rates of the reactive species hydroxyl radical (OH •), singlet oxygen ( 1O 2) and dissolved organic matter triplet states ( 3DOM ⁎) were determined by irradiation (UV-A) of wet-only rainwater samples collected in Turin (Italy) in the presence of specific scavengers (benzene, furfuryl alcohol and phenol, respectively). Photo-formation rates of OH • (≈ 3 · 10 − 11 M s − 1) and 1O 2 (≈ 10 − 14 M s − 1) were lower (1 or 2 orders of magnitude) or largely lower (4 to 10 orders of magnitude) than those determined for fog and cloud samples in previous studies. 3DOM ⁎ formation rate values were either negligible or quite low (≈ 10 − 12 M s − 1) by comparison with those evaluated for surface water samples. Deduced steady-state [OH •] were in the same range as those reported for fog samples in the literature (8.7 · 10 − 16 to 1.5 · 10 − 15 M), while [ 1O 2] was often several orders of magnitude lower and, therefore, could be considered as negligible. Nitrite (NO 2 −) constituted the main source of OH • (69 ± 21 to 138 ± 36%), and the deduced contribution of DOM was low or nil. All the results obtained in this study tend to demonstrate that DOM (including HUmic LIke Substances, HULIS) present in rainwater is poorly or not photoactive. Therefore, there could be considerable difference between rainwater DOM (HULIS included) and the organic matter present in surface waters, particularly the humic substances, as far as the photochemical activity is concerned.

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