Characterization of Products from the Aqueous-Phase Photochemical Oxidation of Benzene-Diols

Chemical processing in atmospheric aqueous phases, including cloud and fog drops, might be significant in reconciling the gap between observed and modeled secondary organic aerosol (SOA) properties. In this work, we conducted a relatively comprehensive investigation of the reaction products generated from the aqueous-phase photochemical oxidation of three benzene-diols (resorcinol, hydroquinone, and methoxyhydroquinone) by hydroxyl radical (center dot OH), triplet excited state (C-3*) 3,4-dimethoxybenzaldehyde (3,4-DMB), and direct photolysis without any added oxidants. The results show that OH-initiated photo-degradation is the fastest of all the reaction systems. For the optical properties, the aqueous oxidation products generated under different reaction conditions all exhibited photo-enhancement upon illumination by simulated sunlight, and the light absorption was wavelength dependent on and increased as a function of the reaction time. The oxygen-to-carbon (O/C) ratio of the products also gradually increased against the irradiation time, indicating the persistent formation of highly oxygenated low-volatility products throughout the aging process. More importantly, aqueous-phase products from photochemical oxidation had an increased oxidative potential (OP) compared with its precursor, indicating they may more adversely impact health. The findings in this work highlight the importance of aqueous-phase photochemical oxidation, with implications for aqueous SOA formation and impacts on both the chemical properties and health effects of OA.