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Brown carbon (BrC) absorbs radiation in the near-UV and visible ranges, affecting atmospheric photochemistry andradiative forcing. Our understanding on the photochemicaltransformation of BrC is still limited, especially when mixed withthe abundant and photochemically labile inorganic salt, nitrate.Herein, we investigate the photochemical reactions of four BrCchromophores, including two methoxyphenols and two nitro-phenols. Experiments were conducted in the absence and presenceof different concentrations of H2O2and nitrate with lights of 254and 313 nm. The results show that the pseudo-first-order decayrate constants (k) of these four BrC compounds at 313 nmillumination were approximately 10 times lower than those at 254nm, demonstrating longer lifetimes of these BrC chromophoresunder tropospherically relevant irradiation. Photo-enhancement in the visible range was observed in most experiments, with thoseunder 313 nm illumination lasting longer, indicating the prolonged effects of nascent and transformed BrC chromophores onradiative forcing. Methoxyphenols had higher averagedkvalues than nitrophenols during direct photolysis with 254 or 313 nmlights, but thekvalues for nitrophenols under high-nitrate (or high-H2O2) conditions approached those of methoxyphenols. Thephoto-enhancement in the visible range for methoxyphenols in the presence of nitrate was substantially contributed by nitroproducts, while that for nitrophenols was mainly contributed by hydroxylated and/or dimerized products. Our results reveal thesimilarity and difference between the photolysis of methoxyphenols and nitrophenols, which may help better understand the aging ofdifferent types of BrC for better model representation of their effects on radiative forcing.

来源平台：ACS EARTH AND SPACE CHEMISTRY