文摘
Recent work has shown that the atmospheric oxidation ofisoprene (2-methyl-1,3-butadiene, C5H8) leads to theformation of secondary organic aerosol (SOA). In thisstudy, the mechanism of SOA formation by isoprenephotooxidation is comprehensively investigated, bymeasurements of SOA yields over a range of experimentalconditions, namely isoprene and NOx concentrations.Hydrogen peroxide is used as the radical precursor,substantially constraining the observed gas-phase chemistry;all oxidation is dominated by the OH radical, and organicperoxy radicals (RO2) react only with HO2 (formed in the OH+ H2O2 reaction) or NO concentrations, including NOx-free conditions. At high NOx, yields are found to decreasesubstantially with increasing [NOx], indicating theimportance of RO2 chemistry in SOA formation. Under low-NOx conditions, SOA mass is observed to decay rapidly,a result of chemical reactions of semivolatile SOA components,most likely organic hydroperoxides.