Atmospheric chemistry and physics · 2015 · 51 citations · 57 references
Natural SciencesChemistryEnvironmental SciencesAir PollutionAtmospheric ChemistryAtmospheric ScienceAerosol ChemistryAerosol ScienceAtmospheric Oxidation ProcessesPhotochemistrySecondary Aerosol FormationSecondary Organic AerosolsAerosol Chemical CompositionAging PhenomenaAging ProcessesAtmospheric Aerosol ChemistryOxidationPhotooxidationSecondary Organic Aerosol AgingSecondary Organic Aerosol Formation
Abstract. It has recently been established that unsaturated water-soluble organic compounds (UWSOCs) might efficiently form oligomers in polluted fogs and wet aerosol particles, even for weakly soluble ones like methyl vinyl ketone (MVK). The atmospheric relevance of these processes is explored by means of multiphase process model studies in a companion paper. In the present study, we investigate the aging of these aqueous-phase MVK oligomers formed via •OH oxidation, as well as their ability to form secondary organic aerosol (SOA) upon water evaporation. The comparison between aqueous-phase composition and aerosol composition after nebulization of the corresponding solutions shows similar trends for oligomer formation and aging. The measurements reveal that oligomer aging leads to the formation of organic diacids. Quantification of the SOA mass formed after nebulization is performed, and the obtained SOA mass yields seem to depend on the spectral irradiance of the light used to initiate the photochemistry. Investigating a large range of initial MVK concentrations (0.2–20 mM), the results show that their •OH oxidation undergoes competition between functionalization and oligomerization that is dependent on the precursor concentration. At high initial MVK concentrations (≥ 2 mM), oligomerization prevails over functionalization, while at lower initial concentrations, oligomerization is not the major process, and functionalization dominates, resulting in small carbonyls, dicarbonyls and monoacids. The atmospheric implications of these processes are discussed.
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