Organosulfates (OSs) formed from heterogeneous reactions of organic-derived oxidation products with sulfate ions are an important component of secondary organic aerosol (SOA) mass, primarily in submicron particles with long atmospheric lifetimes. Fundamental understanding of OS evolution in particles, including the formation of new compounds via oxidation, is limited, particularly across relative humidities above and below the deliquescence of typical sulfate aerosol particles. By generating aqueous particulate OSs and other SOA products from the acid-driven reactive uptake of isoprene epoxydiols (IEPOX) onto inorganic sulfate aerosols in a 2-m3 indoor chamber at various relative humidities (30 – 80%) and injecting them into an oxidation flow reactor under the presence of hydroxyl radicals (·OH), we investigate the modification of particle size distributions, extent of inorganic sulfate conversion to organosulfates, and single-particle physicochemical properties. Chemical composition of particle-phase species, as well as aerosol morphological changes, are analyzed as a function of relative humidity and oxidant exposure times to better understand OS formation and destruction mechanisms in the ambient atmosphere.
Aqueous-phase reactive species formed by fine particulate matter from remote forests and polluted urban air
Abstract. In the aqueous phase, fine particulate matter can form reactive species (RS)that influence the aging, properties, and health effects of atmosphericaerosols. In this study, we explore the RS yields of aerosol samples froma remote forest (Hyytiälä, Finland) and polluted urban locations(Mainz, Germany; Beijing, China), and we relate the RS yields to differentchemical constituents and reaction mechanisms. Ultra-high-resolution massspectrometry was used to characterize organic aerosol composition, electronparamagnetic resonance (EPR) spectroscopy with a spin-trapping technique wasapplied to determine the concentrations of ⚫OH,O2⚫-, and carbon- or oxygen-centered organic radicals, anda fluorometric assay was used to quantify H2O2. The aqueousH2O2-forming potential per mass unit of ambient PM2.5(particle diameter < 2.5 µm) was roughly the same for allinvestigated samples, whereas the mass-specific yields of radicals werelower for sampling sites with higher concentrations of PM2.5. Theabundances of water-soluble transition metals and aromatics in ambientPM2.5 were positively correlated with the relative fraction of⚫OH and negatively correlated with the relative fraction ofcarbon-centered radicals. In contrast, highly oxygenated organic molecules(HOM) were positively correlated with the relative fraction ofcarbon-centered radicals and negatively correlated with the relativefraction of ⚫OH. Moreover, we found that the relative fractionsof different types of radicals formed by ambient PM2.5 were comparableto surrogate mixtures comprising transition metal ions, more »
- Authors:
- ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; more »
- Award ID(s):
- 1808125
- Publication Date:
- NSF-PAR ID:
- 10274458
- Journal Name:
- Atmospheric Chemistry and Physics
- Volume:
- 21
- Issue:
- 13
- Page Range or eLocation-ID:
- 10439 to 10455
- ISSN:
- 1680-7324
- Sponsoring Org:
- National Science Foundation
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