Characterisation of lightly oxidised organic aerosol formed from the photochemical aging of diesel exhaust particles
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Author(s) • • •
Kroll, Jesse
Smith, Jared D.
Worsnop, Douglas R.
Wilson, Kevin R.
Date Issued
June 2012
Journal
Environmental Chemistry
Publisher
CSIRO Publishing
Citation
Kroll, Jesse H. et al. “Characterisation of Lightly Oxidised Organic Aerosol Formed from the Photochemical Aging of Diesel Exhaust Particles.” Environmental Chemistry 9.3 (2012): 211. Web.
Version
Author's final manuscript
Abstract
The oxidative aging of the semivolatile fraction of diesel exhaust aerosol is studied in order to better understand the influence of oxidation reactions on particle chemical composition. Exhaust is sampled from an idling diesel truck, sent through a denuder to remove gas-phase species and oxidised by hydroxyl (OH•) radicals in a flow reactor. OH• concentrations are chosen to approximately match the OH• exposures a particle would experience over its atmospheric lifetime. Evolving particle composition is monitored using aerosol mass spectrometry in two different modes, electron impact ionisation (EI) for the measurement of elemental ratios and vacuum ultraviolet (VUV) photoionisation for the measurement of molecular components. Changes to mass spectra in both modes indicate major changes to particle composition over the range of OH• exposures studied. The product aerosol is only lightly oxidised (O/C < 0.3), suggesting an intermediate oxidation state between primary organics and the highly oxidised organic aerosol observed in the atmosphere. These lightly oxidised organics appear to be composed of secondary organic aerosol from semivolatile species, as well as from heterogeneously oxidised particle-phase organics. Key chemical characteristics (elemental ratios, oxidation kinetics and mass spectrometric features) of the reaction system are examined in detail. Similarities between this laboratory-generated aerosol and ‘hydrocarbon-like organic aerosol’ (HOA) reported in ambient studies suggest that HOA might not be entirely primary in origin, as is commonly assumed, but rather might include a significant secondary component.
MIT Department
Massachusetts Institute of Technology. Department of Chemical Engineering
Massachusetts Institute of Technology. Department of Civil and Environmental Engineering
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DOI of Published Version
https://doi.org/10.1071/EN11162