4.7 Article

Contribution of Isoprene Epoxydiol to Urban Organic Aerosol: Evidence from Modeling and Measurements

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY LETTERS
Volume 1, Issue 6, Pages 278-283

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ez5001353

Keywords

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Funding

  1. U.S. Environmental Protection Agency's Air, Climate, and Energy Program
  2. Oak Ridge Institute for Science Education
  3. NASA Applied Sciences Program through the NASA Air Quality Applied Sciences Team (AQAST)

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In a region heavily influenced by anthropogenic and biogenic atmospheric emissions, recent field measurements have attributed one-third of urban organic aerosol by mass to isoprene epoxydiols (IEPOX). These aerosols arise from the gas-phase oxidation of isoprene, the formation of IEPOX, the reactive uptake of IEPOX by particles, and finally the formation of new compounds in the aerosol phase. Using a continental-scale chemical transport model, we find a strong temporal correspondence between the simulated formation of IEPOX-derived organic aerosol and these measurements. However, because only a subset of isoprene-derived aerosol compounds have been specifically identified in laboratory studies, our simulation of known IEPOX-derived organic aerosol compounds predicts a mass 10-fold lower than the field measurements, despite abundant gas-phase IEPOX. Sensitivity studies suggest that increasing the effective IEPOX uptake coefficient and including aerosol-phase reactions that lead to the addition of functional groups could increase the simulated IEPOX-derived aerosol mass and account for the difference between the field measurements and modeling results.

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