| Literature DB >> 32328536 |
Ben H Lee1, Emma L D'Ambro2, Felipe D Lopez-Hilfiker1, Siegfried Schobesberger1, Claudia Mohr1, Maria A Zawadowicz3, Jiumeng Liu3, John E Shilling3, Weiwei Hu4, Brett B Palm4, Jose L Jimenez4, Liqing Hao5, Annele Virtanen5, Haofei Zhang6, Allen H Goldstein6, Havala O T Pye7, Joel A Thornton1.
Abstract
Organic aerosol (OA) constitutes a significant fraction of atmospheric fine particle mass. However, the precursors and chemical processes responsible for a majority of OA are rarely conclusively identified. We use online observations of hundreds of simultaneously measured molecular components obtained from 15 laboratory OA formation experiments with constraints on their effective saturation vapor concentrations to attribute the VOC precursors and subsequent chemical pathways giving rise to the vast majority of OA mass measured in two forested regions. We find that precursors and chemical pathways regulating OA composition and volatility are dynamic over hours to days, with their variations driven by coupled interactions between multiple oxidants. The extent of physical and photochemical aging, and its modulation by NOx, were key to a uniquely comprehensive combined composition-volatility description of OA. Our findings thus provide some of the most complete mechanistic-level guidance to the development of OA descriptions in air quality and Earth system models.Keywords: ambient measurements; atmospheric simulation chamber; source and chemistry attribution
Year: 2020 PMID: 32328536 PMCID: PMC7180062 DOI: 10.1021/acsearthspacechem.9b00302
Source DB: PubMed Journal: ACS Earth Space Chem Impact factor: 3.475