Unexpected significance of a minor reaction pathway in daytime formation of biogenic highly oxygenated organic compounds

• Published in: Science advances Vol. 8; no. 42; p. eabp8702
• Main Authors: Shen, Hongru, Vereecken, Luc, Kang, Sungah, Pullinen, Iida, Fuchs, Hendrik, Zhao, Defeng, Mentel, Thomas F
• Format: Journal Article
• Language: English
• Published: United States American Association for the Advancement of Science 21.10.2022
• Subjects: Atmospheric Science; Earth, Environmental, Ecological, and Space Sciences; Environmental Studies; SciAdv r-articles
• ISSN: 2375-2548; 2375-2548
• DOI: 10.1126/sciadv.abp8702

Secondary organic aerosol (SOA), formed by oxidation of volatile organic compounds, substantially influence air quality and climate. Highly oxygenated organic molecules (HOMs), particularly those formed from biogenic monoterpenes, contribute a large fraction of SOA. During daytime, hydroxyl radicals initiate monoterpene oxidation, mainly by hydroxyl addition to monoterpene double bonds. Naturally, related HOM formation mechanisms should be induced by that reaction route, too. However, for α-pinene, the most abundant atmospheric monoterpene, we find a previously unidentified competitive pathway under atmospherically relevant conditions: HOM formation is predominately induced via hydrogen abstraction by hydroxyl radicals, a generally minor reaction pathway. We show by observations and theoretical calculations that hydrogen abstraction followed by formation and rearrangement of alkoxy radicals is a prerequisite for fast daytime HOM formation. Our analysis provides an accurate mechanism and yield, demonstrating that minor reaction pathways can become major, here for SOA formation and growth and related impacts on air quality and climate.