Molecular identification of organic vapors driving atmospheric nanoparticle growth

Particles formed in the atmosphere via nucleation provide about half the number of atmospheric cloud condensation nuclei, but in many locations, this process is limited by the growth of the newly formed particles. That growth is often via condensation of organic vapors. Identification of these vapor...

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Veröffentlicht in:Nature communications 2019-09, Vol.10 (1), p.4442-4442, Article 4442
Hauptverfasser: Mohr, Claudia, Thornton, Joel A., Heitto, Arto, Lopez-Hilfiker, Felipe D., Lutz, Anna, Riipinen, Ilona, Hong, Juan, Donahue, Neil M., Hallquist, Mattias, Petäjä, Tuukka, Kulmala, Markku, Yli-Juuti, Taina
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Sprache:eng
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Zusammenfassung:Particles formed in the atmosphere via nucleation provide about half the number of atmospheric cloud condensation nuclei, but in many locations, this process is limited by the growth of the newly formed particles. That growth is often via condensation of organic vapors. Identification of these vapors and their sources is thus fundamental for simulating changes to aerosol-cloud interactions, which are one of the most uncertain aspects of anthropogenic climate forcing. Here we present direct molecular-level observations of a distribution of organic vapors in a forested environment that can explain simultaneously observed atmospheric nanoparticle growth from 3 to 50 nm. Furthermore, the volatility distribution of these vapors is sufficient to explain nanoparticle growth without invoking particle-phase processes. The agreement between observed mass growth, and the growth predicted from the observed mass of condensing vapors in a forested environment thus represents an important step forward in the characterization of atmospheric particle growth. Condensation of organic vapors is a main factor controlling the growth of atmospheric particles. Here the authors identify a distribution of organic vapors in a forested environment able to explain nanoparticle growth at the same location, contributing to understanding aerosol climate effects.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-019-12473-2