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  Hydroxyl radicals from secondary organic aerosol decomposition in water

Tong, H., Arangio, A. M., Lakey, P. S. J., Berkemeier, T., Liu, F., Kampf, C. J., et al. (2016). Hydroxyl radicals from secondary organic aerosol decomposition in water. Atmospheric Chemistry and Physics, 16(3), 1761-1771. doi:10.5194/acp-16-1761-2016.

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Tong, H.1, Autor           
Arangio, Andrea M.1, Autor           
Lakey, Pascale S. J.1, Autor           
Berkemeier, T.1, Autor           
Liu, Fobang1, Autor           
Kampf, Christopher J.1, Autor           
Brune, W. H.2, Autor
Pöschl, U.1, Autor           
Shiraiwa, M.1, Autor           
Affiliations:
1Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society, ou_1826290              
2external, ou_persistent22              

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 Zusammenfassung: We found that ambient and laboratory-generated secondary organic aerosols (SOA) form substantial amounts of OH radicals upon interaction with liquid water, which can be explained by the decomposition of organic hydroperoxides. The molar OH yield from SOA formed by ozonolysis of terpenes (alpha-pinene, beta-pinene, limonene) is similar to 0.1% upon extraction with pure water and increases to similar to 1.5% in the presence of Fe2+ ions due to Fenton-like reactions. Upon extraction of SOA samples from OH photooxidation of isoprene, we also detected OH yields of around similar to 0.1 %, which increases upon addition of Fe2+. Our findings imply that the chemical reactivity and aging of SOA particles is strongly enhanced upon interaction with water and iron. In cloud droplets under dark conditions, SOA decomposition can compete with the classical H2O2 Fenton reaction as the source of OH radicals. Also in the human respiratory tract, the inhalation and deposition of SOA particles may lead to a substantial release of OH radicals, which may contribute to oxidative stress and play an important role in the adverse health effects of atmospheric aerosols.

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 Datum: 2016-02-152016
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: We found that ambient and laboratory-generated secondary organic aerosols (SOA) form substantial amounts of OH radicals upon interaction with liquid water, which can be explained by the decomposition of organic hydroperoxides. The molar OH yield from SOA formed by ozonolysis of terpenes (α-pinene, β-pinene, limonene) is  ∼  0.1 % upon extraction with pure water and increases to  ∼  1.5 % in the presence of Fe2+ ions due to Fenton-like reactions. Upon extraction of SOA samples from OH photooxidation of isoprene, we also detected OH yields of around  ∼  0.1 %, which increases upon addition of Fe2+. Our findings imply that the chemical reactivity and aging of SOA particles is strongly enhanced upon interaction with water and iron. In cloud droplets under dark conditions, SOA decomposition can compete with the classical H2O2 Fenton reaction as the source of OH radicals. Also in the human respiratory tract, the inhalation and deposition of SOA particles may lead to a substantial release of OH radicals, which may contribute to oxidative stress and play an important role in the adverse health effects of atmospheric aerosols.
 Art der Begutachtung: -
 Identifikatoren: ISI: 000371284100034
DOI: 10.5194/acp-16-1761-2016
 Art des Abschluß: -

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Titel: Atmospheric Chemistry and Physics
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Katlenburg-Lindau, Germany : European Geosciences Union
Seiten: - Band / Heft: 16 (3) Artikelnummer: - Start- / Endseite: 1761 - 1771 Identifikator: ISSN: 1680-7316
CoNE: https://pure.mpg.de/cone/journals/resource/111030403014016