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Are organic films from atmospheric aerosol and sea water inert to oxidation by ozone at the air-water interface?
Royal Holloway Univ London, Dept Earth Sci, Egham TW20 0EX, Surrey, England.;Rutherford Appleton Lab, STFC, Cent Laser Facil, Res Complex Harwell, Didcot OX11 0FA, Oxon, England..
Royal Holloway Univ London, Dept Earth Sci, Egham TW20 0EX, Surrey, England..
Rutherford Appleton Lab, STFC, Cent Laser Facil, Res Complex Harwell, Didcot OX11 0FA, Oxon, England..
Uppsala University, Disciplinary Domain of Science and Technology, Physics, Department of Physics and Astronomy, Materials Physics.
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2017 (English)In: Atmospheric Environment, ISSN 1352-2310, E-ISSN 1873-2844, Vol. 161, 274-287 p.Article in journal (Refereed) Published
Abstract [en]

The heterogeneous oxidation of thin films of organic material extracted from real aerosol and sea-water samples was studied at the air-water interface using X-ray reflectivity. Oxidation of thin films of organic material extracted from real aerosol and sea-water is important in further understanding the impact of coated aerosols on the climate of the Earth. Surface active insoluble organic material extracted from the atmosphere was found to form stable films at the air-water interface (thickness measured as 10-14 nm). On exposure of the films to gas-phase ozone, no reaction (or change in the relative scattering length of the interface) was observed, indicating a potential lack of unsaturated organic material in the samples. Gas chromatography and electrospray ionization mass spectrometry showed the presence of saturated compounds in the samples. It is therefore proposed that the amount of unsaturated compounds as compared to saturated compounds in the atmospheric material is so low that the mass spectrometry analyses, as well as gas-phase oxidation are dominated by saturated material. A reaction was observed on exposure of the same films to aqueous phase hydroxyl and nitrate radicals and a film thinning mechanism is proposed to explain the change in scattering length of the film at the air-water interface. It can be suggested tentatively that oxidation by gas-phase ozone is not important in the atmosphere for organic films on aqueous atmospheric aerosol and that further studies should focus on radical induced oxidation of saturated organic material instead of unsaturated proxies that are typically studied.

Place, publisher, year, edition, pages
PERGAMON-ELSEVIER SCIENCE LTD , 2017. Vol. 161, 274-287 p.
Keyword [en]
Atmospheric aerosol, Sea-water, Thin film, Heterogeneous oxidation, Ozone, OH radical, X-ray reflectivity
National Category
Environmental Sciences Meteorology and Atmospheric Sciences
Identifiers
URN: urn:nbn:se:uu:diva-335680DOI: 10.1016/j.atmosenv.2017.04.025ISI: 000403515900026OAI: oai:DiVA.org:uu-335680DiVA: diva2:1168140
Available from: 2017-12-20 Created: 2017-12-20 Last updated: 2017-12-20

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