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Are organic films from atmospheric aerosol and sea water inert to oxidation by ozone at the air-water interface?

Jones, Stephanie H. (author)
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.
King, Martin D. (author)
Royal Holloway Univ London, Dept Earth Sci, Egham TW20 0EX, Surrey, England.
Ward, Andrew D. (author)
Rutherford Appleton Lab, STFC, Cent Laser Facil, Res Complex Harwell, Didcot OX11 0FA, Oxon, England.
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Rennie, Adrian R., 1957- (author)
Uppsala universitet,Materialfysik
Jones, Alex C. (author)
Royal Holloway Univ London, Dept Earth Sci, Egham TW20 0EX, Surrey, England.
Arnold, Thomas (author)
Diamond Light Source, Harwell Campus, Didcot OX11 0DE, Oxon, England.
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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. (creator_code:org_t)
PERGAMON-ELSEVIER SCIENCE LTD, 2017
2017
English.
In: Atmospheric Environment. - : PERGAMON-ELSEVIER SCIENCE LTD. - 1352-2310 .- 1873-2844. ; 161, s. 274-287
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • 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.

Subject headings

NATURVETENSKAP  -- Geovetenskap och miljövetenskap -- Miljövetenskap (hsv//swe)
NATURAL SCIENCES  -- Earth and Related Environmental Sciences -- Environmental Sciences (hsv//eng)
NATURVETENSKAP  -- Geovetenskap och miljövetenskap -- Meteorologi och atmosfärforskning (hsv//swe)
NATURAL SCIENCES  -- Earth and Related Environmental Sciences -- Meteorology and Atmospheric Sciences (hsv//eng)

Keyword

Atmospheric aerosol
Sea-water
Thin film
Heterogeneous oxidation
Ozone
OH radical
X-ray reflectivity

Publication and Content Type

ref (subject category)
art (subject category)

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