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Krischke et al. 2000
Krischke, U., Staubes, R., Brauers, T., Gautrois, M., Burkert, J., Stöbener, D. and Jaeschke, W. (2000). Removal of SO2 from the marine boundary layer over the Atlantic Ocean: A case study on the kinetics of the heterogeneous S(IV) oxidation on marine aerosols. Journal of Geophysical Research 105: doi: 10.1029/1999JD900957. issn: 0148-0227.

Measurements of SO2 and NSS-SO42- were made over the Atlantic Ocean on board the RV Polarstern from October 9 to November 2, 1996, as part of the ALBATROSS campaign. The measurements were performed between 66.7 ¿N and 37.8 ¿S with a mean longitude of approximately 30 ¿W. The most frequent background values for SO2 were found to be 13 parts per trillion by volume (pptv) (0.54 nmol m-3 at standard ambient temperature and pressure (SATP)) in the Southern Hemisphere, and 15 pptv (0.62 nmol m-3 SATP) in the Northern Hemisphere. The mean values for total NSS-SO42- in particles with a d>0.2 μm were (5.99¿2.93) nmol m-3 (SATP) in the Southern Hemisphere, and (8.93¿5.29) nmol m-3(SATP) in the Northern Hemisphere. An analysis of the size-fractionated aerosol samples (d>1 μm and 0.2 μm1 μm. The main fraction of this NSS-SO42- is most likely produced by the oxidation of dissolved SO2 via heterogeneous reactions occurring in the aqueous phase of coarse mode marine aerosols. A case study on the kinetics of this oxidation pathway was conducted during ALBATROSS. October 12, 1996, the ship sailed in the plume of a volcano on Iceland during its eruption from September 30 to October 13, 1996, as indicated by trajectory analysis and by the measurements of NSS-SO42-, SO2, CO, and Hg. An empirical physicochemical approach considering the atmosphere as a natural flow reactor is used for the presented case study. The determined pseudo-first-order reaction rate constant for the oxidation of SO2 on marine aerosols is 3.31¿10-4 s-1 at 25 ¿C. Assuming that the occurrence of coarse mode marine aerosols is the rate-limiting variable of the reaction, the second-order reaction rate constant is found to be 1.32¿10-6 cm3 s-1 particle-1 at 25 ¿C. These values are in good agreement with results of previous field experiments as well as with the results of model studies. ¿ 2000 American Geophysical Union

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Abstract

Keywords
Atmospheric Composition and Structure, Aerosols and particles (0345, 4801), Atmospheric Composition and Structure, Chemical kinetic and photochemical properties, Atmospheric Composition and Structure, Constituent sources and sinks, Atmospheric Composition and Structure, Troposphere—composition and chemistry, Atmospheric Composition and Structure, Cloud physics and chemistry
Journal
Journal of Geophysical Research
http://www.agu.org/journals/jb/
Publisher
American Geophysical Union
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