Journal of Geophysical Research Atmospheres · 1997 · 173 citations · 33 references
Natural SciencesChemistryEarth SciencesAir PollutionAtmospheric ChemistryAtmospheric ScienceAerosol ChemistryAerosol Radiative EffectsAtmospheric Oxidation ProcessesOzone ChemistryStratospheric ChemistryTropospheric ChemistryAmorphous CarbonAtmospheric Carbon DioxideOzoneOzone Loss ProcessesStratospheric Ozone ChemistryTraffic-related Air PollutionTropospheric AttenuationTropospheric Ozone Chemistry
Carbon aerosols are produced by all combustion processes. This paper investigates some possible effects of heterogeneous reduction of atmospheric constituents on carbon aerosols. Reduction of HNO 3 , NO 2 , and O 3 on carbon aerosols may be an important effect of increased air traffic that has not been considered to date. It is shown that if HNO 3 , NO 2 and O 3 are heterogeneously reduced on atmospheric amorphous carbon aerosols, then a significant, lower stratospheric ozone loss mechanism could exist. This ozone loss mechanism is almost independent of temperature and does not require the presence of sunlight. The mechanism can operate at all latitudes where amorphous carbon aerosols are present. The relative importance of the mechanism increases with nightlength. The reduction of HNO 3 on carbon aerosols could also be a significant renoxification process wherever carbon aerosols are present. Owing to the very different soot levels in the two hemispheres, this implies that there should be a hemispheric assymetry in the role of these mechanisms. The renoxification leads to simulated tropospheric HNO 3 /NO x ratios that are close to those observed. In contrast to the stratospheric response, the tropospheric production of NO x due to the reduction of HNO 3 would lead to tropospheric ozone production.
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The Initial Composition of Jet Condensation Trails
B. Kärcher, Thomas Peter, U. M. Biermann et al. · Journal of the Atmospheric Sciences · 1996 · 199 citations · Full text