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  • Peroxyacetylnitrate  (1)
  • free troposphere  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of atmospheric chemistry 28 (1997), S. 319-337 
    ISSN: 1573-0662
    Keywords: convection ; free troposphere ; ozone ; oxides of nitrogen ; three-dimensional model
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The fluxes of ozone and NOx out of the atmospheric boundary layer (ABL) over Europe are calculated in a mesoscale chemical transport model (MCT) and compared with the net chemical production or destruction of ozone and the emissions of precursors within the ABL for two 10 days' periods which had quite different synoptic situations and levels of photochemical activity (1–10 July 1991 (JUL91) and 26 October–4 November 1994 (ON94)). Over the European continent, about 8% of the NOx emissions were brought from the ABL to the free troposphere as NOx, while about 15% of the NOx emissions were brought to the free troposphere as NOy–NOx, i.e. as PAN or HNO3. The convection dominates over the synoptic scale vertical advection as a transport mechanism both for NOx and NOy out of the boundary layer in the summertime high pressure situation (JUL91), while in the fall situation (ON94) the convective part was calculated to be the smallest. NOx was almost completely transformed to NOy–NOx or removed within the ABL. Also for NOy the major part of the atmospheric cycle is confined to the ABL both for JUL91 and ON94. The vertical transport time out of the ABL is of the order of 100h both for the total model domain and over the European continent. The net convective exchange of ozone from the ABL is not a dominant process for the amount of ozone in the ABL averaged over 10 days and the whole domain, but convection reduces the maximum ozone concentration in episodes significantly. The ozone producing efficiency of NOx is calculated to increase with height to typically 15–20 in the upper half of the troposphere from around 5 in the ABL, but in the middle free troposphere the concentration of NOx is often too low to cause net chemical formation of ozone there.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of atmospheric chemistry 1 (1984), S. 187-202 
    ISSN: 1573-0662
    Keywords: Peroxyacetylnitrate ; long-range transport ; model ; measurements
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Model calculations and field measurements have shown that when air masses accumulate emissions of hydrocarbons and nitrogen oxides from sources in continental Europe and then move towards Scandinavia without any synoptic scale break-up of the atmospheric boundary layer (e.g. frontal passages), elevated PAN concentrations in southern Norway or Sweden in the range 1–5 ppb may be caused by long-range transport. The model calculations showed that over sea, the persistence of PAN was comparable to that of ozone in an ageing air mass when the temperatures were fairly low (5–10°C). At higher temperatures the thermal decomposition of PAN made the compound less persistent than ozone. Over land, the situation may be different since the ground removal is typically three times more efficient for ozone than for PAN. According to the model, the concentration of PAN did not change very much when an ageing air mass was exposed to moderate emissions of hydrocarbons, nitrogen oxides, or both. The concentration of PAN decreased less than the concentration of ozone when an ageing air mass was exposed to high emissions of nitrogen oxides.
    Type of Medium: Electronic Resource
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