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Träfflista för sökning "L773:1352 2310 ;pers:(Ljungström Evert 1949)"

Search: L773:1352 2310 > Ljungström Evert 1949

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1.
  • Fischer, Andreas, et al. (author)
  • Ozone removal by occupants in a classroom
  • 2013
  • In: Atmospheric Environment. - : Elsevier BV. - 1352-2310 .- 1873-2844. ; 81, s. 11-17
  • Journal article (peer-reviewed)abstract
    • Ozone concentrations were measured in a classroom with and without occupants, with the purpose to quantify effects on indoor O3 concentrations. The teacher and 24 11-year old pupils each removed O3 at a rate, first order in O3, corresponding to a rate constant of (2.5±0.6)×10-5s-1 in the present locality and to a deposition velocity of 0.45cms-1. The O3-removal caused by the occupants was approximately 2.6 times larger than that of the available surfaces belonging to the classroom and its furniture. Observation of 6-methyl-5-hepten-2-one and 4-oxopentanal at maximum concentrations of 0.2ppb and 0.7ppb, respectively, suggested squalene from human skin oil as a reactive, ozone-consuming substance. There are indications of a source of 4-oxopentanal in the classroom, even some time after the pupils left for the day. The work presented is important for a proper description of indoor exposure, both to ozone itself and some of its reaction products when trying to quantify relations between exposure and health effects.
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2.
  • Hak, Claudia S., 1976, et al. (author)
  • A new approach to in-situ determination of roadside particle emission factors of individual vehicles under conventional driving conditions
  • 2009
  • In: Atmospheric Environment. - : Elsevier BV. - 1352-2310. ; 43:15, s. 2481-2488
  • Journal article (peer-reviewed)abstract
    • A method for continuous on-road measurements of particle number emissions for both diesel- and petrol-fuelled vehicles is presented. The setup allows the determination of particle number emission factors on an individual vehicle basis by the simultaneous measurement of CO2 and particle concentrations. As an alternative to previous measurements on the kerbside, the sample is taken directly in the street, with the advantage of sampling in-situ within the exhaust plumes of passing vehicles, allowing the separation of the individual high-concentration plumes. The method was tested in two experiments that were conducted in the Gothenburg area. In the first study, which was performed at an urban roadside, we were able to determine particle emission factors from individual vehicles in a common car fleet passing the measurement site. The obtained emission factors were of the same order of magnitude (between 1.4 × 1012 and 1.8 × 1014 particles km−1) as values published in the recent literature for light duty vehicles. An additional on-road experiment was conducted at a rural road with four light duty reference vehicles (three of them petrol-powered and one diesel-powered) at driving speeds of 50 and 70 km h−1, realised with different engine speeds. The results of the traffic emission studies show that the method is applicable provided that instruments with an adequate dynamic range are used and that the traffic is not too dense. In addition, the variability in particle emissions for a specified driving condition was estimated.
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4.
  • Olofson, K. Frans G., 1976, et al. (author)
  • Urban aerosol evolution and particle formation during wintertime temperature inversions
  • 2009
  • In: Atmospheric Environment. - : Elsevier BV. - 1352-2310. ; 43, s. 340-346
  • Journal article (peer-reviewed)abstract
    • Aerosol temporal and spatial distributions during wintertime temperature inversions in Gothenburg, Sweden, have been characterized by ground-based and airborne particle measurements combined with lidar measurements. Ground inversions frequently developed during evenings and nights with stable cold conditions, and the low wintertime insolation often resulted in near neutral boundary layer conditions during day-time. Under these conditions ground level aerosol concentrations peaked during morning rush hours and often remained relatively high throughout the day due to inefficient ventilation. The particle number concentrations decreased slowly with increasing altitude within the boundary layer, and measurements slightly above the boundary layer suggested limited entrainment of polluted air into the free troposphere. High concentrations of ultrafine particles were observed throughout the boundary layer up to altitudes of 1100 m, which suggested that nucleation took place within the residual layer during the night and early morning. Recently formed particles were also observed around midday when the layer near ground was ventilated by mixing into the boundary layer, which indicated that ultrafine particles were either transported down from the residual layer to ground level or formed when the polluted surface layer mixed with the cleaner air above.
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5.
  • Olofsson, Marcus, 1968, et al. (author)
  • The flux of isoprene from a willow coppice plantation and the effect on local air quality
  • 2005
  • In: Atmospheric Environment. - : Elsevier BV. - 1352-2310. ; 39:11, s. 2061-2070
  • Journal article (peer-reviewed)abstract
    • Isoprene fluxes from a Salix viminalis (willow) plantation in western Sweden were measured using the relaxed eddy accumulation (REA) technique. Fluxes of up to 0.23 mu g m(-2) s(-1) could be observed. A standard emission factor at 303 K and a PAR flux of 1000 mu mol m(-2) s(-1) was estimated to 0.98 mu g m(-2) s(-1) by using the G93 algorithm. The chemistry of an air parcel passing over a willow coppice plantation was investigated utilising a Lagrangian box model in which the measured isoprene fluxes were used as input data. Dispersion after the field was accounted for by a procedure based on the Gaussian plume model. The calculations indicate that, in most cases, the isoprene emissions have a small effect on the local air quality.
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