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Träfflista för sökning "L773:1352 2310 ;pers:(Sällsten Gerd 1952)"

Sökning: L773:1352 2310 > Sällsten Gerd 1952

  • Resultat 1-7 av 7
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1.
  • Molnár, Peter, 1967, et al. (författare)
  • Domestic wood burning and PM2.5 trace elements: Personal exposures, indoor and outdoor levels
  • 2005
  • Ingår i: Atmospheric Environment. - : Elsevier BV. - 1352-2310. ; 39:14, s. 2643-2653
  • Tidskriftsartikel (refereegranskat)abstract
    • Personal exposures as well as indoor and outdoor levels of PM2.5 were measured with cyclones and impactors simultaneously in the winter of 2003 in a residential area where wood burning for domestic space heating is common. Twenty-four-hour samples from both wood-burning households ("wood burners") and a reference group were analysed for mass and elemental concentration using energy dispersive X-ray fluorescence (EDXRF) and for black smoke (BS) concentration using an EEL 43 reflectometer. Wood-smoke particles made statistically significant contributions of K, Ca, and Zn for both personal exposure and indoor concentration, the median levels of these elements being 66-80% higher for the wood-burning group. In addition, Cl, Mn, Cu, Rb, and Pb were found to be possible markers of wood smoke, though levels of these were only significantly higher among the wood-burning group for either personal exposure or indoor concentrations. PM2.5 mass and S levels were not significantly elevated in wood burners, probably due to large variations in outdoor concentrations from long-distance transported air pollution. Personal exposure and indoor levels showed high correlations for all species, and the personal exposure levels were usually higher than or equal to the indoor levels. The associations between personal exposure and outdoor levels were generally weak except for outdoor S and PM2.5 levels that were both highly correlated with personal S exposure levels (r(s) > 0.8). (c) 2005 Elsevier Ltd. All rights reserved.
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2.
  • Molnár, Peter, 1967, et al. (författare)
  • Residential NOx exposure in a 35-year cohort study. Changes of exposure, and comparison with back extrapolation for historical exposure assessment
  • 2015
  • Ingår i: Atmospheric Environment. - : Elsevier BV. - 1352-2310 .- 1873-2844. ; 115, s. 62-69
  • Tidskriftsartikel (refereegranskat)abstract
    • In this study we aimed to investigate the effects on historical NOx estimates on time trends, spatial distributions, exposure contrasts, the effect of relocation patterns and the effects of back extrapolation. Historical levels of nitrogen oxides (NOx) from 1975 to 2009 were modeled with high resolution in Gothenburg, Sweden, using historical emission databases and Gaussian models. Yearly historical addresses were collected and geocoded from a population-based cohort of Swedish men from 1973 to 2007, with a total of 160,568 address years. Of these addresses, 146,675 (91%) were within our modeled area and assigned a NOx level. NOx levels decreased substantially from a maximum median level of 43.9μg/m3 in 1983 to 16.6μg/m3 in 2007, mainly due to lower emissions per vehicle km. There was a considerable variability in concentrations within the cohort, with a ratio of 3.5 between the means in the highest and lowest quartile. About 50% of the participants changed residential address during the study, but the mean NOx exposure was not affected. About half of these moves resulted in a positive or negative change in NOx exposure of >10μg/m3, and thus changed the exposure substantially. Back extrapolation of NOx levels using the time trend of a background monitoring station worked well for 5-7 years back in time, but extrapolation more than ten years back in time resulted in substantial scattering compared to the "true" dispersion models for the corresponding years. These findings are important to take into account since accurate exposure estimates are essential in long term epidemiological studies of health effects of air pollution.
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4.
  • Strandberg, Bo, 1960, et al. (författare)
  • Field evaluation of two diffusive samplers and two adsorbent media to determine 1,3-butadiene and benzene levels in air
  • 2006
  • Ingår i: Atmospheric Environment. - : Elsevier. - 1352-2310 .- 1873-2844. ; 40:40, s. 7686-7695
  • Tidskriftsartikel (refereegranskat)abstract
    • Two types of diffusive samplers, both of which are compatible with thermal desorption, but differ in their geometry-SKC-Ultra (badge-type) and Radiello (radial symmetry-type)-were evaluated indoors and outdoors under varying temperature, humidity and wind speed conditions, using the graphitized adsorbents Carbopack X or Carbograph 5 to measure 1,3-butadiene and benzene in ambient air. The results obtained by diffusive sampling were compared with results obtained using a conventional active sampling method over both long (1 week) and shorter periods (6-24 h). Analysis and detection were performed using an automatic thermal desorber (ATD) connected to a gas chromatograph-flame ionization detector (GC/FID). Results from each sampler and adsorbent combination were examined using ordinary or multiple linear regression analysis. The overall uncertainty (OU) was also determined. In general, the results obtained with both samplers showed good agreement with those obtained by active sampling. Carbopack X appeared to be a more efficient adsorbent than Carbograph 5 for 1,3-butadiene, but the two adsorbents were equivalent for benzene. No effects of either humidity or air velocity were observed. Minor temperature effects were observed for both samplers for 1,3-butadiene. In summary, the results confirmed the accuracy of sampling rates previously determined for the two samplers and adsorbents. We consider the two samplers to be suitable for stationary and personal monitoring for the general population of 1,3-butadiene and benzene in various environments, indoors and outdoors. They are almost independent of meteorological conditions and may be suitable for monitoring industrial atmospheres.
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5.
  • Tang, L., et al. (författare)
  • Estimation of the long-range transport contribution from secondary inorganic components to urban background PM10 concentrations in south-western Sweden during 1986-2010
  • 2014
  • Ingår i: Atmospheric Environment. - : Elsevier BV. - 1352-2310. ; 89, s. 93-101
  • Tidskriftsartikel (refereegranskat)abstract
    • The contribution of long-range transported (LRT) to urban background PM10 concentrations was investigated from a long-term view from 1986 to 2010. Regional air concentrations of sulphate (SO42-), nitrate (NO3-), and ammonium (NH4+) were used as a sum (C-ion) to investigate the contribution from these ions to the LRT PM10 concentrations at an urban background site in Gothenburg, Sweden. Utilizing backwards trajectory analysis, the LRT contribution from C-ion to the urban background PM10 concentrations (LRTCion) was estimated for six unique transport pathways and related source areas. Air masses transported over eastern Europe, UK/North Sea/Denmark and the vicinity of Scandinavia were associated with high C-ion concentrations observed in Gothenburg. For each pathway, multiple linear models based on the C-ion concentrations were used to estimate LRTCion and PM10 at the urban background site. The performances of the multiple linear models were satisfying with R-2 between estimated and observed annual mean PM10 concentrations of 0.81 during the monitoring years 1990-2010. The models were able to describe the main features of the day-to-day average PM10 concentrations, but underestimated high level values. The annual estimated LRTCion contribution decreased from 7 +/- 2 mu g/m(3) for 1986-2000 to 5 +/- 1 mu g/m(3) for 2001-2010. The higher LRTCion contribution was related to the transport cluster from eastern Europe, UK/North Sea/Denmark and the vicinity of South Scandinavia. (C) 2014 Elsevier Ltd. All rights reserved.
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6.
  • Wierzbicka, Aneta, et al. (författare)
  • Detailed diesel exhaust characteristics including particle surface area and lung deposited dose for better understanding of health effects in human chamber exposure studies
  • 2014
  • Ingår i: Atmospheric Environment. - : Elsevier BV. - 1352-2310. ; 86, s. 212-219
  • Tidskriftsartikel (refereegranskat)abstract
    • Several diesel exhaust (DE) characteristics, comprising both particle and gas phase, recognized as important when linking with health effects, are not reported in human chamber exposure studies. In order to understand effects of DE on humans there is a need for better characterization of DE when performing exposure studies. The aim of this study was to determine and quantify detailed DE characteristics during human chamber exposure. Additionally to compare to reported DE properties in conducted human exposures. A wide battery of particle and gas phase measurement techniques have been used to provide detailed DE characteristics including the DE particles (DEP) surface area, fraction and dose deposited in the lungs, chemical composition of both particle and gas phase such as NO, NO2, CO, CO2, volatile organic compounds (including aldehydes, benzene, toluene) and polycyclic aromatic hydrocarbons (PAHs). Eyes, nose and throat irritation effects were determined. Exposure conditions with PM1 (<1 mu m) mass concentration 280 mu g m(-3), number concentration 4 x 10(5) cm(-3) and elemental to total carbon fraction of 82% were generated from a diesel vehicle at idling. When estimating the lung deposited dose it was found that using the size dependent effective density (in contrast to assuming unity density) reduced the estimated respiratory dose by 132% by mass. Accounting for agglomerated structure of DEP prevented underestimation of lung deposited dose by surface area by 37% in comparison to assuming spherical particles. Comparison of DE characteristics reported in conducted chamber exposures showed that DE properties vary to a great extent under the same DEP mass concentration and engine load. This highlights the need for detailed and standardized approach for measuring and reporting of DE properties. Eyes irritation effects, most probably caused by aldehydes in the gas phase, as well as nose irritation were observed at exposure levels below current occupational exposure limit values given for exhaust fumes. Reporting detailed DE characteristics that include DEP properties (such as mass and number concentration, size resolved information, surface area, chemical composition, lung deposited dose by number, mass and surface) and detailed gas phase including components known for their carcinogenic and irritation effect (e.g. aldehydes, benzene, PAHs) can help in determination of key parameters responsible for observed health effects and comparison of chamber exposure studies. (C) 2013 The Authors. Published by Elsevier Ltd. All rights reserved.
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7.
  • Wängberg, I, et al. (författare)
  • Emissions, dispersion and human exposure of mercury from a Swedish chlor-alkali plant
  • 2005
  • Ingår i: Atmospheric Environment. - : Elsevier BV. - 1352-2310. ; 39:39, s. 7451-7458
  • Tidskriftsartikel (refereegranskat)abstract
    • Mercury in air near a mercury cell chlor-alkali plant in Sweden has been measured within the EU-project EMECAP. Based on the measurements and modelling the annual distributions of GEM and RGM have been calculated for the local area around the plant. The average concentration of GEM in residential areas near the plant was found to be 1-3.5 ng m(-3) higher in comparison to the background concentration in this part of Sweden. The emission of RGM (0.55 kg year(-1)) results in elevated RGM concentrations close to the plant. The greatest impact on the local area is due to wet deposition of RGM. However, only a small fraction (0.4%) of all mercury being emitted was found to be deposited in the local area. No impact on urinary mercury could be demonstrated in the population living close to the plant. (c) 2005 Elsevier Ltd. All rights reserved.
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