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Träfflista för sökning "WFRF:(Strandberg Bo 1960) "

Sökning: WFRF:(Strandberg Bo 1960)

  • Resultat 1-10 av 36
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1.
  • Langer, Sarka, 1960, et al. (författare)
  • Impacts of fuel quality on indoor environment onboard a ship: From policy to practice
  • 2020
  • Ingår i: Transportation Research Part D-Transport and Environment. - : Elsevier BV. - 1361-9209 .- 1879-2340. ; 83
  • Tidskriftsartikel (refereegranskat)abstract
    • Environmental considerations, concerning the negative impacts of ship exhaust gases and particles on ambient air quality, are behind the requirements of cleaner marine fuels currently applied in designated emission control areas (ECAs). We investigated the impact of a ship operating on two types of fuel on the indoor air quality onboard. Gaseous and particulate air pollutants were measured in the engine room and the accommodation sections on-board an icebreaker operating first on Heavy Fuel Oil (HFO, 1%-S), and later Marine Diesel Oil (MDO, 0.1%-S). Statistically significant decrease of SO2, NOx, PM2.5 and particle number concentration were observed when the ship was operating on MDO. Due to the higher content of alkylated PAHs in MDO compared to HFO, the concentration of PAHs increased during operation on MDO. The particulate PAHs classified as carcinogens, were similar to or lower in the MDO campaign. Chemical analysis of PM2.5 revealed that the particles consisted mainly of organic carbon and sulfate, although the fraction of metals was quite large in particles from the engine room. Principal Component Analysis of all measured parameters showed a clear difference between HFO and MDO fuel on the indoor environmental quality on-board the ship. This empirical study poses a first example on how environmental policy-making impacts not only the primary target at a global level, but also brings unexpected localized benefits at workplace level. The study emphasizes the need of further investigations on the impact of new marine fuels and technologies on the indoor air environments on board.
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2.
  • Stockfelt, Leo, 1981, et al. (författare)
  • Effects on airways of short-term exposure to two kinds of wood smoke in a chamber study of healthy humans.
  • 2012
  • Ingår i: Inhalation toxicology. - : Informa UK Limited. - 1091-7691 .- 0895-8378. ; 24:1, s. 47-59
  • Tidskriftsartikel (refereegranskat)abstract
    • Introduction: Air pollution causes respiratory symptoms and pulmonary disease. Airway inflammation may be involved in the mechanism also for cardiovascular disease. Wood smoke is a significant contributor to air pollution, with complex and varying composition. We examined airway effects of two kinds of wood smoke in a chamber study. Materials and Methods: Thirteen subjects were exposed to filtered air and to wood smoke from the start-up phase and the burn-out phase of the wood-burning cycle. Levels of PM(2.5) were 295 µg/m(3) and 146 µg/m(3), number concentrations 140 000/cm(3) and 100 000/cm(3). Biomarkers in blood, breath and urine were measured before and on several occasions after exposure. Effects of wood smoke exposure were assessed adjusting for results with filtered air. Results: After exposure to wood smoke from the start-up, but not the burn-out session, Clara cell protein 16 (CC16) increased in serum after 4 hours, and in urine the next morning. CC16 showed a clear diurnal variation. Fraction of exhaled nitric oxide (FENO) increased after wood smoke exposure from the burn-out phase, but partly due to a decrease after exposure to filtered air. No other airway markers increased. Conclusions: The results indicate that relatively low levels of wood smoke exposure induce effects on airways. Effects on airway epithelial permeability was shown for the start-up phase of wood burning, while FENO increased after the burn-out session. CC16 seems to be a sensitive marker of effects of air pollution both in serum and urine, but its function and the significance need to be clarified.
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3.
  • Almerud, Pernilla, 1978, et al. (författare)
  • Low personal exposure to benzene and 1,3-butadiene in the Swedish petroleum refinery industry
  • 2017
  • Ingår i: International Archives of Occupational and Environmental Health. - : Springer Science and Business Media LLC. - 0340-0131 .- 1432-1246. ; 90:7, s. 713-724
  • Tidskriftsartikel (refereegranskat)abstract
    • Petroleum refinery workers are exposed to the carcinogens benzene and 1,3-butadiene. Declining exposures have been reported internationally but information on current exposure in the Swedish refinery industry is limited. The aim was to examine refinery workers' personal exposure to benzene and 1,3-butadiene and increase awareness of exposure conditions by collaboration with involved refineries. Altogether 505 repeated personal exposure measurements were performed among workers at two refineries. Full-shift measurements were conducted in different exposure groups using Perkin Elmer diffusive samplers filled with Carbopack X. Mean levels were calculated using mixed-effects models. A large fraction of measurements below the limit of detection (LOD) required imputation of computer-generated data. Mean benzene exposure among process technicians was 15.3 A mu g/m(3) (95% CI 10.4-22.5 A mu g/m(3)) and 13.7 A mu g/m(3) (95% CI 8.3-22.7 A mu g/m(3)) for Refinery 1 and 2, respectively. Process technicians working outdoors had higher exposure than maintenance workers (20.7 versus 5.9 A mu g/m(3), p < 0.01). Working in the harbour and tank park (Refinery 1), compared with the process area, was associated with higher exposure. The 1,3-butadiene exposure was low, 5.4 and 1.8 A mu g/m(3), respectively. The total variation was generally attributed to within-worker variability. Low benzene and 1,3-butadiene levels were found among refinery workers. Mean benzene exposure was about 1% of the Swedish occupational limit (1500 A mu g/m(3)) and for 1,3-butadiene, exposure was even lower. A large fraction of values below the LOD can be managed by carefully modelled, computer-generated data.
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4.
  • Bergemalm-Rynell, kerstin, 1949, et al. (författare)
  • Laboratory and field evaluation of a diffusive sampler for measuring halogenated anesthetic compounds
  • 2008
  • Ingår i: J Environ Monit. - : Royal Society of Chemistry (RSC). - 1464-0325. ; 10, s. 1172-78
  • Tidskriftsartikel (refereegranskat)abstract
    • Anesthetic gases such as desflurane, sevoflurane, isoflurane, enflurane, and halothane are used on a daily basis in operating theaters. Active sampling has historically been used to control the level of exposure to personnel. SKC 575-002 is a diffusive passive sampler filled with Anasorb 747. We validated this sampler in both laboratory and field experiments. Parameters tested were desorption efficiency, concentration, sampling time, relative humidity, and reverse diffusion, as well as storage stability for up to 8 weeks. Uptake rates were achieved by comparison with active sampling for each passive sampling trial of 1, 4, or 8 h. Analysis and detection were performed using gas chromatography with flame ionization detection (GC/FID). Multiple regression analysis was used to evaluate the influence of time, concentration, dose, and relative humidity. In the field evaluation experiments, intraclass correlation coefficients (ICC) were estimated. In the laboratory experiments, no problems were found with storage stability or reverse diffusion. The sampling rates for the five anesthetics vary, however, with exposure time and exposure level, with generally higher uptake rates at low concentrations and short sampling times. In the field experiments there was high agreement between the active and passive samplers for halothane, sevoflurane, and isoflurane (ICC > 0.83). When performing whole-day workplace measurements (TWA measurements) the SKC 575-002 can be recommended, and at levels around 1 ppm the following uptake rates should be used: enflurane and halothane, 12.3 mL min−1; desflurane, 13.6 mL min−1; isoflurane, 12.0 mL min−1; and sevoflurane, 11.9 mL min−1.
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  • Bohlin, Pernilla, 1976, et al. (författare)
  • Observations on persistent organic pollutants in indoor and outdoor air using passive polyurethane foam samplers
  • 2008
  • Ingår i: Atmospheric Environment. - : Elsevier BV. - 1352-2310. ; 42:31, s. 7234-7241
  • Tidskriftsartikel (refereegranskat)abstract
    • Air quality data of persistent organic pollutants (POPs) indoors and outdoors are sparse or lacking in several parts of the world, often hampered by the cost and inconvenience of active sampling techniques. Cheap and easy passive air sampling techniques are therefore helpful for reconnaissance surveys. As a part of the Megacity Initiative: Local and Global Research Observations (MILAGRO) project in Mexico City Metropolitan Area in 2006, a range of POPs (polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs), and polybrominated diphenyl ethers (PBDEs)) were analyzed in polyurethane foam (PUF) disks used as passive samplers in indoor and outdoor air. Results were compared to those from samplers deployed simultaneously in Gothenburg (Sweden) and Lancaster (United Kingdom). Using sampling rates suggested in the literature, the sums of 13 PAHs in the different sites were estimated to be 6.1–180 ng m−3, with phenanthrene as the predominant compound. Indoor PAH levels tended to be higher in Gothenburg and outdoor levels higher in Mexico City. The sum of PCBs ranged 59–2100 ng m−3, and seemed to be highest indoors in Gothenburg and Lancaster. PBDE levels (sum of seven) ranged 0.68–620 ng m−3, with the highest levels found in some indoor locations. OCPs (i.e. DDTs, HCHs, and chlordanes) were widely dispersed both outdoors and indoors at all three studied areas. In Gothenburg all POPs tended to be higher indoors than outdoors, while indoor and outdoor levels in Mexico City were similar. This could be due to the influence of indoor and outdoor sources, air exchange rates, and lifestyle factors. The study demonstrates how passive samplers can provide quick and cheap reconnaissance data simultaneously at many locations which can shed light on sources and other factors influencing POP levels in air, especially for the gaseous fractions.
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