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Träfflista för sökning "WFRF:(Nordin J) srt2:(1995-1999)"

Sökning: WFRF:(Nordin J) > (1995-1999)

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  • Somppi, J.L., et al. (författare)
  • Ultrafine ash particle formation during waste sludge incineration in fluidized bed reactors
  • 1998
  • Ingår i: Combustion Science and Technology. - : Informa UK Limited. - 0010-2202 .- 1563-521X. ; 134, s. 433-455
  • Tidskriftsartikel (refereegranskat)abstract
    • Ash formation during the bubbling fluidized bed (BFB) combustion of bark and pulp mill sludge has been studied on an industrial and bench scale. During co-firing in an industrial BFB a submicron fly ash mode was formed via condensation of volatilized K, Na, S and Cl species at 0.05-0.3 μm. The submicron mass mode below 0.3 μm made up 2.2-5.0% of the fly ash, while the share of the supermicron mass fraction was 93.6-97.2%. Elements depleted in the ultrafine ash were Ca, Si, Al, Mg, Fe, Mn, P and Ti. The bench-scale test showed that the ultrafine particle concentration was increased by a higher bed temperature and decreased due to sludge moisture. As, Cd, Pb and Rb were enriched in the ultrafine ash on a bench scale, while Ba, Co, Sr and V were depleted. Cu and Zn were enriched in the ultrafine ash during the combustion of dried sludge, but not when wet sludge was fired. Micron-size ash particles composed of non-volatile species, Ca, Si, Mg, Al, P and Mn, adhered to the bed sand, presumably by surface forces, and sintering densified the ash layer. © 1998 OPA (Overseas Publishers Association) N.V. Published by license under the Gordon and Breach Science Publishers imprint.
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  • DeJongh, J, et al. (författare)
  • Estimation of systemic toxicity of acrylamide by integration of in vitro toxicity data with kinetic simulations.
  • 1999
  • Ingår i: Toxicology and Applied Pharmacology. - : Elsevier BV. - 0041-008X .- 1096-0333. ; 158:3, s. 261-268
  • Tidskriftsartikel (refereegranskat)abstract
    • Neurodegenerative properties of acrylamide were studied in vitro by exposure of differentiated SH-SY5Y human neuroblastoma cells for 72 h. The number of neurites per cell and the total cellular protein content were determined every 24 h throughout the exposure and the subsequent 96-h recovery period. Using kinetic data on the metabolism of acrylamide in rat, a biokinetic model was constructed in which the in vitro toxicity data were integrated. Using this model, we estimated the acute and subchronic toxicity of acrylamide for the rat in vivo. These estimations were compared to experimentally derived lowest observed effect doses (LOEDs) for daily intraperitoneal exposure (1, 10, 30, and 90 days) to acrylamide. The estimated LOEDs differed maximally twofold from the experimental LOEDs, and the nonlinear response to acrylamide exposure over time was simulated correctly. It is concluded that the integration of the present in vitro toxicity data with kinetic data gives adequate estimates of acute and subchronic neurotoxicity resulting from acrylamide exposure.
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  • Nordin-Andersson, M, et al. (författare)
  • Neurite degeneration in differentiated human neuroblastoma cells.
  • 1998
  • Ingår i: Toxicology in Vitro. - 0887-2333 .- 1879-3177. ; 12:5, s. 557-60
  • Tidskriftsartikel (refereegranskat)abstract
    • We have studied neurite degeneration in differentiated human neuroblastoma (SH-SY5Y) cells. The axonopathy-inducing potency in vitro of caffeine, diazepam, methylmercury chloride (MeHg), triethyltin chloride (TET) and acrylamide (ACR) was elucidated. After 72 hours of exposure the neurite degeneration was determined (by morphological quantification) as well as the total protein content (general cytotoxicity). The concentrations that caused 20% reduction of number of neurites (ND(20)) for ACR (250+/-36 mum) and TET (0.097+/-0.03 mum) was significantly lower, 63% and 35%, respectively (P
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  • Resultat 1-10 av 17

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