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Sökning: AMNE:(NATURAL SCIENCES Chemistry Environmental chemistry) > Övrigt vetenskapligt/konstnärligt > Engelska

  • Resultat 1-10 av 584
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  • Olsman [Takner], Helena, et al. (författare)
  • Relative differences in aryl hydrocarbon receptor-mediated response for 18 polybrominated and mixed halogenated dibenzo-p-dioxins and -furans in cell lines from four different species
  • 2007
  • Ingår i: Environmental Toxicology and Chemistry. - 0730-7268 .- 1552-8618. ; 26:11, s. 2448-2454
  • Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
    • As a consequence of ubiquitous use of brominated organic chemicals, there is a concern for persistent or increasing environmental levels of polybrominated dibenzo-p-dioxins/furans (PBDD/Fs) and mixed polychlorinated and polybrominated dibenzo-p-dioxins/furans (PXDD/Fs). Hence, there is a need to broaden the toxicological and environmental knowledge about these compounds, as a basis for risk assessment. In the study presented here, the relative potencies (REPs) for 18 PBDD/F and PXDD/ F congeners were determined in four dioxin-specific bioassays from different species: dioxin receptor chemically activated luciferase expression assay (DR-CALUX, rat hepatoma cells), TV101L (human hepatoma cells), and GPC.2D (guinea pig adenoma cells), as well as ethoxyresorufin-O-deethylase induction in the fish cell line RTL-W1 (rainbow trout liver cells). The bioassay specific REP factors presented here enable the assessment of the contribution from PBDD/Fs and PXDD/Fs to total 2,3,7,8-tetrachl orodibenzop-dioxin (TCDD) equivalents (TEQs: toxic equivalents), using bioassay analysis. The PBDD/Fs were found to be equally potent as their chlorinated analogues in the three mammalian assays, whereas the PXDD/Fs showed relatively higher potencies. Of special concern were the 2,3,7,8-substituted penta- and tetrahalogenated congeners, for which mean REPs were >= 1. The 2-B-1,3,7,8-CDD (2-bromo-1,3,7,8-tetrachlorodibenzo-p-dioxin) was up to three times more potent than TCDD in individual experiments (on weight basis). The RTL-W1 was less sensitive to the tested compounds with overall 10-fold lower REPs than the mammalian cell lines. Although the REP factors exhibited species-specific differences, overall resembling rank orders of dioxin-like potency were obtained.
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  • Dario, Mårten, et al. (författare)
  • Effects of cement additives on radionuclide mobility
  • 2004
  • Ingår i: Scientific basis for radioactive waste management XXVII. - Warrendale, Pa : Materials Research Society. - 1558997520 ; , s. 639-644
  • Konferensbidrag (övrigt vetenskapligt/konstnärligt)
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  • Ericson Jogsten, Ingrid, 1980- (författare)
  • Assessment of human exposure to per- and polyfluorinated compounds (PFCs) : exposure through food, drinking water, house dust and indoor air
  • 2011
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • Per- and polyfluorinated compounds (PFCs) are detected in humans worldwide but all sources of human exposure have not been fully characterized. The aim of this thesis was to evaluate the contributions from food, water, air and dust as sources for human PFC exposure in the general population. Per- and polyfluorinated compounds (PFCs) are detected in humans worldwide but all sources of Up to 27 PFCs were determined at trace levels in blood (ng/mL), water (ng/L), foods (ng/g), dust (ng/g) and air (pg/m3) in a selected Catalan population and PFC intake was estimated from the measured PFC concentrations of the different sources of exposure. The major compounds detected in human blood of the studied population were perfluorooctane sulfonate (PFOS; 7.6 ng/mL), perfluorohexane sulfonate (PFHxS; 3.6 ng/mL) and perfluorooctanoic acid (PFOA; 1.8 ng/mL). In general, PFOS was also the major compound detected in most sources of exposure. Food was found to be the dominant pathway for human PFC exposure accounting for more than 70 % of the total intake of both PFOS and PFOA. In the most populated area (the Barcelona Province) where the highest levels were measured, tap water can contribute to the total exposure substantially with more than 50 % for adults. Indoor sources were negligible in the selected area for most PFCs when compared to food and water intake, except for toddlers under a worst case scenario where contribution from dust and food intake were equal (19 %). Pharmacokinetic (PK) modelling resulted in exposure of 103 ng PFOS/day and 33 ng PFOA/day of adults from the internal PFC blood concentrations. This agrees well with the intake estimated from external exposure through food, drinking water, house dust and indoor air of 80 ng PFOS/day and 32 ng PFOA/day and evidently all major exposure sources for the general population were included (in this study).
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7.
  • García García, Sandra, 1977- (författare)
  • Generation, stability and migration of montmorillonite colloids in aqueous systems
  • 2010
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • In Sweden the encapsulated nuclear waste will be surrounded by compacted bentonite in the granitic host rock. In contact with water-bearing fractures the bentonite barrier may release montmorillonite colloids that may be further transported in groundwater. If large amounts of material are eroded from the barrier, the buffer functionality can be compromised. Furthermore, in the scenario of a leaking canister, strongly sorbing radionuclides, can be transported by montmorillonite colloids towards the biosphere. This thesis addresses the effects of groundwater chemistry on the generation, stability, sorption and transport of montmorillonite colloids in water bearing rock fractures. To be able to predict quantities of montmorillonite colloids released from the bentonite barrier in contact with groundwater of varying salinity, generation and sedimentation test were performed. The aim is first to gain understanding on the processes involved in colloid generation from the bentonite barrier. Secondly it is to test if concentration gradients of montmorillonite colloids outside the barrier determined by simple sedimentation experiments are comparable to generation tests. Identical final concentrations and colloid size distributions were achieved in both types of tests. Colloid stability is strongly correlated to the groundwater chemistry. The impact of pH, ionic strength and temperature was studied. Aggregation kinetics experiments revealed that for colloid aggregation rate increased with increasing ionic strength. The aggregation rate decreased with increasing pH. The temperature effect on montmorillonite colloid stability is pH-dependent. At pH≤4, the rate constant for colloid aggregation increased with increasing temperature, regardless of ionic strength. At pH≥10, the aggregation rate constant decreased with increasing temperature. In the intermediate pH interval, the aggregation rate constant decreased with increasing temperature except at the highest ionic strength, where it increased. The relationship between the rate constant and the ionic strength allowed the critical coagulation concentration (CCC) for Na- and Ca-montmorillonite to be determined. In order to distinguish the contribution of physical filtration and sorption to colloid retention in transport, the different retention mechanisms were quantified. Sorption on different representative minerals in granite fractures was measured for latex colloids (50, 100, 200 nm) and montmorillonite colloids as a function of ionic strength and pH. Despite of the negative charge in mineral surfaces and colloids, sorption was detected. The sorption is correlated to the mineral point of zero charge and the zeta potential of the colloids, and increases with increasing ionic strength and decreasing pH. In transport experiments with latex colloids in columns packed with fracture filling material, the retention by sorption could clearly be seen. In particular at low flow rates, when the contact time for colloids with the mineral surfaces were the longest, sorption contributed to retention of the transport significantly. The retention of latex colloids appeared to be irreversible in contrary to the reversible montmorillonite colloid retention. Generation, stability and sorption of the montmorillonite colloids are controlled by electrostatic forces; hence, the results were in qualitative agreement with DLVO.
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  • Greis, Christina, 1975- (författare)
  • Rapid analysis of actinide isotopes using quadrupole ICP-MS for emergency preparedness and environmental monitoring
  • 2007
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • Transuranium elements in the environment are mainly derived from nuclear weapons testing and the nuclear fuel cycle. Of growing concern are illicit nuclear trafficking and the threat of terror acts. The development of rational methods, for environmental monitoring and for tracing sources of nuclear and radioactive materials in the environment, is constantly required. Traditionally, the actinides have been determined by radiometric techniques. These analyses can be time consuming for elements at low concentrations and with long half-lives. This thesis addresses the determination of actinides, especially plutonium, in environmental samples with ICP-QMS (inductively coupled plasma quadrupole mass spectrometry). The ICP-QMS instrument was equipped with an USN (ultrasonic nebuliser), which proved to be a successful combination for the determination of plutonium at low concentrations in acidified solutions after separation with anion exchange. The detection limit for plutonium was in the range 10-30 pg/l with a RSD of 1-10%. The suitability of chemical separation was evaluated for anion exchange, liquid-liquid-extraction and extraction chromatography. The outlined procedure, including sample dissolution, chemical separation and analysis, for determination of actinides in environmental matrices proved to be accurate and reliable. Quality assurance of the procedure was performed during an intercomparison exercise and with reference materials. The detection accuracy has also been validated with α-spectrometry and ICP-SFMS. The procedure has been applied to saline sediments and fresh water sediments as well as several fresh water matrices.
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10.
  • Rotander, Anna, 1978- (författare)
  • Monitoring persistent organic pollutants (POPs) in sub-Arctic and Arctic marine mammals, 1984 - 2009
  • 2011
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • The Arctic has become an important indicator region for assessing persistence and bioaccumulation properties of persistent organic pollutants (POPs). This thesis is aimed at evaluating the occurrence of persistent halogenated POPs in seven species of sub-Arctic and Arctic marine mammals over a 25-year period. The emphasis is on studying temporal variations in concentration of three categories of POPs, including naturally occurring organobromine compounds. Polybrominated diphenyl ethers (PBDEs), Metoxylated diphenyl ethers (MeO-PBDEs), and polychlorinated naphtalenes (PCNs) were extracted from blubber tissue and analyzed by GC/MS. Polyfluoroalkyl substances (PFAS) were extracted from livers and analyzed by LC-MS/MS. Although restricted by the number of pooled samples, survey points, and species available from the specimen banks, the results showed some interesting contamination patterns. Overall, pollutant concentrations showed signs of declining or levelling out, indicating a decrease in POP exposure in the studied areas in recent years. However, increasing levels of long-chain fluorinated compounds (PFCAs) present in most species is a finding of concern, and implies that a continuous monitoring of these compounds is important. Interestingly, a shift over time in the relative abundance of PFOS isomers in ringed seals was observed, indicating a change in exposure to PFOS in recent years. In many of the investigated species the MeO-PBDE levels equalled or exceeded the levels of PBDEs, showing that MeO-PBDEs can be major contributors to the organobromine load in marine mammal species. No apparent relation was found between PBDE and MeO-PBDE levels, adding further support for a natural origin of MeO-PBDEs.
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