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  • 1.
    Andersson, Maria E.
    et al.
    Univ Gothenburg, Dept Chem, Gothenburg, Sweden..
    Gårdfeldt, Katarina
    Univ Gothenburg, Dept Chem, Gothenburg, Sweden.;GMV Ctr Environm & Sustainabil, SE-41296 Gothenburg, Sweden..
    Wängberg, Ingvar
    IVL Swedish Environm Res Inst, Gothenburg, Sweden..
    Strömberg, Dan
    GMV Ctr Environm & Sustainabil, SE-41296 Gothenburg, Sweden..
    Determination of Henry's law constant for elemental mercury2008In: Chemosphere, ISSN 0045-6535, E-ISSN 1879-1298, Vol. 73, no 4, p. 587-592Article in journal (Refereed)
    Abstract [en]

    The assessment of the global mercury cycle involves estimations of the evasion of mercury form oceanic waters. In such estimations Henry's law constant is often used. In this study the Henry's law constant for elemental mercury has been re-determined in MQ water and artificial sea water. Moreover, for the first time it has been determined for 1.5 M sodium chloride (NaCl) solution which is of relevance for modeling of atmospheric waters at coastal locations. For all solutions, experiments has been conducted at five different temperatures between 278 and 308 K, using a novel technique, for mercury, based on direct measurements of the portioning of mercury between the aqueous and gaseous phase. Elemental mercury was extracted from the water column and the logarithm of the mass of extracted mercury was plotted against time. A dimensionless Henry's law constant, defined as: k(H') = [Hg((g))]/[Hg((aq))] was obtained from the slope of the curve. Almost no difference was observed in the values comparing the Milli-Q water and artificial sea water, however for the 1.5 M NaCl solution a salting-out effect was seen, i.e. the solubility of mercury in the water phase decreased. The decreased solubility will generate an increase in the value of Henry's law constant. (C) 2008 Elsevier Ltd. All rights reserved.

  • 2. Gustafsson, O
    et al.
    Axelman, J
    Broman, D
    Eriksson, M
    Dahlgaard, H
    Process-diagnostic patterns of chlorobiphenyl congeners in two radiochronologically characterized sediment cores from the northern Baffin Bay2001In: Chemosphere, ISSN 0045-6535, E-ISSN 1879-1298, Vol. 45, no 6-7, p. 759-766Article in journal (Refereed)
    Abstract [en]

    Polychlorinated biphenyl (PCB) patterns were interpreted in two radioisotopically constrained sediment cores from the Arctic ocean in order to seek clues about their large-scale environmental fates. Low but clearly measurable fluxes of individual PCB congeners were observed in deeper layer sediments, corresponding to the past 170 years, in a single dated core from the Baffin Bay shelf. Fluxes of the dominant individual congeners in the surface sediments were 20-100 mug m(-2) d(-1). Combining these data with the sediment data from the Arctic Monitoring and Assessment Program, it appears that the PCB distribution in Arctic surface sediments is governed by the organic carbon (OC) content of the sediments. The historical development of the PCB congener fingerprint suggests that the modern sediments are enriched in medium-chlorinated congeners, implying that there are at least two significant, but distinctly different, sink processes acting on the PCB pool. The relative abundance of light-to-heavy congeners, in mid-shelf marine sediments of similar ages, between 40 degreesN and 76 degreesN latitude suggests a northward dilution of PCBs which is stronger attenuated for heavier congeners, consistent with a temperature-driven global fractionation process. The significant presence of PCB in historical archives pre-dating the organochlorine society, as observed in this and several previous studies, awaits a fuller explanation. (C) 2001 Elsevier Science Ltd. All rights reserved.

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