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- Arp, Hans Peter H., et al.
(författare)
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Review of polyoxymethylene passive sampling methods for quantifying freely dissolved porewater concentrations of hydrophobic organic contaminants
- 2015
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Ingår i: Environmental Toxicology and Chemistry. - : Wiley. - 0730-7268 .- 1552-8618. ; 34:4, s. 710-720
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Forskningsöversikt (refereegranskat)abstract
- Methods involving polyoxymethylene (POM) as a passive sampler are increasing in popularity to assess contaminant freely dissolved porewater concentrations in soils and sediments. These methods require contaminant-specific POM-water partition coefficients, K-POM. Certain methods for determining K-POM perform reproducibly (within 0.2 log units). However, other methods can give highly varying K-POM values (up to 2 log units), especially for polycyclic aromatic hydrocarbons (PAHs). To account for this variation, the authors tested the influence of key methodological components in K-POM determinations, including POM thickness, extraction procedures, and environmental temperature and salinity, as well as uptake kinetics in mixed and static systems. All inconsistencies in the peer-reviewed literature can be accounted for by the likelihood that thick POM materials (500m or thicker) do not achieve equilibrium (causing negative biases up to 1 log unit), or that certain POM extraction procedures do not ensure quantitative extraction (causing negative biases up to 2 log units). Temperature can also influence K-POM, although all previous literature studies were carried out at room temperature. The present study found that K-POM values at room temperature are independent (within 0.2 log units) of POM manufacture method, of thickness between 17m and 80m, and of salinity between 0% and 10%. Regarding kinetics, monochloro- to hexachloro-polychlorinated biphenyls (PCBs) were within 0.2 log units of equilibrium after 28d in the mixed system, but only dichloro-PCBs achieved near equilibrium after 126d in the static system. Based on these insights, recommended methods and K-POM values to facilitate interlaboratory reproducibility are presented.
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| 2. |
- Cornelissen, Gerard, et al.
(författare)
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Remediation of Contaminated Marine Sediment Using Thin-Layer Capping with Activated Carbon-A Field Experiment in Trondheim Harbor, Norway
- 2011
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Ingår i: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 45:14, s. 6110-6116
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Tidskriftsartikel (refereegranskat)abstract
- In situ amendment of contaminated sediments using activated carbon (AC) is a recent remediation technique, where the strong sorption of contaminants to added AC reduces their release from sediments and uptake into organisms. The current study describes a marine underwater field pilot study in Trondheim harbor, Norway, in which powdered AC alone or in combination with sand or clay was tested as a thin-layer capping material for polycyclic aromatic hydrocarbon (PAH)-contaminated sediment. Several novel elements were included, such as measuring PAH fluxes, no active mixing of AC into the sediment, and the testing of new manners of placing a thin AC cap on sediment, such as AC+clay and AC+sand combinations. Innovative chemical and biological monitoring methods were deployed to test capping effectiveness. In situ sediment-to-water PAH fluxes were measured using recently developed benthic flux chambers. Compared to the reference field, AC capping reduced fluxes by a factor of 2-10. Pore water PAH concentration profiles were measured in situ using anew passive sampler technique, and yielded a reduction factor of 2-3 compared to the reference field. The benthic macrofauna composition and biodiversity were affected by the AC amendments, AC + clay having a lower impact on the benthic taxa than AC-only or AC + sand. In addition, AC + clay gave the highest AC recoveries (60% vs 30% for AC-only and AC + sand) and strongest reductions in sediment-to-water PAH fluxes and porewater concentrations. Thus, application of an AC-clay mixture is recommended as the optimal choice of the currently tested thin-layer capping methods for PAHs, and more research on optimizing its implementation is needed.
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| 5. |
- Elmquist, Marie, et al.
(författare)
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A 700 year sediment record of black carbon and polycyclic aromatic hydrocarbons near the EMEP air monitoring station in Aspvreten, Sweden
- 2007
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Ingår i: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 41:20, s. 6926-6932
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Tidskriftsartikel (refereegranskat)abstract
- In view of poor constraints on historical combustion emissions, past environmental loadings of black carbon (BC) and polycyclic aromatic hydrocarbon (PAH) were reconstructed from dated lake sediment cores collected 70 km south of Stockholm, Sweden. Compared to several dramatic variations over the recent 150 years, the preindustrial loading were steady within +/-50% through the entire medieval with BC fluxes of 0.071 g m(-2) yr(-1) and PAH fluxes of 6 mu g m(-2) yr(-1). In the wood-burning dominated century leading up to the industrial revolution around 1850, increasing BC fluxes were leading PAH fluxes. BC fluxes reached their millennial-scale maximum around 1920, whereas PAH fluxes increased exponentially to its record maximum around 1960, 50-fold above preindustrial values. For 19201950, BC fluxes consistently decreased as PAH fluxes kept increasing. Coal and coke represented >50% of the Swedish energy market in the 1930s. Combined with sharply decreasing (1,7-)/(1,7-+2,6-dimethylphenanthrene), indicative of diminishing wood combustion, and decreasing methylphenanthrenes/phenahthrene, indicative of higher-temperature combustion (coal instead of wood), the sediment archive suggests that the relative BC/PAH emission factors thus are lower for coal than for wood combustion. For the first time, both BC and PAH fluxes decreased after 1960. This trend break is a testament to the positive effects of decreasing reliance on petroleum fuels and a number of legislative actions aimed at curbing emissions and by 1990, the loading of BC was back at preindustrial levels, whereas that of PAH were the lowest since the 1910s. However, for the most recent period (1990-2004) the BC and PAH fluxes are no longer decreasing, putatively reflecting a slight increase in diesel consumption and a doubling of softwood-pellet burners for home heating.
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| 7. |
- Elmquist, Marie
(författare)
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Measurement and source apportionment of ubiquitous soot black carbon in sediments
- 2007
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- The pyrogenic particles formed from incomplete combustion of organic matter are often termed black carbon (BC) and they partake in many important biogeochemical processes. For instance, BC in water and sediment affects the solid-water partitioning of hydrophobic organic pollutants reducing their bioavailability.The key objective of this thesis was to test the chemothermal oxidation method (CTO) to quantify soot-BC in sediments. In the CTO method, sedimentary BC is isolated by removing non-pyrogenic organic matter through thermal combustion at 375°C under active airflow and subsequent removal of inorganic carbonates by adding hydrochloric acid. The CTO method was here shown to work well for quantifying the thermally more stable soot-BC phase.Another objective was to study sediment samples to measure the historical and spatial distribution of combustion products. First, historical fluxes of BC and polycyclic aromatic hydrocarbons (PAH) were investigated in a Swedish lake sediment. Increasing fluxes of BC and PAH were seen in sediment dated to the industrial revolution in the 1850s, the high coal usage in the early 1900s lead to a 5 time increase in BC flux relative to the pre-industrial flux, and the switch from coal to oil usage in the 1950s lead to a 46 time increase in PAH flux relative to the pre-industrial flux. Further, lower fluxes came from stricter emission controls in the 1960s, improvements in combustion technology and the usage of catalytic filters from mid-1980s. Modern sediment measured 20% lower BC flux and 5 times higher PAH flux relative to the pre-industrial fluxes.Secondly, the spatial distribution and sources of sedimentary soot-BC were studied in rivers in the Arctic region. The estimated BC flux was highest in the McKenzie (99 kton yr-1) whereas it was lowest in Yukon (1.1 kton yr-1). Contemporary biomass-derived BC was detected for the Yenisey, whereas fossil fuel derived BC was found for the Lena, Yukon and McKenzie.
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