| 1. |
- Agrell, Cecilia, et al.
(författare)
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Polybrominated diphenyl ethers (PBDES) at a solid waste incineration plant I: Atmospheric concentrations
- 2004
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Ingår i: Atmospheric Environment. - : Elsevier BV. - 1352-2310. ; 38:30, s. 5139-5148
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Tidskriftsartikel (refereegranskat)abstract
- In the first of two papers, the atmospheric poly brominated diphenyl ether (PBDE) concentrations at a municipal solid waste incineration (MSW) plant with electronic recycling is compared with that at an industrial urban reference site producing asphalt and concrete. In the second paper, atmospheric deposition and washout behaviour is presented (Atmos. Environ. (2004a)). PBDEs (BDE28, -47, -66, -100, -154, -153, -183, -209) in the gaseous and particulate phase were measured with high resolution in time during the colder parts of the year to minimise the influence of potential historical pollution at the sites through volatilisation. This also means that reported levels are lower compared to other reported data. Results of BDE47 (TetraBDE) and BDE209 (DecaBDE) as representatives of "old" vs. "new" PBDEs as well as SigmaPBDE, excluding BDE209, are presented. Median SigmaPBDE, BDE47 and BDE209 concentration were 6.3, 2.1 and 10.4 pg m(-3) at the MSW and 3.5, 1.7 and 6.5 pg m-3 at the reference site. The total concentrations (gaseous and particulate phase) were significantly higher at the MSW compared to the reference site for SigmaPBDE and BDE47 but not for BDE209. The same results were obtained regarding concentrations in the gaseous phase. Particle concentrations were significantly higher at the MSW for SigmaPBDE, BDE47 and BDE209. Within each site, the gaseous-phase concentration was significantly higher than the particulate-phase concentration except for BDE209 at the MSW. Thus, the proportion of BDE209 detected in the particulate phase was higher at the MSW compared to the reference site. Together with the results of the second paper, we suggest that treatment of waste is presently a source of "old" PBDEs to the environment, whereas the rather similar BDE209 concentrations at the two sites are more a result of proximity to potential diffuse sources.
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| 2. |
- Butt, CM, et al.
(författare)
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Spatial distribution of polybrominated diphenyl ethers in southern Ontario as measured in indoor and outdoor window organic films
- 2004
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Ingår i: Environmental Science & Technology. - : American Chemical Society (ACS). - 1520-5851 .- 0013-936X. ; 38:3, s. 724-731
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Tidskriftsartikel (refereegranskat)abstract
- Organic films were collected from indoor and outdoor window surfaces, along an urban-rural transect extending northward from Toronto, Ontario, Canada, and analyzed for 41 polybrominated diphenyl ether congeners (PBDE). For exterior films, urban SigmaPBDE concentrations were similar to10x greater than rural concentrations, indicating an urban-rural gradient and greater PBDE sources in urban areas. Urban films ranged from 2.5 to 14.5 ng/m(2) (mean = 9.0 ng/m(2)), excluding the regional "hotspot" Electronics Recycling Facility, compared to 1.1 and 0.56 ng/m(2) at the Suburban and Rural sites. Interior urban films (mean = 34.4 ng/m(2)) were 3 times greater than rural films (10.3 ng/m(2)) and were representative of variations in building characteristics. Indoor films were 1.5-20 times greater than outdoor films, consistent with indoor sources of HOES and enhanced degradation in outdoor films. Congener profiles were dominated by BDE-209 (51.1%), consistent with deca-BDE as the main source mixture, followed by congeners from the penta-BDE mixture (BDE-99:13.6% and -47:9.4%) and some octa-BDE (BDE-183:1.5%). Congener patterns suggest a degradative loss of lower brominated compounds in outdoor films versus indoor films. Gas-phase air concentrations were back-calculated from film concentrations using the film-air partition coefficient (K-FA). Mean calculated air concentrations were 4.8 pg/m(3) for outdoor and 42.1 pg/m(3) for indoor urban sites, indicating that urban indoor air is a source of PBDEs to urban outdoor air and the outdoor regional environment.
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| 3. |
- ter Schure, Arnout, et al.
(författare)
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Atmospheric transport of polybrominated diphenyl ethers and polychlorinated biphenyls to the Baltic sea
- 2004
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Ingår i: Environmental Science & Technology. - : American Chemical Society (ACS). - 1520-5851 .- 0013-936X. ; 38:5, s. 1282-1287
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Tidskriftsartikel (refereegranskat)abstract
- The atmospheric transport of polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) was compared by measuring concentrations in air and deposition on an island located in the central basin of the Baltic Sea. Median SigmaPBDE and SigmaPCB concentrations (gaseous + particle) were 8.6 and 7.4 pg m(-3), respectively. Airborne PCBs were mainly found in the gaseous phase, while most of the PBDEs were detected on particles, which agrees with predicted particle/gas distributions. SigmaPBDE levels were dominated by the decabrominated BDE209 followed by the tetrabrominated BDE47 and pentabrominated BDE99. BDE209 is a marker for the environmental distribution of the commercial deca-BDE formulation (>99.5% BDE209), whereas BDE47 and BDE99 are markers for the commercial penta-BDE mixture. General correlations between PBDEs and PCBs suggested similarities in sources and transport mechanism, while more detailed examination of the data identified notable behaviors and exceptions. Differences in regression slopes among tetra-, penta-, and decabrominated PBDEs may reflect different transport processes and the change in usage pattern. Tetra- and pentabrominated PBDEs may originate from secondary sources such as air surface exchange in a manner similar to that of the PCBs, while the deca-BDE209 formulation still has primary sources. The tribrominated BDE17 was also detected and is proposed to be a breakdown product due to atmospheric debromination processes. PBDEs had higher washout ratios than PCBs, explaining their higher concentrations compared to PCBs in precipitation (median of 6.0 and 0.5 ng L-1 for SigmaBDE and SigmaPCB concentrations ("dissolved" + particle), respectively) than in air. The calculated yearly deposition of PBDEs and PCBs indicated that the atmospheric input of PBDEs to the Baltic Proper is currently exceeding that of the PCBs by a factor of 40, while that of the PCBs is decreasing.
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| 4. |
- ter Schure, Arnout, et al.
(författare)
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Polybrominated diphenyl ethers at a solid waste incineration plant II: atmospheric deposition
- 2004
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Ingår i: Atmospheric Environment. - : Elsevier BV. - 1352-2310. ; 38:30, s. 5149-5155
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Tidskriftsartikel (refereegranskat)abstract
- In the second of two papers, the atmospheric polybrominated diphenyl ethers (PBDE) deposition (wet and dry) at a municipal solid waste incineration (MSW) plant with electronics recycling is compared with that at an industrial urban reference site (URS) producing asphalt and concrete. Results of BDE209 and SigmaPBDE excluding BDE209 as representatives of "new" vs. "old" PBDEs are presented. Volume weighted mean SigmaPBDE and BDE209 concentrations at the MSW were 6.2 and 14.4 ng l(-1), and at the URS were 2.5 and 14.1 ng l(-1). Median SigmaPBDE and BDE209 deposition fluxes were 21.3, 63.8 and 7.0, 14.7 ng m(-2) day(-1) at the MSW and URS, respectively. The concentrations in precipitation and the deposition fluxes were significantly higher at the MSW compared to the URS. Measured total washout- ratios (W-T) were dependent on particle scavenging and the median WT for all congeners was 5.4x 10(5). Median dry particle deposition velocities ranged from 0.4 to 49 cm s(-1), depending on congener, showing that PBDEs are effectively removed from the atmosphere by particle deposition. PBDE fluxes increased at the reference site when winds were blowing from west south-west, i.e. from the direction of the MSW. PBDE deposition and washout ratios were not influenced by temperature or rain volume, suggesting a constant emission from the MSW regardless of weather conditions. Together with the results of paper I (Agrell et al., 2004, Atmospheric Environment, this issue) we therefore suggest that treatment of waste, e.g. electronics recycling, is more a source of "old" PBDEs to the environment, whereas the rather similar BDE209 concentrations at the two urban sites are more a result of proximity to potential diffuse sources. (C) 2004 Elsevier Ltd. All rights reserved.
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