benzofurans and decabromobiphenyl-ether

The thermal treatment of waste electrical and electronic equipment (WEEE) is regarded as the largest potential contributor to the environmental release of polybrominated dibenzo-p-dioxins/dibenzofurans (PBDD/Fs). Herein, the pyrolysis of decabromodiphenyl ether (deca-BDE), polyethylene (PE) and metal blends was conducted to investigate the emission characteristics of PBDD/Fs at different thermal treatment conditions. The total yield of polybrominated dibenzo-p-dioxins (PBDDs) was less than that of polybrominated dibenzofurans (PBDFs) during the pyrolysis of the PE matrix and metal blends. 2,3,7,8-TBDF and 1,2,3,7,8-PBDF were the dominant congeners emitted from the pyrolysis. Temperature, presence of oxygen and type of added metal were the critical influencing factors for the PBDD/F formation rates and speciation in the pyrolysis process.

Topics: Air Pollutants; Benzofurans; Dioxins; Electronic Waste; Halogenated Diphenyl Ethers; Incineration; Metals; Polyethylene

Photolytic transformation profiles of technical hexabromocyclododecane (HBCD) and technical decabromodiphenyl ether (DecaBDE) in flame-retarded textiles exposed to natural sunlight were compared. Textiles that contained approximately 4% HBCDs by weight showed no substantial loss of any of the HBCD diastereomers during the entire exposure period (371 days), indicating that they were resistant to sunlight, that is, that debromination and isomerization of HBCD diastereomers did not occur under the experimental conditions. Exposure of a textile treated with technical DecaBDE resulted in the formation of polybrominated dibenzofurans (PBDFs) as products of photodecomposition of polybrominated diphenyl ethers present in the technical DecaBDE. After 329 days of exposure, the total PBDF concentration reached a maximum of 27 000 ng g(-1), which was approximately 10 times the initial concentration. During the experiment, di- to hexa-BDF congener concentrations increased continuously. Although the concentrations of PBDFs in the textiles were 4–5 orders of magnitude lower than the concentrations of polybrominated diphenyl ethers, it is important to note that PBDFs were formed as a result of sunlight exposure during normal use of products treated with technical DecaBDE.

Topics: Benzofurans; Flame Retardants; Halogenated Diphenyl Ethers; Halogenation; Hydrocarbons, Brominated; Isomerism; Photolysis; Sunlight; Textiles

The analysis of temporal trends is a key tool to assess the success of national and international regulations on chemical pollution. Persistent organic pollutants (POPs) are chemical pollutants, which are not only harmful, but also because of their slow environmental degradation they pose a long-time risk. In this study, concentrations of selected POPs were measured between 1993 and 2012 in digested sewage sludge from eight municipal waste water treatment plants. Polychlorinated biphenyls (PCBs) and polychlorinated dibenzo-dioxins and furans (PCDD/Fs), which have been banned or restricted for decades, exhibited decreasing trends with apparent half-lives between 9 and 12years. Polybrominated diphenyl ethers (PBDEs) and long-chain perfluorinated acids showed no clear trend, which reflects the recent introduction of regulations. The analysis of octabromodiphenyl ethers did not reveal indications for reductive debromination of decabromodiphenyl ether; however the analysis of total bromine showed that up to 14% of the total bromine load in sewage sludge originated from PBDEs (average 2%). This is the first study to report temporal trends for more than 20years of series POPs in sewage sludge.

Topics: Benzofurans; Bromine Compounds; Conservation of Natural Resources; Dioxins; Environmental Monitoring; Environmental Pollutants; Halogenated Diphenyl Ethers; Polychlorinated Biphenyls; Polychlorinated Dibenzodioxins; Sewage; Switzerland; Time Factors

The study presented the concentrations and distributions of polybrominated dibenzo-p-dioxins and polybrominated dibenzofurans (PBDD/Fs) as impurities in some commercial decabromodiphenyl ether (DBDE) mixtures that were produced by several manufacturers. The total concentrations of 12 2,3,7,8-substituted tetra- to octa-BDD/F congeners were found to be in the range of 3.4-13.6 (mean 7.8) μg/g, averagely accounting for 99% of total PBDD/Fs. OBDF was the prevailing congener, followed by 1,2,3,4,6,7,8-HpBDF. In addition, OBDD and 1,2,3,4,7,8-HxBDF were also obviously detectable. The total concentrations of PBDD/Fs varied both between the manufacturers and between the lots. On the basis of the global demand for the commercial DBDE in 2001, the annual potential emissions of PBDD/Fs were calculated coarsely to be 0.43 (range: 0.21-0.78) tons. The major dioxin congeners, OBDF and 1,2,3,4,6,7,8-HpBDF, presenting in DBDE, were estimated to be formed from BDE-209, BDE-206, and/or BDE-207 via an intra-molecular elimination of Br2/HBr.

Topics: Benzofurans; Bromobenzenes; Dioxins; Environmental Pollution; Halogenated Diphenyl Ethers

Topics: Benzofurans; Bromobenzenes; Chromatography, Gas; Flame Retardants; Halogenated Diphenyl Ethers; Hexanes; Mass Spectrometry; Phenyl Ethers; Photolysis; Polybrominated Biphenyls; Sunlight; Ultraviolet Rays