benzofurans and 1-4-dioxin

Polychlorinated dibenzo-p-dioxins, dibenzofurans (PCDD/F) and their precursors - pentachlorophenol (PCP) and triclosan (TCS), constitute a group of persistent, highly toxic multimedia pollutants, being easily transported via atmosphere over long distances, thus particularly threatening to the polar areas. The global fate of PCDD/Fs is temperature-dependent, and their transfer and immobilization at the Poles are described by the grasshopper effect and the cold trap phenomenon. The aim of this interdisciplinary study was to perform a preliminary assessment of the present state of pollution of Arctic and Antarctic marine sediments by PCP and TCS along with determination of PCDD/Fs contamination by immunoassay. Sediments from 20 stations were collected during two polar expeditions (2013-2016). The study area covered Hornsund Fjord and the southwest coast of Wedel-Jarlsberg Land (Arctic) - Skodde Bay, Nottingham Bay, Isbjørnhamna Bay and Admiralty Bay (Antarctica) - Suszczewski Cove, Halfmoon Cove and Herve Cove. The studied contaminants were quantified in 60% of the collected sediments, with almost half exceeding the environmentally safe levels according European regulations and worldwide literature. The determined levels of PCP, TCS and PCDD/F in Arctic and Antarctic sediments were to be comparable to those reported in the southern Baltic Sea located in the intense industrialized mid-latitudes. Maximum concentrations were observed in the vicinity of retreating, marine terminating glaciers. This observation confirms reemission of POPs into the global cycle with respect to the worldwide ocean warming. The results of this study should gain attention of the international and regional environmental agencies as well as the main chlorine production decision makers.

Topics: Antarctic Regions; Benzofurans; Climate Change; Dibenzofurans; Dibenzofurans, Polychlorinated; Dioxins; Environmental Monitoring; Environmental Pollutants; Environmental Pollution; Geologic Sediments; Pentachlorophenol; Polychlorinated Dibenzodioxins

The homogeneous, gas-phase oxidative thermal degradation of a 50:50 mixture of 2-bromophenol and 2-chlorophenol was studied in a 1 cm i.d., fused silica flow reactor at a concentration of 88 ppm, with a reaction time of 2.0 s, over a temperature range of 300 to 1000 degrees C. Observed products in order of decreasing yield included the following: dibenzo-p-dioxin (DD), 4-bromo-6-chlorodibenzofuran (4-B,6-CDF), phenol, 4,6-dibromodibenzofuran (4,6-DBDF), 2,6-dibromophenol, 4,6-dichlorodibenzofuran (4,6-DCDF), 2-bromo-4-chlorophenol, 2,4-dibromophenol, 2-chloro-4-bromophenol, 4-monobromodibenzofuran (4-MBDF), 4-monochlorodibenzofuran (4-MCDF), dibenzofuran (DF), 1-monobromodibenzo-p-dioxin (1-MBDD), 1-monochlorodibenzo-p-dioxin (1-MCDD), 2,4,6-tribromophenol, naphthalene, chloronaphthalene, bromonaphthalene, chlorobenzene, bromobenzene, and benzene. The results are compared and contrasted with previous results reported for the oxidations of pure 2-chlorophenol and 2-bromophenol as well as results for the pyrolysis of the mixture of 2-chlorophenol and 2-bromophenol. 4,6-DBDF and 4,6-DCDF were observed in higher yields than under pyrolytic conditions but considerably less than the yields observed for the individual oxidation of 2-chlorophenol and 2-bromophenol. The effect on chlorine and bromine on the concentration of hydroxyl radical is shown to control the dioxin-to-furan ratio.

Topics: Benzofurans; Chlorophenols; Dioxins; Environment; Gases; Hydroxyl Radical; Models, Chemical; Naphthalenes; Oxygen; Phenols; Polychlorinated Dibenzodioxins; Temperature

A rapid, sensitive and accurate method has been developed for the determination of seventeen 2, 3, 7, 8-substituted congeners of polychlorinated dibenzo-p-dioxins and dibenzo-furans (PCDD/Fs) in sediment using isotope dilution high resolution gas chromatography/high resolution mass spectrometry (HRGC/HRMS). Dibenzo-p-dioxins and dibenzo-furans were extracted from samples by accelerated solvent extraction (ASE) and then purified by fluid management systems (FMS) with silica column, alumina column and carbon column. Confirmation and quantitative analysis at pg/g level of PCDD/Fs were performed by HRGC/HRMS using voltage selective ion record (VSIR) mode. Recoveries of fifteen isotopically labeled compound solutions (LCS) and the precision and recovery standards (PAR) were found to be in the range of 49.8% -85.3% and 93.2% - 113.8%, respectively. The detection limits of the method for both 2, 3, 7, 8-tetrachloro-dibenzo-furan (TCDF) and 2, 3, 7, 8-tetrachloro-dibenzo-p-dioxin (TCDD) were determined to be 0.1 pg/g. This method not only meets the requirements of international standards, but also shortens analysis time from 2 weeks to 2 days.

Topics: Benzofurans; Chromatography, Gas; Dibenzofurans, Polychlorinated; Dioxins; Furans; Limit of Detection; Mass Spectrometry; Plant Oils; Polychlorinated Dibenzodioxins