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Tropospheric concentrations of the chlorinated solvents,tetrachloroethene and trichloroethene,measured in the remote northern hemisphere
Institution:1. School of Chemistry, University of Bristol, Bristol BS8 1TS, UK;2. ICI Chemicals & Polymers Ltd., P.O. Box 13, The Heath, Runcorn, Cheshire WA7 4QF, UK;3. Department of Physics, University of Toronto, 60, St. George St., Toronto, Canada M5S 1A5;4. Southampton Ocenography Centre, Empress Dock, Southampton SO14 3ZH, UK;1. College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen 518060, PR China;2. State Key Laboratory of Pollution Control and Resource Reuse, Shanghai Institute of Pollution Control and Ecological Security, College of Environmental Science and Engineering, Tongji University, 1239 Siping Road, Shanghai 200092, PR China;1. College of Oceanology, Harbin Institute of Technology (Weihai), Weihai, 264209, PR China;2. Division of Ocean Science and Technology, Graduate School at Shenzhen, Tsinghua University, Shenzhen, 518055, PR China;3. School of Marine Sciences, Ningbo University, Ningbo, 315211, PR China
Abstract:A fully automated twin ECD gas chromatograph system with sample enriching adsorption–desorption primary stage was deployed on two field campaigns – Ny-Ålesund, Svalbard, Arctic Norway (July–September 1997), and the RRS Discovery CHAOS cruise of the northeast Atlantic (April–May 1998). Concentrations of an extensive set of halocarbons were detected at hourly intervals at pptv levels. We present here the results obtained for the chlorinated solvents, tetrachloroethene (PCE) and trichloroethene (TCE). Average baseline PCE and TCE concentrations of 1.77 and 0.12 pptv, respectively, were recorded in Ny-Ålesund. During pollution incidences, concentrations rose to 5.61 (PCE) and 3.18 pptv (TCE). The cruise data showed average concentrations ranging from 4.26 (PCE) and 1.66 pptv (TCE) for air masses originating over the North Atlantic and Arctic open oceans, to maxima of 15.59 (PCE) and 17.51 pptv (TCE) for polluted air masses from Northern Europe. The data sets emphasise the difficulties in defining remote sites for background tropospheric halocarbon measurements, as Ny-Ålesund research station proved to be a source of tetrachloroethene. The data also suggest possible oceanic emissions of trichloroethene in the sub-tropical ocean.
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