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First Day of an Oil Spill on the Open Sea: Early Mass Transfers of Hydrocarbons to Air and Water

机译:公海溢油的第一天:碳氢化合物向空气和水中的早期传质

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摘要

During the first hours after release of petroleum at sea, crude oil hydrocarbons partition rapidly into air and water. However, limited information is available about very early evaporation and dissolution processes. We report on the composition of the oil slick during the first day after a permitted, unrestrained 4.3 m~3 oil release conducted on the North Sea. Rapid mass transfers of volatile and soluble hydrocarbons were observed, with >50% of ≤C_(17) hydrocarbons disappearing within 25 h from this oil slick of <10 km~2 area and <10 μm thickness. For oil sheen, >50% losses of ≤C_(16) hydrocarbons were observed after 1 h. We developed a mass transfer model to describe the evolution of oil slick chemical composition and water column hydrocarbon concentrations. The model was parametrized based on environmental conditions and hydrocarbon partitioning properties estimated from comprehensive two-dimensional gas chromatography (GC×GC) retention data. The model correctly predicted the observed fractionation of petroleum hydrocarbons in the oil slick resulting from evaporation and dissolution. This is the first report on the broad-spectrum compositional changes in oil during the first day of a spill at the sea surface. Expected outcomes under other environmental conditions are discussed, as well as comparisons to other models.
机译:在海上释放石油后的最初几个小时,原油中的碳氢化合物迅速分配到空气和水中。但是,关于非常早期的蒸发和溶解过程的信息有限。在北海进行了4.3 m〜3的无限制放油后的第一天,我们报告了浮油的组成。观察到挥发性和可溶性碳氢化合物的快速传质,在小于10 km〜2的面积和小于10μm的浮油中,≥50%的≤C_(17)碳氢化合物在25小时内消失。对于油光泽,在1 h后观察到≤C_(16)碳氢化合物损失> 50%。我们开发了质量转移模型来描述浮油化学成分和水柱碳氢化合物浓度的演变。该模型是根据环境条件和根据全面二维气相色谱(GC×GC)保留数据估算的烃分配特性进行参数化的。该模型正确预测了由于蒸发和溶解而导致的油中石油烃的分馏现象。这是关于海面溢油的第一天油的广谱成分变化的第一份报告。讨论了在其他环境条件下的预期结果,以及与其他模型的比较。

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  • 来源
    《Environmental Science & Technology》 |2014年第16期|9400-9411|共12页
  • 作者单位

    Environmental Chemistry Modeling Laboratory (LMCE), GR C2 544, Swiss Federal Institute of Technology at Lausanne (EPFL), Station 2, CH-1015 Lausanne, Switzerland,Department of Environmental Chemistry, Swiss Federal Institute of Aquatic Science and Technology (Eawag), UEberlandstrasse 133, CH-8600 Duebendorf, Switzerland;

    Environmental Chemistry Modeling Laboratory (LMCE), GR C2 544, Swiss Federal Institute of Technology at Lausanne (EPFL), Station 2, CH-1015 Lausanne, Switzerland,Department of Environmental Chemistry, Swiss Federal Institute of Aquatic Science and Technology (Eawag), UEberlandstrasse 133, CH-8600 Duebendorf, Switzerland;

    Department of Environmental Microbiology, Helmholtz Centre for Environmental Research - UFZ, Permoserstrasse 15, D-04318 Leipzig, Germany;

    Department of Environmental Microbiology, Helmholtz Centre for Environmental Research - UFZ, Permoserstrasse 15, D-04318 Leipzig, Germany;

    Department of Biological Oceanography, Royal Netherlands Institute for Sea Research (NIOZ), P.O. Box 59, 1790 AB Den Burg, The Netherlands,Aquatic Microbiology, Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, P.O. Box 94248, 1090 GE Amsterdam, The Netherlands;

    Response Organisation, RWS Zee&Delta, Postbus 5807, 2280 HV Rijswijk, The Netherlands;

    Department of Fundamental Microbiology, Batiment Biophore, University of Lausanne, CH-1015 Lausanne, Switzerland;

    Department of Marine Chemistry & Geochemistry, Woods Hole Oceanographic Institution, Woods Hole, Massachusetts 02543, United States;

    Environmental Chemistry Modeling Laboratory (LMCE), GR C2 544, Swiss Federal Institute of Technology at Lausanne (EPFL), Station 2, CH-1015 Lausanne, Switzerland,Department of Environmental Chemistry, Swiss Federal Institute of Aquatic Science and Technology (Eawag), UEberlandstrasse 133, CH-8600 Duebendorf, Switzerland;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-17 14:01:14

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