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Bubble bursting as an aerosol generation mechanism during an oil spill in the deep-sea environment: molecular dynamics simulations of oil alkanes and dispersants in atmospheric air/salt water interfaces

机译:气泡破裂是深海环境中溢油过程中的一种气溶胶生成机理:大气/盐水界面中油烷烃和分散剂的分子动力学模拟

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Potential of mean force (PMF) calculations and molecular dynamics (MD) simulations were performed to investigate the properties of oil n-alkanes [i.e., n-pentadecane (C15), n-icosane (C20) and n-triacontane (C30)l, as well as several surfactant species [i.e., the standard anionic surfactant sodium dodecyl sulfate " (SDS), and three model dispersants similar to the Tween and Span species present in Corexit 9500A1 at air/salt water interfaces. This study was motivated by the 2010 Deepwater Horizon (DWH) oil spill, and our simulation results show that, from the thermodynamic point of view, the n-alkanes and the model dispersants have a strong preference to remain at the air/salt water interface, as indicated by the presence of deep free energy minima at these interfaces. The free energy minimum of these n-alkanes becomes deeper as their chain length increases, and as the concentration of surfactant species at the interface increases. The n-alkanes tend to adopt a flat orientation and form aggregates at the bare air/salt water interface. When this interface is coated with surfactants, the n-alkanes tend to adopt more tilted orientations with respect to the vector normal to the interface. These simulation results are consistent with the experimental findings reported in the accompanying paper [Ehrenhauser et at., Environ. Sci.: Processes Impacts 2013, in press, (DOI: 10.1039/c3em00390f)]. The fact that these long-chain n-alkanes show a strong thermodynamic preference to remain at the air/salt water interfaces, especially if these interfaces are coated with surfactants, makes these species very likely to adsorb at the surface of bubbles or droplets and be ejected to the atmosphere by sea surface processes such as whitecaps (breaking waves) and bubble bursting. Finally, the experimental finding that more oil hydrocarbons are ejected when Corexit 9500A is present in the system is consistent with the deeper free energy minima observed for the n-alkanes at the air/salt water interface at increasing concentrations of surfactant species.
机译:进行了平均力(PMF)的计算和分子动力学(MD)的模拟,以研究油性正构烷烃(即,正十五烷(C15),正二十烷(C20)和正三二十烷(C30)l ,以及几种表面活性剂种类[即标准阴离子表面活性剂十二烷基硫酸钠“(SDS),和三种模型分散剂,类似于气/盐水界面处存在于Corexit 9500A1中的Tween和Span种类。 2010年Deepwater Horizo​​n(DWH)漏油事件,我们的模拟结果表明,从热力学角度看,正构烷烃和模型分散剂非常希望保留在空气/盐水界面,如存在这些正构烷烃的自由能最小值随着链长的增加和界面活性剂种类浓度的增加而变得更深,正构烷烃倾向于采用平面取向并形成在裸露的空气/盐水界面处聚集。当该界面涂有表面活性剂时,正构烷烃倾向于相对于垂直于界面的向量采取更多的倾斜取向。这些模拟结果与所附论文[Ehrenhauser等,Environ.Environ.Chem.Sci。,, 1995,9,3,3,3,5,5,5,6,5,6,7,6,7,6,7,8,9,7,8,8,9,8,9,8,9,8,9,8,8,9均]中报道的实验结果一致。 Sci .: Processes Impacts 2013,印刷中(DOI:10.1039 / c3em00390f)]。这些长链正构烷烃表现出强烈的热力学偏好,可保留在空气/盐水界面上,特别是如果这些界面涂有表面活性剂,这一事实使得这些物质很可能吸附在气泡或液滴的表面并成为通过海面过程(如白浪(破浪)和气泡破裂)喷射到大气中。最后,实验发现,当系统中存在Corexit 9500A时,会喷射出更多的石油烃,这与在表面活性剂种类浓度升高时在空气/盐水界面处观察到的正构烷烃的更深的自由能最小值相一致。

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