首页> 外文会议>Air Waste Management Association's Annual Conference Exhibition >ADSORPTION OF AROMATIC HYDROCARBON VAPORS AT THE GAS- SOLID AND GAS-WATER INTERFACE
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ADSORPTION OF AROMATIC HYDROCARBON VAPORS AT THE GAS- SOLID AND GAS-WATER INTERFACE

机译:气固气体界面芳烃蒸气吸附

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It is apparent that there is a lack of experimental data on the adsorption of polycyclic aromatic hydrocarbons at the gas-water environmental interface such as fog droplets that offers a high surface area for potential accumulation of these hydrophobic organic compounds. An inverse gas chromatography (IGC) technique using Chromosorb P NAW as the packing support to obtain the thermodynamic properties of adsorption for three aromatic compounds (benzene, naphthalene and phenanthrene) at gas/water and gas/solid interfaces. The partition constant and free energy at different temperatures were measured and used to compute the enthalpy and entropy of adsorption using the Gibbs-Duhem equation. The enthalpy of adsorption at the gas/water interface for all three compounds was larger than the enthalpy of liquefaction and enthalpy of aqueous solvation. This supports the prevailing "critical cluster" model for the dynamics of the transfer of compounds to the gas/water interface. The thermodynamics of adsorption at the gas/solid interface was more favorable than the gas/water interface.
机译:显然存在关于在气水环境界面处的多环芳烃吸附的实验数据,例如雾滴,其提供高表面积,用于这些疏水性有机化合物的潜在积累。一种逆气相色谱(IGC)技术,使用染色体P naw作为填料载体,以获得气/水和天然气/固体界面在气体/水/固体界面中吸附的吸附热力学性质。测量不同温度下的分区常数和自由能,并使用使用GIBBS-DUEM方程来计算吸附的吸附焓和熵。对于所有三种化合物的气/水界面上吸附的吸附焓大于液化焓和含水溶剂化的焓。这支持了将化合物转移到气/水界面的动态的主要的“关键集群”模型。气/固体界面的吸附热力学比气/水界面更有利。

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