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Elucidation of retention processes governing the transport of volatile organic compounds in unsaturated soil systems

机译:阐明支配非饱和土壤系统中挥发性有机化合物迁移的保留过程

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摘要

There is evidence to suggest that the air-water interface serves as an important retention domain for volatile organic compounds (VOCs) in vadose-zone soil systems. Gas-phase solute transport experiments were conducted to evaluate the influence of air-water interfacial adsorption on trichloroethene transport and retention. Mechanical mixing and diffusion were observed to contribute significantly to the transport of gases and vapors in unsaturated soils. The relative contribution of individual dispersion processes was governed largely by the differences in their diffusion coefficients, while changes in gas-phase tortuosity and linear velocity due to soil-water content changes represented secondary effects. Difluoromethane (DFM) was shown to hold promise as a reactive tracer for the in-situ measurement of soil-water content, as there was shown to be a linear relationship between DFM-estimated and measured soil-water contents. Heptane was shown here to exhibit nonideal tracer behavior that complicate its use in estimating air-water interfacial areas. Conversely, relatively ideal interfacial tracer properties were exhibited by decane. In excess of 90% of the decane retardation factor was contributed by adsorption at the air-water interface, rendering other forms of retention entirely secondary. Decane retardation factors were in an appropriate range for soil-water contents greater than ∼2.5%. Specific air-water interfacial areas estimated from decane retention data appear to be reasonable, based on comparison with the measured N₂√BET specific surface area of the porous media and comparison with literature data. The retention of TCE vapor in unsaturated soil systems to be influenced by several processes, including sorption to the solid surfaces, dissolution into bulk soil-water, and adsorption at the air-water interface. The retention of TCE in the system under various conditions was not predicted well by the traditional retardation equation. However, use of DFM (water-partitioning tracer) data and decane (interfacial tracer) data were observed to further improve agreement between predicted and experimental TCE retardation factors. Interfacial processes were shown to influence TCE retention most significantly at soil-water contents less than 5%, contributing 87% of the total measured retardation factor at 2% soil-water content.
机译:有证据表明,空气-水界面是渗流带土壤系统中挥发性有机化合物(VOC)的重要保留域。进行了气相溶质迁移实验,以评估空气-水界面吸附对三氯乙烯迁移和保留的影响。观察到机械混合和扩散对气体和蒸气在非饱和土壤中的传输有显着贡献。各个分散过程的相对贡献在很大程度上取决于其扩散系数的差异,而土壤水含量变化引起的气相曲折度和线速度的变化则代表了次级效应。二氟甲烷(DFM)被证明有望作为一种反应性示踪剂用于土壤水含量的原位测量,因为表明DFM估算的土壤水含量与测量的土壤水含量之间存在线性关系。此处显示的庚烷表现出非理想的示踪剂行为,这使其在估算气水界面面积方面的使用变得复杂。相反,癸烷显示出相对理想的界面示踪剂性质。超过90%的癸烷阻滞因子是由空气-水界面处的吸附引起的,从而使其他形式的保留完全变为次要。癸烷阻滞因子在土壤水分含量大于约2.5%的合适范围内。根据与多孔介质的N 2√BET比表面积的比较以及与文献数据的比较,根据癸烷保留数据估算出的特定的空气-水界面面积似乎是合理的。 TCE蒸气在非饱和土壤系统中的保留受到多种过程的影响,包括吸附到固体表面,溶解到大量的土壤-水中以及在空气-水界面处的吸附。传统的延迟方程无法很好地预测TCE在各种条件下在系统中的保留率。但是,观察到使用DFM(水分配示踪剂)数据和癸烷(界面示踪剂)数据可以进一步改善预测的和实验的TCE延迟因子之间的一致性。结果表明,在土壤含水量小于5%的情况下,界面过程对TCE保留的影响最大,在土壤含水量为2%的情况下,界面作用占总测量延迟因子的87%。

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    Costanza Molly Susan;

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  • 年度 2001
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