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Transport of nonreactive and volatile Solutes in unsaturated porous media under wetting and draining conditions

机译:润湿和排水条件下非反应性和挥发性溶质在不饱和多孔介质中的传输

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摘要

The effect of water content and soil-water hysteresis on transport of unreactive water-tracers and volatile organic compounds (VOCs) in porous media is investigated under steady-state water-flow conditions. Specifically, this research addresses the effect on dispersive and mass transfer processes affecting the movement of NaC1 and trichloroethene (ICE) and how these processes influence the approach to Fickian flux conditions. Transport experiments were conducted in a 25-cm column packed with silica sand. Based on the results, it is concluded that water content (0), pore-water velocity, and flow history affect the average movement and spread of water-tracers and VOCs. It is suggested that non-volatile solutes in unsaturated media travel longer distances or times to achieve a Fickian state. Consequently, a greater number of averaged heterogeneities are encountered and solute flux is characterized by a greater dispersion coefficient (D). A power (n) law relationship (D(m) = η(v(m)/ θ(m))ⁿ), found between mobile dispersion coefficients (D(m_), pore-water velocity (v(m)), and water content (θ(m)) for different porous media, indicates that dispersivity (η) is not only a function of the media, but also of θ(w). TCE transport is controlled by advection processes for Ow greater than 50% saturation. Lower θ(w) result in greater TCE dispersion, retardation, mass-transfer resistance, vapor diffusion, and spreading. Consequently, VOCs reach the Fickian regime at shorter distances than unreactive solutes in water. Although VOC transport is influenced by multiple rate-limited mass transfer, the mechanisms controlling the overall mass-transfer resistance vary as a function of θ(w). The hysteretic behavior of solute transport parameters is attributed to a greater degree of irregular flow paths and entrapped air, higher air-water interfacial areas, and thicker water-films for wetting than draining scenarios. Consequently, wetting conditions result in slower mixing (up to 98% lower mass-transfer coefficients) of dissolved solutes. Since TCE transport at low water contents and wetting conditions is dominated by diffusion and dispersion mechanisms, the TCE velocity distribution in the liquid phase is normalized by velocity distributions in the gas-phase and becomes closer to Fickian conditions.
机译:在稳态水流条件下,研究了含水量和土壤水滞后对未反应水示踪剂和挥发性有机化合物(VOC)在多孔介质中迁移的影响。具体而言,这项研究致力于解决分散和传质过程对NaCl和三氯乙烯(ICE)运动的影响,以及这些过程如何影响Fickian通量条件的方法。运输实验是在装有硅胶砂的25 cm色谱柱中进行的。根据结果​​可以得出结论,含水量(0),孔隙水速度和流动历史会影响示水剂和VOC的平均运动和扩散。建议不饱和介质中的非挥发性溶质行进更长的距离或次数以达到菲克状态。因此,会遇到更多的平均异质性,并且溶质通量的特征在于更大的分散系数(D)。在移动弥散系数(D(m_),孔隙水速度(v(m))之间发现幂(n)律关系(D(m)=η(v(m)/θ(m))ⁿ)和水含量(θ(m))对于不同的多孔介质,表明分散度(η)不仅是介质的函数,而且还是θ(w)的函数。TCE的传输受平流过程控制,Ow大于50%较低的θ(w)会导致更大的TCE分散,阻滞,传质阻力,蒸气扩散和扩散,因此,VOC到达Fickian态的距离比水中的非反应性溶质更短。有限的传质,控制总传质阻力的机制随θ(w)的变化而变化溶质传递参数的滞后行为归因于更大程度的不规则流动路径和截留的空气,较高的气水界面区域,以及比排水方案更厚的水膜。稀释会使溶解的溶质的混合速度变慢(传质系数最多降低98%)。由于TCE在低水分含量和润湿条件下的传输受扩散和弥散机制的支配,因此液相中TCE的速度分布通过气相中的速度分布进行归一化,并且变得更接近菲克条件。

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