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Implications of non-equilibrium transport in heterogeneous reactive barrier systems : evidence from laboratory denitrification experiments

机译:异质反应性屏障系统中非平衡迁移的影响:实验室反硝化实验的证据

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摘要

Organic substrates in reactive barrier systems are often heterogeneous material mixtures with relatively large contrasts in hydraulic conductivity and porosity over short distances. These short-range variations in material properties imply that preferential flow paths and diffusion between regions of higher and lower hydraulic conductivity may be important for treatment efficiency. This paper presents the results of a laboratory column experiment where denitrification is investigated using a heterogeneous reactive substrate (sawdust mixed with sewage sludge). Displacement experiments with a non-reactive solute at three different flow rates are used to estimate transport parameters using a dual porosity non-equilibrium model. Parameter estimation from breakthrough curves produced relatively consistent values for the fraction of the porosity consisting of mobile water (β) and the mass transfer coefficient (α), with average values of 0.27 and 0.42 d-1, respectively. The column system removes > 95% of the influent nitrate at low and medium flow, but only 50 – 75% of the influent nitrate at high flow, suggesting that denitrification kinetics and diffusive mass transfer rates are limiting the degree of treatment at lower hydraulic residence times. Reactive barrier systems containing dual porosity media must therefore consider mass transfer times in their design; this is often most easily accommodated by adjusting flowpath length.
机译:反应性阻隔系统中的有机基质通常是异质材料混合物,在短距离内的水力传导率和孔隙率存在较大差异。材料特性的这些短距离变化意味着,较高的和较低的水力传导率区域之间的优先流动路径和扩散对于处理效率可能很重要。本文介绍了实验室柱实验的结果,该实验使用非均相反应性底物(木屑与污水污泥混合)研究了反硝化作用。使用非反应性溶质在三种不同流速下进行的置换实验用于使用双重孔隙度非均衡模型估算运输参数。根据穿透曲线进行的参数估算得出了由流动水(β)和传质系数(α)组成的孔隙率的相对一致值,平均值分别为0.27和0.42 d-1。在低流量和中流量时,该色谱柱系统可去除> 95%的硝酸盐,但在高流量时,仅可去除50–75%的硝酸盐,这表明反硝化动力学和扩散传质速率限制了较低水力停留时间下的处理程度次。因此,包含双重孔隙介质的反应性阻隔系统必须在设计中考虑传质时间。通常,通过调整流路长度可以很容易地适应这一点。

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  • 作者

    Herbert, Roger;

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  • 年度 2011
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  • 原文格式 PDF
  • 正文语种 eng
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