首页> 外文OA文献 >Impact of multicomponent ionic transport on pH fronts propagation in saturated porous media
【2h】

Impact of multicomponent ionic transport on pH fronts propagation in saturated porous media

机译:多组分离子迁移对饱和多孔介质中pH前沿传播的影响

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Multicomponent ionic interactions have been increasingly recognized as important factors for the displacement of charged species in porous media under both diffusion- [1,2] and advection-dominated flow regimes [3,4]. In this study we investigate the propagation of pH fronts during multicomponent ionic transport in saturated porous media under flow-through conditions. By performing laboratory bench-scale experiments combined with numerical modeling we show the important influence of Coulombic effects on proton transport in the presence of ionic admixtures. The experiments were performed in a quasi two-dimensional flow-through setup under steady-state flow and transport conditions. Dilute solutions of hydrochloric acid with MgCl2 (1:2 strong electrolyte) were used as tracer solutions to experimentally test the effect of electrochemical cross-coupling on the migration of diffusive/dispersive pH fronts. We focus on two experimental scenarios, with different composition of tracer solutions, causing remarkably different effects on the propagation of the acidic fronts with relative differences in the penetration depth of pH fronts of 36% between the two scenarios and of 25% and 15% for each scenario with respect to the transport of ions at liberated state (i.e. without considering the charge effects). Also significant differences in the dilution of the distinct ionic plumes, quantified using the flux-related dilution index at the laboratory bench scale [5], were measured at the outflow of the flow-through system. The dilution of the pHplumes also changed considerably (26% relative difference) in the two flow-through experiments only due to the different composition of the pore water solution and to the electrostatic coupling of the ions in the flow-through setups. Numerical transport simulations were performed to interpret the laboratory experiments. The simulations were based on a multicomponent ionic formulation accurately capturing the Coulombic interactions between the transported ions in the flow-through system. The results of purely forward simulations show a very good agreement with the high-resolution measurements performed at the outlet of the flow-through setup and illustrate the importance of charge effects on pH fronts propagation in porous media.
机译:在扩散[1,2]和以对流为主的流态下[3,4],多组分离子相互作用已逐渐被认为是带电物质在多孔介质中位移的重要因素。在这项研究中,我们研究了流通条件下饱和多孔介质中多组分离子迁移过程中pH前沿的传播。通过进行实验室规模的实验与数值模拟相结合,我们显示了在存在离子混合物的情况下库仑效应对质子传输的重要影响。实验是在稳态流动和运输条件下以准二维流通装置进行的。使用盐酸与MgCl2(1:2强电解质)的稀溶液作为示踪剂溶液,以实验方式测试电化学交叉偶联对扩散/分散pH前沿迁移的影响。我们专注于两种实验方案,其示踪剂溶液的组成不同,对酸性前沿的传播造成明显不同的影响,两种方案之间pH前沿渗透深度的相对差异分别为36%和25%和15%。关于在自由状态下离子传输的每种情况(即,不考虑电荷效应)。在流通系统的流出处,还测量了不同离子羽流的稀释率的显着差异,这些差异是在实验室工作台规模下使用与通量相关的稀释指数进行定量的[5]。在两个流通实验中,pH柱的稀释度也发生了很大变化(相对差异为26%),这仅是由于孔隙水溶液的组成不同以及流通设置中离子的静电耦合所致。进行了数值运输模拟以解释实验室实验。该模拟基于多组分离子配方,可准确捕获流通系统中运输的离子之间的库仑相互作用。纯正向模拟的结果表明,与流通设置出口处执行的高分辨率测量非常吻合,并说明了电荷效应对pH值在多孔介质中传播的重要性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号