电场作用下非饱和黄土中铅离子迁移机理研究

STUDY ON THE MIGRATION LAW OF LEAD IONS IN UNSATURATED LOESS UNDER ELECTROOSMOSIS

  • 摘要: 研究了电场作用下非饱和黄土中铅离子的迁移机理。通过等温吸附试验确定黄土对铅离子的吸附类型;基于固、液、气三相系统建立了电场作用下非饱和土中污染物迁移的多场耦合数学模型,利用COMSOL Multiphysics软件对模型进行数值求解,结合室内土柱试验验证了模型可靠性,参数分析了各因素对污染物迁移的影响。研究表明:Langmuir非线性吸附模型较符合黄土颗粒对铅离子的吸附特征;土柱高度方向铅离子浓度和吸附浓度随电压、电渗透率及离子扩散系数的增大而增大,电压增大1倍,浓度和吸附浓度增大约11%,电渗透率增大2倍,浓度和吸附浓度增大约10%,离子扩散系数增大1倍,浓度和吸附浓度均增大约8%;土体最大吸附量增大1倍,浓度减小约33%,吸附浓度增大约52%;电泳作用引起负极处浓度出现富集,电压越大,富集越明显,但电泳对吸附浓度影响不明显。

     

    Abstract: The migration mechanism of lead ions in unsaturated loess under the action of electric field was studied in this paper. The adsorption type of lead ions on loess was determined through isothermal adsorption tests; A multi field coupled mathematical model for pollutant migration in unsaturated soil under the action of electric field was established based on a three-phase system of solid, liquid and gas. The model was numerically solved using COMSOL Multiphysics software, and the reliability of the model was verified through indoor soil column tests. The influence of various factors on pollutant migration was analyzed through parameter analysis. Research has shown that the Langmuir nonlinear adsorption model is more in line with the adsorption characteristics of loess particles for lead ions; The lead ion concentration and adsorption concentration in the height direction of the soil column increase with the increase of voltage, electrical permeability and ion diffusion coefficient. When the voltage increases by one time, the concentration and the adsorption concentration increase by about 11%, the electrical permeability increases by two times, the concentration and the adsorption concentration increase by about 10%, the ion diffusion coefficient increases by one time, and the concentration and the adsorption concentration increase by about 8%. When the maximum adsorption capacity of the soil increases by one time, the concentration decreases by about 33%, and the adsorption concentration increases by about 52%; Electrophoresis causes concentration enrichment at the negative electrode, and the higher the voltage, the more obvious the enrichment, but the effect of electrophoresis on adsorption concentration is not significant.

     

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