污染场地铬迁移规律及铬对地下水源地影响的数值模拟研究

Chromium Migration in Contaminated Site and Numerical Simulation of Its Effect on Groundwater Source Area

  • 摘要: 铬(Cr)污染已经成为土壤和地下水的重金属污染之一。为研究污染场地地下水中铬的迁移规律,分析预测六价铬Cr(Ⅵ)迁移到水源地保护区的时间,本文以河南省新乡市某铬污染场地为研究区,利用GMS软件建立地下水流数值模拟模型和溶质运移模型,对在不考虑吸附和考虑吸附情况下Cr(Ⅵ)的迁移进行分析预测。结果表明:不考虑吸附时浅层潜水含水层中Cr(Ⅵ)迁移到水源地保护区的时间为78年,深层潜水含水层中Cr(Ⅵ)迁移到水源地保护区的时间为70年;考虑吸附时,采用Langmuir吸附模型,可得浅层、深层潜水含水层中Cr(Ⅵ)迁移到水源地保护区的时间比不考虑吸附作用时慢约4年时间。此外,在考虑吸附作用条件下,对污染源持续释放、污染源10年后消失以及污染源不断衰减三种污染源浓度变化的情景进行模拟,模拟结果为:前期地下水中原有Cr(Ⅵ)浓度迅速升至峰值后快速下降,而在后期铬渣堆经过淋滤再次入渗时,三种情景下Cr(Ⅵ)浓度变化呈现出差异。污染源持续释放时浓度缓慢增长、污染源10年后消失时两个观测点先后出现浓度略微增长后逐渐趋近于0的情况,污染源不断衰减时浓度先上升后下降最终趋近0;同时可得,污染源与观测点距离的缩短会显著降低Cr(Ⅵ)的迁移耗时,其抵达观测点的时间与水动力条件呈负相关关系,这一现象主要受污染羽扩散特征及含水介质渗透系数等关键水文地质参数控制。本研究结果可为污染场地中铬污染范围的预测和防治提供科学依据。

     

    Abstract: Chromium pollution has become one of the heavy metal pollutions in soil and groundwater. To study the migration law of chromium (Cr) in the groundwater of contaminated sites and analyze and predict the time for hexavalent chromium to migrate to the water source protection area, a certain chromium-contaminated site in Xinxiang City, Henan Province was taken as the research area. The grounder modeling systems (GMS) software was used to establish the numerical simulation model of groundwater flow and the solute transport model to analyze and predict the migration of hexavalent chromium without considering adsorption and with adsorption considered. The conclusions show that without considering adsorption, the time for Cr(Ⅵ) in the shallow phreatic aquifer to migrate to the water source protection area is 78 years, and in the deep phreatic aquifer, it is 70 years. When adsorption is considered and the Langmuir adsorption model is adopted, the time for hexavalent chromium in both the shallow and deep phreatic aquifers to migrate to the water source protection area is about 4 years slower than that without considering adsorption. In addition, under the condition of considering adsorption, the scenarios of three changes in the source concentration, namely continuous release of the pollution source, disappearance of the pollution source after 10 years, and continuous attenuation of the pollution source, were simulated. The simulation results are as follows: In the early stage, the original concentration of Cr(Ⅵ) in the groundwater rapidly rises to a peak and then drops rapidly. When the chromium slag pile infiltrates again after leaching in the later stage, the concentration changes of Cr(Ⅵ) under the three scenarios show differences. When the pollution source is continuously released, the concentration slowly increases; when the pollution source disappears after 10 years, the concentrations at the two observation points first slightly increase and then gradually approach 0; when the pollution source continuously attenuates, the concentration first rises and then falls and finally approaches 0. At the same time, it can be obtained that shortening the distance between the pollution source and the observation point will significantly reduce the migration time of Cr(Ⅵ), and the time for it to reach the observation point is negatively correlated with the hydrodynamic conditions. This phenomenon is mainly controlled by key hydrogeological parameters such as the diffusion characteristics of the pollution plume and the permeability coefficient of the aquifer medium. The results of this study can provide a scientific basis for the prediction, prevention, and control of the chromium pollution range in contaminated sites.

     

/

返回文章
返回