MacKinnon L K, Thomson N R
Department of Civil Engineering, University of Waterloo, ON, Canada.
J Contam Hydrol. 2002 May;56(1-2):49-74. doi: 10.1016/s0169-7722(01)00203-0.
In situ chemical oxidation (ISCO) is an emerging technology for the destruction of some chlorinated solvents present in subsurface environments. A laboratory investigation using a physical model was designed to assess the effectiveness of using permanganate as an oxidant to reduce the mass of a perchloroethylene (PCE) pool. The physical model was filled with silica sand overlying a silica flour base, simulating a two-dimensional saturated sand zone overlying a capillary barrier. PCE was introduced into the model so that it rested on top of the silica flour base, forming a dense nonaqueous phase liquid pool. The experimental methodology involved flushing the model with a permanganate solution for 146 days. During this period, measurements of chloride were used to assess the extent of pool oxidation. Before and after the oxidant flush, the quasi-steady state dissolution from the PCE pool was evaluated. Additionally, tracer studies were completed to assess changes in the flow field due to the oxidation process. At the termination of the experiment nine soil cores extracted from the model were used to detect the presence of MnO2 deposits and to quantify the mass of PCE remaining in the system. Excavation of the remaining material in the model revealed that the MnO2 distribution throughout the model was consistent with that observed in the cores. The oxidant flush was concluded before all of the pure phase PCE had been completely oxidized; however, approximately 45% of the PCE mass was removed, resulting in a fourfold decrease in the quasi-steady state aqueous phase mass loading of PCE from the pool. Measurements of chloride during the oxidant flush and of PCE in the soil cores suggested that the oxidation reaction occurred primarily at the upgradient edge of the PCE pool. MnO2 deposits within the model aquifer decreased the velocity of water directly above the pool, and the overall mass transfer from the remaining PCE pool. The results of this experimental study indicate that ISCO using permanganate is capable of removing substantial mass from a DNAPL pool; however, the performance of ISCO as a pool removal technology will be limited by the formation and precipitation of hydrous MnO2 that occurs during the oxidation process.
原位化学氧化(ISCO)是一种新兴技术,用于破坏地下环境中存在的某些氯化溶剂。设计了一项使用物理模型的实验室研究,以评估使用高锰酸盐作为氧化剂来减少全氯乙烯(PCE)池质量的有效性。物理模型用覆盖在硅粉基底上的硅砂填充,模拟覆盖在毛细屏障上的二维饱和砂层。将PCE引入模型中,使其位于硅粉基底顶部,形成一个致密的非水相液体池。实验方法包括用高锰酸盐溶液冲洗模型146天。在此期间,通过测量氯离子来评估池氧化的程度。在氧化剂冲洗前后,评估了PCE池的准稳态溶解情况。此外,还完成了示踪剂研究,以评估氧化过程引起的流场变化。实验结束时,从模型中提取了九个土壤岩心,用于检测MnO₂沉积物的存在并量化系统中剩余PCE的质量。对模型中剩余材料的挖掘表明,整个模型中MnO₂的分布与岩心中观察到的一致。在所有纯相PCE完全氧化之前就结束了氧化剂冲洗;然而,大约45%的PCE质量被去除,导致PCE从池中准稳态水相质量负荷下降了四倍。在氧化剂冲洗期间对氯离子的测量以及对土壤岩心中PCE的测量表明,氧化反应主要发生在PCE池的上坡边缘。模型含水层中的MnO₂沉积物降低了池上方直接的水流速度以及剩余PCE池的整体传质。这项实验研究的结果表明,使用高锰酸盐的ISCO能够从DNAPL池中去除大量物质;然而,ISCO作为一种池去除技术的性能将受到氧化过程中发生的水合MnO₂的形成和沉淀的限制。