Ecohydrology Research Group, Department of Earth and Environmental Sciences and Water Institute, University of Waterloo, Waterloo, ON, Canada.
Department of Chemical Engineering and Analytical Science, The University of Manchester, Manchester, M13 9PL, UK.
Chemosphere. 2022 Feb;289:133177. doi: 10.1016/j.chemosphere.2021.133177. Epub 2021 Dec 7.
In this paper, the dissolution and mobilization of non-aqueous phase liquid (NAPL) blobs in the Surfactant-Enhanced Aquifer Remediation (SEAR) process were upscaled using dynamic pore network modeling (PNM) of three-dimensional and unstructured networks. We considered corner flow and micro-flow mechanisms including snap-off and piston-like movement for two-phase flow. Moreover, NAPL entrapment and remobilization were evaluated using force analysis to develop the capillary desaturation curve (CDC) and predict the onset of remobilization. The corner diffusion mechanism was also applied in the modeling of interphase mass transfer to represent NAPL dissolution as the dominant mass transfer process. In addition, the effect of pore-scale heterogeneity on mass transfer rate coefficient and recovered residual NAPL was considered in the simulations. Sodium dodecyl sulfate (SDS) and Triton X-100 were used as the surfactant for the SEAR process. The results indicate that although surfactants enhance NAPL recovery during two-phase flow, surfactant-enhanced remediation of residual NAPL through dissolution is highly dependent on surfactant type. When SDS ─as a surfactant with high critical micelle concentration (CMC) and low micelle partition coefficient (K)─ was injected into a NAPL contaminated site, the mass transfer rate coefficient decreased (due to considerable changes in interface chemical potentials) which leads to a significant reduction in NAPL recovery after the end of two-phase flow. In contrast, Triton X-100 (with low CMC and high K) improved NAPL recovery, by enhancing solubility at surfactant concentrations greater than CMC which overcompensates the interphase mass transfer reduction.
本文采用三维非结构化动态孔隙网络模型(PNM)研究了非水相液体(NAPL)液滴在表面活性剂强化含水层修复(SEAR)过程中的溶解和迁移。考虑了角流和微流动机制,包括两相流中的断开和活塞状流动。此外,通过力分析评估 NAPL 捕获和再迁移,以开发毛细饱和度曲线(CDC)并预测再迁移的开始。角扩散机制也应用于相间传质的建模中,以表示 NAPL 溶解是主要的传质过程。此外,还考虑了孔隙尺度非均质性对传质速率系数和回收残余 NAPL 的影响。十二烷基硫酸钠(SDS)和 Triton X-100 被用作 SEAR 过程中的表面活性剂。结果表明,尽管表面活性剂在两相流中增强了 NAPL 的回收,但通过溶解进行的残余 NAPL 的表面活性剂强化修复高度依赖于表面活性剂类型。当 SDS ─作为一种具有高临界胶束浓度(CMC)和低胶束分配系数(K)的表面活性剂─被注入 NAPL 污染场地时,传质速率系数降低(由于界面化学势发生了相当大的变化),这导致两相流结束后 NAPL 回收显著减少。相比之下,Triton X-100(CMC 低且 K 高)通过在大于 CMC 的表面活性剂浓度下提高溶解度,从而增强了 NAPL 的回收,从而弥补了相间传质的减少。