International Postgraduate Programs in Environmental Management, Graduate School, Chulalongkorn University, Bangkok, Thailand.
J Environ Sci Health A Tox Hazard Subst Environ Eng. 2013;48(13):1619-27. doi: 10.1080/10934529.2013.815093.
This work evaluates the behavior of surfactant and alcohols in combination with a mixture of tributyltinchloride (TBT) and tetrachloroethylene (PCE) with the goal of modifying the mixed oil from being a dense non-aqueous phase liquid (DNAPL) to a light non-aqueous phase liquid (LNAPL). Phase behavior of the mixed oil was studied under various combinations of surfactant, alcohol, and salinity. Phase density conversion was examined using pseudo-ternary phase diagrams constructed between the mixed oil, surfactant solution (4 wt%), and two types of alcohols (n-butyl alcohol (BuOH) and tert-butyl alcohol (TBA)). Aqueous phase solubilization and oil phase density modification were studied at varying alcohol to surfactant (A/S) ratios. The results showed that the optimum surfactant system was sodium dihexylsulfosuccinate (SDHS) and hexadecyl diphenyloxidedisulfonate (C16DPDS) (3.6 wt% and 0.4 wt%, respectively) with salt (NaCl) of 3 wt%. From pseudo-ternary phase diagrams, BuOH was found to produce a larger LNAPL region than TBA. From solubilization studies, the surfactant system plus either TBA or BuOH caused PCE preferential solubilization and this preference was more pronounced at higher total surfactant concentration in the system with TBA addition. In terms of density modification, BuOH produced lower oil density than TBA at high A/S ratio. This phase behavior knowledge can be used to optimize site remediation of organometallic DNAPLs.
本研究旨在通过表面活性剂和醇类的组合,对三丁基锡氯化物(TBT)和四氯乙烯(PCE)混合物进行处理,以期将混合油从致密非水相液体(DNAPL)转化为轻质非水相液体(LNAPL)。通过对不同表面活性剂、醇类和盐度组合下混合油的相行为进行研究,考察了混合油的相密度转化。通过构建混合油、表面活性剂溶液(4wt%)和两种醇类(正丁醇(BuOH)和叔丁醇(TBA))之间的拟三元相图,研究了水相溶解和油相密度的变化。在不同醇与表面活性剂(A/S)比值下研究了油相密度的变化。结果表明,最优的表面活性剂体系为十二烷基磺基琥珀酸钠(SDHS)和十六烷基二苯醚二磺酸钠(C16DPDS)(分别为 3.6wt%和 0.4wt%),盐度(NaCl)为 3wt%。从拟三元相图中可以看出,BuOH 比 TBA 产生的 LNAPL 区域更大。从增溶研究来看,表面活性剂体系与 TBA 或 BuOH 共同作用导致 PCE 优先增溶,且在 TBA 存在下,体系中总表面活性剂浓度较高时,这种优先性更为明显。就密度改性而言,高 A/S 比下 BuOH 比 TBA 产生的油密度更低。这些相行为知识可用于优化有机金属 DNAPL 的场地修复。