Li Zhaohui, Hanlie Hong
Geosciences Department, University of Wisconsin-Parkside, Kenosha, WI 53144, USA.
Water Res. 2008 Feb;42(3):605-14. doi: 10.1016/j.watres.2007.08.010. Epub 2007 Aug 17.
A combination of surfactant solubilization with permanganate oxidation of trichloroethylene (TCE) was studied in batch, flow-through column, and three-dimensional (3-D) tank tests. Batch results showed that chloride production, an indication of TCE degradation, followed a pseudo-first-order reaction kinetics with respect to KMnO4 in the presence of free-phase TCE. A higher chloride production rate was achieved when anionic surfactants were present. The observed pseudo-first-order reaction rate constant increased as the concentrations of anionic surfactants Ninate 411 and Calfax increased from 0% to 0.1%, 0.3%, and 1.0%. Column experiments on TCE reduction by permanganate in the presence and absence of surfactants were carried out using well-sorted coarse Ottawa sand. The peak effluent TCE concentration reached 1700 mg/L due to enhanced solubilization when both sodium dodecyl sulfate (SDS) and permanganate were used, in contrast to less than 300 mg/L when only permanganate solution was used. In addition, the effluent TCE concentration decreased much faster when SDS was present in the permanganate solution, compared with the case when SDS was absent. With an initial 1 mL of TCE emplaced in the columns, the effluent TCE concentration dropped to <5mg/L after 29-31h of flushing with 1% SDS and 0.1% KMnO4 solution in contrast to 37-73 h when only 0.1% KMnO4 was used. Furthermore, KMnO4 breakthrough occurred after 21-25 h of injection when SDS was present compared with 45-70 h later when SDS was absent. A slightly higher chloride concentration was observed in the earlier stage of the column experiment and the chloride concentration decreased quickly once KMnO4 was seen in the effluent. The 3-D tank test showed that the MnO2 precipitation front formed more quickly when 1% SDS was present, which further confirmed the observation from the column study.
在间歇式试验、流通柱试验和三维(3-D)水槽试验中,研究了表面活性剂增溶与高锰酸钾氧化三氯乙烯(TCE)相结合的方法。间歇式试验结果表明,在存在游离相TCE的情况下,作为TCE降解指标的氯化物生成遵循相对于KMnO4的准一级反应动力学。当存在阴离子表面活性剂时,氯化物生成速率更高。随着阴离子表面活性剂Ninate 411和Calfax的浓度从0%增加到0.1%、0.3%和1.0%,观察到的准一级反应速率常数增加。在有和没有表面活性剂的情况下,使用分选良好的粗渥太华砂进行了高锰酸钾还原TCE的柱实验。当同时使用十二烷基硫酸钠(SDS)和高锰酸钾时,由于增溶作用增强,流出物中TCE的峰值浓度达到1700 mg/L,而仅使用高锰酸钾溶液时该浓度低于300 mg/L。此外,与不存在SDS的情况相比,当SDS存在于高锰酸钾溶液中时,流出物中TCE的浓度下降得更快。在柱中初始注入1 mL TCE后,用1% SDS和0.1% KMnO4溶液冲洗29 - 31小时后,流出物中TCE的浓度降至<5mg/L,而仅使用0.1% KMnO4时为37 - 73小时。此外,存在SDS时,注入21 - 25小时后出现KMnO4穿透,而不存在SDS时则在45 - 70小时后出现。在柱实验的早期阶段观察到氯化物浓度略高,一旦在流出物中看到KMnO4,氯化物浓度迅速下降。三维水槽试验表明,当存在1% SDS时,MnO2沉淀前沿形成得更快,这进一步证实了柱研究中的观察结果。