Friis A K, Heron G, Albrechtsen H-J, Udell K S, Bjerg P L
Institute of Environment & Resources, Technical University of Denmark, building 115, Bygningstorvet, DK-2800 Kgs Lyngby, Denmark.
J Contam Hydrol. 2006 Dec 15;88(3-4):219-34. doi: 10.1016/j.jconhyd.2006.07.001. Epub 2006 Sep 26.
The effects of Electrical Resistance Heating (ERH) on dechlorination of TCE and redox conditions were investigated in this study. Aquifer and groundwater samples were collected prior to and after ERH treatment, where sediments were heated to approximately 100 degrees C. Sediment samples were collected from three locations and examined in microcosms for 250 to 400 days of incubation. Redox activities, in terms of consumed electron acceptors, were low in unamended microcosms with field-heated sediments, although they increased upon lactate-amendment. TCE was not dechlorinated or stalled at cDCE with field-heated sediments, which was similar or lower compared to the degree of dechlorination in unheated microcosms. However, in microcosms which were bioaugmented with a mixed anaerobic dechlorinating culture (KB-1) and lactate, dechlorination past cDCE to ethene was observed in field-heated sediments. Dechlorination and redox activities in microcosms with field-heated sediments were furthermore compared with controlled laboratory-heated microcosms, which were heated to 100 degrees C for 10 days and then slowly cooled to 10 degrees C. In laboratory-heated microcosms, TCE was not dechlorinated and redox activities remained low in unamended and lactate-amended sediments, although organic carbon was released to the aqueous phase. In contrast, in field-heated sediments, high aqueous concentrations of organic carbon were not observed in unamended microcosms, and TCE was dechlorinated to cDCE upon lactate amendment. This suggests that dechlorinating microorganisms survived the ERH or that groundwater flow through field-heated sediments carried microorganisms into the treated area and transported dissolved organic carbon downstream.
本研究调查了电阻加热(ERH)对三氯乙烯脱氯及氧化还原条件的影响。在ERH处理前后采集了含水层和地下水样本,其中沉积物被加热到约100摄氏度。从三个地点采集了沉积物样本,并在微观世界中进行了250至400天的培养研究。就消耗的电子受体而言,在含有现场加热沉积物的未添加修正物的微观世界中,氧化还原活性较低,不过在添加乳酸后活性有所增加。对于现场加热的沉积物,三氯乙烯未发生脱氯或仅停滞在顺式二氯乙烯阶段,与未加热微观世界中的脱氯程度相比,这一程度相似或更低。然而,在添加了混合厌氧脱氯培养物(KB - 1)和乳酸进行生物强化的微观世界中,观察到现场加热的沉积物中三氯乙烯从顺式二氯乙烯进一步脱氯为乙烯。此外,还将含有现场加热沉积物的微观世界中的脱氯和氧化还原活性与受控的实验室加热微观世界进行了比较,后者被加热到100摄氏度并持续10天,然后缓慢冷却至10摄氏度。在实验室加热的微观世界中,在未添加修正物和添加乳酸的沉积物中,三氯乙烯未发生脱氯,氧化还原活性仍然较低,尽管有机碳释放到了水相中。相比之下,在现场加热的沉积物中,未添加修正物的微观世界中未观察到高浓度的水溶有机碳,并且在添加乳酸后三氯乙烯被脱氯为顺式二氯乙烯。这表明脱氯微生物在电阻加热过程中存活了下来,或者是地下水流经现场加热的沉积物将微生物带入了处理区域,并将溶解的有机碳输送到了下游。