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Fate of Chlorinated Compounds in a Fractured Sandstone Aquifer in the U.S. Midwest

机译:美国中西部裂缝砂岩含水层中氯化化合物的命运

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A fractured sandstone site located in the U.S. Midwest was impacted beginning before 1970 by a multicomponent DNAPL mainly composed of 1,1,1-TCA, PCE, TCE and BTEX. A groundwater VOC plume containing the above-mentioned compounds and degradation products extends for more than 3 km from the DNALP input area. In September 2007, groundwater samples were collected for evaluation of redox parameters and VOC and carbon isotope analyses as part of a study aiming to evaluate the fate of the VOC in the plume. The VOC data indicated almost complete degradation of PCE/TCE to cis-DCE and around 80% transformation of 1,1,1-TCA to 1,1-DCA in the area from the source to the middle of the plume which is consistent with anaerobic condition reported for this area. The leading edge of the plume was characterized by much less degradation. The VOC degradation pattern was confirmed by the carbon isotopes data. In the area between the source and the middle of the plume, the δ13C values of the daughter product, cis-DCE and 1,1-DCA, tend to the isotope composition of the precursors, PCE/TCE and 1,1,1-TCA, which indicates that cis-DCE or 1,1-DCA are not been affected by biodegradation. The δ13C values at the fringes of the plume indicated the degree of biodegradation is much less than in the middle of plume, which is consistent with the more aerobic condition measured at the fringes of the plume. Degradation of 1,1,1-TCA to 1,1-DCA showed much less degradation of TCE to cis-DCE and a clear trend of decreasing extent along the flow path. This is also confirmed by the δ13C values of 1,1,1-TCA and 1,1-DCA. This study showed that a combined approach of VOC concentration and carbon isotopes analyses significantly improved the understanding of the fate of chlorinated ethenes and ethanes in a regional VOC plume developed in a fractured rock aquifer.
机译:位于美国中西部的裂缝砂岩遗址在1970年以来,由多组分DNAPL开始影响,主要由1,1,1-TCA,PCE,TCE和BTEX组成。含有上述化合物和降解产物的地下水VOC羽流量距离DNALP输入区域超过3公里。 2007年9月,收集地下水样品以评估氧化还原参数和VOC和碳同位素分析,作为旨在评估羽流中VOC的命运的研究的一部分。 VOC数据表明,从源到羽流的源区的区域中,PCE / TCE对CIS-DCE的几乎完全降低了1,1,1-TCA至1,1-DCA的大约80%。厌氧条件报告了这一领域。羽流的前缘特征在于降低较小的降解。碳同位素数据证实了VOC降解模式。在羽流的源和中间之间的区域中,女儿产品,CIS-DCE和1,1-DCA的δ13C值倾向于前体,PCE / TCE和1,1,1-的同位素组成TCA表明CIS-DCE或1,1-DCA不受生物降解的影响。羽流条纹的δ13C值表示生物降解程度远小于羽流的中间,这与在羽流的条件下测量的更具有氧病症一致。 1,1,1-TCA至1,1-DCA的降解表现出降低TCE对CIS-DCE的降低以及沿着流动路径的降低程度的明显趋势。这也通过1,1,1-TCA和1,1-DCA的Δ13C值来证实。本研究表明,VOC浓度和碳同位素的组合方法分析了在碎裂岩含水层中产生的区域VOC羽流中的氯化替代品和乙醇的命运的理解。

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