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模拟天然存在的有机碳对氯乙烯向公共供水井迁移的影响。

Modeling the effects of naturally occurring organic carbon on chlorinated ethene transport to a public supply well.

作者信息

Chapelle Francis H, Kauffman Leon J, Widdowson Mark A

机构信息

U.S. Geological Survey, Montana Water Science Center, Bozeman, MT, 59601.

出版信息

Ground Water. 2014 Sep;52 Suppl 1(Suppl 1):76-89. doi: 10.1111/gwat.12152. Epub 2013 Dec 23.

Abstract

The vulnerability of public supply wells to chlorinated ethene (CE) contamination in part depends on the availability of naturally occurring organic carbon to consume dissolved oxygen (DO) and initiate reductive dechlorination. This was quantified by building a mass balance model of the Kirkwood-Cohansey aquifer, which is widely used for public water supply in New Jersey. This model was built by telescoping a calibrated regional three-dimensional (3D) MODFLOW model to the approximate capture zone of a single public supply well that has a history of CE contamination. This local model was then used to compute a mass balance between dissolved organic carbon (DOC), particulate organic carbon (POC), and adsorbed organic carbon (AOC) that act as electron donors and DO, CEs, ferric iron, and sulfate that act as electron acceptors (EAs) using the Sequential Electron Acceptor Model in three dimensions (SEAM3D) code. SEAM3D was constrained by varying concentrations of DO and DOC entering the aquifer via recharge, varying the bioavailable fraction of POC in aquifer sediments, and comparing observed and simulated vertical concentration profiles of DO and DOC. This procedure suggests that approximately 15% of the POC present in aquifer materials is readily bioavailable. Model simulations indicate that transport of perchloroethene (PCE) and its daughter products trichloroethene (TCE), cis-dichloroethene (cis-DCE), and vinyl chloride (VC) to the public supply well is highly sensitive to the assumed bioavailable fraction of POC, concentrations of DO entering the aquifer with recharge, and the position of simulated PCE source areas in the flow field. The results are less sensitive to assumed concentrations of DOC in aquifer recharge. The mass balance approach used in this study also indicates that hydrodynamic processes such as advective mixing, dispersion, and sorption account for a significant amount of the observed natural attenuation in this system.

摘要

公共供水井对氯化乙烯(CE)污染的脆弱性部分取决于天然有机碳消耗溶解氧(DO)并引发还原脱氯的能力。通过构建柯克伍德 - 科汉西含水层的质量平衡模型对其进行了量化,该含水层在新泽西州广泛用于公共供水。此模型是通过将校准后的区域三维(3D)MODFLOW模型缩放到一个有CE污染历史的单一公共供水井的近似捕获区而构建的。然后使用这个局部模型,通过三维顺序电子受体模型(SEAM3D)代码来计算作为电子供体的溶解有机碳(DOC)、颗粒有机碳(POC)和吸附有机碳(AOC)与作为电子受体(EA)的DO、CE、铁离子和硫酸根之间的质量平衡。SEAM3D通过改变通过补给进入含水层的DO和DOC浓度、改变含水层沉积物中POC的生物可利用部分以及比较DO和DOC的观测和模拟垂直浓度剖面来进行约束。该过程表明,含水层物质中约15%的POC易于生物利用。模型模拟表明,全氯乙烯(PCE)及其子产物三氯乙烯(TCE)、顺式二氯乙烯(cis - DCE)和氯乙烯(VC)向公共供水井的迁移对假设的POC生物可利用部分、随补给进入含水层的DO浓度以及流场中模拟PCE源区的位置高度敏感。结果对含水层补给中假设的DOC浓度不太敏感。本研究中使用的质量平衡方法还表明,诸如平流混合、弥散和吸附等水动力过程在该系统中观察到的自然衰减中占了很大一部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7b8/4265263/a9b4ad7f0fea/gwat0052-0076-f1.jpg

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