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Modelling of iron cycling and its impact on the electron balance at a petroleum hydrocarbon contaminated site in Hnevice, Czech Republic

机译:铁循环模型及其对捷克共和国赫内维斯市石油烃污染场所电子平衡的影响

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Over a period of several decades multiple leaks of large volumes from storage facilities located near Hnevice (Czech Republic) have caused the underlying Quaternary aquifer to be severely contaminated with nonaqueous phase liquid (NAPL) petroleum hydrocarbons. Beginning in the late 1980's the NAPL plume started to shrink as a consequence of NAPL dissolution exceeding replenishment and due to active remediation. The subsurface was classified geochemically into four different zones, (ⅰ) a contaminant-free zone never occupied by NAPL or dissolved contaminants, (ⅱ) a re-oxidation zone formerly occupied by NAPL, (ⅲ) a zone currently occupied by NAPL, and (ⅳ) a lower fringe zone between the overlying NAPL and the deeper underlying contaminant-free zone. The study investigated the spatial and temporal variability of the redox zonation at the Hnevice site and quantified the influence of iron-cycling on the overall electron balance. As a first step inverse geochemical modelling was carried out to identify possible reaction models and mass transfer processes. In a subsequent step, two-dimensional (forward) multi-component reactive transport modelling was performed to evaluate and quantify the major processes that control the geochemical evolution at the site. The study explains the observed enrichment of the lower fringe zone with ferrihydrite as a result of the re-oxidation of ferrous iron. It suggests that once the NAPL zone started to shrink the dissolution of previously formed siderite and FeS by oxygen and nitrate consumed a significant part of the oxidation capacity for a considerable time period and therefore limited the penetration of electron acceptors into the NAPL contaminated zone.
机译:在几十年的时间里,位于赫内维斯(捷克共和国)附近的存储设施多次大量泄漏,导致其下的第四纪含水层被非水相液态(NAPL)石油烃严重污染。从1980年代后期开始,NAPL羽流开始减少,这是由于NAPL溶解度超过补给量和积极的补救措施所致。根据地球化学将地下分为四个不同区域:(ⅰ)从未被NAPL占据或溶解的污染物所占据的无污染区,(ⅱ)先前被NAPL占据的再氧化区,(ⅲ)当前被NAPL占据的区,以及(ⅳ)上覆NAPL与下层较深的无污染区之间的较低边缘区域。该研究调查了Hnevice站点氧化还原带的时空变化,并量化了铁循环对整体电子平衡的影响。第一步,进行逆地球化学建模以识别可能的反应模型和传质过程。在随后的步骤中,进行了二维(正向)多组分反应性运输建模,以评估和量化控制现场地球化学演化的主要过程。该研究解释了由于亚铁的再氧化,观察到的下部边缘区域富含亚铁水合物。这表明一旦NAPL区开始收缩,先前形成的菱铁矿和FeS在氧气和硝酸盐中的溶解会在相当长的时间内消耗掉大部分氧化能力,因此限制了电子受体向NAPL污染区的渗透。

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