Vencelides Zbynek, Sracek Ondra, Prommer Henning
OPV, Belohorská 31, 169 00 Praha 6, Czech Republic.
J Contam Hydrol. 2007 Jan 30;89(3-4):270-94. doi: 10.1016/j.jconhyd.2006.09.003. Epub 2006 Oct 27.
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.
在几十年的时间里,位于赫涅维采(捷克共和国)附近的储存设施多次发生大量泄漏,导致下伏的第四纪含水层被非水相液体(NAPL)石油烃严重污染。从20世纪80年代末开始,由于NAPL溶解超过补给以及积极的修复措施,NAPL羽状物开始收缩。地下被地球化学划分为四个不同区域:(i)一个从未被NAPL或溶解污染物占据的无污染区;(ii)一个以前被NAPL占据的再氧化区;(iii)一个目前被NAPL占据的区域;(iv)上覆NAPL与更深层无污染区之间的下部边缘区。该研究调查了赫涅维采场地氧化还原分带的空间和时间变异性,并量化了铁循环对整体电子平衡的影响。第一步进行了反地球化学建模,以确定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)多组分反应输运建模,以评估和量化控制该场地地球化学演化的主要过程。该研究解释了观察到的下部边缘区由于亚铁离子的再氧化而富含水铁矿的现象。研究表明,一旦NAPL区开始收缩,先前形成的菱铁矿和FeS被氧气和硝酸盐溶解,在相当长的一段时间内消耗了很大一部分氧化能力,因此限制了电子受体向下穿透到NAPL污染区。