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Processes Affecting the Fate of Monoaromatic Hydrocarbons in an Aquifer Contaminated by Crude Oil

机译:影响被原油污染的含水层中单芳烃命运的方法

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Crude oil spilled from a subsurface pipeline in north-central Minnesota has dissolved in the groundwater, resulting in the formation of a plume of aliphatic, aromatic, and alicyclic hydrocarbons. Comparison of paired oil and groundwater samples collected along the central axis of the residual oil body shows that the trailing edge of the oil is depleted in the more soluble aromatic hydrocarbons (e.g., benzene, toluene, etc.) when compared with the leading edge. At the same time, concentrations of monoaromatic hydrocarbons in groundwater beneath the oil increase as the water moves toward the leading edge of the oil. Immediately downgradient from the leading edge of the oil body, certain aromatic hydrocarbons (e.g., benzene) are found at concentrations near those expected of a system at equilibrium, and the concentrations exhibit little variation overtime (≈8-20%). Other compounds (e.g., toluene) appear to be undersaturated, and their concentrations show considerably more temporal variation (≈20-130%). The former are persistent within the anoxic zone downgradient from the oil, whereas concentrations of the latter decrease rapidly. Together, these observations suggest that the volatile hydrocarbon composition of the anoxic groundwater nearthe oil body is controlled by a balance between dissolution and removal rates with only the most persistent compounds reaching saturation. Examination of the distributions of homologous series and isomeric assemblages of alkylbenzenes reveals that microbial degradation is the dominant process controlling the fate of these compounds once groundwater moves away from the oil. For all but the most persistent compounds, the distal boundary of the plume at the water table extends no more than 10-15 m down-gradient from the oxic/anoxic transition zone. Thus, transport of the monoaromatic hydrocarbons is limited by redox conditions that are tightly coupled to biological degradation processes.
机译:从明尼苏达州中北部的地下管线泄漏的原油已溶解在地下水中,从而形成脂肪族,芳香族和脂环族烃羽状流。沿剩余油体中心轴收集的成对的石油和地下水样品的比较表明,与前缘相比,石油的后缘贫化了更易溶的芳烃(例如苯,甲苯等)。同时,随着水向油的前沿移动,油下方的地下水中单芳烃的浓度会增加。从油体的前缘立即降级,发现某些芳香烃(例如苯)的浓度接近平衡时系统预期的浓度,并且浓度随时间变化很小(≈8-20%)。其他化合物(例如甲苯)似乎不饱和,其浓度显示出更大的时间变化(约20-130%)。前者在缺氧区域内持续存在,并因油而下降,而后者的浓度迅速下降。总之,这些观察结果表明,油体附近缺氧地下水的挥发性碳氢化合物组成受溶解和去除速率之间的平衡控制,只有最持久的化合物达到饱和。对烷基苯的同源系列和异构体组合的分布进行的研究表明,一旦地下水离开石油,微生物降解是控制这些化合物命运的主要过程。对于除最持久性化合物以外的所有化合物,水柱中烟羽的远端边界从有氧/缺氧过渡区向下延伸的斜度不超过10-15 m。因此,单芳烃的运输受到与生物降解过程紧密相关的氧化还原条件的限制。

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