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Geochemical heterogeneity of a gasoline--contaminated aquifer

机译:汽油污染的含水层的地球化学非均质性

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The scale of biogeochemical reactions was studied in a physically and chemically heteroge- neous surficial Coastal Plain aquifer contaminated by a gasoline spill. The physical heterogeneity of the aquiter is manifested in two hydrologic units, a shallow local aquifer of perched water and a regional sandy aquifer. Over the studied vertical interval of 21.3 ft (6.5 m), concentrations of reactive species varied by orders of magnitude, and the impact of biodegradation was expressed to widely varying degrees. A thin (3 ft thick) section of the perched-water zone was the most contaminated; total aromatic hydrocarbons were as high as 19.4 mg/l. Hydrocarbons were degraded by microbially mediated reactions that varied over short vertical distances and time. Anaerobic processes dominated within the low--permeability clay unit, whereas in the more permeable sandy layers nitrate reduction and aerobic degradation occurred. Hydrocarbons were more persistent over time in the low--permeability layer due to the limited availability of electron acceptors for degradation. The microbial degradation of hydrocarbons was linked to sulfate and iron reduction in the clay unit and led to alterations in the aquifer solids; electron microscopy revealed the presence of FeS minerals encrusting primary aquifer grains. High concentrations of Fe~2+ in groundwater, up to 34.5 mg/l, persist in kinetic disequilibrium in the presence of elevated H_2S levels of 1.0 mg/l. Assessment of aquifer heterogeneities and groundwater contamination was possible due to sample discrimination at a scale of approximately 2 ft (~ 0.6 m), a much finer resolution than is attempted in many remedial investigations of polluted aquifers. The information obtained in this type of study is essential to the development of models capable Of estimating the fate of hydrocarbons at a site scale.
机译:在被汽油泄漏污染的物理和化学异质表面沿海平原含水层中研​​究了生物地球化学反应的规模。食水体的物理异质性表现在两个水文单元中,一个是浅水区的局部栖息水层,另一个是区域性砂质含水层。在研究的垂直间隔21.3英尺(6.5 m)内,反应性物质的浓度变化了几个数量级,并且生物降解的影响表达的程度也相差很大。栖息水区的薄薄部分(3英尺厚)受污染最严重。总芳烃含量高达19.4 mg / l。碳氢化合物通过微生物介导的反应而降解,该反应在较短的垂直距离和时间范围内变化。在低渗透性粘土单元中,厌氧过程占主导地位,而在渗透性更高的沙层中,硝酸盐还原和需氧降解发生。随着时间的推移,碳氢化合物在低渗透层中的持久性更高,这是因为电子受体的降解能力有限。碳氢化合物的微生物降解与粘土单元中的硫酸盐和铁的还原有关,并导致含水层固体的改变。电子显微镜显示,FeS矿物包裹着初级含水层。在H_2S浓度升高至1.0 mg / l的情况下,地下水中高达24.5 mg / l的高浓度Fe〜2 +在动力学失衡中持续存在。由于样品的分辨范围约为2英尺(〜0.6 m),因此可以评估含水层的非均质性和地下水污染,这比许多污染含水层的补救研究所尝试的分辨率要精细得多。在这种研究中获得的信息对于开发能够估算站点规模的碳氢化合物命运的模型至关重要。

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