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A PCE plume discharging to a river: Investigations of flux, geochemistry, and biodegradation in the streambed.

机译:PCE羽流向河流的排放:河床中通量,地球化学和生物降解的调查。

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A tetrachloroethene (PCE) groundwater plume emanates from beneath a dry cleaner facility and discharges to a 60 m-long reach of the Pine River in Angus, Ontario, Canada. The streambed and near-stream zone were shown to be a dynamic and unique environment that modified the distribution, concentration, and composition of the plume. The plume and hydrogeology were characterized using a Waterloo Profiler, mini-profilers, bundle multilevel samplers, driveable multilevel samplers, Ground Penetrating Radar surveys (of the streambed), streambed temperature mapping (to identify discharge zones), drivepoints, and sediment coring. Low hydraulic conductivity silt, clay, and peat deposits underlying the sandy streambed deposits caused the plume to discharge over a large area of the streambed and extend across the full width (11 to 14 m) of the river at some locations. Spatial variations in the geology resulted in groundwater fluxes that varied from 0.03 to at least 446 L/m2d. Although no appreciable biodegradation of the plume occurred in the upgradient aquifer, anaerobic biodegradation in the top 2.5 m of the streambed dramatically altered the plume composition by transforming PCE primarily to cis-1,2-dichloroethene (cDCE) and vinyl chloride (VC) and to a lesser extent trichloroethene (TCE), 1,1-dichloroethene (11DCE), trans-1,2-dichloroethene (tDCE), ethene, and ethane. Transformation of PCE generally occurred over relatively short vertical distances (0.45 m) and was associated with sharp changes in redox conditions. The degree of biodegradation was highly correlated with the redox conditions and the magnitude of fluxes because the low hydraulic conductivity deposits that caused the low fluxes were also organic-rich and strongly reducing. High amounts of dechlorination (i.e. production of ethene and ethane) occurred where fluxes were very low and sulfate reducing to methanogenic conditions existed. Virtually no biodegradation occurred in high flux areas where water was anaerobic to nitrate reducing. A new method of calculating groundwater fluxes based on streambed temperature measurements and testing of mini-piezometers was developed and used to create a conceptual flow model that was based on the magnitude and direction of the fluxes. PCE was detected at concentrations ≤3.1 μg/L and on one occasion was as high as 23.2 μg/L whereas no cDCE or VC was detected in surface water. This study demonstrates the complex interaction of hydrogeologic, geochemical, and biochemical processes that occur in streambeds and the resulting fine scale spatial variability in plume discharge. (Abstract shortened by UMI.)
机译:四氯乙烯(PCE)地下水羽流从干洗店的设施下方散发出来,并排放到加拿大安大略省安格斯的松树河长60 m。流域和近流带被证明是一个动态而独特的环境,可以改变羽流的分布,浓度和组成。使用滑铁卢剖面仪,小型剖面仪,束状多级采样器,可驱动的多级采样器,探地雷达勘测(河床),河床温度测绘(以识别排放区),驱动点和沉积物取心来表征羽状流和水文地质。沙质河床沉积物下方的低水力传导性淤泥,粘土和泥炭沉积物导致羽流在河床的大面积上排出,并在某些位置延伸到河流的整个宽度(11至14 m)。地质学的空间变化导致地下水通量从0.03变化到至少446 L / m 2 d。尽管在上升的含水层中没有明显的羽流生物降解,但在河床顶部2.5 m的厌氧生物降解通过将PCE主要转变为顺式1,2,2-二氯乙烯(cDCE)和氯乙烯(VC)而显着改变了羽流组成。在较小程度上,三氯乙烯(TCE),1,1-二氯乙烯(11DCE),反式1,2-二氯乙烯(tDCE),乙烯和乙烷。 PCE的转变通常发生在相对较短的垂直距离(<0.45 m)上,并且与氧化还原条件的急剧变化有关。生物降解的程度与氧化还原条件和通量的大小高度相关,因为引起低通量的低水力传导性沉积物也富含有机物并且强烈还原。在通量很低并且存在硫酸盐还原成甲烷的条件下,发生大量的脱氯反应(即生产乙烯和乙烷)。实际上,在高通量区域,其中水是厌氧的,硝酸盐还原的,没有发生生物降解。提出了一种基于流床温度测量和微型管道仪测试计算地下水通量的新方法,并将其用于创建基于通量大小和方向的概念性水流模型。检测到的PCE浓度≤3.1μg/ L,有一次高达23.2μg/ L,而在地表水中未检测到cDCE或VC。这项研究证明了在河床中发生的水文地质,地球化学和生化过程的复杂相互作用,以及在羽流中产生的精细尺度的空间变异性。 (摘要由UMI缩短。)

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