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Laboratory and field investigation of chlorinated solvents remediation in soil and groundwater.

机译:土壤和地下水中氯化溶剂修复的实验室和现场调查。

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Chlorinated solvents are the second most ubiquitous contaminants, next to petroleum hydrocarbons, and many are carcinogens. Tetrachloroethylene or perchloroethene (PCE) has been employed extensively in the dry cleaning industry and carbon tetrachloride (CT) has been used as a fumigant in grain storage facilities. In this work, remediation feasibility studies were conducted by mesocosm experiments; a chamber was divided into six channels and filled with soil, and plants were grown on top. Each channel was fed with contaminated water near the bottom and collected at the outlet, simulating groundwater flow conditions. The contaminants were introduced starting from March 12, 2004. PCE was introduced at a concentration of about 2 mg/L (∼12 micromoles/L) in three channels, two of them with alfalfa plants and the other with grass. CT was introduced at a concentration of about 2 mg/L (∼13 micromoles/L) in the other three channels, two of them with alfalfa plants and the other with grass. After the system had attained steady state, the concentrations of PCE and CT at inlet and outlet were monitored and the amount of PCE and CT disappearing in the saturated zone was studied. Since no degradation products were found at the outlet after about 100 days, one channel-each for PCE and CT (with alfalfa) was made anaerobic by adding one liter of 0.2% glucose solution. The glucose solution was fed once every month starting from July 1, 2004 and continued until February 2005. From October 1, 2004, one liter of 0.1% emulsified soy oil methyl esters (SOME) was fed to two other channels (with alfalfa), one exposed to PCE and another exposed to CT. The SOME addition dates were the same as that for glucose. The outlet liquid of the channel fed with PCE and SOME started to contain some of the degradation compounds of PCE; however, the extent of degradation was not as great as that of the glucose fed channel. No degradation compounds were observed in the outlet solution of the channel (grass grown on top) in which no carbon and energy supplements were added. Similar trend was observed in the CT fed channels also. KB-1, a commercially available microbial culture (a consortium of dehalococcoides) that degrades dichloroethene (DCE), was added through the inlet of the PCE fed channels, but this did not lead to sufficient conversion of DCE. Addition of KB-1 at well 3, located approximately in the middle of the channel, had a greater impact in the degradation of DCE, in both glucose and SOME amended channels, compared to addition at the inlet. KB-1 culture added to the channel was active even 155 days later, suggesting that there is sustainable growth of KB-1 when provided with suitable conditions and substrates.;A pilot field study was conducted for remediation of a tetrachloroethylene (PCE) contaminated site at Manhattan, KS. The aquifer in the pilot study area has two distinct zones, termed shallow zone and deep zone, with groundwater velocities of about 0.3 m/day and 0.1 m/day. Prior to the pilot study, PCE concentration in groundwater at the pilot study area was about 15 mg/L (ppm) in the deep zone and 1 mg/L in the shallow zone. Nutrient solution comprising soy oil methyl esters (SOME), lactate, yeast extract and glucose was added in the pilot study area for biostimulation, on August 18, 2005. Potassium bromide (KBr) was added to the nutrient solution as a tracer. PCE was converted to DCE under these conditions. To carry out complete degradation of PCE, KB-1, a consortium of Dehalococcoides, and a second dose of nutrient solution were added on October 13, 2005. After addition of KB-1, both PCE and DCE concentrations decreased. Nutrients were again injected on March 3, 2006 (with KBr) and on August 1, 2006. The total chlorinated ethenes (CEs) have decreased by about 80% in the pilot study area due to bioremediation. Biodegradation of CEs continued for a long time (several months) after the addition of nutrients. The insoluble SOME may be retained at the feeding area and provide a long time source of electron donors. Biostimulation and bioaugmentation of PCE contaminated soil and groundwater was evaluated in the laboratory and this technique was implemented successfully in the pilot field study.;Modeling of the tracer study was performed using an advection-dispersion equation (ADE) and traditional residence time distribution (RTD) methods. Based on data collected from several wells the hydrologic parameter values obtained from tracer studies appear to vary spatially. (Abstract shortened by UMI.)
机译:氯化溶剂是仅次于石油烃的第二大普遍污染物,其中许多是致癌物。四氯乙烯或全氯乙烯(PCE)已广泛用于干洗行业,四氯化碳(CT)已用作谷物存储设施中的熏蒸剂。在这项工作中,通过介观实验进行了修复可行性研究。一个小室被分成六个通道并充满了土壤,在上面生长了植物。每个通道的底部都注入了污水,并在出口处收集,模拟了地下水的流动情况。从2004年3月12日开始引入污染物。在三个通道中引入PCE的浓度约为2 mg / L(〜12微摩尔/ L),其中两个通道用于苜蓿植物,另一个通道用于草。在其他三个通道中引入CT的浓度约为2 mg / L(约13微摩尔/ L),其中两个通道用于苜蓿植物,另一个通道用于草。系统达到稳态后,监测入口和出口的PCE和CT浓度,并研究饱和区中PCE和CT消失的数量。由于约100天后在出口处未发现降解产物,因此通过添加一升0.2%葡萄糖溶液,使PCE和CT(使用苜蓿)的每个通道成为厌氧的。从2004年7月1日开始,每月喂一次葡萄糖溶液,一直持续到2005年2月。从2004年10月1日起,将一升0.1%的乳化大豆油甲酯(SOME)喂入另外两个通道(使用苜蓿),一个暴露于PCE,另一个暴露于CT。某些添加日期与葡萄糖相同。进料PCE和SOME的通道出口液体开始包含一些PCE降解化合物。然而,降解程度不如葡萄糖进料通道的降解程度大。在未添加碳和能量补充剂的通道(草生长在顶部)的出口溶液中未观察到降解化合物。在CT进料通道中也观察到了类似的趋势。通过PCE进料通道的入口添加了降解二氯乙烯(DCE)的商业微生物培养物KB-1(脱卤球菌的财团),但这并未导致DCE的充分转化。与在入口处添加相比,在葡萄糖和SOME修正通道中,大约位于通道中间的第3孔中添加KB-1对DCE的降解具有更大的影响。添加到通道中的KB-1培养物甚至在155天后仍处于活动状态,这表明在提供合适条件和底物的情况下KB-1可以持续生长。;进行了中试研究,以修复受四氯乙烯(PCE)污染的场所在堪萨斯州曼哈顿。试点研究区域的含水层有两个不同的区域,分别称为浅层区域和深层区域,地下水流速分别约为0.3 m / day和0.1 m / day。在试点研究之前,试点研究区域的地下水中PCE浓度在深区约为15 mg / L(ppm),在浅区约为1 mg / L。 2005年8月18日,在试验研究区中添加了包含大豆油甲酯(SOME),乳酸,酵母提取物和葡萄糖的营养液,以进行生物刺激。将溴化钾(KBr)作为示踪剂添加至营养液中。在这些条件下,PCE已转换为DCE。为了完全降解PCE,2005年10月13日添加了KB-1,脱卤球菌财团和第二剂营养液。添加KB-1后,PCE和DCE浓度均降低。在2006年3月3日(含KBr)和2006年8月1日再次注入了营养素。由于生物修复,试验研究区的总氯化乙烯(CE)减少了约80%。添加营养素后,CE的生物降解持续了很长时间(数月)。不溶性SOME可能保留在进料区,并提供了长期的电子供体来源。在实验室中对PCE污染土壤和地下水的生物刺激和生物强化进行了评估,并成功地在中试研究中实施了该技术。示踪剂研究的模型使用对流扩散方程(ADE)和传统停留时间分布(RTD) ) 方法。根据从几口井收集的数据,从示踪剂研究获得的水文参数值似乎在空间上变化。 (摘要由UMI缩短。)

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