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Electrical Resistance Heating Remediation at a Carbon Tetrachloride Site

机译:四氯化碳位点处的电阻加热修复

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Carbon tetrachloride was used as a carrier for the fumigant carbon disulfide in the grain industry during the 1950s to early 1980s. This practice left a carbon tetrachloride legacy at a number of grain storage facilities across the United States. At this Kansas facility, a significant source remained, including undissolved product extending 52 ft below grade adjacent to a grain elevator. Geology was dominated by clays. Those below 39 ft were associated with heaving clays. An estimated 3,220 lbs of carbon tetrachloride was present within the source area. Given the difficult geology and a stringent performance standard of mass reduction of carbon tetrachloride to less than 19 lbs total and less than 7 mg/kg remaining in all soil samples, the remedial technology selected was Electrical Resistance Heating. Carbon tetrachloride undergoes a hydrolysis reaction at elevated temperatures resulting in destruction in situ, and thus negating the need for off-gas treatment. In addition, a remedial groundwater goal of achieving 0.5 mg/L carbon tetrachloride and 0.5 mg/L chloroform in the source area was agreed upon with the regulatory agency. The geology resulted in variable heating within the source area. From the increase in chlorides in the source area monitoring wells, an estimated 8,100 pounds of carbon tetrachloride was destroyed via the hydrolysis reaction. However, the reaction rate proved slower than the literature suggested. Not all carbon tetrachloride was destroyed by hydrolysis, and an estimated 1,000 to 2,500 lbs of carbon tetrachloride and chloroform was extracted by a near-surface soil vapor extraction system. Overall destruction of contaminants exceeded 99.4 percent, resulting in meeting the mass remedial goal for carbon tetrachloride (8 lbs remaining) and meeting the 7 mg/kg goal on average, but not on every individual soil sample.
机译:在20世纪50年代到20世纪80年代初,将四氯化碳用作谷物工业中蒸发碳二硫化碳的载体。这种做法在美国各地的粮食储存设施中留下了四氯化物遗产。在此堪萨斯工厂,一个重要的来源仍然存在,包括未溶解的产品在谷物电梯附近延伸52英尺的52英尺。地质以粘土为主。低于39英尺的人与起伏粘土相关。估计的3,220磅的四氯化碳存在于源区内。鉴于难度地质和严格的物质降低的碳四氯化碳的严格性能标准,总共小于19磅,留在所有土壤样品中剩余的少于7毫克/千克,所选择的补救技术是电阻加热。四氯化碳在升高的温度下经历水解反应,导致原位破坏,从而否定对废气处理的需求。另外,在源区实现0.5毫克/升四氯化碳和0.5毫克/升氯仿的补救地下水目标是在与管理机构同意。地质导致源区内的可变加热。从源区域监测孔中的氯化物的增加,通过水解反应破坏了估计的8,100磅的四氯化碳。然而,反应率证明比文献所示的慢。并非所有碳四氯化碳通过水解破坏,并且通过近表面土蒸气提取系统提取估计的1,000至2,500磅的四氯化碳和氯仿。整体破坏污染物超过99.4%,导致满足四氯化碳的质量补救目标(剩余8磅),平均会满足7毫克/千克的目标,但不在每个单独的土壤样本上。

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