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Contaminant mass transfer during boiling in fractured geologic media.

机译:破裂地质介质中沸腾过程中的污染物传质。

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The objective of this study is to understand the contaminant mass transfer due to boiling in fractured geologic media.;Local-scale matrix boiling and contaminant mass transfer during the process were demonstrated using a sandstone core, where the unfractured core represents the matrix and an end the fracture. The core was contaminated by pumping water dissolved with 1,2-DCA and NaBr. When boiling occurred in the matrix, a temperature gradient toward the fracture was observed, indicating, under saturated vapor condition, a pressure gradient pushing the steam (water and vapor mixture) towards the fracture. When boiling occurred, 1,2-DCA was removed at a rate 6 times higher than before heating. The nonvolatile bromide concentration, as an indicator of the steam quality, showed a reverse correlation with the volatile 1,2-DCA concentration, indicating that the majority of 1,2-DCA was removed by partitioning to the vapor phase.;To accurately predict the partitioning of contaminant between aqueous and gaseous phase at high temperature, Henry's law constants were measured for 12 chlorinated solvents (tetrachloroethylene, trichloroethylene, chloroform, 1,2-dichloroethane, 1,1,1-trichloroethane, 1,1-dichloroethane, dichloromethane, carbon tetrachloride, cis-1,2-dichloroethylene, chloromethane, chloroethane, and vinyl chloride) over temperatures from 8 to 93 °C. The measured results show that Henry's law constant is strongly dependent on temperature, increasing by factors from 3 (chloromethane) to 30 fold (1,2-DCA) as temperature increases from 8 to 93 °C. The temperature dependency of Henry's law constants was modeled with the Van't Hoff equation. Better fitting is obtained by assuming the enthalpy of dissolution is a function of temperature, suggesting the inappropriateness of extrapolating the Henry's law constant from measurements at low temperature using a linear function. Using measured data for solubility, a vapor pressure-solubility model gives a reasonable prediction of the Henry's law constants. With improved data on Henry's law constants at high temperatures for the 12 common CVOCs measured in this study, it will be possible to more accurately model subsurface remediation processes that operate near the boiling point of water.;The laboratory experiment was simulated with a 2-D multiphase numerical model using the TMVOC code. The simulated results are in reasonable agreement with the experiment, provideing confidence for the TMVOC code in predicting the CVOC removal from fractured geologic media by boiling. A 1-D numerical model was further used to demonstrate the contaminant mass transfer from a core without end effects. Similar to the experiment results, a temperature gradient was observed while pore water in the matrix was boiled. After opening to the atmosphere, a high proportion of steam vapor was produced, corresponding to a high removal rate of 1,2-DCA. All of the 1,2-DCA mass was removed after boiling out around 50 mL pore water. The contaminant removal from fractured geologic media at field scale was simulated using the MINC method. After about 35 days of treatment, 27.8% of the pore water (including both steam vapor and liquid water) was extracted, and essentially all the 1,2-DCA mass (more than 99%) was removed from the fractured site. The simulation shows boiling is an effective mechanism for CVOC removal from fractured geologic media.;Effects of chemicals, fracture spacing, fracture aperture, diameter of heating pattern, matrix permeability, extent of vacuum, and different operational strategies on the performance of thermal treatment of a fractured site were investigated. The simulation results show that, under the same boiling conditions, the contaminant removal rates vary for different chemicals, depending on their Henry's law constants. The higher the Henry's law constant for a chemical, the higher the contaminant removal rate. Variations of fracture properties (aperture and spacing), size of heating pattern, and the extent of extraction vacuum have larger effects on the system temperature than the matrix permeability due to the different percentages of heat extracted from the system. (Abstract shortened by UMI.)
机译:这项研究的目的是了解裂缝性地质介质中沸腾引起的污染物传质。使用砂岩岩心演示了过程中局部尺度的基质沸腾和污染物传质,其中未破裂的岩心代表基质,一端骨折。泵入溶解有1,2-DCA和NaBr的水,污染了堆芯。当基质中发生沸腾时,观察到朝向裂缝的温度梯度,表明在饱和蒸汽条件下,压力梯度将蒸汽(水和蒸汽混合物)推向裂缝。当发生沸腾时,以比加热前高6倍的速率除去1,2-DCA。非挥发性溴化物浓度作为蒸汽质量的指标,与挥发性1,2-DCA浓度呈反相关关系,表明大部分1,2-DCA通过分配至气相而被去除。在高温下水相和气相之间污染物的分配方面,测量了12种氯化溶剂(四氯乙烯,三氯乙烯,氯仿,1,2-二氯乙烷,1,1,1-三氯乙烷,1,1-二氯乙烷,二氯甲烷)的亨利定律常数(例如四氯化碳,顺式1,2-二氯乙烯,氯甲烷,氯乙烷和氯乙烯)的温度范围为8至93°C。测量结果表明,亨利定律常数强烈依赖于温度,随着温度从8升高到93°C,亨利定律常数从3(氯甲烷)增加到30倍(1,2-DCA)。亨利定律常数的温度依赖性通过Van't Hoff方程建模。假设溶解焓是温度的函数,则可以得到更好的拟合度,这表明用线性函数从低温下的测量值推断亨利定律常数是不合适的。使用溶解度的测量数据,蒸气压-溶解度模型可以合理地预测亨利定律常数。利用这项研究中测得的12种常见CVOC在高温下亨利定律常数的改进数据,将可能更准确地对在水沸点附近运行的地下修复过程进行建模。;实验室实验是使用2-使用TMVOC代码的D多相数值模型。模拟结果与实验结果基本吻合,为TMVOC编码提供了预测通过沸腾从裂缝性地质介质中去除CVOC的信心。一维数值模型还被用来证明污染物从核中的传质没有末端效应。与实验结果相似,当基质中的孔隙水沸腾时观察到温度梯度。向大气开放后,产生了高比例的蒸汽,对应于1,2-DCA的高去除率。在沸腾约50 mL孔隙水后,将所有1,2-DCA物质除去。使用MINC方法模拟了在野外从裂缝性地质介质中去除污染物的过程。处理约35天后,抽出了27.8%的孔隙水(包括蒸汽和液态水),并且基本上从裂缝处去除了所有的1,2-DCA团块(超过99%)。模拟表明沸腾是从裂缝性地质介质中去除CVOC的有效机制。;化学品,裂缝间距,裂缝孔径,加热模式直径,基质渗透率,真空程度以及不同操作策略对热处理性能的影响对骨折部位进行了调查。仿真结果表明,在相同的沸腾条件下,不同化学物质的污染物去除率会有所不同,具体取决于它们的亨利定律常数。化学品的亨利定律常数越高,污染物去除率越高。断裂特性(孔径和间距),加热方式的大小以及抽真空的程度的变化比基质渗透率对系统温度的影响更大,这是因为从系统中提取的热量百分比不同。 (摘要由UMI缩短。)

著录项

  • 作者

    Chen, Fei.;

  • 作者单位

    Clemson University.;

  • 授予单位 Clemson University.;
  • 学科 Geology.;Environmental Sciences.;Engineering Environmental.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 187 p.
  • 总页数 187
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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