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Time-lapse monitoring of DNAPL in a controlled cell

机译:受控细胞中DNAPL的延时监控

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A multi-component GPR antenna is used to perform time-lapse measurements in a controlled experiment simulating DNAPL release. The DNAPL monitoring is based on the delay time of a reflection from the back side of a cell and on spectral analysis of traces. The study shows that co-polar and cross-polar antennas detect a similar pull-up of the reflection from the back of the cell induced by the DNAPL. The amplitude of the reflection from the DNAPL is weaker in the cross-polar data with respect to the co-polar data and in actual cases it could not be detected by both antenna configurations. In addition we observe a change in the amplitude spectra of the traces collected at the DNAPL release with respect to those collected in an uncontaminated area. The amplitude spectrum variations occurred mainly in the co-polar antennas. The spectra of cross-polar antennas show variations over time that are not easily linked to the DNAPL position. We observed that the data collected 141 hours after the first DNAPL injection and two hours of water flow, show a pull-up of the reflection from the back of the cell and variations in the amplitude spectra of the traces located at the same position as the DNAPL injection. This suggests that the DNAPL probably remained trapped by sediments and was not totally removed by the water flow. Forward models, simulating the experiment, confirmed that the DNAPL induces a pull-up of the reflection from the back of cell and showed that in a controlled experiment the DNAPL produces a reflection whose amplitude depends on the DNAPL saturation. In a real case the presence of small amounts of DNAPL can be at best barely visible because of induced small amplitude reflections. This is truer if no GPR data are available from before the DNAPL spill, so there is little chance that GPR responses can be positively attributed to DNAPL presence.
机译:在模拟DNAPL释放的受控实验中,多组件GPR天线用于执行延时测量。 DNAPL监控基于从电池背面反射的延迟时间以及痕量光谱分析。研究表明,同极化和交叉极化天线检测到由DNAPL引起的细胞背面反射的类似上拉。相对于同极性数据,来自DNAPL的反射幅度在交叉极性数据中较弱,在实际情况下,两种天线配置都无法检测到。此外,我们观察到在DNAPL释放时收集的迹线的振幅谱相对于在未污染区域中收集到的迹线的幅度谱发生了变化。幅度频谱变化主要发生在同极化天线中。交叉极化天线的频谱显示了随时间变化的变化,这些变化很难与DNAPL位置关联。我们观察到,第一次DNAPL注入和两个小时的水流经过141小时后收集到的数据显示,来自细胞背面的反射波呈上拉趋势,并且迹线的振幅谱中的变化与DNAPL注射。这表明DNAPL可能仍被沉积物所困,并没有被水流完全清除。模拟实验的正向模型证实了DNAPL引起细胞背面反射的上拉,并表明在受控实验中DNAPL产生的反射幅度取决于DNAPL饱和度。在实际情况下,由于诱导了小幅度的反射,因此几乎看不到少量DNAPL的存在。如果在DNAPL泄漏之前没有可用的GPR数据,则情况更是如此,因此,将GPR响应肯定归因于DNAPL的存在的可能性很小。

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