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Pilot-scale study of in-situ chemical oxidation of trichloroethene with sidium permanganate

机译:高锰酸钾原位化学氧化三氯乙烯的中试研究

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This study indicates that the dissolved-phase TCE was rapidly oxidizat by permanganate while the destruction of source free phase TCE appeared to be controlled by the rate of mass transfer of both permanganate and TCE toward their interface. The oxidation of dissolved-phase TCE by permanaganate had caused a significant decrease in pH (e.g., from 6.5 (background) to 3.5 (at approx pore volume)) and an increase in chloride (e.g., from 83 mg/L (background) to 380 mg/L (at approx 1 pore volume) in the extracted water in the beginning of the test. The downward migration of permanganate fronts near the aquitard provides evidences for the destruction of source free phase TCE. Two sets of soil cores collected near the aquitard at different times reveal that MnO_2 layers were formed above the source TCE zones and increased as the test proceeded.
机译:这项研究表明,高锰酸盐可快速溶解溶解相三氯乙烯,而高锰酸盐和三氯乙烯向其界面的传质速率可控制游离源三氯乙烯的破坏。高锰酸盐对溶解相TCE的氧化导致pH值显着降低(例如,从6.5(背景)降低到3.5(在大约孔体积下))和氯离子的升高(例如,从83 mg / L(背景)降低到试验开始时,提取水中的浓度为380 mg / L(约1孔体积),高锰酸盐前沿在阿奎塔德附近的向下迁移提供了源自由相TCE破坏的证据。从不同的时间来看,Aquitard结果表明MnO_2层在源TCE区域上方形成,并随着测试的进行而增加。

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