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首页> 外文期刊>Separation and Purification Technology >Enhanced nano-Fe3O4/S2O8~(2-) oxidation of trichloroethylene in a clayey soil by electrokinetics
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Enhanced nano-Fe3O4/S2O8~(2-) oxidation of trichloroethylene in a clayey soil by electrokinetics

机译:电动学增强黏土中三氯乙烯的纳米Fe3O4 / S2O8〜(2-)氧化

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摘要

The effectiveness of electrokinetically enhanced persulfate oxidation for destruction of trichloroethylene (TCE) in a spiked sandy clay soil was evaluated in this work. In addition, the effect of nanoscale Fe3O4 on activating persulfate oxidation was also evaluated. The TCE-spiked soil was compacted in the soil column of the electrokinetic (EK) treatment system, and both the anode and cathode reservoirs were filled with simulated groundwater. The electrode material for both the anode and cathode was graphite. An electrical potential gradient of 1 V cm~(-1) was applied to the EK treatment system by a DC power supply for a period of 7-14 d. Sodium persulfate (Na2S2O8) was injected daily at a dose of 1.0-10.0 g L~(-1) into the anode or cathode reservoir, starting from the very beginning of the treatment. To evaluate the performance of persulfate alone in chemical oxidation of TCE in the EK treatment system, EK-alone test was also carried out for comparison. Experimental results have shown that the EK process greatly enhances the transport of injected persulfate from the anode reservoir to the cathode reservoir via the soil compartment by means of electroosmotic flow, aiding in situ chemical oxidation of TCE. In addition, nanoscale Fe3O4 was found to play a significant role in activating persulfate oxidation. Such a coupled process was found to be capable of effective destruction of TCE in the soil compartment and electrode compartments. Under optimal conditions, the residual TCE concentration in the soil compartment was found to be lower than Taiwan EPA's regulatory threshold (i.e., 60 mg kg~(-1)). The residual TCE concentrations in both electrode reservoirs (i.e., not detectable and 0.01-1.74 mg L~(-1) for the anode and cathode reservoirs, respectively) also met the local regulatory standards for Type II groundwater quality (i.e., <0.05 mgL~(-1)).
机译:在这项工作中,评估了电动增强过硫酸盐氧化对破坏尖峰砂质粘土中三氯乙烯(TCE)的有效性。此外,还评估了纳米级Fe3O4对活化过硫酸盐氧化的影响。将TCE掺加的土壤压实在电动(EK)处理系统的土壤柱中,阳极和阴极储层均充满模拟地下水。阳极和阴极的电极材料均为石墨。通过直流电源向EK处理系统施加1 V cm〜(-1)的电势梯度,持续时间为7-14 d。从处理开始就每天以1.0-10.0 g L〜(-1)的剂量将过硫酸钠(Na2S2O8)注入阳极或阴极容器中。为了评估过硫酸盐在EK处理系统中TCE的化学氧化中的性能,还进行了EK单独测试以进行比较。实验结果表明,EK工艺通过电渗流大大增强了注入的过硫酸盐从阳极储库到土壤储库的渗透,通过电渗流,有助于TCE的原位化学氧化。另外,发现纳米级的Fe 3 O 4在活化过硫酸盐氧化中起重要作用。发现这种偶联过程能够有效破坏土壤室和电极室中的TCE。在最佳条件下,发现土壤区室中的残留三氯乙烯浓度低于台湾环保局的规定阈值(即60 mg kg〜(-1))。两个电极储层中的残留三氯乙烯浓度(即,阳极和阴极储层中均不可检出,分别为0.01-1.74 mg L〜(-1))也符合当地II类地下水水质的监管标准(即<0.05 mgL 〜(-1))。

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