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Trichloroethylene Degradation by Zero Valent Iron Activated Persulfate Oxidation

机译:零价铁活化过硫酸盐氧化降解三氯乙烯

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摘要

The present study describes the use of zero valent iron (Fe0 ) as a source for ferrous ion activated persulfate (PS) oxidation of trichloroethylene (TCE). The experimental results indicated that in the absence of TCE there was a lag time for persulfate decomposition when the reaction was activated by Fe0 . An initial pH drop in the Fe0 /PS system to acidic conditions was accompanied by the persulfate decomposition and a decrease in oxidation-reduction potential (ORP) values. Furthermore, in the TCE/Fe0 /PS system, the rapid TCE degradation was accompanied by the rapid persulfate decomposition and chloride ion formation as evidence of TCE mineralization. SEM images of Fe0 before and after persulfate oxidation exhibited significant corrosions of Fe0 . Acicular aggregate formation in the absence of TCE and coarse aggregate formation in the presence of TCE were observed. Moreover, the XRD spectrum revealed the formation of magnetite over the surface of Fe0 after contact with persulfate. Thus, Fe0 activated persulfate oxidation offers a fast and effective way for remediation of TCE contamination.
机译:本研究描述了使用零价铁(Fe0)作为三氯乙烯(TCE)的亚铁离子活化过硫酸盐(PS)氧化的来源。实验结果表明,在没有TCE的情况下,当反应被Fe0活化时,过硫酸盐分解会有滞后时间。 Fe0 / PS系统中最初的pH下降到酸性条件会伴随着过硫酸盐的分解和氧化还原电位(ORP)值的降低。此外,在TCE / Fe0 / PS系统中,TCE的快速降解伴随着过硫酸盐的快速分解和氯离子的形成,这是TCE矿化的证据。过硫酸盐氧化前后的Fe0的SEM图像显示出Fe0的明显腐蚀。在不存在TCE的情况下观察到针状聚集体的形成,而在存在TCE的情况下观察到粗聚集体的形成。而且,XRD谱图显示了与过硫酸盐接触后在Fe0的表面上形成了磁铁矿。因此,Fe0活化的过硫酸盐氧化为补救TCE污染提供了一种快速有效的方法。

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