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低频交流电磁场下硫化微米级零价铁对三氯乙烯的强化脱氯

Enhanced dechlorination of trichloroethene by sulfidated microscale zero-valent iron under low-frequency AC electromagnetic field.

作者信息

He Feng, Yu Ye, Wan Wubo, Liang Liyuan

机构信息

College of Environment, Zhejiang University of Technology, Hangzhou 310014, China.

College of Environment, Zhejiang University of Technology, Hangzhou 310014, China.

出版信息

J Hazard Mater. 2022 Feb 5;423(Pt A):127020. doi: 10.1016/j.jhazmat.2021.127020. Epub 2021 Aug 24.

Abstract

In this study an electromagnetic heating strategy is proposed for remediation of trichloroethene (TCE) by ball milled, sulfidated microscale zero valent iron (S-mZVI) particles. S-mZVI is ferromagnetic, which generates heat under the application of a low-frequency alternating current electromagnetic field (AC EMF). We found that the temperature reached up to ~120 ℃ during 30-min electromagnetic induction heating of 10 g/L S-mZVI (with S/Fe molar ratio of 0.1), compared with ~55 ℃ and ~80 ℃ for ZVI and ball milled mZVI, respectively. The application of AC EMF accelerated the TCE degradation rate (k = 5.5 × 10 h) by up to 4-fold without compromising or even enhancing electron efficiency of S-mZVI compared to no-heating. Furthermore, this process halved the generation of chlorinated intermediate, cis-DCE. In contrast, water-bath heating only increased the dechlorination rate 2-fold with unchanged cis-DCE generation and lowered electron efficiency. This is attributed to both rising temperature by induction heating and accelerated ZVI corrosion and surface Fe exposure caused by AC EMF. In real groundwater, the AC EMF maintained the same promoting effects for TCE dechlorination by S-mZVI. This study shows that combination of filed-scale available AC EMF with S-mZVI provides a promising approach for remediation of chlorinated hydrocarbons in contaminated groundwater.

摘要

在本研究中,提出了一种电磁加热策略,用于通过球磨硫化的微米级零价铁(S-mZVI)颗粒修复三氯乙烯(TCE)。S-mZVI具有铁磁性,在低频交变电流电磁场(AC EMF)作用下会产生热量。我们发现,在对10 g/L S-mZVI(S/Fe摩尔比为0.1)进行30分钟的电磁感应加热过程中,温度高达约120℃,相比之下,零价铁(ZVI)和球磨微米级零价铁(mZVI)分别约为55℃和80℃。与不加热相比,施加AC EMF使TCE降解速率(k = 5.5×10 h)提高了4倍,同时不影响甚至提高了S-mZVI的电子效率。此外,该过程使氯化中间产物顺式二氯乙烯(cis-DCE)的生成量减半。相比之下,水浴加热仅使脱氯速率提高了2倍,cis-DCE生成量不变,且电子效率降低。这归因于感应加热导致的温度升高以及AC EMF引起的ZVI腐蚀加速和表面铁暴露。在实际地下水中,AC EMF对S-mZVI脱氯TCE保持相同的促进作用。本研究表明,现场可用的AC EMF与S-mZVI相结合为修复受污染地下水中的氯代烃提供了一种有前景的方法。

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