Yu Binbin, Zhang Huimin, Xu Wei, Li Gang, Wu Zucheng
Department of Environmental Engineering, Laboratory of Electrochemistry and Energy Storage; State Key Laboratory of Clean Energy Utilization, Zhejiang University, Hangzhou 310058, P. R. China.
Sci Rep. 2014 Aug 29;4:5860. doi: 10.1038/srep05860.
Chromium pollution has been historically widespread throughout the world. Most available remediation technologies often require energy consumption. This study is aimed to develop electrochemical remediation for Cr(VI) in chromium-slag leakage with self-generated electricity. Dynamic leaching experiments of chromium-slag samples were conducted to survey the release and leaching behavior of Cr(VI). Based on previous work, a unique urea-Cr(VI) was designed, in which urea was employed as the fuel and Cr(VI) from the leakage of the dichromate slag served as the oxidant. Furthermore, the electrochemical results showed that the removal percent of Cr(VI) was more than 96% after 18 h with the leakage Cr(VI) concentration of 2.69 mM. The open circuit potential (OCP) varied in the range of 1.56 ~ 1.59 V under different initial Cr(VI) leakage concentrations. The approach explores the feasibility of the promising technique without the need of energy input for simultaneous chromium-slag remediation and generation of electricity.
铬污染在历史上曾在全球广泛存在。大多数现有的修复技术通常需要消耗能源。本研究旨在开发利用自生电力对铬渣渗滤液中的六价铬进行电化学修复的方法。进行了铬渣样品的动态浸出实验,以研究六价铬的释放和浸出行为。基于之前的工作,设计了一种独特的尿素-六价铬体系,其中尿素用作燃料,重铬酸盐渣渗滤液中的六价铬用作氧化剂。此外,电化学结果表明,在六价铬泄漏浓度为2.69 mM的情况下,18小时后六价铬的去除率超过96%。在不同的初始六价铬泄漏浓度下,开路电位(OCP)在1.56~1.59 V范围内变化。该方法探索了这种有前景的技术在无需能量输入的情况下同时进行铬渣修复和发电的可行性。