Key Laboratory of Groundwater Resources and Environment of Ministry of Education, College of New Energy and Environment, Jilin University, Changchun 130021, China; Jilin Provincial Key Laboratory of Water Resources and Environment, College of New Energy and Environment, Jilin University, Changchun 130021, China; National and Local Joint Engineering Laboratory for Petrochemical Contaminated Site Control and Remediation Technology, Jilin University, Changchun 130021, China.
Key Laboratory of Groundwater Resources and Environment of Ministry of Education, College of New Energy and Environment, Jilin University, Changchun 130021, China; Jilin Provincial Key Laboratory of Water Resources and Environment, College of New Energy and Environment, Jilin University, Changchun 130021, China; National and Local Joint Engineering Laboratory for Petrochemical Contaminated Site Control and Remediation Technology, Jilin University, Changchun 130021, China.
Sci Total Environ. 2022 Jul 1;828:154422. doi: 10.1016/j.scitotenv.2022.154422. Epub 2022 Mar 8.
Micron zero valent iron (mZVI) was an underground remediation material, which had great application potential to replace nano zero valent iron (nZVI) from the perspective of economic and health benefits. However, mZVI was highly prone to gravitational settling, which limited its wide application for in situ remediation of contaminated groundwater. This paper was devoted to develop an efficient and economical groundwater remediation material based on mZVI, which should possess excellent stability, reactivity, and transportability. Thereby xanthan gum (XG) stabilized and NaSO sulfidated mZVI (XG-S-mZVI) was synthesized and characterized with SEM, XRD, XPS, and FTIR techniques. In terms of stability, the adsorbed XG and the dispersed XG worked together to resist the sedimentation of S-mZVI. In terms of reactivity, sulfidation enhanced the electron transfer rate and electron selectivity of XG-S-mZVI, thereby improved the reactivity of XG-S-mZVI. The hexavalent chromium (Cr(VI)) removal rate constant by XG-S-mZVI was determined to be 832.4 times than bare mZVI. In terms of transportability, the transportability of XG-S-mZVI was greatly improved (~80 cm in coarse sand and ~50 cm in medium sand). Straining was the main mechanism of XG-S-mZVI retention in porous media. XG-S-mZVI in situ reactive zone (XG-S-mZVI-IRZ) was only suitable to the media with a grain size larger than 0.25 mm. This study could provide theoretical support and guidance for the implementation of IRZ technology based on mZVI.
微米零价铁(mZVI)是一种地下修复材料,从经济和健康效益的角度来看,它具有很大的应用潜力,可以替代纳米零价铁(nZVI)。然而,mZVI极易发生重力沉降,这限制了其在污染地下水的原位修复中的广泛应用。本文致力于开发一种基于 mZVI 的高效、经济的地下水修复材料,该材料应具有优异的稳定性、反应性和迁移性。因此,合成并表征了黄原胶(XG)稳定和 NaSO 硫化的 mZVI(XG-S-mZVI),采用 SEM、XRD、XPS 和 FTIR 技术。在稳定性方面,吸附的 XG 和分散的 XG 共同作用抵抗 S-mZVI 的沉降。在反应性方面,硫化增强了 XG-S-mZVI 的电子转移速率和电子选择性,从而提高了 XG-S-mZVI 的反应性。XG-S-mZVI 的六价铬(Cr(VI))去除速率常数是 bare mZVI 的 832.4 倍。在迁移性方面,XG-S-mZVI 的迁移性大大提高(在粗砂中约为 80cm,在中砂中约为 50cm)。滤失是 XG-S-mZVI 在多孔介质中保留的主要机制。XG-S-mZVI 原位反应区(XG-S-mZVI-IRZ)仅适用于粒径大于 0.25mm 的介质。本研究可为基于 mZVI 的 IRZ 技术的实施提供理论支持和指导。