Mechanistic insights into manganese oxide impacting the oxidation and transport of Cr(III) immobilized by nano-zero valent charged ion particles in water-saturated porous media

零价铁 化学 环境修复 浸出(土壤学) 金属 氧化物 吸附 纳米颗粒 色散(光学) 无机化学 化学工程 污染 土壤水分 工程类 生态学 土壤科学 有机化学 物理 光学 生物 环境科学
作者
Wu Sun,Nan Xu,Wenxin Jiang,Gongbi Cheng
出处
期刊:Journal of Hazardous Materials [Elsevier BV]
卷期号:469: 134050-134050 被引量:11
标识
DOI:10.1016/j.jhazmat.2024.134050
摘要

The presence of manganese oxide (MnO2) could influence the stability of green-synthesized nano-zero valent iron (nZVI@GT) associated with trivalent chromium (Cr(III)) after its excess application in the in situ remediation of hexachromium (Cr(VI)) contaminated soil. The research findings revealed that the co-transport of the remaining nZVI@GT with Cr(III) was substantially inhibited by high δ-MnO2 concentrations due to the formation of hetero-aggregates between nZVI@GT and δ-MnO2, resulting in an increased irreversible attachment parameter at second-site in a two-site kinetic attachment model. Simultaneously, the Cr(III) complex immobilized on nZVI@GT could be oxidized leading to high levels of Cr(VI) leaching at high δ-MnO2 concentrations. During this process, Mn(IV) was converted to Mn(III)/Mn(II). Subsequently, leachate containing a partial amount of Cr(VI) preferentially adsorbed onto the nZVI@GT surface, enhancing the dispersion of the nZVI@GT and δ-MnO2 agglomerates. Thereafter, nZVI@GT transportability was enhanced with a decreased second-site attachment parameter and the flow content of dissolved Cr(VI) was increased to double, also increasing the potential risk of Cr(VI) being carried by nZVI@GT to underground water systems. This study provides theoretical support for preserving the long-term stability of nZVI@GT after the in situ remediation of heavy metal-contaminated sites in the presence of δ-MnO2.
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