麦金纳维
铁质
氧化还原
硫化铁
吸附
硫化物
环境修复
鳞片岩
纳米颗粒
无机化学
零价铁
化学
水溶液
部分氧化
化学工程
针铁矿
催化作用
污染
有机化学
硫黄
工程类
生物
生态学
作者
Yaqi Liu,Haibo Gan,Li Tian,Zhenhai Liu,Yunyun Ji,Tong Zhang,Pedro J. J. Alvarez,Wei Chen
标识
DOI:10.1021/acs.est.2c02406
摘要
Iron sulfide nanoparticles (nano-FeS) have shown great potential for in situ remediation of Cr(VI) pollution by reducing Cr(VI) to the less soluble and toxic Cr(III). However, material oxidation that inevitably occurs during storage and application alters its reactivity. Herein, we show that partial oxidation of nanoparticulate mackinawite (FeS) significantly enhances its capability in sequestering Cr(VI). Oxidation of nano-FeS increases its binding affinity to Cr(VI), likely due to preferential inner-sphere complexation of Cr(VI) oxyanions to ferric over ferrous iron in mackinawite/lepidocrocite (FeS/γ-FeOOH) nanocomposites. A trade-off is that oxidation mitigates Cr(VI) reduction by lowering the electron-donating potential of the material and the electron transfer at a solution-material interface and consequently hinders the transformation of adsorbed Cr(VI) to Cr(III). Notably, the rate-limiting step of Cr(VI) sequestration transitions from adsorption to reduction during oxidation, as demonstrated with batch experiments coupled with kinetic modeling. Thus, an optimum oxidation degree exists, wherein the gain in the overall performance from enhanced adsorption overcompensates the loss from inhibited reduction, resulting in maximum sequestration of aqueous Cr(VI) as solid-phase Cr(III). Our findings inform better assessment and design of nanomaterials for Cr(VI) remediation and may be extended to interactions of other oxyanions with natural and engineered nanoparticles during oxidative aging.
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