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层状双氢氧化物负载纳米零价铁增强地下水除钒(V)。

Enhanced removal of vanadium(V) from groundwater by layered double hydroxide-supported nanoscale zerovalent iron.

机构信息

School of Environment, Tsinghua University, Beijing, 100084, PR China.

College of Life and Environmental Sciences, Minzu University of China, Beijing 100081, PR China.

出版信息

J Hazard Mater. 2020 Jun 15;392:122392. doi: 10.1016/j.jhazmat.2020.122392. Epub 2020 Feb 24.

Abstract

To reduce the toxicity of vanadium(V) [V(V)] and inhibit the desorption of adsorbed vanadium in groundwater, we synthesized nanoscale zerovalent iron (nZVI) dispersed on layered double hydroxide (LDH) composites (nZVI@LDH) to remove V(V) from simulated groundwater. We found that nZVI@LDH could reduce high-valence vanadium to low-valence vanadium, then forming vanadium-containing precipitation to reduce the toxicity and inhibiting vanadium from returning to groundwater. SEM and XRD characterizations exhibited the uniform dispersal of nZVI on the surface of LDH. nZVI@LDH with nZVI/LDH at a mass ratio of 1:2 provided the maximum adsorption capacity of 93.7 mg g at pH 3.0. Coexisting anions and dissolved oxygen in groundwater have little effect on V(V) removal. nZVI@LDH performed well across a wide pH range (3.0-8.0). The surface characterizations and XPS analysis revealed that LDH as supporting materials inhibited the aggregation and passivation of nZVI. The adsorbed V(V) was reduced to V(IV) and V(III) by nZVI and spontaneously transformed into insoluble VO and VO. The DFT calculations indicated the strong complexation and better stability of the V(IV) and V(III) species with nZVI@LDH than V(V). This work suggests that nZVI@LDH has the potential to serve as an efficient material for the immobilization of V(V) in groundwater.

摘要

为降低钒(V)[V(V)]的毒性并抑制地下水中吸附态钒的解吸,我们合成了纳米零价铁(nZVI)分散在层状双氢氧化物(LDH)复合材料(nZVI@LDH)上,以去除模拟地下水中的 V(V)。我们发现 nZVI@LDH 可以将高价态钒还原为低价态钒,然后形成含钒沉淀,从而降低毒性并抑制钒返回地下水。SEM 和 XRD 表征显示 nZVI 在 LDH 表面均匀分散。当 nZVI/LDH 的质量比为 1:2 时,nZVI@LDH 的最大吸附容量为 93.7mg/g,pH 值为 3.0。地下水中共存的阴离子和溶解氧对 V(V)的去除影响不大。nZVI@LDH 在较宽的 pH 范围内(3.0-8.0)表现良好。表面特性和 XPS 分析表明,LDH 作为支撑材料抑制了 nZVI 的聚集和钝化。吸附的 V(V)被 nZVI 还原为 V(IV)和 V(III),并自发转化为不溶性 VO 和 VO。DFT 计算表明,与 V(V)相比,V(IV)和 V(III)物种与 nZVI@LDH 的强络合作用和更好的稳定性。这项工作表明,nZVI@LDH 有可能成为固定地下水中 V(V)的有效材料。

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