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用于去除马里亚纳矿难后污染河水中 Cr(VI)和 Pb(II)的氧化铁纳米材料。

Iron Oxide Nanomaterials for the Removal of Cr(VI) and Pb(II) from Contaminated River After Mariana Mining Disaster.

机构信息

Instituto de Ciência, Engenharia e Tecnologia, Universidade Federal dos Vales do Jequitinhonha e Mucuri, 39803-371 Teófilo Otoni, Minas Gerais, Brazil.

Centro de Ciências Naturais e Humanas, Universidade Federal do ABC, 09210-580 Santo André, São Paulo, Brazil.

出版信息

J Nanosci Nanotechnol. 2021 Mar 1;21(3):1711-1720. doi: 10.1166/jnn.2021.19089.

Abstract

If not properly treated, water contaminated with chromium (Cr(VI)) and lead (Pb(II)) can cause severe damage to health due to the accumulation of those toxic metals in the human body. Therefore, in this work, three iron oxides, i.e., δ-FeOOH, cystine-functionalized δ-FeOOH (Cys-δ-FeOOH), and Fe₃O₄, were synthesized and used as adsorbents for Cr(VI) and Pb(II) in water. The results indicated that the Cr(VI) is best adsorbed on cys-δ-FeOOH followed by δ-FeOOH and Fe₃O₄. It was because of the enhanced interaction between Cr(VI) and the cysteine functional groups on the δ-FeOOH surface. The Cr(VI) adsorption capacity of cys-δ-FeOOH, δ-FeOOH, and Fe₃O₄ was 217, 14, and 8 mg g, respectively. On the other hand, Pb(II) was preferentially adsorbed directly on δ-FeOOH achieving a maximum Pb(II) adsorption capacity of 174 mg g. The Pb(II) adsorption capacity of cys-δ-FeOOH and Fe₃O₄ was 97 and 74 mg g, respectively. The Cr(VI) adsorption on cys-δ-FeOOH was best described by the Langmuir-Freundlich model, whereas Pb(II) adsorption on δ-FeOOH followed the Langmuir model. Both Cr(VI) and Pb(II) adsorption on the adsorbents was well-fitted to pseudo-second-order kinetics. The Cr(VI) was more quickly adsorbed by cys-δ-FeOOH ( = 0.10 mg g min) while the initial adsorption rate of Pb(II) onto δ-FeOOH was significantly faster ( = 16.34 mg g min). Finally, the synthesized adsorbents were efficient to remove Cr(VI) and Pb(II) from water samples of the Doce river after the environmental disaster of Mariana city, Brazil, thus showing its applicability to remediate real water samples.

摘要

如果得不到妥善处理,受铬(Cr(VI))和铅(Pb(II))污染的水会因这些有毒金属在人体内积累而对健康造成严重损害。因此,在这项工作中,我们合成了三种氧化铁,即 δ-FeOOH、半胱氨酸功能化的 δ-FeOOH(Cys-δ-FeOOH)和 Fe₃O₄,并将其用作水中 Cr(VI) 和 Pb(II) 的吸附剂。结果表明,Cr(VI) 在 Cys-δ-FeOOH 上的吸附效果最好,其次是 δ-FeOOH 和 Fe₃O₄。这是因为 Cr(VI) 与 δ-FeOOH 表面的半胱氨酸官能团之间的相互作用得到了增强。Cys-δ-FeOOH、δ-FeOOH 和 Fe₃O₄ 的 Cr(VI) 吸附容量分别为 217、14 和 8 mg g。另一方面,Pb(II) 优先直接吸附在 δ-FeOOH 上,达到最大的 Pb(II) 吸附容量 174 mg g。Cys-δ-FeOOH 和 Fe₃O₄ 的 Pb(II) 吸附容量分别为 97 和 74 mg g。Cys-δ-FeOOH 对 Cr(VI) 的吸附最符合 Langmuir-Freundlich 模型,而 δ-FeOOH 对 Pb(II) 的吸附符合 Langmuir 模型。Cr(VI) 和 Pb(II) 在吸附剂上的吸附都很好地符合准二级动力学模型。Cr(VI) 更容易被 Cys-δ-FeOOH 吸附(= 0.10 mg g min),而 Pb(II) 初始吸附到 δ-FeOOH 上的速率明显更快(= 16.34 mg g min)。最后,这些合成的吸附剂对巴西马里亚纳城环境灾难后多西河水中的 Cr(VI) 和 Pb(II) 进行了有效去除,因此表明其可用于修复实际水样。

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