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冯露、侯浩波的论文在MICROPOROUS AND MESOPOROUS MATERIALS 刊出
发布时间:2021-11-04 17:44:44     发布者:易真     浏览次数:

标题: Post-functionalized metal-organic framework for effective and selective removal of Hg(II) in aqueous media

作者: Feng, L (Feng, Lu); Zeng, TY (Zeng, Tianyu); Hou, HB (Hou, Haobo)

来源出版物: MICROPOROUS AND MESOPOROUS MATERIALS : 328 文献号: 111479 DOI: 10.1016/j.micromeso.2021.111479 出版年: DEC 2021

摘要: For the serious hazards to human and natural environment caused by the toxic Hg(II), a new MOF-based adsorption material, UiO-66-AHMT, was designed and synthesized by incorporating the 4-amino-3-hydrazino5-mercapto-1,2,4-triazole molecule into the UiO-66-NH2 matrix and used for the removal of Hg(II) from aqueous media. As expected, UiO-66-AHMT exhibits rapid removal ability toward Hg(II) and maximum uptake capacity of 327.88 mg/g at 298 K and pH = 5, the adsorption capacity is improved significantly compared to the unmodified UiO-66-NH2 and comparable in the excellent UiO-66 based adsorbents reported so far. The adsorption behaviors of UiO-66-AHMT conform well to the pseudo-second-order and Langmuir models, respectively, which indicate that the adsorption process is mainly monolayer chemisorption. Meanwhile, UiO-66AHMT shows strong selectivity to Hg(II) in the coexistence of varieties of metal ions and outstanding recyclability characteristics. To investigate the adsorption mechanism, the Hg(II) loaded UiO-66-AHMT mainly analyzed by XPS suggests that the nitrogen-and sulfur-containing groups in grafted molecule have the synergistic complexation to Hg(II). Furthermore, the binding strength between different function sites and Hg(II) are quantified and the stable complexation patterns are obtained based on the DFT calculation. These results strongly confirm that UiO-66-AHMT is a potential adsorbent in the practical treatment of wastewater containing Hg(II).

作者关键词: UiO-66-AHMT; Maximum uptake capacity; Adsorption behaviors; Adsorption mechanism; DFT calculation

地址: [Feng, Lu; Zeng, Tianyu; Hou, Haobo] Wuhan Univ, Sch Resource & Environm Sci, Wuhan 430072, Hubei, Peoples R China.

[Feng, Lu; Zeng, Tianyu; Hou, Haobo] Wuhan Univ, Zhaoqing GD HK & MO Environ Technol Res INST, Zhaoqing, Guangdong, Peoples R China.

通讯作者地址: Hou, HB (通讯作者)Wuhan Univ, Sch Resource & Environm Sci, Wuhan 430072, Hubei, Peoples R China.

电子邮件地址: hhb-bhh@163.com

影响因子:5.455


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