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苯并三唑修饰氧化石墨烯用于高效去除 U(VI)。

Benzotriazole decorated graphene oxide for efficient removal of U(VI).

机构信息

College of Chemistry, Sichuan University, Chengdu, 610064, China.

College of Chemistry and Material Science, Sichuan Normal University, Chengdu, 610066, China.

出版信息

Environ Pollut. 2019 Oct;253:221-230. doi: 10.1016/j.envpol.2019.06.109. Epub 2019 Jul 9.

DOI:10.1016/j.envpol.2019.06.109
PMID:31310872
Abstract

There is a need to develop highly efficient materials for capturing uranium from nuclear wastewater. Here, 5-methylbenzotriazole modified graphene oxide (MBTA-GO) was used to adsorb U(VI) from aqueous solution. By the trials of different conditions, we found that the removal of U(VI) from acidic solution was strongly dependent on pH but independent of ionic strength. The U(VI) adsorption was perfectly conformed to the pseudo-second-order kinetics and the adsorption isotherms were simulated by the Langmuir model well. A high removal capacity (q = 264 mg/g) for U(VI) at pH 3.5 was obtained. XPS, EXAFS analyses and DFT calculations revealed that the mechanism of uranium capture was ascribed to (i) the surface complexation by benzotriazole and carboxyl groups (providing lone pair electrons) on MBTA-GO and (ii) enhanced synergistic coordination ability of delocalized π-bond of triazole group toward U due to the transfer of electrons from graphene sheet to benzotriazole. DFT calculations further demonstrated that benzotriazole displayed stronger binding with U(VI) compared to carboxyl group due to higher binding energy of [Side/Surface-U-MBTA-GO] (79.745, 54.986 kcal/mol) than [MBTA-GO-COOH-U] (27.131 kcal/mol). This work will provide valuable insight into designing novel nitrogen-containing adsorbents for practical application in wastewater treatment.

摘要

需要开发高效的材料来从核废水中捕获铀。在这里,使用 5-甲基苯并三唑修饰的氧化石墨烯(MBTA-GO)从水溶液中吸附 U(VI)。通过不同条件的试验,我们发现从酸性溶液中去除 U(VI)强烈依赖于 pH 值,而与离子强度无关。U(VI)的吸附完全符合准二级动力学,吸附等温线很好地通过 Langmuir 模型进行模拟。在 pH 为 3.5 时,U(VI)的去除容量达到了 264 mg/g。XPS、EXAFS 分析和 DFT 计算表明,铀捕获的机制归因于:(i) 苯并三唑和 MBTA-GO 上的羧基(提供孤对电子)与表面的络合作用;(ii) 由于电子从石墨烯片转移到苯并三唑,三唑基团的离域π键对 U 的协同配位能力增强。DFT 计算进一步表明,苯并三唑与 U(VI)的结合比羧基更强,因为 [Side/Surface-U-MBTA-GO](79.745,54.986 kcal/mol)的结合能高于 [MBTA-GO-COOH-U](27.131 kcal/mol)。这项工作将为设计用于实际废水处理的新型含氮吸附剂提供有价值的见解。

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