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Hydrolytically Stable Luminescent Cationic Metal Organic Framework for Highly Sensitive and Selective Sensing of Chromate Anions in Natural Water Systems

机译:用于高敏感和选择性感应的水解稳定的发光阳离子金属有机框架,用于天然水系统中的铬酸盐阴离子

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摘要

Effective detection of chromate anions in aqueous solution is highly desirable because of their high solubility, environmental mobility, carcinogenicity, and bioaccumulation effect. A new strategy for precise detection of chromate anions in the presence of a large excess of other anions, such as Cl-, NO3-, and HCO3-, in drinking water and natural water systems remains a challenge. Herein, a hydrolytically stable cationic luminescent europium(III)-based metal organic framework (MOP), 1, was successfully synthesized and investigated as a luminescent sensor that exhibits instant and selective luminescence quenching properties toward chromate ions in aqueous solutions. Moreover, 1 can be introduced into high-ionic-strength water system (e.g., seawater) for chromate detection as a consequence of the excellent sensing selectivity. The real environmental application of 1 as a chromate probe is studied in deionized water, lake water, and seawater. The detection limits in these aqueous media are calculated to be 0.56, 2.88, and 1.75 ppb, respectively. All of these values are far below the maximum contamination standard of Cr(VI) in drinking water of 100 ppb, defined by the U.S. Environmental Protection Agency. This excellent chromate sensing capability originates from the fast enrichment of chromate ions in solids of 1 from solutions, followed by efficient energy transfer from the MOF skeleton to the chromate anion, as demonstrated by solution absorption spectroscopy, X-ray diffraction, and chromate uptake kinetics and isotherm investigations. To the best of our knowledge, 1 possesses the lowest chromate detection limit among all reported MOFs up to date and is the only MOF material reported for chromate sensing application under environmentally relevant conditions with high ionic strengths.
机译:由于其高溶解度,环境迁移率,致癌性和生物累积效应,高度理想地检测水溶液中铬酸盐阴离子的有效检测。在饮用水和天然水系统中,在大量的其​​他阴离子存在下精确地检测铬酸盐阴离子的新策略仍然是挑战。这里,成功地合成了水解稳定的阳离子发光铕(III)基础的金属有机骨架(MOP),1作为发光传感器,其表现出瞬间和选择性发光淬火性质,其致铬水溶液中的铬酸盐离子。此外,由于优异的感测选择性,可以将1引入高离子强度水系统(例如,海水)中,用于铬酸盐检测。在去离子水,湖水和海水中,研究了1作为铬酸盐探针的真实环境施用。将这些含水介质中的检测限制分别计算为0.56,2.88和1.75ppb。所有这些值远远低于100ppb饮用水中Cr(vi)的最大污染标准,由美国环境保护局定义。这种优异的铬酸盐感测能力来自溶液中的1个固体中的铬酸盐离子的快速富集,然后通过溶液吸收光谱,X射线衍射和铬酸盐摄取动力学证明,从MOF骨架到铬酸盐的有效能量转移和等温手续的调查。据我们所知,1个迄今为止拥有最低铬酸盐检测限,迄今为止,尚未在具有高离子强度的环境相关条件下进行铬酸盐传感施用的唯一MOF材料。

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