铀酰
三吡啶
化学
选择性
纳米纤维
水溶液中的金属离子
氢键
金属
发光
无机化学
分子间力
离子
化学工程
分子
纳米技术
有机化学
材料科学
催化作用
工程类
光电子学
作者
Seonae Lee,Ka Young Kim,Na Young Lim,Junoh Jung,Ji Ha Lee,Myong Yong Choi,Jong Hwa Jung
标识
DOI:10.1016/j.jhazmat.2019.05.106
摘要
Uranyl is a radioactive, toxic pollutant commonly found in the waste remaining after nuclear fuel reprocessing, and it poses several types of risks to human health; therefore, developing absorbents and chemical probes for this compound is crucial to overcoming these issues. This study examined the sensing abilities of terpyridine-appended benzenetricarboxyamide (T-BTA) as a chromogenic probe for detecting uranyl ions (UO22+). The complex with Eu3+ (1–Eu) spontaneously formed nanostructured fibers in H2O owing to the triamide groups of T-BTA, which induced intermolecular hydrogen-bonding interactions. The strong blue emission of these nanofibers in H2O was quenched upon adding UO22+ but not upon adding any other metal ion. This high selectivity was probably because of the interactions between the nitrigen atoms of the terpyridine moieties of 1 and UO22+. Furthermore, the 1–Eu nanofibers assumed spherical morphologies when UO22+ was added. To develop a convenient UO22+ sensor, an electrospun film incorporating 1–Eu (ESF–1–Eu) was manufactured, and it exhibited high selectivity for UO22+ over a variety of rival metal ions. The plot for luminescence change of ESF–1–Eu vs UO22+ concentrations in seawater samples showed a good linearty. Thus, the ESF–1–Eu shows potential as a useful sensor for detecting and removing UO22+ in H2O.
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