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A proof-of-concept fluorescent strategy for highly selective detection of Cr(vi) based on inner filter effect using a hydrophilic ionic chemosensor

机译:基于亲水离子化学传感器基于内部滤光效应的高选择性检测Cr(vi)的概念验证荧光策略

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摘要

In this article, a facile and versatile strategy for highly selective detection of Cr(vi) in 100% aqueous solution was developed based on fluorescence inner filter effect (IFE) using a hydrophilic ionic chemosensor. In the presence of Cr(vi), remarkable fluorescence quenching of the chemosensor could be observed because of the strong absorption of Cr(vi) to both the excitation and emission light of the fluorophore (in this work, acridine was chosen as the model fluorophore). By utilizing the modified Benesi-Hildebrand equation, not only was the efficiency of IFE quantitatively calculated, but also the calibration curve used for Cr(vi) determination was vastly broadened. A linear range of 5.0 × 10~(-6) to 1.4 × 10~(-3) M for Cr(vi), along with a detection limit of 8.9 × 10~(-7) M and a RSD of 3.6% at 2.5 × 10~(-5) M in 100% aqueous solution were obtained. In addition, the detection limit could be as low as 9,2 × 10~(-8) M in MeCN aqueous solution. Meanwhile, the present method possesses an excellent selectivity for Cr(vi) detection. It was also successfully applied in Cr(vi)-spiked tap water samples and wastewater samples.
机译:在本文中,使用亲水性离子化学传感器,基于荧光内部过滤效应(IFE),开发了一种简便,通用的策略,可选择性地检测100%水溶液中的Cr(vi)。在存在Cr(vi)的情况下,由于Cr(vi)对荧光团的激发光和发射光都有很强的吸收,因此可以观察到化学传感器的荧光猝灭(在这项工作中,选择,啶为模型荧光团)。通过使用改进的Benesi-Hildebrand方程,不仅可以定量计算IFE的效率,而且可以大大拓宽用于Cr(vi)测定的校准曲线。 Cr(vi)的线性范围为5.0×10〜(-6)至1.4×10〜(-3)M,检出限为8.9×10〜(-7)M,RSD为3.6%得到2.5×10〜(-5)M的100%水溶液。另外,在MeCN水溶液中的检出限可低至9.2×10〜(-8)M。同时,本方法对于Cr(vi)检测具有极好的选择性。它也已成功应用于加标六价铬的自来水样品和废水样品中。

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