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Determination of dissolved oxygen based on photoinduced electron transfer from quantum dots to methyl viologen

机译:基于光致电子从量子点转移到甲基紫精中的溶解氧的测定

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A rapid colorimetric methodology based on photoinduced electron transfer from excited CdS quantum dots (CdS QDs) to methyl viologen (MV~(2+)) has been developed for the sensitive determination of dissolved oxygen (DO) content. The reduction of MV~(2+) is initiated by light excitation of CdS QDs, which induces the electron transfer from sacrificial donor glutathione (GSH) to the photogenerated hole of CdS QDs. Due to the presence of oxygen, the reduced radical-cation of methyl viologen (MV~(+·)) could be rapidly reoxidized, thus turning into the original methyl viologen dication (MV~(2+)). The existence of MV~(+·) is confirmed by electron paramagnetic resonance technique. This proposed colorimetric methodology has been applied to quantify the concentration of DO in real water samples. The result is consistent with the value obtained while adopting the traditional standard Winkler's methodology. A linear response of the absorbance of CdS QDs-GSH-MV system to the different concentrations of DO is obtained in the range of 0.75~7.95 ppm, with a detection limit of 0.23 ppm in pH 7.5.
机译:为了灵敏地确定溶解氧(DO)的含量,已开发出一种基于光敏电子从激发的CdS量子点(CdS QDs)转移至甲基紫精(MV〜(2+))的快速比色法。 MV〜(2+)的还原是由CdS QDs的光激发引发的,它诱导电子从牺牲供体谷胱甘肽(GSH)转移到CdS QDs的光生空穴。由于存在氧,还原后的甲基紫精自由基(MV〜(+·))可以迅速被再氧化,从而转变为原始的甲基紫精指示剂(MV〜(2+))。 MV〜(+·)的存在通过电子顺磁共振技术得以证实。该拟议的比色方法已用于量化真实水样中溶解氧的浓度。结果与采用传统标准Winkler方法获得的价值一致。 CdS QDs-GSH-MV系统的吸光度对不同浓度DO的线性响应在0.75〜7.95 ppm范围内,pH 7.5下的检出限为0.23 ppm。

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