基于量子点荧光探针的重金属离子Hg2+检测方法
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国家重点研发计划项目(2016YFD0800907)


Detection Method of Heavy Metal Ions Hg2+ Based on Quantum Dots Fluorescence Probe
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    摘要:

    以重金属离子Hg2+为研究对象,使用经过L半胱氨酸修饰的CdTe量子点溶液对Hg2+进行检测,Hg2+与表面采用修饰剂的量子点结合使得量子点发生荧光猝灭现象,Hg2+浓度与荧光猝灭的变化强度呈一定的线性关系,利用这种线性关系实现量子点对溶液中Hg2+含量的定量检测,检测波段为400~800nm。在优化条件下测得方法检出限为6.11×10-9mol/L (S/N=3,n=11),线性范围为9×10-9~5×10-6mol/L,相对标准偏差(RSD)为286%。在实验环境下,对特征波段进行变量标准化(SNV)预处理,再进行偏最小二乘(PLS) 建模分析,得到较好的自预测能力和实际预测能力,其中校正集的决定系数为0.8784,RMSEC为11.6313μmol/L,验证集的决定系数为0.7287,RMSEP为18.7174μmol/L。结果表明,实验建模效果良好,操作简单、方便,实验快速、可靠、无污染,表明利用量子点荧光探针检测 Hg2+方法可行。

    Abstract:

    The subject of this experiment was Hg2+, Hg2+ was detected by L cysteinemodified CdTe quantum dot solution, and Hg2+ was combined with the surfacemodified quantum dots to cause fluorescence quenching of quantum dots, Hg2+ concentration and fluorescence. The intensity of annihilation had a linear relationship. This linear relationship was used to quantitatively detect the Hg2+ content in the solution by quantum dots. The detection band was 400~800nm.The detection limit of the method under optimized conditions was 6.11×10-9mol/L (S/N=3, n=11), and the linear range was 9×10-9~5×10-6mol/L. The deviation (RSD) was 2.86%. In a certain experimental environment, the variable normalization (SNV) preprocessing of the characteristic band and the partial least squares (PLS) modeling analysis can obtain better selfprediction ability and actual prediction ability, and the determination coefficient of the correction set reached 0.8784. The standard deviation was 11.6313μmol/L, the determination coefficient of the validation set was 0.7287, and the standard deviation was 18.7174μmol/L. The results showed that the modeling effect was good, the operation was simple and convenient, the experiment was fast, reliable and nonpolluting, which indicated that the method of detecting Hg2+ by quantum dot fluorescent probe was feasible.

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漆明星,杨普,邹铃,孙明.基于量子点荧光探针的重金属离子Hg2+检测方法[J].农业机械学报,2019,50(Supp):195-199.

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  • 收稿日期:2019-04-21
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  • 在线发布日期: 2019-07-10
  • 出版日期: 2019-07-10