利用掺杂 N 的碳量子点和分子内电荷转移效应检测谷物中的甲草胺

Jinchen Wang, Liyuan Zhang, Runzhong Yu
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引用次数: 0

摘要

本文采用水热法在碳量子点(N-CQDs)中掺入氮元素,用于快速检测谷物中的甲草胺。然后分别利用透射电子显微镜、X 射线光电子能谱和荧光光谱分析和研究了 N-CQDs 的形态特征、元素组成和光学性质。根据分子内电荷转移原理,构建了一种快速检测甲草胺的荧光探针。在最佳实验条件下,当甲草胺浓度在 0.0125-2.5 μg mL-1 范围内时,N-CQDs 的荧光强度变化值与甲草胺浓度具有良好的线性关系。该方法的选择性、重现性和稳定性良好,检出限为 1.63 μg kg-1,定量限为 3.92 μg kg-1。采用加标回收率测定法检测了6个实际样品的加标回收率,加标回收率范围为105.05%~87.13%,相对标准偏差(n=3)为4.62%~0.61%,表明该方法可用于实际样品的检测,具有良好的精密度和稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metolachlor Detection in Grain Using N‐Doped Carbon Quantum Dots and the Intramolecular Charge Transfer Effect
Herein, nitrogen is doped into carbon quantum dots (N‐CQDs) using a hydrothermal method for the rapid detection of metolachlor in grain. The morphological features, elemental compositions, and optical properties of the N‐CQDs are then analyzed and investigated using transmission electron microscopy, X‐ray photoelectron spectroscopy, and fluorescence spectroscopy, respectively. Based on the principle of intramolecular charge transfer, a fluorescent probe is constructed for the rapid detection of metolachlor. Under optimal experimental conditions, the fluorescence intensity change values of the N‐CQDs and metolachlor concentration have a good linear relationship when the concentration of metolachlor is in the range of 0.0125−2.5 μg mL−1. An evaluation of the method shows that the method has good selectivity, reproducibility, and stability, with a limit of detection of 1.63 μg kg−1 and a limit of quantification of 3.92 μg kg−1. The spiked recoveries of six real samples are tested using a spiked recovery assay that yielded spiked recoveries in the range of 105.05−87.13%, and their relative standard deviations (n = 3) ranged from 4.62% to 0.61%, indicating that the method can be used for detection in actual samples with good precision and stability.
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