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Quantitative P-31 NMR for Simultaneous Trace Analysis of Organophosphorus Pesticides in Aqueous Media Using the Stir Bar Sorptive Extraction Method

机译:搅拌棒吸附萃取法同时定量分析水介质中有机磷农药的定量P-31 NMR

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摘要

The analysis of pesticides in water samples is of primary concern for quality control laboratories due to the toxicity of these compounds and their associated public health risk. A novel analytical method based on stir bar sorptive extraction (SBSE), followed by P-31 quantitative nuclear magnetic resonance (P-31 QNMR), has been developed for simultaneously monitoring and determining four organophosphorus pesticides (OPPs) in aqueous media. The effects of factors on the extraction efficiency of OPPs were investigated using a Draper-Lin small composite design. An optimal sample volume of 4.2 mL, extraction time of 96 min, extraction temperature of 42A degrees C, and desorption time of 11 min were obtained. The results showed reasonable linearity ranges for all pesticides with correlation coefficients greater than 0.9920. The limit of quantification (LOQ) ranged from 0.1 to 2.60 mg/L, and the recoveries of spiked river water samples were from 82 to 94% with relative standard deviation (RSD) values less than 4%. The results show that this method is simple, selective, rapid, and can be applied to other sample matrices.
机译:由于水样中农药的毒性及其相关的公共健康风险,因此水质样品中农药的分析是质量控制实验室的主要关注点。已经开发了一种基于搅拌棒吸附萃取(SBSE),然后进行P-31定量核磁共振(P-31 QNMR)的新颖分析方法,用于同时监测和测定水性介质中的四种有机磷农药(OPP)。使用Draper-Lin小型复合设计研究了因素对OPP提取效率的影响。最佳样品体积为4.2 mL,萃取时间为96分钟,萃取温度为42A摄氏度,解吸时间为11分钟。结果表明,所有农药的相关系数均大于0.9920,具有合理的线性范围。定量限(LOQ)为0.1至2.60 mg / L,加标河水样品的回收率为82至94%,相对标准偏差(RSD)值小于4%。结果表明,该方法简单,选择性,快速,可用于其他样品基质。

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