Shi Zhihong, Hu Junda, Li Qi, Zhang Shulan, Liang Yuhuan, Zhang Hongyi
College of Chemistry and Environmental Science, Hebei University, Key Laboratory of Analytical Science and Technology of Hebei Province, Baoding 071002, China.
College of Chemistry and Environmental Science, Hebei University, Key Laboratory of Analytical Science and Technology of Hebei Province, Baoding 071002, China.
J Chromatogr A. 2014 Aug 15;1355:219-27. doi: 10.1016/j.chroma.2014.05.085. Epub 2014 Jun 12.
In this paper, graphene, a new sorbent material, was synthesized and used for solid-phase extraction (SPE) of the six carbamate pesticides (pirimicarb, baygon, carbaryl, isoprocarb, baycarb and diethofencarb) in environmental water samples. The target analytes can be extracted on the graphene-packed SPE cartridge, and then eluted with acetone. The eluate was collected and dried by high purity nitrogen gas at room temperature. 1mL of 20% (v/v) acetonitrile aqueous solution was used to redissolve the residue. The final sample solution was analyzed by ultra performance liquid chromatography-tandem quadrupole mass spectrometry (UPLC-MS/MS) system. Under optimum conditions, good linearity was obtained for the carbamates with correlation coefficient in the range of 0.9992-0.9998. The limits of detection (S/N=3) for the six carbamate pesticides were in the range of 0.5-6.9ngL(-1). Relative standard deviations (RSD) for five replicate determinations were below 5.54%. RSD values for cartridge-to-cartridge precision (n=7) were in the range of 1.27-8.13%. After proper regeneration, the graphene-packed SPE cartridge could be re-used over 100 times for standard solution without significant loss of performance. The enrichment factors for the target analytes were in the range of 34.2-51.7. The established method has been successfully applied to the determination of carbamate pesticide residues in environmental water samples such as river water, well water and lake water.
在本文中,合成了一种新型吸附剂材料石墨烯,并将其用于环境水样中六种氨基甲酸酯类农药(抗蚜威、残杀威、西维因、异丙威、恶虫威和乙霉威)的固相萃取(SPE)。目标分析物可在填充有石墨烯的SPE柱上进行萃取,然后用丙酮洗脱。收集洗脱液,在室温下用高纯氮气吹干。用1mL 20%(v/v)乙腈水溶液重新溶解残留物。最终样品溶液通过超高效液相色谱-串联四极杆质谱(UPLC-MS/MS)系统进行分析。在最佳条件下,氨基甲酸酯类农药具有良好的线性,相关系数在0.9992 - 0.9998范围内。六种氨基甲酸酯类农药的检测限(S/N = 3)在0.5 - 6.9 ngL⁻¹范围内。五次重复测定的相对标准偏差(RSD)低于5.54%。柱间精密度(n = 7)的RSD值在1.27 - 8.13%范围内。经过适当再生后,填充有石墨烯的SPE柱可重复使用100多次来分析标准溶液,且性能无明显损失。目标分析物的富集因子在34.2 - 51.7范围内。所建立的方法已成功应用于河水、井水和湖水等环境水样中氨基甲酸酯类农药残留的测定。