Key Laboratory of Bioinorganic Chemistry, College of Science, Agricultural University of Hebei, Baoding 071001, Hebei, China.
J Chromatogr A. 2011 Nov 4;1218(44):7936-42. doi: 10.1016/j.chroma.2011.09.027. Epub 2011 Sep 16.
A graphene-based magnetic nanocomposite was synthesized and used for the first time as an effective adsorbent for the preconcentration of the five carbamate pesticides (metolcarb, carbofuran, pirimicarb, isoprocarb and diethofencarb) in environmental water samples prior to high performance liquid chromatography-diode array detection. The properties of the magnetic nanocomposite were characterized by scanning electron microscopy and X-ray diffraction. This novel graphene-based magnetic nanocomposite showed great adsorptive ability towards the analytes. The method, which takes the advantages of both nanoparticle adsorption and magnetic phase separation from the sample solution, could avoid some of the time-consuming experimental procedures related to the traditional solid phase extraction. Various experimental parameters that could affect the extraction efficiencies have been investigated. Under the optimum conditions, the enrichment factors of the method for the analytes were in the range from 474 to 868. A linear response was achieved in the concentration range of 0.1-50 ng mL(-1). The limits of detection of the method at a signal to noise ratio of 3 for the pesticides were 0.02-0.04 ng mL(-1). Compared with the dispersive liquid-liquid microextraction and the ultrasound-assisted surfactant-enhanced emulsification microextraction, much higher enrichment factors and sensitivities were achieved with the developed method. The method has been successfully applied for the determination of the carbamate pesticides in environmental water samples.
一种基于石墨烯的磁性纳米复合材料被合成,并首次被用作环境水样中五种氨基甲酸酯类农药(甲萘威、克百威、丙溴磷、异稻瘟净和二噻农)高效液相色谱-二极管阵列检测的预浓缩有效吸附剂。通过扫描电子显微镜和 X 射线衍射对磁性纳米复合材料的性质进行了表征。这种新型基于石墨烯的磁性纳米复合材料对分析物具有很强的吸附能力。该方法结合了纳米颗粒吸附和从样品溶液中磁性相分离的优点,可以避免一些与传统固相萃取相关的耗时实验步骤。研究了各种可能影响萃取效率的实验参数。在最佳条件下,该方法对分析物的富集因子范围为 474 至 868。在 0.1-50ng mL(-1)的浓度范围内得到了线性响应。该方法对农药的信噪比为 3 时的检出限为 0.02-0.04ng mL(-1)。与分散液-液微萃取和超声辅助表面活性剂增强乳液萃取相比,该方法获得了更高的富集因子和灵敏度。该方法已成功应用于环境水样中氨基甲酸酯类农药的测定。