Department of Chemistry, College of Basic Sciences, Agricultural University of Hebei, Baoding, Hebei, China.
Talanta. 2013 May 15;109:133-40. doi: 10.1016/j.talanta.2013.02.008. Epub 2013 Feb 8.
In this study, a magnetic microsphere-confined graphene (Fe3O4@SiO2-G) was prepared as a novel adsorbent for the preconcentration of some phthalate esters in environmental water and soybean milk samples prior to high performance liquid chromatography analysis. The properties and morphology of the Fe3O4@SiO2-G were characterized by transmission electron microscopy and X-ray diffraction. This novel graphene-based magnetic nanocomposite showed great adsorptive ability toward the analytes. The method, which takes the advantages of both the high adsorption capacity of G and easy phase separation of the magnetic adsorbent from the sample solution, could avoid the time-consuming experimental procedures related to the traditional solid phase extraction. Various experimental parameters that could affect the extraction efficiencies, such as the amount of Fe3O4@SiO2-G, the extraction time, the pH of sample solution and the desorption conditions, were investigated. Under the optimum conditions, the limits of detection (S/N=3) of the method for the compounds were between 0.07 and 0.10 ng mL(-1) in water samples, and between 0.15 and 0.30 ng mL(-1) in soybean milk samples. The relative standard deviations (RSDs) varied from 2.7% to 6.1% (n=5). The recoveries of the method were in the range between 87.2% and 109.0% for environmental water and soybean milk samples. The method is suitable to determine the five phthalate esters (diallyl phthalate, di-n-propyl-phthalate, benzyl butyl phthalate, dicyclohexyl-phthalate and diethyl-hexyl-phthalate) in environmental water and soybean milk samples.
在这项研究中,制备了一种磁性微球限制的石墨烯(Fe3O4@SiO2-G),作为一种新型吸附剂,用于高效液相色谱分析前环境水样和豆浆样品中一些邻苯二甲酸酯的预浓缩。通过透射电子显微镜和 X 射线衍射对 Fe3O4@SiO2-G 的性质和形态进行了表征。这种新型基于石墨烯的磁性纳米复合材料对分析物表现出很强的吸附能力。该方法结合了 G 的高吸附能力和磁性吸附剂从样品溶液中易于分离的优点,可以避免与传统固相萃取相关的耗时实验程序。研究了各种可能影响萃取效率的实验参数,如 Fe3O4@SiO2-G 的用量、萃取时间、样品溶液的 pH 值和洗脱条件。在最佳条件下,该方法对水中化合物的检测限(S/N=3)在 0.07 和 0.10ng mL(-1)之间,在豆浆样品中在 0.15 和 0.30ng mL(-1)之间。方法的相对标准偏差(RSD)在 2.7%至 6.1%(n=5)之间变化。该方法对环境水样和豆浆样品中五种邻苯二甲酸酯(邻苯二甲酸二烯丙酯、邻苯二甲酸二正丙酯、邻苯二甲酸苄丁酯、邻苯二甲酸二环己酯和邻苯二甲酸二乙酯)的回收率在 87.2%至 109.0%之间。该方法适用于测定环境水样和豆浆样品中的五种邻苯二甲酸酯(邻苯二甲酸二烯丙酯、邻苯二甲酸二正丙酯、邻苯二甲酸苄丁酯、邻苯二甲酸二环己酯和邻苯二甲酸二乙酯)。