Department of Chemistry, Faculty of Sciences, Ferdowsi University of Mashhad, Iran.
J Adv Res. 2015 Nov;6(6):957-66. doi: 10.1016/j.jare.2014.10.010. Epub 2014 Nov 8.
Surfactant-enhanced hollow fiber liquid phase (SE-HF-LPME) microextraction was applied for the extraction of melamine in conjunction with high performance liquid chromatography with UV detection (HPLC-UV). Sodium dodecyl sulfate (SDS) was added firstly to the sample solution at pH 1.9 to form hydrophobic ion-pair with protonated melamine. Then the protonated melamine-dodecyl sulfate ion-pair (Mel-DS) was extracted from aqueous phase into organic phase immobilized in the pores and lumen of the hollow fiber. After extraction, the analyte-enriched 1-octanol was withdrawn into the syringe and injected into the HPLC. Preliminary, one variable at a time method was applied to select the type of extraction solvent. Then, in screening step, the other variables that may affect the extraction efficiency of the analyte were studied using a fractional factorial design. In the next step, a central composite design was applied for optimization of the significant factors having positive effects on extraction efficiency. The optimum operational conditions included: sample volume, 5 mL; surfactant concentration, 1.5 mM; pH 1.9; stirring rate, 1500 rpm and extraction time, 60 min. Using the optimum conditions, the method was analytically evaluated. The detection limit, relative standard deviation and linear range were 0.005 μg mL(-1), 4.0% (3 μg mL(-1), n = 5) and 0.01-8 μg mL(-1), respectively. The performance of the procedure in extraction of melamine from the soil samples was good according to its relative recoveries in different spiking levels (95-109%).
表面活性剂强化中空纤维液相微萃取(SE-HF-LPME)与高效液相色谱法-紫外检测(HPLC-UV)联用,用于提取三聚氰胺。首先在 pH 值为 1.9 的样品溶液中加入十二烷基硫酸钠(SDS),与质子化的三聚氰胺形成疏水离子对。然后,质子化的三聚氰胺-十二烷基硫酸离子对(Mel-DS)从水相萃取到固定在中空纤维孔和内腔中的有机相中。萃取后,将富含分析物的 1-辛醇吸入注射器并注入 HPLC。初步采用单变量法选择萃取溶剂的类型。然后,在筛选步骤中,使用部分因子设计研究可能影响分析物萃取效率的其他变量。下一步,采用中心组合设计优化对萃取效率有积极影响的显著因素。最佳操作条件包括:样品体积,5 mL;表面活性剂浓度,1.5 mM;pH 值 1.9;搅拌速度,1500 rpm;萃取时间,60 min。在最佳条件下,对该方法进行了分析评价。检测限、相对标准偏差和线性范围分别为 0.005 μg mL(-1)、4.0%(3 μg mL(-1),n=5)和 0.01-8 μg mL(-1)。根据不同添加水平的相对回收率(95-109%),该程序在土壤样品中提取三聚氰胺的性能良好。