Rahmani Mashaallah, Kaykhaii Massoud, Ghasemi Elham, Tahernejad Mohadeseh
Department of Chemistry, Faculty of Sciences, University of Sistan and Baluchestan, Zahedan 98135-674, Iran
Department of Chemistry, Faculty of Sciences, University of Sistan and Baluchestan, Zahedan 98135-674, Iran.
J Chromatogr Sci. 2015 Aug;53(7):1210-6. doi: 10.1093/chromsci/bmu163. Epub 2015 Jan 16.
Two new simple and effective methods based on dispersive liquid-liquid microextraction (DLLME) procedure, termed "in-syringe DLLME (IS-DLLME)" and "narrow-bore tube DLLME (NB-DLLME)", were developed and applied for rapid and simultaneous separation and preconcentration of trace amounts of benzene, toluene, ethylbenzene and xylene isomers in water samples followed by gas chromatographic analysis. Different parameters influencing the extraction efficiency of both methods such as type and volume of the extraction solvent and the disperser solvent; pH, temperature and volume of sample solution and ionic strength of samples were investigated and optimized. Under optimal condition, the limits of detection ranged from 1.7 to 2.4 µg L(-1) for IS-DLLME and 1.5 to 2.2 µg L(-1) for NB-DLLME. Precision (as relative standard deviation) of the two techniques was between 2.1 and 4.6% for IS-DLLME and between 1.5 and 4.5% for NB-DLLME. The enrichment factors found to be between 20-29 and 31-73 for IS- and NB-DLLME, respectively. The applicability of the proposed methods was investigated by analyzing real water samples.
基于分散液液微萃取(DLLME)技术开发了两种新的简单有效的方法,即“注射器内DLLME(IS-DLLME)”和“窄孔管DLLME(NB-DLLME)”,并将其应用于水样中痕量苯、甲苯、乙苯和二甲苯异构体的快速同时分离和预富集,随后进行气相色谱分析。研究并优化了影响两种方法萃取效率的不同参数,如萃取溶剂和分散剂溶剂的类型和体积;样品溶液的pH值、温度和体积以及样品的离子强度。在最佳条件下,IS-DLLME的检测限为1.7至2.4 μg L(-1),NB-DLLME的检测限为1.5至2.2 μg L(-1)。两种技术的精密度(相对标准偏差),IS-DLLME为2.1%至4.6%,NB-DLLME为1.5%至4.5%。发现IS-DLLME和NB-DLLME的富集因子分别在20-29和31-73之间。通过分析实际水样研究了所提出方法的适用性。