Nojavan Saeed, Bidarmanesh Tina, Memarzadeh Farkhondeh, Chalavi Soheila
Faculty of Chemistry, Shahid Beheshti University, Tehran, Iran.
Electrophoresis. 2014 Sep;35(17):2446-53. doi: 10.1002/elps.201400072. Epub 2014 Aug 6.
A simple electromembrane extraction (EME) procedure combined with ion chromatography (IC) was developed to quantify inorganic anions in different pure water samples and water miscible organic solvents. The parameters affecting extraction performance, such as supported liquid membrane (SLM) solvent, extraction time, pH of donor and acceptor solutions, and extraction voltage were optimized. The optimized EME conditions were as follows: 1-heptanol was used as the SLM solvent, the extraction time was 10 min, pHs of the acceptor and donor solutions were 10 and 7, respectively, and the extraction voltage was 15 V. The mobile phase used for IC was a combination of 1.8 mM sodium carbonate and 1.7 mM sodium bicarbonate. Under these optimized conditions, all anions had enrichment factors ranging from 67 to 117 with RSDs between 7.3 and 13.5% (n = 5). Good linearity values ranging from 2 to 1200 ng/mL with coefficients of determination (R(2) ) between 0.987 and 0.999 were obtained. The LODs of the EME-IC method ranged from 0.6 to 7.5 ng/mL. The developed method was applied to different samples to evaluate the feasibility of the method for real applications.
开发了一种结合离子色谱(IC)的简单电膜萃取(EME)方法,用于定量分析不同纯水样品和与水混溶的有机溶剂中的无机阴离子。对影响萃取性能的参数进行了优化,如支撑液膜(SLM)溶剂、萃取时间、供体和受体溶液的pH值以及萃取电压。优化后的EME条件如下:使用正庚醇作为SLM溶剂,萃取时间为10分钟,受体和供体溶液的pH值分别为10和7,萃取电压为15V。IC使用的流动相是1.8 mM碳酸钠和1.7 mM碳酸氢钠的混合物。在这些优化条件下,所有阴离子的富集因子在67至117之间,相对标准偏差(RSD)在7.3%至13.5%之间(n = 5)。获得了2至1200 ng/mL的良好线性值,测定系数(R²)在0.987至0.999之间。EME-IC方法的检测限在0.6至7.5 ng/mL之间。将所开发的方法应用于不同样品,以评估该方法在实际应用中的可行性。