University of Cumhuriyet, Faculty of Science, Department of Chemistry, TR-58140, Sivas, Turkey.
Anal Chim Acta. 2011 Oct 10;703(2):137-44. doi: 10.1016/j.aca.2011.07.026. Epub 2011 Jul 23.
Cloud point extraction (CPE) methodology has successfully been employed for the preconcentration of ultra-trace arsenic species in aqueous samples prior to hydride generation atomic absorption spectrometry (HGAAS). As(III) has formed an ion-pairing complex with Pyronine B in presence of sodium dodecyl sulfate (SDS) at pH 10.0 and extracted into the non-ionic surfactant, polyethylene glycol tert-octylphenyl ether (Triton X-114). After phase separation, the surfactant-rich phase was diluted with 2 mL of 1M HCl and 0.5 mL of 3.0% (w/v) Antifoam A. Under the optimized conditions, a preconcentration factor of 60 and a detection limit of 0.008 μg L(-1) with a correlation coefficient of 0.9918 was obtained with a calibration curve in the range of 0.03-4.00 μg L(-1). The proposed preconcentration procedure was successfully applied to the determination of As(III) ions in certified standard water samples (TMDA-53.3 and NIST 1643e, a low level fortified standard for trace elements) and some real samples including natural drinking water and tap water samples.
浊点萃取(CPE)方法已成功应用于氢化物发生原子吸收光谱法(HGAAS)前水样中超痕量砷形态的预富集。在 pH 值为 10.0 时,As(III)与十二烷基硫酸钠(SDS)形成离子对配合物,并在非离子表面活性剂聚乙二醇辛基苯基醚(Triton X-114)中被萃取。分相后,用 2 mL 1M HCl 和 0.5 mL 3.0%(w/v)的消泡剂 A 稀释富含表面活性剂的相。在优化条件下,校准曲线范围为 0.03-4.00 μg L(-1)时,可获得 60 的富集因子和 0.008 μg L(-1)的检测限,相关系数为 0.9918。该预富集程序成功应用于测定认证标准水样(TMDA-53.3 和 NIST 1643e,微量元素低水平强化标准)和一些实际样品中的 As(III)离子,包括天然饮用水和自来水样品。