Hosoda Akihiro, Tsuyoshi Akira, Akiba Kenichi
Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, Katahira-2, Aoba, Sendai 980-8577, Japan.
Anal Sci. 2002 Aug;18(8):897-901. doi: 10.2116/analsci.18.897.
The capability of high-speed countercurrent chromatography (HSCCC) has been investigated for enrichment and determination of metal ions at trace levels. Separation of selected divalent metal ions was performed using a small coiled column. A hexane solution of 2-ethylhexylphosphonic acid mono-2-ethylhexyl ester (EHPA) was employed as the stationary phase. Loaded divalent metal ions such as Ni, Co, Cu, and Zn were chromatographically eluted in the order of increasing extractability by passing a mobile phase buffered at a desired pH. Individual metal ions showed good linearity between concentrations and chromatographic peak areas of the absorbance, as detected by postcolumn reaction with 4-(2-pyridylazo)resorcinol (PAR). Metal ions enriched into the stationary phase from a sample solution were separated into individual metal ions. The trace quantity of zinc in natural mineral water was determined by enrichment separation through an HSCCC column.
已对高速逆流色谱法(HSCCC)富集和测定痕量金属离子的能力进行了研究。使用小型盘管柱对选定的二价金属离子进行分离。以2-乙基己基膦酸单2-乙基己酯(EHPA)的己烷溶液作为固定相。通过使处于所需pH值缓冲的流动相通过,使负载的二价金属离子(如Ni、Co、Cu和Zn)按照萃取率增加的顺序进行色谱洗脱。通过与4-(2-吡啶偶氮)间苯二酚(PAR)进行柱后反应检测,各个金属离子在浓度与吸光度的色谱峰面积之间显示出良好的线性关系。从样品溶液中富集到固定相中的金属离子被分离成单个金属离子。通过HSCCC柱的富集分离测定了天然矿泉水中痕量的锌。