Yokota Kuriko, Fukushi Keiichi, Ishio Nobuhiro, Sasayama Nobukazu, Nakayama Yusuke, Takeda Sahori, Wakida Shin-Ichi
Research Institute for Marine Cargo Transportation, Kobe University of Mercantile Marine, Kobe, Japan.
College of Analytical Chemistry, Osaka, Japan.
Electrophoresis. 2003 Jun;24(12-13):2244-2251. doi: 10.1002/elps.200305420.
We describe an application of capillary zone electrophoresis (CZE) with transient isotachophoresis (ITP) as the on-line concentration procedure for the determination of iodide in seawater. The effective mobility of iodide was decreased by the addition of 10 mM cetyltrimethylammonium chloride (CTAC) to an artificial seawater background electrolyte (BGE) so that transient ITP functioned and iodide was separated from other coexisting anions such as bromide, nitrite, and nitrate in seawater samples. After sample injection, 600 mM acetate was separately injected into the capillary as the terminating ion to generate transient ITP. The limit of detection (LOD) for iodide was 3.0 microg/L. The LOD was obtained at a signal-to-noise ratio (S/N) of 3. The values of the relative standard deviation (RSD) of peak area, peak height, and migration time for iodide were 2.9, 2.1, and 0.6%. The proposed method was applied to the determination of iodide in seawater collected around the Osaka Bay. The results obtained by use of the calibration graph were agreed with those obtained by the addition of the standard solutions for iodide.
我们描述了一种将毛细管区带电泳(CZE)与瞬态等速电泳(ITP)联用作为在线浓缩方法来测定海水中碘化物的应用。通过向人工海水背景电解质(BGE)中添加10 mM十六烷基三甲基氯化铵(CTAC),碘化物的有效迁移率降低,从而使瞬态ITP发挥作用,碘化物得以与海水中其他共存阴离子(如溴化物、亚硝酸盐和硝酸盐)分离。进样后,将600 mM乙酸盐作为终止离子单独注入毛细管中以产生瞬态ITP。碘化物的检测限(LOD)为3.0 μg/L。该检测限是在信噪比(S/N)为3时获得的。碘化物峰面积、峰高和迁移时间的相对标准偏差(RSD)值分别为2.9%、2.1%和0.6%。所提出的方法应用于大阪湾周边采集的海水中碘化物的测定。使用校准曲线获得的结果与添加碘化物标准溶液获得的结果一致。