Fukushi Keiichi, Miyado Takashi, Ishio Nobuhiro, Nishio Hideaki, Saito Keiitsu, Takeda Sahori, Wakida Shin-ichi
Research Institute for Marine Cargo Transportation, Kobe University of Mercantile Marine, Kobe, Japan.
Electrophoresis. 2002 Jun;23(12):1928-34. doi: 10.1002/1522-2683(200206)23:12<1928::AID-ELPS1928>3.0.CO;2-K.
We describe a combination of selected ions as a terminating ion which is useful for transient isotachophoresis (ITP) in capillary zone electrophoresis (CZE) for the determination of nitrite and nitrate in seawater. In addition to 150 mM sulfate as the principal terminating ion, 10 mM bromate was added to a sample solution as the additional terminating ion. Artificial seawater containing 3 mM cetyltrimethylammonium chloride (CTAC) was adopted as a background electrolyte (BGE). The limits of detection (LODs) for nitrite and nitrate were 2.2 and 1.0 microg/L (as nitrogen), respectively. The LODs were obtained at a signal to noise ratio (S/N) of 3. The values of the relative standard deviation (RSD) of peak area for these ions were 1.9 and 1.4%. The RSDs of peak height were 1.7 and 1.9%, the RSDs of migration time 0.11%. The proposed method was applied to the determination of nitrite and nitrate in a proposed certified reference material for nutrients in seawater, MOOS-1, distributed by the National Research Council of Canada (NRC). The results almost agreed with the assigned tolerance interval.
我们描述了一种选定离子的组合作为终止离子,该组合对于毛细管区带电泳(CZE)中的瞬态等速电泳(ITP)测定海水中的亚硝酸盐和硝酸盐很有用。除了150 mM的硫酸盐作为主要终止离子外,还向样品溶液中添加了10 mM的溴酸盐作为额外的终止离子。采用含有3 mM十六烷基三甲基氯化铵(CTAC)的人工海水作为背景电解质(BGE)。亚硝酸盐和硝酸盐的检测限(LOD)分别为2.2和1.0 μg/L(以氮计)。检测限是在信噪比(S/N)为3时获得的。这些离子的峰面积相对标准偏差(RSD)值分别为1.9%和1.4%。峰高的RSD为1.7%和1.9%,迁移时间的RSD为0.11%。该方法应用于测定加拿大国家研究委员会(NRC)分发的一种拟议的海水营养物质有证标准物质MOOS-1中的亚硝酸盐和硝酸盐。结果几乎与规定的公差区间一致。