Fukushi K, Ishio N, Sumida M, Takeda S, Wakida S, Hiiro K
Research Institute for Marine Cargo Transportation, Kobe, Japan.
Electrophoresis. 2000 Aug;21(14):2866-71. doi: 10.1002/1522-2683(20000801)21:14<2866::AID-ELPS2866>3.0.CO;2-V.
We describe capillary zone electrophoresis (CZE) with transient isotachophoresis (ITP) for the determination of low concentrations of nitrite and nitrate ions in seawater. Bromide-free artificial seawater was adopted as background electrolyte (BGE) to eliminate the interference of high concentrations of salts in seawater. To reverse the electroosmotic flow (EOF), 3 mM cetyltrimethylammonium chloride (CTAC) was added to the BGE. High concentrations of chlorate were added to sample solutions as the terminating ion to generate the ITP process before the CZE separation. In general, the stacking effect increased with increasing amounts of chlorate injected into the capillary. The limits of detection (LODs) for nitrite and nitrate were 0.063 and 0.033 mg/L when the chlorate concentration was 600 and 200 mM, respectively; these were half of those obtained by CZE without the transient ITP. The LODs were obtained at a signal to noise ratio (S/N) of 3. The relative standard deviations (RSD, n = 10) of the peak areas for these ions were 3.2 and 2.9%. The RSDs of peak heights for these ions were 1.6 and 2.1%. The RSDs of migration times for these ions were 0.67 and 0.46%.
我们描述了采用毛细管区带电泳(CZE)结合瞬态等速电泳(ITP)来测定海水中低浓度的亚硝酸根离子和硝酸根离子。采用无溴人工海水作为背景电解质(BGE)以消除海水中高浓度盐分的干扰。为了反转电渗流(EOF),向BGE中加入了3 mM十六烷基三甲基氯化铵(CTAC)。向样品溶液中加入高浓度的氯酸盐作为终止离子,以便在CZE分离之前产生ITP过程。一般来说,随着注入毛细管的氯酸盐量增加,堆积效应增强。当氯酸盐浓度分别为600 mM和200 mM时,亚硝酸根和硝酸根的检测限(LOD)分别为0.063 mg/L和0.033 mg/L;这些检测限是未采用瞬态ITP的CZE方法所获检测限的一半。检测限是在信噪比(S/N)为3时获得的。这些离子峰面积的相对标准偏差(RSD,n = 10)分别为3.2%和2.9%。这些离子峰高的RSD分别为1.6%和2.1%。这些离子迁移时间的RSD分别为0.67%和0.46%。