Takayanagi Toshio, Ishida Makoto, Mbuna Julius, Driouich Rim, Motomizu Shoji
Graduate School of Natural Science and Technology, Okayama University, 3-1-1 Tsushimanaka, Okayama 700-8530, Japan.
J Chromatogr A. 2006 Sep 22;1128(1-2):298-302. doi: 10.1016/j.chroma.2006.06.056. Epub 2006 Jul 3.
Bromate ion in drinking water was determined by capillary zone electrophoresis (CZE) with direct photometric detection. Bromate ion in the sample solution was introduced and concentrated into the capillary by electrokinetic injection for 50s at -10 kV. Electrophoretic separation was made at an applied voltage of -25 kV and bromate ion was detected at wavelength 193 nm, at which the baseline was stabilized with less UV-absorbing acidic phosphate buffer. Bromate ion was detected within 5 min in the electropherogram. By increasing the electric conductivity in the migrating solution with 10 mM Na2SO4, a limit of detection (LOD) of 9 x 10(-10)M (0.1 microg/L BrO3-) was achieved. The proposed method was applied to the analysis of tap water and river water samples, but bromate ion was not detected. Because the practical samples contain relatively large amount of foreign ionic substances, the tap water sample was diluted to avoid the matrix ions. Bromate ion added in a tap water at the concentration of 8 x 10(-8)M was quantitatively recovered by diluting it 1/10.
采用直接光度检测的毛细管区带电泳(CZE)法测定饮用水中的溴酸根离子。将样品溶液中的溴酸根离子通过电动进样在-10 kV下进样50 s引入并浓缩到毛细管中。在-25 kV的施加电压下进行电泳分离,在193 nm波长处检测溴酸根离子,在此波长下,使用吸光性较小的酸性磷酸盐缓冲液可使基线稳定。在电泳图中5分钟内检测到溴酸根离子。通过在迁移溶液中加入10 mM Na2SO4提高电导率,实现了9×10(-10)M(0.1 μg/L BrO3-)的检测限。该方法应用于自来水和河水样品的分析,但未检测到溴酸根离子。由于实际样品中含有相对大量的外来离子物质,为避免基质离子的干扰,将自来水样品进行了稀释。将浓度为8×10(-8)M的溴酸根离子添加到自来水中,通过将其稀释1/10可实现定量回收。