Ion chromatographic determination of trace iodate, chlorite, chlorate, bromide, bromate and nitrite in drinking water using suppressed conductivity detection and visible detection

被引:116
作者
Zhu, Binghui [1 ]
Zhong, Zhixiong [1 ]
Yao, Jing [1 ]
机构
[1] Ctr Dis Control & Prevent Guangdong Province, Guangzhou 510300, Peoples R China
关键词
ion chromatography; iodate; chlorite; chlorate; bromide; bromate; nitrite; tap water; mineral water; bottled water;
D O I
10.1016/j.chroma.2006.01.139
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
An ion chromatography method for the simultaneous determination of trace iodate, chlorite, chlorate, bromide, bromate and nitrite in drinking water has been developed using an anion-exchange column and the suppressed conductivity detector, followed by post-column addition of reagent to enhance visible absorbance detection of ions. A high capacity anion exchange Ion Pac9-HC column (250 mm x 4 mm I.D.) was used. Eight millimole per liter sodium carbonate was used as eluent, an auto-suppression external water mode was selected, 0.5 g/l o-dianisidine-2HCl (ODA) + 4.5 g/l KBr + 25% methanel + 5.6% nitric acid was used as post-column reagent. The post-column reaction (PCR) temperature was at 60 degrees C, and the visible absorbance detected wavelength at 450 nm. The sample's pH and coexist anions had no influence on determination. The method enjoyed a wide linear range and a good linear correlation coefficient (r > 0.999). The method detection limits were between 0.023 and 2.0 mu g/l. The average recoveries ranged from 87.5 to 110.0%, and the relative standard deviations (RSD) were in the range of 1.1-4.6%. The analytical results by the method of post-column addition of reagent to enhance visible absorbance detection of anions was compared with that of the suppressed conductivity detection, and the former was proved to be better in sensitivity and selectivity. The results showed that this method was accurate, sensitive and might be good for application and suitable for trace analysis at the level of mu g/l. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:106 / 110
页数:5
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