Yebra M C, Cespón R M
Department of Analytical Chemistry, Nutrition and Bromatology, Chemistry Faculty, University of Santiago, Santiago de Compostela, Spain.
Fresenius J Anal Chem. 2000 May;367(1):24-8. doi: 10.1007/s002160051593.
A continuous flow atomic absorption spectrometric system was used to develop an efficient on-line preconcentration-elution procedure for the determination of iodide traces. Chromium (VI) is introduced into the flow system and is reduced to chromium (III) in acid medium proportionally to the iodide present in the sample. The Cr(III) reduced by iodide is retained on a minicolumn packed with a poly(aminophosphonic acid) chelating resin, while unreduced Cr(VI) is not retained. Reduced Cr(III) is preconcentrated by passing the sample containing iodide through the system during 3 min, and is then eluted with 0.5 mol L(-1) hydrochloric acid and determined by flame atomic absorption spectrometry (FAAS). The detection limit (3sigma) obtained is 2.5 microg L(-1). Other ions typically present in waters do not interfere. The proposed method allows the determination of iodide in the range 6-220 microg L(-1) with a relative standard deviation of 2.7% at a rate of 17 samples h(-1). The method has been applied to the determination of iodide in tap and sea waters.
采用连续流动原子吸收光谱系统开发了一种高效的在线预富集-洗脱方法,用于测定痕量碘化物。将铬(VI)引入流动系统,并在酸性介质中与样品中存在的碘化物成比例地还原为铬(III)。由碘化物还原产生的Cr(III)保留在填充有聚(氨基膦酸)螯合树脂的微型柱上,而未还原的Cr(VI)则不被保留。通过使含碘化物的样品在3分钟内通过系统对还原的Cr(III)进行预富集,然后用0.5 mol L(-1)盐酸洗脱并用火焰原子吸收光谱法(FAAS)测定。获得的检测限(3σ)为2.5 μg L(-1)。水中通常存在的其他离子不产生干扰。所提出的方法能够测定6-220 μg L(-1)范围内的碘化物,在17个样品 h(-1)的速率下相对标准偏差为2.7%。该方法已应用于自来水和海水中碘化物的测定。