碘
检出限
化学
碘化物
线性范围
色谱法
盐(化学)
氧化还原
溶剂
无机化学
有机化学
作者
Joana L.A. Miranda,Raquel B.R. Mesquita,Edwin Palacio,José Manuel Estela,Vı́ctor Cerdà,António O.S.S. Rangel
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2022-02-16
卷期号:27 (4): 1325-1325
被引量:3
标识
DOI:10.3390/molecules27041325
摘要
In this work, a flow-based spectrofluorimetric method for iodine determination was developed. The system consisted of a miniaturized chip-based flow manifold for solutions handling and with integrated spectrofluorimetric detection. A multi-syringe module was used as a liquid driver. Iodide was quantified from its catalytic effect on the redox reaction between Ce(IV) and As(III), based on the Sandell-Kolthoff reaction. The method was applied for the determination of iodine in salt, pharmaceuticals, supplement pills, and seaweed samples without off-line pre-treatment. An in-line oxidation process, aided by UV radiation, was implemented to analyse some samples (supplement pills and seaweed samples) to eliminate interferences and release iodine from organo-iodine compounds. This feature, combined with the fluorometric reaction, makes this method simpler, faster, and more sensitive than the classic approach of the Sandell-Kolthoff reaction. The method allowed iodine to be determined within a range of 0.20-4.0 µmol L-1, with or without the in-line UV digestion, with a limit of detection of 0.028 µmol L-1 and 0.025 µmol L-1, respectively.
科研通智能强力驱动
Strongly Powered by AbleSci AI