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Trace ion analysis of seawater by capillary electrophoresis: Determination of iodide using transient isotachophoretic preconcentration

✍ Scribed by Takeshi Hirokawa; Teppei Ichihara; Kazuaki Ito; Andrei R. Timerbaev


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
151 KB
Volume
24
Category
Article
ISSN
0173-0835

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✦ Synopsis


Abstract

An improved transient isotachophoresis (tITP) procedure for the preconcentration of iodide from highly saline matrices was developed with the objective to quantify iodide in seawater by capillary electrophoresis (CE). The procedure takes advantage of introducing cetyltrimethylammonium chloride into the high‐sodium chloride background electrolyte, which due to a specific interaction with iodide amended placement of the analyte at a large distance from the matrix chloride (the latter performed the role of a leading anion). Computer simulation showed that 2‐(N‐morpholino)ethanesulfonate could be adopted as a suitable terminating ion to enable isotachophoretic focusing at the beginning of the CE run. Under optimized tITP conditions, the sensitivity response of iodide was improved by a factor of 140 over normal CE mode. This allowed for direct UV detection of as low as 0.6Β ΞΌg/L iodide and made feasible CE analysis of undiluted surface seawater samples where iodide was found at a 30Β ΞΌg/L level. The applicability of the proposed tITP‐CE method could apparently be extended to the determination of other trace seawater anions (e.g., iodate).


πŸ“œ SIMILAR VOLUMES


Simultaneous determination of metal ions
✍ Hikaru Okamoto; Andrei R. Timerbaev; Takeshi Hirokawa πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 838 KB

CE with indirect UV detection was used for the simultaneous determination of lithium, magnesium, calcium, creatinine, carnitine, and a number of amino acids in human serum. The target analytes, positively charged under acidic electrolyte conditions, were separated with positive separation voltage po