An on-line sample pretreatment method was developed to preconcentrate trace metal ions from water samples. complexes of metal ions with butane-2,3-dione bis(N-pyridinoacetyt hydrazone) were retained on a column packed with Amberlite XAD-4 resin at pH 8-9. The metal complexes were removed from the co
On-line preconcentration of selenium(IV) and selenium(VI) in aqueous matrices followed by liquid chromatography-inductively coupled plasma mass spectrometry determination
✍ Scribed by Yong Cai; Mercè Cabañas; JoséL Fernández-Turiel; Manoli Abalos; Josep M Bayona
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 893 KB
- Volume
- 314
- Category
- Article
- ISSN
- 0003-2670
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✦ Synopsis
A study was carried out for the determination of selenite and selenate from water matrices using ion-pairing reversed-phase or anion exchange liquid chromatography followed by determination with inductively coupled plasma mass spectrometry (LC-ICP-MS), which used conventional pneumatic nebulization as sample introduction technique. The detection limits and background levels for the anion exchange chromatography were lower than those for the ion-pairing separation method. Based on the optimum conditions obtained with a 25 /*l sample injection loop, a preconcentration column was coupled on-line with the anion exchange LC-ICP-MS system. The capability of this simple on-line preconcentration procedure was demonstrated for the analysis of various water matrices spiked with selenite and selenate including high salt-containing water, river, tap, and well water samples. The detection limits (3~) obtained by preconcentration of 2-10 ml of the high salt-containing water and other aqueous matrices were 0.16-0.42 and 0.08-0.19 pg 1-l of Se for selenite and selenate, respectively. These relative detection limits were ca. two orders of magnitude better than those obtained with a 25 ~1 sample loop.
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