Sequential injection chromatography with post-column reaction/derivatization for the determination of transition metal cations in natural water samples
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
25702988
DOI
10.1016/j.talanta.2015.01.001
PII: S0039-9140(15)00006-5
Knihovny.cz E-resources
- Keywords
- On-column stacking, Post-column reaction, Sequential Injection Chromatography, Spectrophotometric detection, Transition metal cations,
- MeSH
- Water Pollutants, Chemical analysis MeSH
- Chromatography methods MeSH
- Formates chemistry MeSH
- Picolinic Acids MeSH
- Copper analysis MeSH
- Mineral Waters analysis MeSH
- Drinking Water analysis MeSH
- Pyridines chemistry MeSH
- Resorcinols chemistry MeSH
- Sulfates chemistry MeSH
- Fresh Water analysis MeSH
- Iron analysis MeSH
- Zinc analysis MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 4-(2-pyridylazo)resorcinol MeSH Browser
- Water Pollutants, Chemical MeSH
- dipicolinic acid MeSH Browser
- Formates MeSH
- formic acid MeSH Browser
- Picolinic Acids MeSH
- Copper MeSH
- Mineral Waters MeSH
- Drinking Water MeSH
- Pyridines MeSH
- Resorcinols MeSH
- Sulfates MeSH
- sodium sulfate MeSH Browser
- Iron MeSH
- Zinc MeSH
In this work, the applicability of Sequential Injection Chromatography for the determination of transition metals in water is evaluated for the separation of copper(II), zinc(II), and iron(II) cations. Separations were performed using a Dionex IonPAC™ guard column (50mm×2mm i.d., 9 µm). Mobile phase composition and post-column reaction were optimized by modified SIMPLEX method with subsequent study of the concentration of each component. The mobile phase consisted of 2,6-pyridinedicarboxylic acid as analyte-selective compound, sodium sulfate, and formic acid/sodium formate buffer. Post-column addition of 4-(2-pyridylazo)resorcinol was carried out for spectrophotometric detection of the analytes׳ complexes at 530nm. Approaches to achieve higher robustness, baseline stability, and detection sensitivity by on-column stacking of the analytes and initial gradient implementation as well as air-cushion pressure damping for post-column reagent addition were studied. The method allowed the rapid separation of copper(II), zinc(II), and iron(II) within 6.5min including pump refilling and aspiration of sample and 1mmol HNO3 for analyte stacking on the separation column. High sensitivity was achieved applying an injection volume of up to 90µL. A signal repeatability of<2% RSD of peak height was found. Analyte recovery evaluated by spiking of different natural water samples was well suited for routine analysis with sub-micromolar limits of detection.
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