Sequential injection chromatography with post-column reaction/derivatization for the determination of transition metal cations in natural water samples
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25702988
DOI
10.1016/j.talanta.2015.01.001
PII: S0039-9140(15)00006-5
Knihovny.cz E-zdroje
- Klíčová slova
- On-column stacking, Post-column reaction, Sequential Injection Chromatography, Spectrophotometric detection, Transition metal cations,
- MeSH
- chemické látky znečišťující vodu analýza MeSH
- chromatografie metody MeSH
- formiáty chemie MeSH
- kyseliny pikolinové MeSH
- měď analýza MeSH
- minerální vody analýza MeSH
- pitná voda analýza MeSH
- pyridiny chemie MeSH
- resorcinoly chemie MeSH
- sírany chemie MeSH
- sladká voda analýza MeSH
- železo analýza MeSH
- zinek analýza MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 4-(2-pyridylazo)resorcinol MeSH Prohlížeč
- chemické látky znečišťující vodu MeSH
- dipicolinic acid MeSH Prohlížeč
- formiáty MeSH
- formic acid MeSH Prohlížeč
- kyseliny pikolinové MeSH
- měď MeSH
- minerální vody MeSH
- pitná voda MeSH
- pyridiny MeSH
- resorcinoly MeSH
- sírany MeSH
- sodium sulfate MeSH Prohlížeč
- železo MeSH
- zinek 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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