Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/8573
Title: Determination of cobalt, nickel and iron at trace level in natural water samples by in-column chelation-reversed phase high-performance liquid chromatography
Authors: Höl, Ayşen
Divrikli, Ümit
Elçi, Latif
Keywords: 4-(2-Pyridylazo) resorcinol
Cobalt
Iron
Nickel
RP-HPLC-DAD
Water
4-(2-Pyridylazo )resorcinol
Ammonium acetate
Certified reference materials
Chelating reagent
Derivatizations
Detection limits
Full optimization
Mobile phase
Natural water samples
Ni ions
Peak area
Photodiode array detectors
Relative standard deviations
Retention time
Reversed phase
Spiked water samples
Trace level
Ammonium compounds
Chelation
Chromatography
Diodes
High performance liquid chromatography
Methanol
Phenols
Trace analysis
4 (2 pyridylazo)resorcinol
cobalt
iron
nickel
resorcinol derivative
unclassified drug
4-(2-pyridylazo)resorcinol
chelating agent
heavy metal
chelation
liquid chromatography
water
article
chemical analysis
chemical structure
derivatization
limit of detection
metal recovery
pH
phase separation
reversed phase high performance liquid chromatography
validation process
waste water
water analysis
water quality
water sampling
chemistry
environmental monitoring
high performance liquid chromatography
methodology
reversed phase liquid chromatography
water pollutant
Chelating Agents
Chromatography, High Pressure Liquid
Chromatography, Reverse-Phase
Environmental Monitoring
Metals, Heavy
Resorcinols
Water Pollutants, Chemical
Abstract: This paper reports the utilization of 4-(2-pyridylazo) resorcinol (PAR) as a chelating reagent for in-column derivatization and the determination of trace Co, Fe, and Ni ions by reversed-phase highperformance liquid chromatography with photodiode array detector. A good separation of Co, Fe, and Ni chelates were achieved by using an Inertsil ODS-3 column and a mobile phase, consisted of methanol- THF-water mixture (50:5:45) containing ammonium acetate buffer (pH 5.0) and PAR. After full optimization, good repeatability of retention times (relative standard deviation (RSD)<0.05%) and peak areas (RSD<1.7%) was achieved as well as a good linearity (r 2>0.9991). The detection limits (S/N=3), expressed as micrograms per liter, were 0.50 (Co), 9.07 (Fe), and 2.00 (Ni). The applicability and the accuracy of the developed method were estimated by the analysis of spiked water samples and certified reference material BCR 715 wastewater-SRM. © Springer Science+Business Media B.V. 2011.
URI: https://hdl.handle.net/11499/8573
https://doi.org/10.1007/s10661-011-2201-9
ISSN: 0167-6369
Appears in Collections:Fen-Edebiyat Fakültesi Koleksiyonu
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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