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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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