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https://hdl.handle.net/11499/4204
Title: | A multi-element solid-phase extraction method for trace metals determination in environmental samples on Amberlite XAD-2000 | Authors: | Bulut, V.N. Gundogdu, A. Duran, C. Senturk, H.B. Soylak, M. Elçi, Latif Tufekci, M. |
Keywords: | Amberlite XAD-2000 Diethyldithiocarbamate Flame atomic absorption spectrometry Preconcentration Trace metals Water Acetone Concentration (process) Extraction pH effects Trace elements acetone amberlite xad 2000 cadmium chelate cobalt copper ion diethyldithiocarbamic acid iron ligand manganese metal ion nitric acid polacrilin resin trace metal transition element unclassified drug zinc ion adsorption amber atomic absorption spectroscopy chemical compound detection method ion exchange trace element absorption spectrophotometry acidity alkalinity article cabbage elution flame atomic absorption spectrometry flow rate kale solid phase extraction validation process water analysis water sampling Brassica Ditiocarb Environmental Monitoring Hydrogen-Ion Concentration Metals, Heavy Polystyrenes Resins, Synthetic Solid Phase Extraction Turkey Water Pollutants, Chemical Brassica oleracea var. acephala |
Abstract: | A method for the preconcentration of some transition elements at trace level was proposed using a column filled with Amberlite XAD-2000 resin. Metal ions were adsorbed on XAD-2000 as their diethyldithiocarbamate chelates, then analytes retained on the resin were eluted by 1 mol L-1 nitric acid in acetone and determined by flame atomic absorption spectrometry (FAAS). The influences of some analytical parameters including pH of sample solution, ligand amount, the type, concentration and volume of elution solution, flow rates of the sample and eluent solutions, adsorption capacity of the resin and sample volume on the preconcentration efficiency have been investigated. The influences of some matrix elements were also examined. The detection limit (N = 20, 3 sigma) for Mn(II), Fe(II), Co(II), Cu(II), Cd(II), Zn(II), Pb(II) and Ni(II) were found as 0.20, 0.35, 0.25, 0.20, 0.20, 0.15, 0.45 and 0.25 µg L-1, respectively. The validation of the procedure was carried out by analysis of certified reference materials. The proposed method was applied to natural waters and kale vegetable (Brassica oleracea var. acephala). © 2006 Elsevier B.V. All rights reserved. | URI: | https://hdl.handle.net/11499/4204 https://doi.org/10.1016/j.jhazmat.2006.12.013 |
ISSN: | 0304-3894 |
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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