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https://hdl.handle.net/11499/37335
Title: | Determination of cobalt in food by magnetic solid-phase extraction (MSPE) preconcentration by polyaniline (PANI) and polythiophene (PTH) coated magnetic nanoparticles (MNPs) and microsample injection system–flame atomic absorption spectrometry (MIS-FAAS) | Authors: | Elçi, Şükrü Gökhan | Keywords: | Cobalt magnetic nanoparticles (MNPs) magnetic solid-phase extraction (MSPE) microsample injection system–flame atomic absorption spectrometry (MIS-FAAS) polyaniline (PANI) polythiophene (PTH) Absorption spectroscopy Atomic absorption spectrometry Beverages Chlorine compounds Cobalt compounds Iron oxides Magnetic nanoparticles Magnetism Magnetite Phase separation Polyaniline Synthesis (chemical) Adsorption capacities Certified reference materials Fe3O4 nanoparticles Flame atomic absorption spectrometry Magnetic nanoparti cles (MNPs) Magnetic solidphase extraction (MSPE) Polyanilines (PAni) Real sample analysis Extraction |
Publisher: | Taylor and Francis Inc. | Abstract: | Magnetic nanoparticles (MNPs) named Fe3O4@coPANI-PTH were synthesized by coating Fe3O4 nanoparticles (NPs) with a polyaniline (PANI)/polythiophene (PTH) co-polymer. The feasibility of Fe3O4@coPANI-PTH as the nanosorbent for magnetic solid-phase extraction (MSPE) was evaluated for the determination of Co(II) in real samples using microsample injection system–flame atomic absorption spectrometry (MIS-FAAS). Parameters (sample pH, adsorbent mass, eluent volume, sample volume, and co-existing ion effects) influencing the preconcentration of cobalt were optimized. Under the optimum conditions at pH 10, cobalt was completely adsorbed by 100 mg Fe3O4@coPANI-PTH from 60 mL sample and eluted quantitatively (? 95%) using 1.0 mL of 0.2% thiourea solution in a mixture of 2 mol L-1 HCl and 1 mol L-1 HNO3. The adsorption capacity and characteristics of Fe3O4@coPANI-PTH for cobalt were evaluated with isotherm studies. The accuracy of the optimized method was evaluated by measuring certified reference materials (CRMs) and spiked real samples. The relative error and standard deviation were below 6.0% for the CRM and real sample analyses. The limit of detection was 1.6 µg L-1. The determination of ultra-trace cobalt amounts in various soft drinks, spice, vegetable, and water samples was achieved satisfactorily with this method. © 2020 Taylor & Francis Group, LLC. | URI: | https://hdl.handle.net/11499/37335 https://doi.org/10.1080/10739149.2020.1818577 |
ISSN: | 1073-9149 |
Appears in Collections: | Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Teknoloji Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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