Abstract

Magnetically driven separation technology has received considerable attention in recent decade for its great potential application. In this study, we investigate the application of silica-modified magnetite nanoparticles (NPs) coated with a cationic surfactant as adsorbent for microextraction and determination of trace amounts of Cu(II), Ni(II), Co(II), Cd(II), Pb(II) and Mn(II) from environmental water samples. The synthesized silica-coated NPs in combination with cetylpyridinium bromide have the ability to adsolubilize the metal ions after complexation with 8-hydroxyquinoline. The NPs bearing the target metals are easily separated from the aqueous solution by applying an external magnetic field and the complexed metals were desorbed using acidic methanol. The desorbed analytes are introduced into the graphite furnace of an atomic absorption spectrometer. The effect of pH, complexing agent, amount of cetylpyridinium bromide, microextraction time, desorption conditions, ionic strength on extraction efficiency of the metal ions are investigated and optimized. Under the optimized conditions, the detection limits for Cu(II), Ni(II), Co(II), Cd(II), Pb(II) and Mn(II) are 4.7, 9.1, 9.5, 2.3, 7.4 and 15.3 ng L −1, respectively and the relative standard deviations ( n = 6) are less than 3.6%. The accuracy of the method was evaluated by recovery measurements on the spiked samples and good recoveries (93–113%) with low RSDs were achieved.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.