Amin-functionalized magnetic-silica core-shell nanoparticles for removal of Hg2+ from aqueous solution. Issue 5 (4th May 2017)

• Record Type: Journal Article
• Authors: Afraz, Ahmadreza; Hajian, Ali; Niknam, Zahra; Mosayebi, Elham; Yusefi, Amin; Sillanpää, Mika
• Is Part Of: Journal of dispersion science and technology. Volume 38:Issue 5(2017)
• Page Start: 750
• Page End: 756
• Publication Date: 2017-05-04
• Subjects: Adsorption -- adsorption kinetic -- heavy metal -- isotherm model -- magnetic adsorbent; Emulsions -- Periodicals; Suspensions (Chemistry) -- Periodicals; Emulsions; Suspensions; 541.34
• DOI: 10.1080/01932691.2016.1193815
• Languages: English
• ISSNs: 0193-2691

Abstract

ABSTRACT: Magnetic nanoparticles with monodisperse shape and size were prepared by a simple method and covered by silica. The prepared core-shell Fe3 O4 @silica nanoparticles were functionalized by amino groups and characterized by scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, Brunauer-Emmett-Teller (BET) and Fourier transform infrared spectroscopy (FT-IR) techniques. The synthesized nanoparticles were employed as an adsorbent for removal of Hg 2+ from aqueous solutions, and the adsorption phenomena were studied from both equilibrium and kinetic point of views. The adsorption equilibriums were analyzed using different isotherm models and correlation coefficients were determined for each isotherm. The experimental data were fitted to the Langmuir–Freundlich isotherm better than other isotherms. The adsorption kinetics was tested for the pseudo-first-order, pseudo-second-order and Elovich kinetic models at different initial concentrations of the adsorbate. The pseudo-second-order kinetic model describes the kinetics of the adsorption process for amino functionalized adsorbents. The maximum adsorption occurred at pH 5.7 and the adsorption capacity for Fe3 O4 @silica-NH2 toward Hg 2+ was as high as 126.7 mg/g which was near four times more than unmodified silica adsorbent. GRAPHICAL ABSTRACT: