Rapid hydrothermal synthesis of magnetic CoxNi1−xFe2O4 nanoparticles and their application on removal of Congo red

•A rapid synthesis method for Co–Ni nanoparticles is suggested.•The quickest adsorption of CR onto CoxNi1−xFe2O4 appears at x=0.5.•The largest adsorption capacity of CR occurs at x=0.3.•All samples show excellent adsorbent ability to CR.•Detailed adsorbent characterization and adsorption mechanisms...

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Veröffentlicht in:Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2014-04, Vol.242, p.226-233
Hauptverfasser: Chen, Ri, Wang, Wei, Zhao, Xiruo, Zhang, Yajun, Wu, Sizhu, Li, Feng
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Sprache:eng
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Zusammenfassung:•A rapid synthesis method for Co–Ni nanoparticles is suggested.•The quickest adsorption of CR onto CoxNi1−xFe2O4 appears at x=0.5.•The largest adsorption capacity of CR occurs at x=0.3.•All samples show excellent adsorbent ability to CR.•Detailed adsorbent characterization and adsorption mechanisms are presented. A rapid synthesis method for magnetic nanoparticles CoxNi1−xFe2O4 (x=0, 0.3, 0.7, 0.9, 1.0) (Co–Ni) using the colloid mill and hydrothermal technique is investigated. The structure and magnetic performance of as-synthesized samples are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Raman spectrum, BET surface area method and vibrating sample magnetometer (VSM). The adsorption capability of Co–Ni ferrite to remove Congo Red (CR) dye from aqueous solution is examined carefully by UV spectrophotometer at room temperature. Research indicates that the substitution of Co2+ has a marked effect on the magnetic properties and CR adsorption of the Co–Ni ferrite nanoparticles. VSM shows that all samples, synthesized at 140°C for a short reaction time 2h, have excellent magnetic properties. Also, all samples show high adsorption capacity for CR dye. The CR adsorption isotherms and kinetics are studied. It is worth noticing that the largest adsorption capacity of the as-synthesized Co–Ni ferrite nanoparticles occurs at x=0.3, and the quickest adsorption appears at x=0.5. The corresponding adsorption mechanisms are analyzed.
ISSN:1385-8947
1873-3212
DOI:10.1016/j.cej.2013.12.016