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Articles

Superparamagnetic nanomaterial Fe3O4–TiO2 for the removal of As(V) and As(III) from aqueous solutions

Pages 1790-1801 | Received 25 May 2015, Accepted 12 Dec 2015, Published online: 05 Feb 2016
 

ABSTRACT

A magnetically separable nanomaterial Fe3O4–TiO2 was synthesized and characterized which was subsequently used for the removal of arsenic (V) from aqueous solutions. The surface morphology, magnetic properties, crystalline structure, thermal stability and Brunauer–Emmet–Teller surface area of the synthesized Fe3O4–TiO2 nanoparticles (NPs) are characterized by scanning electron microscope and high-resolution transmission electron microscope, vibrating sample magnetometry, X-ray diffractometer, thermogravimetric analysis and multi point function surface area analyzer. The saturation magnetization of Fe3O4–TiO2 NPs was determined to be 50.97 emu/g, which makes them superparamagnetic. The surface area of Fe3O4–TiO2 NPs was as much as 94.9 m2/g. The main factors affecting adsorption efficiency, such as solution pH, reaction time, initial As(V) concentration and adsorbent concentration are investigated. When the adsorption isotherms were analyzed by the Langmuir, Freundlich and Dubinin-Radushkevich models, equilibrium data were found to be well represented by Freundlich isotherm, and adsorption on Fe3O4–TiO2 NPs fitted well with pseudo-second-order kinetic model. The maximum adsorption capacity of As(V) on Fe3O4–TiO2 NPs, calculated by the Freundlich model was determined at 11.434 µg/g. 1.0 g/L of Fe3O4–TiO2 NPs was efficient for complete removal of 100 µg/L As(V) in 1 h. Fe3O4–TiO2 NPs was also effective for 93% removal of 100 µg/L As(III). Matrix effect was determined using As(V)-contaminated well water. Successfull results were obtained for purification of real well water containing 137.12 µg/L As(V). Results show that Fe3O4–TiO2 NPs are promising adsorbents with an advantage of magnetic separation.

Acknowledgement

The author thanks KOSKI for their help in taking well water sample and performing chemical composition analyses.

Disclosure statement

No potential conflict of interest was reported by the authors.

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