Preparation and characterization of chitosan/Fe2O3 nano composite for the adsorption of thorium (IV) ion from aqueous solution

Author:

Broujeni B. Rouhi1,Nilchi A.2,Hassani A. H.3,Saberi R.2

Affiliation:

1. Environmental Engineering, Department of Natural Resources and Environment, Tehran Science and Research Branch, Islamic Azad University, P.O. BOX 1478814656, Tehran, Iran

2. Faculty Member of Materials and Nuclear Fuel Research School, Nuclear Science and Technology Research Institute, P.O. BOX 11365-8486, Tehran, Iran

3. Tehran Science and Research Branch, Department of Natural Resources and Environment, Islamic Azad University, Tehran, Iran

Abstract

Abstract In this study, novel chitosan/Fe2O3nano composite Ch/Fe-Onc was synthesized and evaluated as an adsorbent for removing thorium (IV) (Th4+) ion from aqueous solution. The Ch/Fe-Onc was characterized by X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET), Fourier transform infrared (FTIR) and scanning electron microscopy (SEM). Response surface methodology (RSM) was used in the optimization of Th4+ adsorption for parameters such as pH, the initial metal ion concentration (Th4+ concentration) and contact time. The statistical measures (i.e. analysis of variance, R2, the lack of fit test and the P value) specify that the developed model is proper. Furthermore, the adsorption kinetics was well defined by the pseudo-second-order equation, while the adsorption isotherms were better fitted by the Langmuir model. The adsorption capacity of Ch/Fe-Onc was 430 mg Th4+g−1 composite which leads to 99% removal at 25 °C. Moreover, thermodynamic parameters which state the natural and endothermic nature of the reactions were determined. The loaded Th4+ can be easily regenerated with HNO3 and the Ch/Fe-Onc can be used repeatedly without any significant reduction in its adsorption capacity. The desorption level of Th4+ from the Ch/Fe-Onc by using 0.1 M HNO3, was more than 95%.

Publisher

IWA Publishing

Subject

Water Science and Technology,Environmental Engineering

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