Synthesis and characterization of magnetic hexacyanoferrate (II) polymeric nanocomposite for separation of cesium from radioactive waste solutions

Nanocrystalline potassium zinc hexacyanoferrate loaded on nanoscale magnetite substrate was successfully synthesized for significantly enhanced removal of cesium from low-level radioactive wastes. A description was given for preparation and properties of these precursors. The physicochemical properties of these nanocomposites were determined using different techniques including Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS). Data clarified that supporting potassium zinc hexacyanoferrates on iron ferrite nanoparticles increased their thermal stability. Further, Fourier transform infrared spectra confirmed that the nanocomposites were well coordinated and incorporated in the polymer matrix. The average particle sizes, of these nanoparticles, determined by SEM had a good agreement with XRD results. Based on characterization data, the prepared zinc hexacyanoferrates were proposed to have a zeolitic rhombohedral structure with cavities can host alkali metal ions and water molecules. The magnetic analysis showed a super-paramagnetic behavior. Batch technique was applied to evaluate the influences of initial pH value, contact time, and competing cations on the efficiency of cesium removal. The sorption process was fast initially, and maximum separation was attained within 2 h of contact. Cesium exchange was independent from pH value and deviate from ideal exchange phenomena. In neutral solutions, Cs+ was retained through exchange with K+; however, in acidic solution, phase transformation was proposed. Sorption capacity of these materials attained values amounted 1965 mg g(-1). The synthesized nanocomposites exhibited different affinities toward Cs(I), Co(II), and Eu(III) elements and showed a good ability to separate them from each other. (C) 2012 Elsevier Inc. All rights reserved.