Microstructure, ion adsorption and magnetic behavior of mesoporous γ-Fe(2)O(3) ferrite nanoparticles

Magnetic nanoparticles with capacity for surface functionalisation have potential applications in water purification and biomedicine. Here, a simple co-precipitation technique was used to synthesize mesoporous ferrite nanoparticles in the presence of cetyltrimethylammonium bromide (CTAB) micellular surfactant. The as-synthesized ferrite nanoparticles were calcined at 250 °C for 5, 10, 15, and 24 h to remove the surfactant and create a mesoporous structure. The prepared samples were characterised using a wide range of analytical techniques. Microscopical images showed that all uncalcined particles have cauliflower shape without porosity. However, after calcination, surface and deep pores were created on the synthesized nanoparticles. In addition, transmission electron microscope (TEM) images of calcined nanoparticles revealed a wormhole-like structure, which is typical for the mesoporous architectures. Based on X-ray diffraction (XRD), the uncalcined and calcined samples exhibit pure Fe(3)O(4) (magnetite) and γ-Fe(2)O(3) (maghemite) ferrite phases, respectively. The γ-Fe(2)O(3) nanoparticles demonstrated a high Brunauer–Emmett–Teller (BET) surface area with pore diameters smaller than 10 nm and a type IV isotherm similar to the mesopores. Hysteresis loops measured by vibrating sample magnetometry (VSM) showed the superparamagnetic nature for mesoporous γ-Fe(2)O(3) nanoparticles. The first-order reversal curve (FORC) diagram revealed the formation of a mesoporous structure in calcined materials which reduces coercive distribution (H(c)) and magnetostatic interaction (H(u)) once compared to non-calcined samples. Mesoporous γ-Fe(2)O(3) nanoparticles were successfully employed as an adsorbent for the removal of heavy metal ions of Pb(ii) from an aqueous solution. The highest lead ion adsorption was observed in mesoporous γ-Fe(2)O(3) nanoparticles prepared with 3% CTAB.