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The CoFe2O4 nanoparticles have been synthesized by using a stable ferric salt of FeCl3 with a micellar microemulsion method. The normal micelles are formed by sodium dodecyl sulfate (NaDS) in aqueous solutions. The mean size of the nanoparticles can be controlled from less than 4 nm to about 10 nm through controlling the concentrations of the reagents. The neutron diffraction in combination with the Rietveld refinement shows that these CoFe2O4 nanoparticles have a high degree of inversion with 66% of the tetrahedral sublattice occupied by Fe3+. Magnetic measurements and neutron diffraction studies demonstrate the superparamagnetic nature of these CoFe2O4 nanoparticles. The size-dependent superparamagnetic properties of CoFe2O4 nanoparticles have also been systematically studied. The blocking temperature and coercive field of the nanoparticles increase with increasing size of the nanoparticles. The superparamagnetic behaviors of CoFe2O4 nanoparticles are consistent with the Stoner-Wohlfarth theory of single domain particles.

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A highly effective adsorbent with phosphate groups bound to cellulose microspheres was designed by an improved solid-phase modification method to adsorb lead ions from water by a batch and fixed-bed column method. The phosphorylated cellulose microsphere adsorbents were prepared through esterification by which phosphate groups were introduced to the interface of regenerated cellulose microspheres which were previously prepared through a sol–gel transition process from a simple cellulose solution. Their morphological, structural, and physicochemical properties were characterized by SEM, FTIR, XRD, and DSC, etc. Furthermore, EDX and XPS were used to confirm the chemical modification process and to investigate their phosphate adsorption mechanism. In the batch adsorption experiments, the equilibrium time and adsorption capacity were determined by both equilibrium and kinetic adsorption experiments, which were also conducted to investigate the adsorption mechanism. In the dynamic adsorption experiments, multiple operation conditions such as flow rate, initial concentration, bed height, and pH were evaluated, and the experiment data were fitted to several dynamic adsorption models, such as Adams–Bohart, Thomas, Yoon–Nelson, Bed Depth Service Time (BDST), and Dose Response, to study the performance of adsorption of Pb2+ onto the adsorbents. The results suggested that chemical adsorption was the main controlled process during the adsorption process and that the adsorbents could highly effectively capture Pb2+ from water via chelation.