Aqueous Solution Preparation, Structure, and Magnetic Properties of Nano-Granular ZnxFe3−xO4 Ferrite Films

This paper reports a simple and novel process for preparing nano-granular ZnxFe3−xO4 ferrite films (0 ≤ x ≤ 0.99) on Ag-coated glass substrates in DMAB-Fe(NO3)3-Zn(NO3)2 solutions. The deposition process may be applied in preparing other cations-doped spinel ferrite films. The Zn content x in the ZnxFe3−xO4 films depends linearly on the Zn2+ ion concentration ranging from 0.0 to 1.0 mM in the aqueous solutions. With x increasing from 0 to 0.99, the lattice constant increases from 0.8399 to 0.8464 nm; and the microstructure of the films changes from the non-uniform nano-granules to the fine and uniform nano-granules of 50–60 nm in size. The saturation magnetization of the films first increases from 75 emu/g to the maximum 108 emu/g with x increasing from 0 to 0.33 and then decreases monotonously to 5 emu/g with x increasing from 0.33 to 0.99. Meanwhile, the coercive force decreases monotonously from 116 to 13 Oe

Synthesis and characterization of BaTiO3/-Fe2O3 core/shell structure

Multiferroic materials attracted a lot of attention in recent years because of their significant scientific interest and technological applications. The multiferroic core/shell powders have a better connectivity between the phases, resulting in superior dielectric and magneto electric properties. In this study, the influence of preparation condition on structure and properties of BaTiO3/-Fe2O3 core/shell composite materials was examined. The five samples were obtained by varying synthesis conditions, such as synthesized method (co-precipitation and sonochemical method) and pH values of solution. XRD and Raman spectroscopy analyses were performed in order to determine phase composition and structural changes within samples. Morphology modifications were examined by SEM and EDS analyses. Finally, effect of structural and microstructural changes on magnetic and electrical properties was detected and explained

Surface Modification and Planar Defects of Calcium Carbonates by Magnetic Water Treatment

Powdery calcium carbonates, predominantly calcite and aragonite, with planar defects and cation–anion mixed surfaces as deposited on low-carbon steel by magnetic water treatment (MWT) were characterized by X-ray diffraction, electron microscopy, and vibration spectroscopy. Calcite were found to form faceted nanoparticles having 3x () commensurate superstructure and with well-developed {} and {} surfaces to exhibit preferred orientations. Aragonite occurred as laths having 3x () commensurate superstructure and with well-developed () surface extending along [100] direction up to micrometers in length. The (hkil)-specific coalescence of calcite and rapid lath growth of aragonite under the combined effects of Lorentz force and a precondensation event account for a beneficial larger particulate/colony size for the removal of the carbonate scale from the steel substrate. The coexisting magnetite particles have well-developed {011} surfaces regardless of MWT

Magnetically induced demulsification of water and castor oil dispersions stabilized by Fe3O4-coated cellulose nanocrystals

Superparamagnetic iron oxide (Fe3O4) nanoparticle (NP) coated cellulose nanocrystals (CNCs) were synthesized and used to prepare emulsions with magnetically controlled stability. Magnetite NPs were deposited onto the surface of wood pulp CNCs (WCNCs) and bacterial CNCs (BCNCs) by a one-step coprecipitation method. The effect of the CNC to Fe3O4 mass ratio (1:1, 1:2, and 1:4) was varied to optimize the colloidal, magnetic and emulsifying properties of the hybrid NPs. TEM images showed that the 1:4 ratios lead to greater coverage of Fe3O4 than lower Fe3O4 loadings (1:1, and 1:2). The CNCs and Fe3O4 appeared to interact via hydrogen bonding between the hydroxyl groups on the surfaces of both particles. The hybrid NPs had high saturation magnetizations of 56 emu/g for WCNC/Fe3O4 (1:4) and 60 emu/g for BCNC/Fe3O4 (1:4). In addition, they were efficient stabilizers for castor oil and water emulsions. The magnetite lowered the colloidal stability of the CNCs while providing superparamagnetic properties which allowed stabilization of Pickering emulsions and the subsequent depletion of the Pickering effect by an external magnet. Water-in-oil emulsions, with oil contents of 70% and 90% V/V, were broken by an external magnet, while the CNC/ Fe3O4 NPs were recovered and recycled. The 30% and 50% V/V oil emulsions were oil-in-water and could not be broken by the magnet, probably due to higher emulsion stability. The fabricated magnetic CNCs have potential use in magnetically driven separations, drug delivery, and oil recovery