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The composites containing various iron compounds and highly microporous carbon spheres were produced and investigated for structural and magnetic properties. Iron citrate, nitrate and chloride were used to prepare samples and the obtained products contained iron, iron carbide or magnetite. All the produced samples were characterized by high porosity and good magnetic properties. The coupling of the high porosity of carbon spheres with magnetic properties of iron compounds provides a potential application of the composites to removal of impurities from water, followed by a magnetic separation of the sorbent.

O-Carboxymethylchitosan-N-lauryl/γ-Fe2O3 magnetic nanoparticles (OCh-LM) were synthesized and characterized using FT-IR, TGA, SEM and VSM. The OCh-LM was essentially spherical in shape, with a mean particle size of 11.1 ± 3.4 nm and saturated magnetization of 18.4 emu/g. The nanoparticle was used to remove the anionic dye Remazol Red 198 (RR198) from aqueous solution by the batch system. The kinetic data and adsorption isotherm were best fitted by the pseudo-second order kinetic model, and the Langmuir–Freundlich isotherm, respectively. Thermodynamic parameters such as change in enthalpy, change in Gibbs free energy and change in entropy were estimated, and the results indicated that the adsorption process was spontaneous and endothermic. The maximum adsorption capacity, calculated through the Langmuir–Freundlich model at 25 °C, was 216 mg/g. Desorption of the dye and reuse of the adsorbent were performed in four cycles. These results show that OCh-LM can be potentially used as a magnetic adsorbent to remove RR198 and probably other anionic reactive dyes from aqueous solution for avoiding the secondary pollution. Keywords: Dye adsorption, Magnetic nanoparticle, Magnetic separation, O-Carboxymethylchitosan-N-lauryl/γ-Fe2O3, Remazol Red 198

We present the study of pristine and calcined f-MWCNTs functionalized by nitrogen-containing functional groups. We focus on the structural and microstructural modification tuned by the previous annealing. However, our primary goal was to analyze the electronic structure and magnetic properties in relation to the structural properties using a multi-technique approach. The studies carried out by X-ray diffraction, XPS, and 57Fe Mössbauer spectrometry revealed the presence of γ-Fe nanoparticles, Fe3C, and α-FeOOH as catalyst residues. XPS analysis based on the deconvolution of core level lines confirmed the presence of various nitrogen-based functional groups due to the purification and functionalization process of the nanotubes. The annealing procedure leads to a structural modification mainly associated with removing surface impurities as purification residues. Magnetic studies confirmed a significant contribution of Fe3C as evidenced by a Curie temperature estimated at TC = 452 ± 15 K. A slight change in magnetic properties upon annealing was revealed. The detailed studies performed on nanotubes are extremely important for the further synthesis of composite materials based on f-MWCNTs.

Abstract Two sets of core/shell magnetic nanoparticles, CoFe2O4/Fe3O4 and Fe3O4/CoFe2O4, with a fixed diameter of the core (~ 4.1 and ~ 6.3 nm for the former and latter sets, respectively) and thickness of shells up to 2.5 nm were synthesized from metal chlorides in a diethylene glycol solution. The nanoparticles were characterized by X-ray diffraction, transmission electron microscopy, and magnetic measurements. The analysis of the results of magnetic measurements shows that coating of magnetic nanoparticles with the shells results in two simultaneous effects: first, it modifies the parameters of the core-shell interface, and second, it makes the particles acquire combined features of the core and the shell. The first effect becomes especially prominent when the parameters of core and shell strongly differ from each other. The results obtained are useful for optimizing and tailoring the parameters of core/shell spinel ferrite magnetic nanoparticles for their use in various technological and biomedical applications.

Thermal treatment is a post-synthesis treatment that aims to improve the crystallinity and interrelated physical properties of as-prepared materials. This process may also cause some unwanted changes in materials like their oxidation or contamination. In this work, we present the post-synthesis annealing treatments of the amorphous Fe1−xCox (x = 0.25; 0.50; 0.75) Wire-like nanochains performed at 400 °C in two different atmospheres, i.e., a mixture of 80% nitrogen and 20% hydrogen and argon. These processes caused significantly different changes of structural and magnetic properties of the initially-formed Fe-Co nanostructures. All of them crystallized and their cores were composed of body-centered cubic Fe-Co phase, whereas their oxide shells comprised of a mixture of CoFe2O4 and Fe3O4 phases. However, the annealing carried out in hydrogen-containing atmosphere caused a decomposition of the initial oxide shell layer, whereas a similar process in argon led to its slight thickening. Moreover, it was found that the cores of thermally-treated Fe0.25Co0.75 nanochains contained the hexagonal closest packed (hcp) Co phase and were covered by the nanosheet-like shell layer in the case of annealing performed in argon. Considering the evolution of magnetic properties induced by structural changes, it was observed that the coercivities of annealed Fe-Co nanochains increased in comparison with their non-annealed counterparts. The saturation magnetization (MS) of the Fe0.25Co0.75 nanomaterial annealed in both atmospheres was higher than that for the non-annealed sample. In turn, the MS of the Fe0.75Co0.25 and Fe0.50Co0.50 nanochains annealed in argon were lower than those recorded for non-annealed samples due to their partial oxidation during thermal processing.

This work presents a growth of Fe3O4 nanoparticle films on silicon substrate. The iron oxide is deposited applying a pulsed laser deposition technique. The process is performed in open air in the absence and presence of external magnetic field. In fact, the morphologies of the obtained Fe3O4–Si samples are similar. The Fe3O4 nanoparticles are spherical with average diameters of 30 nm and are densely agglomerated on the Si substrate. The Fe3O4–Si material prepared in the absence of magnetic field has revealed more intense signals during X‐ray diffraction and Raman measurements. The magnetic investigations indicate that the Fe3O4 nanoparticles are significantly coupled with the Si substrate and do not exhibit superparamagnetic behavior. Moreover, the Verwey transition is 98 K for both investigated Fe3O4–Si samples. [ABSTRACT FROM AUTHOR]