Efficient visible light magnetic modified iron oxide photocatalysts

Magnetite iron oxide (Fe₃O₄) nanoparticles were synthesized via simple co-precipitation method using ferrous and ferric ions salts. Fe₃O₄ nanoparticles were modified by silica and titania. Pure and modified nanoparticles were employed for dye degradation under visible light. X-ray diffraction analysis indicated inverse spinel structure of Fe₃O₄ nanoparticles. The particle size of magnetite nanoparticles is decreased due to coating of silica and titania. Scanning and transmission electron microscopy indicated the spherical morphology for all samples. The synthesized Fe₃O₄ nanoparticles were ferromagnetic in nature with highest saturation magnetization value of 1.1034 emu as compared to silica and titania coated samples. Fourier transform infra-red spectra confirmed the incorporation of magnetite nanoparticles with silica and titania. Titania modified magnetite sample showed the highest photocatalytic activity as compared to silica modified magnetite nanoparticles and bare iron oxide under visible light irradiations.     

Influence of process variables on biooxidation of ferrous sulfate by an indigenous Acidithiobacillus ferrooxidans. Part II: Bioreactor experiments

The oxidation of ferrous iron in solution using Acidithiobacillus ferrooxidans has industrial applications in the regeneration of ferric iron as an oxidant agent for the removal of hydrogen sulfide from waste gases, desulphurization of coal, leaching of non-ferrous metallic sulfides and treatment of acid mine drainage. The aim of this attempt was to increase the biooxidation rate of ferrous sulfate by using immobilized cells. Rate of ferrous iron oxidation was determined in a packed-bed reactor configuration with low density polyethylene (LDPE) particles as support material in order to find the most practical system for scale-up. The present work studies the influence of basic parameters on the ferrous iron biooxidation process using an indigenous iron-oxidizing microorganism, namely A. ferrooxidans, in a 2 L packed-bed bioreactor. Effects of several process variables such as initial pH, temperature, dilution rate, initial concentrations of ferrous and ferric ions on oxidation of ferrous sulfate were investigated. Experimental results indicate that in the temperature range of 31–34 °C the biooxidation of ferrous ions to ferric ions could be resulted efficiently. A pH range of 2–2.2 was optimum for the growth of the culture and effective bacterial activity for oxidation of ferrous ions to ferric ions. The highest oxidation rate of 2.9 g Fe²⁺ L⁻¹ h⁻¹ was obtained using a culture initially containing 25 g L⁻¹ Fe⁺² at the dilution rate of 0.4 h⁻¹. This rate is very high compared to that achieved in other bioreactors found in the literature. In addition the biooxidation of Fe²⁺ to Fe³⁺ conversion could be achieved effectively in the presence of the Fe³⁺ in the concentration range of 0.1–0.7 g/L.     

Preparation of titanium oxide,iron oxide,and aluminium oxide from sludge generated from Ti-salt,Fe-salt and Al-salt flocculation of wastewater

In this study, the settled floc (sludge) produced by aluminum sulfate (Al₂(SO₄)₃), ferric chloride (FeCl₃) and titanium tetrachloride (TiCl₄) flocculation was recycled with a novel flocculation process, which has a significant potential to the lower cost of waste disposal, protect the environment and public health and yield economically useful by-products. Three coagulants removed 70% of organic matter in synthetic wastewater. The settled floc was incinerated in the range from 100 °C to 1000 °C. Alumina (Al₂O₃), hematite (Fe₂O₃), titanium oxide (TiO₂) which are the most widely used metal oxides were produced from the wastewater sludge generated by the flocculation in wastewater with Al₂(SO₄)₃, FeCl₃ and TiCl₄, respectively. TiO₂ particles produced from the sludge consisted of the large amount of nano size particles. Hematite (Fe₂O₃) and grattarolaite (Fe₃ (PO₄)O₃ or Fe₃PO₇) included the majority of micro size (40%) particles. Alumina (Al₂O₃) also consisted of micro size (40%). Due to TiO₂ usefulness of the application, detailed characterisation of TiO₂ after calcination at different temperatures were investigated in terms of X-ray diffraction, energy dispersive X-ray, surface area and photoactivity.     

Phase compositions and equilibria in the CaO–Al2O3–Fe2O3–SO3 system,for assemblages containing ye'elimite and ferrite Ca2(Al,Fe)O5

Phase equilibria in the CaO–Al₂O₃–Fe₂O₃–SO₃ system have been studied, mainly at 1325 °C. In particular the solid solution compositions of ye'elimite Ca₄(Al₆O₁₂)SO₄ and brownmillerite (C₂(A,F)) phases have been analysed and used to estimate the composition boundaries of these phases in their co-existence with liquid at 1325 °C. Sulfate and iron oxide facilitate the formation of a liquid phase, whose amount increases with overall Fe₂O₃ content. However, the solubility of sulfate in this liquid phase is very low and liquid formation tends to lead to the volatilisation of sulfate in unsealed samples.     

Effect of the milling process on the properties of CoFe2O4 pigment

In this study, CoFe₂O₄ pigments were synthesised using both co-precipitation and conventional ceramic methods. Pigment particles prepared using the conventional ceramic method were subsequently milled to submicron size. The effects of the solvent, dispersant and milling type in the milling process were investigated. This study showed that planetary milling in a diethylene glycol (DEG) medium with sodium tripolyphosphate (STPP) was an effective method for producing submicron-sized pigment powders from pigments synthesised using the conventional method. With this method, submicron-sized pigment particles (approximately 190 nm) were obtained after milling for 4 h. Planetary milling was more efficient in reducing particle size compared to attrition milling. Co-precipitated pigment had a more intense black colour, due to the nanoscale particle size (<100 nm). However, conventional ceramic pigments also had an adequately intense black colour that increased after milling compared to unmilled conventional pigments. When considering production of industrial scale submicron-sized pigments, the milling of these pigments to submicron size can be a good alternative method for the production of ink colourants.     

Promoting role of transition metal oxide on ZnTiO3–TiO2 nanocomposites for the photocatalytic activity under solar light irradiation

Transition metal oxide (Fe₂O₃, Co₃O₄ and CuO) loaded ZnTiO₃–TiO₂ nanocomposites were successfully prepared by solid state dispersion method. The structural, morphological and optical properties of samples were characterized by TGA/DTA, XRD, BET, FT-IR, DRS, PL, XPS and SEM techniques. The photocatalytic activity of samples was investigated by degradation of 4-chlorophenol in water under sunlight. The Fe₂O₃ loaded sample was found to exhibit much higher photocatalytic activity than the other composite powders. 7Fe₂O₃/ZnTi sample has the highest percentage of 4-chlorophenol degradation (100%) and highest reaction rate (1.27 mg L⁻¹ min⁻¹) was obtained in 45 min. The enhancement of photocatalytic activity for ZnTiO₃–TiO₂ sample with Fe₂O₃ addition may be attributed to its small particle size, the presence of more surface OH groups, lower band gap energy than other samples in this paper and the presence of more hexagonal ZnTiO₃ phase in the morphology.     

Influence of iron content on the color of the C3A–Fe2O3 system synthesized under different conditions of temperature,atmosphere and cooling

The 3CaO·Al₂O₃–Fe₂O₃ (C₃A–Fe₂O₃) system is important for the production of white clinker. In the present study this system was examined from the perspective of improving the sustainability of the production process. Microstructural evaluation was employed to explain the changes in color caused by variation of: iron content; temperature; type of atmosphere; and cooling conditions. It was found that color was more significantly affected by the iron content, temperature and type of atmosphere than by the type of cooling used. It was also observed that the utility of iron-rich raw materials could be maximized by understanding and enhancing the solubility of Fe₂O₃ in C₃A. It was found that a 2 wt.% Fe₂O₃ solid solution was stable only under kiln open to atmospheric conditions and remained clear at temperatures up to 1370 °C. However, the same 2 wt.% Fe₂O₃ solid solution suffered a significant change in color when the temperature rose to 1400 °C. Mössbauer spectroscopy showed that the oxidation state of Fe was Fe³⁺, which did not change between 1370 and 1400 °C; however, a structural change in the C₃A–Fe₂O₃ solid solution was detected as a result of the alteration of the thermal treatment. The distinction between the structures at these two temperatures was that at 1370 °C, all of the Fe³⁺ had a tetrahedral coordination, while at 1400 °C, 19 wt.% of the Fe³⁺ appeared in octahedral sites, a result that was corroborated by Rietveld analysis.     

Crystallization kinetics and magnetic properties of iron oxide contained 25Li2O–8MnO2–20CaO–2P2O5–45SiO2 glasses

With crystallization at 850 °C for 4 h, LiMn₂O₄, β-wollastonite (β-CaSiO₃), lithium silicate (Li₂SiO₃), Ca(Ca, Mn)Si₂O₆ and Li₂Ca₄Si₄O₁₃ phases were found in 25Li₂O–8MnO₂–20CaO–2P₂O₅–45SiO₂ (LMCPS) glass ceramics. The (Li, Mn)ferrite phase was obtained in the iron oxide contained LMFCPS glass ceramic and Li₂FeMn₃O₈ phase was found in that containing 8 at.% Fe₂O₃. TEM investigations showed that (Li, Mn)ferrite particles dispersed in the β-wollastonite matrix (Li, Mn)ferrite particles, with an average size of 40 nm, were found in the glass ceramics containing 4 at.% Fe₂O₃. The (Li, Mn)ferrite particle sizes in the glass ceramics containing 8 at.% Fe₂O₃ varied from a few μm to 5 nm. The SQUID result showed that only the glass ceramic containing 4 at.% Fe₂O₃ exhibited super-paramagnetic behavior at temperature 300 K and ferromagnetic behavior at 4 K. The LMCPS glass ceramic containing 8 at.% Fe₂O₃ exhibited ferromagnetic behavior at both temperatures.     

Structural,magnetic, and textural properties of iron oxide-reduced graphene oxide hybrids and their use for the electrochemical detection of chromium

Superparamagnetic Fe₃O₄ nanoparticles were anchored on reduced graphene oxide (RGO) nanosheets by co-precipitation of iron salts in the presence of different amounts of graphene oxide (GO). A pH dependent zeta potential and good aqueous dispersions were observed for the three hybrids of Fe₃O₄ and RGO. The structure, morphology and microstructure of the hybrids were examined by X-ray diffraction, transmission electron microscopy (TEM), Fourier transform infrared spectroscopy, Raman and X-ray photoelectron spectroscopy. TEM images reveal lattice fringes (d₃₁₁ = 0.26 nm) of Fe₃O₄ nanoparticles with clear stacked layers of RGO nanosheets. The textural properties including the pore size distribution and loading of Fe₃O₄ nanoparticles to form Fe₃O₄–RGO hybrids have been controlled by changing the concentration of GO. An observed maximum (～10 nm) in pore size distribution for the sample with 0.25 mg ml^?1 of GO is different from that prepared using 1.0 mg ml^?1 GO. The superparamagnetic behavior is also lost in the latter and it exhibits a ferrimagnetic nature. The electrochemical behavior of the hybrids towards chromium ion was assessed and a novel electrode system using cyclic voltammetry for the preparation of an electrochemical sensor platform is proposed. The textural properties seem to influence the electrochemical and magnetic behavior of the hybrids.     

Synthesis of black pigments containing chromium from leather sludge

The black ceramic pigments with spinel structure have been prepared by using Cr-rich leather sludge in this paper. The washed Cr-rich leather sludge calcined at 1100 °C for 1 h as chromium oxide precursor (named as CA) was mixed with an appropriate proportion of other industrial metallic oxides, followed synthesizing black ceramic pigment by sintering. Both non-washed and washed sludge fired at 1100 °C were characterized by X-ray fluorescence (XRF) in order to determine their chemical compositions and X-ray diffraction (XRD) analysis to confirm that CA mainly contains Cr₂O₃ crystal phase. The results show that CA could be used as a source of chromium to prepare black pigment. The crystalline phases of obtained pigments were characterized by XRD. Furthermore, the morphology as well as the composition of pigments was investigated by scanning electron microscopy (SEM) and energy dispersion spectroscopy (EDS). The color coordinates of pigments were examined and compared with the commercial pigments based on CIE-L* a* b* values measured using UV–vis spectroscopy. The obtained pigments sintered at 1200 °C with 35–55 wt% content of CA possess the excellent black spinel structure and color effect. Under optimized conditions, the pigment has low average spectral reflectance (7%).     

Fabrication of graphene nanosheet (GNS)–Fe3O4 hybrids and GNS–Fe3O4/syndiotactic polystyrene composites with high dielectric permittivity

Graphene nanosheet–Fe₃O₄ (GNS–Fe₃O₄) hybrids were obtained by a one-step solvothermal reduction of iron (III) acetylacetonate [Fe(acac)₃] and graphene oxide (GO) simultaneously, which had several advantages: (1) the Fe₃O₄ nanoparticles were firmly anchored on GNS surface even after mild ultrasonication; (2) the loading amount of Fe₃O₄ nanoparticles could be effectively controlled by changing the initial feeding weight ratio of Fe(acac)₃ to GO; (3) the Fe₃O₄ nanoparticles were homogeneously distributed on the GNS surface without much aggregation. Composites based on syndiotactic polystyrene (sPS) and GNS–Fe₃O₄ were prepared by a solution-blending method and the electric and dielectric properties of the resultant GNS–Fe₃O₄/sPS composites were investigated. The percolation threshold of GNS–Fe₃O₄ in the sPS matrix was determined to be 9.41 vol.%. Slightly above the percolation threshold with 9.59 vol.% of GNS–Fe₃O₄, the GNS–Fe₃O₄/sPS composite showed a high dielectric permittivity of 123 at 1000 Hz, which was 42 times higher than that of pure sPS. The AC electrical conductivity at 1000 Hz increased from 3.6 × 10⁻¹⁰ S/m for pure sPS to 2.82 × 10⁻⁴ S/m for GNS–Fe₃O₄/sPS composite containing 10.69 vol.% of GNS–Fe₃O₄, showing an obvious insulator-semiconductor transition.     

Iron and chromium doped perovskite (CaMO3 M = Ti,Zr) ceramic pigments,effect of mineralizer

Solid solutions Ca(D_xM_1?x)O₃ (M = Ti, Zr and D = Fe,Cr), have been studied as ceramic pigment in conventional ceramic glazes using 0.5 mol/mol of NH₄Cl as flux agent by solid state reaction and by ammonia coprecipitation route. Ca(Cr_xTi_1?x)O₃ compositions obtained without addition of NH₄Cl as mineralizer, produce pink color in glazes at low x but CaCrO₄ crystallizes when x increases, producing undesired green colors. The crystallization of chromates can be avoided using NH₄Cl as mineralizer, giving a complete solid solution that produce pink color in glazes at low x and dark blue shades at high x. Coprecipitated sample produce blue colors at low x and at low temperature than ceramic sample (1000 °C instead 1200 °C for CE sample). Cr⁴⁺ ion acts as red chromophore, but at higher x values (blue samples) Cr³⁺ ion entrance affects the color. Ca(Fe_xTi_1?x)O₃ system crystallizes perovskite CaTiO₃ and pseudobrookite Fe₂TiO₅ together with rutile as residual crystalline phase, glazed samples change from a yellow to a pink color associated to the increase of pseudobrookite with firing temperature. Ca(Fe_xTi_1?x)O₃ and Ca(Cr_xZr_1?x)O₃ systems crystallize perovskite CaZrO₃ and zirconia (ZrO₂) in both monoclinic and cubic polymorphs, but iron or chromium oxides are not detected in the powders. Coprecipitated sample stabilises cubic form. The solid solution is not reached completely in these samples and is not stable in glazes.     

One-pot dual product synthesis of hierarchical Co3O4@N-rGO for supercapacitors,N-GDs for label-free detection of metal ion and bio-imaging applications

Cobalt oxide nanoparticles@nitrogen-doped reduced graphene oxide (Co₃O₄@N-rGO) composite and nitrogen-doped graphene dots (N-GDs) were synthesized by a one-pot simple hydrothermal method. The average sizes of the synthesized bare cobalt oxide nanoparticles (Co₃O₄ NPs) and Co₃O₄ NPs in the Co₃O₄@N-rGO composite were around 22 and 24 nm, respectively with an interlayer distance of 0.21 nm, as calculated using the XRD patterns. The Co₃O₄@N-rGO electrode exhibits superior capacitive performance with a high capability of about 450 F g^?1 at a current density of 1 A g^?1 and has excellent cyclic stability, even after 1000 cycles of GCD at a current density of 4 A g^?1. The obtained N-GDs exhibited high sensitivity and selectivity towards Fe²⁺ and Fe³⁺, the limit of detection was as low as 1.1 and 1.0 μM, respectively, representing high sensitivity to Fe²⁺ and Fe³⁺. Besides, the N-GDs was applied for bio-imaging. We found that N-GDs were suitable candidates for differential staining applications in yeast cells with good cell permeability and localization with negligible cytotoxicity. Hence, N-GDs may find dual utility as probes for the detection of cellular pools of metal ions (Fe³⁺/Fe²⁺) and also for early detection of opportunistic yeast infections in biological samples.     

Synthesis and characterization of magnetic polyHIPEs with humic acid surface modified magnetic iron oxide nanoparticles

Magnetic macroporous polymer monoliths have been prepared using styrene/divinylbenzene (S/DVB) high internal phase emulsions (HIPEs) as templates. Humic acid surface modified iron oxide magnetic nanoparticles (Fe₃O₄@HA) have been used to prepare magnetic emulsion templates. The effect of magnetic particle concentration has been investigated by changing the ratio of Fe₃O₄@HA nanoparticles in the continuous phase. Highly macroporous polymers with magnetic response were obtained by the removal of the internal phase after the curing of emulsions at 80 °C. Fe₃O₄@HA particles were characterized by XRD and FTIR. The porosity, pore morphology and magnetic properties of the macroporous polymers were characterized as a function of the Fe₃O₄@HA concentration by scanning electron microscopy (SEM), Brunauer–Emmet–Teller (BET) molecular adsorption method and vibrating sample magnetometry (VSM), respectively. BET and VSM measurements demonstrated that the specific surface area and the saturation magnetization of the polymer monoliths were changed according to the Fe₃O₄@HA concentration between 8.77–35.08 m² g^?1 and 0.63–11.79 emu g^?1, respectively. Resulting magnetic monoliths were tested on the adsorption of Hg(II) and atomic absorption spectroscopy (AAS) was used to calculate the adsorption capacities. The maximum adsorption capacity of the magnetic monoliths was calculated to be 20.44 mmol g^?1 at pH 4.     

Effectiveness of Ni incorporation in iron oxide crystal structure towards thermochemical CO2 splitting reaction

In this study, Ni-doped iron oxide (Ni_xFe_3−xO₄) materials were synthesized via the 1,2-epoxypropane assisted sol-gel method by varying the molar concentration of Ni from x=0.2 to 1. Sol-gel derived Ni_xFe_3−xO₄ gels were dried and the dried powder was further calcined upto 600 °C in air for 90 min. Obtained calcined Ni_xFe_3−xO₄ powders were further analyzed to determine the phase composition, crystallite size, specific surface area, pore volume, and morphology via powder X-ray diffraction (PXRD), BET surface area analysis (BET), as well as scanning and transmission electron microscopy (SEM and TEM). The obtained results in the synthesis and characterization section indicate formation of Ni_xFe_3−xO₄ nanoparticles with high specific surface area. Thermal reduction and re-oxidation of the sol-gel synthesized Ni_xFe_3−xO₄ materials were determined by using the high temperature thermogravimetry. Obtained results indicate that the amount of O₂ released during the thermal reduction step (at 1400 °C) and quantity of CO produced during the CO₂ splitting step (at 1000 °C) increases as the concentration of Ni inside the iron oxide crystal structure increases. The highest amounts of O₂ released (221.88 μmol/g) and CO produced (375.01 μmol/g) in case of NiFe₂O₄ (NF10 material).     

A comparative study of the magnetic and microwave properties of Al3+ and In3+ substituted Mg–Mn ferrites

The effect of substitution of diamagnetic Al³⁺ and In³⁺ ions for partial Fe³⁺ ions in a spinel lattice on the magnetic and microwave properties of magnesium–manganese (Mg–Mn) ferrites has been studied. Three kinds of Mg–Mn based ferrites with compositions of Mg_0.9Mn_0.1Fe₂O₄, Mg_0.9Mn_0.1Al_0.1Fe_1.9O₄, and Mg_0.9Mn_0.1In_0.1Fe_1.9O₄ were prepared by the solid-state reaction route. Each mixture of high-purity starting materials (oxide powders) in stoichiometric amounts was calcined at 1100 °C for 4 h, and the debinded green compacts were sintered at 1350 °C for 4 h. XRD examination confirmed that the sintered ferrite samples had a single-phase cubic spinel structure. The incorporation of Al³⁺ or In³⁺ ions in place of Fe³⁺ ions in Mg–Mn ferrites increased the average particle size, decreased the Curie temperature, and resulted in a broader resonance linewidth as compared to un-substituted Mg–Mn ferrites in the X-band. In this study, the In³⁺ substituted Mg–Mn ferrites exhibited the highest saturation magnetization of 35.7 emu/g, the lowest coercivity of 4.1 Oe, and the highest Q×f value of 1050 GHz at a frequency of 6.5 GHz.     

Study on orientation in EVA/Fe3O4 composite hot-melt adhesives

EVA hot melt adhesives have tackiness to both external anticorrosion coating made by cross-linked polyethylene and iron-base petroleum pipeline. But, traditional EVA hot melt adhesives cannot meet the requirement of external anticorrosion coating for weaker tackiness. Two types of Fe₃O₄ particles with different particle sizes and magnetic strengths were added in adhesives. One is of 3.665 μm^{Laser particle size analyzer (LPSA)} and 8.403×10¹ emu/g^{vibrating sample magnetometer (VSM)} and the other one is of 0.426 μm^LPSA and 3.997×10¹ emu/g^VSM. The result of peel test indicated that peel strength of composite adhesives increased as Fe₃O₄ content increased when particles size was 3.665 μm^LPSA but the tackiness of composite adhesive decreased as Fe₃O₄ content increased when particles size was 0.426 μm^LPSA. Also, microphotos of SEM revealed that the composite adhesive with 3.665 μm^LPSA Fe₃O₄ was more likely to distribute in a region near the tackiness surface between the adhesive and iron layers, but the one with 0.426 μm^LPSA Fe₃O₄ was more likely to aggregate in the middle region of adhesive. The movement of 3.665 μm^LPSA Fe₃O₄ particles could induce EVA molar chain orientation and this orientation was confirmed by infrared dichroism and XRD. Results of infrared dichroism and XRD showed that the orientation degree of EVA increased as 3.665 μm^LPSA Fe₃O₄ content increased. Furthermore, crystallinity tests by XRD and DSC indicated that crystallinity of PE segment of EVA also increased as 3.665 μm^LPSA Fe₃O₄ content increased, which could support increase of orientation tested by infrared dichroism and XRD.     

Effect of core-shell reversal on the structural,magnetic and adsorptive properties of Fe2O3-GO nanocomposites

Effect of core-shell reversal on the nanocomposites of graphene oxide (GO) and ferric oxide (Fe₂O₃) was studied. Fe₂O₃@GO core-shell nanosheets were synthesized by sonication method, while the GO@Fe₂O₃ core-shell nanospheres by employing N,N′-dicyclohexylcarbodimide as the binding agent for the wrapping of GO sheets on pre-formed Fe₂O₃ nanoparticles (NPs). The phase composition, crystallinity and morphology of the nanocomposites were characterized by FT-IR, TEM, SEM-EDS, VSM, BET surface area study and XRD techniques. The saturation magnetization (M_s) was 1.25 and 0.51 emu g⁻¹ for GO@Fe₂O₃ and Fe₂O₃@GO respectively owing to the dependence of magnetic properties on the reversal of core-shell. BET analysis revealed the surface area of 100.32 m² g⁻¹ and 45.69 m² g⁻¹ for GO@Fe₂O₃ and Fe₂O₃@GO nanocomposites respectively. The fabricated nanocomposites were analyzed as adsorbents for the uptake of Pb (II) ions. The impact of various factors affecting adsorption process such as pH, adsorbent dose, contact time, temperature and metal ion concentration was also investigated. GO@Fe₂O₃ core-shell nanospheres showed a higher adsorption capacity for Pb (II) ions as compared to Fe₂O₃@GO core-shell nanosheet with the maximum adsorption capacities (q_m) of 303.0 and 125.0 mg g⁻¹ respectively. The equilibrium data was estimated by Freundlich, Langmuir, D-R and Temkin isotherm models. Thermodynamic analysis confirmed the spontaneous and exothermic nature of the adsorption process. The adsorption kinetics was significantly fitted to pseudo-second order model. The results confirmed that core-shell reversal can significantly alter the adsorptive properties of Fe₂O₃-GO nanocomposite     

Magnetic reduced graphene oxide nanocomposite as an effective electromagnetic wave absorber and its absorbing mechanism

A magnetic reduced graphene oxide (MRGO) composite consisting of graphene oxide and Fe₃O₄ particles in the range of 5–20 nm has been prepared by the one-pot hydrothermal process. RGO nanosheets provide flexible substrates for nanoparticle decoration, while Fe₃O₄ nanoparticles can also effectively prevent nanosheets to restack each other. Compared with previously literature, the synthesized RGO-Fe₃O₄ composite exhibits excellent electromagnetic wave absorption. The minimum reflection loss (R_L) value of −49.05 dB has been observed at 14.16 GHz with a thickness of 2.08 mm. The absorption bandwidth (R_L<−10 dB) corresponding to the minimum R_L is 4.60 GHz. The electromagnetic wave absorption properties of the RGO-Fe₃O₄ composite have been interpreted through the quarter-wavelength matching model.     

Fe3O4 nanoparticles encapsulated in electrospun porous carbon fibers with a compact shell as high-performance anode for lithium ion batteries

Fe₃O₄ nanoparticles encapsulated in porous carbon fibers (Fe₃O₄@PCFs) as anode materials in lithium ion batteries are fabricated by a facile single-nozzle electrospinning technique followed by heat treatment. A mixed solution of polyacrylonitrile (PAN) and polystyrene (PS) containing Fe₃O₄ nanoparticles is utilized to prepare hybrid precursor fibers of Fe₃O₄@PS/PAN. The resulted porous Fe₃O₄/carbon hybrid fibers composed of compact carbon shell and Fe₃O₄-embeded honeycomb-like carbon core are formed due to the thermal decomposition of PS and PAN. The Fe₃O₄@PCF composite demonstrates an initial reversible capacity of 1015 mAh g⁻¹ with 84.4% capacity retention after 80 cycles at a current density of 0.2 A g⁻¹. This electrode also exhibits superior rate capability with current density increasing from 0.1 to 2.0 A g⁻¹, and capacity retention of 91% after 200 cycles at 2.0 A g⁻¹. The exceptionally high performances are attributed to the high electric conductivity and structural stability of the porous carbon fibers with unique structure, which not only buffers the volume change of Fe₃O₄ with the internal space, but also acts as high-efficient transport pathways for ions and electrons. Furthermore, the compact carbon shell can promote the formation of stable solid electrolyte interphase on the fiber surface.