scholarly journals Structural, Optical, and Catalytic Properties of MgCr2O4 Spinel-Type Nanostructures Synthesized by Sol–Gel Auto-Combustion Method

Catalysts ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 1476
Author(s):  
Vasyl Mykhailovych ◽  
Andrii Kanak ◽  
Ştefana Cojocaru ◽  
Elena-Daniela Chitoiu-Arsene ◽  
Mircea Nicolae Palamaru ◽  
...  

Spinel chromite nanoparticles are prospective candidates for a variety of applications from catalysis to depollution. In this work, we used a sol–gel auto-combustion method to synthesize spinel-type MgCr2O4 nanoparticles by using fructose (FS), tartaric acid (TA), and hexamethylenetetramine (HMTA) as chelating/fuel agents. The optimal temperature treatment for the formation of impurity-free MgCr2O4 nanostructures was found to range from 500 to 750 °C. Fourier transform infrared (FTIR) spectroscopy was used to determine the lattice vibrations of the corresponding chemical bonds from octahedral and tetrahedral positions, and the optical band gap was calculated from UV–VIS spectrophotometry. The stabilization of the spinel phase was proved by X-ray diffraction (XRD) and energy-dispersive X-ray (EDX) analysis. From field-emission scanning electron microscopy (FE-SEM), we found that the size of the constituent particles ranged from 10 to 40 nm. The catalytic activity of the as-prepared MgCr2O4 nanocrystals synthesized by using tartaric acid as a chelating/fuel agent was tested on the decomposition of hydrogen peroxide. In particular, we found that the nature of the chelating/fuel agent as well as the energy released during the auto-combustion played an important role on the structural, optical, and catalytic properties of MgCr2O4 nanoparticles obtained by this synthetic route.

2014 ◽  
Vol 3 (3) ◽  
pp. 267-277 ◽  
Author(s):  
Ahmad Amirabadizadeh ◽  
Mohammad Rasouli ◽  
Reza Sarhaddi

In this study, Co0.5Ni0.5-xMnxFe2O4 (x=0, 0.15, 0.25, 0.35, 0.5) ferrite nanoparticles were prepared by sol-gel auto-combustion method. Structural, magnetic and morphology properties of obtained nanoparticles were investigated with X-ray Diffraction (XRD), Vibrating Sample Magnetometer (VSM) and Transmission Electron Microscopy(TEM), respectively. The XRD results show that the most dominant peaks for samples is related to the Spinel phase. Crystalline size using Scherrer's equation for different values of x were obtained between 44 to 64 nm. VSM results showed that the saturation magnetization and coercivity values changed with increasing Mn. TEM images obtained results are in good agreement with the XRD results.


Cerâmica ◽  
2019 ◽  
Vol 65 (374) ◽  
pp. 274-281 ◽  
Author(s):  
S. S. Satpute ◽  
S. R. Wadgane ◽  
S. R. Kadam ◽  
D. R. Mane ◽  
R. H. Kadam

Abstract Y3+ substituted strontium hexaferrites having chemical composition SrYxFe12-xO19 (x= 0.0, 0.5, 1.0, 1.5) were successfully synthesized by sol-gel auto-combustion method. The structural and morphological studies of prepared samples were investigated by using X-ray diffraction technique, energy dispersive X-ray spectroscopy, field emission scanning electron microscopy (FE-SEM) and high-resolution transmission electron microscopy. The X-ray diffraction pattern confirmed the single-phase hexagonal structure of yttrium substituted strontium ferrite and the lattice parameters a and c increased with the substitution of Y3+ ions. The crystallite size also varied with x content from 60 to 80 nm. The morphology was studied by FE-SEM, and the grain size of nanoparticles ranged from 44 to 130 nm. The magnetic properties were investigated by using vibrating sample magnetometer. The value of saturation magnetization decreased from 49.60 to 35.40 emu/g. The dielectric constant decreased non-linearly whereas the electrical dc resistivity increased with the yttrium concentration in strontium hexaferrite.


2020 ◽  
Vol 43 (1) ◽  
pp. 26-42 ◽  
Author(s):  
Zahra Hajian Karahroudi ◽  
Kambiz Hedayati ◽  
Mojtaba Goodarzi

AbstractThis study presents a preparation of SrFe12O19– SrTiO3 nanocomposite synthesis via the green auto-combustion method. At first, SrFe12O19 nanoparticles were synthesized as a core and then, SrTiO3 nanoparticles were prepared as a shell for it to manufacture SrFe12O19–SrTiO3 nanocomposite. A novel sol-gel auto-combustion green synthesis method has been used with lemon juice as a capping agent. The prepared SrFe12O19–SrTiO3 nanocomposites were characterized by using several techniques to characterize their structural, morphological and magnetic properties. The crystal structures of the nanocomposite were investigated via X-ray diffraction (XRD). The morphology of SrFe12O19– SrTiO3 nanocomposite was studied by using a scanning electron microscope (SEM). The elemental composition of the materials was analyzed by an energy-dispersive X-ray (EDX). Magnetic properties and hysteresis loop of nanopowder were characterized via vibrating sample magnetometer (VSM) in the room temperature. Fourier transform infrared spectroscopy (FTIR) spectra of the samples showed the molecular bands of nanoparticles. Also, the photocatalytic behavior of nanocomposites has been checked by the degradation of azo dyes under irradiation of ultraviolet light.


2015 ◽  
Vol 29 (14) ◽  
pp. 1550090 ◽  
Author(s):  
O. Mirzaee ◽  
R. Mohamady ◽  
A. Ghasemi ◽  
Y. Alizad Farzin

Nanostructure of Y-type hexaferrite with composition of Sr 2 Ni 2 Al x/2 Cr x/2 Fe 12-x O 22 (where x are 0, 0.6, 1.2, 1.8, 2.4 and 3) were prepared by sol–gel auto-combustion method. The influence of Al and Cr doping on the structural and magnetic properties has been investigated. The X-ray diffraction (XRD) patterns confirm phase formation of Y-type hexaferrite. The microstructure and morphology of prepared samples were studied by high resolution field emission scanning electron microscope (FESEM) which shows the hexagonal shape for all of the samples. Magnetic properties were characterized using vibrating sample magnetometer (VSM). The magnetic results revealed that by increasing the Al and Cr to the structure, the coercivity was also increased from 840 Oe to 1160 Oe. Moreover it has been shown that with addition of dopants, saturation magnetization (Ms) and remnant magnetization (Mr) were decreased from 39.61 emu/g to 30.11 emu/g and from 17.51 emu/g to 14.62 emu/g, respectively, due to the entrance of nonmagnetic ions into Fe 3+ sites.


2013 ◽  
Vol 209 ◽  
pp. 177-181 ◽  
Author(s):  
Ram S. Barkule ◽  
D.V. Kurmude ◽  
A.V. Raut ◽  
N.N. Waghule ◽  
K.M. Jadhav ◽  
...  

Abstract: The magnetic nano-particles of nickel ferrite were synthesized successfully by sol-gel auto-combustion method using high purity metal nitrates and citric acid as chelating agent. The as prepared powder of nickel ferrite was sintered at 5500C for 5 hr to obtain good crystalline phase and was used for further study. The X-ray diffraction technique was employed to confirm the single phase formation of nickel ferrite nano-particles. The X-ray diffraction pattern shows the Bragg’s peak which belongs to cubic spinel structure. The values of lattice constant, X-ray density, oxygen parameter and radii of tetrahedral and octahedral sites were calculated from XRD data. The average crystallite size was estimated using Scherrer’s formula and found to be 6 nm. The temperature dependence of the electrical conductivity plot shows the kink, which can be attributed to ferromagnetic-paramagnetic transition. The activation energy obtained from resistivity plots in paramagnetic region is found to be more than that in ferrimagnetic region. The conduction mechanism in these nickel ferrite nano-particles has been discussed on the basis of hopping of electrons.


2015 ◽  
Vol 815 ◽  
pp. 141-146 ◽  
Author(s):  
Gui Fang Liu ◽  
Run Hua Fan ◽  
Ke Lan Yan ◽  
Xu Ai Wang ◽  
Kai Sun ◽  
...  

Barium ferrite fibers and barium ferrite powders were successfully prepared respectively via Electrospinning method and sol-gel auto-combustion method by using Fe (NO3)3·9H2O, Ba (NO3)2 as one of the main raw materials. X-ray diffraction (XRD) and field emission scanning electron microscope (FSEM) were used to study the phase composition and microstructure of barium ferrite. The results showed that barium ferrite fibers consist of a mixture of barium ferrite particles, the diameter of fibers is about 200 nm; barium ferrite powders prepared by sol-gel auto-combustion method were flake barium ferrite compositing of rod-like grains of less than 100 nm in size stacking disorderly. Magnetic properties were investigated by vibrating sample magnetometer (VSM), the results showed that the values of Mr, Ms, and Hc of barium ferrite fibers and powders are quite different due to their different morphologies.


2019 ◽  
Vol 24 (7) ◽  
pp. 52
Author(s):  
Ibrahim F. Waheed ◽  
Faiz M. AL-Abady ◽  
Baidaa M. Ali

Magnesium ferrite (MgFe2O4) nanoparticles is prepared by sol-gel auto combustion method and calcinated at (200,450, 900) °C. The capping agent was urea and (Mg(NO3)2.6H2O) and (Fe(NO3)3.9H2O) nitrates as sources of metal. X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR) characteristic show clear modes of the cubic Mg-ferrite structure formation. Infrared spectrum of metal-oxygen vibration at (703-636) and (574-433) cm−1 show the tetrahedral and octahedral site of Mg-ferrite structure. Scanning Electron Microscope (SEM) images shown pure crystalline microstructure with polyhedral shapes and very small numbers of globular small particles. The crystallite size of Mg-ferrite is calculated using Debye-Scherrer relation and was in the range of 29 nm.   http://dx.doi.org/10.25130/tjps.24.2019.129


2014 ◽  
Vol 8 (2) ◽  
pp. 87-92 ◽  
Author(s):  
Unikoth Megha ◽  
Karakat Shijina ◽  
George Varghese

LaCo0.6Fe0.4O3 (LCFO) nanopowder was synthesized from constituent metal nitrates, citric acid and ethylene glycol by citrate sol gel autocombustion method and calcined at different temperatures. The powders were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDAX) and Fourier transform infrared spectra (FTIR), whereas dielectric properties were investigated with LCR-meter. The FTIR spectra, taken for the xerogel and the sample calcined at 1000?C, confirm that the organic groups were removed during calcination and oxide structure was formed. The XRD result shows that LCFO has rhombhohedral crystal structure with R-3C space group and forms single phase after calcination at 600?C. The activation energy of crystallite growth, determined from the Arrhenius plot, was 17?2 kJ/mol. Surface feature studies of the powders were obtained from SEM. At 1000?C, dense microstructure with wellshaped grain boundaries was obtained and the average grain size was around 400 nm. EDAX confirms the elemental composition. Finally, from the dielectric studies, it was found that the dielectric constant (?r) as well as dielectric loss tangent (tan ?) decreases with increase in frequency.


2012 ◽  
Vol 463-464 ◽  
pp. 1052-1056
Author(s):  
Ai Xiang Zeng ◽  
Jun Yuan

Ni0.6-xZn0.4MgxFe2O4were synthesized by sol-gel auto-combustion method with Zn(NO3.) 2 •6H2O. , Ni(NO3.) )2•6H2O. , Mg(NO3.) )2•6H2O. , Fe(NO3.) )3•9H2O. , COOO2. and NH3•H2O. X-ray diffraction (XRD) analysises show that the sample is single phase and the doping of magnesium makes no difference to nickel-zinc ferrite’s crystal structure; nickel-zinc ferrite has formed after auto-combustion. Scanning electron microscope analysises show that after sintered the sample’s size is more even and the doping of magnesium makes the size smaller and more even too.


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