Structural, Morphological, and Magnetic Properties of Nickel Substituted Cobalt Zinc Nanoferrites at Different Sintering Temperature

2021 ◽  
Vol 7 (2) ◽  
pp. 24-32
Author(s):  
D. Parajuli ◽  
N. Murali ◽  
K. Samatha
Keyword(s):  
Particle Size ◽  
Magnetic Properties ◽  
Sintering Temperature ◽  
Compositional Analysis ◽  
Sintered Sample ◽  
Lattice Parameter ◽  
Nickel Concentration ◽  
Ionic Radii ◽  
X Ray ◽  
Average Lattice

Co-precipitation was used for the preparation of Co0.5-xNixZn0.5Fe2O4 (x = 0 to 0.3) nanoferrites. The inverse spinel structure of the samples was clearly shown by the structural analysis of X-ray Diffractometer (XRD) and Fourier Transform Infrared (FTIR) Spectroscopy. We have studied the effect of sintering temperature (500oC) on the lattice constant and particle size using XRD. The average lattice parameters for the non-sintered and sintered samples were 8.377 Å and 8.354 Å respectively. For the non-sintered sample, the nickel concentration decreases the lattice parameter from 8.354 Å to 8.310 Å due to its smaller ionic radii than that of cobalt. While for a sintered sample at 500oC, the lattice parameter increases for concentration x=0.3 due to the thermal effect. The particle size calculated by Transmission Electron Microscope (TEM) agrees well with that of XRD. The morphological and compositional analysis was done with the help of Scanning Electron Microscopy (SEM) and the attached Energy Dispersive X-ray (EDX) Analyzer. The increasing percentage of nickel with decreasing percentage of cobalt shows that the cobalt is substituted by Nickel. The magnetic properties were studied by Vibrational Spectrometer (VSM). The value of saturation magnetization is higher for x=0.1 but lower for x=0.2 and 0.3 due to their particle size. The hysteresis loop of the samples their superparamagnetic behavior at room temperature.

Annealing Effects on the Physical and Magnetic Properties of Tb1.5Y1.5Fe5O12 Films Nanoparticles Prepared by Sol-Gel Method

2013 ◽  
Vol 756 ◽  
pp. 91-98 ◽  
Author(s):  
Ftema W. Aldbea ◽  
Noor Bahyah Ibrahim ◽  
Mustafa Hj. Abdullah
Keyword(s):  
Particle Size ◽  
Magnetic Properties ◽  
Annealing Temperature ◽  
Quartz Substrate ◽  
Sol Gel ◽  
Lattice Parameter ◽  
Gel Method ◽  
X Ray ◽  
Sol Gel Method ◽  
Iron Garnet

Terbium –substituted yttrium iron garnet (Tb1.5Y1.5Fe5O12) films nanoparticles were successfully prepared by a sol-gel method. The films were deposited on the quartz substrate using spin coating technique. To study effect of annealing temperature, the annealing process was executed at 700, 800 and 900 °C in air for 2 hours. The X-ray diffraction (XRD) proved that the pure phase of garnet structure was detected for the film annealed at 900 °C. The lattice parameter increased with the increment of annealing temperature and the highest value of 12.35 Å was obtained at 900 °C. Field Emission Scanning Electron Microscope (FE-SEM) results showed that the particle size increased from 43nm to 56nm as annealing temperature increased from 700 to 900°C. The film’s thickness also affected by increasing of annealing temperature and become thin at 900 °C due to densification process occurred at high annealing temperature. The elemental compositions of the Tb1.5Y1.5Fe5O12 film were detected using an Energy Dispersive X-raySpectroscopy (EDX). Magnetic properties at room temperature were measured using a Vibrating Sample Magnetometer (VSM).The saturation magnetization Ms increased with the annealingtemperature and showed a high value of 104emu/cm3, but the coercivity Hc of the film was decreased due to the increment of the particle size. Normal 0 21 false false false MS X-NONE X-NONE MicrosoftInternetExplorer4 Terbium –substituted yttrium iron garnet (Tb1.5Y1.5Fe5O12) films nanoparticles were successfully prepared by a sol-gel method. The films were deposited on the quartz substrate using spin coating technique. To study effect of annealing temperature, the annealing process was executed at 700, 800 and 900°C in air for 2 hours. The X-ray diffraction (XRD) proved that the pure phase of garnet structure was detected for the film annealed at 900 °C. The lattice parameter increased with the increment of annealing temperature and the highest value of 12.35 Å was obtained at 900 °C. Field Emission Scanning Electron Microscope (FE-SEM) results showed that the particle size increased from 43nm to 56nm as annealing temperature increased from 700 to 900 °C. The film’s thickness also affected by increasing of annealing temperature and become thin at 900 °C due to densification process occurred at high annealing temperature. The elemental compositions of the Tb1.5Y1.5Fe5O12 film were detected using an Energy Dispersive X-ray Spectroscopy (EDX). Magnetic properties at room temperature were measured using a Vibrating Sample Magnetometer (VSM).The saturation magnetization Ms increased with the annealing temperature and showed a high value of 104emu/cm3, but the coercivity Hc of the film was decreased due to the increment of the particle size. st1\:*{behavior:url(#ieooui) } /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0cm 5.4pt 0cm 5.4pt; mso-para-margin:0cm; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi;}

scholarly journals Ferroelectromagnetic Properties of PbFe1/2Nb1/2O3 (PFN) Material Synthesized by Chemical-Wet Technology

Materials ◽  
2018 ◽  
Vol 11 (12) ◽  
pp. 2504 ◽  
Author(s):  
Dariusz Bochenek ◽  
Przemysław Niemiec
Keyword(s):  
Magnetic Properties ◽  
Electron Microscope ◽  
Scanning Electron Microscope ◽  
Sintering Temperature ◽  
Closed Porosity ◽  
X Ray ◽  
Synthesis Conditions ◽  
Ceramic Samples ◽  
Sem Microstructure ◽  
Scanning Electron

In this work, PbFe1/2Nb1/2O3 (PFN) ceramic samples synthesized by chemically wet method (precipitation from the solution) were obtained. Due to the tendency to form powder agglomerates, the synthesized powder was subjected to ultrasound. The sintering was carried out under various technological conditions, mainly through controlling the sintering temperature. -X-ray powder-diffraction (XRD), scanning electron microscope (SEM) microstructure analysis, as well as the examinations of dielectric, ferroelectric, and magnetic properties of the PFN ceramics were carried out. Studies have shown that hard ceramic agglomerates can be partially minimized by ultrasound. Due to this treatment, closed porosity decreases, and the ceramic samples have a higher density. Optimization and improvement of the technological process of the PFN material extends the possibility of its use for the preparation of multiferroic composites or multicomponent solid solutions based on PFN. Such materials with functional properties find applications in microelectronic applications, e.g., in systems integrating ferroelectric and magnetic properties in one device. The optimal synthesis conditions of PFN ceramics were determined to be 1050 °C/2 h.

Effect of Process on the Dielectric Properties of BaTiO3-Based X9R Ceramics

2014 ◽  
Vol 906 ◽  
pp. 18-24 ◽  
Author(s):  
Bao Lin Zhang ◽  
Bin Bin Zhang ◽  
Ning Ning Wang ◽  
Jing Ming Fei
Keyword(s):  
Particle Size ◽  
Dielectric Properties ◽  
Milling Time ◽  
Sintering Temperature ◽  
Sintering Process ◽  
X Ray Diffraction ◽  
Sintered Ceramic ◽  
X Ray ◽  
Particle Size Analyzer

The effect of milling time and sintering process on the dielectric properties of BaTiO3-based X9R ceramics was investigated. The characterization of the raw powders and the sintered ceramic was carried out by X-ray diffraction and scanning electron microscopy. The particle size distribution of the mixed powders was examined by Laser Particle Size Analyzer. The results shown that with the milling time extended, the Cruie Peak was depressed, or even disappeared. Moreover, with the rise of sintering temperature, the dielectric constant of the ceramics increased and the dielectric loss decreased gradually. Eventually, by milling for 11h and sintering at 1090°Cfor 2h, good dielectric properties were obtained, which were ε25°C≥ 2526, εr/εr25°C≤± 12% (–55~200°C), tanδ≤1.12% (25°C).

ZnFe2O4 Modified by Fe(NO3)3 for the Synthesis of Ionic Ferrofluids

2010 ◽  
Vol 177 ◽  
pp. 32-36 ◽  
Author(s):  
An Rong Wang ◽  
Jian Li ◽  
Qing Mei Zhang ◽  
Hua Miao
Keyword(s):  
Particle Size ◽  
Magnetic Properties ◽  
Electron Microscope ◽  
Transmission Electron Microscope ◽  
Photoelectron Spectroscopy ◽  
Vibrating Sample Magnetometer ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Znfe2o4 Nanoparticles

Weak magnetic ZnFe2O4 nanoparticles were prepared by coprecipitation and treated with different concentrations of Fe(NO3)3 solution. Untreated and treated particles were studied using a vibrating sample magnetometer, transmission electron microscope, by X-ray diffraction, X-ray energy dispersive spectroscopy and X photoelectron spectroscopy. The results showed that, after treatment, the ZnFe2O4/γ-Fe2O3 forms disphase nanoparticles, with enlarged size, enhanced magnetic properties and with a surface parceled with Fe(NO3)3. The size of the particles and their magnetic properties are related to the concentration of the treatment solution. The particle size and magnetic properties could be controlled by controlling the concentration of treating solution, therefore nanoparticles can be more widely used.

Preparation and Properties of CaF2 Nano-Powder

2016 ◽  
Vol 680 ◽  
pp. 257-260
Author(s):  
Meng Yun Dong ◽  
Cheng Zhang ◽  
Jin Feng Xia ◽  
Hong Qiang Nian ◽  
Dan Yu Jiang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Particle Size ◽  
Sintering Temperature ◽  
Raw Materials ◽  
X Ray Diffraction ◽  
X Ray ◽  
Nano Powder ◽  
Direct Precipitation ◽  
Scanning Electron

CaF2 nano-power was prepared by direct precipitation methods with Ca(NO3)2 and KF as raw materials. The influences of presintering temperature and sintering temperature on the particle size and distribution of CaF2 nano-power were studied by X-ray diffraction (XRD) and field-emission scanning electron microscopy (FESEM). This study provided an experimental method for preparation of CaF2 nano-power. The results show that the best presintering temperature of CaF2 nano-power is 500°C and the best sintering temperature of CaF2 ceramic is 900°C.

Preparation of LaFeO3 particles by sol-gel technology

1998 ◽  
Vol 13 (2) ◽  
pp. 451-456 ◽  
Author(s):  
C. Vázquez-Vázquez ◽  
P. Kögerler ◽  
M. A. López-Quintela ◽  
R. D. Sánchez ◽  
J. Rivas
Keyword(s):  
Particle Size ◽  
Magnetic Properties ◽  
Infrared Spectroscopy ◽  
Sol Gel ◽  
Diffraction Peak ◽  
Gel Formation ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ferromagnetic Component ◽  
Peak Broadening

The study of submicroscopic particles in already known systems has resulted in a renewed interest due to the large differences found in their properties when the particle size is reduced, and because of possible new technological applications. In this work we report the preparation of LaFeO3 particles by the sol-gel route, starting from a solution of the corresponding metallic nitrates and using urea as gelificant agent. Gels were decomposed at 200 °C and calcined 3 h at several temperatures, T, in the range 250–1000 °C. The samples were structurally characterized by x-ray diffraction (XRD) showing that the orthoferrite crystallizes at T as low as 315 °C. From the x-ray diffraction peak broadening, the particle size was determined. The size increases from 60 to 300 nm as the calcination T increases. Infrared spectroscopy was used to characterize gels and calcined samples. From these studies a mechanism for the gel formation is proposed. Study of the magnetic properties of LaFeO3 particles shows the presence of a ferromagnetic component which diminishes as the calcination temperature increases, vanishing at T = 1000 °C.

Structural and Dielectric Analysis of La0.88Bi0.12Mn0.80Ni0.20O3 Composite

2021 ◽  
Vol 317 ◽  
pp. 35-45
Author(s):  
Aaliyawani Ezzerin Sinin ◽  
Walter Charles Primus ◽  
Zainal Abidin Talib ◽  
Chen Soo Kien ◽  
Abdul Halim Shaari ◽  
...  
Keyword(s):  
Dielectric Loss ◽  
Sintering Temperature ◽  
Solid State Reaction Method ◽  
Lattice Parameter ◽  
Rhombohedral Structure ◽  
X Ray Diffraction ◽  
Conventional Solid State Reaction ◽  
X Ray ◽  
A Value ◽  
Electric Behavior

Composite La0.88Bi0.12Mn0.80Ni0.20O3 was synthesized using the conventional solid-state reaction method with sintering temperature of 1200 °C for 12 hours and the dielectric properties investigated. The X-ray diffraction result shows that the composite has a rhombohedral structure with lattice parameter of a = b = c = 5.5136 Ǻ. Scanning electron microscope shows grains with approximately from 0.8 to 5.4 μm in size with presence of voids. The dielectric permittivity, εʹ and dielectric loss, εʺ were measured in the range of 298 K to 473 K where both are temperature and frequency dependent. At 1 kHz to 100 kHz, the εʹ is around 10000 and the dielectric loss tangent, tan δ is below 1.5. The electric behavior of this composite is best represented by Quasi-dc model which consists of two universal capacitors in parallel. Parameters value from the fitting indicated that high correlations of electrons between inter and intra-clusters. The activation energy, Ea calculated from the conductivity of the sample gives a value of 0.116 eV. Vibrating sample magnetometer shows that the La0.88Bi0.12Mn0.80Ni0.20O3 has a magnetic coercivity, Hc of 36.109 G and retentivity, Br, valued 2.7504 x 10-3 emu/g.

Dependence on cation distribution of particle size, lattice parameter, and magnetic properties in nanosize Mn–Zn ferrite

2002 ◽  
Vol 91 (4) ◽  
pp. 2211-2215 ◽  
Author(s):  
Chandana Rath ◽  
S. Anand ◽  
R. P. Das ◽  
K. K. Sahu ◽  
S. D. Kulkarni ◽  
...  
Keyword(s):  
Particle Size ◽  
Magnetic Properties ◽  
Cation Distribution ◽  
Lattice Parameter ◽  
Zn Ferrite

Analyzing structure factor phases in pure and doped single crystals by synchrotron X-ray Renninger scanning

2013 ◽  
Vol 47 (1) ◽  
pp. 160-165 ◽  
Author(s):  
Zohrab G. Amirkhanyan ◽  
Claúdio M. R. Remédios ◽  
Yvonne P. Mascarenhas ◽  
Sérgio L. Morelhão
Keyword(s):  
Small Difference ◽  
Accurate Determination ◽  
Nickel Sulfate ◽  
Lattice Parameter ◽  
Metallic Ions ◽  
Multiple Diffraction ◽  
Ionic Radii ◽  
X Ray ◽  
Model Structures

X-ray multiple diffraction has been applied to study the substitutional incorporation of Mg2+ions into NSH crystals (nickel sulfate hexahydrate, NiSO4·6H2O). Intensity profiles provide information on invariant phases, while angular positions of the multiple diffractions allow accurate determination of lattice parameters. By increasing the atomic disordering only of O2−sites in model structures of doped NSH, the sense and magnitude of induced phase shifts match those necessary to justify the observed changes in the intensity profiles. Causes of disordering and lattice parameter variation are discussed. Although the amount of extra oxygen disordering is relatively large with respect to the small difference in the ionic radii of the metallic ions, this disordering is beyond the resolution power achievable by analyzing diffracted intensities of isolated reflections, such as in standard crystallographic techniques.

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