Physical, Electrical and Magnetic Properties of Nanocrystalline Zr-Mn-Co Prepared by Co-Precipitation Route

2011 ◽  
Vol 14 ◽  
pp. 113-121
Author(s):  
Ashari Maqsood ◽  
Kishwar Khan ◽  
M. Anis-ur-Rehman ◽  
Muhammad Ali Malik
Keyword(s):  
Activation Energy ◽  
Particle Size ◽  
Electrical Resistivity ◽  
Drift Mobility ◽  
Spinel Ferrites ◽  
Average Particle ◽  
Dc Electrical Resistivity ◽  
X Ray ◽  
General Chemical ◽  
Co Precipitation

Spinel ferrites, which have the general chemical composition MeFe2O4, (Me = Co, Zn, Ni) are of interest due to their electronic, magnetic and optical properties. Nanosized Co-Zr-Mn spinel ferrites with nominal composition CoFe2-2xZrxMnxO4 (0.1≤ x≤0.4) have been prepared by the co-precipitation route. The products are characterized by X-ray diffraction, scanning electron microscopy (SEM) at room temperature, dc electrical resistivity as a function of temperature and dielectric parameters in the frequency range of 100 Hz to 3 MHz are also measured. The lattice constants agree with usual spinel ferrites. The particle size calculated from X-ray data by the Scherrer formula is in the range of 28-30 nm, while the average particle size varies from 15-25 nm obtained from the SEM measurements, X-ray density (Dx), Porosity (P) and bulk density (Dm) for all the samples are calculated. The dc electrical resistivity decreased with the rise in temperature for all the samples, showing a semiconductor like behavior. From the dc electrical resistivity the activation energy and drift mobility are determined. Both the drift mobility and activation energy increase with a rise in x. The dielectric constant, dielectric loss and ac electrical resistivity as a function of frequency are also reported. The low field ac magnetic susceptibility measurement showed that the ferrimagentic transition temperature is in the range of 439±5 K to 658±5 K.

Preparation, Structural and Electrical Properties of Nanocrystalline Zr-Mn Cobalt-Ferrite Synthesized by the Co-Precipitation Method

2012 ◽  
Vol 510-511 ◽  
pp. 248-254
Author(s):  
K. Khan
Keyword(s):  
Activation Energy ◽  
Electrical Resistivity ◽  
Frequency Band ◽  
Electrical Characterization ◽  
Drift Mobility ◽  
Precipitation Method ◽  
Dc Electrical Resistivity ◽  
Ft Ir ◽  
Ir Study ◽  
Co Precipitation

The present study describes the preparation, structural and electrical characterization of nanosized Zr-Mn cobalt-ferrites. The nominal compositions CoFe2-2xZrxMnxO4 (0.10.4) have been synthesized by the co-precipitation method. These nanopowder products were sintered in furnace at temperature of 800 °C for 8 hour with a heating rate of 10οC/min to obtain these ferrites. The nanopowder was evaluated using XRD, FT-IR and SEM. The XRD data showed that all the samples are of single phase and the crystallite size is found in the range of 2630 nm. The lattice constant (a), X-ray density (dx), porosity (P) and bulk density (dm) are also calculated from XRD data. FT-IR study confirms the presence of ferrite functional groups. The IR spectra of Zr-Mn ferrite system have been analyzed in the frequency range 400650 cm-1. It revealed two prominent bands υ1 and υ2 which are assigned to tetrahedral and octahedral metal complexes, respectively. The position of the highest frequency band is around 550 cm-1 while the lower frequency band is around 425 cm-1. The structural properties are also analyzed on scanning electron microscopy (SEM) at room temperature. Additionally, the dc electrical resistivity decreased with the rise in temperature for all the samples, showing a semiconductor like behavior. From the dc electrical resistivity the activation energy and drift mobility are determined. Both the drift mobility and activation energy increase with a rise in x.

Morphology-Controlled CaCO3 Nanostructures by Modified Co-Precipitation in Pulsed Mode

2015 ◽  
Vol 752-753 ◽  
pp. 148-153
Author(s):  
M.M. Nassar ◽  
Taha Ebrahiem Farrag ◽  
M.S. Mahmoud ◽  
Sayed Abdelmonem
Keyword(s):  
Particle Size ◽  
Calcium Carbonate ◽  
Rotation Speed ◽  
Average Particle Size ◽  
Calcium Nitrate ◽  
Precipitation Method ◽  
Average Particle ◽  
X Ray ◽  
Co Precipitation ◽  
Pulsed Mixing

Calcium carbonate nanoparticles and nanorods were synthesized by precipitation from saturated sodium carbonate and calcium nitrate aqueous solutions through co precipitation method. A new rout of synthesis was done by both using pulsed mixing method and controlling the addition of calcium nitrate. The effect of the agitation speed, and the temperature on particle size and morphology were investigated. Particles were characterized using X-ray Microanalysis, X-ray analysis (XRD) and scanning electron microscopy (SEM). The results indicated that increasing the mixer rotation speed from 3425 to 15900 (rpm) decreases the average particle size to 64±7 nm. A rapid nucleation then aggregation induced by excessive shear force phenomena could explain this observation. Moreover, by increasing the reaction temperature, the products were converted from nanoparticle to nanorods. The maximum attainable aspect ratio was 6.23 at temperature of 75°C and rotation speed of 3425. Generally, temperature raise promoted a significant homoepitaxial growth in one direction toward the formation of calcite nanorods. Overall, this study can open new avenues to control the morphology of the calcium carbonate nanostructures.

Electrical, Dielectrical and Magnetic Properties of Zr-Mn Doped Nano-Ferrites

2012 ◽  
Vol 510-511 ◽  
pp. 301-306
Author(s):  
K. Khan ◽  
Ashari Maqsood
Keyword(s):  
Activation Energy ◽  
Electrical Resistivity ◽  
Drift Mobility ◽  
Nominal Composition ◽  
Frequency Range ◽  
Energy Increase ◽  
Dielectric Parameters ◽  
Dc Electrical Resistivity ◽  
Low Field ◽  
Mn Doped

We measured the dc electrical resistivity as a function of temperature and dielectric parameters in the frequency range 100 Hz to 3 MHz of nanosized Zr-Mn spinel ferrites with nominal composition CoFe2-2xZrxMnxO4(0.1x0.4). The dc electrical resistivity decreased with the rise in temperature for all the samples, showing a semiconductor like behavior. From the dc electrical resistivity the activation energy and drift mobility are determined. Both the drift mobility and activation energy increase with a rise inx. The dielectric constant, dielectric (losses) and ac electrical resistivity as a function of frequency are also reported. The low field ac magnetic susceptibility measurement showed that the ferrimagentic transition temperature is in the range of 4395 K to 6585 K.

scholarly journals Thermal, Structural, and Physical Properties of Freeze Dried Tropical Fruit Powder

2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
K. A. Athmaselvi ◽  
C. Kumar ◽  
M. Balasubramanian ◽  
Ishita Roy
Keyword(s):  
Particle Size ◽  
Physical Properties ◽  
Average Particle Size ◽  
Average Particle ◽  
X Ray Diffraction ◽  
Tropical Fruit ◽  
X Ray ◽  
Freeze Dried ◽  
Fruit Powder ◽  
Lcr Meter

This study evaluates the physical properties of freeze dried tropical (guava, sapota, and papaya) fruit powders. Thermal stability and weight loss were evaluated using TGA-DSC and IR, which showed pectin as the main solid constituent. LCR meter measured electrical conductivity, dielectric constant, and dielectric loss factor. Functional groups assessed by FTIR showed presence of chlorides, and O–H and N–H bonds in guava, chloride and C–H bond in papaya, and chlorides, and C=O and C–H bonds in sapota. Particle size and type of starch were evaluated by X-ray diffraction and microstructure through scanning electronic microscopy. A semicrystalline profile and average particle size of the fruit powders were evidenced by X-ray diffraction and lamellar/spherical morphologies by SEM. Presence of A-type starch was observed in all three fruits. Dependence of electric and dielectric properties on frequency and temperature was observed.

Nitrocellulose Catalyzed With Manganese Oxide Nanoparticles: Advanced Energetic Nanocomposite With Superior Decomposition Kinetics

2021 ◽  
Author(s):  
Sherif Elbasuney ◽  
M. Yehia ◽  
Shukri Ismael ◽  
Yasser El-Shaer ◽  
Ahmed Saleh
Keyword(s):  
Activation Energy ◽  
Particle Size ◽  
Manganese Oxide ◽  
Energetic Materials ◽  
Average Particle Size ◽  
Active Surface ◽  
Propagation Rate ◽  
Hydroxyl Groups ◽  
Average Particle ◽  
Decomposition Enthalpy

Abstract Nanostructured energetic materials can fit with advanced energetic first-fire, and electric bridges (microchips). Manganese oxide, with active surface sites (negatively charged surface oxygen, and hydroxyl groups) can experience superior catalytic activity. Manganese oxide could boost decomposition enthalpy, ignitability, and propagation rate. Furthermore manganese oxide could induce vigorous thermite reaction with aluminium particles. Hot solid or liquid particles are desirable for first-fire compositions. This study reports on the facile fabrication of MnO2 nanoparticles of 10 nm average particle size; aluminium nanoplates of 100 nm average particle size were employed. Nitrocellulose (NC) was adopted as energetic polymeric binder. MnO2/Al particles were integrated into NC matrix via co-precipitation technique. Nanothermite particles offered an increase in NC decomposition enthalpy by 150 % using DSC; ignition temperature was decreased by 8 0C. Nanothemrite particles offered enhanced propagation index by 261 %. Kinetic study demonstrated that nanothermite particles experienced drastic decrease in NC activation energy by - 42, and - 40 KJ mol-1 using Kissinger and KAS models respectively. This study shaded the light on novel nanostructured energetic composition, with superior combustion enthalpy, propagation rate, and activation energy.

scholarly journals Preparation, Characterization and Performance Properties of Polydodecylmethylsilsesquioxane Nanoparticles

Coatings ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 1045
Author(s):  
Fuquan Deng ◽  
Hua Jin ◽  
Wei Xu
Keyword(s):  
Thermal Stability ◽  
Particle Size ◽  
Electron Microscope ◽  
Contact Angles ◽  
Process Conditions ◽  
Average Particle ◽  
Gravimetric Analysis ◽  
Laser Scattering ◽  
Excellent Thermal Stability ◽  
X Ray

A series of polydodecylmethylsilsesquioxane (PDMSQ) nanocomposite latexes were prepared via emulsion polymerization of methyltriethoxysilane (MTES) and dodecyltrimethoxysilane (DTMS) and sodium hydroxide as the catalyst, and sodium dodecyl benzene sulfonate/Tween 80 as the mixed emulsifiers. Effects of the emulsifier doses, the reaction temperature, the catalyst concentration and the oil/water ratio on the particle size and distribution of the PDMSQ nanoparticles were discussed. Particle size and micromorphology, structure, thermal stability, crystallinity and hydrophobicity of PDMSQ nanoparticles (PDMSQ NPs) were investigated by dynamic laser scattering (DLS), Fourier transform infrared spectroscopy (FTIR), silicon-nuclear magnetic resonance (28Si-NMR), X-ray photoelectron spectroscope (XPS), scanning electron microscope (SEM), transmission electron microscope (TEM), atomic force microscope (AFM), thermo gravimetric analysis (TGA), X-ray diffraction (XRD) and contact angle tester. Results showed that a series of PDMSQ NPs could be obtained with an average particle size of less than 80 nm and narrow distribution as well as spherical structure under the optimal process conditions. PDMSQ NPs exhibited excellent thermal stability and were mainly amorphous but also contained some crystal structures. Importantly, the static water contact angles (WCAs) on its latex films were larger than 150° and the WCAs hysteresis were less than 10°, thus those PDMSQ nanocomposite latexes show potential in the field of superhydrophobic coatings.

scholarly journals Preparation of ultrafine iron phosphate micro-powder from phosphate slag

2018 ◽  
Vol 238 ◽  
pp. 02002
Author(s):  
Fangjing Sun ◽  
Yi Zhang ◽  
Jiawei Zhang ◽  
Xixi Yan ◽  
Xiaoyu Liu ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Particle Size ◽  
Electron Microscope ◽  
Average Particle Size ◽  
Iron Phosphate ◽  
Average Particle ◽  
X Ray ◽  
Particle Size Analyzer ◽  
Phosphate Slag ◽  
Scanning Electron

In this experiment, ultrafine iron phosphate micro-powder was prepared by hydrothermal method which used phosphate slag as an iron source. The effects of reaction temperature, surfactants type and amount on its particle size were explored. The samples were characterized by using Malvern Laser Particle Size Analyzer (MS2000), X-Ray Diffractometer (XRD), Scanning Electron Microscope (SEM) and Energy Dispersive X-Ray Spectroscopy (EDX).The results showed that at 160 °C, 1 wt%CTAB, monoclinic iron phosphate micro-powder was obtained with an average particle size about 0.4 μm which also has a good dispersion in aqueous solution.

The Influence of Calcination Temperature on Quantitative Phase of Hematite from Iron Stone Tanah Laut

2015 ◽  
Vol 1112 ◽  
pp. 489-492
Author(s):  
Ali Mufid ◽  
M. Zainuri
Keyword(s):  
Particle Size ◽  
Calcination Temperature ◽  
Thermo Gravimetric Analysis ◽  
Precipitation Method ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Particle Size Analyzer ◽  
Co Precipitation

This research aims to form particles of hematite (α-Fe2O3) with a basis of mineral iron ore Fe3O4 from Tanah Laut. Magnetite Fe3O4 was synthesized using co-precipitation method. Further characterization using X-ray fluorescence (XRF) to obtain the percentage of the elements, obtained an iron content of 98.51%. Then characterized using thermo-gravimetric analysis and differential scanning calorimetry (TGA-DSC) to determine the calcination temperature, that at a temperature of 445 °C mass decreased by 0.369% due to increase in temperature. Further Characterization of X-ray diffraction (XRD) to determine the phases formed at the calcination temperature variation of 400 °C, 445 °C, 500 °C and 600 °C with a holding time of 5 hours to form a single phase α-Fe2O3 hematite. Testing with a particle size analyzer (PSA) to determine the particle size distribution, where test results indicate that the α-Fe2O3 phase of each having a particle size of 269.7 nm, 332.2 nm, 357.9 nm, 412.2 nm. The best quantity is shown at a temperature of 500 °C to form the hematite phase. This result is used as the calcination procedure to obtain a source of Fe ions in the manufacture of Lithium Ferro Phosphate.

scholarly journals Gas-Phase Hydrogenation of Furfural to Furfuryl Alcohol over Cu-ZnO-Al2O3 Catalysts Prepared from Layered Double Hydroxides

Catalysts ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 486
Author(s):  
Guillermo R. Bertolini ◽  
Carmen P. Jiménez-Gómez ◽  
Juan Antonio Cecilia ◽  
Pedro Maireles-Torres
Keyword(s):  
Gas Phase ◽  
Aging Time ◽  
Layered Double Hydroxides ◽  
Furfuryl Alcohol ◽  
Precipitation Method ◽  
Molar Ratio ◽  
X Ray ◽  
General Chemical ◽  
Co Precipitation ◽  
Double Hydroxides

Several layered double hydroxides (LDHs) with general chemical composition (Cu,Zn)1−xAlx(OH)2(CO3)x/2·mH2O have been synthesized by the co-precipitation method, maintaining a (M2+/M3+) molar ratio of 3, and varying the Cu2+/Zn2+ molar ratio between 0.2 and 6.0. After calcination and reduction steps, Cu/ZnO/Al2O3 catalysts were synthesized. These catalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), H2 thermoprogrammed reduction (H2-TPR), N2 adsorption-desorption at −196 °C, N2O titration, X-ray photoelectron miscroscopy (XPS), NH3-thermoprogramed desorption (NH3-TPD) and CO2- thermoprogrammed desorption (CO2-TPD). The characterization data revealed that these catalysts are mainly meso-and macroporous, where Cu, ZnO and Al2O3 are well dispersed. The catalytic results show that these catalysts are active in the gas-phase hydrogenation of furfural, being highly selective to furfuryl alcohol (FOL) and reaching the highest FOL yield for the catalyst with a Cu2+/Zn2+ molar ratio of 1. In an additional study, the influence of the aging time on the synthesis of the LDHs was also evaluated. The catalytic data revealed that the use of shorter aging time in the formation of the LDH has a beneficial effect on the catalytic behavior, since more disordered structures with a higher amount of available Cu sites is obtained, leading to a higher yield towards FOL (71% after 5 h of time-on-stream at 210 °C).

Fabrication and Characterization of Nanospinel ZnCr2O4 Using Thermal Treatement Method

2015 ◽  
Vol 1107 ◽  
pp. 301-307 ◽  
Author(s):  
Salahudeen A. Gene ◽  
Elias B. Saion ◽  
Abdul Halim Shaari ◽  
Mazliana A. Kamarudeen ◽  
Naif Mohammed Al-Hada
Keyword(s):  
Particle Size ◽  
Calcination Temperature ◽  
Average Particle Size ◽  
Treatment Method ◽  
Esr Spectra ◽  
Resonance Spectroscopy ◽  
Average Particle ◽  
Face Centered Cubic ◽  
X Ray ◽  
Xrd Patterns

The fabrication of nanospinel zinc chromite (ZnCr2O4) crystals by the means of thermal treatment method from an aqueous solution containing metal nitrates, polyvinyl pyrrolidone (PVP), and deionized water was described in this study. The samples were calcined at various temperatures ranging from 773 to 973 K for the decomposition of the organic compounds and crystallization of the nanocrystals. PVP was used as capping agent to control the agglomeration of the particles. The characterization studies of the fabricated samples were carried out by X-ray diffraction spectroscopy (XRD), transmission electron microscopy (TEM), energy dispersed X-ray spectroscopy (EDX) and electron spin resonance spectroscopy (ESR). The corresponding peaks of Zn, Cr and O were observed in the EDX spectrum of the sample which confirms the formation of ZnCr2O4. The XRD patterns also confirmed the formation of the single faced nanocrystallines of spinel ZnCr2O4 with a face-centered cubic structure. The average particle size of the synthesized crystals was also determined from the XRD patterns using the Scherers formula which shows that the crystallite sizes increases with increase in calcination temperature and was in good agreement with the TEM images which shows cubical ZnCr2O4 nanocrystals with uniform morphology and particle size distributions. The ESR spectra confirmed the existence of unpaired electron in the fabricated samples and the increase in g-factor and decreases in resonant magnetic field (Hr) were observed as the calcination temperature increases.

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