S. Safi, Dr G. H. Akbari,
Volume 36, Issue 1 (6-2017)
Abstract
Strengthening of copper matrix by dispersion of metallic oxides particles as an efficient way to increase strength without losing thermal and electrical conductivities has been recognized for many years. Such a composite can withstand high temperatures and keep its properties. Such copper alloys have many applications especially in high temperature including resistance welding electrodes, electrical motors and switches. In the present work, at first, the Cu-1%Al solid solution was prepared by the mechanical alloying process via 48 hours of milling. Subsequently, 0.66 gr of copper oxide was added to Cu-1%Al solid solution and mechanically milled for different milling times of 0,16, 32, 48 hours. The milled powder mixtures were investigated by X-Ray Diffraction and scanning electron microscopy techniques. The lattice parameter of Cu increased at first, but then decreased at longer milling times. The internal strain increased and the average Cu crystal size decreased during milling process.The particle size decreased during the whole process. With increasing annealing temprature from 450°C to 750°C, the microhardness values of samples decreased at the beginning but then increased. From these results, it can be concluded that nanosize aluminaparticles are formed in the copper matrix.
S. Alamolhoda, S. M. Mirkazemi, T. Shahjooyi, N. Benvidi,
Volume 36, Issue 2 (9-2017)
Abstract
In this research, nickel ferrite nanoparticles were synthesized by sol-gel auto-combustion route, and the effect of calcination temperature on phase constituents, magnetic properties and microstructure of the synthesized nanoparticles was evaluated using X-ray Diffraction (XRD), Vibrating Sample Magnetometer (VSM) and Scanning Electron Microscopy (SEM). XRD results were submitted to quantitative analysis. Microstructural studies and crystallite size calculations showed formation of nanoparticles. XRD results showed that the combustion product consisted of NiFe2O4, α-Fe2O3, NiO, and FeNi3 phases. FeNi3 was eliminated by calcination, and the amounts of NiO and α-Fe2O3 were modvlated by changing in calcination temperature. Saturation magnetization changed from 37emu/g in combustion product to 30emu/g by calcination at 600°C, due to decomposition of FeNi3 magnetic phase and formation of higher amount of antiferromagnetic hematite phase. Also, the coercivity values increased, that could be due to increasing the amount of nickel ferrite phase and eliminating FeNi3 phase. Saturation magnetization reached to 43emu/g in calcinated sample at 1000°C due to the reaction between hematite and NiO phases that led to formation of higher amount of nickel ferrite to 43emu/g. Coercivity value dropped out to 127Oe by calcination at 1000°C, the reason of which could be incresing of particle size and formation of multi domain magnetic particles.
S. E. Mousavi Ghahfarokhi, F. Bazdar, I. Kazeminezhad,
Volume 36, Issue 2 (9-2017)
Abstract
In this paper, Ni-doped lead hexaferrites (PbFe12-xNixO19) nanoparticles with x = 0.2 were prepared by sol- gel method. Then, the effect of annealing temperature on its structural, magnetic and dielectric properties was studied. First, the dryed gel was evaluated by Thermogravimetry-Differential Thermal Analysis (TG/DTA) and then, the structural morphology, magnetic and dielectric properties of samples have been characterized by Fourier Transform Infrared (FT-IR) spectroscopy, X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Vibrating Sample Magnetometer (VSM) and LCR meter. The results of x-ray diffraction patterns show that by increasing annealing temperature up to 800 °C, PbFe11.8Ni0.2O19 phase percentage in the samples increases. Also, by increasing annealing temperature, the magnetization increases because the unwanted phases disappear and pure and single-phase lead hexaferrite are formed. By increasing frequency, first the AC electrical conductivity of the samples decreases and then increases. These variations have been explained by Maxwell- Wanger model. The result measurements show that the best sample is PbFe11.8Ni0.2O19 with annealing temperature of 800 °C for 3 h.
F. Ebrahimi, F. Ashrafizade, S. R. Bakhshi,
Volume 36, Issue 3 (11-2017)
Abstract
In this research, ordered porous anodic templates with 30 nm diameter and 15 µm thickness were prepared by using double anodization process. Dip coating method was employed to synthesize strontium ferrite in the form of nanowires in sol dilution. Ferrite nanopowders were also synthesized using sol gel method. The characterization of the nanostructures were examined by X-Ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM) and Energy Dispersive Spectroscopy (EDS). Hysteresis loops of nanopowders and nanowires, parallel and perpendicular to the wires axes, were measured by Superconducting Quantom Interference Device (SQUID). The results showed that double anodization in 0.3 M oxalic acid at 4 oC with a single anodization for 12 hours could produce ordered template. Dip coating in 80 oC for two hours could form fine and uniform strontium ferrite nanowires. The produced material showed parallel anisotropy.
D. Haghshenas, A. Amirjani,
Volume 36, Issue 4 (3-2018)
Abstract
In this study, null and one-dimensional nanoparticles and nanostructures of Ag and Ag-Cu were synthesized using polyol method. In order to prepare different nanostructures with the same synthesis route, thermodynamics and kinetic conditions of the system were manipulated. In the thermodynamics approach, the nanostructures with the minimum surface energy were obtained as the final product, while in kinetic approach, the nanostructures with the lower activation energy were formed. By using these appraoches, Ag and Ag-Cu spherical and cubical nanostructures were produced in the size range of 90-100 nm. Also, by manipulating the kinetic conditions of the system, silver nanowires with the diameters in the range of 100-200 nm and the length of several microns were obtained successfully. The effect of Cu ions (Cu2+) on aspect ratio of the synthesized silver nanowires by polyol method was evaluated.
S. Yousefi, B. Ghasemi, M. Tajalli, A. Asghari,
Volume 36, Issue 4 (3-2018)
Abstract
In this paper, high purity magnesium hydroxide nanoplates were successfully synthesized by using brine rich in magnesium ions as precursor and NaOH as precipitating agent without using dispersant agent in the room temoerature. The study and characterization of various properties of obtained nanopowder was carried out by X-Ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), Energy Dispersive X-ray Fluorescence Spectrometer (EDX), Fourier Transform Infrared Spectrophotometer (FTIR) and Ultraviolet–visible spectroscopy (UV-Vis). The FESEM and XRD analysis results showed that magnesium hydroxide powder had nanoplates with the average crystallite size 17.1nm and no impurity; that was in agreement with the result of EDX and FTIR perfectly. Furthermore, optical characteristics of magnesium hydroxide nanoplates by UV-Vis spectroscopy showed an optical band gap of 5.5 eV. This wide band gap can be a useful innovation in optoelectronic sub-micron devices.
M. Mirhaj, M. Mahmoodi, A. Shybani,
Volume 36, Issue 4 (3-2018)
Abstract
In this research, keratin (Kr)/ poly caprolactone (PCL)/ hydroxyapatite (HA) scaffold was made by electrospinning method. Then, the effect of HA nanoparticles on properties of scaffold B (Kr 33%, PCL 50% and HA 17%) and scaffold A (Kr 40% and PCL 60%) were studied. The surface morphology, functional groups on the surface of samples, porosity, and specific surface area were evaluated by Scanning Electron Microscopy (SEM), Fourier Transform Infrared Spectrophotometer (FTIR), liquid displacement method, and BET test, respectively. The mean diameter of fibers in samples A and B was measured 184 nm and 108 nm, respectively. Results showed that the specific surface area in scaffolds with HA nanoparticles was almost 2 times higher than that of the scaffold without HA. The biodegradability of scaffolds was examined in phosphate buffer solution (PBS) and the results showed an increase in the weight loss percentage of the scaffold B. The cell viability and adherence of osteosarcoma cell line (Saos-2) on the scaffold surface was observed via MTT assay and the results showed an increase in cell growth on PCL/Kr scaffolds with HA nanoparticles. Thus, scaffolds containing HA nanoparticles can be a good choice for tissue engineering applications.
H. Salehi, P. Amiri, Y. Loveimi Motlagh,
Volume 37, Issue 1 (6-2018)
Abstract
In this article, the electronic and optical properties of bulk TiC and its narrow nanowires were investigated using Quantum-Espresso/PWSCF computational package in the framework of density functional theory. According to the results, this compound showed a metallic behavior in the bulk structure, but the small diameters of the nanowires against the bulk structure showed a semiconducting behavior. This deviation became negligible at the higher diameters. In both structures, the electronic results were compatible with the optical calculations of the structure under consideration. Considering the optical results, the structure of bulk TiC had the maximum amount of refractive index value and this amount could be decreased by a reduction in the nanowire diameters. Also, the optical results indicated that by increasing the size of nanowires, the ELLOS value was raised toward the corresponding bulk value
S. Faraji, Gh. Dini, M. Zahraei,
Volume 37, Issue 1 (6-2018)
Abstract
Manganese ferrite nanoparticles (NPs) have different applications, especially in medical diagnosis and treatment as well as the biomolecule separation,. In this research, the effects of various parameters such as the pH of reaction solution and the hydrothermal process duration on the synthesis of spinel phase in NPs were evaluated. Crystal structure, chemical composition, morphology and size of synthesized particles were investigated by the X-ray diffraction (XRD) analysis and field-emission scanning electron microscopy (FE-SEM) equipped with energy dispersive spectroscopy (EDS). The XRD results showed that the process duration of 12 h and pH=11 were suitable for the formation of monophase manganese ferrite NPs. The FE-SEM investigations showed that the average size of the synthesized NPs was about 50 nm. Moreover, the EDS analysis showed the presence of about 20% of manganese in the NPs structure. Hydrothermally synthesized manganese ferrite NPs in this researchcould be, therefore, a good candidate for the biomedical application due to their small size and narrow size distribution.
Z. Talebi, Mahin Karimi, Negar Habibi,
Volume 37, Issue 1 (6-2018)
Abstract
In the present study, silica aerogel was evaluated by a two-step catalytic process at the ambient pressure drying, under different synthesis conditions. The effects of the catalyst and water content in the hydrolysis step on the physical properties of silica aerogel, including density, porosity and shrinkage, were investigated. The results showed that increasing the water content in the hydrolysis step increased the shrinkage of gel network and density of obtained aerogel. Moreover, in the presence of insufficient water, NH4OH as the condensation catalyst in the gel formation step was more effective on the physical properties of silica aerogel, as compared to HCl as thehydrolysis catalyst; Moreover, the increase in the NH4OH content led to lower density and higher porosity. On the other hand, NH4OH effect on the physical properties of silica aerogel was not noticeable in the presence of enough water content. In the NH4OH/HCl molar ratio of 6, the best silica aerogel sample was obtained with the density of 0.214 g/cm3, porosity of 90% and shrinkage of 23%
Z. Khosroshahi, F. Karimzadeh, M. Kharaziha,
Volume 37, Issue 2 (9-2018)
Abstract
Due to electrical properties (high electron mobility) and electrochemical characteristics (high electron transport rate), graphene-based materials have been widely applied for various scientific fields. However, due to their two-dimensional structures, these materials have low active sites for reaction. Therefore, changing from two-dimensional sheets dimensional to the three-dimensional ones could provide graphene-based materials with high specific surface and electron and mass transport particles. For these purpose, reduced graphene oxide (rGO) and polystyren (PS) aqueous solution were mixed with two different weight ratios kinetic. In this study, the three-dimensional graphene (3DG) was synthesized with graphene oxide using sacrificial PS particles. For this purpose, rGO and the PS aqueous solution were mixed with two different weight ratios of 95:5 and 85:15. Then, the 3DG-PS scaffolds were synthesized by controlling the pH value in the range of 6-8. Subsequently, PS particles were removed by immersing the synthesized scaffolds in toluene. In this research, the effect of filtering through the member filter and centrifuge on the morphology of the scaffolds was investigated. The scaffolds were characterized with X-ray diffraction and scanning electron microscopy. The results showed the formation of 3DG with a uniform distribution of porosities by using the centrifuge procedure. Moreover, the sacrificial PS particles were completely removed when the rGO to PS weight ratio was 95:5. So, 3DG with the uniform distribution of microscopy porosity could be synthesized through the sacrificial mold method and the centrifuge procedure; graphene oxide was also reduced with the PS weight ratio of 95:5. Further, based on the electrochemical evaluation of this optimized sample, as compared to the rGO , it was found that the 3DG had better electrochemical properties than the rGO. Therefore, 3DG with the optimized rGO to PS weight ratio of 95:5 could be an ideal substitute for rGO in electrochemical applications
S. Daneshvar E Asl, S. Kh. Sadrnezhaad,
Volume 37, Issue 2 (9-2018)
Abstract
Rutile-phase titanium dioxide nanorod arrays were prepared by the hydrothermal method. Then, anatase-phase nanoleaves were successfully synthesized on the nanorod arrays via mild aqueous chemistry. Nanorod arrays scanning electron microscopy revealed that the thin film is uniform and crack free and the average diameter and height of the nanorods are 90 nm and 2 µm, respectively. Furthermore, nanorods are vertical to the substrate surface and have desired coverage density due to the predeposition of TiO2 seed layer which leaded to decrease the surface roughness of the substrate. Nanoleafed nanorods scanning electron microscopy indicated that the nanoleaves were grown uniformly on the entire surface of nanorods and the specific surface area and roughness factor of those are significantly improved. Energy dispersive spectrums suggested that F- and Cl- ions are partially doped into TiO2 crystals. Raman and X-ray spectra confirmed the formation of anatase-phase nanoleaves on the rutile-phase nanorods. X-ray diffraction also indicated that the nanorod arrays are highly oriented with respect to the substrate surface. The diffused reflectancetransmittance data revealed the incident light was more efficiently harvested by the nanoleafed nanorod thin film and the values of energy gap are 2.78 and 2.82 eV for rutile TiO2 nanorod and rutile+anatase TiO2 nanoleafed nanorod thin films, respectively. Synthesized nanostructure, having improved charge separation and transfer (due to the presence of the surface anatase/rutile junctions), high specific surface area and light harvesting (due to the presence of the nanoleaves) and low band gap energy (due to the nonmetallic elements doping), is viable alternative to traditional single crystalline TiO2 nanorods for highly efficient photoelectrochemical applications.
G. Pishevarz, H. Erfan Niya, E. Zaminpayma,
Volume 37, Issue 3 (12-2018)
Abstract
Abstract: In this work, the amounts of the adsorption of conjugated polymers onto graphene/ graphene oxide were examined by reactive force-field molecular dynamics simulation. The polymers were poly(3-hexylthiophene) (P3HT) and poly(phenothiazine vinylene-polythiophene)(PTZV-PT). The length and width of the graphene sheet were 95.19 Å and 54.16 Å, respectively. The graphene oxide sheets with different oxidation percentages were considered. The molecular dynamics simulation results demonstrated a higher amount of adsorption onto graphene oxide sheets in comparison to graphene; furthermore, poly(phenothiazine vinylene-polythiophene) revealed a larger amount of adsorption in comparison with poly(3-hexylthiophene) in both functionalized groups of hydroxyl and epoxy. Also, some structural properties of polymers, such as radius of gyration of polymer and radial distribution function, were calculated at different reactive sites.
M. Eshraghi, Z. Mosleh, M. Rahimi,
Volume 38, Issue 1 (6-2019)
Abstract
In this investigation, the structural and magnetic properties of Cr and Zn substituted Co ferrite with the general formula Co1-xZnxFe2-xCrxO4 (x= 0.1, 0.3, 0.5, 0.7) as prepared by sol- gel method were studied. The structural, morphological and magnetic properties of the samples were characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR), Scanning electron microscopy (SEM) and Vibrating sample magnetometer (VSM). XRD measurements along with the Rietveld refinement indicated that the prepared samples were single phase with the space group of Fd-3m. Results of SEM images also showed that the particles were in the nanosize range. Also, the magnetic properties of the samples indicated that the magnetization was first decreased, reaching the minimum value for x=0.1 sample; then it was increased. This behavior was related to the cation distribution at the tetrahedral and octahedral sites. Moreover, coercivity was significantly decreased with increasing the doping level due the decrease of magnetocrystalline anisotropy because of the nonmagnetic Zn ion substitution.
A. Jafari, S. Khademi, M. Farahmandjou, A. Darudi, R. Rasuli,
Volume 38, Issue 2 (9-2019)
Abstract
Titanium dioxide nanoparticles (TiO2) are known as a widely used photocatalyst. In order to improve the performance of these nanoparticles, the recombination of the electron-cavity pair must be reduced and the absorption rate of the visible region should be expanded. One way to increase the performance of these nanoparticles is using cerium doped TiO2. In the present study, pure and doped titanium dioxide nanoparticles were made by the electrical discharge method. The effect of cerium dopants on the structural, morphological and optical properties were studied by x-ray diffraction (XRD), scanning electron microscopy (FESEM), diffused reflection spectroscopy (DRS), photoluminescence (PL) and infrared fourier transform (FTIR) spectroscopy analyses. XRD analysis revealed that the size of TiO2 nanocrystals was decreased to 7.7 nm. The FESEM morphology of the samples also showed that the uniformity of the Ce doped TiO2 was decreased. Further, the DRS results indicated that the band gap energy of Ce-TiO2 was decreased to 2.24 eV. The photoluminescence results demonstrated that the intensity of PL was reduced for the Ce-TiO2 sample, which reduced the recombination of the electron-hole coupling and increased the photocatalytic activity in the doped sample.
F. Mohammadi Bodaghabadi, M. R. Loghman Estarki, M. Ramazani, A. Alhaji,
Volume 38, Issue 3 (12-2019)
Abstract
In this research, synthesis of lithium fluoride (LiF) nanoparticles by fluorolytic sol-gel method has been studied. Moreover, the effect of lithium ion to fluorine source molar ratio and calcination temperature on particle size and phase of LiF nanoparticles were investigated. Lithium acetate (C2H3LiO2), trifluoroacetic acid (TFA), ethylene glycol monobutyl ether and oleic acid were used as sources of Li+ and F- ions, solvent and growth inhibitor, respectively. Thermal and X-ray diffraction (XRD) analyses as well as field emission scanning electron microscopy (FESEM) were used to investigate thermal behavior of the primary gel and to determine the phase and morphology of samples, respectively. The results showed that the 2: 1 molar ratio of Li+/ TFA and the calcination temperature of 400 °C result in LiF nanoparticles with a mean particle size of 80-100 nm.
N. Poursharifi, D. Semnani, P. Soltani, S. Amanpour,
Volume 38, Issue 4 (1-2020)
Abstract
In this study, seven-layer nanofiber structures consisting of polycaprolactone/ chitosan polymers loaded with methotrexate and 5-fluorouracil anti-cancer drugs, for controlled drug delivery, were produced and evaluated. For this purpose, the second, fourth and sixth layers were loaded with drug and placed between the drug-free layers. The surface morphology of drug-free and drug-loaded nanofibers was investigated by scanning electron microscopy (SEM) and Fourier transform infrared spectrometry (FTIR) was used to study their chemical structure. The drug release rate in phosphate buffered saline (pH=7.4) and the released drug concentration were measured by spectrophotometry. Mechanical properties of single- and multi-layered samples were also investigated. SEM images showed formation of uniform and beadless fibers. FTIR spectrum confirmed presence of the drugs in the polymer mixture with no interaction. It was found that by increasing the chitosan content, a brittle structure with decreased elongation is formed. The release behavior of methotrexate and 5-Fluoracil drugs in neutral pH environment for 26 days was evaluated and the results exhibited a slow and sustained release.
M. Shirvani, M. Mashhadi, M. Yosofi,
Volume 38, Issue 4 (1-2020)
Abstract
In this research, solid state carbothermal synthesis of HfB2 Nano powders was investigated. For this purpose, HfO2,H3BO3, carbon active or phenolic resin were used as raw materials for carbothermal reaction. After 2-4 hours of milling the raw materials by a planetary ball in an ethanol media, the mixture was heat dried and pressed in to disks under pressure of 20-30 bar. The disks were then placed in a graphite crucible and heat-treated at 1500–1600 °C for 1 hour under flowing Ar atmosphere. The powder product was analyzed by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS) and backscattered electron (BSE) imaging. The heat treatment temperature, amount of boric acid, milling and heat treatment time were recognized as four factors influencing synthesis and size of HfB2 powder particles. SEM images reported irregular morphologies with a particle size of about 2-4 µm for HfB2 powder. The best sample was obtained at a molar ratio of HfO2 : phenolic resin carbon: boric acid = 1:5:5 at 1600 °C after 1 hour of heat treatment. XRD results confirmed synthesis of pure HfB2 with a crystallite size of about 60 nm.
M. Mahallati, M. Khosravi,
Volume 39, Issue 2 (8-2020)
Abstract
In this research, using phenolic resin as the precursor of carbon and various amounts of ethylene glycol as a pore former, porous samples of hard carbon were synthesized. Samples were characterized by x-ray diffraction (XRD) and N2 adsorption-desorption methods. Broad diffraction peaks represent the amorphous structure of samples. Moreover, the gas adsorption-desorption curves showed that the adsorption isotherms of samples were of type IV and all samples had meso-micro porous structure. Charge-discharge tests were performed on samples to obtain their capacities. The sample with higher capacity, broader XRD pattern and appropriate porosity, was selected for silicon incorporation. Silicon nanoparticles were obtained by mechanical milling of its micro particles. According to XRD patterns, silicon nanoparticles had a crystalline structure. Field emission scanning electron microscopy (FESEM) images approved uniform distribution of nanoparticles. XRD patterns of nanocomposites evidenced the existence of hard carbon and silicon. The electrochemical test results showed that the capacity, coulombic efficiency and cycle life of nanocomposites were improved by increasing the amount of silicon.
A. H. Kianfar, N. Eskandari, M. A. Arayesh,
Volume 39, Issue 2 (8-2020)
Abstract
In this research the synthesis of [Co(Salen)(PPh3)(H2O)]4[Fe(CN)6] and [Co(Salophen)(PPh3)(H2O)]4[Fe(CN)6] schiff base complexes was reported. Co3O4/CoFe2O4 magnetic nanoparticles were prepared by calcination of these complexes at 500, 550 and 600°C. Precursor complexes were identified by FT-IR and UV-Vis spectroscopy and their thermal behavior was studied via TG/DTA. Nanomagnetic samples were characterized by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), and Fourier Transform Infrared Spectroscopy (FT-IR). Magnetic properties of the synthesized nanoparticles were studied using Vibrating Sample Magnetometer (VSM). Magnetic parameters such as saturation magnetization (Ms), remanent magnetization (Mr), coercive field (Hc) and squareness ratio (SQ = Mr/Ms) were determined at room temperature. Stoichiometry and approximate composition of the prepared samples were studied by Electron Diffraction X-ray spectroscopy (EDX). The prepared nanocomposites could be useful in some practical applications due to their high magnetization, good chemical stability and dispersion.
