Showing 110 results for Ge
A. Rostamnejadi, M. K. Esmaeilzadeh,
Volume 36, Issue 3 (11-2017)
Abstract
In this research, nanoparticles of La0.8Sr0.2MnO3 with mean crystallite size of 20 nm have been prepared by sol gel method. The sample has been characterized by X-Ray Diffraction (XRD) using Rietveld refinement, Field Emission Scanning Electron Microscope (FESEM) and Fourier Transform Infrared (FTIR) spectroscopy. The static magnetic properties such as saturation magnetization, effective magnetic moment and ferromagnetic phase fraction of the nanoparticles are determined by different techniques using magnetic hysteresis loop at room temperature. The magnetic dynamic properties of crystalls are studied by measuring AC magnetic susceptibility versus temperature at different frequencies. Néel-Brown, Vogel-Fulcher, critical slowing down models and empirical parameters are used to distinguish between superparamagnetic and superspin glass behaviour in the nanoaprticles. By fitting the experimental data with the models, relaxation time, critical view, magnetic anisotropy energy and effective magnetic anisotropy constant have been estimated. The obtained results support the presence of interacting superparamagnetic behaviour between magnetic nanoparticles of La0.8Sr0.2MnO3.
S. Daneshvar E Asl, S. K. Sadrnezhaad,
Volume 36, Issue 3 (11-2017)
Abstract
TiO2/MWCNT nanocomposite thin films containing different percentages of multi-walled carbon nanotubes were coated on fluorinated tin oxide substrates by sol-gel dip coating method. Results of X-ray diffraction analysis indicated that the crystal structure of the coatings was anatase TiO2. It was also understood that the size of crystallites reduced with CNT but structural properties and equilibrium phase remain intact. Field emission scanning electron microscope images showed that CNTs dispersed uniformly among 45 nm spherical TiO2 particles of close relations. These images also showed that CNT promoted cracks on the coated surface. Results of the UV-Vis spectroscopy showed that the visible light range adsorption increased with CNT and the absorption edge did not significantly differ with the pure TiO2 layers.. Results of the photoluminescence spectroscopy revealed that the presence of CNT could reduce the pair electron–electron holes recombination which is considered totally undesirable.
M. Kouhi, M. Shamanian, M. Fathi, Molamma Prabhakaran, Seeram Ramakrishna,
Volume 36, Issue 3 (11-2017)
Abstract
In this work, poly (hydroxybutyrate co hydroxyvalerate) (PHBV) composite nanofibrous scaffold containing hydroxyapatite/bredigite (HABR) nanoparticles was fabricated through electrospining method. The morphology of prepared nanofibers and the state of the nanoparticles dispersion in nanofiber matrix were investigated using scanning and transmission electron microscopy, respectively. Evaluation of the mechanical properties of the nanofibrous scaffolds revealed that there is a limit to the nanoparticle concentration at which nanoparticles can improve the mechanical properties of the nanofibrous scaffolds. According to the results, PHBV/HABR nanofibers showed higher wettability compared to PHBV nanofibers. In vitro cell culture assay was done using human fetal osteoblast cells on nanofibrous scaffold. MTS assay revealed that cell proliferation on the composite nanofibrous scaffold was significantly higher than those on the pure scaffold after 10 and 15 days. Scanning electron microscopy- Energy dispersive X-ray spectroscopy and CMFDA colorimeter assay analysis showed that the cells on the PHBV/HABR scaffolds acquired higher mineral deposition than the cells on the pure PHBV and control sample scaffold. Based on the results we concluded that PHBV/HABR nanofibers scaffold with higher wettability, improved mechanical properties and cell behavior hold great potential in bone regeneration applications.
M. R. Pakmanesh, M. Shamanian, S. Asghari,
Volume 36, Issue 4 (3-2018)
Abstract
In the present study, the optimization of pulsed Nd:YAG laser welding parameters was done on a lap-joint of a 316L stainless steel foil in order to predict the weld geometry through response surface methodology. For this purpose, the effects of laser power, pulse duration, and frequency were investigated. By presenting a second-order polynomial, the above-mentioned statistical method was managed to be well employed to evaluate the effect of welding parameters on weld width. The results showed that the weld width at the upper, middle and lower surfaces of weld cross section increases by increasing pulse durationand laser power; however, the effects of these parameters on the mentioned levels are different. The effect of pulse duration in the models of weld upper, middle and lower widths was calculated as 76, 73 and 68%, respectively. Moreover, the effect of power on theses widths was determined as 18, 24 and 28%, respectively. Finally, by superimposing these models, optimum conditions were obtained to attain a full penetration weld and the weld with no defects.
F. Z. Akbarzadeh, M. Rajabi,
Volume 36, Issue 4 (3-2018)
Abstract
In this study, the composite material with composition of MgH2-10 wt% (25Ce-75Ni) has been prepared by co-milling of magnesium hydride powder with Ce-Ni alloy produced by vacuum arc remelting method. The effect of milling time and additive on magnesium hydride structure, i.e. crystallite size, lattice strain and particle size, and also hydrogen desorption properties of obtained composite were evaluated and compared with pure milled MgH2. It has been shown that the addition of 25Ce-75Ni alloy to magnesium hydride yielded a finer particle size. As a consequence, the desorption temperature of mechanically activated MgH2 decreased from 340 °C to 280 °C for composite 1(5 h mechanical alloying) and to 290 °C for composite 2 (15 h mechanical alloying). Further improvement in the hydrogen desorption tempreture of composite 1 can be related to finer particle size and higher Mg2NiH4 phase value, which corresponded with calculated enthalpy results.
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%
M. Akbari Taemeh, B. Akbari, J. Nourmohammadi,
Volume 37, Issue 3 (12-2018)
Abstract
In gradient scaffolds, changes in porosity, pore size or chemical composition occur gradually. Recently, different methods have been applied to create gradient in the scaffolds, but they have some disadvantages such as high cost and control. The main purpose of this research was to fabricate porous gradient scaffolds by a novel, functional, simple, and low-cost method. Two homogenous scaffolds (Homog 1 and Homog 2) and two gradient scaffolds (Grad 1 and Grad 2) were fabricated and compared. Polycaprolactone scaffolds with the pore size gradient along the radial direction were fabricated by combining layer-by-layer assembly and porogen leaching techniques. Paraffin micro particles were used as porogen in two size ranges: 250 to 420 µm and 420 to 600 µm. The average pore size of Homog 1 and Homog 2 was 278.48 ± 11.23 µm and 417.79 ± 14.62, which were suitable for bone tissue engineering. The porosity of the samples was: Homog 1: 77.5 ± 1.25 %, Homog 2: 61.3 ± 3.5 %, Grad 1: 74 ± 0.5 % and Grad 2: 79.8 ± 4 %. It should be stated that the required porosity for cell survival and growth was above 70 %. Compressive strength at 80% strain and compressive modulus for Homog 1, Homog 2, Grad 1 and Grad 2 were 0.16 ± 0.16 MPa and 0.25 ± 0.11 MPa, 0.26 ± 0.20 MPa and 0.53 ± 0.34 MPa, 0.19 ± 0.34 MPa and 0.33 ± 0.43 MPa, 0.12 ± 0.28 MPa and 0.16 ± 0.51 MPa, respectively. The results showed that pore size gradient had a negligible effect on the mechanical properties of the scaffolds and using polycaprolactone (PCL) as the only material of scaffold was not appropriate. The structure of gradient scaffolds showed the radial pore size gradient with a good adhesion between layers without any detectable interface; the result of the compression test also confirmed it.
A. Baradaran, M. Tavoosi,
Volume 37, Issue 3 (12-2018)
Abstract
In the present study, the structural, optical and thermal behaviors of GeO2-PbO-CaO-SrO glasses were investigated to achieve the highest optical properties and thermal stability. Accordingly, different 50GeO2-(50-x)PbO-xCaO and 50GeO2-(50-x)PbO-xSrO (x=0, 10, 20) germanate glasses were prepared by the conventional melt and quench technique between two steel sheets. The produced samples were characterized using X-ray diffraction (XRD), differential thermal analysis (DTA), Fourier transform infrared (FTIR) and UV-Vis spectroscopy. Based on the obtained results, the addition of CaO to glass composition reduced the glass phase forming ability as well as optical and thermal behaviors of the prepared glasses. In contrast, the presence of SrO had no destructive effect on the optical properties of the prepared glasses; the highest values of glass transition (580 oC) and crystallization temperature (831 oC) were achieved in the sample containing 20 mole% of SrO.
M. Haghshenas Gorgani, M. Mirkazemi, F. Golestanifard,
Volume 37, Issue 4 (3-2019)
Abstract
In this research, the rheological behavior and stability of suspensions containing Si3N4, Al2O3, Y2O3 and starch were investigated in order to use them in the starch consolidation casting of porous silicon nitride. Dolapix CE64 was used as the dispersant. Then, the effect of some parameters such as Si3N4 surface oxidation, dispersant content, solid loading and starch content on the viscosity and rheological behavior of Si3N4-starch slurry was determined. Surface oxidation of Si3N4 powder at 800°C for 2 hours reduced the viscosity of the slurry, effectively. The best dispersant content was 0.4 wt. %, relative to ceramic powders. Slurries containing 30 to 40 vol. % and 7.5 to 25 vol. % starch, relative to total solid loading, had the suitable viscosity and the sufficient stability for casting by the starch consolidation method.
M. Hajfarajzadeh, A. Eshaghi, A. Aghaei,
Volume 37, Issue 4 (3-2019)
Abstract
A TEOS-GPTMS nano-hybrid thin film was deposited on the polymethyl methacrylate (PMMA) substrate by a sol-gel dip coating method. Morphology, roughness and surface chemical bonding of the thin films were evaluated by X-ray diffraction (XRD), field emission scanning electron microscopy(FE-SEM), atomic force microscopy, and Fourier transform infrared spectroscopy methods, respectively. UV-vis spectrophotometer was used to measure the transmittance spectra of the samples. Also, the adhesion and hardness of the coatings were investigated using pencil hardness the adhesion tape test and the test, respectively. XRD results proved that the thin film had an amorphous structure. Also, FE-SEM images indicated that addition of GPTMS to the TEOS yielded a crack-free thin film. Based on the UV-vis spectroscopy results, the transmittance of the polymer substrate in the visible region was increased by the deposition of the nano-hybrid coating. Moreover, the hardness of the PMMA substrate was increased from 3H to 6H by the deposition of the nano-hybrid thin film. Also, tape test confirmed the high adhesion of the nano-hybrid thin film on the PMMA substrate. Consequently, the transparent organic-inorganic GPTMS-TEOS hybrid coating can be used as a scratch resistant coating on the PMMA substrate.
H. R. Shahverdi, R. Alipour Mogadam,
Volume 38, Issue 2 (9-2019)
Abstract
Creep age forming (CAF) process is a novel metal forming method with major benefits including improved mechanical properties and cost reduction for aviation industry applications. CAF happens due to creep phenomenon and stress-release during the artificial aging of heat-treatable aluminum alloys. In this work, the creep age forming of 7075 Aluminum alloy at 120, 150 and 180 °C for 6, 24 and 48 h was done; tensile and hardness tests were used to characterize the samples. Results on spring-back revealed that it was influenced by time and temperature; by increasing the time and temperature, it was reduced from 54.1 to 39.51. Mechanical property evaluation also showed that by increasing the time, the strength and hardness could be enhanced due to microstructural evolution and precipitation during the CAF process. According to the mechanical and CAF results, two samples were selected as the optimum ones and their work hardening behavior and fracture surfaces were investigated
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.
M. Afrashi, D. Semnani, Z. Talebi,
Volume 38, Issue 2 (9-2019)
Abstract
In this study, adsorption of fluconazole on silica aerogel was performed successfully by the immersion method in the 1% solution of fluconazole-ethanol at the ambient condition and without using the supercritical method. The hydrophobic and hydrophilic silica aerogels were synthesized by the two-stage sol-gel method and dried at the ambient temperature. This method had most of drug loading at 24 h. It was 1.92% and 1.98% for the hydrophilic and hydrophobic silica aerogels, respectively. Physical properties of the synthesized aerogels were studied by the nitrogen absorption and desorption tests. The presence of fluconazole and the chemical structure of the samples were determined by fourier-transform infrared spectroscopy (FTIR). As well, the loading and release of the drug were investigated using a spectrophotometer. The results showed the structure of the synthesized aerogels had a pore diameter of 6-8 nm and a surface area of about 800-100 m2/g. The study of the drug release also revealed that the release rate of fluconazole in the hydrophilic silica aerogel was higher than that of the hydrophobic sample.
N. Alirezaei Varnosfaderani, S. E. Mousavi Ghahfarokhi, M. Zargar Shoushtari,
Volume 38, Issue 3 (12-2019)
Abstract
In this paper, W-type SrCo2Fe16O27 hexaferrite nanostructures were synthesized by sol-gel auto-combustion method. Effect of annealing temperature on the structural, magnetic and optical properties of these SrCo2Fe16O27 nanostructures was investigated. In order to determine the annealing temperature of samples, the prepared gel was examined by thermo-gravimetric and differential-thermal analyses. Morphology and crystal structure of the prepared samples were characterized by field emission scanning electron microscopy and X-ray diffraction pattern. Based on X-ray diffraction results, at annealing temperature of 1000 °C, the maximum amount of main phase formed. A planar morphology was spectroscopy for the synthesized samples through scanning electron microscope images. Fourier transform infrared analysis was used to confirm the synthesis of the main properties obtained of samples were measured by the vibrating sample magnetometer and the results showed that by increasing temperature, magnetic saturation increases. Moreover, optical properties of samples were investigated by ultraviolet–visible absorption and photoluminescence spectroscopies. The result of measurements of the energy gap approximately is same in the ultraviolet- visible and photoluminescence spectroscopes and also the energy gap is constant with increasing temperature.
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.
M. H. Musazadeh, R. Vafaei, E. Mohammad Sharifi, Kh. Farmanesh,
Volume 38, Issue 3 (12-2019)
Abstract
Finite element (FE) simulations in conjunction with experimental analysis were carried out to characterize the deformation behavior of an AISI 321 austenitic stainless steel (ASS) during cold pilgering process. The effect of process parameters including feed rate (4 and 8 mm) and turn angle (15, 30 and 60°) on damage build-up were also evaluated. The Johnson-cook model was used to simulate the flow behavior of material. By considering compressive stresses, a new revised Latham-Cockcraft damage was calculated and used to determine the optimum process parameters. It was found that the radial and hoop strains in all friction conditions were compressive, while the axial strains were observed to be tensile. The amount of strain (whether it is compressive or tensile strain) was also higher on the outside of the tube compared to its inside. By considering fatigue cycles of a tube element during the process, the feed rate of 8mm, turn angle of 60° and the lowest coefficient of friction were determined as optimum parameters.
M. Emami, Sh. Hayashi,
Volume 38, Issue 3 (12-2019)
Abstract
The outer surface of heat exchanger tubes that work under fluidized bed waste or biomass incineration is exposed to severe high-temperature erosion-corrosion (E-C). To evaluate the behavior and enhance the service life of the tubes, the real service conditions ought to be simulated in the laboratory. In this study a test rig with a fluidized bed of hot sand was designed and manufactured to expose nickel-based SFNi4 alloy to high-temperature E-C. In order to increase the corrosiveness of the environment, the silicon oxide sand was mixed with 0, 0.5 and 1 wt.% of a mixture of NaCl and KCl salts with 1:1 molar ratio. The erosive conditions of the environment were changed by altering air flow rate from 20 to 25 L/min and changing the sand incident angle from 45 to 90 degrees. The rate of material removal was calculated by measuring the thickness of each sample before and after the test. After each experiment, the surface and cross-section of specimens were studied using SEM and EDS analysis. Finally, the optimum E-C parameters to ensure actual industrial conditions were obtained.
M. R. Loghman Estarki, H. Ghalibaf Tousi, E. Mohammad Sharifi, H. Sheikh, A. Alhaji,
Volume 38, Issue 4 (1-2020)
Abstract
The purpose of this study was to evaluate the effect of glycyrol (tri-dentate, GLY) and ethylenediamine (double- dentate clay, en) chelating agents on phase and morphology changes of spinel nanoparticles synthesized by sol-gel method. Characterization of samples was performed by X-ray diffraction (XRD) and field-emission scanning electron microscope (FESEM) equipped with energy dispersive X-ray spectrometer (EDX). The results showed that both samples synthesized with GLY and en contain cubic spinel phase. The sample synthesized with ethylenediamine has a pyramidal morphology with particle size in the range of 20-25 nm whereas the specimen prepared with glycerol is spherical with particle size in the range of 20-25 nm. Finally, suggested mechanism for morphological changes of spniel nanoparticles was discussed.
A. Karimian, Kalantar,
Volume 39, Issue 1 (5-2020)
Abstract
In this research, barium calcium hexaferrite (Ba1-xCaxFe12O19 , 0≤x£1) nanoparticles were synthesized through a sol-gel combustion method. The dried gel samples were then calcined at 950ºC for 4:30h. The phase and microstructural evolution of calcined samples were investigated by X-ray powder diffraction (XRD) and scanning electron microscopy (SEM), respectively. The results revealed formation of calcium -barium hexaferrite phase with a small amount of hematite as a secondary phase. The average particle size is between 60-100 nm and the particle morphology is hexagonal or plate like structure. Results of a vibrating sample magnetometer (VSM) showed that the sample with x=0.4, exhibited the lowest value of saturation magnetization in comparison with others. This could be due to structural heterogeneity and presence of higher amounts of non- magnetic phases (BaFe2O4 and Fe2O3) in this sample compared to others. The results of sensory testing in acetone gas showed that the barium-calcium hexaferrite sample with x=0.2 had the highest sensitivity (0.28) and shortest response (15s) at a concentration of 900 ppm and a temperature of 200 °C despite of the long recovery time.
F. Davar, Z. Enteshari,
Volume 39, Issue 1 (5-2020)
Abstract
In this research, Zinc oxide nanoparticles with semi-spherical morphology were synthesized by modified sol-gel method using rosemary extract as a stabilizing agent. The effect of the amount of rosemary extract and calcination temperature on size and shape of the particles was investigated. The samples were characterized by X-ray diffraction (XRD), infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) and elemental analysis (EDX). X-ray diffraction results showed hexagonal structure (wurtzite phase) of zinc oxide. According to the SEM results semi-spherical nanoparticles of 18 nm in size were obtained using 75 ml of rosemary extract. The photocatalytic activity of the modified ZnO nanoparticles was investigated for degradation of the methylene blue dye solution. The results showed 96.87% of dye degradation in the 135 min that confirmed suitable efficiency of as-synthesized nanoparticles in the photocatalytic degradation process of dyes.
