Showing 306 results for Co
M. Maniei, A. Eshaghi, A. Aghaei,
Volume 38, Issue 2 (9-2019)
Abstract
In this research, MgF2-2%SiO2/MgF2 thin films were applied on a glass substrate. At first, MgF2 thin films with the optical thickness were deposited on the glass slide substrates. Then, MgF2-2%SiO2 thin films were deposited on the glass coated with MgF2 thin films. Finally, the nanocomposite thin films were surface treated by the PFTS solution. Characterization of the thin film was done by X-Ray defractometry (XRD), attenuated total reflectance fourier transform infrared spectroscopy (ATR-FTIR), UV-Vis spectroscopy, and atomic force microscopy (AFM) techniques. Also, the hydrophobic properties of the samples were investigated by measuring the contact angle of the water. The results showed that the deposition of the six layer MgF2 thin films on the two sides of the glass substrate increased the transmission up to 96.4%. For the glass deposited by MgF2-2%SiO2 nanocomposite thin films, transmission was reduced to 94.4%, with its transmission being higher than the pure glass. Also, the water contact angle (WCA) analysis determined that the contact angle of the water droplet on the MgF2-2%SiO2 nanocomposite thin film coated glass was decreased. On the other hand, the contact angle of the water droplet on the MgF2-2%SiO2 nanocomposite thin film coated glass after modification with the PFTS solution was increased up to 119o. So, MgF2-2%SiO2 nanocomposite thin films could be used as an antireflective and self-cleaning coating on the surface of the optical devices.
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. Soleimani, R. Emadi,
Volume 38, Issue 3 (12-2019)
Abstract
In this study, polycaprolactone/chitosan/1% baghdadite composite coating was applied on anodized AZ91 alloy to improve the corrosion rate of AZ91 alloy in simulated body fluid (SBF) solution for long immersion times, control its degradability and enhance its bioactivity. By applying the composite coating and after seven days of immersion in a phosphate buffer solution, the corrosion rate decreased from 0.21 mg/h.cm2 (for AZ91 sample) to 0.1 mg/h.cm2 (for anodized AZ91 sample). Formation of apatite layer on the surface of specimens is considered a criterion for bioactivity. In order to evaluate the ability of specimens to get covered by an apatite, the SBF test was used. Application of the composite coating yielded the highest ability for apatite formation, controlled release of ions, and the lowest corrosion rate in the SBF so that it could be considered a good choice for bone implants.
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.
A. R. Parvanian, H. R. Salimijazi, M. H. Fathi,
Volume 38, Issue 4 (1-2020)
Abstract
The concentrated solar power (CSP) is one of the renewable energy sources in which solar irradiation heat energy will be used in a steam turbine to generate electrical grid. Solar radiation is absorbed by a solar receiver reactor on the surface of a porous solar absorber. In this survey, synthesis and mechanical/thermal characterization of micro-porous silicon carbide (SiC) absorber to be used in solar reactor is carried out. SiC foams were synthesized and categorized based on three different pore sizes i.e. 5, 12 and 75 ppi. Mechanical behavior and thermal shock resistance of porous foams in the working temperature range for absorber (25-1200 °C) were evaluated. Results revealed that the specific compressive strength (σc/ρ) of foams increase exponentially by a decrement in the porosity percentage and the average pore size. Moreover, for foams with smaller pore size, a considerable decrease in mechanical strength due to thermal shock was observed. This could be due to increase in the number of struts per unit volume i.e. more weak struts to withstand the mechanical loading. So, porous foams with coarser pore sizes were distinguished to be more capable of tolerating thermal shock while serving as solar absorbers.
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.
M. Zarchi, Sh. Ahangarani ,
Volume 39, Issue 1 (5-2020)
Abstract
The structural and optical properties of polycrystalline silicon films obtained on a silicon wafer by electron beam physical vapor deposition (EBPVD), were studied in this paper. These films were initially amorphous and changed to a crystalline solid phase during annealing. Annealing was performed in an inert gas atmosphere tube furnace at different temperatures. Micro-structure of the films was analyzed to know the relationship between the crystalline / amorphous composition, grain size and characteristics of the films. The results showed a decrease in roughness with increasing annealing temperature and structural density. Moreover, results of Micro-Raman spectrum showed formation and increase of silicon nanocrystals in the annealed condition when the thickness of the coating increased due to structural defects.
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. Shahriari Nogorani, M. Afari, M. A. Taghipoor, A. Atefi,
Volume 39, Issue 1 (5-2020)
Abstract
Practical applications of thermal barrier coatings with aluminide bond-coats are limited due to oxide scale spallation of the aluminide coating under applied thermal stresses. Considering the positive effects of oxygen-active elements or their oxides on the high temperature oxidation behavior, in this research zirconia was introduced into an aluminide coating. For this purpose, a Watts type bath was used to electroplate a layer of Ni-ZrO2 composite on a Ni-based substrate. Aluminizing was performed using the conventional two-step process at 760 and 1080 °C. Microstructural characterization of coatings in the as-coated conditions and after cyclic oxidation via 5-hour cycles at 1050 °C was performed using electron microscopy, energy dispersive spectroscopy and X-ray diffractometry. The results showed that the general three-zone microstructure of the simple high activity aluminide coatings develops below the pre-deposited nickel-zirconia layer and latter converts to a nearly un-alloyed porous NiAl. In spite of its porous surface layer, the zirconia modified coating has a higher oxidation resistance than the unmodified aluminide coating.
F. Mansouri, M. Mehran,
Volume 39, Issue 1 (5-2020)
Abstract
In this paper, synthesis of inverted nano-pyramids on a single crystal silicon surface through a simple and cost-effective wet chemical method is surveyed. These structures were synthesized by MACE process using Cu as the assisted metal in the solution of copper nitrate, hydrogen peroxide and hydrofluoric acid for different etching times. FE-SEM images of the samples show that time is an important factor in the formation of silicon inverted nano-pyramids and by extending synthesis time the structures gradually fade. After synthesis, some samples were etched in KOH 2% and IPA 6% for one minute which resulted in formation of nano-pyramids besides inverted nano-pyramids on the silicon surface. Formation of these combinational structures affected the self-cleaning behavior of the silicon surface. X-ray diffraction (XRD) was utilized for studying the crystalline characteristics of the synthesized structures. Moreover, the self-cleaning behavior of them was studied using the contact angle goniometer. The results showed that the inverted nano-pyramids improve the hydrophilic behavior of the silicon surface while post-synthesized etching improves the hydrophobic behavior of the surface. These textures improve the performance of solar cells due to their self-cleaning and light adsorption properties
N. Bahremandi Tolou, H. R. Salimi Jazi, M. Kharaziha, N. Lisi, G. Faggio, A. Tamburrano,
Volume 39, Issue 1 (5-2020)
Abstract
In recent years, graphene has been considered in various tissue engineering applications such as nerve guide conduits because of its unique properties such as high electrical and mechanical properties, porous structure for exchange of nutritious and waste materials, biocompatible, capability of drug and growth factor delivery. In the current study, nerve guide conduits based on a 3D graphene were synthesized by induction heating chemical vapor deposition (ICVD). Graphene was synthesized on Ni foam template at 1080 ͦC. Fabricated samples were characterized by Raman analysis and Scanning Electron Microscopy. Raman analysis showed that the synthesized graphene is in the form of a turbostratic multilayered graphene with little defects. Cyclododecane (CD) as a temporary protective layer was used to remove nickel. After removing nickel, the free-standing 3D-graphene structure was coated with a polymer (PCL) by drop and dip coating methods to obtain the composite conduit. A comparison of the electromechanical results of the 3D-graphene/PCL conduit and PCL conduit indicated that firstly, grapheme increased the electrical conductivity of the composite conduit which will help promote nerve regeneration and axon growth. Secondly, tensile strength and flexibility of the 3D-graphene/PCL conduit was improved compared to the PCL conduit.
M. Toorani Farani,
Volume 39, Issue 1 (5-2020)
Abstract
In this study, Plasma Electrolytic Oxidation (PEO) at three frequencies of 500, 1000 and 3000 Hz was applied on Mg surface and the effect of PEO surface preparation on protective behavior of three types of epoxy, fusion bond epoxy (FBE) and polyurethane coatings was investigated. The microstructural and protective properties of PEO coatings were studied by SEM, potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). The results showed that the coating formed at frequency of 3000 Hz had smaller pore size and better protection properties. EIS test in 3.5 Wt.% NaCl solution was also used to investigate the protective behavior of the two-layered coatings. The results showed that PEO process had a favorable effect on the protective behavior of the polymer layers. Moreover, the best protection behavior was related to the PEO/FBE coating system.
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.
M. Farhadian, K. Raeissi, M. A. Golozar,
Volume 39, Issue 2 (8-2020)
Abstract
This work is focused on the effect of amorphous SiO2 addition on the phase transformation and microstructural evolution of ZrO2 particles. Considering the structural similarities between the amorphous ZrO2 and its tetragonal structure, XRD results showed initial nucleation of metastable tetragonal ZrO2 from its amorphous matrix upon heat treatment. This metastable phase is unstable in pure ZrO2 sample and transforms to a stable monoclinic phase at around 600 oC. However, addition of amorphous SiO2 to ZrO2 structure causes metastable tetragonal phase to remain stable up to around 1100 oC. The temperature range for stability of metastable tetragonal ZrO2 structure increased from about 150 oC in pure ZrO2 particles to around 500 oC in ZrO2-10 mol.% SiO2 composite powders. A further increase in SiO2 content up to 30 mol.% did not change the stabilization temperature range but the average particle size reduced around 1.6 times compared to pure ZrO2 particles. Stabilization of metastable tetragonal ZrO2 explained by constrained effect of SiO2 layer surrounding zirconia nuclei. The thickness of this SiO2 layer enhanced by increasing SiO2 content which limited the growth of ZrO2 nuclei resulting in finer particle sizes.
M. Etminan, M. Morakabati, S. M. Qazi Mir Saeid,
Volume 39, Issue 2 (8-2020)
Abstract
The aim of this study was to investigate the effect of temperature and time of homogenization treatment on the microstructure, distribution of alloying elements and hardness of the novel Co-based superalloy Co-7Al-7W-4Ti-2Ta. For this purpose, the specimens were first homogenized at 1250 and 1300 °C for 2, 4, 6 and 8 hours and then water-cooled. Subsequently, the specimens were subjected to hardness testing and microstructural examinations by optical and electron microscopy. The results showed that by increasing the homogenization temperature to 1300 °C, the porosity created by Ti oxidation and local melting of the Co-Al-Ti eutectic compounds led to a decrease in hardness to 90 Vickers. This phenomenon was due to high segregation of alloying elements in the cast structure. The intensity and destructive effects of this segregation were reduced by remelting of alloy. However, by homogenization at 1250 °C, no local melting of eutectic zones or porosity were observed in the specimens and a more uniform structure was obtained with increasing time. Minimum and maximum hardness values after homogenization at 1250°C were 348 and 406 Vickers, respectively. Moreover, the microstructure became more homogenous by increasing the homogenization treatment time at this temperature.
A. Zolriasatein, S. Navazani, M. Rezaei Abdadchi, N. Riahi Noori ,
Volume 39, Issue 3 (12-2020)
Abstract
In this paper, the effect of adding aluminum trihydrate (ATH) on electrical (including dielectric constant, dielectric loss and strength, volume and surface resistivity) and hydrophobic properties of two-part room temperature volcanized (RTV) silicone rubber resin coatings were investigated. For this purpose, the RTV-ATH nanocomposite was made by physical mixing and its electrical and hydrophobic properties were compared with those of pure RTV. The results showed an increase in the dielectric constant (from 3.11 to 4.13), the dielectric loss (by ~ 0.06) and the dielectric strength (by ~ 4 KV/mm) of the RTV-ATH composite compared to the pure RTV. Moreover, ATH increased volume resistivity and reduced the surface resistivity of composite coatings. On the other hand, by spraying of coatings, no improvement in the hydrophobicity class of composite coating compared to pure RTV was observed and both samples were standardized in the HC2 standard class. Structural analysis of samples was performed by X-ray diffraction, optical microscopy and scanning electron microscopy and the presence of the main phases in them was confirmed.
S. Arjmand, M. Tavoosi,
Volume 39, Issue 3 (12-2020)
Abstract
The present work aims to modify surface properties of pure Ti by development of Ti-Al-N intermetallic composite coatings. In this regard, tungsten inert gas (TIG) cladding process was carried out using Al 1100 as filler rod with Ar and Ar+N2 as shielding gases. Phase and structure of the samples were investigated by X-ray diffraction (XRD) technique, optical microscopy (OM) and scanning electron microscopy (SEM). Hardness values and corrosion behavior of the obtained coatings were also compared using Vickers microhardness tester and potentiostat, respectively. The results showed that composite structure containing Al3Ti, Ti3Al2N2 and Ti3Al intermetallic compounds could be formed on the surface of pure Ti. Amounts of brittle phases and welding defects at the titanium-coating interface were least by welding under pure Ar shielding. Despite the increasing amount of structural defects such as porosity and non-uniformity under Ar+N2 shielding, the prepared coatings had higher hardness (more than 100 HV) and corrosion resistance (more than twice) compared with those obtained under Ar shielding.
A. Zamani, M. R. Loghman Estraki, S. R. Hosseini, M. Ramezani, A. Al-Haji,
Volume 39, Issue 3 (12-2020)
Abstract
The aim of the study was to investigate the effect of temperature, time, pH, capping agent concentration (mercaptoacetic acid), Zn to Se and Se to reducing agent (NaBH4) mole ratios on morphology, phase developments and size of zinc selenide nanoparticles prepared by hydrothermal method. Characterization of zinc selenide nanoparticles was performed by Field Emission Electron Microscopy (FESEM), Energy Dispersive X-ray Spectrometry (EDS), X-ray Diffraction (XRD), Induced Coupled Plasma Spectrometry (ICP), Fourier Transform Infrared spectroscopy (FTIR) and Simultaneous Thermal Analysis (STA). The results of EDS showed that the ratio of atomic percentage of Zn to Se in the optimized zinc selenide nanoparticles is 1: 1 and elements are evenly distributed in the nanoparticles. Based on the results of FTIR and STA thermal analyses, MAA as the stabilizing agent binds to and stabilizes zinc selenide nanoparticles. Finally, fine nanoparticles of zinc selenide with narrow size distribution, spherical shape and cubic crystal structure were obtained at the minimum temperature (130 °C) and processing time (15 hours) with the least amount of reducing and capping agents compared to previous researches.
