Showing 19 results for Glass
D. Mostofinejad,
Volume 20, Issue 1 (7-2001)
Abstract
The paper presents the results of casting and testing of 264 GFRC specimens. The glass fibers were 25 mm long, with the aspect ratio (L/D) ranging between 1250 and 3570. The parameters studied were the ratio (by weight) of fibers to cement, i.e. F/C=0%, 1.5%, 3%, and 4.5%, and the ratio of coarse to fine aggregates (gravel to sand), i.e. G/S=1.1, 0.7 and 0.2. In total, 12 mix designs were selected for GFRC specimens while the water-cement ratio was constant and equal to W/C=0.4. The balling of glass fibers in the mix was overcome by using adequate and sufficient antistatic agents. The specimens were tested under compressive, tensile and flexular loading at the ages of 7 and 28 days. Furthermore, the modulus of elasticity and the absorption of the concretes were determined. Finally, the mechanical and physical properties of the GFRC specimens were analysed and an empirical expression describing the modulus of elasticity of the GFRC was proposed.
H. Edris , M. H. Fathi,
Volume 29, Issue 2 (12-2010)
Abstract
Fabrication of biomaterials with ability to form a bond with bone tissue for bone skeletal system repair is one of the biomaterial science aims. Bioactive glasses containing CaO-SiO2-P2O5 are among the most important groups used in biomedicine and dentistry such as bone defect repair and maxillo-facial reconstruction. The aim of this work was preparation and characterization of nano particle bioactive glass with optimum bioactivity. Bioactive glasses with three different compositions (45S, 49S and 58S) were prepared via sol- gel technique. X- ray diffraction (XRD) technique and X- ray fluorescent (XRF) method were utilized for the phase analysis and also to investigate the chemical composition of the obtained bioactive glass nanopowders. Transmision electron microscopy (TEM) and Scanning electron microscopy (SEM) were utilized to study the structure, morphology and particle size of synthesized bioactive glass nanopowders. In order to investigate the bioactivity, the prepared bioactive glasses were immersed in the simulated body fluid (SBF) solution at 37◦C for 30 days. Scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) were utilized to recognize and confirm the apatite layer on the prepared bioactive glass nanopowders. TEM images showed that the prepared bioactive glasses had the particle sizes less than 100 nanometers. SEM, FTIR and XRD confirmed the formation of bone-like apatite layer formed on the bioactive glass nanopowders surface, confirming the bioactivity of synthesized bioactive glass nanopowders. It was concluded that the amount of apatite on the 45S bioactive glasse was greater in comparison with 49S and 58S bioactive glasses. It is notable that by optimizing the chemical composition, bioactive glass nanopowder could be used in applications such as repair of bone defects and bone replacement.
M. Ashuri, F. Moztarzadeh, N. Nezafati, A. Ansari Hamedani, M. R. Tahriri,
Volume 31, Issue 1 (6-2012)
Abstract
In the present study, a bioceramic-based composite with remarkable mechanical properties and in vitro apatite forming ability was synthesized by sintering compacts made up of mixtures of hydroxyapatite (HA) and sol-gel derived bioactive glass (64SiO2-26CaO-5MgO-5ZnO) (based on mole %). HA was synthesized through co-precipitation method. The stabilization temperature of the bioactive glass was set to be 700 ºC according to simultaneous thermal analysis (STA). Laser Particle Size Analysis (LPSA) was used to compare the particle size distributions of the synthetic powders. HA matrix was mixed with different weight percentages of bioactive glass (5, 10, 15, 20, 25 and 30 wt. %) and compressed by 80 MPa pressure. After sintering the uniaxial compression test of the samples was done and the specimen with the highest compressive strength (20 wt. % bioactive glass) was selected to be immersed in the Simulated Body Fluid (SBF) for 3, 7 and 14 days. The results showed that the compressive strength of the sample decreased after keeping it in the SBF. Also, inductively coupled plasma analysis (ICP) was used to study the ion release behavior of the sample in the SBF. Finally, phase composition, microstructure and functional groups in the composite were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier transform infra-red spectroscopy (FTIR) techniques, respectively.
M. Mazrooei Sebdani, M. H. Fathi ,
Volume 31, Issue 2 (12-2012)
Abstract
Despite excellent bioactivity of bioactive ceramics such as hydroxyapatite, their clinical applications have been limited due to their poor mechanical properties. Using composite coatings with improved mechanical properties could be a solution to this problem. Therefore, the strength of metal substrate and the bioactivity of the improved composite coating combined could yield suitable results. The aim of this work was fabrication and characterization of hydroxyapatite-forsterite-bioactive glass nanocomposite coating. The sol-gel technique was used to prepare hydroxyapatite-forsterite-bioactive glass nanocomposite in order to coat on 316L stainless steel (SS) by deep coating technique. The X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM) and energy dispersive X-ray analysis (EDX) techniques were used to investigate the microstructure and morphology of the prepared coating. The results obtained from XRD analysis showed that the suitable temperature for calcination is 600 °C. At this temperature, the homogenous and crack-free coating could attach to the 316L SS substrate. The crystallite size of composite coatings determined via AFM was lower than 100 nm. Overall, the results obtained from this work indicate that hydroxyapatite-forsterite-bioactive glass nanocomposite coating can be a good candidate for biomedical applications.
A. M. Molavi, S. M. Mirkazemi, A. Beitollahi,
Volume 32, Issue 1 (6-2013)
Abstract
The effects of temperature, time and atmosphere on microstructure and magnetic properties of NiFe2O4 glassceramic were investigated utilizing differential thermal analysis, X-ray diffraction, vibrating sample magnetometer and scanning electron microscope techniques. Various compositions were studied in the Na2O-NiO-Fe2O3-B2O3-SiO2 system to obtain amorphous phase. The sample heat-treated in graphite bed at 510°C for 1 hr showed higher magnetization than the one heattreated in the air under the same condition. XRD analysis showed the presence of nickel ferrite and some non-magnetic phases such as sodium borate and silicate phases in the heat treated samples. The maximum magnetization of samples reduced by increasing the holding time from 1hr to 3 hr at 510°C. Increment of temperature to 700°C increased the amount of NiFe2O4 and maximum magnetization.
F.s. Sayyedan, M.h. Fathi, H. Edris, A. Doostmohamadi, V.s., Mortazavi, F. Shirani,
Volume 33, Issue 3 (3-2015)
Abstract
The objective of this study was to synthesize glass ionomer–forsterite nanocomposite and study the effect of
incorporating forsterite nanoparticles to the ceramic part of glass ionomer cement in order to improve mechanical properties and
bioactivity. So, Forsterite nanoparticles were made by the sol-gel process using different weight percentages added to the ceramic
part of commercial GIC (Fuji II GC). X-ray diffraction (XRD) was used in order to characterize and determine grain size of the
produced forsterite nanopowder. In order to study the mechanical properties of the produced glass ionomer cement-forsterite
nanocomposite, the compressive strength (CS), three-point flexural strength (FS) and diametral tensile strength (DTS) of
specimens were measured. Statistical analysis was done by one Way ANOVA and differences were considered significant if
P‹0.05. The morphology of fracture surface of specimens was studied using scanning electron microscopy (SEM) technique.
Bioactivity of specimens was investigated by Fourier transitioned-infrared spectroscopy (FTIR), scanning electron microscopy
(SEM), and Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES). The results of XRD analysis confirmed the
nanocrystalline and pure forsterite synthesis. According to the mechanical properties measurements, the optimum weight
percentages of forsterite nanoparticles for enhancement of CS, FS, and DTS were obtained equal to 3, 1 and 1 wt.%, respectively.
Statistical analysis showed that the differences between all the groups were significant (P<0.05). SEM images and results of the
ICP-OES and FTIR tests confirmed the bioactivity of the nanocomposite. Glass ionomer-forsterite nanocomposite containing 1 to
3 wt.%-forsterite nanoparticles can be a suitable candidate for dentistry and orthopedic applications due to the improvement of
mechanical properties and bioactivity.
M. Tehrani Dehkordi, S. H. Bahrami, R. Nategi Jahromi,
Volume 33, Issue 3 (3-2015)
Abstract
In this study, the effects of different parameters on charpy impact properties of pure and hybrid composite laminates reinforced with basalt and glass filaments were investigated. For this purpose, five types of basalt and glass laminates with
quasi-isotropic stacking sequence, namely, a pure basalt, a pure glass, two inter-ply hybrid and one intra-ply hybrid composites were produced. Epoxy resin was used as matrix material. After that, the impact test was performed and the average absorbed energy of each type of specimens was determined. The results indicated that the pure basalt and nylon laminates had the highest and least absorbed energy, respectively. The hybrid laminates had the absorbed energy somewhere between the pure basalt and glass ones. Also, between the hybrid composites, the intra-ply laminate had a better impact performance than the inter-ply ones.
H. Amiri, S. M. Mirkazemi, A. Beitollahi ,
Volume 34, Issue 2 (7-2015)
Abstract
In this investigation, the effect of heat treatment on magnetic properties of glass and nano-structured cobalt-ferrite glass-ceramic was studied. The glass was synthesized in the system of Na2O-Fe2O3-CoO-B2O3-SiO2. Based on DTA results, heat treatment was done at different times and temperatures. X-ray diffraction pattern of glass-ceramic showed the crystallization of CoFe2O4 and some nonmagnetic phases. The highest magnetization of 11.8 emu/g was obtained for the sample heat-treated for 2 hr at 670C in graphite bed. Average crystallite size of CoFe2O4 in this sample was 50 nm. Scanning Electron Microscopy (SEM) confirmed the formation of cobalt ferrite nanoparticles in the glass matrix.
A. Abdolahi, M. R. Saeri, F. Tirgir, A. Doostmohammadi, H. Sharifi,
Volume 35, Issue 1 (6-2016)
Abstract
In this study, NBG was successfully achieved through a sol-gel technique, and to further improve its dispersibility, a crylate coupling agent was coupled onto the surface of the NBG. The 3-(Trimethoxysilyl)Propylmethacrylate coupling agent was used to the surface modification of the synthesized NBG by a wet-chemical method in a dynamic inert nitrogen atmosphere. The surface properties of the biomaterials before and after modification were characterized and compared using FTIR and AFM techniques. The characteristic peaks in FTIR spectra indicated that –CH2, –CH3 and C=O groups appeared on the surface of modified NBG, and also, AFM analysis revealed that the dispersibility of surface modified NBG was improved, significantly. The above results proved that the desired groups of 3-(Trimethoxysilyl)Propyl methacrylate had been covalently bonded onto the surface of NBG. Besides, a nanocomposite scaffold was synthesized using the synthesized NBG and polyurethane foam as raw materials. The morphology of pores, porosity contents, compress strength and bioactivity of the scaffold were studied. The results showed that the biological scaffolds for use in bone tissue engineering with the basic requirements (90% porosity and 200-600 μm pore diameter) were successfully prepared. The polymer component had no effect on the relationship between the scaffold pores and bioactivity of bioglass nanoparticles. Improvement of compressive strength and proper bioactivity of the resulted scaffold showed that it is an acceptable candidate for biomaterials applications.
S. Nikbakht Katouli, A. Doostmohammadi, F. Esmaeili,
Volume 35, Issue 1 (6-2016)
Abstract
The aim of this study was to fabricate carbon nanotube (CNT) and bioactive glass nanoparticles (BG) (at levels of
5 and 10 wt%) incorporated electrospun chitosan (CS)/polyvinyl alcohol (PVA) nanofibers for potential neural tissue engineering applications.The morphology, structure, and mechanical properties of the formed electrospun fibrous mats were characterized using scanning electron microscopy (SEM) and mechanical testing, respectively. In vitro cell culture of embryonal carcinoma stem cells (P19) were seeded onto the electrospun scaffolds. The results showed that the incorporation of CNTs and BG nanoparticles did not appreciably affect the morphology of the CS/PVA nanofibers. The maximum tensile strength (7.9 MPa) was observed in the composite sample with 5 %wt bioactive glass nanoparticles. The results suggest that BG and CNT-incorporated CS/PVA nanofibrous scaffolds with small diameters, high porosity, and promoted mechanical properties can potentially provide many possibilities for applications in the fields of neural tissue engineering and regenerative medicine.
M. Shamsi, N. Nezafati, S. Zavareh, A. Zamanian,
Volume 35, Issue 1 (6-2016)
Abstract
Ternary (%mol) (64SiO2-31CaO-5P2O5) system of sol-gel derived bioactive glass fibers was prepared by electrospinning method. X-ray Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and nitrogen adsorption test (BET) analyses were performed to investigate the phase and chemical group of the composition, morphology of the surface and specific surface area of the fibers, respectively. SEM observations confirmed that the fibers were nano size. The amorphous nature and the presence of silanol groups in the composition were confirmed by XRD and FTIR, respectively. Apatite formation and biodegradability of the fibers were studied using various analyses after different days of soaking in simulated body fluid (SBF). The results affirmed the presence of apatite layers on the surface of the fibers. Cell culture evaluation indicated that MG-64 human osteoblast-like cells were attached and spread well on the surface. Furthermore, cell viability and cell growth demonstrated that the cells were grown and reproduced well on the fibers.
S. Ahmadi, H. R. Shahverdi,
Volume 35, Issue 2 (9-2016)
Abstract
In this research, Glass Form Ability (GFA) has been investigated in the new class of Fe-based amorphous
alloys. Indeed, the main purpose is to evaluate the effects of alloying with niobium on glass form ability of Fe55-xCr18Mo7B16C4Nbx (X=0, 3, 4, 5) alloys. Vacuum induction melting (VIM) was utilized for production of primary ingots and melt spinning process was used for production of thin ribbons required for kinetic and structural investigations. Kinetic analysis was done using
the data obtained from Differential Scanning Calorimetry (DSC) tests. Results showed that GFA and viscosity were enhanced by Nb alloying. It was also determined that devitrification transformation was accomplished in alloys by nucleation and growth mechanisms.
M. Rezazadeh, M.r. Saeri, F. Tirgir Malkhlifeh, A. Doostmohammdi,
Volume 35, Issue 2 (9-2016)
Abstract
The aim of the present study is to study the effects of adding diopside (CaMgSi2O6) as well as silica sulfuric acid nanoparticles to ceramic part of glass ionomer cement (GIC) in order to improve its mechanical properties. To do this, firstly, diopside (DIO) nanoparticles with chemical formula of CaMgSi2O6 were synthesized using sol-gel process and then, the structural and morphological properties of synthesized diopside nanoparticles were investigated. The results of scanning electron microscopy (SEM) and particle size analyzing (PSA) confirmed that synthesized diopside are nanoparticles and agglomerated. Besides, the result of X-ray diffraction (XRD) analyses approved the purity of diopside nanoparticles compounds. Silica sulfuric acid (SSA) nanoparticles are also prepared by chemical modification of silica nanoparticles by means of chlorosulfonic acid. Fourier transform infrared spectroscopy (FTIR) technique was used to find about the presence of the (SO3H) groups on the surface of silica sulfuric acid nanoparticles. Furthermore, various amounts (0.1, 3 and 5 wt.%) of diopside and silica sulfuric acid nanoparticles were added to the ceramic part of GIC (Fuji II GIC commercial type) to produce glass ionomer cement nanocomposites. The mechanical properties of the produced nanocomposites were measured using the compressive strength, three-point flexural strength and diametral tensile strength methods. Fourier transform infrared spectroscopy technique confirmed the presence of the (SO3H) groups on the surface of silica nanoparticles. The compressive strength, three-point flexural strength and diametral tensile strength were 42.5, 15.4 and 6 MPa, respectively, without addition. Although adding 1% silica solfonic acid improved nanocomposite mchanical properties by almost 122%, but maximum increase in nanocomposite mechanical properties was observed in the nanocomposites with 3% diposid, in which 160% increase was seen in the mechanical properties.
M. Illbeigi, A. R. Fazlali, M. Kazazi, A. H. Mohammadi,
Volume 36, Issue 1 (6-2017)
Abstract
In this research, new lithium ion conductor glass-ceramics with NASICON-type structure (Li1+x+yAlxCryGe2-x-y (PO4)3, x+y=0.5) were synthesized using melt-quenching method and converted to glass-ceramics through heat treatment. Influence of addition of different concentrations of aluminum and chromium in LiGe2(PO4)3 glass-ceramic was investigated for ionic conduction improvement. Substitution of Ge4+ ions in NASICON structure by Al3+ and Cr3+ ions induced more Li+ ions in A2 vacant sites to obtain charge balance and also changed the unit cell parameters. These two factors led to ionic conductivity improvement of synthesized glass-ceramics. The glass-ceramics were characterized and the amorth structures were investigated by X-ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), Energy-Dispersive X-ray spectroscopy (EDX), Differential Scanning Calorimetry (DSC) and Complex Impedance Spectroscopy (CIS). The highest lithium ion conductivity of 8.82×10-3 S/cm was obtained for x=0.4 and y=0.1 (Li1.5Al0.4Cr0.1Ge1.5(PO4)3) crystallized at 850 oC for 8 h with minimum activation energy of 0.267 eV.
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.
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. T. Asadi Khanouki, R. Tavakoli , H. Aashuri,
Volume 38, Issue 2 (9-2019)
Abstract
In this research, the effect of temperature on the mean size of fracture surface features, as well as the relation between fracture surface morphologies and ductility of a La-based BMG as a relatively brittle alloy, was systematically investigated. After producing the alloy, three-point bending experiments, over a wide range of temperatures, were conducted on the samples; then the fracture surfaces were analyzed using scanning electron microscopy. The results demonstrated that the width of stable crack growth region (ΔW) was increased upon ductility (δp). Conversely, the mean size of the features on both stable (Ds) and fast (Df) crack growth regions and also, shear offset width (ΔL) were found to decrease with increasing ductility. In this case, the shear band instability was reduced, and the plastic strain could be more homogeneously distributed on the shear bands. The similarity of ΔL and Ds values suggested that the formation of vein pattern was caused by steak-slip behavior and multiple-step sliding inside the shear band through the fluid meniscus instability mechanism. Furthermore, the results obtained from correlation between ductility and fracture surface morphologies in the BMG indicated that the size of features was reduced with increasing ductility.
A. Faeghinia, H. Mardi,
Volume 38, Issue 4 (1-2020)
Abstract
Amorphous steel slag was blended with different concentrations of waste glass (20, 40, 50, 60, 70 wt.%) and SiC to obtain a composite. According to Hot Stage Microscopy images, slag-glass composite contractions started at 1050 ºC. scanning electron microscope micrographs of slag-SiC (foaming agent) composite revealed tunnel-like porosities of 500 to 1000 microns. Gaseous products of carbide decomposition led to the formation of these tunnel-like porosities. By adding up to 50 wt. % of waste glass to this composite and sintering at 1200 ° C, the size of cavities decreased by 10 times and achieved 50 microns to form spherical cavities. By increasing glass content, the total porosity of slag-glass-SiC increased to 80 wt.% followed by a decrease in the strength to 3.2 MPa. Having an overall density of 0.8 g/cm3, the slag-glass composite could be classified as a porous foam material. Pseudo Waltonite phase was also detected in this composite after sintering.
M. T. Asadi Khanouki,
Volume 39, Issue 3 (12-2020)
Abstract
In this study, the influence of temperature and strain rate on plastic flow of a Zr-based bulk metallic glass (BMG) during the three-point bending test was studied to find a correlation between strain rate sensitivity (m) and flow behavior. The flexural stress-deflection curves revealed two distinct types of dynamics, serrated and non-serrated flow, related to temperature and strain rate. The serrated flow which appeared at temperatures higher than a critical value or strain rates lower than a critical value, was simultaneously due to activation of shear transformation zones (STZs) and time-dependent structural relaxations. Further results indicated negative and positive values of m at temperatures above and below 0.4 Tg, respectively. The main reason for negative strain rate sensitivity was insufficient time of structural relaxation at high strain rates which lead to generation of free volume inside shear bands making the BMG softer. Comparison of STZ activation energy with activation energy for the onset of serration indicated almost equal values and there was a close relationship between serrated flow and STZ operation.
