Showing 26 results for Nanocomposite
B. Karami, M. Imani, A. Seifalian, M.a.shokrgozar, S.bonakdar, A. Khavandi,
Volume 32, Issue 1 (6-2013)
Abstract
This study aims to characterize and evaluate the applicability of Polyhedral OligomericSilsesquioxane (POSS)/ Poly (carbonate-urea) Urethane (PCU) nanocomposite films as a temporary skin substitute by means of FTIR, MTT assay, cell proliferation assay and SEM studies. FTIR spectra showed all the characteristic peaks of POSS/PCU nanocomposite. The indirect cytotoxicity of membranes was investigated by MTT assay. In MTT test, L929 mouse fibroblasts were exposed to the extract of the films for 24 h. MTT results showed no sign of cell cytotoxicity for the extracts at the extraction times up to14 days. Menwhile, it was found that POSS nanocages have a stimulating effect on L929s. In cell proliferation assay, L929s were cultured on the films for 3, 7 and 14 days. The cells showed a high rate of proliferation in direct contact with the biomaterial after 7 and 14 days. Morphology and density of the cells on the nancomposite surface was investigated through SEM observations. SEM micrographs showed that the cells adhered well on the surface after 3 days of culture. Moreover, after 7 days, cell density increased so substantially that a cell layer was formed on the membranes.
M. Raz, F. Moztarzadeh, M.a. Shokrgozar, M. Ashuri, M. Tahriri,
Volume 32, Issue 2 (12-2013)
Abstract
In this project, we prepared biomimetic nanocomposite scaffolds from gelatin and chitosan and hydroxyapatite and subsequently the scaffolds were evaluated by common used bulk technique. For this purpose, the nanocomposite hydrogel/apatite bone tissue engineering scaffolds were fabricated using applied biomimetic method accompanied with freeze drying technique. The apatite was precipitated using double diffusion mechanism within gelatin hydrogel in similar pH and temperature to the human body. Chitosan initial percentage (20, 30 and 40%) was set as variables. Nanocomposites were soaked in glutaraldehyde solution in order to enhance mechanical properties and make them insoluble in water. Diffusion of calcium and phosphate from lateral hydrogel into the middle hydrogel caused formation of parallel white layer-formed precipitate. Analysis of precipitates formed within middle hydrogel for the samples, showed that detected materials are composed of carbonated hydroxyapatite and dicalcium phosphate dihydrate (DCPD, brushite). Also, mechanical behavior obtained for the scaffolds were comparable with spongy bone. With increasing chitosan in the composite scaffold, the water up-take was increased from 379 to 661%. Phase composition, microstructure and structural groups in the composite samples were also characterized by X-Ray Diffraction (XRD), scanning electron microscopy (SEM) and Fourier transform infra-red (FTIR) analyses. Eventually, the obtained results showed that the composite contains 20% chitosan had appropriate properties for fabricating bone scaffold.
R. Esmaeili, M.r. Dashtbayazi,
Volume 32, Issue 2 (12-2013)
Abstract
In the present work, molecular dynamics simulation method was used for determining Young's modulus, Shear modulus and Poisson’s ratio of Al-SiC nanocomposites, with different volume fractions of the reinforcements. For simulation, the open source package, LAMMPS, was used. After putting Aluminum and Silicon Carbide atoms in their initial positions, interatomic potentials between them were defined. EAM potential was used for Aluminum atoms, Morse potential was used for Al-C and Al-Si, and for C-C, Si-C, and Si-Si Tersoff potential was used. According to the elastic bounding principal, and the comparison between the simulations results and Voigt, Ruess and Halpin-Tsai micromechanical models showed that the results were close to the upper bound Voigt model.
S.s. Sayyedain, H.r. Salimijazi, M.r. Toroghinejad, F. Karimzadeh.,
Volume 33, Issue 1 (7-2014)
Abstract
Due to their superior properties such as high specific strength, high creep resistance and high strength at elevated temperatures, aluminum composites reinforced with alumina nano particles are widely used for advanced purposes such as aerospace and auto industries. Lack of an appropriate welding process limits their applications. Transient liquid phase (TLP) bonding is one of the state-of-the-art joining processes. It is used for welding composites and advanced materials. Microstructure and mechanical properties of TLP bonding depend on the bonding time and temperature. In the current study, the effect of bonding time on the microstructure and bonding strength of the TLP diffusion bonded of Al2O3p/Al nanocomposite was investigated. A thin layer of copper deposited by electroplating was used as an interlayer. The bonding times of 20 and 40 min were not sufficient for completing the isothermal solidification, and the bonding strengths were not satisfactory. By increasing the bonding time to 60 min at constant bonding temperature of 580 ºC, the isothermal solidification was completed and the final joint microstructure consisted of soft α-Al phase with dispersed CuAl2 precipitated particles. Decreasing the amount of brittle eutectic structures in the joint seam by increasing the bonding time was the main reason for improvement of the joint shear strength. The maximum joint shear strength was achieved at 580 ºC for 60 min which was about 85% of the shear strength of the base material.
M. Ahmadi, Sh. Ebrahimi, M. Ahmadi,
Volume 33, Issue 2 (3-2015)
Abstract
This research aimed at producing microcellular foams (with cell size of 1-10 μm and cell density above 10 9 cell/cm3)
from PC/EPDM in order to use in medical devices. Due to the weak nucleation behavior of microcellular polycarbonate foams, it is difficult to prepare them. This research provides valuable information regarding the possibility of making microcellular foams from this polymer by using multiwalled carbon nanotubes (MWNT,s) as nucleating agents (the value of 1-3 phr). The nanocomposite samples were prepared in an internal mixer and foamed via a batch processing method using supercritical carbon dioxide as the foaming agent. The results showed that the addition of nanoparticles up to 3 phr improves the foamability of PC/EPDM blend. Furthermore, as nanoparticle content increased a decrease in cell size and hence an increase in cell density were observed. Another finding showed that cell size distribution is directly related to uniform dispersion of carbon nanotubes.
M.godarzi, A. Saidi,
Volume 33, Issue 2 (3-2015)
Abstract
In recent years, much research has been performed in the field of nanomaterials synthesis using mechanochemical process. In this research, TixAly/Al2O3 ceramic matrix nanocomposite was produced by the mechanochemical method. Aluminum and inexpensive titanium oxide powders were used as raw materials, and milling was performed under N2 atmosphere. The results showed that reduction of TiO2 by Al is the first step of synthesis process, and then Ti reacts with residual Al. The synthesis after 10 hours of milling resulted in titanium aluminide and aluminium oxide. With the increase of milling time to 80 hours, titanium aluminide quantity was increased. Also, the results showed that the heating of samples containing titanium aluminide in the argon and nitrogen atmospheres does not lead to complete decomposition of aluminides.
S. Mirtalebi , D. Ghasemi ,
Volume 33, Issue 2 (3-2015)
Abstract
In the present study, pure Aluminum powder with 5%wt Titanium Dioxide was mechanically milled at different times. Using phase analysis through X-ray diffraction (XRD), it was found that increasing of the milling times over 10 hours causes the reduction of Titanium by Aluminum and formation of Al2O3 in the structure. Also, it was shown that if the process persists, Aluminum reacts with Titanium and causes the formation of Al3Ti in the composition. The reactions were studied through the thermodynamic relations. Furthermore, after distribution of reinforcement particles in the matrix,
using X-ray diffraction peak broadening, according to Williamson-Hall equation, the mean crystallite size and lattice strain were determined, and by scanning electron microscopy (SEM), the structure and morphology of the powder particles were studied.
M.r. Dehnavi, B. Niroumand, F. Ashrafizadeh,
Volume 34, Issue 1 (5-2015)
Abstract
Effects of discontinuous ultrasonic treatment on the microstructure, nanoparticle distribution, and mechanical properties of cast Al413-SiCnp nanocomposites were studied. The results showed that discontinuous ultrasonic treatment was more effective in improving the mechanical properties of the cast nanocomposites than the equally timed continuous treatment. The yield and ultimate tensile strengths of Al413-2%SiCnp nanocomposites discontinuously treated for two 20 minute periods increased by about 126% and 100% compared to those of the monolithic sample, respectively. These improvements were about 107% and 94% for the nanocomposites continuously treated for a single 40 minute period. The improvement in the mechanical properties was associated with severe refinement of the microstructure, removal of the remaining gas layers on the particles surfaces, more effective fragmentation of the remaining agglomerates as well as improved wettability and distribution of the reinforcing particles during the first stage of solidification.
M.r. Dashtbayazi, R. Esmaeili,
Volume 34, Issue 2 (7-2015)
Abstract
Based on molecular dynamics simulation results, a model was developed for determining elastic properties of aluminum nanocomposites reinforced with silicon carbide particles. Also, two models for prediction of density and price of nanocomposites were suggested. Then, optimal volume fraction of reinforcement was obtained by genetic algorithm method for the least density and price, and the highest elastic properties. Based on optimization results, the optimum volume fraction of reinforcement was obtained equal to 0.44. For this optimum volume fraction, optimum Young’s modulus, shear modulus, the price and the density of the nanocomposite were obtained 165.89 GPa, 111.37 GPa, 8.75 $/lb and 2.92 gr/cm3, respectively.
M.r. Dashtbayazi, M. Mahmoudi Meymand,
Volume 34, Issue 3 (12-2015)
Abstract
In this research, stiffness of polymer-clay nanocomposites was simulated by Mori-Tanaka and two and three dimensional finite element models. Nanoclays were dispersed into polymer matrix in two ways, namely parallel and random orientations toward loading direction. Effects of microstructural parameters including volume fraction of nanoclays, elastic modulus of nanoclays and interphase, thickness of interphase, aspect ratio of nanoclays and random orientation of nanoclays on elastic modulus of the nanocomposite were investigated by finite element model. Comparing the simulation with experimental results showed that the Mori-Tanak simulation results were closer to the experimental results. Analysis of results showed that the volume fraction of nanoclay, elastic modulus of nanoclay, deviation of nanoclay layers with respect to loading direction, nanoclays aspect ratio, thickness of interphase and the elastic modulus of interphase had respectively the most to the least effect on elastic modulus of nanocomposite.
A. Mosleh, H. Shahverdi, R. Poursalehi,
Volume 35, Issue 2 (9-2016)
Abstract
In this study, electrical wire explosion has been used to produce aluminum carbon nanotube (Al-CNT) nanocomposite particles in acetone medium. In order to synthesize Al-CNT nanocomposites, initially, CNTs were ultrasonically dispersed. Then, aluminum wire was exploded in this medium. Synthesized samples were characterized by Fourier Transform Infrared (FTIR) spectroscopy and Transmission Electron Microscopy (TEM) methods. The results exhibited formation of spherical nanoparticles in the medium. The average diameter of nanoparticles was 4 nm. Moreover, attained nanoparticles remained stable in acetone. Results revealed a good interaction between aluminum nanoparticles and CNTs in this medium. It is concluded that acetone is a suitable medium for synthesizing Al-CNT nanocomposite as appropriate dispersion of Al-CNT nanoparticles can be achieved in this medium.
Mrs M. Akbari, Dr S. Sabooni, Dr M. H. Enayati, Dr F. Karimzadeh,
Volume 36, Issue 2 (9-2017)
Abstract
In the present study, FeAl/Al2O3 nanocomposite coating was produced on the carbon steel plate using mechanical alloying (MA) technique via a mechanochemical reaction. Stoichiometric ratios of Fe, Al and Fe2O3 as well as a substrate were mixed and milled up to 22h in a vibrating high energy mill with a 4 mm ball. Samples prepared after 18h of MA were subjected to annealing at 773 K for 1-3 h. X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM) and microhardness measurements were carried out to study mechanochemical reaction and coating formation characterization. The results showed that mechanochemical reactions were started after 10h of MA, which finally caused the slight formation of FeAl/Al2O3 nanocomposite. Increasing the milling time to 18 hours led to the continuous increase of the coating thickness up to 80 μm, while the coating layer fractured and began to peel by further milling. The microhardness of the coating after 18h milling was 1050 vickers. Annealing of the 18h milled powders at 773K for 3h led to the complete formation and synthesis of the FeAl/Al2O3 nanocomposite. The results showed that the annealing treatment had considerable effects on the hardness increase up to 1200 vickers as well as adhesion strength of the composite coating.
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.
Sh. Tavakoli Dehaghi, S. Darvishi, Sh. Nemati, M. Kharaziha,
Volume 37, Issue 3 (12-2018)
Abstract
Abstract: With the advances in the development of biomaterials for tissue replacement, the attention of scientists has been focused on the improvement of clinical implant properties. In this regard, despite the appropriate properties of the stainless steel, the application of stainless steel as implants has been limited due to the weak corrosion resistivity. The purpose of this paper was preparation and characterization of hydrophobic polydimethylsiloxane (PDMS)-SiO2-CuO nanocomposite coating on the 316L stainless steel surface. The 316L stainless steel was coated by SiO2 nanoparticles (20 wt. %), CuO nanoparticles (0.5, 1 and 2 wt. %) and biocompatible PDMS. In this research, x-ray diffraction (XRD) and scanning electron microscopy (SEM) were applied to characterize the coating. Moreover, the roughness and water contact angle of the coatings consisting of various amounts of CuO nanopowder were estimated. Finally, the effects of various amounts of the CuO nanopowder on the corrosion resistivity of nanocomposite coatings were investigated. XRD patterns confirmed the presence of crystalline CuO nanoparticles on the substrate. Due to the non-crystalline nature of silica nanoparticles and the semi-crystalline PDMS polymer, no peak confirming the presence of these phases was detected on the XRD pattern of the nanocomposite coating. SEM images showed the formation of a lotus leaf-like layer on the surface of the nanocomposite coating containing 1 and 2 wt. % CuO. Moreover, water contact angle evolution revealed that while contact angle was 81 degree without CuO nanoparticles, it was enhanced to 146 degree in the presence of 1 wt. % CuO. Moreover, the corrosion study showed the nanocomposite containing 2 wt.% CuO had the best corrosion resistance, the corrosion current density of 2.1E-7 A.cm-2, and the corrosion potential of 0.22 V.
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.
N. Zakeri, H.r. Rezaie, J. Javadpour, M. Kharaziha,
Volume 39, Issue 4 (2-2021)
Abstract
In recent years, nanoceramics have been used in scaffolds to emulate the nanocomposite with a three-dimensional structure of natural bone tissue. In this regard, polycaprolactone biopolymer is widely used as a scaffold in bone tissue engineering. The goal of this research is to produce porous scaffolds of polycaprolactone - zeolite biocomposite with suitable mechanical, bioactive and biological properties for bone tissue engineering applications. The nanocomposite scaffolds were synthesized by solvent casting/particulate leaching and freeze-drying approaches. Microscopic investigations showed generation of pores with an average size of 200-400μm after addition of ceramic phase. Energy dispersive X-ray analysis confirmed uniform distribution of ceramic phase in polycaprolactone matrix. FTIR results determined the binding type of zeolite nanoparticles to the polycaprolactone matrix as physical bonding. The results of mechanical tests showed the increase in young’s modulus after addition of ceramic phase (from 0.04 to 0.3 and 3 to 7 MPa, respectively). The hydrophilicity of polycaprolactone increased after adding nanozeolite and more weight loss was observed for scaffold containing 20% zeolite (53.52 6 1.6%) with an increase in the rate of hydroxyapatite formation. The results showed that the prepared scaffolds have potential for cancellous bone tissue engineering application.
I. Forooghi , M. Mashhadi,
Volume 39, Issue 4 (2-2021)
Abstract
Due to their unique features, Ultra-High Temperature Ceramics (UHTCs) have potential applications in aerospace, military and industry. ZrB2-SiC composite as one of these ceramics has been at the center of researches due to its attractive mechanical, thermal and oxidation resistance. In this study, the effect of ZrC addition on pressureless sintering behavior, mechanical, microstructural and thermal properties of ZrB2-SiC nanocomposite were investigated. For this purpose, micron-sized ZrB2 and ZrC powders and nano-sized SiC powder were used. ZrB2-20vol% SiC nanocomposites with addition of (3, 6, 9, 12, 15) vol% ZrC were sintered by pressureless sintering method at 2100 ºC. The results showed that the addition of ZrC improved relative density, hardness and fracture toughness of ZrB2-20vol% SiC nanocomposite. Optimum properties were obtained in a sample containing 12 vol% ZrC and the relative density, hardness and fracture toughness of this sample were reported to be 99.01%, 16.95 Gpa and 5.43 Mpa.m0.5, respectively. Thermal analysis of the samples showed that by adding ZrC, thermal diffusivity of this nanocomposite reduced. The highest thermal diffusivity at room temperature equaled 35.3 mm2 /s and was obtained for ZS composite.
S. Borhani Esfahani, H. R. Salimi Jazi, M. H. Fathi, A. Ershad Langroudi, M. Khoshnam,
Volume 40, Issue 1 (5-2021)
Abstract
In this research, a kind of environmentally-friendly inorganic-organic hybrid nanocomposite coating based on silica containing titania/silica core/shell nanoparticles was synthesized and characterized for conservation of facade tiles in historical buildings. The matrix of the composite was prepared by sol-gel process via two methods of ultrasonic and reflux stirring. Tetraethyl orthosilicate (TEOS) and poly-dimethyl siloxane hydroxy-terminated (PDMS-OH) were used for the formation of silica network and creation of flexibility and hydrophobicity, respectively. Titania nanoparticles were used in the form of titania/silica core/shell as ultraviolet absorber. The synthesized nanocomposite was applied on the microscope slides and tiles by dip coating technique. The properties of nanoparticles and coatings were characterized by Fourier-transform infrared spectroscopy (FTIR), Transmission electron microscopy (TEM) and water contact angle measurement. The results revealed that formation of titania/silica core/shell structure was successful. The investigation of PDMS content effect on transparency, cohesion and hydrophobicity of the coating confirmed that the optimum content of this siloxane was around 20 wt.%. In general, the results showed that the silica-based hybrid nanocomposite reinforced with TiO2/SiO2 core/shell nanoparticles could produce a transparent and hydrophobic coating for tile and glass protection.
R. Zarei, E. Mohammadsharifi, M. R. Loghman, M. Ramazani, Kh. Zamani,
Volume 41, Issue 1 (8-2022)
Abstract
The present research has examined the effect of adding Si3N4 on the mechanical and structural properties of NiCrAlY alloy. The structural and mechanical properties of the manufactured samples were characterized by SEM, XRD, micro-hardness evaluation and pin on disk wear test. Various concentrations of Si3N4 powder (1, 3, and 5 wt.%) were mixed with NiCrAlY powder using a mechanical ball mill. Next, the mixtures were sintered at 1100 °C using the spark plasma sintering (SPS) technique. The XRD patterns indicated that the samples were composed of two phases of solid solution γ-Ni(Cr) and intermetallic compounds β-NiAl. The results of micro-hardness measurements showed that adding 1% Si3N4 to NiCrAlY enhanced the hardness from 418 to 614 HV. However, with an increase in the Si3N4 content from 1 to 5 wt%, the hardness diminished from 614 to 543 HV, and by Adding Si3N4 to the NiCrAlY, its tribological properties were significantly improved.
A. Azimi-Fouladi , S.a. Hasanzadeh-Tabrizi,
Volume 41, Issue 2 (11-2022)
Abstract
Water pollution is one of the big problems of human societies, and the need to find new ways to remove these pollutants has been given much attention in recent years. One of the methods is the use of photocatalysts. In this research, TiO2 and TiO2-CdO nanoparticles were prepared by a sol-gel method as nano photocatalysts. The produced samples have been used to degrade methylene blue under UV light. To characterize the prepared samples, X-ray Diffraction (XRD), Field Emission Scanning Electron Microscope (FESEM), X-ray Energy Diffraction Spectroscopy (EDS), and Ultraviolet-Visible Spectroscopy (UV-Vis) were used. Microstructural results revealed nanoparticles with dimensions of 18 to 32 nm. XRD results showed that the main phase formed was the anatase. TiO2-4 wt.% CdO nanocomposite showed more photocatalytic activity compared to pure TiO2. Also, the effect of pH, irradiation time, and amount of powder on photocatalytic activity was investigated. The results showed that at pH=9, time of 75 min, and using 0.02 g TiO2-4 wt.% CdO photocatalyst, the maximum photocatalytic activity of about 92 % was obtained.
