Journal of Advanced Materials in Engineering (Esteghlal)

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The addition of ZrO2 particles to the HA coating has received considerable attention because ZrO2 particles increase the bonding strength between HA coating and substrate. In this study, nanostructured hydroxyapatite (HA)/yttria stabilized zirconia (YSZ) coatings were prepared by a sol–gel method. It was found that at 950ºC, the dominant phases were HA and tetragonal (t)-zirconia in 3YSZ, cubic (c)-zirconia in 8 YSZ and t-c-Zirconia in 5YSZ phases with the small amounts of β-tricalcium phosphate (β-TCP) and CaZrO3. The crystallite size of the coating was about ~20-30 nm for tetragonal and cubic zirconia grain size and 40-80 nm for hydroxyapatite grain size. Crack-free and homogeneous HA/YSZ composite coatings were obtained with no observable defects. In vitro evaluation in 0.9% NaCl showed that Ca2+ dissolution rate of composite coatings was lower than that of pure HA coatings. The decrease in electrochemical performance of these coated samples in comparison with the uncoated type 316L St.St could be associated with chloride ion and water penetration into the coating, transport of ions through the coating, and the subsequent electrochemical reactions at the coating–metal interface.

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In the present study, in-situ synthesis of carbon nanotube/hydroxyapatite nano composite powder with stable homogeneous dispersions of carbon nanotubes (CNTs) was carried out using surfactant as dispersing agent. By applying sol-gel method, dispersion in the hydroxyapatite matrix and its effects on the microstructure were investigated. The chemical and phase composition, structure and morphological and size analyses were performed using XRD, FT-IR, SEM, TEM/SAED/EDX, Raman, UV-Vis spectroscopy and differential scanning calorimetry (DSC). The influences of different dispersing agents (sodium dodecyl sulfate, SDS) as a benchmark for future dispersion experiments) and excitation wavelength are discussed and the results are compared to the commonly used UV-Visible spectroscopic analysis. The results indicated that synthesis of hydroxyapatite particles in the presence of the carbon nanotubes had the best homogenization of the carbon nanotube dispersion and faster crystallization of hydroxyapatite, and the use of SDS for dispersion carbon nanotubes at hydroxyapatite matrix rendered formation of hydroxyapatite coating on CNTs surface. The average crystallite size of heat-treated (at 600°C) samples, estimated by Scherrer,s equation, was found to be ~50-60 nm that was confirmed by TEM.

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In recent years, much research in the field of advanced materials synthesis using the mechanochemical process has been performed. In this study, Al2O3-TiN nanocomposite was produced by the mechanochemical method and using inexpensive material TiO2 (instead of pure titanium which is too expensive). Also, aluminum and titanium oxide powders were used as raw materials. Milling under N2 atmosphere with 5 atmospheric pressure was performed and the products were evaluated by the SEM and XRD. Milling results showed that in the first stage of the synthesis process, titanium oxide is reduced by aluminum and the process continues, producing titanium reaction with nitrogen. When the Al/TiO2 ratio molar is equal to 1.2 and 1.3, after 20 hours of milling, TiN peaks in the XRD appears. Moreover, the results showed that milling leads to the formation of fine and spherical particles.

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In this article, the role of nano-size calcium carbonate in penetration resistance of medium- density polyethylene (PE) was investigated through experiments. In order to study the penetration resistance of PE and its nanocomposites, perforation test was carried out. The results of tests showed that penetration resistance depends strongly on calcium carbonate amount. As a matter of fact, addition of CaCO3 to PE increases resistance against penetration as CaCO3 amount reaches to 5 percent of weight. Stereomicroscope was used to evaluate the damage and plastic zone around the perforated area in all the samples including neat polyethylene and its nanocomposites. The plastic zone was measured using an image analysis as an effective technique. The results of image analysis techniques proved that the addition of calcium carbonate to PE makes a damaged zone around the perforated area. The results of microscopic evaluations showed that the area of plastic zone rises as the amount of calcium carbonate increases up to 7.5 percent of weight. By increasing the amount of CaCO3, resistance against penetration decreases more and some micro cracks appear around the perforated area. For further clarification of the fracture mechanism of MDPE nanocomposites, scanning electron microscopy was employed. Fracture surface images showed that when calcium carbonate is higher than 5 percent of weight, agglomeration of nanoparticles occurs, resulting in lower resistance against penetration to the samples.

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The aim of this work was synthesis of MCM-41/HA nanocomposite and biodegradation behavior of pure silica-mesoporous in attendance of hydroxyapatite crystals. These materials were synthsized by sol-gel method and ageing at 100°C for 24hr. A surfactant was used as template. The pores were formed after removal of surfactant by calcination at 550°C. FTIR results demonstrated formation of silanol and siloxan groups of silica network and hydroxyl and phosphate groups of HA network. Also SEM, TEM and EDS results confirmed presence of HA crystals within MCM-41 structure. Finally biodegradation behavior was examined by ICP and FTIR analysis. The results indicated biodegradable HA phase in the nanocomposite (with release of Ca2+ inos in water and the increasing of the pH value) can increase non-bridging oxygens of the silica network and therefore, it improves biodegradation behavior of silica network.

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Composite and nanocomposite Ni-Co/SiC coatings were synthesized by electro-codeposition of micro and nano-sized SiC particles with average diameter of 10m and 20nm using horizontal electrodes. Surface morphology, chemical composition, phase composition, hardness and corrosion resistance of the deposited coatings were studied using SEM observations and EDX, XRD, microhardness and polarization measurements as a function of the electrodeposition current density. The results indicated that the nanocomposite coatings exhibit higher hardness and corrosion resistance compared with the composite coatings containing micro-sized SiC particles despite their lower percentage of the SiC content. The maximum hardness values of 615HV and 490HV were obtained for nanocomposite and composite coatings deposited at current density of 3A/dm2. The observed properties were discussed based on the structural details.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.
 

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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.
 

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