Iranian Journal of Materials Science and Engineering

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Electrochemical coating processes are significantly affected by applied magnetic fields due to the generation of electromagnetic forces. The present research work has been undertaken to study the effect of coating parameters such as current density and alumina concentration on the characteristics of Ni-Al2O3 composite coating under static magnetic field. Ni-Al2O3 composite coating was applied on a mild steel substrate using conventional Watts solution containing Al2O3 particles with and without magnetic field. The coating microstructure and Al2O3 particle density in the coating layer were examined by scanning electron microscopy (SEM). It was found that the applied magnetic field made the coating structure finer and leads to the increases of the particle content in the coating. However, the results confirmed that the magnetic forces inversely affected the particle density in the coating at higher current density than that of normal coating process.

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C-SiC composites with carbon-based mesocarbon microbeads (MCMB) preforms are new type of highpreformance and high-temperature structural materials for aerospace applications. In this study MCMB-SiC composites with high density (2.41 g.cm-3) and high bending strength (210 MPa,) was prepared by cold isostatic press of mixed mesophase carbon powder derived from mesophase pitch with different amount (0, 2.5, 5%) nano SiC particles. All samples were carbonized under graphite bed until 1000 °C and finally liquid silicon infiltration (LSI). Microstructure observations resultant samples were performed by scanning electron microscopy and transition electron microscopy (SEM & TEM). Density, porosity and bending strength of final samples were also measured and calculated. Results indicates that the density of samples with nano additive increased significantly in compare to the free nano additives samples.

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Metal matrix composite coatings reinforced with nano-particles have attracted scientific and technological interest due to the enhanced properties exhibited by these coatings. Cobalt/hexagonal boron nitride nano-composite coatings were prepared by means of the pulse current electroplating from a chloride electrolyte on copper substrates and a comparison was made with the pure cobalt in terms of structure and tribological properties. Effects of particles concentration (5-20 gL-1) and current density (50-200 mA cm-2) on the characterization of electroplated coatings were investigated via X-ray diffraction analysis, energy dispersive spectroscopy and Vickers micro-hardness. Moreover, the tribological behavior was studied using pin-on-disc method. The results showed that cobalt/hexagonal boron nitride nano-composite coatings have higher hardness, wear resistance and lower friction coefficient than pure cobalt and the plating parameters strongly affect the coating’s properties

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In the present study, bioceramic composites based hydroxyapatite (HAp) reinforced with carbon nanotubes (CNTs) was synthesized via sol-gel technique. The dried gels were individually heated at a rate of 5°C/min up to 600°C for 2 h in a muffle furnace in order to obtain HAp-MWCNTs mixed powder. Composites were characterized by XRD, FT-IR, SEM, TEM/SAED/EDX and Raman spectroscopy techniques. Results showed the synthesis of HAp particles in the MWCNTs sol which was prepared in advance, leads to an excellent dispersion of MWCNTs in HAp matrix. Apparent average size of crystallites increased by increasing the percentage of MWCNTs. The average crystallite size of samples (at 600°C), estimated by Scherrer’s equation was found to be ~50-60 nm and was confirmed by TEM. MWCNTs kept their cylindrical graphitic structure in composites and pinned and fastened HAp by the formation of hooks and bridges.

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Accumulative roll-bonding process (ARB) is an important severe plastic deformation technique for production of the ultrafine grained, nanostructured and nanocomposite materials in the form of plates and sheets. In the present work, this process used for manufacturing Al/SiO 2 nanocomposites by using Aluminum 1050 alloy sheets and nano sized SiO 2 particles, at ambient temperature. After 8 cycles of ARB process, the tribological properties and wear resistance of produced nanocomposites were investigated. The wear tests by abrasion were performed in a pinon-disc tribometer. Results show that by increasing ARB cycles and the amount of nano powders, the friction coefficient of produced nanocomposites decreases.

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Ni-P Electroless coatings provide appropriate resistance to wear and corrosion. Co-deposition of particles between layers can improve their properties, especially general corrosion and erosion-corrosion behavior by means of nano diamond as reinforcing particles. In this study Ni-P/nano diamond composite deposition were deposited on steel substrate. Structure of the coatings and corrosion resistance of theme were investigated by scanning electron microscopy and corrosion tests in salty media. The composite structure of the deposit was evaluated as nano size without using any surfactants. Also results for the composite coating show better corrosion protection and higher hardness comparing with as -deposited Ni-P. The optimum concentration of diamond nanometer particles were found by evaluation of scanning electron microscopy pictures, hardness measurement, linear polarization and electrochemical impedance spectroscopy results

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In the present paper, the influence of cobalt additive on the sintering/infiltration behavior of W-Cu composite was studied. For this purpose, the mixed powders of tungsten and cobalt were compacted by CIP method and then sintered at 1450, 1550 and 1600 °C in a hydrogen atmosphere. The sintered specimens at 1550 °C were subsequently infiltrated with liquid copper at 1250 °C for 10, 60 and 120 min. The microstructure and composition of samples were evaluated using SEM, EDS as well as XRD techniques. The density of the sintered samples was measured by Archimedes method. Vickers indentation test was used to measurement hardness. It was found that sintering mechanism of tungsten powder depends on temperature and cobalt additive content. Also, the best infiltration behavior was observed in the samples with optimum cobalt value. In addition, it was found that the W-W contiguity as well as dihedral angle decreases as cobalt increases. Density and hardness of infiltrated specimens are attained 16.28-16.79 g.cm-3 and 220-251 VHN, respectively.

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In this research, infiltration behavior of W-Ag composite compacts with Nickel and Cobalt as additives has been investigated. Nickel and Cobalt were added to Tungsten powder by two distinct methods: mixing elementally and reduction of salt solution. The coated Tungsten powders were compacted under controlled pressures to make porous skeleton with 32-37 vol. % porosity. Infiltration process was carried out at 1100 ̊C under a reducing atmosphere for 1h. The effect of additives on infiltration of Ag and density were evaluated by SEM and Archimedes methods. Properties of the specimens were compared following two distinct processes namely: I) sintering simultaneously with infiltration process and II) sintering prior to infiltration (pre-sintering process). It was found that specimens which were pre-sintered and then infiltrated with molten silver represent higher hardness and finer microstructure than the specimens infiltrated simultaneously with sintering.

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Metallic-intermetallic laminate (MIL) composites are promising materials for structural applications especially in the aerospace industry. One of the interesting laminate composites is the Ti-TiAl 3 multilayer. In this work, commercially pure sheets of aluminum and titanium with almost equal thickness of around 0.5 mm were explosively joined. The achieved multilayers were annealed at 630 ℃in different times so that an intermetallic layer was formed at the Ti/Al interface. The resulting microstructure was studied by optical and scanning electron microscopy and Energy Dispersive Spectroscopy (EDS). TiAl3 was the only intermetallic phase that was observed in all annealing times. The kinetics of the formation of TiAl 3 was investigated and compared to previous research studies performed on Ti-Al multilayers which were fabricated using methods other than explosive welding.

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Achieving extreme hardness in the newly synthetic steel formed by converting from initial amorphous state to subse-quent crystalline structure –named as devitrification process- was studied in this research work. Results of TEM observa-tions and XRD tests showed that crystallized microstructure were made up four different nano-scale phases i.e., α-Fe, Fe 36 Cr12 Mo10 , Fe 3 C and Fe3 B. More, Vickers hardness testing revealed a maximum hardness of 18.6 GPa which is signifi-cantly harder than existing hardmetals. Detailed kinetic and structural studies have been proof that two key factors were contributed to achieve this extreme hardness supersaturation of transition metal alloying elements (especially Nb) and also reduction in the structure to the nano-size crystals.

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B4C and its composites with TiB2 as second phase continues to be extensively used as the preferred ceramic material in military applications as armor systems for absorbing and dissipating kinetic energy from high velocity projectiles. It also exhibits a high melting point (2427 °C), and high neutron absorption cross section. Pressureless sintering of the B 4C-nanoTiB2 nanocomposite using small amount of Fe and Ni (≤3 Wt%) as sintering aids was investigated in order to clarify the role of Fe and Ni additions on the mechanical and microstructural properties of B4C-nanoTiB2 nanocomposites. Different amount of Fe and Ni, mainly 1 to 3 Wt% were added to the base material. Pressureless sintering was conducted at 2175, 2225 and 2300 °C. It was found that Addition of 3 Wt% Fe and 3 wt% Ni and sintering at 2300 °C resulted in improving the density of the samples to about 99% of theoretical density. The nanocomposite samples exhibited high density, hardness, and microstructural uniformity.

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This study was undertaken to investigate the effects of Cu and solution heat treatment on the microstructure and hardness of cast Al-Al4Sr metal matrix composite. Different amounts of Cu (0.3, 0.5, 1, 3 and 5 wt.%) were added to the composite. Specimens were heat treated at 500 °C for 4 hours followed by water quenching. Microstructural studies were assessed by the use of optical microscope, scanning electron microscope (SEM) and x-ray diffractometry (XRD). The results showed that addition of 5 wt.% Cu reduces the length of large needle-like Al4Sr phase and refines the microstructure. In addition, the presence of Cu-intermetallics increases hardness of the composite. Cu mainly forms θ phase which segregates at the grain boundaries. Heat treatment partially dissolves Cu-intermetallics and homogenizes the distribution of θ phase in the matrix.

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In this study, corrosion behaviour of A356-10 vol.% SiC composites casted by gravity and squeeze casting is evaluated. For this purpose, prepared samples were immersed in HCl solution for 1h at open circuit potential. Tafel polarization and electrochemical impedance spectroscopy (EIS) were carried out to study the corrosion resistance of composites. The Tafel polarization and EIS studies of the corrosion behaviour of the A356-10 vol.% SiC composites showed that the corrosion resistance of the composite casted by squeeze casting was higher than that of the composites casted by gravity in selected corrosion media. Also, the Tafel polarization and EIS studies revealed that the corrosion current densities of both composites increase with the increase in the concentration of HCl. The micrographs of scanning electron microscope (SEM) clearly showed the squeeze casting composite exhibits a good dispersion/matrix interface compared to that of the composites produced by gravity casting

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Aluminium base alloy (Al-Cu-Si) was reinforced with silicon carbide (SiC) particles, in various percentage compositions from 0-20 wt%. Silicon carbide particle size of 20µm was selected. The molten slurry of SiC reinforced base aluminium metal was casted through green and dry sand casting methods and solidification process was carried out under ambient conditions. A selected population of total casted samples were subjected to T6 heat treatment process, followed by evaluation of mechanical properties of hardness, tensile strength and impact loading. The micro sized SiC particles were preheated up to 300C prior pouring into the melted metal, for subsequent removal of residual gases and moisture content. A continuous manual stirring method was used for homogenous distribution of reinforced particle in molten slurry. The experimental results revealed that the highest parameters of hardness, impact energy and tensile strength were achieved in the T6 heat treated specimens having highest percentage composition (20%) of Silicon Carbide (SiC) particles

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In this research, two different carbonaceous materials (Graphite:G and Petrocoke:P) were separately compared in terms of the carbothermic reduction of hematite and anatase in order to synthesize Fe-TiC nanocrystalline composite by mechanically activated sintering method. Powders were activated in a planetary high-energy ball mill under argon atmosphere for 0, 2, 5, 10,and 20 h. Then, the activated powders were analyzed by XRD and SEM to investigate phase constituents and microstructure of the mixtures. Results proved that Fe 2 O 3 and TiO 2 were not reduced by carbonaceous materials even after 20h of milling. SEM investigations showed that G-mixture was more homogenous than P-mixture after 20h of milling, meaning that graphite-anatase-hematite was mixed satisfactorily. Thermogravimetry analysis was done on 0 and 20h milled powders. TG and DTG curves showed that mechanical activation led to almost 300°C decrease in the reduction temperature of hematite and anatase in both mixtures. In the next step, the powders were sintered in a tube furnace under argon atmosphere. In the G-mixture, anatase was reduced to titanium carbide at 1100°C but, in the P-mixture, temperature of 1200°C was essential for completely reducing anatase to titanium carbide.Results of phase identification of the sintered powders showed that anano-crystalline ironbased composite with titanium carbide, as the reinforcement was successfully synthesized after 20 h high-energy milling of the initial powders and subsequent sintering occurred at 1200˚C for 1h

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Lead zirconate titanate (PZT) as a piezoelectric ceramic has been used widely in the fields of electronics, biomedical engineering, mechatronics and thermoelectric. Although, the electrical properties of PZT ceramics is a major considerable, but the mechanical properties such as fracture strength and toughness should be improved for many applications. In this study, lead monoxide, zirconium dioxide and titanium dioxide were used to synthesize PZT compound with chemical formula Pb(Zr 0.52 ,Ti 0.48 )O 3 by calcination heat treatment. Planetary mill with zirconia balls were used for homogenization of materials. Two-stage calcination was performed at temperatures of 600˚C and 850˚C for holding time of 2h. In order to improve the mechanical properties of PZT, various amount of ZnO and/or Al 2 O 3 particles were added to calcined materials and so PZT/ZnO, PZT/Al 2 O 3 and PZT/ZnO+Al 2 O 3 composites were fabricated. Composites samples were sintered at 1100˚C for 2 h in the normal atmosphere. Microstructural component and phase composition were analyzed by XRD and SEM. The density, fracture strength, toughness and hardness were measured by Archimedes method, three-point bending, direct measurement length crack and Vickers method, respectively. Dielectric and piezoelectric properties of the samples were also measured by LCR meter and d33metet tester, respectively. The results showed that by addition of ZnO and Al 2 O 3 to composite materials, the relative density of PZT based composites was increased in conjunction with a signification improvement of mechanical properties such as flexural strength, toughness and hardness. Moreover, the dielectric and piezoelectric properties of PZT such as dielectric constant, piezoelectric coefficient and coupling factor were decreased while the loss tangent was also increased.

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In the present study, the feasibility of α-Fe ferromagnetic phase formation in glass and glass-ceramic by reduction in hydrogen atmosphere have been investigated. The glass with the composition of 35Na 2 O–24Fe2O3–20B 2O3 – 20SiO 2 –1ZnO (mol %) was melted and quenched by using a twin roller technique. As quenched glass flakes were heat treated in the range of 400-675 °C for 1-2 h in hydrogen atmosphere, which resulted in reduction of iron cations to α-Fe and FeO. The reduction of iron cations in glass was not completely occurred. Saturation magnetization of these samples was 8-37 emu g -1 . For the formation of glass ceramic, As quenched glass flakes heat treated at 590 °C for 1 h. Heat treatment of glass ceramic containing magnetite at 675°C in hydrogen atmosphere for 1 h led to reduction of almost all of the iron cations to α-Fe. Saturation magnetization of this sample increased from 19.8 emu g -1 for glass ceramic to 67 emu g -1

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MgAl2O4/Ti(C,N) composites were synthesized through aluminothermic reaction between Al,TiO 2,MgO powders and phenolic resin in coke bed condition. Effect of addition of carbon black and sugar into the mixture at different temperatures were investigated. The phases and microstructures of samples were investigated by X-ray diffraction (XRD) and scanning electron microscopy (SEM). MgAl 2O4 /Ti(C,N) composites without additive were obtained after heat treatment at 1600˚C. With addition of carbon black TiC, TiN and Ti(C,N) were appeared after firing at 1400˚C and formation of spinel/Ti(C,N) composites were completed at 1600˚C. In sample containing sugar, MgAl2O4 -Ti(C,N) composite were completely synthesized at 1400˚C. In this sample crystallite size of Ti(C,N) were 32 nm and carbon content of titanium carbonitride (Ti(C,N)) reached to 0.442 value.

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Different volume fractions (1.3, 2.6, and 7.6 Vol.%) of carbon nanotubes (CNTs) were dispersed within 8Y-TZP nanopowders. Mixed powder specimens were subsequently processed by spark plasma sintering (SPS) and effects of CNTs on the sintering process of 8Y-TZP/CNT composites was studied. Maintenance of CNTs through the SPS process was confirmed using TEM and Raman Spectroscopy. Studies on the sintering profile of zirconia-CNT composites (Z-xC composites) could, to some extent, clarify the effect of CNTs’ volume fraction on the densification rates of Z-xC composites. The specimen with the highest content of CNT (Z-7.6C) showed the lowest sintering rate while it was unable to reach full density.

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The epoxy coatings containing multi-walled carbon nanotube/ poly ortho aminophenol nanocomposite were prepared and used as anticorrosive coatings. The nanocomposites with different contents of carbon nanotube were synthesized in a solution of sodium dodecyl sulfate and ammonium peroxy disulfate as a surfactant and an oxidant, respectively. The morphology and structural properties were confirmed by Fourier transform infrared spectroscopy and scanning electron microscopy methods. The mean size of nanocomposite particles was 20-35 nm determined by scanning electron microscopy. The epoxy coatings containing the nanocomposites were applied over mild steel panels and their corrosion performance was investigated using electrochemical impedance spectroscopy and potentiodynamic polarization measurements in a 3.5 % sodium chloride solution. The results showed that epoxy coatings consisting of nanocomposite with 1 wt.% multi-walled carbon nanotube exhibited higher anticorrosive properties than other prepared coatings of different carbon nanotube contents, which could be due to the strong interaction between the mild steel surface and the conjugated nanocomposite.