Iranian Journal of Materials Science and Engineering

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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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n this paper a finite element model has been proposed for evaluation of primary and secondary current density values on the cathode surface in nickel electroplating operation of a revolving part. In addition, the capability of presented electroplating simulation has been investigated in order to describe the electroplated thickness of the nickel sulfate solution. Nickel electroplating experiments have been carried out. A good agreement between the simulated and experimental results was found. Also the results showed that primary current density can describe the general form of thickness distribution but the relative value of current density using secondary current density can present better description of thickness distribution

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High energetic aluminum nanoparticles are mainly used as additive in solid rocket propellants. However, fabrication of these aluminized energetic materials is associated with decreasing the burning rate of propellants due to problems such as oxidation and agglomeration of nanoparticles. In this study, to improve combustion performance of aluminum nanoparticles, coating by metallic Ni shell was studied. Nickel coating of aluminum nanoparticles was performed through electroless deposition (ED) subsequently, morphology and chemical composition of Ni-coated nanoparticles were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS) and X-ray diffraction (XRD). These studies show that a uniform Ni layer with a thickness of 10nm is coated on the surface of Al nanoparticles. Thermal analysis of uncoated and Ni-coated aluminum nanoparticles was done using differential thermal analysis (DTA) and thermo gravimetric analysis (TGA). The results of thermal analysis indicate that, coating the aluminum particles by Ni, leads to improvement in combustion performance of aluminum nanoparticles through decreasing critical ignition temperature, ignition delay time of the nanoparticles and promoting the ignition by exothermic chemical reactions between Al and Ni

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In the present study, CrN, TiN and (Ti, Cr)N coatings were deposited on D6 tool steel substrates. Physical and mechanical properties of coatings such as microstructure, thickness, phase composition, and hardness were evaluated. Phase compositions were studies by X-ray diffraction method. Mechanical properties were determined by nano-indentation technique. The friction and wear behaviour of the coatings were investigated using ball-on-disc tests under normal loads of 5, 7 and 9 N at sliding distance of 500 m, at room temperature. Scanning electron microscope equipped with energy dispersive spectroscopy, optical microscope, and 2D/3D profilometry were utilized to investigate the microstructures and wear mechanisms. Wear test results clarified that the wear resistance of (Ti, Cr)N and TiN coatings was better than that of CrN coating. The wear resistance of the (Ti, Cr)N coatings was related to the Ti content in the coatings and reduced by decreasing the Ti content. The dominant wear mechanisms were characterized to be abrasive and tribochemical wear

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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 mechanical characterization of short E- glass fiber reinforced, graphite and sintered bronze filled epoxy composite was carried out in this study. The aim of the present study was to develop tribological engineering material. In this study the flexural strength, theoretical and experimental density, Hardness and Impact strength of composites was investigated experimentally. The results showed that the increased percentage of graphite (10 to 15%Vol) and Eglass fiber (10 to 15%Vol) enhanced flexural strength (149 MPa) of the composite and the maximum flexural modulus (13.3 GPa and 13.1 GPa) was obtained for composite C2 and C5 respectively. Maximum hardness (84 on L scale) and impact energy (90 Joule) was obtained for the composite C6 with increased percentage of glass fiber and graphite filler. The metallurgical electron microscopic images were discussed to interpret the effect of graphite and sintered bronze on mechanical characterization of composite

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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.

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The micro layers micaceous iron oxide and nano-TiO 2 were incorporated into the epoxy resin by mechanical mixing and sonication process. Optical micrographs showed that the number and diameter size of nanoparticle agglomerates were decreased by sonication. The structure and composition of the nanocomposite was determined using transmission electron microscopy which showed the presence of dispersed nano-TiO 2 in the polymer matrix. The anticorrosive properties of the synthesized nano-composites coating were investigated using salt spray, electrochemical impedance spectroscopy and polarization measurement. The EIS results showed that coating resistance increased by addition of micaceous iron oxide micro layers and nano-TiO 2 particles to the epoxy coatings. It was observed that higher corrosion protection of nanocomposite coatings obtained by the addition of 3 %wt micaceous iron oxide and 4%wt nano-TiO 2 into epoxy resin.

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In situ Al2024- Mg₂Si composite was fabricated by spark plasma sintering (SPS) of reactive powder. Reactive powder was obtained from mechanical alloying (MA) of elemental powders. Clad layers of in situ composite were fabricated on Al substrates by spark plasma sintering (SPS). Structural evolution during MA process and after SPS was investigated by X-ray diffractometery (XRD). Scanning electron microscopy (SEM) was utilized to study the microstructure of sintered samples. Hardness and tensile behavior of sintered samples were investigated. The results showed that SPS of mechanically alloyed unreacted powder can result in the in situ formation of Mg₂Si and Mg₂Al₃ within the Al matrix. SPSed clad layer showed a sound and clear interface to the Al substrate with a hardness of about 140 HV. Sintered in situ composite exhibited a tensile strength of 288 MPa.

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In this study, polyaniline-graphene composites with different nano-structures are synthesized and the behaviour of the obtained composites serving as electrode materials in electrochemical capacitors is studied. The morphology, crystal structure, and thermal stability of the composites are examined using scanning electron microscopy (SEM), X-ray diffraction (XRD), and Thermal gravimetric analysis (TGA). Electrochemical properties are characterized by cyclic voltammetry (CV). According to the results, the obtained composites show different crystal structures and different thermal stabilities, and consequently different electrochemical capacities, when used as electrodes in electrochemical capacitors. A nano-fibre composite is shown to have a good degree of crystallization, 5.17% water content, 637oC degradation onset temperature, and 379 Fg-1 electrochemical capacity.

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A homogenous TiO₂ / multi-walled carbon nanotubes(MWCNTs) composite film were prepared by electrophoretic co-deposition from organic suspension on a stainless steel substrate.  In this study, MWCNTs was incorporated to the coating because of their long structure and their capability to be functionalized by different inorganic groups on the surface. FTIR spectroscopy showed the existence of carboxylic groups on the modified carbon nanotubes surface. The effect of applied electrical fields, deposition time and concentration of nanoparticulates on coatings morphology were investigated by scanning electron microscopy. It was found that combination of MWCNTs within TiO₂ matrix eliminating micro cracks presented on TiO₂ coating. Also, by increasing the deposition voltages, micro cracks were increased. SEM observation of the coatings revealed that TiO₂/multi-walled carbon nanotubes coatings produced from optimized electric field was uniform and had good adhesive to the substrate.