Iranian Journal of Materials Science and Engineering

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Abstracts:

nanoparticles. All the extracts were used separately for the synthesis of gold nanoparticles through the reduction of

aqueous AuCl

gold ions to gold nanoparticles. The ethanol extract of black tea and its tannin free ethanol extract produced gold

nanoparticles in the size ranges of 2.5-27.5 nm and 1.25-17.5 nm with an average size of 10 nm and 3 nm, respectively.

The prepared colloid gold nanoparticles, using the ethanol extract of black tea, did not show the appropriate stability

during storage time (24 hours) at 4

showed no particle aggregation during short and long storage times at the same conditions. To the best of our

knowledge, this is the first report on the rapid synthesis of gold nanoparticles using ethanol extract of black tea and

its tannin free fraction.

In this research the ethanol extract of black tea and its tannin free fraction used for green synthesis of gold4¯. Transmission electron microscopy and visible absorption spectroscopy confirmed the reduction ofoC. In contrast, gold colloids, which were synthesized by a tannin free fraction

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Abstract:

nanocrystalline nickel samples with the grain size of ~25 nm were prepared via direct current electrodeposition and

aluminized for different durations by pack cementation method at 500

means of SEM, EDS and XRD techniques. According to results, short time aluminizing resulted in the formation of a

single aluminide layer whereas at long duration two distinct aluminide layers were formed. The growth kinetics of the

coating was non-parabolic at short times while it obeyed the parabolic law at long duration. The parabolic growth

rate constant of single phase coating formed on electrodeposited samples was about 30 ìm / h1/2 approximately 3 times

greater than the data reported for coarse grained nickel (8.4 ìm / h1/2). Meanwhile, the overall growth rate constant

was decreased to 11.7 ìm / h1/2, when double aluminide layers formed on nanocrystalline nickel.

In this research, aluminizing behavior of ultra fine-grained nickel was investigated. For this purpose,oC. The aluminide layers were examined by

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The effects of anodizing condition and post treatment on the growth of nickel nanowires, were investigated. A two-step anodizing process was applied in phosphoric and oxalic acid solution. Nickel electrochemical plating was applied to fill Anodic Aluminum Oxide (AAO) pores. For pore filling enhancement, AAO surfaces were treated by silver predeposition. After electroplating, aluminum and oxide layer of some specimens were removed. The results showed that silver preplating increases the pore filling and as the applied voltage becomes higher, the pores diameter decreases.

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In this research an ultra-fine grained composite structure consisting of an intermetallic matrix together with dispersed nano-sized Al2O3 obtained via mechanical activation of TiO2 and Al in a high energy ball mill and sintering of consolidated samples. Phase composition and morphology of the milled and sintered samples were evaluated by XRD and SEM techniques Thermal behavior of the powder sample milled for 8 hours was evaluated by DTA technique. DTA results showed that, the reaction happens in two steps. The first step is the aluminothermic reduction of TiO2 with Al. XRD observations reveals that minor amount of Ti3Al phase formed during reduction reaction together with TiAl and Al2O3 major phases. This intermetallic phase disappeared when sintering temperature was increased to 850 ºC. The second step in DTA is related to a reaction between residual Al in the system (partly dissolved in TiAl lattice) and the Ti3Al phase produced earlier at lower temperatures. SEM micrographs reveal that by completion of the reduction reaction more homogeneous and finer microstructure is observable in sintered samples.

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Abstract:

current densities. Electrochemical impedance spectroscopy (EIS) results showed that the codeposition mechanism of

tungsten in Ni-W deposition is the reduction of tungsten oxide which changed to the reduction of tungsten-containing

ion complexes at higher current densities. In Co-W electrodeposition, the tungsten codeposition takes place via

reduction of tungsten oxide, although, the role of tungsten-containing complexes at higher current densities cannot be

ruled out. The surface morphology of Ni-W coatings was crack-free and was strongly dependent on deposition current

density. In addition, higher grain size and lower tungsten content were obtained by increasing the current density. In

Co-W coatings, no obvious variation in surface morphology was observed except for the fine cracks appeared at

higher current densities. In this system the grain size remained almost constant with increasing current density. The

microhardness values of Ni-W and Co-W coatings decreased due to the increase in the grain size and/or decrease in

tungsten content.

Ni-W and Co-W alloy nanocrystalline coatings were electrodeposited on copper substrate at different

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Abstract: Nano pore Mordenite membranes were prepared on the outer surface of ceramic tubular tubes via hydrothermal synthesis and evaluated for dehydration pervaporation of water unsymmetrical dimethylhydrazine UDMH mixtures. Highly water-selective mordenite membranes were prepared and the optimum reaction condition was found to be 24 h crystallization time and 170 °C crystallization temperature. Effect of gel composition on separation factor and water flux of the water-UDMH mixtures was investigated. X-ray diffraction (XRD) patterns showed that mordenite is the only zeolite material which presents in the membrane. Morphology of the supports subjected to crystallization was characterized by Scanning electron microscopy (SEM). In PV of the water-UDMH mixtures, the membrane exhibits a hydrophilic behavior, with a high selectivity towards water and a good flux. The best membranes had a water flux of 2.67 kg/m2.h at 27 °C. The best PV selectivity was obtained to be 264.

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Abstract: In this study Al-5 (Vol) % SiCp nanocomposite powder has been successfully synthesized by high-energy planetary milling of Al and SiC powders for a period of 25 h at a ball-to-powder ratio of 15:1. The changes of the lattice strain, the crystallite size of the matrix phase, and the nanocomposite powder microstructure with time have been investigated by X-ray diffraction (XRD), X-ray mapping, and scanning electron microscopy (SEM) analyses. The morphologies of the nanocomposite powders obtained after 25 h of milling have also been studied by transmission electron microscopy (TEM). The results showed that nanocomposite powders were composed of near-spherical particles and, moreover, the SiC particles were uniformly distributed in the aluminum matrix.

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Abstract: SiC nano particles with mono dispersed distribution were synthesized by using of silicon alkoxides and phenolic resin as starting materials. After synthesis of sample, characterizations of the obtained powder were investigated via Fourier Transform Infrared Spectroscopy (FTIR) with 400-4000 cm-1, X-ray Diffractometry (XRD), Laser Particle Size Analyzing (LPSA), Si29 NMR analysis, Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM). FTIR and Si29 NMR results of the gel powder indicated that Si-O-C bonds were formed due to hydrolysis and condensation reactions . FTIR results showed a very strong peak for heat treated powder at 1500°C after carbon removal which is corresponded to Si-C bond. Obtained pattern from X-ray diffractometry showed that the final products contain -SiC phase with poly crystalline planes and little amounts of residual carbon. PSA results showed that the average particles size were 50.6 nm with monosized distribution. Also microstructural studies showed that the SiC nano powders have semi spherical morphology with mean particles size of 30-50 nm and also there are some agglomerates with irregular shape.

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Abstract: Most properties of nanoparticles are size-dependent. In fact, the novel properties of nanoaprticles do not prevail until the size has been reduced to the nanometer scale. The particle size and size distribution of alumina nanoparticle, as a critical properties, have been determined by transmission electron microscopy (TEM), photon correlation spectroscopy (PCS), surface area analysis (BET) and x-ray diffraction peak broadening analysis. The particle size was found to be in the range of 5-95nm. Cumulative percentage frequency plot of the data extracted form TEM images indicates that particle size distribution obeys the log-normal function. The TEM images also reveal that particles are spherical in shape and loosely agglomerated. Comparing of the XRD and TEM results shows that the particles are single-crystal. The HRTEM images also verify that the particles have a single-crystal nature. In comparison, there is a good correlation between the BET, XRD and TEM measurements other than PCS that is sensitive to the presence of the agglomerates.

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Abstract:

composition of MgO and nano boehmite. The reactant and potassium chloride, as the reaction media, were fired at

800-1000 °C at different dwell times (0.5-5 h) in the ambient atmosphere. After washing and filtration, the spinel nano

powder was characterized by X-ray diffraction (XRD), Scanning electron microscopy (SEM), and Brunauer-Emmett-

Teller (BET) techniques. It was demonstrated that the formation temperature decreased to 850

particles revealed an average size of 30 nm with a narrow size distribution. The mechanism of MgAl

was found to be a template type where the morphology and size of product were similar to those of alumina formed

from boehmite decomposition. Prolonging the reaction time from 0.5 to 3 h, the reaction was further completed and

crystallinity was improved. However, the increase of temperature was more effective in this regard.

MgAl2O4 (MA) nano powder was synthesized via molten salt technique, by heating stochiometric°C. The nano spinel2O4 formation

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Abstract: In this study, carbon nanotubes (CNTs) were grown directly in the pores of micro porous pyrex membranes
and consequently ceramic membranes with very fine pores and high porosity were achieved. Our experiment was done
in two stages. Initially cobalt powder with different percent was homogeneously mixed with pyrex powder. In order to
produce row membranes, each of these mixtures were compacted in the form of tablet by use of a uniaxial cold press
and in a stainless steel mould, and then the tablets were sintered at different temperature in an electric furnace. In
second stage chemical vapor deposition (CVD) method was used to grow CNTs within the pores of the membranes.
Argon and ammonia were used as carrier and reactive gas respectively and acetylene was used as the carbon
feedstock. Morphology of the membranes before and after CVD process was studied by scanning electron microscopy
(SEM). After CVD process CNTs were grown in the pores of membranes and the pores size was decreased but total
porosity of the membrane was not changed considerably. In this way membranes with high porosity and fine pores were
fabricated.

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Ultraviolet–Visible (UV–Vis) spectroscopy was used, in the current investigation, to explore the dispersion and stability of titania nanoparticles in an aqueous media with different types of dispersants. Hydrochloric and nitric acids as well as ammonia were used to determine the stability of the suspension in the acidic region (pH=2.5) and basic area (pH=9.5), respectively. In addition, for measuring sustainability of suspension and creating steric, and electrosteric repulsive forces, ethylene glycol and ethylene glycol plus ammonia were employed, respectively. UV–V is
spectrometry was applied to realize the effect of nano titania concentrations and different types of dispersants of samples containing different amounts of nano titania and different types of dispersants on stability of TiO2-containing suspensions. In addition, the stability of dispersion could be evaluated in colloidal mixtures containing ethylene glycol plus ammonia. It was demonstrated that the mixtures containing ethylene glycol plus ammonia were stable over a period of 4 days. To support the UV–Vis results, other techniques such as atomic force microscopy (AFM) and scanning electron microscopy (SEM) were employed to study the degree of agglomeration of titania nanoparticles in terms ofmorphology and size.

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Abstract: Nickel was electrodeposited onto copper substrates with high {111} and {400} peak intensities. The grain size of coatings deposited onto the copper substrate with a higher {111} peak intensity was finer. Spheroidized pyramid morphology was obtained at low current densities on both copper substrates. By increasing the deposition current density, grain size of the coating was increased for both substrates and eventually a mixed morphology of pyramids and blocks was appeared without further increase in grain size. This decreased the anodic exchange current density probably due to the decrease of surface roughness and led to a lower corrosion rate.

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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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Yellow-colored nitrogen doped TiO2 photocatalyst and a pure TiO2 powder were synthesized via sol-gel method using TiCl4 and urea as raw materials. However, the synthesis procedure for nitrogen doped TiO2 was catalyzed by acid that dialed with controlled precipitation and slow nucleation. According to XRD analysis, the nitrogen doped TiO2 consisted of anatase phase of titania which was a significant achievement regarding its possible photocatalytic applications. The band gaps of nitrogen doped TiO2 and pure TiO2 were estimated from UV-Vis spectroscopy data to be 2.8 and 3.3 ev, respectively. Photocatalytic properties of the nitrogen doped TiO2 nanocatalyst and pure TiO2 were compared for degradation of crystal violet dye in visible light irradiation. In comparison to pure TiO2, nitrogen doped TiO2 showed superior photocatalytic efficiency towards the dye.

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Abstract:Nanostructured titania was synthesized by colloidal and polymeric sol-gel routes. Stable colloidal and polymeric titania sols were prepared by adjusting the proper values of the acid/alkoxide and the water/alkoxide molar ratios. The properties of sols were determined by dynamic light scattering technique and synthesized titania was characterized by thermogravimetry and differential thermal analysis, X-ray diffraction, Fourier transform infrared spectroscopy, optical microscopy and field emission scanning electron microscopy. The results showed particle size distribution of colloidal sol 10-50 nm compared to polymeric one which was 0.5-2 nm. Phase analysis of the colloidal sample revealed anatase as the major phase up to 550 °C, while the polymeric route resulted only anatase phase up to 750 °C. On the basis of results, titania prepared by the polymeric route showed better thermal stability against phase transformation than the sample prepared by the colloidal route. Also, microstructural studies showed that titania nanopowder can be produced by both sol-gel routes

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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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Abstract:In recent years, there have been many attempts to improve the properties of dental amalgam. The aim of the present investigation was fabrication and characterization of dental amalgams containing TiO2 nanoparticles and evaluation of their compressive strength, antibacterial and corrosion behavior. In this experimental research, TiO2 nanoparticles (TiO2 NPs) were added to reference amalgam alloy powder and then, dental amalgam was prepared. In order to investigate the effect of TiO2 NPs on properties of dental amalgam, 0, 0.5, 1, 2 and 3 wt. % of TiO2 NPs were added to amalgam alloy powder and the prepared composite powder was triturated by a given percent of mercury. Xray diffraction (XRD), Scanning Electron Microscopy (SEM) and Energy-Dispersive Spectroscopy (EDS) techniques were used to characterize the prepared specimens. Potentiodynamic polarization corrosion tests were performed in the Normal Saline (0.9 wt. % NaCl) Solutions as electrolytes at 37°C. The results showed that the corrosion behavior of the dental amalgam with 0.5 or 1 wt. % TiO2 NPs is similar to the corrosion behavior of the reference amalgam, while with increasing the weight percent of TiO2 NPs, the corrosion rate increases. Also, the results of this investigation indicated that adding TiO2 NPs in amounts of up to 1 wt. % to amalgam alloy powder improve compressive strength of dental amalgam and has no destructive influence on its corrosion behavior. As well as, according to antibacterial results, TiO2 NPs can increase the biocompatibility and antibacterial activity of dental amalgam. The results of present study suggest that amalgam/ TiO2 NPs nanocomposite with 1% of TiO2 NPs could be regarded as a biocompatible and bioactive dental material that provide better characters for dental applications.

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Ni and Cu elemental powder mixtures containing 25, 50, and 75% at Cu were subjected to mechanical alloying in a planetary ball mill under various milling times. Structural evolution was analyzed by means of X-ray diffraction and scanning electron microscopy. Experimental results indicated that nanostructured solid solution alloy powders having homogeneous distribution of Ni and Cu were formed by milling-induced interdiffusion of the elements. Average crystallite size of the as-milled powders was decreased with increasing Ni content and milling duration, and found to be in the order of 15-40 nm after 30 h of milling for all powder compositions. Moreover, lattice parameter and lattice strain of solid solutions were increased with the time of MA, which was more intense for nickel-rich alloys

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Mono dispersed nano SiC particles with spherical morphology were synthesized in this project by hydrolysis and condensation mechanism during sol gel processing. pH, temperature and precursor’s ratio considered as the main parameters which could influence particles size. According to DLS test results, the smallest size of particles in the sol (<5nm) was obtained at pH<4. It can be observed from rheology test results optimum temperature for achieving nanometeric gel is about 60 ˚C. The optimum pH values for sol stabilization was (2-5) determined by zeta potentiometery. Si 29NMR analysis was used in order to get more details on final structure of gel powders resulted from initial sol. X-ray diffraction studies showed sythesized powder consists of β-SiC phase. Scanning electron microscopy indicated agglomerates size in β-SiC synthesis is less than 100 nm. Finally, TEM studies revealed morphology of β-SiC particles treated in 1500˚C and after 1hr aging is spherical with (20-30) nm size