Iranian Journal of Materials Science and Engineering

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Two commercial methods are used for the production of strontium carbonate:1) Direct conversion of Celsetite to strontium carbonate by hot sodium carbonate,2) Carbothermic reduction of celestite with coal followed by water leaching of strontium sulfide(SrS) and its conversion to strontium carbonate.The present study has been made on the carbothermic reduction of celestite ores of Varamin (Iran) mines. Effects of temperature, time, pellet size, particle size of celestite ore, pellet compactness and type of reducing agent have been studied. In the range of 800-1100°C, reduction rate increases notably with temperature, which may mean that the reduction is predominantly chemical controlled. Activation energy of around 22.5 kcal/mol supports the idea of chemical control mechanism. Further support for this postulation is provided by the following facts:1) Increasing rate with carbon reactivity (graphite, coal, and charcoal)2) Small dependency of rate on pellet compactness.3) Small dependency of rate on pellet size

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The synergistic behavior of molybdate and phosphate ions in mitigating the corrosion of mild steel in simulated cooling water was evaluated performing potentiodynamic polarization and impedance spectroscopy tests. Phosphate and molybdate showed a synergistic effect on corrosion inhibition of steel in simulated cooling water. The observed reduction in anodic and cathodic current densities could be the consequence of incorporation of both phosphate and molybdate ions in forming a protective layer on the surface. The charge transfer resistance of the protective layer formed on steel surface was much greater in presence of both ions in solution than that when each inhibitor used alone.

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Abstract:Optimization of specimen geometry before subjecting it to hot torsion test (HTT) is essential for minimizingnon-uniform temperature distribution and obtaining uniform microstructure thought the specimen.In the present study, a nonlinear transient analysis was performed for a number of different geometries andtemperatures using the commercial finite element (FE) package ANSYSTM. FE thermal results then were applied tooptimize HTTspecimen produced from API-X 70 microalloyed steel taking into account the microstructurehomogeneity.  The thermodynamic software Thermo-calcTM was also used to analysis solubility of microalloyingelements and their precipitates that may exist at different equilibrium conditions. In addition the behavior of austenitegrain size during reheating was investigated. The results show high temperature gradient occurred in long specimens.This could lead to non homogeneous initial austenite grain size and alloying element or precipitates within the gaugesection of the specimen. The proposed optimization procedure can in general be used for other materials and reheatingscenarios to reduce temperature. This then creates more homogeneous initial microstructure prior to deformation andreduces errors in post processing of the HTTresults

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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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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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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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The microstructure and mechanical properties of 7075 wrought aluminum alloy produced by strain induced melt activation (SIMA) route were investigated.Also liquid volume fraction measurement was studied by three procedures. Remelting process was carried out in the range of 560 to 610 °C for 20 min holding. The microstructure in the semi-solid state consists of fine spherical solid grains surrounded byliquid.The mechanical properties of the alloy vary with the grain size and weak mechanical properties of globular samples would appear if an alloy reheated at a high temperature. Thermodynamic simulation is a fast and efficient tool for the selection of alloys suitable for semi-solid processing

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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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In this paper, the influence of heat treatment on PH17-7 stainless steel spring was evaluated. Precipitation hardening phenomenon of  PH 17-7 steel was evaluated in three stages. First, the spring constant changes with time and temperature was evaluated. Second, the spring constant changes with respect to its original length at constant temperature and time with blocking (spring length after compression, 18 and 21 mm) were investigated.  And finally, the spring heat treatment at 480 °C for 80 min and then holding at 230 °C in oil bath for 60 min without blocking were investigated. The results showed that the use of 18 mm block have large spring constant than 21 mm block. The optimal conditions (480°C for 80 min) for this spring to reaching maximum spring constant were determined.

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Relations between the microstructure, mechanical properties and machinability of as-cast 65Cu-35Zn brass with various amounts of Al from 0 to 4.72 and Si from 0 to 3.62 wt% were investigated. Both Si and Al initially enhanced the UTS and toughness of the brass samples, which led to improvement in machinability due to a reduction in the main cutting force. A duplex brass with random oriented α plates in β’ matrix was found to have the best machinability among the other microstructures. It was found that beside the presence of brittle phases, such as β’ phase in the microstructure, the morphology and hardness of the phases involved had significant influence on machinability.

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The combined influence of both melt filtration and cooling rate on the microstructure features and mechanical properties of A356 cast alloy was studied. A step casting model with five different thicknesses was used to obtain different cooling rates. The effect of melt filtration was studied by using of 10 and 20 ppi ceramic foam filters in the runner. Results showed that secondary dendrite arm spacing decreased from 80 μm to 34 μm with increasing cooling rate. Use of ceramic foam filters in the runner led to the reduction of melt velocity and surface turbulence, which prevented incorporation of oxide films and air in the melt, and consequently had an overall beneficial effect on the quality of the castings. A matrix index, which is the representative of both SDAS and microporosity content, was defined to consider the simultaneous effect of melt filtration and cooling rates on UTS variations. Also, the fracture surface study of test bars cast using 10 and 20 ppi ceramic foam filters showed features associated with ductile fracture.
 

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Modification of MnFe₂O₄@SiO₂ core-shell nanoparticles with (3-aminopropyl) triethoxysilane (APTES) was investigated. The magnetite MnFe₂O₄ nanoparticles with an average size of ~33 nm were synthesized through a simple co-precipitation method followed by coating with silica shell using tetraethoxysilane (TEOS); that has resulted in a high density of hydroxyl groups loaded on nanoparticles. The prepared MnFe₂O₄@SiO₂ nanoparticles were further functionalized with APTES via silanization reaction. For having suitable surface coverage of APTES, controlled hydrodynamic size of nanoparticles with a high density of amine groups on the outer surface, the APTES silanization reaction was investigated under different reaction temperatures and reaction times. Based on dynamic light scattering (DLS) and zeta potential results, the best conditions for the formation of APTES-functionalized MnFe₂O₄@SiO₂ nanoparticles were defined at a reaction temperature of 70 °C and the reaction time of 90 min. The effectiveness of our surface modification was established by X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), Fourier transforms infrared spectroscopy (FTIR), and vibrating sample magnetometer (VSM). The prepared magnetite nanostructure can be utilized as precursors for synthesizing multilayered core-shell nanocomposite particles for numerous applications such as medical diagnostics, drug, and enzyme immobilization, as well as molecular and cell separation.

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The hot deformation behavior of the heat-treated AA6061 and AA 6063 aluminum alloys by T6-1, T6-2 artificial aging treatment, and O annealing treatment were studied by compression testing over a temperature range of 350–550  and strain rates of 0.005-0.1 s^-1. It was observed that the flow stresses of the studied aluminum alloys treated by the T6-1 and T6-2 heat treatments were significantly higher than those of the O annealing treatment. Moreover, the stress-strain curves of the heat-treated alloys by the T6-1, T6-2, and O heat treatments demonstrated significant softening during deformation at the lowest strain rate under any of the deformation conditions. For several strains, the activation energy of hot deformation was specified and obtained to vary significantly with strain for the heat-treated alloys by the T6-1 and T6-2 treatments. The stress-strain data calculated from a linear equation, with strain-dependent parameters, shows a great fit with the experimental data for the heat-treated aluminum alloys.

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A full factorial design of experiment was applied running 36 experiments to investigate the effects of milling parameters including cutting speed with three levels of 62.83, 94.24 and 125.66 m/min, feed rate with three levels of 0.1, 0.2 and 0.3 mm/tooth, cutting depth with two levels of 0.5 and 1 mm and machining media with two levels, on surface integration properties of magnesium AZ91C alloy such as grain size, secondary phase percent, surface microhardness and surface roughness. In all cases, a fine grained surface with higher secondary phase sediment and microhardness obtained comparing the raw material. According to analysis of variance results, the most effective parameter on grain size, secondary phase percent and microhardness was cutting depth and the most effective parameter on surface roughness was feed rate. although the grain size in all machined samples was smaller than that of the raw material but due to the dual effect of cryogenic conditions, which both cool and lubricate and reduce the temperature and strain rate at the same time, the direct effect of this parameter on grain size was not significant. Also, the all interaction effects of parameters on grain size and microhardness were significant.

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Abstract
The power line insulators are permanently exposed to various environmental pollutants such as dust and fine particles. This may lead to flashovers and therefore widespread power blackouts and heavy economic damage. One way to overcome this problem is to make the insulator surface superhydrophobic. In this research, the superhydrophobic properties of the insulators were improved by applying room-temperature cured composite coatings consisting of epoxy and hydrophobic nano-silica particles. Either octadecyl trichlorosilane (ODTS) or hexamethyldisilazane (HMDS) was used to coat the silica nanoparticles and make them hydrophobic. Then, the hydrophobic silica was added to a mixture of epoxy resin and hardener. The suspension was applied on the surfaces of a commercial porcelain insulator and cold cured at ambient temperature. The coating increased the water contact angle from 50° to 149°. Even after 244 h exposure to the UV light, the samples preserved their hydrophobic properties. The adhesion of the coating was rated as 4B according to the ASTM D3359 standard. The coating decreased the leakage current by 40% and increased the breakdown voltage by 86% compared to the uncoated sample and showed promise for making power line insulators self-cleaning.