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Showing 164 results for Tic

A. Poladi, M. Zandrahimi,
Volume 5, Issue 3 (9-2008)
Abstract

Abstract: Austenitic stainless steels exhibit a low hardness and weak tribological properties. The wear behaviour of austenitic stainless steel AISI 316 was evaluated through the pin on disc tribological method. For investigating the effect of wear on the changes in microstructure and resistance to wear, optical microscopy and scanning electron microscope were used. The hardness of the worn surfaces was measured with a micro-hardness tester. Worn surfaces were analyzed through X-ray diffraction. Results showed that with increasing the sliding distance and applied load, the austenite phase partially transformed to ά martensite, and there was no trace of ε phase detected. Due to the formation of probably hard and strong martensite phase, as the sliding distance and applied load increased, the hardness and the wear resistance of the material was increased. Wear mechanism was on the base of delamination and abrasion.
M. Mossanef, M. Soltanieh,
Volume 5, Issue 4 (12-2008)
Abstract

Abstract: The possibility of vanadium carbide coating formation on AISI L2 steel was studied in molten salt bath containing 33 wt% NaCl- 67 wt% CaCl2. In this research, the effects of time, temperature and bath composition on growing layer thickness were studied. The vanadium carbide coating treatment was performed in the NaCl-CaCl2 bath at 1173, 1273 and 1373 K temperatures for 3, 6, 9 hours and in bath containing 5, 10, 15, 25 wt% ferrovanadium. The presence of VC formed on the surface of the steel substrate was confirmed by optical microscopy, scanning electron microscopy (SEM) and X-ray diffraction analysis. The layer thickness of vanadium carbide and surface hardness ranged between 4.8 to 25.7 µm and 2645 to 3600 HV, respectively. The kinetics of layer growth was analyzed by measuring the depth of vanadium carbide layer as a function of time and temperature. The mean activation energy for the process is estimated to be 133 kJ/ mol.


S.h.r. Fatemi Nayeri, J. Vahdati Khaki, M. R. Aboutalebi,
Volume 6, Issue 1 (3-2009)
Abstract

Abstract:A combination of mechanical activation and Differential Thermal Analysis (DTA) together with X-Ray Diffraction (XRD), and various microstractural characterization techniques were used to evaluate the starting reaction in the combustion synthesis of TiC-Al2O3 composite in TiO2-Al-C system. The mechanical activation was performed on the mixtures of two components of TiO2/Al, Al/C and TiO2/C and then the third component was added according to the stoichiometric reaction for 3TiC+2Al2O3 composite formation. The powder mixtures were heated up to 1450 °C under Argon atmosphere at a heating rate of 10 °C/min. The combustion synthesis temperature was observed to decrease from 962 °C to 649 °C after milling of TiO2/Al mixture for 16 hr. On the contrary, the mechanical activation of Al/C and TiO2/C mixtures for 16 hr made the reaction temperature increase to 995 °C and 1024 °C, respectively. The decrease in reaction temperature as a result of milling the TiO2/Al mixture could be due to an increase of TiO2 and Al interface area as confirmed by TEM micrographs and XRD patterns of milled powder mixture. In addition, DTA experiments showed that for the sample in which TiO2 and Al were mechanically activated the reaction occurred at the temperature even lower than that of Al melting point.
M. Pirhadi Tavandashti, M. Zandrahimi, B. Akbari,
Volume 6, Issue 1 (3-2009)
Abstract

Abstract: Nanoparticles exhibit a high reactivity and strong tendency towards agglomeration. In this study, aluminum oxide (alumina) nanoparticles were characterized by gas adsorption (BET), transmition electron microscopy (TEM) and photon correlation spectroscopy (PCS) techniques to assess the agglomeration of the particles. There is a good correlation between the BET and TEM measurements but PCS was larger in the mean and median size and with a degree of agglomerates being detected. Some agglomeration was evident, but most of the particles existed as discrete objects as observed in the (HR) TEM images which were in good agreement with the agglomeration factor.
M. Ebrahimi-Basabi,, J. Javadpour,, H. Rezaie, M. Goodarzi,
Volume 6, Issue 1 (3-2009)
Abstract

Abstract: Nano- size alumina particles have been synthesized by mechanical activation of a dry powder mixture of AlCl3 and CaO. Mechanical milling of the above raw materials with the conditions adopted in this study resulted in the formation of a mixture consisting of crystalline CaO and amorphous aluminum chlorides phases. There was no sign of chemical reaction occurring during milling stage as evidenced by x-ray diffraction studies. Subsequent heat treatment of the milled powder at 350ºC resulted in the occurrence of displacement reaction and the formation of Al2O3 particles within a water soluble CaCl2 matrix. The effect of higher temperature calcinations on the phase development in this powder mixture was followed by X-ray diffraction (XRD) analysis and scanning electron microscope ( SEM). Differential thermal analysis (DTA) was used to compare the thermal behavior between the milled and unmilled powders. Perhaps the most important result in this study was the observation of á-Al2O3 phase at a very low temperature of 500ºC.
M. Goodarzi, S. M. A. Boutorabi, M. A. Safarkhanian,
Volume 6, Issue 3 (9-2009)
Abstract

Abstract:In this study, an effort has been made to determine the influence of rotational speed of tool on themicrostructure and hardness values of friction stir welded 2024-T851 aluminum alloy. The microstructure of stir zonein the joints has been investigated. It was found that the particles such as Al6(CuFeMn) particles are broken up duringfriction stir welding, and the degree of break up of these particles in the stir zone increases with increasing rotationalspeed. Since the break up of these particles and the recrystallization of new grains happen simultaneously, the brokenparticles would be placed in the grain boundaries. Moreover, the hardness value in the stir zone increases withincreasing rotational speed
B. Tolaminejad, A. Karimi Taheri, H. Arabi, M. Shahmiri,
Volume 6, Issue 4 (12-2009)
Abstract

Abstract: Equal channel angular extrusion (ECAE) is a promising technique for production of ultra fine-grain (UFG) materials of few hundred nanometers size. In this research, the grain refinement of aluminium strip is accelerated by sandwiching it between two copper strips and then subjecting the three strips to ECAE process simultaneously. The loosely packed copper-aluminium-copper laminated billet was passed through ECAE die up to 8 passes using the Bc route. Then, tensile properties and some microstructural characteristics of the aluminium layer were evaluated. The scanning and transmission electron microscopes, and X-ray diffraction were used to characterize the microstructure. The results show that the yield stress of middle layer (Al) is increased significantly by about four times after application of ECAE throughout the four consecutive passes and then it is slightly decreased when more ECAE passes are applied. An ultra fine grain within the range of 500 to 600 nm was obtained in the Al layer by increasing the thickness of the copper layers. It was observed that the reduction of grain size in the aluminium layer is nearly 55% more than that of a ECA-extruded single layer aluminium billet, i.e. extruding a single aluminium strip or a billet without any clad for the same amount of deformation. This behaviour was attributed to the higher rates of dislocations interaction and cell formation and texture development during the ECAE of the laminated composite compared to those of a single billet
Javad Bahrami, Mohammad Hossein Paydar, Nader Setoudeh, Mohammad Hossein Shariat,
Volume 6, Issue 4 (12-2009)
Abstract

  Abstract

  The effect of mechanical activation using an attrition mill on the particle size of an ilmenite concentrate and its effect on the ability of the concentrate for Iron separation during hydrochloric acid leaching and the kinetics of the dissolution process have been investigated. It was observed that mechanical activation in an attritor significantly enhances the dissolution of iron in hydrochloric acid while have a slight effect on dissolution of titanium. With the mechanically activated ilmenite using an attrition mill, leaching conversion at 90 oC reached to 80%. The kinetic data of leaching of mechanically activated ilmenite was found to follow shrinking core model. Mechanically activating ilmenite using the attrition mill was found to cause the activation energy of leaching to be decrease from 43.69 , found for samples leached without mechanically activated, to 18.23 .


Bahman Mirzakhani, Hossein Arabi, Mohammad Taghi Salehi,seyed Hossein Seyedein, Mohammad Reza Aboutalebi, Shahin Khoddam, Jilt Sietsma,
Volume 6, Issue 4 (12-2009)
Abstract

  Abstract

  Recovery and recrystallization phenomena and effects of microalloying elements on these phenomena are of great importance in designing thermomechanical processes of microalloyed steels. Thus, understanding and modeling of microstructure evolution during hot deformation leads to optimize the processing conditions and to improve the product properties.

  In this study, finite element method was utilized to simulate thermomechanical parameters during hot deformation processes. FEM results then were integrated with physically based state variable models of static recovery and recrystallization combined with a realistic microstructural geometry. The thermodynamic software Thermo-calc was also used to predict present microalloying elements at equilibrium conditions.

The model performance was validated using stress relaxation tests. Parametric studies were carried out to evaluate the effects of deformation process parameters on the microstructure development following hot deformation of the API-X70 steel
R. Khoshhal, M. Soltanieh, M. Mirjalili,
Volume 7, Issue 1 (3-2010)
Abstract

Abstract:

titanium sheets in pure molten aluminum at 750

and X-Ray Diffraction Analysis results, TiAl

intermetallic layer thickness increases slowly at primary stages. After that an enhanced growth rate occurs due to layer

cracking and disruption. Presumably, reaction starts with solving titanium into the molten aluminum causing in

titanium super saturation and TiAl

intermetallic layer which consequently leads to TiAl

energy of intermetallic layer formation and growth was developed by measuring titanium thickness decreases.

In this work, kinetics of intermetallic compounds formation in Al-Ti system was studied by immersingoC, 850 oC and 950 oC. According to Scanning Electron Microscopy3 is the only phase can form at the interface. Observations revealed that3 formation. At this stage, growth may be controlled by aluminum diffusion through3 formation at the interface of Ti-TiAl3. Furthermore, activation

M. Banoee,z. Ehsanfar, N. Mokhtari,m. R. Khoshayand, A. Akhavan Sepahi, P. Jafari Fesharaki,h. R. Monsef-Esfahani,, A. R. Shahverdi,
Volume 7, Issue 1 (3-2010)
Abstract

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

A.m. Rashidi, A. Amadeh,
Volume 7, Issue 2 (6-2010)
Abstract

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

M.sh. Bafghi, A.h. Emami, A. Zakeri, J. Vahdati Khaki,
Volume 7, Issue 2 (6-2010)
Abstract

Abstract:

has been investigated. It has been shown that the mechanism of leaching reaction is diffusion through the product layer

and does not undergo any change as a result of mechanical activation in a wide range of experimental conditions.

Leaching rate is strongly influenced by milling intensity and the effect of ball to powder mass ratio is stronger than

milling time. Curve fitting of experimental data shows that leaching rate constant is approximately a linear function

of ball to powder mass ratio, while it obeys a power function with regard to the milling time.

The kinetics of chalcopyrite leaching in a ferric sulfate media for raw and mechanically activated samples

M. Nusheh*, H. Yoozbashizadeh,
Volume 7, Issue 2 (6-2010)
Abstract

Abstract:

the competition between the precipitation of cobalt ions and evolution of hydrogen gas on the cathode surface during

the reduction process in a sulfate bath, investigation on the mechanism of metal precipitation is of great importance.

In the present work, study on the kinetics of cobalt electrowinning and the mechanism of the involved reactions have

been carried out. The obtained results, confirm the mechanism of cobalt precipitation by depletion of hydroxides. The

effects of temperature and scan rate parameters were studied on electrowinning of cobalt by cyclic voltammetry

technique. The diffusion coefficient and rate constant of the reactions were measured and calculated by performed

experiments.

Nowadays cobalt is mostly produced through the electrowinning process of sulfate solutions. Regarding to

S. Ahmadi,, H. R. Shahverdi*, S. S. Saremi,
Volume 7, Issue 4 (10-2010)
Abstract

Abstract: In this research work, crystallization kinetics of Fe55Cr18Mo7B16C4 alloy was evaluated by X-ray diffraction, TEM observations and differential scanning calorimetric tests. In practice, crystallization and growth mechanisms were investigated using DSC tests in four different heating rates. Results showed that a two -step crystallization process occurred in the alloy in which - Fe phase was crystallized in the first step after annealing treatments. Activation energy for the first step of crystallization i.e. - Fe was measured to be 276 (kj/mol) according to Kissinger model. Further, avrami exponent calculated from DSC curves was 2 and a three -dimensional diffusion controlled mechanism with decreasing nucleation rate was observed in the alloy. It is also known from the TEM observations that crystalline á – Fe phase nucleated in the structure of the alloy in an average size of 10 nm and completely mottled morphology.


R. Alizadeh, O. Ostrovski,
Volume 8, Issue 1 (3-2011)
Abstract

Abstract: Reduction of the Titanium dioxide, TiO2, by methane was investigated in this work. The thermodynamic of reaction was examined and found favorable. The reaction of titanium dioxide with methane was carried out in the temperature range 1150°C to 1450°C at atmospheric pressure with industrial high porosity pellets prepared from titanium dioxide powder. The evolved gas analyzing method was used for determination of the extent of reduction rate. The gas products of the reaction are mostly CO and trace amount of CO2 and H2O. The synthesized product powder was characterized by X-ray diffraction (XRD) for elucidating solid phase compositions. The effect of varying temperature was studied during the reduction. The conversion-time data have been interpreted by using the grain model. For first order reaction with respect to methane concentration, the activation energy of titanium dioxide reduction by methane is found to be 51.4 kcal/gmole. No detailed investigation of kinetic and mechanism of the reaction was reported in literatures.
A. Najafi, F. Golestani-Fard, H. R. Rezaie, N. Ehsani,
Volume 8, Issue 2 (6-2011)
Abstract

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.
B. Akbari, M. Pirhadi Tavandashti, M. Zandrahimi,
Volume 8, Issue 2 (6-2011)
Abstract

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.
M. Sh. Bafghi, A. Yarahmadi, A. Ahmadi, H. Mehrjoo,
Volume 8, Issue 3 (9-2011)
Abstract

Abstract:

the reduction agent. Pellets of barite ore containing about 95% BaSO

temperature, time, ore grain size and the type and grain size of the carbon materials. Graphite, coke and charcoal have

been used as the reducing agent and the reduction experiments have been performed in the temperature range of 925-

1150 °C. Apart from conducting the experiments using pellets made of ore powder, kinetic analysis of the experimental

data by use of the reduced (dimensionless) time method has been another unique feature of the present study.

Experimental results show that grain size of either carbon material or barite ore has not appreciable effect on the

reaction rate. Kinetic analysis of the experimental data revealed the rate is strongly controlled by the chemical reaction

of carbon gasification (Boudouard reaction). The reaction rate is very considerably related to the type of carbon

material so that the activation energy varies from 15.6 kcal.mol

kcal.mol

gasification.

The present study deals with the reduction of barium sulfate (Barite) to barium sulfide by use of carbon as4 has been reduced under different conditions of-1 for charcoal to 26.3 kcal.mol-1 for graphite and 20.8-1 for coke. This behavior provides further support for the postulated reaction mechanism, i.e., carbon
A. Namiranian , M. Kalantar,
Volume 8, Issue 3 (9-2011)
Abstract

The process of mullitization of kyanite concentrate was studied at different conditions of heat treatment (1400
– 1600 °C and 0.5 – 3.5 hours) and particle size of raw materials (38-300 ?m). Kyanite concentrate was obtained from
ore-dressing of kyanite deposits of Mishidowan-Bafgh region at 100 km northeastern part of Yazd. The results of
microstructure (shape, distribution and size of the grains) and phase evolution studies by SEM and XRD showed that
total transformation of kyanite to mullite takes place by heat treatment between 1500 –1550 °C during 2.5 hours.. At
temperatures below 1500 °C need-like mullite grains are always produced. At higher temperatures the mullite grains
reveal rounded and platelet morphology. At 1550 °C, the rate of mullitization and densification were improved by
increasing soaking time from 1h to 3h and decreasing particle size of materials from 300 to 38 m

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