Showing 28 results for Activation
Tavakoli A. H., Goudarzi M.,
Volume 1, Issue 3 (9-2004)
Abstract
The synthesis of advanced materials from low cost minerals concentrates is a new field of study that has great potential applications. In this paper, the effect of milling time on the temperature of initiation and amount of carbothermic reduction of ilmenite has been investigated. The stoichiometric molar ratio (1:4) of ilmenite to graphite was mixed and mechanically activatedfor 30-70 hours at room temperature. Then homogenized mixture heated for one hour at 1000-1400°C in coal reducing atmosphere. The results show that complete conversion of ilmenite to Fe and TiC can not be achieved in the unmilled powder at 1400°C, while with milling of mixture for 30 hours, complete reduction of ilmenite to Fe and TiC at 1400° C was observed. With increasing milling time from 30 to 70 hours the temperature of complete reduction decreases from 1400 to 1200° C. Leaching of final product in HCI 3% solution dissolve Fe but leave pure titanium carbide intact. Determination of TiC unit cell size from X-ray diffraction pattern shows that unit cell size of synthesized TiC is less than stoichiometric one, which suggests that some oxycarbide phases (TiCxO1-x), is present into the final product.
Bafghi M. Sh., Adeli M., Mohammadi Nikoo H.,
Volume 1, Issue 3 (9-2004)
Abstract
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
A. Ataie1,, S. Heshmati-Manesh1,, S. Sheibani1,, G. R. Khayati,y. Firozbakht,
Volume 5, Issue 1 (3-2008)
Abstract
Abstract: In this paper solid state reduction of high carbon ferrochromium-chromite composite
pellets in the temperature range of 900-1350°C was investigated. A two stage reduction
mechanism is proposed. The first stage is likely to be controlled by the chemical reaction with
activation energy of 127.2kJ/mol. In the second stage, solid state diffusion of carbon through the
reaction product layer is suggested to be rate controlling. The activation energy of this stage was
calculated to be 93.1kJ/mol. The reduction process was found to be favored by high temperatures
as well as high vacuum. The results also show that pre-milling of initial mixture has a negative
effect on the reduction degree.
A. Allahverdi, E. Najafi Kani, S. Esmaeilpoor,
Volume 5, Issue 2 (6-2008)
Abstract
Abstract: The use of alkali-activated cementitious materials especially over the past decades has
significantly been increased. The goal of this research is to investigate the effects of silica modulus
and alkali concentration on alkali-activation of blast-furnace slag. In this research, the most
important physical characteristics of cementitious systems, i.e. the 28-day compressive strength
and final setting time, were studied by changing influencing parameters such as silica modulus,
i.e. SiO2/Na2O, (0.44, 0.52, 0.60, and 0.68) and Na2O concentration (4, 6, 8 and 10% by weight of
dry binder) at a constant water-to-dry binder ratio of 0.25. Final setting time of the studied
systems varies in the range between 55-386 minutes. The obtained results show that systems cured
at an atmosphere of more than 95% relative humidity at room temperature exhibit relatively high
28-day compressive strengths up to 107 MPa.
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.
A. Shokuhfar, S. Ahmadi, H. Arabi, S. Nouri,
Volume 6, Issue 3 (9-2009)
Abstract
Abstract: Guinier-Preston (GP) zone formation and precipitation behavior of T1 (Al2CuLi) phase during the ageingof an Al-Cu-Li-Zr alloy was studied by differential scanning calorimetry (DSC) technique and electrical resistancemeasurement of the samples. Results show that endothermic effects in the thermograms of the alloy between 180°Cand 240°C can be related to the enthalpy of GPzones dissolution. Formation of GPzones in the structure increasedhardness, tensile strength and electrical resistance of the Al-Cu-Li-Zr alloy. Furthermore, precipitation of T1 phaseoccurred in temperature range of 250ºC to 300ºC whereas its dissolution occurred within the temperature of 450-530ºC. Activation energies for precipitation and dissolution of T1 phase which were determined for the first time inthis research, were 122.1(kJ/mol) and 130.3(kJ/mol) respectively. Results of electrical resistance measurementsshowed that an increase in the aging time resulted in the reduction of electrical resistance of the aged samples.
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 .
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.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. 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
M. M. Kashani Motlagh, A. A. Youzbashi, Z. Amiri Rigi,
Volume 8, Issue 4 (12-2011)
Abstract
A natural bentonite obtained from Khorasan, Iran, was submitted to acid activation with sulphuric acid. Sample aliquots (5gr)
were leached with 100 ml H2SO4 solutions of various concentrations (2–7N) at 80±2 oC for 2 hours. X–ray diffraction, chemical analysis, infrared spectroscopy and specific surface area measurements were performed in order to evaluate important structural modifications occurring as a result of acid attack. Octahedral sheet was affected by acid activation resulting into the dissolution of cations (Mg2+, Fe2+, Al3+) and consequent decomposition of montmorillonite structure. Bentonite samples were then tested in order to verify their capacity to bleach colza–soybean oil, and their performances were compared to that of a commercial bleaching clay. The bleaching ability of the natural clay was poor when compared with that of the industrial adsorbent. Acid activation of the bentonite sample with 7N sulphuric acid yielded an adsorbent material which was highly efficient in the bleaching of the oil functioned better than the commercial clay product under the same conditions.
Dr Ali Darehkordi, Mr Mohammad Sadegh Hosseini,
Volume 9, Issue 3 (9-2012)
Abstract
Montmorillonite modified is an efficient environmental friendly catalyst under one-pot-three-component synthesis of 3,4-dihydropyrimidine-2(1H) ones. The preparation was performed with an aldehyde, 1,3-dicarbonyl compounds, urea or thiourea under solvent-free conditions. In comparison with the other methods of Biginelli reaction, this new method has short reaction time inexpensive catalyst and in addition excellent yields were obtained.
M. S. Kaiser,
Volume 10, Issue 3 (9-2013)
Abstract
Precipitation behaviour of wrought Al-6Mg alloys with ternary scandium and quaternary zirconium and titanium has been studied. Hardness measurements and resistivity studies are employed to assess the precipitation behaviour of scandium doped Al-6Mg alloy without or with quaternary additions of zirconium and titanium. Further, the kinetics of precipitations are studied by differential scanning calorimetric technique. Scandium has been observed to form fine coherent Al3Sc precipitates during ageing and these are responsible for strengthening of the alloys. The precipitation kinetics of Al3Sc depends on the diffusion of scandium in aluminium. Presence of fine coherent precipitates of Al3Sc impedes the migration of dislocations and increase the recovery temperature. The kinetics of recrystallisation is also delayed.
M. Sheikhshab Bafghi, M. Karimi, M. Adeli,
Volume 10, Issue 4 (12-2013)
Abstract
In the present study, reduction of zinc oxide from the pellets made of steelmaking electric arc furnace dust has been investigated. Effects of such parameters as the type of carbon material (graphite, coke and charcoal) as well as time and temperature on the reduction reaction have been examined. The reduced (dimensionless) time method was applied to perform a kinetic analysis of the system. Experimental results showed that increasing the temperature in the range of 925-1150°C results in a remarkable increase in the reduction rate. It was also shown that the reduction process is controlled by chemical reaction. Meaningful difference in the activation energy values calculated for reduction with graphite (24.75 kcal/mol), coke (18.13 kcal/mol) and charcoal (11.52 kcal/mol) indicate the predominant role of chemical reaction (carbon gasification) in the overall reaction rate and its rate-controlling mechanism. Carbothermal reduction of pelletized EAF dust proved to be an efficient reduction method, so that above 90% reduction was achieved in about one hour at temperatures around 1100°C.
A Fattah-Alhosseini, M Asadi Asadabad,
Volume 11, Issue 4 (12-2014)
Abstract
Four compositions of austenitic Mn-Cr steels have been developed successfully for in-vessel component materials in power plant industry. The phase stability of these Mn-Cr steels was studied by and X-ray diffraction (XRD) patterns. XRD patterns have shown that the matrix of these Mn-Cr steels is a single γ-phase structure. The potentiodynamic polarisation curves suggested that these fabricated Mn-Cr steels showed passive behaviour in 0.1M H2SO 4solution. Therefore, semiconducting behaviour of passive film formed on these fabricated Mn-Cr steels in 0.1M H2SO 4 solution was evaluated by Mott–Schottky analysis. This analysis revealed that passive films behave as n-type and p-type semiconductors. Based on the Mott–Schottky analysis, it was also shown that donor and acceptor densities are in the order of 1021 cm -3 and are comparable for other austenitic stainless steels in acidic environments
S. Niksirat, Sh. Raygan, S. Moradi Ghiassabadi,
Volume 12, Issue 2 (6-2015)
Abstract
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
N. Ghanbarpourabdoli, Sh. Raygan, H. Abdizadeh,
Volume 13, Issue 4 (12-2016)
Abstract
In this study, the adsorption of hexavalent chromium and zinc ions from the solution is investigated by raw red mud and mechanical-chemical activated red mud along with the possibility of selective reclamation of these ions from the solution. The mechanical-chemical activation of red mud was done by employing high-energy milling and subsequent acid treatment with HNO3. Raw red mud (RRM) and mechanical-chemical activated red mud (MCARM) adsorbents were characterized with Fourier transform infrared spectroscopy (FTIR), X-ray fluorescence (XRF), X-ray diffraction (XRD), scanning electron microscope (SEM), and Brunauer–Emmett–Teller (BET) methods. In order to determine the suitable adsorption conditions, effects of pH of the solution, amount of adsorption, temperature, and time of adsorption were investigated. It was found that the optimum pH for the adsorption of hexavalent chromium and zinc ions by MCARM adsorbent was 2 and 6, respectively. According to these pH values, MCARM had the ability to separately adsorb more than 95 and 79% of hexavalent chromium and zinc ions from the solution, respectively. Experimental results were in good agreement with Langmuir and Freundlich isotherms. By considering the kinetic models of adsorption, the kinetics of the adsorption of both ions followed the pseudo-second-order reaction model. It was also determined that almost 25.8 and 61.8% of the hexavalent chromium and zinc ions adsorbed in MCARM could be recovered
E. Mohammadi, M. Pourabdoli,
Volume 16, Issue 2 (6-2019)
Abstract
The effect of mechanical activation on the kinetics of ammoniacal thiosulfate leaching of a refractory oxide gold ore containing 2.8 ppm Au was investigated. The gold extraction of 99.81% was achieved by 16 h leaching of a sample mechanically activated for 60 minutes. The gold extraction observed for a similar reference sample without mechanical activation was only 55%. Studies revealed that leaching progresses at two different rates depending on the leaching time (0-2 h and 2-16 h). It was observed that diffusion through an ash layer as a dominant mechanism controls the leaching of samples mechanically activated up to 45 minutes during total leaching time, while reaction control and liquid film diffusion are dominant mechanisms for leaching of a sample mechanically activated for 60 minutes during 0-2 h and 2-16 h, respectively. The extraction observed during the ash diffusion step depends significantly upon mechanical activation time. Mechanical activation of 60 minutes results in high gold extraction in this step which when combined with subsequent chemical reaction gives close to 100% gold extraction in a 16 hour leach. Mechanical activation for up to 45 minutes leads to a modest improvement in overall gold extraction compared with the reference test without mechanical activation
A. R. Abbasian, M. R. Rahimipour, Z. Hamnabard,
Volume 16, Issue 4 (12-2019)
Abstract
In this work, lithium meta titanate (Li2TiO3) nanocrystallites were synthesized by hydrothermal method and subsequent heat treatment. The shrinkage of the powder compact was measured under constant heating rate in order to study the sintering behavior of the synthesized powders. Densification curves of the synthesized powders were also constructed via the dilatometry analysis and evaluated at several heating rates. Two separate methods of analytical procedure and master curve sintering were employed to determine the activation energy of the initial sintering stage. The activation energy values were estimated based on these two distinct methods as 229±14 and 230 kJ/mol respectively, consistenting with each other. Moreover, surface diffusion was determined as the dominant mechanism of densification on initial sintering of Li2TiO3 nanocrystallites.
A. Allahverdi, H. Hashemi, M. Mahinroosta,
Volume 17, Issue 1 (3-2020)
Abstract
This work evaluates the resistance of alkali-activated slag (AAS) mortar against sodium sulfate attack. The effects of immersion in 5% sodium sulfate solution under room temperature and wetting-drying cycles on the compressive strength of mortar specimens were considered for evaluating the extent of degradation. Mortar specimens prepared from type II and V Portland cements (PC2 and PC5) in accordance with ASTM standard were also used as reference. To characterize the chemical products of the degradation process due to sodium sulfate attack, the specimens were also studied by X-ray diffractometry, scanning electron microscopy, and the elemental analysis by energy dispersive X-ray spectroscopy. After 360 days of exposure to the sodium sulfate solution, PC2, PC5 and AAS cements showed 71, 52 and 45% reduction in compressive strength, respectively. According to the obtained results, AAS cement exhibits a higher sulfate resistance compared to PC2 and PC5.
