Showing 28 results for Kinetic
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.
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
M. Rezvani,
Volume 8, Issue 4 (12-2011)
Abstract
The effect of Y2O3, CeO2, P2O5, ZrO2 and TiO2 in single, double and triple form on crystallization mechanism of Li2OAl2O3- SiO2(LAS) glass-ceramic system was investigated .The nucleation and crystallization peak temperatures of optimized samples in each group were determined by Ray & Day method .The crystalline phase was determined by the X-ray diffractometery .The micro-structure of the samples was studied by SEM techniqe .Crystallization activation energy ,E, and kinetic constants(n ,m) were determined by differential thermal analysis (DTA) through Marotta and Augis-Bennet methods .According to the results ,the Avrami constants(m ,n) derived from the Marotta and Augis- Bennett, glasses containing both ZrO2 and TiO2 nuclei were showed bulk crystallization .The crystallization mechanism of specimens containing ZrO2, TiO2 and CeO2 in the triple nuclei series represent two-dimensional bulk crystallization .By comparison of Avrami constants and activation energy of crystallization of optimized samples with other results they gave much lower value of E(255.5 kJ/mol) and higher value of n in 4.38.The lattice constants of the main phase( -eucryptite solid solution)in samples were determined according to the XRD results
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.
M. Ghobeiti Hasab, F. Rashchi, Sh. Raygan,
Volume 11, Issue 2 (6-2014)
Abstract
In this paper, gold leaching of a refractory sulfide concentrate by chloride–hypochlorite solution was
investigated and effects of stirring speed, temperature and particle size on the leaching rate were reported.
Experimental data for leaching rate of gold were analyzed with the shrinking–core model. Results were consistent with
chemical reaction control mechanism in the first 1 h of leaching and diffusion control mechanism in the second 1 h.
Apparent activation energy also was found to be 22.68 kJ/mol in the first step and 3.93 kJ/mol in the second step of
leaching.
M. Nouri, P. Alizadeh, M. Tavoosi,
Volume 14, Issue 3 (9-2017)
Abstract
In this study, the crystallization behavior of a 65GeO2-15PbO-10MgF2-10MgO glass (prepared by the conventional melt quenching technique) has been investigated. The microstructure and crystallization behaviors of this glass were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), non-isothermal differential thermal analysis (DTA) and Fourier transform infrared spectroscopy (FTIR). The results demonstrated that a fully glassy phase can successfully be prepared by the conventional melt quenching technique exhibiting one-stage crystallization on heating, i.e., the glassy phase transforms into crystalline MgGeO3 and Pb5GeO7 phases. The activation energy for the crystallization, evaluated from the Kissinger equation, was approximately 202±5 kJ/mole using the peak temperature of the exothermic reaction. The Avrami exponent or reaction order, n, indicates the nucleation rate in this glass to increase with time and the crystallization to be governed by a three-dimensional interface-controlled growth.
M. Krishna, R. Nandini, A.v. Suresh, K. Narasimha Rao ,
Volume 15, Issue 2 (6-2018)
Abstract
An efficient solid-state approach was established to synthesize (K0.5Na0.5) NbO3 ceramics using calcination kinetics and microwave assisted sintering. Milling of carbonate and oxide raw materials were carried out for 15h to obtain homogeneous nano particles. The crystallite size of 5.30 nm was obtained for the KNN system after calcination through optimized parameters and observed to be stoichiometric in nature. The obtained nano particles showed phase transition from orthorhombic to tetragonal crystal structure without any secondary phases. The high relative density and tetragonality ratio of KNN ceramics obtained through optimized sintering parameters yielded with significant piezoelectric and ferroelectric properties.
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
E. Shahmohamadi, A. Mirhabibi, F. Golestanifard,
Volume 16, Issue 3 (9-2019)
Abstract
An accurate prediction of reaction kinetics of silicon nitridation is of great importance in designing procedure of material production and controlling of reaction. The main purpose of the present study is to investigate the effect of temperature on the kinetics of reaction bonded silicon nitride (RBSN) formation. To achieve this, nitrogen diffusion in the silicon nitride layer is considered as a reaction controlling factor and sharp interface method based on this theory is used to develop the analytical model. In the developed model, the variations in the size of silicon particles are calculated for the whole reaction. In the experimental phase, the extent of nitridation is measured for different reaction temperatures and 4 different reaction times and then, the occurrence of full nitridation is shown by EDS analysis. Furthermore, an analytical approach was established for describing the kinetics of compound formation and the performance of the developed model is evaluated through statistical analysis. There was good agreement between experimental data and predictions of the developed model which demonstrates the accuracy of considered presumptions and reaction mechanisms. An accurate prediction of reaction kinetics of silicon nitridation is of great importance in designing procedure of material production and controlling of reaction. The main purpose of the present study is to investigate the effect of temperature on the kinetics of reaction bonded silicon nitride (RBSN) formation. To achieve this, nitrogen diffusion in the silicon nitride layer is considered as a reaction controlling factor and sharp interface method based on this theory is used to develop the analytical model. In the developed model, the variations in the size of silicon particles are calculated for the whole reaction. In the experimental phase, the extent of nitridation is measured for different reaction temperatures and 4 different reaction times and then, the occurrence of full nitridation is shown by EDS analysis. Furthermore, an analytical approach was established for describing the kinetics of compound formation and the performance of the developed model is evaluated through statistical analysis. There was good agreement between experimental data and predictions of the developed model which demonstrates the accuracy of considered presumptions and reaction mechanisms.
A. Bahrami, F. Kazemi, J. Abdolahi Sharif,
Volume 17, Issue 1 (3-2020)
Abstract
Kinetic models are the most important instruments for predicting and evaluating the performance of flotation circuits. To determine the kinetic order and rate of flotation of a gilsonite sample, flotation experiments were carried out in both rougher and cleaner stages. Experiments conducted using the combinations of petroleum-MIBC, gas oil-pine oil, and one test without any collector and frother. Five first order kinetic models were applied to the data obtained from the flotation tests by using the Matrix Laboratory software. Statistical analysis showed that the classic first order model perfectly matched the rougher and cleaner results performed using petroleum-MIBC combination. The kinetic constants (k) were calculated as 0.04 (s-1) and 0.01 (s-1) for the rougher and cleaner, respectively. Rougher and cleaner tests without collector and frother also matched with the modified gas/solid adsorption and rectangular models with the k values of 0.05 (s-1), and 0.01 (s-1), respectively. The relationship between flotation rate constant, maximum combustible recovery and particle size were also studied. The results showed that the maximum flotation combustible recovery and flotation rate were obtained with an intermediate particle size both in the rougher and cleaner flotation processes. The combustible recovery and flotation rate in the rougher flotation process were higher than that in the cleaner flotation process.
E. Shahmohamadi, A. Mirhabibi, F. Golestanifard,
Volume 17, Issue 1 (3-2020)
Abstract
In the present study, a soft computing method namely the group method of data handling (GMDH) is applied to develop a new and efficient predictive model for prediction of conversion percentage of silicon. A comprehensive database is obtained from experimental studies in literature. Several effective parameters like time, temperature, nitrogen percentage, pellet size and silicon particle size are considered. The performance of the model is evaluated through statistical analysis. Moreover, the silicon nitridation was performed in 1573 k and results were evaluated against model results for validation of the model. Furthermore, the performance and efficiency of the GMDH model is confirmed against the two most common analytical models. The most effective parameters in estimating the conversion percentage are determined through sensitivity analysis based on the Gamma Test. Finally, the robustness of the developed model is verified through parametric analysis.
A. Kazazi, S. M. Montazeri, S. M. A. Boutorabi,
Volume 17, Issue 4 (12-2020)
Abstract
In the present study, austempering heat treatment was performed on compacted graphite aluminum cast iron with the chemical composition of 4.8%wt Al, 3.2%wt C, 0.81%wt Ni, 0.37%wt Mn, and 0.02%wt Mg. This study aims to investigate the effect of aluminum additions and removal of silicon on the kinetics of austempering transformation of Fe-3.2%C alloy. The cast samples were austenitized at 900 °C for 120 min and the isothermal austempering heat treatment was performed at 200 °C, 300 °C and 400 °C for 5, 30, 60, 120 and 180 minutes, respectively. Kinetics of this transformation was studied by X-Ray diffraction (XRD) analysis. The effect of temperature and time on the microstructure and hardness of the austempered samples was investigated and discussed. The presence of Al was seen to prolonged formation of the carbides from high carbon austenite, and that expanded the process window in the austempering transformation. Besides, the lower bainitic ferrite phase was observed in the austempered samples at 200 °C and 300 °C. Increasing austempering temperature to 400 °C changed the lower bainite to upper bainite structure. The volume fraction of austenite reached its maximum level (34.6 %) after austempering the samples at 400 °C for 30 minutes.
Shadi Moshayedi, Hossein Sarpoolaky, Alireza Khavandi,
Volume 19, Issue 2 (6-2022)
Abstract
In this paper, chemically-crosslinked gelatin/chitosan hydrogels containg zinc oxide nanoparticles (ZNPs), were loaded with curcumin (CUR), and their microstructural features, physical properties, curcumin entrapment efficiency, and drug release kinetics were evaluated using scanning electron microscopy (SEM), the liquid displacement method, and UV–Vis spectroscopy. The in vitro kinetics of drug release was also studied using First-order, Korsmeyer-Peppas, Hixon-Crowell, and Higuchi kinetic models. The SEM micrographs confirmed the formation of highly porous structures possessing well-defined, interconnected pore geometries. A significant reduction in the average pore sizes of the drug-loaded hydrogels was observed with the addition of ZNPs and CUR to the bare hydrogels. High value of drug loading efficiency (~ 72 %) and maximum drug release of about 50 % were obtained for the drug-loaded scaffolds. It was found that curcumin was transported via the non-Fickian diffusion mechanism. It was also shown that the kinetics of curcumin release was best described in order by Hixon-Crowell, Higuchi, and Korsmeyer-Peppas models, demonstrating that drug release was controlled by diffusion, degradation, and swelling of the drug carrier. However, lower degree of fitting was observed with First-order kinetic model.
Yaser Moazzami, Mahdi Gharabaghi, Ziadin Shafaei Tonkaboni,
Volume 19, Issue 4 (12-2022)
Abstract
Ionic liquids as green solvents with high thermal stability, recyclability, low flash point, and low vapor
pressure, have been considered as a viable alternative in hydrometallurgical processes. In this study the leaching
kinetics of chalcopyrite concentrate was investigated using 1-Butyl-3-methylimidazolium hydrogen sulfate
(BmimHSO4) as an acidic ionic liquid. The Effect of operational parameters, including temperature, BmimHSO4
concentration, H2O2 concentration, stirring speed, solid-to-liquid ratio, and particle size on the rate of copper
dissolution of CuFeS2 were examined systematically. The highest Cu efficiency (ca. 97%) was achieved using 40%
(w/v) BmimHSO4, 30 %v/v H2O2, and 10 g.L-1 solid to liquid ratio for particle sizes less than 37 μm at 300 rpm and
45°C after 180 min leaching time. Kinetics study using Shrinking Core Model (SCM) revealed that CuFeS2 leaching
process using BmimHSO4 follows chemical reaction-controlled process. Under these circumstances, the calculated
activation energy was 46.66 KJ/mol. Moreover, the orders of reaction with respect to BmimHSO4 and H2O2
concentration, solid to liquid ratio and particle size were estimated to be 0.539, 0.933, −0.676 and −1.101
respectively. The obtained Arrhenius constant was found to be 0.26 106. The calculation of apparent activation
energy using “time given to a fraction method” revealed that the leaching mechanism remains the same over the
course of time.
Chouchane Toufik, Sana Chibani, Ouahida Khireddine, Atmane Boukari,
Volume 20, Issue 1 (3-2023)
Abstract
In this work, blast furnace slag (BFS) was used as an adsorbent material for the removal of Pb(II) ions in solution in batch mode. The physico-chemical analyzes used indicated that the BFS is essentially composed of silica, lime, and alumina. Its specific surface area corresponds to 275.8m2/g and its PZC is around 3.8.
The adsorption study indicated that the maximum amount of Pb(II) adsorbed under optimum conditions (agitation speed (Vag): 150rpm; pH: 5.4; particle size (Øs): 300µm, T: 20°C) is 34.26mg/g after 50 minutes of agitation, and adsorption yield is best for feeble initial concentrations. The most appropriate isothermal model was that of Langmuir, and the adsorption speed was better characterized by the pseudo-second order kinetic model. The adsorption mechanism revealed that internal diffusion is not the only mechanism that controls the adsorption process; there is also external diffusion, which contributes enormously in the transfer of Pb(II) from solution to adsorbent. Thermodynamic study indicated that the Pb(II) adsorption on the blast furnace slag (BFS) was spontaneous, exothermic, and that the adsorbed Pb(II) is more ordered at the surface of the adsorbent. Finally, we estimate that BFS is a superb adsorbent for water containing Pb(II).
Mohammad Javad Sohrabi, Hamed Mirzadeh, Saeed Sadeghpour, Reza Mahmudi,
Volume 20, Issue 4 (12-2023)
Abstract
Deformation-induced α΄-martensite generally forms at shear bands in the coarse-grained austenite, while it nucleates at grain boundaries in the ultrafine-grained (UFG) austenite. The available kinetics models are related to the nucleation on the shear band intersections, and hence, their application to investigating the kinetics of α΄-martensite formation for the UFG regime cannot be justified. Accordingly, in the present work, the general Johnson–Mehl–Avrami–Kolmogorov (JMAK-type) model was implemented for comparing the kinetics of α΄-martensite formation in the UFG and coarse-grained regimes using an AISI 304L stainless steel. On the experimental front, the X-ray diffraction (XRD) patterns and the electron backscattered diffraction (EBSD) maps were used for phase and microstructural analyses, respectively. It was revealed that the simple JMAK-type model, by considering the dependency of the volume fraction of α΄-martensite on the strain, is useful for modeling the experimental data, predicting the nucleation sites based on the theoretical Avrami exponents, and characterizing the transformation kinetics at low and high strains.
Dewi Qurrota A'yuni, Hadiantono Hadiantono, Velny Velny, Agus Subagio, Moh. Djaeni, Nandang Mufti,
Volume 21, Issue 0 (3-2024)
Abstract
Rice husk carbon by-product from the industrial combustion is a promising source to produce a vast amount of activated carbon adsorbent. This research prepared rice husk-activated carbon adsorbent by varying the concentration of potassium hydroxide solution (5, 10, 15, 20 % w/v) and activation time (2, 4, 6, 8 hours). Fourier-transform infrared spectral characterization (FTIR) indicated a significant effect before and after activation, especially the presence of hydroxyl groups. Based on the iodine adsorption, the specific surface area of the produced-activated carbon was approximately 615 m2/g. Experimental results showed that increasing potassium hydroxide concentration and activation time increases the water vapor adsorption capacity of the activated carbon. Compared with the rice husk carbon, the KOH-activated carbon enhanced the water vapor adsorption capacity to 931%. In the adsorption observation, changing the temperature from 15 to 27 ℃ caused a higher water vapor uptake onto the activated carbon. Two adsorption kinetics (pseudo-first- and pseudo-second-order models) were used to evaluate the adsorption mechanism. This research found that rice husk-activated carbon performed a higher water vapor adsorption capacity than other adsorbents (silica gel, zeolite, and commercially activated carbon).
