Showing 21 results for Energy
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. 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.
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. 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
Karmous Mohamed Salah,
Volume 9, Issue 2 (6-2012)
Abstract
Atomistic simulations are carried out for zeolite with ABW framework. The structure is modeled and force field simulations are preformed to investigate its elastic properties, bulk, shear modulus and auxeticity. Bulk moduli (Ks), Shear moduli (G), and Poissons ratios (ν) were found to be Ks=79.71725 GPa, G=16.93265 GPa, νxy = -0.2207, νxz= -0.5730, νyx= -0.71717, νyz=0.87013, νzx= -0.33097 and νzy=1.54568 for ABW the negative value of Poisson’s ratios reflects an auxetic behavior of material. An evaluation of the directional young’s moduli shows that the compressibility of ABW is not uniform along [100], [010] and [001] axes. All calculations were performed using GULP program.
A. Karimbeigi, A. Zakeri, A. Sadighzadeh,
Volume 10, Issue 3 (9-2013)
Abstract
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
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.
R. Zarei Moghadam, M.h. Ehsani, H. Rezagholipour Dizaji, M.r. Sazideh,
Volume 15, Issue 3 (9-2018)
Abstract
In this work, Cadmium Telluride (CdTe) thin films were deposited on glass substrates at room temperature by vacuum evaporation technique. The deposited CdTe thin films were characterized by X-ray diffraction, UV-Visible spectroscopy and Field emission scanning electron microscope (FESEM) techniques. Structural studies revealed that the CdTe films deposited at various thicknesses are crystallized in cubic structure. The results showed the improvement of the film crystallinity upon grain size increment. Optical constants such as refractive index (n), extinction coefficient (k), real and imaginary parts of dielectric constant, volume energy loss function (VELF), and surface energy loss function (SELF) were calculated using UV-Vis spectra. In addition, band gap and Urbach energies were calculated by Tauc and ASF methods. The band gap energy of the specimens was found to decrease from 1.8 to 1.4eV with increasing the thickness of films. The absorption coefficient, computed and plotted versus the photon energy (hν) and tailing in the optical band gap, was observed which is understood based on Urbach law. Urbach energy variation from 0.125 to 0.620 eV in the samples with higher thicknesses is concluded.
H. Esfandiar, S. M. Hashemianzadeh, S. Saffary, S. Ketabi,
Volume 15, Issue 3 (9-2018)
Abstract
Gold nanoparticles have become common in many applications of biotechnology due to their specific properties. Shape and size are important attributes which affect their solubility in water. In this study, the outcomes of Monte Carlo Simulation for the solvation of gold nanorods in aqueous solution with the different radii, in terms of solvation free energy, are discussed. Simulation results show a negative solvation free energy for all the samples with radii of 4 to 9Å. The results show that the absolute values of solvation free energy for gold nanorods with smaller radius are larger, which indicate the dependency between the gold nanorods solvation and their radius.
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.
T. Mandal, D. Roy,
Volume 17, Issue 1 (3-2020)
Abstract
Magnetic iron oxide nanomaterials (MIONs) have been extensively investigated for the various important applications. Coprecipitation, hydrothermal, high temperature decomposition of organic precursors, microemulsions, polyol methods, electrochemical methods, aerosol method, sonolysis and green synthesis processes for the fabrication of MIONs have been reviewed. Different characterization methods like XRD, SEM, EDX and TEM for the as prepared MION materials have been studied. Important applications of MIONs in the field of biomedical, nanorobotics and energy devices have also been addressed in this review. Target oriented drug delivery and hyperthermia applications of MIONs have also focused
Mohammad Ali Maghsoudlou, Reza Barbaz Isfahani, Saeed Saber-Samandari, Mojtaba Sadighi,
Volume 18, Issue 2 (6-2021)
Abstract
The low velocity impact (LVI) response of pure and glass fiber reinforced polymer composites (GFRP) with 0.1, 0.3 and 0.5 wt% of functionalized single-walled carbon nanotubes (SWCNTs) was experimentally investigated. LS-DYNA simulation was used to model the impact test of pure and incorporated GFRP with 0.3 wt% of SWCNT in order to compare experimental and numerical results of LVI tests. All tests were performed in two different levels of energy. In 30J energy, the specimen containing 0.5 wt% SWCNT was completely destructed. The results showed that the incorporated GFRP with 0.3 wt% SWCNT has the highest energy absorption and the back-face damage area of this sample was smaller than other specimens. TEM images from specimens were also analyzed and showed the incorporation of well-dispersed 0.1 and 0.3 wt% of SWCNT, while in specimens containing 0.5 wt% of CNT, tubes tended to be agglomerated which caused a drop in LVI response of the specimen. The contact time of impactor in numerical and experimental results was approximately equal; however, the maximum contact forces in LS DYNA simulation results were higher than the experimental results which could be due to the fact that in the numerical modeling, properties are considered ideal, unlike in experimental conditions.
Sara Ahmadi, Bijan Eftekhari Yekta, Hossein Sarpoolaky, Alireza Aghaei,
Volume 18, Issue 4 (12-2021)
Abstract
In the present work, monolithic gels were prepared through different drying procedures including
super critical, infrared wavelengths and traditional drying methods. Dense and transparent glasses
were obtained after controlled heat treatment of the dried porous xerogels in air atmosphere.
The chemical bonding as well as different properties of the prepared gels and the relevant glasses
were examined by means of Fourier transform infrared spectroscopy (FTIR), Brunauer-Emmitt-
Teller (BET) and UV-Vis spectrometer. Based on the obtained results, different drying conditions
affect the average pore size and the total pore volume of the studied gels. The mean pore size was
found to be 8.7 nm, 2.4 nm and 3.2 nm for super critical, IR radiation and slow drying in air
atmosphere, respectively. The glass network structure was significantly changed by heat treatment temperature so that the B-O-Si bonds were formed only after 450 °C. It was found that the gel dried under super critical condition was unable to reach to its full density all over the selected sintering temperature interval.
Nihel Hsouna, Mohsen Mhadhbi, Chaker Bouzidi,
Volume 19, Issue 1 (3-2022)
Abstract
Phosphate glass with different Al2O3 and Na2CO3 compositions [80NaH2PO4-(20-x) Na2CO3-xAl2O3 with a step from 0 to 4] were prepared through melt quenching technique furnace at 900 °C. In order to determine the structure and microstructure modification of the samples after heat treatment the IR and Raman spectroscopy were performed. The X-ray diffraction (XRD) result shows an amorphous character of the prepared glass. The result obtained by differential scanning calorimetry (DSC) reveals a good thermal stability in the temperature range of 25 to 400 °C. The impedance Nyquist diagrams were investigated and modeled by resistors and constant phase elements (CPE) equivalent circuits. These measurements show a non-Debye type dielectric relaxation. Both AC and DC conductivity, dielectric constant, and loss factors were determined. Thermal activation energies were also calculated. A changes in the electrical conductivity and activation energy depend upon the chemical composition were observed. Also, a transition in the conduction mechanism from ionic to mixed ionic polaronic was noted. In the same line, electrical modulus and dielectric loss parameters are also deduced. Their frequency and temperature dependency exhibited relaxation behavior. Likewise, activation energies value obtained from the analysis of M’’ and those obtained from the conductivity are closes, which proves the optimal character of the preparation conditions.
Nouar Sofiane Labidi,
Volume 19, Issue 1 (3-2022)
Abstract
The synthesed foam-shaped zeolite ZSM-5 material w:::as char:::acterized by X-ray diffraction (XRD), (FTIR) spectroscopy, scanning electron microscopy (SEM) and BET technique. The adsorption performances of the material were evaluated for the basic blue-41 dye removal. A maximum removed amount of 161.29 mg/g at 323K was achieved. Experimental kinetic data of this new adsorbent fitted well the pseudo-second order model. The apparent diffusion coefficient values was in the range of 10-12 cm2/s. The regeneration tests revealed that the adsorption efficiency of the foam-shaped zeolite was retained after three regeneration runs, with a loss of 6% of the original adsorbed value.
Sonali Wagh, Umesh Tupe, Anil Patil, Arun Patil,
Volume 19, Issue 4 (12-2022)
Abstract
Temperature is one of the key factor that affecting the electrical, physical, structural, and morphological properties as well as the crystallinity of the nanomaterials. The current study investigates the effect of annealing temperature on the structural and electrical properties of lanthanum oxide (La2O3) thick films. La2O3 thick films were prepared on a glass substrate using a conventional screen printing technique. In this work, T1 is an unannealed prepared film, whereas T2 and T3 are annealed in a muffle furnace for 3 hours at 350°C and 450°C, respectively. XRD technique was exploited to investigate the crystallization behavior of the films. It was found that the crystal structure of La2O3 thick films are pure hexagonal phase. The annealing temperatures were revealed to have influence on the crystallite sizes of the films. SEM and EDS was used to study the morphology and elemental analysis of the films respectively. The electrical properties of the films were explored by measuring resistivity, temperature coefficient of resistivity (TCR), and activation energy at lower and higher temperatures regions. The film annealed at 450°C has high resistivity, a high TCR, and small crystallite size. The thickness of the La2O3 thick films was also found to decrease as the annealing temperature increased.
Bijan Eftekhari Yekta, Omid Banapour Ghafari,
Volume 20, Issue 4 (12-2023)
Abstract
Glasses in the B2O3-Li2 (O, Cl2, I2) system were prepared through the conventional melt-quenching method. Then, the conductivity of the molten and glassy states of these compositions was evaluated. Furthermore, the thermal and crystallization behavior of the glasses was determined using simultaneous thermal analysis (STA) and X-ray diffractometry (XRD). The electrical conductivity of the melts was measured at temperatures ranging from 863 to 973 K, and the activation energy of the samples was calculated using the data obtained from ion conduction in the molten state and found to be in the vicinity of 32 kcal/mol. In glassy states, electrical conductivity was also measured. To determine this property, the electrochemical impedance spectroscopy method (EIS) was used. In the molten state, temperature played an important role in the ion conductivity; however, at lower temperatures, other factors became important. Based on the results, the addition of LiI and LiCl to the B2O3-Li2O base glass system (75 B2O3, 10 Li2O, 7.5 LiI, 7.5 LiCl) (mol%) increases the ionic conductivity of the glass from 3.2 10-8 S.cm-1 to 1.4 10-7 S.cm-1 at 300 K.
Yugen Kulkarni, Niketa Pawar, Namrata Erandole, Muskan Mulani, Mujjamil Shikalgar, Swapnil Banne, Dipali Potdar, Ravindra Mane, Smita Mahajan, Prashant Chikode,
Volume 21, Issue 1 (3-2024)
Abstract
The paper investigates the solar photodegradation of Methylene Blue dye using copper oxide (CuO) thin films synthesized by the Successive Ionic Layer Adsorption and Reaction (SILAR) method. The structural, morphological, and optical characteristics of the CuO thin films have been investigated by employing a variety of methods, such as Fourier transform Infrared (FTIR) spectroscopy, UV-Vis spectroscopy, Scanning electron microscopy (SEM), and X-ray diffraction (XRD). The outcomes showed that CuO thin films with excellent surface shape and a highly crystalline nature had been successfully deposited. Methylene Blue was subjected to solar radiation during its photodegradation process, and the outcomes showed a significant decrease in the dye's concentration over time. To maximize the photo degradation process, the effects of other experimental factors were also assessed, such as the starting concentration of MB, the quantity of CuO thin film, number of SILAR cycles and the pH of the solution. Good photocatalytic activity is demonstrated by CuO thin films produced using the SILAR approach in the solar photodegradation of methylene blue. The development of affordable and ecologically friendly wastewater treatment technology that can use sun energy to break down persistent organic contaminants is affected by these findings.
