Showing 6 results for Koli
Tavakoli A. H., Goudarzi M.,
Volume 1, Issue 3 (Apr 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.
M.r. Tavakoli Shoushtari, M. Goodarzi, H. Sabet,
Volume 15, Issue 4 (December 2018)
Abstract
In this study, the microstructure, hardness, and dry sliding wear behavior of the hardfaced layers made by a cored wire Fe-B-C-Ti alloy were investigated. St37 steel was used as the substrate and the deposition of the hardfaced layers was conducted by the flux cored arc welding (FCAW) process under single-, two-, and three-pass conditions. Dry sliding wear tests were performed by a pin-on-disk apparatus, based on ASTM-G99, at room temperature (250C) at the normal applied loads of 50, 100, and 150 N with a constant speed of 0.08 m/s for a sliding distance of 1000 m. The microstructural and phase analyses were carried out by field emission scanning electron microscopy (FE-SEM) and X-ray diffraction (XRD), respectively. The results showed that the hardfaced layer produced by the single-pass process contains TiC rectangular phase distributed within a matrix containing ferrite and the eutectic of (α-Fe2B). But, the hardfaced layers produced by the two- and three-pass process contain TiB2 hexagonal phase in addition to TiC, which prevents the formation of detrimental FeB phase around Fe2B and reduces the number of micro-cracks. Moreover, the sample hardfaced by the three-pass process had the best wear resistance due to the greater hardness resulted from the higher amounts of TiC and TiB2 phases. In addition, increasing the number of passes has led to the reduction of wear rate at all the three applied loads. At the applied load of 100 N, the wear mechanism for the all three hardfaced samples was an oxidation wear. However, at the applied load of 150 N, the wear mechanism was a combination of oxidation and delamination.
M. Tavakoli Harandi, M. Askari-Paykani, H. Shahverdi, M. Nili Ahmadabadi,
Volume 16, Issue 1 (March 2019)
Abstract
One-step and two-step annealing techniques were used to examine the relationship between microstructure and mechanical properties during compression tests in iron-based ribbons and nanostructured 1- and 2.5mm cylindrical rods. The X-ray diffraction, microstructural, and mechanical results showed that substituting Nb for Fe had a minor effect on glass-forming ability but increased the formability index. The novel two-step annealing process resulted in a remarkable formability index of 16.62 GPa, yield stress of 2830 MPa, ultimate strength of 3866 MPa, and 4.3% plastic strain. A ductile nanosized α-Fe framework and boron-containing nano precipitations, which caused Zener pinning effect, were responsible for these novel mechanical properties.
Hamed Tavakoli, Mohammad Reza Aboutalebi, Seyed Hosein Seyedein, Seyed Nezameddin Ashrafizadeh,
Volume 18, Issue 1 (March 2021)
Abstract
Separation of samarium and lutetium was investigated through solvent extraction from their mixed aqueous species using commercial extractants of D2EHPA and PC88A. The Response Surface Method (RSM) was utilized to design the solvent extraction experiments. In which, a Central Composite Design (CCD) was applied to set the optimum conditions for highest separation factors between Sm and Lu. Design of Experiments (DOE) was conducted by making use of four operating variables, namely initial pH of the aqueous solutions (A: 0.2–2.6), extractant concentration (B: 0.01-0.09 molar), mole fraction of D2EHPA in the extractant mixture (C: 0 - 0.8) and a type of acidic solution (D: sulfuric and nitric acid) at three levels. The results indicated that the initial pH was the most paramount variable in solvent extraction of samarium and lutetium, while in the case of lutetium, the molar fraction of D2EHPA in the mixed extractants was non-influential. The statistical model predictions were confirmed by experiments for both samarium and lutetium extraction with high validity parameter of 97 and 98%, respectively. The optimum conditions for samarium and lutetium separation were identified as: A=0.8, B= 0.05, C= 0.2 and D= sulfuric acid. According to the findings of the model, the desirability value at the optimum conditions was evaluated as about 0.93, in which 71% of lutetium was extracted while the amount of extracted samarium was only less than 1%.
Hamed Tavakoli, Mohammad Reza Aboutalebi, Hossein Seyedein, Seyed Nezameddin Ashrafizadeh,
Volume 18, Issue 3 (September 2021)
Abstract
Solvent extraction of samarium from aqueous solutions by two different types of extractants, namely D2EHPA and PC88A, in kerosene was investigated. Through identification of speciation diagrams, the chemically stable complexes of samarium in different acidic solutions (H2SO4, HCl and HNO3) were first investigated. Regarding the various types of samarium species in sulfate medium in comparison with other acidic environments, H2SO4 and HNO3 media were chosen to examine the extraction behavior of samarium complexes. Thermodynamic parameters of samarium extraction reactions by D2EHPA and PC88A from aqueous solutions of HNO3 and H2SO4 were calculated as ∆G∘ (D2EHPA-HNO3), , ∆G∘ (D2EHPA-H2SO4) , ∆G∘ (PC88A-HNO3), ∆G∘ (PC88A-H2SO4) equal to -5.58, 3.40, 6.70 and 14.26, and respective ΔHº values equal to -9.38, -2.75, 4.01 and 16.95 kJ/mol, respectively. According to the results, D2EHPA seemed to be a more efficient extractant than PC88A and nitric aqueous solution was a better media than the sulfuric one. The synergistic effect of binary extractants revealed that synergistic factors were 2.94 and 5.74 in sulfuric and nitric solutions, respectively, for a D2EHPA:PC88A ratio of 2:3. The compositions of extracted complexes by D2EHPA and PC88A in sulfuric and nitric solutions were SmH3A6 and SmH3B6, respectively. Thermodynamic parameters of extraction reactions were calculated to be Ke equal to 9.513, 0.254, 0.067, and 0.003 and ∆S∘ (D2EHPA-HNO3), , ∆S∘ (D2EHPA-H2SO4) , ∆S∘ (PC88A-HNO3), ∆S∘ (PC88A-H2SO4) equal to -12.75, -20.64, -9.03, and 9.03 (J mol-1), respectively.
Satish Ahire, Ashwini Bachhav, Bapu Jagdale, Thansing Pawar, Prashant Koli, Dnyaneshwar Sanap, Arun Patil,
Volume 21, Issue 2 (June 2024)
Abstract
Hybrid photocatalysts, comprising both inorganic and organic polymeric components, are the most promising photocatalysts for the degradation of organic contaminants. The nanocomposite, Titania-Polyaniline (TiO2-PANI) was synthesized using the chemical oxidative polymerization method. Various characterization techniques were employed to assess the properties of the catalysts. The ultraviolet diffuse reflectance spectroscopy (UV-DRS) analysis revealed that the TiO2 absorbs only UV light while the TiO2-PANI nanocomposite absorbs light from both UV and visible regions. The X-ray diffraction (XRD) results confirmed the presence of TiO2 (anatase) in both TiO2 nanoparticles and TiO2-PANI (Titania-Polyaniline) nanocomposite. The phases of the catalysts were verified through Raman, TEM, and SAED techniques where all results are in good agreement with each other. The average crystallite size of TiO2 nanoparticle and TiO2-PANI nanocomposite were 13.87 and 10.76 nm. The thermal stability of the catalysts was assessed by the Thermal gravimetric analysis (TGA) technique. The order of the thermal stability is TiO2 > TiO2-PANI > PANI. The crystal lattice characteristics were confirmed using Transmission electron microscopy (TEM). The surface area measurements were confirmed from the Brunauer-Emmett-Teller (BET) study and were employed for the evaluation of the photocatalytic efficiency of both, TiO2 nanoparticles and TiO2-PANI nanocomposite catalysts. The energy dispersive spectroscopy (EDS) study was employed for elemental detection of the fabricated materials. While Raman spectroscopy was employed for the chemical structure and the phase characteristics of the materials. The standard conditions for the degradation of the CF dye were 8 g/L of catalyst dosage, 20 mg/L of dye concentration, and a pH of 7. The TiO2-PANI nanocomposite exhibited superior efficiency as compared to pure TiO2 nanoparticles, achieving almost 100 % degradation in just 40 minutes.
