Showing 7 results for Catalyst
Barzegar Alamdarit B., Ashrafi Zadeh S.n., Ashrafi Zadeh F.,
Volume 1, Issue 2 (6-2004)
Abstract
In the current research, the optimum conditions for the electrolytic deposition of TiO2 coatings on titanium pieces were experimentally investigated. Flat pieces of commercially available titanium with dimensions of 50 x20 x3 mm were used as the anode and cathode electrodes. The coatings were applied on the cathode in an electrolyte solution essentially from water and methanol, containing different amounts of TiCI4, and H202. Coatings of sufficient thickness and adequate adhesion to the substrate were obtained at the optimum conditions of theELD process. The latter conditions were electrode gap distance of 3 cm, TiCl4 concentration of 0.005M, H202 concentration of 0.1 M, current density of 35 mA/cm2, methanol/water volume ratio of 9, and pH of the electrolyte in the vicinity of 1.40. Results of XRD analysis revealed the presence of anatase crystals of titanium oxide in the coated layers, where the deposited coating was treated at some temperatures in the range of 400 to 600°C for a period of at least 2 hours. Scanning electron microscopy (SEM) pictures also confirmed the formation of a uniform coating layer with cracked suiface area. At the optimum conditions of the process coatings with thicknesses of up to 10 flm were easily obtained through the application of one to three deposited layers.
F. Torknik, M. Keyanpour-Rad, A. Maghsoudipour, G. M. Choi,
Volume 13, Issue 1 (3-2016)
Abstract
In order to further enhance the Ni/Ce 0.8Gd0.2O2-δ (Ni/GDC20) cermet anodic performance for low temperature solid oxide fuel cell (LT-SOFC), a study was conducted on the nanostructuring of NiO/GDC composite by only once wet-infiltration of rhodium chloride precursor. By using electrochemical impedance spectroscopy (EIS) analysis, the effect of only one drop of Rh-infiltrating solution on the anodic polarization resistance was examined using symmetric Ni–GDC20|GDC20|Pt electrolyte-supported cell at 400-600 °C. Nanostructural evolution before and after H 2 reduction at 600 °C and also after anodic performance test was investigated by atomic force microscopy (AFM), field emission scanning electron microscopy (FE-SEM), and transmission electron microscopy (TEM) techniques in comparison to the anode itself. Despite the fine distribution of Rh-infiltrated nanoparticles having average particle size of 11.7 nm, the results showed ineffectiveness and inability of the Rh nanoparticles to succeed in decreasing of anodic polarization resistance for H 2 oxidation reaction in LT-SOFC.
S. Komeili, M. Takht Ravanchi, A. Taeb,
Volume 14, Issue 1 (3-2017)
Abstract
A series of MAl2O4 (M=Ni, Zn, and Cu) aluminates were prepared by using impregnation method; the metal content of the products was ranged between 5wt% to 25wt%. The samples were characterized by x-ray diffraction (XRD), Brunauer Emmett Teller (BET) surface area, NH3 temperature-programmed desorption (NH3-TPD), and inductively coupled argon plasma (ICP).
The specific surface areas of zinc, nickel and copper aluminates were in the ranges of 47-77m2/g, 63-87m2/g and 1.6-3m2/g, respectively. The surface acidity decreased in the order of CuAl2O4<< NiAl2O4< ZnAl2O4<< Al2O3. By increasing the amount of metals in the samples, the number of acidic sites decreased, but their strength did not significantly change. Ni-aluminates have fewer acidic sites than Zn-aluminates, particularly in strong acid sites
M. Palizdar, Z. Aslam, R. Aghababazadeh, A. Mirhabibi, P. Sangpour, Z. Abadi, Y. Palizdar, R. Brydson,
Volume 16, Issue 4 (12-2019)
Abstract
In this paper the chemical interaction between catalyst and support has been studied to understand the observed different growth rate of CNTs in our previous paper. Both pure MgO and Mg(NO3)2 . 6H2O as sources of the MgO catalyst support and Fe2(SO4)3 · xH2O as the source of the Fe catalyst, were employed. A Fe catalyst supported on MgO has been synthesized using the wet impregnation method followed by calcination. To compare the catalyst grain size and its distribution, the sample were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray powder diffraction (XRD) and BET specific surface area (SSA) measurement and X-ray photoelectron spectroscopy (XPS). XPS technique have utilized complementary to demonstrate the existence of chemical interaction between MgO support and Fe catalyst. Results revealed that the type of precursor used to prepare the support has a significant influence on the morphology of the support and the associated distribution of the Fe catalysts. The highest yield of MgFe2O4 phase was obtained using a pure MgO precursor which after calcination results in a homogenous distribution of nano-sized Fe particles over the support surface
Saba Payrazm, Saeid Baghshahi, Zahra Sadeghian, Amirtaymour Aliabadizadeh,
Volume 19, Issue 3 (9-2022)
Abstract
In this research, zinc oxide quantum dots and graphene nanocomposites were synthesized via two different methods; In the first (direct) method, ZnO-graphene Nanocomposites were made mixing the synthesized zinc oxide and graphene. In the second (indirect) method, zinc nitrate, graphene, and sodium hydroxide were used to made ZnO-graphene Nanocomposites. XRD, FTIR and Raman spectroscopy analyses were used for phase and structural evaluations. The morphology of the nanocomposites w::as char::acterized by SEM. The specific surface area and porosity of the samples were characterized by BET analysis. The optical properties of the samples were investigated by photoluminescence and ultraviolet-visible spectroscopy analyses. Results showed that using graphene, increased the photoluminescence property and shifted the photoluminescence spectrum of the composites towards the visible light spectrum. The photoluminescence of the synthesized graphene-zinc oxide composite, in the visible light region, was closer to white light than that of pure zinc oxide. According to the results of BET test, the nanocomposite synthesized by direct method had a higher surface area (25.7 m2.g-1) and a higher porosity (0.32 cm3.g-1) than the nanocomposite synthesized by the indirect method with a specific surface area of (16.5 m2.g-1) and a porosity of 0.23 cm3.g-1).
Salihah Alkhobrani, Hossein Bayahia, Fares T. Alshorifi,
Volume 20, Issue 3 (9-2023)
Abstract
In this study, CoFe2O4 (CoF) and ZnFe2O4 (ZnF) photocatalysts were successfully prepared by a facile and simple chemical precipitation method for degradation of methylene blue (MB) and methyl orange (MO) dyes under direct sunlight irradiation. The obtained ferrites were then characterized through XRD, TEM, EDS, UV-vis, and SEM. XRD and TEM results exhibited cubic nanostructures with sizes ranging from 9 to 16 nm and 11 to 18 nm for ZnF and CoF, respectively. SEM images showed homogenous, porous flat surfaces. EDS spectra confirmed the successful synthesis of ZnF and CoF nanostructures with high purity. UV-vis spectra results of MB and MO dyes showed maximum sunlight absorbance in the absence of ZnF and CoF, while a regular decrease in the sunlight absorbance was observed in the presence of ZnF and CoF within 15-60 min. The UV-vis results also showed that ZnF had higher photocatalytic activity than CoF. The experimental findings showed that the highest % degradation was 92.89% and 96.89% for MO and MB dyes, respectively, over ZnF compared to CoF photocatalyst (87.55% and 88.41% for MO and MB, respectively). These findings confirm that porous ZnF and CoF nanostructures are critical in promoting the degradation of dyes under sunlight instead of UV-vis light lamps that consume/require electrical energy.
Mohammad Derakhshani, Saeed Rastegari, Ali Ghaffarinejad,
Volume 21, Issue 2 (6-2024)
Abstract
In this research, a nickel-tungsten coating as a catalyst for hydrogen evolution reaction (HER) with different current densities was synthesized and the resulting electrocatalytic properties and morphology were assessed. Linear sweep voltammetry (LSV), electrochemical impedance spectroscopy (EIS), and chronoamperometry in 1 M NaOH were used to evaluate the electrocatalytic activity for HER. By increasing the current density of electrodeposition up to 500 mA/cm2, a columnar morphology was observed. The cyclic voltammetry test (CV) revealed that when the plating current density increases, Cdl has increased from 248 to 1310 µF/cm2 and the active surface area increases 5 times. The results showed that by modifying the coating morphology, the current density of the hydrogen evolution increased up to two times.
