Showing 6 results for Tio2
S. Mirtalebi , D. Ghasemi ,
Volume 33, Issue 2 (3-2015)
Abstract
In the present study, pure Aluminum powder with 5%wt Titanium Dioxide was mechanically milled at different times. Using phase analysis through X-ray diffraction (XRD), it was found that increasing of the milling times over 10 hours causes the reduction of Titanium by Aluminum and formation of Al2O3 in the structure. Also, it was shown that if the process persists, Aluminum reacts with Titanium and causes the formation of Al3Ti in the composition. The reactions were studied through the thermodynamic relations. Furthermore, after distribution of reinforcement particles in the matrix,
using X-ray diffraction peak broadening, according to Williamson-Hall equation, the mean crystallite size and lattice strain were determined, and by scanning electron microscopy (SEM), the structure and morphology of the powder particles were studied.
N. Sharifi,
Volume 34, Issue 3 (12-2015)
Abstract
Conventionally, a film of TiO2 particles of ~300 nm size is employed in DSCs as the back reflector film to enhance the light harvesting. In this study, two electrolytes with different transparencies, iodide-based and cobalt-based electrolytes, were used to investigate the transparency effect of electrolytes on light back-scattering from back scattering layer and also to study its effect on the performance of DSCs. The use of cobalt-based electrolyte is recommended from the view point of optical properties as due to the light absorption in electrolytes, the current density losses are 2.9mA/cm2 and 4.2 mA/cm2 in cobalt- and iodide-based electrolytes, respectively, and the transmission of 100% is observed for cobalt-based electrolyte in 500-600 nm in spite of iodide-based electrolyte. Use of light back-scattering layer, unlike iodide-based cell, causes external quantum efficiency in cobalt-base cell to increase for the wavelengths lower than 350 nm since cobalt-base electrolyte has transparency in this region. In addition, optical calculations demonstrate that in the range 400-500 nm, in which dye has a noticeable absorption, absorption loss is 40% and 30% for iodide- and cobalt-based electrolytes, respectively.
S. Bassaki, F. Golestani Fard, R. Naghizadeh, M. Rashidzadeh,
Volume 34, Issue 3 (12-2015)
Abstract
Titanium dioxide-nickel oxide porous coatings were synthesized by Plasma Electrolytic Oxidation (PEO)/ ElectroPhoretic Deposition (EPD) in one step and within a short time. The main purpose of this research was to increase photocatalytic activity of titanium oxide by increasing surface area and coupling of titanium oxide with nickel oxide. Applied voltage effects on phase structure, surface morphology and photocatalytic efficiency of coatings were studied. Phase structure and surface morphology of the synthesized catalysts were investigated by XRD and SEM, respectively. Photocatalytic efficiency of the samples was studied through measuring the decomposition rate of 4-chlorophenol. The results showed that the coatings mainly consisted of anatase and nickel oxide phases whose amounts in coatings increased with the voltage. There was an enhancement of the photocatalytic efficiency in TiO2/NiO composite coatings compared with TiO2 coatings. Besides, there was an optimum amount of NiO to reach maximum photocatalytic efficiently.
S. Daneshvar E Asl, S. Kh. Sadrnezhaad,
Volume 37, Issue 2 (9-2018)
Abstract
Rutile-phase titanium dioxide nanorod arrays were prepared by the hydrothermal method. Then, anatase-phase nanoleaves were successfully synthesized on the nanorod arrays via mild aqueous chemistry. Nanorod arrays scanning electron microscopy revealed that the thin film is uniform and crack free and the average diameter and height of the nanorods are 90 nm and 2 µm, respectively. Furthermore, nanorods are vertical to the substrate surface and have desired coverage density due to the predeposition of TiO2 seed layer which leaded to decrease the surface roughness of the substrate. Nanoleafed nanorods scanning electron microscopy indicated that the nanoleaves were grown uniformly on the entire surface of nanorods and the specific surface area and roughness factor of those are significantly improved. Energy dispersive spectrums suggested that F- and Cl- ions are partially doped into TiO2 crystals. Raman and X-ray spectra confirmed the formation of anatase-phase nanoleaves on the rutile-phase nanorods. X-ray diffraction also indicated that the nanorod arrays are highly oriented with respect to the substrate surface. The diffused reflectancetransmittance data revealed the incident light was more efficiently harvested by the nanoleafed nanorod thin film and the values of energy gap are 2.78 and 2.82 eV for rutile TiO2 nanorod and rutile+anatase TiO2 nanoleafed nanorod thin films, respectively. Synthesized nanostructure, having improved charge separation and transfer (due to the presence of the surface anatase/rutile junctions), high specific surface area and light harvesting (due to the presence of the nanoleaves) and low band gap energy (due to the nonmetallic elements doping), is viable alternative to traditional single crystalline TiO2 nanorods for highly efficient photoelectrochemical applications.
A. Razmjou, F. Noorisafa, N. Emami,
Volume 37, Issue 4 (3-2019)
Abstract
Polyurethane polymer plays an important role in health care, and it is widely used in medical devices and instruments. However, the low biocompatibility and biofilm formation on the surface can be regarded as a challenging issue. Engineering the wetting capability of the surface is an effective way to increase the biodegradability of polymer surfaces with sufficient bulk properties. In this study, the surface modification of polyurethane sheets by a thin layer of polyethylene glycol and trapping of titanium dioxide nanoparticles were carried out by means of physical and chemical changes on the surface to enhance the biocompatibility. The physicochemical properties of the modified surfaces were determined using fourier-transform infrared (FTIR) spectroscopy , scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and contact angle and free surface energy measurement. The biocompatibility of the modified levels was evaluated using the MTT toxicity test on cervical cancer cells (HeLA), bacterial adhesion, biofilm formation, and the protein absorption assay by the Bradford method. A thin, autoclave able and inexpensive thin layer with a solid and stable roughening structure was created covalently on the surface of the polyurethane plates for biological and medical applications. The results, therefore, showed that apart from antibacterial activity, the modified sample also had the ability to reduce the biofilm formation, such that the maximum biofilm attachment inhibition in the first 24 hours was 94% higher than that of the modified sample.
A. Azimi-Fouladi , S.a. Hasanzadeh-Tabrizi,
Volume 41, Issue 2 (11-2022)
Abstract
Water pollution is one of the big problems of human societies, and the need to find new ways to remove these pollutants has been given much attention in recent years. One of the methods is the use of photocatalysts. In this research, TiO2 and TiO2-CdO nanoparticles were prepared by a sol-gel method as nano photocatalysts. The produced samples have been used to degrade methylene blue under UV light. To characterize the prepared samples, X-ray Diffraction (XRD), Field Emission Scanning Electron Microscope (FESEM), X-ray Energy Diffraction Spectroscopy (EDS), and Ultraviolet-Visible Spectroscopy (UV-Vis) were used. Microstructural results revealed nanoparticles with dimensions of 18 to 32 nm. XRD results showed that the main phase formed was the anatase. TiO2-4 wt.% CdO nanocomposite showed more photocatalytic activity compared to pure TiO2. Also, the effect of pH, irradiation time, and amount of powder on photocatalytic activity was investigated. The results showed that at pH=9, time of 75 min, and using 0.02 g TiO2-4 wt.% CdO photocatalyst, the maximum photocatalytic activity of about 92 % was obtained.
