Search published articles


Showing 22 results for Nanoparticles

M. Shayestefar, A. R. Mashreghi, S. Hasani ,
Volume 40, Issue 1 (5-2021)
Abstract

Mn0.8Zn0.2Fe2-xDyxO4 (where x= 0, 0.025, 0.05, 0.075, 0.1) ferrite nanoparticles were synthesized by auto- combustion sol-gel method for the first time in this study. The effect of Dy-doping on the structural and magnetic properties of the produced specimens was examined using the X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), vibrating sample magnetometery (VSM), and field emission scanning electron microscope (FE-SEM). The results showed that a cubic spinel structure was formed in all of the synthesized specimens. It was also found that the addition of Dy increased the lattice parameter while decreased the average of crystallites size. Furthermore, the FE-SEM micrographs showed that Dy not only plays an effective role in reducing the agglomeration of nanoparticles and their distribution, but also reduces the average of particle size. It was also observed that the addition of Dy had no effect on the morphology of the synthesized nanoparticles. Investigation of the magnetic properties revealed a clear decrease in the saturation magnetization and coercivity by the Dy addition. So that the saturation magnetization of the samples decreased from 66.3 to 58.4 emu/g and the coercivity decreased from 78.5 to 71.9 Oe.

R. Bagheri, F. Karimzadeh, A. Kermanpur , M. Kharaziha,
Volume 40, Issue 2 (9-2021)
Abstract

A new method has been presented for the synthesis of copper (Cu)/copper oxide (CuO)-nanoparticles (NPs), based on the process of corrosion and oxidation of Cu-NPs on the surface of the gold electrode by nitric acid. Cu-NPs were deposited on the surface using potentiometric method. The high concentration of Cu-NPs was estimated by Differential Pulse Voltammetry (DPV). The process of growth and distribution of CuO-NPs on the surface of Cu-NPs using structural analysis of Fourier Transform Infrared Spectroscopy (FTIR) and X-ray diffraction (XRD) showed that nitrate was well absorbed and a sharp hydroxyl peak appeared and a phase of CuO NPs formed on the electrode surface. The surface morphology indicated that the average size reduced from about 150 nm to 50 nm in the presence of nitrate. This can be due to the oxidation of Cu nanoparticles on the surface and reduction of particle size compared to the absence of nitric acid. This simple and low-cost method can be used as a surface modification of antibacterial and active catalyst electrodes.


Page 2 from 2     

© 2024 CC BY-NC 4.0 | Journal of Advanced Materials in Engineering (Esteghlal)

Designed & Developed by : Yektaweb