Authors: Hydralyn T. Gammad, Eugenie Marie A. Pranada, Pamela Marielle C. Gahol, Menandro C. Marquez
Abstract: The nanosized samarium doped tin oxide in varying concentration (0%, 0.5%, 1%, 3%, 5%) was successfully synthesized using the wet chemical precipitation approach. X-ray Diffraction (XRD) analysis was done to monitor the effect of the dopant concentration to the host lattice as broadening and narrowing of the formed peaks are seen. Average crystallite sizes of the produced sample are ranging from 9-28 nm, confirming it to be nanoscale. Identified peaks with Miller indices of ((110), (101), (200), (111), (211), (220), and (002) signifies a tetragonal rutile structure of the synthesized samples. Scanning Electron Microscopy (SEM) shows the difference in morphology for the powdered samples as per different samarium loading as well as the shape, which is granular. Energy Dispersive X-ray spectroscopy (EDX) affirms the successful integration of the samarium dopant to the lattice structure of the SnO2.
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Authors: R. Kazemzadeh, Aliasghar Behnamghader, Saeed Hesaraki
Abstract: In this research hydroxyapatite powder was synthesized by wet chemical method using calcium nitrate and diammonium hydrogen phosphate precursors at 2, 20, 50 and 90⁰ C. Phase composition, morphological aspects and particle size have been investigated using X-ray diffraction method (XRD), Fourier transform infra red spectroscopy (FTIR) and scanning electron microscopy (SEM). For the low synthesis temperature, products with low degree of crystallinity were obtained and the phases like calcium deficiency hydroxyapatite (CDHA) and hydroxyapatite were formed. In higher temperature ranges, higher degree of crystallinity was measured. For these samples, crystallite sizes estimated by scherrer formula and measured directly by SEM were found to be less than 100 nm. The synthesis temperature of 90°C has showed better results from crystallinity point of view. Considerable crystallinity of the powders produced in this research is almost comparable to that of conventional heat treatment used for enhancing the crystallinity.
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Authors: Ashari Maqsood, Kishwar Khan, Muhammad Anis-ur-Rehman, Muhammad Ali Malik
Abstract: Spinel ferrites, which have the general chemical composition MeFe2O4, (Me = Co, Zn, Ni) are of interest due to their electronic, magnetic and optical properties. Nanosized Co-Zr-Mn spinel ferrites with nominal composition CoFe2-2xZrxMnxO4 (0.1≤ x≤0.4) have been prepared by the co-precipitation route. The products are characterized by X-ray diffraction, scanning electron microscopy (SEM) at room temperature, dc electrical resistivity as a function of temperature and dielectric parameters in the frequency range of 100 Hz to 3 MHz are also measured. The lattice constants agree with usual spinel ferrites. The particle size calculated from X-ray data by the Scherrer formula is in the range of 28-30 nm, while the average particle size varies from 15-25 nm obtained from the SEM measurements, X-ray density (Dx), Porosity (P) and bulk density (Dm) for all the samples are calculated. The dc electrical resistivity decreased with the rise in temperature for all the samples, showing a semiconductor like behavior. From the dc electrical resistivity the activation energy and drift mobility are determined. Both the drift mobility and activation energy increase with a rise in x. The dielectric constant, dielectric loss and ac electrical resistivity as a function of frequency are also reported. The low field ac magnetic susceptibility measurement showed that the ferrimagentic transition temperature is in the range of 439±5 K to 658±5 K.
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Authors: Muhammad Anis-ur-Rehman, Muhammad Ali Malik, Kishwar Khan, Ashari Maqsood
Abstract: Mg-Co nano crystalline ferrites having general formula Mg1-xCoxFe2O4 (x=0, 0.05, 0.1, 0.15, 0.2, 0.25) were prepared by co-precipitation method. X-ray powder diffraction (XRD) patterns of the prepared samples show the formation single spinel phase. The crystallite size, lattice parameters and porosity of samples were calculated by XRD data analysis as function of cobalt concentration. The crystallite size for each sample was calculated using the Scherrer formula considering the most intense (3 1 1) peak lies in the range 27-35 nm. The lattice parameters increased with increase of cobalt concentration. It is because of the fact that cobalt has greater ionic radius then magnesium. The dielectric constant, dielectric loss tangent and ac electrical conductivity of the prepared samples is also measure. The observed variation in electrical and dielectric properties is explained on the basis of cations distribution among tetrahedral (A) and octahedral (B) sites. The variance in saturation magnetization, remanence magnetization and magnetic moment was also measured from BH curve of samples.
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Authors: Hua Min Kou, Jing Kun Guo, Jing Wang, Yu Bai Pan
Abstract: Coating process is attracting more and more attention in the preparation of
composite materials mainly due to its predominance in the improvement of the
uniformity for different phases. The formation of nanosize alumina shells on the
aluminum core particles by a wet-chemical based route was investigated and the
composite particles were characterized using TG/DSC, XRD, SEM, TEM, XPS. An
enhancement of cermet properties can be expected by using these coated particles as initial powders.
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