Magnesium Ferrite (MgFe2O4) Nanostructures Fabricated by Electrospinning

Magnesium ferrite (MgFe2O4) nanostructures were successfully fabricated by electrospinning method. X-ray diffraction, FT-IR, scanning electron microscopy, and transmission electron microscopy revealed that calcination of the as-spun MgFe2O4/poly(vinyl pyrrolidone) (PVP) composite nanofibers at 500–800 °C in air for 2 h resulted in well-developed spinel MgFe2O4nanostuctures. The crystal structure and morphology of the nanofibers were influenced by the calcination temperature. Crystallite size of the nanoparticles contained in nanofibers increased from 15 ± 4 to 24 ± 3 nm when calcination temperature was increased from 500 to 800 °C. Room temperature magnetization results showed a ferromagnetic behavior of the calcined MgFe2O4/PVP composite nanofibers, having their specific saturation magnetization (Ms) values of 17.0, 20.7, 25.7, and 31.1 emu/g at 10 Oe for the samples calcined at 500, 600, 700, and 800 °C, respectively. It is found that the increase in the tendency ofMsis consistent with the enhancement of crystallinity, and the values ofMsfor the MgFe2O4samples were observed to increase with increasing crystallite size

Preparation of Pectin–ZnO Nanocomposite

Pectin–ZnO nanocomposite was prepared in the aqueous solution condition at room temperature. The Fourier transform infrared, X-ray diffraction, and transmission electron microscope (TEM) measurements confirmed the nanoscaled structure of pectin–ZnO composite. According to the TEM observation, the average composite granules size was about 150 nm and the embedded ZnO nanoparticles were uniform with an average diameter of 70 nm

Magnetic and Cytotoxicity Properties of La1−xSrxMnO3(0 ≤ x ≤ 0.5) Nanoparticles Prepared by a Simple Thermal Hydro-Decomposition

This study reports the magnetic and cytotoxicity properties of magnetic nanoparticles of La1−xSrxMnO3(LSMO) withx = 0, 0.1, 0.2, 0.3, 0.4, and 0.5 by a simple thermal decomposition method by using acetate salts of La, Sr, and Mn as starting materials in aqueous solution. To obtain the LSMO nanoparticles, thermal decomposition of the precursor was carried out at the temperatures of 600, 700, 800, and 900 °C for 6 h. The synthesized LSMO nanoparticles were characterized by XRD, FT-IR, TEM, and SEM. Structural characterization shows that the prepared particles consist of two phases of LaMnO3(LMO) and LSMO with crystallite sizes ranging from 20 nm to 87 nm. All the prepared samples have a perovskite structure with transformation from cubic to rhombohedral at thermal decomposition temperature higher than 900 °C in LSMO samples ofx ≤ 0.3. Basic magnetic characteristics such as saturated magnetization (MS) and coercive field (HC) were evaluated by vibrating sample magnetometry at room temperature (20 °C). The samples show paramagnetic behavior for all the samples withx = 0 or LMO, and a superparamagnetic behavior for the other samples havingMSvalues of ~20–47 emu/g and theHCvalues of ~10–40 Oe, depending on the crystallite size and thermal decomposition temperature. Cytotoxicity of the synthesized LSMO nanoparticles was also evaluated with NIH 3T3 cells and the result shows that the synthesized nanoparticles were not toxic to the cells as determined from cell viability in response to the liquid extract of LSMO nanoparticles

Thermal shock resistance of sintered alumina/silicon carbide nanocomposites

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Thermal shock of ground and polished alumina and Al(2)O(3)/SiC nanocomposites

The thermal shock behaviour of sintered alumina and alumina/SiC nanocomposites with 1, 2.5 and 5 vol.% SiC was studied. The thermal shock testing was carried out by means of quenching into water from high temperatures (ΔT in the range 0-750 °C). Both single shocks and repeated shocks were used. The damage introduced by thermal shock was characterised by degradation of strength in four-point bending and by changes in Young's modulus. The effects of the surface finish of the test specimens (either ground or highly polished surfaces) on the thermal shock resistance were also studied. In both alumina and nanocomposite materials, specimens with ground surfaces showed a better resistance to thermal shocks than specimens with polished surfaces. However, the resistance of the nanocomposite material to single and repeated thermal shocks was no better than that of the pure alumina. © 2002 Elsevier Science Ltd. All rights reserved

Anomalous change in dielectric constant of CaCu3Ti4O12 under violet-to-ultraviolet irradiation

The influence of light illumination on the dielectric constant of CaCu3Ti4O12 (CCTO) polycrystals is studied in this work. When exposed to 405-nm laser light, a reversible enhancement in the room temperature capacitance as high as 22% was observed, suggesting application of light-sensitive capacitance devices. To uncover the microscopic mechanisms mediating this change, we performed electronic structure measurements, using photoemission spectroscopy, and measured the electrical conductivity of the CCTO samples under different conditions of light exposure and oxygen partial pressure. Together, these results suggest that the large capacitance enhancement is driven by oxygen vacancies induced by the irradiation.Publisher PDFPeer reviewe

Thermal shock resistance of sintered alumina/silicon carbide nanocomposites evaluated by indentation techniques

The thermal shock resistance of sintered Al2O3/1, 2.5, and 5 vol% SiC nanocomposites was studied using two indentation techniques. In the first technique, "indentation thermal shock" measurements were made of the extension of median/radial cracks around Vickers indentations after quenching from various temperatures (up to 480°C) into a bath of boiling water. This technique allowed a critical thermal shock temperature, ΔTCInd, to be quantitatively evaluated. In the second technique, "indentation fatigue" tests were conducted on the thermally shocked specimens; repeated indentations were made at the same site, and the number of load cycles needed to initiate lateral fracture was measured. The results showed that nanocomposites with an addition of SiC nanophase as low as 1 vol% had a thermal shock resistance superior to that of pure Al2O3