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1.
Nano-aluminum-phosphate (AlPO4) powder has been synthesized by an ethylene glycol (EG), polymerization, complexation route. The AlPO4 powder has a particle size ≤10 nm via TEM. The differential thermal analysis (DTA) and the thermo-gravimetric analysis (TGA) show complete burn-out of organics is achieved ≤680 °C and crystallization initiates ≤500 °C. X-ray diffraction (XRD) shows crystallization is well developed by 700 °C. Scanning electron microscopy shows a fine grain size with fused edges indicating partial sintering of the powder at 900 °C.  相似文献   

2.
β-Ga2O3 nanocolumns straightened and crossed perpendicularly each other were deposited on MgO (1 0 0) substrate by vapor phase transport method. Growth of the nanocolumns was examined at steps of 1000, 1050, and 1200 °C in elevation of source-boat temperature. We have drawn out the substrate from deposition-tube at each source-boat temperatures of 1000, 1050, and 1200 °C. Scanning electron microscopy of the sample with source-boat temperature of 1200 °C demonstrated that the straightened and elongated nanocolumns are crossing perpendicularly each other. Typical lengths of the nanocolumns were in the range of several hundreds nanometers below 1050 °C, and those of 1200 °C were in the range of ten to fifteen hundreds nanometers. Diameters of the nanocolumns stayed in the range of few hundreds nanometers, notwithstanding variation of the source temperature. X-ray diffraction and transmission electron microscopy with energy dispersive X-ray spectroscopy revealed that the nanocolumns are monoclinic β-Ga2O3 crystal, and the (4 0 0) plane of β-Ga2O3 nanocolumns is parallel to the (1 0 0) plane of MgO substrate.  相似文献   

3.
Calcium phosphate ceramic such as hydroxyapatite (HA) is good candidate for bone substitutes due to their chemical and structural similarity to bone minerals. The bone mineral consists of tiny hydroxyapatite crystals in the nanoregime. Nanostructured hydroxyapatite is also expected to have better bioactivity than coarser crystals. This paper reports on the preparation and in vitro evaluation of bone-like hydroxyapatite nanopowder. The sol–gel prepared hydroxyapatite nanopowder was characterized for its phase purity, chemical homogeneity and bioactivity. Fourier transform infrared (FTIR) spectroscopy was used to identify the functional groups. X-ray diffraction (XRD) analysis was carried out to study the phase composition, crystallinity and the crystallite size of hydroxyapatite nanopowders that were sintered at different temperatures. The in vitro test was performed in a stimulated body fluid (SBF) medium. The changes of the pH of SBF medium were measured at pre-determined time intervals using a pH meter. The dissolution of calcium ions in SBF medium was determined by an atomic absorption spectrometer (AAS). FTIR result combined with the X-ray diffraction exhibited single phase of hydroxyapatite with carbonate peaks in the FTIR spectrum. The results indicate that increasing the sintering temperature increases the crystallinity and the crystallite size of hydroxyapatite nanopowders. Photomicrograph of transmission electron microscopy (TEM) showed that the obtained powder after sintering at 600 °C is composed of hydroxyapatite nanoparticles (20–30 nm). Dissolution rate of hydroxyapatite nanopowders was higher than conventional hydroxyapatite powders and closer to biological apatite due to its nanostructure dimensions. It was concluded that sol–gel prepared hydroxyapatite nanopowders had superior bioresorption and similar chemical and crystal structure to natural bone apatite.  相似文献   

4.
In this study, the influence of the glass addition and sintering parameters on the densification and mechanical properties of tetragonal zirconia polycrystals (3Y-TZP) ceramics were evaluated. High-purity tetragonal ZrO2 powder and La2O3-rich glass were used as starting powders. Two compositions based on ZrO2 and containing 5 wt.% and 10 wt.% of La2O3-rich glass were studied in this work. The starting powders were mixed/milled by planetary milling, dried at 90 °C for 24 h, sieved through a 60 mesh screen and uniaxially cold pressed under 80 MPa. The samples were sintered in air at 1200 °C, 1300 °C, 1400 °C for 60 min and at 1450 °C for 120 min, with heating and cooling rates of 10 °C/min. Sintered samples were characterized by relative density, X-ray diffraction (XRD) and scanning electron microscopy (SEM). Hardness and fracture toughness were obtained by Vickers indentation method. Dense sintered samples were obtained for all conditions. Furthermore, only tetragonal-ZrO2 was identified as crystalline phase in sintered samples, independently of the conditions studied. Samples sintered at 1300 °C for 60 min presented the optimal mechanical properties with hardness and fracture toughness values near to 12 GPa and 8.5 MPa m1/2, respectively.  相似文献   

5.
The formation and chemical leaching effects of a nonequilibrium Al0.6(Fe25Cu75)0.4 powder produced by rod milling is described. X-ray diffraction, transmission electron microscopy, differential scanning calorimetry and vibrating sample magnetometry were used to characterize both the as-milled and leached specimens. After 400 h of milling, only the bcc AlFe phase with an amorphous phase was detected in the XRD patterns. The crystallite size for the bcc AlFe phase (110) after 400 h of milling was about 5.3 nm. The peak temperature and the crystallization temperature of the as-milled powders were 448.7 and 428.0 °C, respectively. Al atoms leaching from the as-milled bcc AlFe powders in the L1 condition did not alter the diffraction pattern significantly, even though Al atoms had been removed. After the L1 specimen was annealed at 500 °C for 1 h, the bcc AlFe phase transformed to the fcc Cu, Fe, and CuFe2O4 phases. The peak widths of L1 and L2 specimens were similar, but became broader than that of the as-milled powder. The saturation magnetization decreased with increasing milling time, and a value of 10.4 emu/g was reached after 400 h of milling. After cooling the specimen from 750 °C, the magnetization slowly increased at approximately 491.4 °C, indicating that the bcc AlFe phase had transformed to the fcc Cu and Fe phases.  相似文献   

6.
Nano-crystalline vanadium disilicide was successfully synthesized using vanadium tetrachloride and silicon as starting materials via reduction–silication route at 650 °C in the molten salt solution of magnesium chloride and sodium chloride in an autoclave. X-ray powder diffraction patterns indicated that the product was hexagonal VSi2 (a=4.572 Å, c=6.372 Å). Transmission electron microscopy images showed that the particle size of the product was in the range of 40–60 nm in diameter. There was a strong absorption peak at 271 nm in the UV-Vis absorption spectra. The oxidation of nano-crystalline VSi2 began to proceed at the temperature of 400 °C in air. But the product had high thermal oxidation stability below 1000 °C. It can be used as an antioxidation coating material.  相似文献   

7.
Pore morphology and pore size distribution in yttria-stabilized zirconia (ZrO2–8 mol% Y2O3) have been investigated, for two sintering temperatures, namely 1200 and 1270 °C, using small-angle neutron scattering. The results show that the reduction in the porosity, at 1270 °C compared to that at 1200 °C, occurs by the elimination of the pores at the lower end of the pore size distribution. In addition, the polydispersity is also lower at 1270 °C and the nature of the distribution is altered significantly near the smaller radius range. The average pore size shifts towards the higher radius range. The specific surface area of the pores is also diminished at 1270 °C because of the elimination of the finer pores.  相似文献   

8.
Four alloys manufactured from different combinations of powders (TiC + TiN + WC; Ti(C,N) + WC; (Ti,W)C + TiN and (Ti,W)(C,N)) were studied using X-ray diffractometry, optical microscopy (OM), scanning electron microscopy (SEM) and analytical electron microscopy (AEM). The alloy manufactured from binary powders had a smaller grain size and a more inhomogeneous microstructure than the other alloys. The alloys manufactured with WC contained an inner rim around Ti(C,N) cores, as well as W-rich cores. Thermodynamic calculations suggest that these are formed during solid-state sintering at 900°C in a low nitrogen activity. The outer rim had a composition that is in good agreement with calculations of the equilibrium during liquid phase sintering at 1450°C.  相似文献   

9.
During exposure of pure Ta to temperatures up to 1800 °C pronounced grain growth combined with embrittlement becomes a major problem. Doping with elements which form nanometer to submicron sized oxide or silicide particles is an appropriate way to prevent, or at least to hamper, uncontrolled grain growth. In the present paper the effects of doping with varying combinations of Si and Y on microstructure and mechanical properties of cold-worked and annealed Ta have been investigated. For these purposes methods including small-angle neutron scattering and transmission electron microscopy as well as light-optical microscopy have been applied. Ta samples doped with Si show a higher hardness and strength than those doped with Y or made from pure Ta powder. However, the grain growth behaviour of all alloy variants is rather similar. The particle size distributions of doped Ta change significantly with varying annealing treatments as coarsening and dissolution of the prevailing particles (oxides and silicides) take place. Therefore, particles do not play a significant role in grain growth kinetics at temperatures as high as 1800 °C. However, this loss in retarding force is partially compensated for by an increased solution drag stemming from elements in solid solution.  相似文献   

10.
Al-Cu-Mg-Ag alloys with different Yb contents were prepared by ingot metallurgy and thermomechanical treatment. The effect of Yb addition on the precipitation and microstructure of the alloys was investigated using mechanical properties testing, optical microscopy, differential scanning calorimetry(DSC), scanning electron microscopy(SEM) and transmission electron microscopy(TEM). The results show that adding 0.10%-0.35% Yb accelerates the aging hardening process, increases the maximum hardness and the tensile strength of the extruded alloys from room temperature to 300 ℃. Trace Yb element addition refines the grains of the casting alloys from 85 μm to 30 μm, decreases the precipitation temperature of Ω phase. Moreover, the addition of Yb into AI-Cu-Mg-Ag alloy decreases the precipitates size, and improves the density and the thermal stability of.Ω phase between 200 ℃ and 300 ℃.  相似文献   

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