Papers by Keyword: Lu₂O₃

Abstract: In this work, the well-known program WinXCom have been performed over 1 keV to 20 MeV to obtain the radiation properties (in case of theoretical calculation) of calcium-silico-borate glass system containing Lu₂O₃ in the composition of xLu₂O₃ : 10.0CaO : 10.0SiO₂ : (80.0-x)B₂O₃ with x are Lu₂O₃ concentrations varying from 0.0, 5.0, 10.0, 15.0, 20.0, and 25.0 mol%. The total mass attenuation and partial attenuation coefficients have been studied as functions of chemical compositions and incoming photon energies. In addition, the obtained data were then used to compute the effective atomic numbers and effective electron densities. The calculated results show the variation of both parameters with photon energy.

Abstract: Spherical submicron SiO2 particles have been coated with luminescent Lu2O3: Eu3+ layers by a Pechini sol-gel process, resulting in the formation of SiO2@Lu2O3: Eu3+ core-shell particles(300, 500 nm). The obtained core–shell phosphors have perfect spherical shape with narrow size distribution, smooth surface and non-agglomeration. The thickness of shells could be easily controlled by changing the number of deposition cycles (50 nm for four deposition cycles). Under the excitation of ultraviolet, the Eu3+ ion mainly shows its characteristic emissions in the core-shell particles from Lu2O3: Eu3+) shells. The PL intensity of Eu3+ increases with the number of coating cycles.

Abstract: The influence of Lu2O3 on phase transformation and seeds morphology was investigated. The result showed that the β-Si3N4 seeds with up to 95% β phase content could be obtained with 2wt% Lu2O3 as the additive content under 1750°C for two hours. The microstructure and mechanical properties of hot-pressed Si3N4 ceramics, using 9wt.% of Lu2O3• additives were investigated by the means of MTS measurements and Vickers indentation crack size measurements, as well as XRD and SEM. It was known that the high fracture toughness of Si3N4 ceramics was attributed to the rodlike morphology of β-Si3N4 grains. And the reinforcement effect and mechanism of β-Si3N4 seed were studied. It was found that the grain size and its distribution influence the property and microstructure of Si3N4 ceramics, namely, the relative narrow distribution of grain diameter in some extent and relative wide range of bimodal distribution of grain aspect ratio could improve the property of Si3N4 ceramics. The improvement in the fracture toughness with the amount of additive was mainly attributed to elongated grain growth during the sintering process.The high temperature properties of self-reinforced Si3N4 with different additives were studied. By this method, self-reinforced Si3N4 ceramics with an increment of 10~20 percent of fracture toughness was successfully fabricated.

Abstract: Yb3+ and Ho3+ co-doped Lu2O3 nanocrystalline powders were synthesized by a reversestrike co-precipitation method. The as-prepared powders were examined by the X-ray diffraction and transmission electron microscopy. The phase composition of the powders was cubic and the particle size was in the range of 30~50 nm. Emission and excitation spectra of the powders were measured by a spectrofluorometer and the possible upconversion luminescence mechanism was also discussed.

Abstract: High-temperature properties of silicon nitride ceramics with Lu-silicon-oxynitride grain boundary phases were investigated. Si3N4 powder with 1.2 mol% (SN12) and 4.8 mol% (SN48) of Lu2O3 were gas-pressure hot-pressed at 1950°C for 2 h under 20 MPa in 1 MPa N2. SN12 consisted of elongated β-Si3N4 and a secondary phase, Lu4Si2O7N2, whilst SN48 consisted of elongated β-Si3N4 and Lu4Si2O7N2 + Lu2SiO5. At 1500°C and 1600°C, the stress-strain curve of SN48 was nonlinear, whilst that of SN12 was linear, indicating that SN12 broke as a brittle fracture at these temperatures. SN12 had excellent oxidation resistance and weight gain during the oxidation at 1500°C for 1000 h was 4 g/m2. Creep lifetime of SN12 at 1500°C under tensile stress of 137 MPa exceeded 1678.5 h.

Abstract: The effects of microstructure and composition on the wear properties of Lu sialon ceramics have been studied under dry sliding conditions through block-on-ring wear tests. Microstructural and compositional effects on wear behaviour were studied by producing both equiaxed and elongated α sialons through the incorporation of additional oxides to promote extended liquid formation and grain growth, and by producing α / β composite materials with elongated β grains. The wear response of the materials is discussed in terms of the dominant wear mechanism under different experimental conditions. Under higher loads, where fracture dominates, materials with improved mechanical properties show better wear resistance and both the composite materials and the elongated α sialons showed lower wear rates than the equiaxed materials due to the elongated grain microstructures. Under low normal loads, fracture does not occur and the dominant wear mechanism is thought to be tribochemically assisted wear. Under these conditions, the equiaxed materials had better wear resistance than the composites, and the Lu-α sialon showed an order of magnitude lower wear rate than an equivalent Y-α sialon, thought to be due to better oxidation resistance and improved refractory nature afforded through the use of the smaller radius cation. The elongated Lu-α sialons under these low load conditions showed wear resistance that was to some extent dependent on the composition of the additional liquid phase, with high SiO2 contents leading to higher wear rates.

Abstract: Nanocrystalline powders of Lu2O3:Eu with activator content varying between 0.2%-10% were prepared using four different methods of synthesis. The products differed in their microstructure and crystallites sizes. Combustion of Lu(NO3)3 with urea produced strongly agglomerated material, most probably with significantly non-uniform distribution of the Eu3+ dopant. Replacing urea with glycine for the combustion produced only slightly agglomerated, voluminous, fluffy powder. Applying the Pechini technique resulted in significantly agglomerated powder while the homogeneous precipitation of Lu(OH)3 with urea at 90 °C and its subsequent decomposition to Lu2O3 at 650 °C resulted in a powder of perfectly spherical particles with a uniform size of about 130 nm with very low agglomeration. The efficiency of X-ray excited luminescence of our nanocrystalline Lu2O3:5%Eu was compared to that of the commercial microcrystalline Gd2O2S:Eu. It was found that the commercial phosphor performed four times more efficiently than our nanocrystalline powder. We consider this to be rather encouraging as the fabrication of our powder is not optimized yet. It seems that Lu2O3:Eu, even in nanocrystalline form, can perform much more efficiently which would make it a promising X-ray phosphor.