LUMINESCENCE OF YAG:Ce DOPED WITH SILVER NANOPARTICLES

В работе впервые было исследовано влияние наночастиц серебра на люминесценцию иттрий-алюминиевого граната, легированного церием. С помощью метода химического восстановления был синтезирован золь с размером наночастиц серебра ≈100 нм. Керамический порошок люминофора иттрий-алюминиевого граната, легированного церием, был получен методом двухстадийного осаждения в уротропин. Золь наночастиц серебра в концентрациях от 0,125 до 0,1 мл вводили в порошок-прекурсор перед прокаливанием. Было показано, что при данном способе введения наночастиц серебра интенсивность фотолюминесценции возрастала по сравнению с эталоном. Оптимальной концентрацией в рамках исследования являлась концентрация 0,25 мл. При данной концентрации увеличение интенсивности фотолюминесценции на длине волны 540 нм составило порядка 10%. Проведенные исследования показали, что наночастицы серебра могут с успехом применяться для увеличения яркости люминофора иттрий-алюминиевого граната, легированного церием, без искажения и ухудшения спектральных характеристик. This work was the first to study the effect of silver nanoparticles on the luminescence of cerium doped yttrium-aluminum garnet. A sol with the size of silver nanoparticles of ≈100 nm was synthesized using the method of chemical reduction. Phosphor ceramic powder of the yttrium-aluminum garnet doped with cerium was obtained by the two-stage precipitation method. The silver nanoparticles sol was introduced into the precursor powder before calcination in concentrations from 0,125 to 0,1 ml. It was shown that the photoluminescence intensity increased in comparison with the reference when we used this method of introducing silver nanoparticles. The optimal concentration within the study was 0,25 ml. At this concentration, the increase in the photoluminescence intensity at a wavelength of 540 nm was about 10 %. Studies have shown that silver nanoparticles can be successfully used to increase the brightness of the phosphor of the yttrium-aluminum garnet doped with cerium without distortion and deterioration of spectral characteristics.

Closed-Cell Rigid Polyimide Foams for High-Temperature Applications: The Effect of Structure on Combined Properties

Closed-cell rigid polyimide foams with excellent thermal stability and combined properties were prepared by thermal foaming of a reactive end-capped polyimide precursor powder in a closed mold. The precursor powder was obtained by thermal treatment of a polyester-amine salt (PEAS) solution derived from the reaction of the diethyl ester of 2,3,3′,4′-biphenyl tetracarboxylic dianhydride (α-BPDE) with an aromatic diamine mixture of p-phenylenediamine (PDA) and 2-(4-aminophenyl)-5-aminobenzimidazole (BIA) in the presence of an end-capping agent (mono-ethyl ester of nadic acid anhydride, NE) in an aliphatic alcohol. The effect of polymer mainchain structures on the foaming processability and combined properties of the closed-cell rigid polyimide foams were systematically investigated. The polyimide foams (100–300 kg/m3) with closed-cell rates of 91–95% show an outstanding thermal stability with an initial thermal decomposition temperature of ≥490 °C and a glass transition temperature of 395 °C. Polyimide foams with density of 250 kg/m3 exhibited compression creep deformation as low as 1.6% after thermal aging at 320 °C/0.4 MPa for 2 h.

Investigation of Microstructure and Mechanical Properties for Ti-6Al-4V Alloy Parts Produced Using Non-Spherical Precursor Powder by Laser Powder Bed Fusion

An unmodified, non-spherical, hydride-dehydride (HDH) Ti-6Al-4V powder having a substantial economic advantage over spherical, atomized Ti-6Al-4V alloy powder was used to fabricate a range of test components and aerospace-related products utilizing laser beam powder-bed fusion processing. The as-built products, utilizing optimized processing parameters, had a Rockwell-C scale (HRC) hardness of 44.6. Following heat treatments which included annealing at 704 °C, HIP at ~926 °C (average), and HIP + anneal, the HRC hardnesses were observed to be 43.9, 40.7, and 40.4, respectively. The corresponding tensile yield stress, UTS, and elongation for these heat treatments averaged 1.19 GPa, 1.22 GPa, 8.7%; 1.03 GPa, 1.08 GPa, 16.7%; 1.04 GPa, 1.09 GPa, 16.1%, respectively. The HIP yield strength and elongation of 1.03 GPa and 16.7% are comparable to the best commercial, wrought Ti-6Al-4V products. The corresponding HIP component microstructures consisted of elongated small grains (~125 microns diameter) containing fine, alpha/beta lamellae.

Development of a Fluorine-Free Polymer-Assisted-Deposition Route for YBa2Cu3O7−x Superconducting Films

Polymer assisted deposition (PAD) was used as an environmentally friendly, non-fluorine, growth method for superconducting YBa2Cu3O7−x (YBCO) films. The kinetics of the thermal decomposition of the precursor powder was studied by thermogravimetry coupled with mass spectrometry (TG-QMS). YBCO films were spin coated on (100) SrTiO3 (STO) single crystalline substrates, followed by a single step thermal treatment under wet and dry O2 and O2/N2 mixture. The as-obtained films were epitaxially grown having a [001]YBCO||[001]STO out-of-plane epitaxial relationship and exhibited good superconducting properties with Tc (R = 0) > 88 K, transition widths, ΔT ≈ 2 K and critical current densities as high as 2.3 MA/cm2 at 77 K and self magnetic field.

Synthesis and characterization of sol-gel derived monophasic mullite powder

High-purity microfine mullite precursor powder of stoichiometric chemical composition, 3Al2O3.2SiO2, was synthesized through the sol-gel route using aluminum isopropoxide and tetraethyl orthosilicate. The derived mullite precursor powder was characterized by BET surface area, particle size distribution, Fourier-transform infrared spectroscopy, thermogravimetry-differential thermal analysis (TG-DTA), X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy. Phase analysis of the precursor powder and calcined samples at different temperatures was done by XRD. Non-isothermal crystallization kinetics of mullite precursor was studied by TG-DTA in static air using heating rates of 5.0, 7.5, 10.0, 12.5, and 15 K.min-1. Grain morphology was studied by SEM. The results showed that synthesized mullite precursor powder possessed homogeneity of Al and Si components, and the amorphous precursor powder was converted to monophasic mullite crystal when heat-treated at 970 °C. Based on Flynn-Wall-Ozawa and Kissinger equations, the activation energy associated with the crystallization of mullite was determined to be 1189.8 and 1189.0 kJ.mol-1, respectively.