Fabrication of polycrystalline (Y0.7Gd0.3)2O3:Eu ceramics: The influence of initial pressure and sintering temperature on its morphology and photoluminescence activity

Nanocrystalline (Y_0.7Gd_0.3)₂O₃ powder, synthetised via polymer complex solution method, was compacted into 25 pellets applying high pressures (173-867 MPa) for 30 s that were subsequently sintered at different temperatures (800-1400 °C) for 18 h. The morphology and optical characteristics of the starting powder and prepared ceramic samples were monitored and discussed in order to identify the changes induced with the variations of initial compacting pressure, which influence is often neglected, and with sintering temperature. The grain size tends to decrease significantly with increasing pressure, even when elevated temperatures are used for annealing, while low compacting pressure resulted in grain coarsening and, in some cases, even in anomalous morphology of ceramic samples. Luminescence emission in ceramic samples decays faster than in nanopowders, that is in complete agreement with the grain formation and gradual transformation to the bulk material. Judd-Ofelt intensity parameters and branching ratios were calculated taking into account the difference in effective refractive index for nanopowder and ceramic samples.     

Oxidation of methane in a wide range of pressures and effect of inert gases

The analysis of methane oxidation in a wide range of pressures (0.05–10 atm) demonstrates that the efficiency of CH₃ radicals recombination is of great importance for high selectivity of C₂ hydrocarbons formation. The relative efficiency of different “colliders” assisting the stabilization of exited C₂H*₆ molecules increases in the series: solid surface> Ar> He. The increase of the overall reaction rate upon increasing pressure of the inert gases in the case of catalysts having a higher surface area and more developed pore structure is likely due to the contribution of the surface-induced chain reaction in the volume of pores.     

Miyaura Borylation and One‐Pot Two‐Step Homocoupling of Aryl Chlorides and Bromides under Solvent‐Free Conditions

Solvent‐free protocols for Miyaura borylation and the one‐pot, two‐step homocoupling of aryl halides are reported for the first time. Bis(dibenzylideneacetone)palladium(0) [Pd(dba)₂] is an optimal source of palladium for Miyaura borylation, while for one‐pot two‐step homocoupling palladium(II) acetate [Pd(OAc)₂] gives highest yields. Aryl bromides are coupled most efficiently using the DPEphos ligand. Chlorides are coupled using XPhos. The developed protocols are robust, versatile and easily reproducible on a large scale.

     

Flash Lamps as Ignition and Initiation Sources of the VS-2 Pyrotechnic Composition

In the present work it is found that the pyrotechnic composition VS-2 can be initiated with flash lamps IFC-500 and EVIS. VS-2 pyrotechnic composition contains 90% of mercury（Ⅱ） 5-hydrazinotetrazolate perchlorate and 10% of optically transparent copolymer of 2-methyl-5-vinyltetrazole and methacrylic acid （PVMT）. We have found that the flash lamps make it possible to initiate combustion of VS-2 composition with its transition to detonation both in cylindrical charges placed in brass caps of 5 mm diameter and 2 mm high， and film charges with 10 mm×80 mm in size and surface weights of 60 mg·cm^-2 and 90 mg·cm^-2， showing ignition delay times 10 μs and 3 μs， respectively. We also measured detonation velocities for VS-2 composition film charges， which were 4375-4505 m·s^-1 （of the charge being surface mass 60 mg·cm^-2） and 4221-4281 m·s^-1 （of the charge being surface mass 90 mg·cm^-2） and their blasting action on the aluminum plate. The depths of the normal shock wave imprints at the charge-barrier interface were 0.6-0.7 mm （for surface mass of the film charges 60 mg·cm^-2） and 1.2-1.3 mm （for surface mass of the film charges 90 mg·cm^-2）.     

The effect of red pigment on the amyloidization of yeast proteins

The intensity of amyloid-bound thioflavine T fluorescence was studied in crude lysates of yeast strains carrying mutations in the ADE1 or ADE2 genes and accumulating the red pigment (a result of polymerization of aminoimidazoleribotide), and in white isogenic strains--either adenine prototrophs or carrying mutations at the first stages of purine biosynthesis. We found that the red pigment leads to a drop of amyloid content. This result, along with the data on separation of protein polymers of white and red strains in PAGE, suggests that the red pigment inhibits amyloid fibril formation. The differences in transmission of the thioflavine T fluorescence pattern by cytoduction and in blot-hybridization of pellet proteins of red and white [PSI(+) ] strains with Sup35p antibodies confirmed this conclusion. Purified red pigment treatment also led to a decrease of fluorescence intensity of thioflavine T bound to insulin fibrils and to yeast pellet protein aggregates from [PSI(+) ] strains. This suggests red pigment interaction with amyloid fibrils. Comparison of pellet proteins from red and white isogenic strains separated by 2D-electrophoresis followed by MALDI analysis has allowed us to identify 48 pigment-dependent proteins. These proteins mostly belong to functional classes of chaperones and proteins involved in glucose metabolism, closely corresponding to prion-dependent proteins that we characterized previously. Also present were some proteins involved in stress response and proteolysis. We suppose that the red pigment acts by blocking certain sites on amyloid fibrils that, in some cases, can lead in vivo to interfere with their contacts with chaperones and the generation of prion seeds.     

Ascorbic Acid-Assisted Eco-friendly Synthesis of NiCo<Subscript>2</Subscript>O<Subscript>4</Subscript> Nanoparticles as an Anode Material for High-Performance Lithium-Ion Batteries

We have synthesized NiCo₂O₄ nanoparticles (NCO NPs) using an ascorbic acid-assisted co-precipitation method for the first time. When NCO NPs are used as an anode material for lithium-ion batteries, the cell exhibits superior lithium storage properties, such as high capacity (700 mA h g^?1 after 300 cycles at 200 mA g^?1), excellent rate capabilities (applied current density range 100–1200 mA g^?1), and impressive cycling stability (at 1200 mA g^?1 up to 650 cycles). The enhanced electrochemical properties of NCO NPs are due to the nanometer dimensions which not only offers a smooth charge-transport pathway and short diffusion paths of the lithium ions but also adequate spaces for volume expansion during Li storage. Hence, this eco-friendly synthesis approach will provide a new strategy for the synthesis of various nanostructured metal oxide compounds, for energy conversion and storage systems applications.     

Metal silicide/poly-Si Schottky diodes for uncooled microbolometers

Nickel silicide Schottky diodes formed on polycrystalline Si 〈P〉 films are proposed as temperature sensors of monolithic uncooled microbolometer infrared focal plane arrays. The structure and composition of nickel silicide/polycrystalline silicon films synthesized in a low-temperature process are examined by means of transmission electron microscopy. The Ni silicide is identified as a multi-phase compound composed of 20% to 40% of Ni₃Si, 30% to 60% of Ni₂Si, and 10% to 30% of NiSi with probable minor content of NiSi₂ at the silicide/poly-Si interface. Rectification ratios of the Schottky diodes vary from about 100 to about 20 for the temperature increasing from 22℃ to 70℃; they exceed 1,000 at 80 K. A barrier of around 0.95 eV is found to control the photovoltage spectra at room temperature. A set of barriers is observed in photo-electromotive force spectra at 80 K and attributed to the Ni silicide/poly-Si interface. Absolute values of temperature coefficients of voltage and current are found to vary from 0.3%℃ to 0.6%/℃ for forward bias and around 2.5%/℃ for reverse bias of the diodes.     

ION EXCHANGE CHARACTERISTICS OP A NEW MANGANESE OXIDE : SELF-DIFFUSION AND TRACE COMPONENT DIFFUSION

The kinetics of self-diffusion and trace component diffusion of Na+ and Cs+ in a new manganese oxide, having the chemical formula Na₄Mn₁₇O₂₇.13 H₂O, was studied. A uniform diffusion process was observed in all cases. The diffusion coefficients increase with particle size at the relatively large sizes, which is attributed to the conglomeration of small particles. The self-diffusion coefficient of Na+ is lower than that of Cs+ whereas the trace diffusion coefficients follow a reverse trend. Besides, the self-diffusion coefficients are not equal to the trace diffusion ones and opposite differences are observed for Na+ and Cs+. These results were tentatively explained in terms of the oxide water content and ion hydration.     

Calculating the strength and estimating the service life of pressure vessels at thermal power stations during investigation of industrial Safety

Matters relating to carrying out strength calculations and estimating the service life of pressure vessels at power stations after this equipment has worked through standardized service life are considered. The need to carry out one kind of calculations or another, depending on the purpose and operating conditions of a vessel, is analyzed. Procedures for carrying out check calculations of vessels taking their actual state and operating conditions into account for substantiating the possibility of their further operation are described.     

Decentralised decision making in heterogeneous teams using anonymous optimisation

This paper considers the scenario where multiple autonomous agents must cooperate in making decisions to minimise a continuous and differentiable team cost function. A distributed and asynchronous optimisation algorithm is presented which allows each agent to incrementally refine their decisions while intermittently communicating with the rest of the team. A convergence analysis provides quantitative requirements on the frequency agents must communicate that is prescribed by the structure of the decision problem. In general the solution method will require every agent to communicate to and have a model of every other agent in the team. To overcome this, a specific subset of systems, called Partially Separable, is defined. These systems only require each agent to have a combined summary of the rest of the team and allows each agent to communicate locally over an acyclic communication network, greatly increasing the scalability of the system.