Role of carbonate-carboxylate species during alumina coking

The role of carbonate-carboxylate species on alumina surface has been studied during alumina coking. The species are intermediates poisoning the active sites. Little O₂ added to the hydrocarbon feedstock causes further oxidation of the species and promotion of the active sites.     

Determination of the size of particles of highly dispersed materials by low temperature nitrogen adsorption

The average size of particles of highly dispersed materials (Al₂O₃, TiO₂, Y₂O₃) is calculated from their specific surface areas. The latter is determined with the analysis of sorption capacity of materials with nitrogen at ?196°C in the ranges of relative equilibrium pressures of 0.05–0.35 (the Brunauer-Emmett-Teller method, BET) and 0.4–0.7 (the comparative method). Good agreement is obtained between results produced with the comparative method and familiar methods of analysis such as scanning and transmission electron microscopy and small-angle X-ray scattering.     

Effect of sulfate synthesis conditions on characteristics of samples with the nanosized η-TiO2 modification

The nanosized titania modification ??-TiO₂ has been obtained from titanyl sulfate with different starting precursor concentration, under different hydrolysis and coagulation conditions. Characteristics of samples (nanoparticle and crystallite size, specific surface, pore volume) have been determined by scanning electron microscopy, small-angle and wide-angle X-ray diffraction, and nitrogen physical adsorption at ?196°C, and their correlation with the synthesis conditions has been established. Optimal technological regimes ensuring fabrication of samples with a high yield of ??-TiO₂ modification and specified functional characteristics have been found.     

Pair scattering of electrons in edge channels of opposite chiralities in the presence of a disorder potential

The nonequilibrium transfer of the energy between electrons of counter-propagating quasi-one-dimensional systems has been perturbatively calculated for edge channels in a two-dimensional system in the integer quantum Hall effect. The processes involving two electrons that are allowed only in the system with disorder have been taken into account. Expressions for the cases of Coulomb scattering and transfer of nonequilibrium phonons have been obtained. The energy transferred per unit time has a quasi-threshold dependence on the degree of nonequilibrium of the hot channel. According to numerical estimates for electrons in GaAs, Coulomb scattering processes dominate in the energy transfer and the expected effect can be experimentally observed.     

Influence of Iron Alloying on the Properties of Vanadium Dioxide

Russian Physics Journal - Results of investigations of the x-ray structural parameters of the crystal lattice and their temperature dependences in the vicinities of the metal-dielectric phase...     

Nonlinear evolution of perturbations in a thin fluid layer during wave formation

A mathematical model is presented for the state of a free surface of a thin fluid layer (a fluid film) in heat-mass-exchange processes of condensation and evaporation. The wave motion of a fluid film is studied under inhomogeneous surface tension. Nonlinear development of perturbations belonging to a continuous band of wave numbers on the surface of a thin fluid layer is investigated within the framework of a non-linear parabolic equation. It is shown that wave packets with carrier wave lying near the harmonic of maximum increment become self-ordered; as a result, a monochromatic wave is generated on the surface of the fluid film. When a wave packet is generated in the neighborhood of the neutral stability curve, one can observe a phenomenon of directed energy transfer to the waves in the neighborhood of the harmonic of maximum increment.     

Monolith catalyst for high-temperature combustion of gaseous hydrocarbon fuels

X-ray, chemical phase analysis, TPR, DRES, adsorption technique, kinetic measurements have been used to study active sites of a combustion catalyst containing iron oxide supported on multihole plate ceramics.     

Structures and Chemical Bonding in Antimony(III) Bromide Complexes with Pyridine

Weakly or “partially” bonded molecules are an important link between the chemical and van der Waals interactions. Molecular structures of six new SbBr₃-Py complexes in the solid state have been determined by single-crystal X-ray diffraction analysis. In all complexes all Sb atoms adopt a pseudo-octahedral coordination geometry which is completed by additional Sb⋅⋅⋅Br contacts shorter than the sum of the van der Waals radii, with Br−Sb⋅⋅⋅Br angles close to 180°. To reveal the nature of Sb–Br and Sb–N interactions, the DFT calculations were performed followed by the analysis of the electrostatic potentials, the orbital interactions and the topological analysis. Based on Natural Bond Orbital (NBO) analysis, the Sb–Br interactions range from the covalent bonds to the pnictogen bonds. A simple structural parameter, non-covalence criterion (NCC) is defined as a ratio of the atom-atom distance to the linear combination of sums of covalent and van der Waals radii. NCC correlates with E(2) values for Sb−N, Sb−Cl and Sb−Br bonds, and appears to be useful criterion for a preliminary evaluation of the bonding situation.