


Vol 2017, No 8 (2017)
- Year: 2017
- Articles: 13
- URL: https://journal-vniispk.ru/0036-0295/issue/view/10453
Article
Solubility of silver in the K–KCl melt at 850°C
Abstract
The solubility of silver in K–KCl melts at 850°C is studied in varying the potassium content from 0 to 100 mol %. It is shown that the solubility linearly increases as the alkali metal content increases; the solubility of silver in potassium melt is 6.0 mol %.



Volumetric thermal expansion coefficients of the equiatomic Na–K and K–Rb melts
Abstract
The volumetric thermal expansion coefficients of the equiatomic Na–K and K–Rb melts at 373 K are calculated using variational method with an additive hard-sphere reference system. It is found that the Krasko–Gurskii model pseudopotential with the exchange-correlation Geldart–Vosko function yields better agreement with the experimental data as compared to the local Animalu–Heine pseudopotential with the exchange-correlation Toigo–Woodruff function.



High-temperature hydrolysis of magnesium nitrate hexahydrate
Abstract
The high-temperature hydrolysis of magnesium nitrate hexahydrate is studied. The presence of basic magnesium nitrate in the decomposition product at 160°C is found by IR spectroscopy and X-ray diffraction analysis. A mechanism for the high-temperature hydrolysis of Mg(NO3)2 · 6H2O is proposed.



Synthesis of new metal-matrix Al–Al2O3–graphene composite materials
Abstract
The mechanism of formation of ceramic microparticles (alumina) and graphene in a molten aluminum matrix is studied as a function of the morphology and type of precursor particles, the temperature, and the gas atmosphere. The influence of the composition of an aluminum composite material (as a function of the concentration and size of reinforcing particles) on its mechanical and corrosion properties, melting temperature, and thermal conductivity is investigated. Hybrid metallic Al–Al2O3–graphene composite materials with up to 10 wt % alumina microparticles and 0.2 wt % graphene films, which are uniformly distributed over the metal volume and are fully wetted with aluminum, are synthesized during the chemical interaction of a salt solution containing yttria and boron carbide with molten aluminum in air. Simultaneous introduction of alumina and graphene into an aluminum matrix makes it possible to produce hybrid metallic composite materials having a unique combination of the following properties: their thermal conductivity is higher than that of aluminum, their hardness and strength are increased by two times, their relative elongation during tension is increased threefold, and their corrosion resistance is higher than that of initial aluminum by a factor of 2.5–4. We are the first to synthesize an in situ hybrid Al–Al2O3–graphene composite material having a unique combination of some characteristics. This material can be recommended as a promising material for a wide circle of electrical applications, including ultrathin wires, and as a structural material for the aerospace industry, the car industry, and the shipbuilding industry.



Surface tension of a titanium-containing oxide–fluoride melt calculated by the polymer theory
Abstract
The surface tension of an aluminum–calcium oxide–fluoride melt is calculated using the polymer theory. It is shown that, at 15 mol % titanium oxide in the melt, aluminum–fluorine–oxygen complexes mainly form. When the titanium oxide content increases further, these complexes disappear and are partly replaced by titanium–oxygen TiO44- and Ti2O76- anions and titanium–fluorine–oxygen groups.



Kinetics of electrolysis current reversal boriding of tool steels in a boron-containing oxychloride melt based on CaCl2
Abstract
The kinetics of thermal diffusion boriding in a melt based on calcium chloride with a boron oxide additive is studied using reversed current. The main temperature, concentration, and current parameters of the process are determined. The phase composition of the coating is determined by a metallographic method.



Electrochemical cell with the reversible electrode–solid electrolyte or ionic melt interface in galvanodynamic and potentiodynamic operating modes
Abstract
This work is aimed at studying the kinetics of the following two simultaneous processes: charging of the double electrical layer and the charge transfer at the reversible silver electrode–sulfate solid electrolyte or corresponding ionic melt interface in two operating modes of electrochemical cell, namely, galvanodynamic and potentiodynamic ones. The electrochemical kinetics has been studied by the method of operational impedance based on the Ohm law of interaction between Laplace transformed current, voltage, and complex resistance (impedance). Using appropriate mathematical calculations, analytical expressions are obtained for the current passing via a cell during linear potential scanning (potentiodynamic mode) as a function of time and for the interface potential as a function of time in the galvanodynamic mode (linear current scanning). The time dependence of the potential of the electrode–solid electrolyte or ionic melt interface is described by an exponential function in the potentiodynamic mode of the cell operation. An analysis and comparison of the results of the two independent electrochemical modes demonstrate that the behavior of the electrochemical cells containing a reversible metallic electrode, i.e., a solid electrolyte or the corresponding ionic melt, obeys the classical Randles–Ershler equivalent circuit. This statement can be proved by both the alternating current method (impedance method) and relaxation galvanodynamic and potentiodynamic methods (linear scanning of potential and current).



Thermal analysis for modeling the aluminothermic reduction of zirconium from oxide
Abstract
The modeling of zirconium reduction from oxide by thermal analysis shows that the congruently stable intermetallic compound Al3Zr is formed as a result of the process. The formation of Al3Zr proceeds via the stage of formation of intermediate zirconium monoxide.



Electroreduction of chromium(III) chloride in a thermal battery
Abstract
The discharge characteristics and the reduction products of the CrCl3 cathodic material in a thermal battery are studied. The maximum discharge capacity of the cathodic material is found to be 0.45 A h g–1 (550°C). A mechanism for the reduction of CrCl3 to metallic chromium via an intermediate formation of the melt of Li3CrCl6x(Br6(1–x)) complexes is proposed.



Synthesis of hafnium carbide by mechanochemistry and irradiation
Abstract
The interaction in the Hf–C system during mechanical activation performed in a high-energy planetary ball mill and the irradiation-assisted fabrication of hafnium carbide from an Hf/C mechanocomposite are studied by synchrotron X-ray diffraction (at a quantum energy of 33.7 keV) and high-resolution scanning electron microscopy. The mechanochemical interaction results in the formation of an Hf/C mechanocomposite at the first stage and mechanical activation for ≥8 min forms hafnium carbide. The irradiation of the Hf/C mechanocomposite with a high-energy electron beam (~150 W/mm2) causes melting and spreading of hafnium over the carbon particle surface and the crystallization of hafnium carbide.



Electrical properties of the LaLiyCo1 – yO3 – δ (0 ≤ y ≤ 0.10) oxides
Abstract
The effect of the Li ion concentration on the phase composition, the electrical conductivity, and the thermoelectric power of the LaLiyCo1–yO3–δ (0 ≤ y ≤ 0.1) oxides synthesized by cocrystallization has been studied. It is found that the region of the perovskite-like solid solution LaLiyCo1–yO3–δ is no higher than y = 0.037. In the temperature range 300–1020 K, lithium alloying leads to an increase in the electrical conductivity and a decrease in the positive thermoelectric power of the single-phase samples compared to LaCoO3–δ. The results are discussed using the density of states model proposed by Senarus Rodriguez and Goodenough for LaCoO3–δ and La1–xSrxCoO3–δ and using the Mott theory of noncrystalline substances.



Estance of gold in molten LiCl and the effect of the nature of cation on the estance zero potentials of Au in molten alkali metal chlorides
Abstract
The dependences estance vs. potential in molten LiCl are obtained. They have three zeros of estance near the melting temperature of the salt. When the temperature increases by 400 K, only one cathode zero is retained for equilibrium estance. A comparison of the potentials of this zero of estance in a row of alkali metal chlorides at the same temperature indicates their nonmonotonic dependence on the cation radius, in contrast to the potentials of the ECC maxima of liquid Pb, Bi, and In and the PZC of gold in this row.



Self-diffusion coefficients of cadmium and indium in liquid
Abstract
The self-diffusion coefficients of liquid Cd and In near melting temperatures are calculated by the Helfand–Devis–Palyvos method using a model square-well pair potential in the random phase approximation. Adequate agreement between the calculated and available experimental data is achieved for both metals under study.


