Mechanism of Dy3+ and Nd3+ Ions Electrochemical Coreduction with Ni2+, Co2+, and Fe3+ Ions in Chloride Melts

The present paper is devoted to the study of the processes of the mechanism of electrochemical coreduction of Dy3+ and Nd3+ ions with Ni2+, Co2+, and Fe3+ ions in the equimolar NaCl-KCl melt at 973 K and characterization of the synthesized samples. The performed voltammetry analysis of the electrochemical coreduction processes elucidated a significant difference in the values of the extraction potentials of the studied metals. This melt testifies that intermetallic compounds of Dy and Nd with Ni, Co, and Fe may be synthesized in the kinetic regime. The intermetallic phases of Dy and Nd with Ni, Co, and Fe are found to be formed along with the phases of metallic Ni, Co, and Fe either during electrolysis at the cathode current densities exceeding the limiting diffusion current of Ni2+, Co2+, and Fe3+ ions or in the potentiostatic regime at the potentials of the corresponding voltammetry curves. Therefore, the following interrelated key parameters affecting the electrochemical synthesis of Dy and Nd intermetallic compounds with Ni, Co, and Fe were determined: (i) composition of the electrolyte, i.e., concentrations of FeCl3, CoCl2, NiCl2, DyCl3, and NdCl3; (ii) cathode current density or electrolysis potential and (iii) electrolysis time. The obtained samples were characterized by micro-X-ray diffraction analysis, cyclic voltammetry, and scanning electron microscopy methods.

Electrochemical deposition of tin-copper alloy coatings

Solderable tin-base alloy coatings are widely used when assembling electronic products. The reorientation of production to lead-free technologies sets the task of developing new technological processes for the formation of coatings for electrical contacts with stable electrical properties, high soldering ability, which lasts for a long time. The features of the process of electrodeposition of coatings with a tin-copper alloy were experimentally investigated and the regularities of the influence of the electrolyte composition, current density, and ultrasound intensity on the cathode current efficiency of the alloy, the deposition rate, elemental composition, structure and functional properties of the precipitation were established. For sonochemical treatment an experimental setup developed at Research Laboratory 5.2 of BSUIR, which makes it possible to vary the intensity of ultrasonic vibrations in the range of 0.058– 1.7 W/cm2 , was used. It has been established that the use of ultrasound changes the formation mechanism of the electrochemical alloy, reduces cathodic polarization, increases the value of the limiting current and makes it possible to control the composition and structure of the precipitates. With an increase in the intensity from 0.12 to 0.95 W/cm2 the amount of copper in the coating increases by 4.5 times. The spreading coefficient of the solder is 92.59–98.44 %.

Conversion Method of Thermionic Emission Current to Voltage for High-Voltage Sources of Electrons

The stability of the electron thermionic emission current is one of the most important requirements for electron sources used, inter alia, in evaporators, production of rare gas excimers, and electron beam objects for high energy physics. In emission current control systems, a negative feedback signal, directly proportional to the emission current is transferred from the high-voltage anode circuit to the low-voltage cathode circuit. This technique, especially for high-voltage sources of electrons, requires the use of galvanic isolation. Alternatively, a method of converting the emission current to voltage in the cathode power supply circuit was proposed. It uses a linear cathode current intensity distribution and multiplicative-additive processing of two voltage signals, directly proportional to the values of cathode current intensity. The simulation results show that a relatively high conversion accuracy can be obtained for low values of the electron work function of the cathode material. The results of experimental tests of the dynamic parameters of the electron source and the steady-state Ie-V characteristic of the converter are presented. The implementation of the proposed Ie-V conversion method facilitates the design of the emission current controller, especially for high-voltage sources of electrons, because a negative feedback loop between the anode and cathode circuits is not required, all controller sub-components are at a common electrostatic potential.

On hybrid type of cathode attachment in high current vacuum arcs

This paper discusses the issues of a possible change of the type of cathode attachment of high-current vacuum arcs (HCVA) with an average cathode current density of more than 105 A/cm2. This type of HCVA is used as pumping plasma gun in experiments with plasma puff z-pinches. These experiments showed that the measured linear mass of the HCVA plasma jet is much higher (by a factor of 10 or more) than the expected mass, which can be obtained from the assumption that cathode attachment occurs only through a multitude of cathode spots emitting supersonic plasma jets. It is shown that in HCVA of the type under consideration, at some time instant there are two types of cathode attachments - cathode spots and thermionic erosion attachment (TEA). It can be said that HCVA of this type have a hybrid cathodic attachment. Unlike cathode spots, TEA produces a subsonic plasma flow, which contributes to an increase in the linear mass of the HCVA plasma jet.

Performance Optimization of μDMFC with Foamed Stainless Steel Cathode Current Collector

The micro direct methanol fuel cell (μDMFC) has attracted more and more attention in the field of new energy due to its simple structure, easy operation, and eco-friendly byproducts. In a μDMFC’s structure, the current collector plays an essential role in collecting the conduction current, and the rational distribution of gas and water. The choice of its material and flow fields would significantly impact the μDMFC’s performance. To this end, four different types of cathode current collector were prepared in this study. The materials selected were stainless steel (SS) and foam stainless steel (FSS), with the flow fields of hole-type and grid-type. The performance of the μDMFC with different types of cathode current collector was investigated by using polarization curves, electrochemical impedance spectroscopy (EIS), and discharging. The experimental results show that the maximum power density of μDMFC of the hole-type FSS cathode current collector is 49.53 mW/cm2 at 70 °C in the methanol solution of 1 mol/L, which is 115.72% higher than that of the SS collector. The maximum power density of the μDMFC with the grid-type FSS collector is 22.60 mW/cm2, which is 27.39% higher than that of the SS collector. The total impedance of the μDMFC of the FSS collector is significantly lower than that of the μDMFC of the SS collector, and the total impedance of the μDMFC with the hole-type flow field collector is lower than that of the grid-type flow field. The discharging of μDMFC with the hole-type FSS collector reaches its optimal value at 70 °C in the methanol solution of 1 mol/L.

Fabrication of Multi-Layered Zn-Fe Alloy Coatings for Better Corrosion Performance

Zn-Fe compositionally modulated multilayer alloy (CMMA) coatings were developed onto low carbon steel from acid sulphate bath; and their corrosion resistance was calculated using Tafel polarization and impedance methods. The deposit layers were formed galvanostatically by single bath technique (SBT), using square current pulses. An optimal configuration for the growth of most corrosion resistant Zn-Fe coating was proposed and discussed. At maximum switching cathode current density (SCCD) (2.0–5.0 A dm−2), the deposit with 300 layers showed ~43 times superior corrosion resistance than the same thickness of monolayer coating. The improved corrosion resistance of multilayered coatings is due to small change in iron content, leading to change the phase structure of the alternate-layers of the alloy coatings. The surface morphology and structure of film and roughness of the deposit were assessed using Scanning Electron Microscopy and Atomic Force Microscopy. Thus, superior corrosion resistance of Zn-Fe multilayer coatings was used for industrial applications including defense, machinery and automobile etc.