Electrode processes during electrodeposition, electropolishing and oxidation of niobium

The electrode processes occurring during the electrodeposition, electropolishing and oxidation of niobium are considered. The discharge of Nb(IV) complexes during Nb electrodeposition was studied by cyclic voltammetry. The anodic polarization curve on niobium in a mixture of acids H2SO4:HF (9:1) was obtained by chronopotentiometry method, the potential range at which the highest quality and speed of electropolishing is achieved was found. The film formation mechanism of niobium pentoxide Nb2O5 on niobium was studied by cyclic voltammetry.

Modeling of electric mass transfer process in controlled electrochemical resistance

The aim of the study is to mathematically simulate the concentration field of an electrolyte in a controlled electrochemical resistance. All processes occurring in the object are considered isothermal, the electric fields in all fragments of the electrochemical resistance are potential, plane-parallel. All physical and chemical parameters of the object’s materials are constant values. The kinetics of all electrode processes in the object of study is controlled by the diffusion stage in the electrolyte. As a research method, the operator method of Laplace and Fourier – expansion is used to obtain an analytical description of the concentration field of the electrolyte. In the course of the study, a mathematical model of the concentration field of the electrolyte with a uniform distribution of the current density was obtained. An analytical expression is obtained that allows to construct the surface of the change in the concentration of the electrolyte in the controlled electrochemical resistance. The concentration profiles of the electrolyte at different temperatures and the time dependences of the change in the concentration of the electrolyte are calculated.

Polimeryzacja aniliny w środowisku stałego pola magnetycznego

Polyaniline is an example of an electronically conducting polymer. During the oxidation of the polymer, positive charges appear in its structure, which must be compensated for e.g. by the presence of anions in the polymer layer. The form of polyaniline depends on both the degree of oxidation and the degree of protonation of the polymer, i.e. the pH of the solution. Due to the ease of electrochemical preparation of polyaniline, as well as the possibility of full control of the course of the process, the influence of the constant magnetic field (s.p.m.) on the reaction of its preparation was additionally investigated. The cyclic voltammetry (CV) method was used for this purpose. Aniline polymerization processes were carried out on platinum, plate electrodes, not insulated (A) and insulated on two different sides with Teflon, with surfaces directed parallel to the line of force of the s.p.m. (To beat). Research on the electrochemical preparation of polyaniline in s.p.m. allowed to conclude that the following factors affect the magnitude of the current in the tested process: (i) the magnitude of the magnetic induction vector B, (ii) the position of the electrode plane in relation to the direction of the vector B, (iii) the type of electrode (insulated on one side or not). Impact on the impact of s.p.m. the magnetic properties (e.g. paramagnetic, diamagnetic) of the particles participating in the electrochemical reaction, as well as their charge (+/-), also had an effect on the electrochemical polymerization processes. Based on the experimental results, the mechanism of the influence of s.p.m. was proposed. on the tested electrochemical reactions. This mechanism was based, inter alia, on the formation of the magnetohydrodynamic effect (MHD), which causes a change in the speed of transport of the reacting substances to the electrode, the magnetohydrodynamic movement of the electrolyte and the change in the kinetics of electrode processes. For the tested process, changes in the rate constants of electrochemical reactions (ks) as a result of external action of s.p.m. were around 30%.

Ultrasound Supported Galvanostatic Deposition of Zn Coatings Reinforced with Nano-, Submicro-, and Micro-SiC Particles—Weak Acidic Chloride Baths

In this paper, we present results concerning the electrochemical deposition of Zn-SiC composite coatings reinforced with nano-, submicro-, and microparticles. The influence of current density, particle size, and ultrasound on functional parameters which are especially important from a practical point of view (i.e., concentration of particles in coatings, current efficiency, morphology, reflectivity, roughness, hardness, and corrosion resistance) are investigated and discussed. Coatings were deposited from commercial, chloride-based electrolytes dedicated for the deposition of Zn coatings in a weakly acidic environment. Electrodeposited composites contained up to 1.58, 4.08, and 1.15 wt. % of SiC for coatings reinforced with nano, submicro, and micrometric particles, respectively. The process proceeded with relatively high efficiency, exceeding 80% in almost all cases. The results indicate that ultrasounds strongly increase Faradaic efficiency and affect the kinetics of electrode processes and the properties of synthesized coatings. Moreover, the obtained results show that it is possible to synthesize composite coatings with slightly higher mechanical properties while retaining corrosion resistance compared to metallic Zn coatings.