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Документ Chemical deposition of CdS films from ammoniac-thiourea solutions(Технологический центр, 2018) Pancheva, Hanna; Khrystych, Olena; Mykhailova, Evgeniia; Ivashchenko, Maryna; Pilipenko, AlexeiThis paper investigates the process of chemical deposition of CdS films from ammonia-thiourea solutions. It was established that a change in the turbidity of solution occurs in the process of chemical deposition. The results of visual observations and measurement of turbidity of solution allowed us to establish that these dependences could be used to monitor the status of the process. Visual observations correlate with the obtained dependences for turbidity and suggest that the chemical deposition of CdS includes the accumulation of colloidal-dispersed precipitate in the volume of solution, agglomeration of CdS particles, and a stationary mode of the CdS film growth at the surface of a sample. The first stage of the process is matched by a sharp increase in the turbidity of solution; the second stage is accompanied by the emergence of a maximum in the dependence. No significant change in turbidity occurs at the third stage. The observation of morphology of the resulting precipitate allowed us to establish working concentrations of reagents in solution, which ensure obtaining a high-quality CdS film with a thickness not less than 100 μm. The working concentrations of cadmium chloride, ammonia, and thiourea are, respectively, 1.8, 0.6, and 8.4 g·l⁻¹. It was assumed that the CdS formation is accompanied by the formation of thiourea. This is confirmed by data on the analysis of a working solution. An analysis of the solution revealed high concentrations of the CO₃²⁻ ions, which are a product of the thiourea decomposition. The data obtained are a preliminary stage in the development of a technology of chemical deposition of CdS films from ammonia-thiourea solutions.Документ Establishing the patterns in the formation of oxide films on the alloy Ti6Al4V in carbonic acid solutions(Технологический центр, 2018) Ivashchenko, Maryna; Smirnova, Olha; Kyselova, Svitlana; Avina, Svetlana; Sincheskul, Alexander; Pilipenko, AlexeiThis paper reports results of studying the features of the formation of thin interference-colored oxide films on the alloy Ti6Al4V alloy in solutions of carboxylic acids. It has been established that a change in voltage on the cell corresponding to the molding dependence of the alloy depends on the anodic current density. At current densities <0.5 A∙dm⁻², a continuous oxide film is not formed at the alloy surface and the assigned voltage value is not reached. An increase in current density to values higher than 0.5 A∙dm⁻² predetermines a linear change in voltage over time with followed by reaching the assigned magnitude U. The maximum film thickness for these conditions is defined by the voltage magnitude and does not depend on the electrolysis mode. Color of the oxide film is defined by the specified value for the molding voltage and does not depend on current density, nature and concentration of carboxylic acid. A match between the molding dependences of oxidation obtained in different electrolytes suggests that the formation of oxide proceeds in line with the same mechanism. The obtained data are explained by the fact that the formation of oxide under the galvanic static mode takes place under conditions of the presence of a constant potential gradient in the oxide film. An increase in the voltage magnitude applied to the cell predetermines a proportional increase in the maximum oxide thickness, since it leads to an increase in the amount of electricity passed through the cell and a corresponding increase in the mass of the oxidized metal. Results of the study into determining the effect of the nature of carboxylic acid on the formation process of an oxide film on the alloy Ti6Al4V using the method of electrochemical oxidation have demonstrated that the nature of the electrolyte does not affect the characteristics of its formation. The obtained data allow us to suggest that the choice of an electrolyte for the development of a technology for electrochemical oxidation of titanium implants should be based on the results of studying the functional properties of the obtained coatings.