ELECTROCHEMICAL DISSOLUTION OF TITANIUM ELECTRODES POLARIZED BY ALTERNATING CURRENT IN A HYDROBROMIC ACID AQUEOUS SOLUTION

R. Nurdillayeva, A. Bayeshov, A. Abdikerim, G. Zhylysbayeva
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Abstract

The work shows the patterns of electrochemical dissolution of titanium electrodes polarized by alternating current in an aqueous solution of hydrogen bromide. The current density (200-1200 A/m2), hydrogen bromide concentration (1.0-5.0 M), electrolysis duration (0.25-2.0 hours), and electrolyte temperature depend on the current rate of the titanium electrode in the alternating current source (20°C-80°C) were considered. The maximum value of current yield was obtained at a current density of 400 A/m2 when titanium electrodes were polarized by an alternating current and it was recorded that the current yield is reduced at a high current density. It is shown that the current output for titanium increases directly proportional to the concentration of hydrogen bromide, i.e., hydrogen ion content. The order of the reaction which occurs during the electrolysis of hydrogen bromide is determined. It is proved that the current efficiency of dissolving titanium in the alternating current source decreases when the electrolysis time is increased, as the electrolysis products in the electrolyte settle down on the electrode surface. It is shown that as the temperature of the electrolyte solution is increased, the current output value for dissolving titanium rises to 48%. The activation energy determined according to the temperature-kinetic regime was 17.76 kJ/mol, the process was carried out according to the diffusion-kinetic regime. It was shown that titanium is dissolved in hydrogen bromide aqueous solution to form titanium (III) ions. The influence of the main parameters on the electrochemical dissolution of a polarized alternating current titanium electrode in hydrochloric acid is investigated and effective ways of titanium dissolution are considered. The results of the research can be used to propose a new method of titanium waste recycling and increase the potential of titanium electrode usage in production.
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交流电极化钛电极在氢溴酸水溶液中的电化学溶解
这项工作显示了钛电极在溴化氢水溶液中被交流电极化的电化学溶解模式。考虑了钛电极在交流电流源(20℃~ 80℃)下的电流速率对电流密度(200 ~ 1200 A/m2)、溴化氢浓度(1.0 ~ 5.0 M)、电解时间(0.25 ~ 2.0 h)和电解液温度的影响。用交流电流极化钛电极时,电流密度为400 a /m2时电流产率达到最大值,并记录了高电流密度时电流产率降低。结果表明,钛的电流输出与溴化氢浓度,即氢离子含量成正比。测定了溴化氢电解过程中反应的顺序。实验证明,随着电解时间的延长,电解液中的电解产物沉积在电极表面,使钛在交流电源中的溶解电流效率降低。结果表明,随着电解液温度的升高,溶解钛的电流输出值提高到48%。根据温度-动力学模式确定的活化能为17.76 kJ/mol,反应过程按照扩散-动力学模式进行。结果表明,钛在溴化氢水溶液中溶解形成钛(III)离子。研究了主要参数对极化交流钛电极在盐酸中电化学溶解的影响,探讨了钛溶解的有效途径。研究结果可为钛废料的回收利用提供新的途径,提高钛电极在生产中的应用潜力。
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