Studying the Insulating Properties of Oxide Films Obtained on the Ti6A14V Alloy in Tartaric Acid Solutions Using the Method of Electrochemical Decoration by Copper

IF 1 Q4 CHEMISTRY, MULTIDISCIPLINARY Chemistry & Chemical Technology Pub Date : 2021-11-25 DOI:10.23939/chcht15.04.526
O. Pylypenko, O. Smirnova, Olga Skorynina-Pohrebna, O. Khoroshev
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引用次数: 3

Abstract

The investigation data of the formation peculiarities of oxide films on the Ti6A14V alloy in tartaric acid solutions have been given. It is shown that the behavior of alloy forming dependences is conditioned by the anode current density. At ja < 0.5 A∙dm-2 the continuous oxide film is not formed on the alloy surface and the preset value of the final voltage on the cell is not reached. With an increase in ja > 0.5 A∙dm-2, alloy forming dependences show a linear behavior that is indicative of the formation of low porous films. In these conditions, the oxide film formation rate is in direct proportion to the value of ja. The electrochemical oxidation of Ti6A14V alloy in tartaric acid solutions results in the formation of interference-colored oxide films. The oxide film ultimate thickness and color are defined by the preset voltage and are independent of the current density and electrolyte concentration. The isolating properties of obtained films were studied by the way of the cathode polarization of oxidized specimens in the sulfate copper-plating electrolyte. The research done allows us to make a conclusion that electrochemical copper deposition is a convenient tool for the detection of defective spots in oxide films. It is shown that due to the specific features of the reduction kinetics of Cu2+ ions on the oxidized titanium it is reasonable to use for the studies the initial sections of polarization dependences that correspond to ΔE = 0.2–0.25 V. The alloy polarization dependences allow us to establish unavailability of apparent dependences between the oxidation current density, the electrolyte concentration, the cell final voltage value and the polarization that occurs during the Cu2+ ion reduction. The anodic connection of copper-coated specimens conditions the reversible dissolution of a greater portion of the specks of copper deposits. It is indicative of the electron conduction of film defects. The obtained data allow us to vary the electrolysis parameters in a wide range with no significant influence of the treatment mode of Ti6A14V alloy on the quality of oxide coatings.
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用铜电化学修饰法研究酒石酸溶液中Ti6A14V合金氧化膜的绝缘性能
给出了Ti6A14V合金在酒石酸溶液中氧化膜形成特性的研究数据。结果表明,合金成形依赖的行为取决于阳极电流密度。在ja < 0.5 A∙dm-2时,合金表面没有形成连续的氧化膜,电池上的最终电压也没有达到预设值。随着ja > 0.5 A∙dm-2的增加,合金形成依赖表现为线性行为,表明形成了低孔膜。在这些条件下,氧化膜的形成速率与ja的值成正比。Ti6A14V合金在酒石酸溶液中电化学氧化,形成干涉色氧化膜。氧化膜的最终厚度和颜色由预设电压决定,与电流密度和电解质浓度无关。采用氧化试样在硫酸盐镀铜电解液中阴极极化的方法,研究了所得膜的隔离性能。研究结果表明,电化学镀铜是检测氧化膜缺陷点的一种方便的工具。结果表明,由于Cu2+离子在氧化钛上还原动力学的特殊性,采用对应于ΔE = 0.2 ~ 0.25 V的极化依赖初始截面进行研究是合理的。合金极化依赖性使我们能够建立氧化电流密度、电解质浓度、电池最终电压值和Cu2+离子还原过程中发生的极化之间的明显依赖性。镀铜试样的阳极连接条件下,大部分的铜沉积斑点的可逆溶解。它指示了薄膜缺陷的电子传导。获得的数据使我们能够在较大范围内改变电解参数,而Ti6A14V合金的处理方式对氧化膜质量没有显著影响。
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来源期刊
Chemistry & Chemical Technology
Chemistry & Chemical Technology CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
1.70
自引率
44.40%
发文量
60
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