Influence of Titanium Additions to Aluminum on the Microhardness Value and Electrochemical Behavior of Synthesized Aluminum-Titanium Alloy in Solutions of HCl and H3PO4

材料科学 塔菲尔方程 腐蚀 冶金 合金 介电谱 扫描电子显微镜 钛合金 电化学 复合材料 物理化学 电极 化学
作者
Abdel-Rahman El-Sayed,Adila E. Mohamed,Fatma S. M. Hassan,Mohamed Sarwat El-Mahdy
出处
期刊:Journal of Materials Engineering and Performance [Springer Science+Business Media]
卷期号:32 (4): 1760-1777 被引量:9
标识
DOI:10.1007/s11665-022-07248-8
摘要

Abstract The effect of Ti content in various concentrations as an alloying element with Al on both microhardness and crystallization structure of aluminum–titanium alloys was studied, utilizing x-ray diffraction (XRD) and a scanning electron microscope (SEM). To study the electrochemical and corrosion performance of Al and its investigated alloys in 0.5 M solutions of HCl and H 3 PO 4, two different techniques were used: extrapolation of Tafel plot and electrochemical impedance spectroscopy (EIS). Tafel plots and EIS revealed a similar trend. Generally, the rate of corrosion of the alloys was higher than that of Al. This investigation exhibited that the corrosion of Al alloying with Ti increased with an increase in both Ti content and temperature, which is due to reducing the growth of oxide film on the surface. Changes in the standard values of both entropy (Δ S ) and enthalpy (Δ H ), in addition to apparent activation energy ( E a ) of corrosion processes of Al and its alloys in HCl and H 3 PO 4, were evaluated. The evaluated data indicated negative values of Δ S, while the values of Δ H were positive. Besides, the decrease in Δ H value with the increase of Ti content in the alloy revealed that the dissolution of the studied alloys was fast. The positive values of Δ H were accompanied by an endothermic process. On the other hand, the activation energy ( E a ) was decreased as a result of Al alloying with Ti in the two mentioned acids. Those results were supported by the corrosion current density ( i corr .) and impedance parameters. By comparing the data obtained for both HCl and H 3 PO 4 in all investigated electrodes, the corrosion current density ( i corr .) in H 3 PO 4 was lower than that in HCl. Such behavior can be ascribed to the aggressive attack of Cl¯ ions on the surfaces of the investigated electrodes, leading to pits formation.

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