Copper corrosion inhibition in 0.1 M nitric acid (HNO3) solution by some secondary amines, namely, dibutyl amine (C8H20N), diethyl amine (C4H11N), and diphenyl amine (C12H11N), was investigated using potentiodynamic polarization, electrochemical impedance spectroscopy (EIS), and electrochemical frequency modulation (EFM) techniques. A significant decrease in the corrosion rate of copper was observed in the presence of the investigated compounds. The corrosion rate was found to depend on the concentration, temperature, and type of inhibitor. The adsorption of these compounds was found to follow the Temkin adsorption isotherm. Tafel polarization data indicated that the investigated amines were inhibiting both cathodic and anodic reactions. The thermodynamic activation parameters of copper dissolution in 0.1 M HNO3 were determined and discussed. The results obtained from the three different techniques were in good agreement. Clear correlation was found between corrosion inhibition efficiency and theoretical parameters obtained from the PM3 semi-empirical method. The experimental results are supported by the theoretical data.
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1 July 2012
Research Article|
May 16 2012
Corrosion Inhibition of Copper in Nitric Acid Solution Using Some Secondary Amines
A.S. Fouda;
‡ Corresponding author. E-mail: [email protected].
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‡ Corresponding author. E-mail: [email protected].
* Department of Chemistry, Faculty of Science, El-Mansoura University, El-Mansoura-35516, Egypt.
** Department of Chemistry, Faculty of Science, Benha University, Egypt. Present address: Department of Chemistry, Faculty of Applied Science, Umm Al-Qura University, KSA.
Received:
May 23 2011
Accepted:
October 15 2011
Online ISSN: 1938-159X
Print ISSN: 0010-9312
© 2012 NACE International
2012
CORROSION (2012) 68 (7): 610–619.
Article history
Received:
May 23 2011
Accepted:
October 15 2011
Citation
A.S. Fouda, M. Abdallah, A.M. Atya, H.D. Sabaa; Corrosion Inhibition of Copper in Nitric Acid Solution Using Some Secondary Amines. CORROSION 1 July 2012; 68 (7): 610–619. https://doi.org/10.5006/0454
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