Kinetics and Thermodynamic Studies on the Anodic Passivation of Ni in H2SO4 Solutions by the Galvanostatic Polarization Method
Int. J. Electrochem. Sci • 2021
Publication Information
Authors
S. Abd El Wanees,M.Abdallah, Arej S Al-Gorair, F.A.A. Tirkistani, S. Nooh, R. Assi
Keywords
Not Available
Journal
Int. J. Electrochem. Sci
Publisher
ESG
Volume
16
Issue
1
Pages
150969
publication.type
Local
Paper Link
Open Link
Supplementary Materials
Not Available
Abstract
The electrochemical passivation behavior of Ni in H2SO4 solutions was studied by the galvanostatic
anodic polarization method. The data of the polarization curves relied on the polarizing current, Iimposed,
acid concentration, C, and the temperature, T. The polarized curve elucidated various characteristic
regions confirming various oxidation processes. The 1st region is recognized by a rapid jump in the Ni
electrode potential E (zone I), due to the decay of H2 over-voltage. A large discrete 1st potential arrest,
a, coincides with the formation of Ni+
ions, while the 2nd potential arrest, b, matches the electro-oxidation
of Ni+
ions to Ni2+ ions. The second increase in the potential, E (zone II), harmonizes the onset of
passivity due to the countenance of Ni2O3. The duration time, τ, of the two arrests a and b decrease with
increasing the Iimposed, T, and the acid concentration, C. The thermodynamics activation parameters, Ea,
∆Ha, and ∆Sa for the dissolution and passivation processes are deduced and discussed.
anodic polarization method. The data of the polarization curves relied on the polarizing current, Iimposed,
acid concentration, C, and the temperature, T. The polarized curve elucidated various characteristic
regions confirming various oxidation processes. The 1st region is recognized by a rapid jump in the Ni
electrode potential E (zone I), due to the decay of H2 over-voltage. A large discrete 1st potential arrest,
a, coincides with the formation of Ni+
ions, while the 2nd potential arrest, b, matches the electro-oxidation
of Ni+
ions to Ni2+ ions. The second increase in the potential, E (zone II), harmonizes the onset of
passivity due to the countenance of Ni2O3. The duration time, τ, of the two arrests a and b decrease with
increasing the Iimposed, T, and the acid concentration, C. The thermodynamics activation parameters, Ea,
∆Ha, and ∆Sa for the dissolution and passivation processes are deduced and discussed.
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