Comparative Electrochemical and Corrosion Inhibition Assessment of Commercial Tannic Acid, Crude Extracts, and n-Butanol Fractions of Quercus robur Stem Bark
DOI:
https://doi.org/10.31489/2959-0663/3-26-13Keywords:
Quercus robur, tannins, corrosion inhibitor, mild steel, potentiodynamic polarization, Langmuir adsorption isotherm, n-butanol fraction, commercial tannic acid, adsorption isothermsAbstract
In this study, crude aqueous-ethanolic extract and n-butanol fraction of Quercus robur stem bark were obtained, and their corrosion-inhibition performance on mild steel in 1 M HCl was evaluated while their performances are compared to the commercial tannic acid used as standard. Corrosion inhibition was assessed by potentiodynamic polarization at 200 mg L⁻¹ after 1 hour of immersion. The n-butanol fraction exceeded the 71.9 % efficiency of the crude extract, though remaining below the 98.2 % maximum efficiency observed for the tannic acid standard at 1000 mg L⁻¹. Polarization curve shifts support classifying the tannin-containing samples as mixed-type inhibitors. Adsorption-isotherm analysis showed model-dependent behavior: the Freundlich model provided the highest R2 for the crude extract, while the Langmuir model provided the highest R2 for the n-butanol fraction and tannic acid. These fits represent empirical descriptions of concentration-dependent inhibition rather than direct molecular mechanisms. For commercial tannic acid, the standard Gibbs free energy of adsorption as approximately -33.3 kJ mol⁻¹, indicating thermodynamically favorable adsorption. Overall, solvent fractionation improved inhibition performance. These findings indicate the n-butanol fraction's potential as a plant-derived inhibitor. Further phytochemical investigation, isolation and characterization are required to properly identify the active constituents underlying the adsorption mechanisms.
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Copyright (c) 2026 Bibisara D. Burkitbayeva, Adewale O. Adeloye, Alfira F. Miftakhova, Raigul Zh. Jumanova, Gulmira S. Beisenova, Akmaral M. Argimbayeva, Gulzhan Seit, Yeldana G. Bakhytzhan, Aruzhan B. Smail

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