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International Journal of Corrosion
Volume 2016 (2016), Article ID 9532809, 21 pages
Research Article

Study of New Thiazole Based Pyridine Derivatives as Potential Corrosion Inhibitors for Mild Steel: Theoretical and Experimental Approach

1Department of Studies in Chemistry, Manasagangotri, University of Mysore, Mysuru, Karnataka 570006, India
2Department of Chemistry, Sri Venkateswara College, Dhaula Kuan, New Delhi 110021, India

Received 11 September 2015; Revised 16 January 2016; Accepted 17 January 2016

Academic Editor: Michael J. Schütze

Copyright © 2016 T. K. Chaitra et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Three new thiazole based pyridine derivatives 5-(4-methoxy-phenyl)-thiazole-2-carboxylic acid pyridin-2-ylmethylene-hydrazide (2-MTPH), 5-(4-methoxy-phenyl)-thiazole-2-carboxylic acid pyridin-3-ylmethylene-hydrazide (3-MTPH), and 5-(4-methoxy-phenyl)-thiazole-2-carboxylic acid pyridin-4-ylmethylene-hydrazide (4-MTPH) were synthesized and characterized. Corrosion inhibition performance of the prepared compounds on mild steel in 0.5 M HCl was studied using gravimetric, potentiodynamic polarisation, and electrochemical impedance techniques. Inhibition efficiency has direct relation with concentration and inverse relation with temperature. Thermodynamic parameters for dissolution and adsorption process were evaluated. Polarisation study reveals that compounds act as both anodic and cathodic inhibitors with emphasis on the former. Impedance study shows that decrease in charge transfer resistance is responsible for effective protection of steel surface by inhibitors. The film formed on the mild steel was investigated using FTIR, SEM, and EDX spectroscopy. Quantum chemical parameters like , , , hardness, softness, and ionisation potential were calculated. Higher value of and lower value of indicate the better inhibition efficiency of the compounds. Lower ionisation potential of inhibitors indicates higher reactivity and lower chemical stability.