Experimental and computational studies on the corrosion inhibition potential of a novel synthesized thiophene and pyridine-based 1,3,4-oxadiazole hybrid against mild steel corrosion in 1 N HClShow others and affiliations
2025 (English)In: Environmental Science and Pollution Research, ISSN 0944-1344, E-ISSN 1614-7499, Vol. 32, no 28, p. 17005-17031Article in journal (Refereed) Published
Abstract [en]
A convenient synthesis of a novel 1,3,4-oxadiazole derivative, specifically known as, 2-(5-methylthiophen-2-yl)-5-(pyridin-3-yl)-1,3,4-oxadiazole (MTPO), is reported along with a comprehensive evaluation of its ability to inhibit the corrosion of mild steel (MS) in a 1 N HCl environment using weight loss, EIS, PDP, SEM, EDX, and UV–Vis spectroscopy. The investigated inhibitor expressed excellent inhibition efficiency (99.05% at 500 ppm, 298 K) with a mixed-type inhibitory mechanism as demonstrated by the PDP technique. Furthermore, MTPO followed Langmuir adsorption isotherm, which provides insights into the adsorption phenomena, demonstrating that it exhibits superior adsorption behavior on the MS surface compared. In silico investigations, using DFT computation and MD simulation complements the experimental outcomes revealing strong adsorbing attributes of the MTPO hybrid with the ω − and ω + values of 8.8882 eV and 4.4787 eV, respectively. In addition, the radial distribution function also addressed the chemisorption behavior of MTPO. This article also takes into consideration the various ways in which the inhibitor interacts with the mild steel, offering potential insights for developing strategies to mitigate metal dissolution in acidic environments.
Place, publisher, year, edition, pages
Springer Nature , 2025. Vol. 32, no 28, p. 17005-17031
Keywords [en]
Computational chemistry, Corrosion inhibition, Inhibitory mechanism, Metal dissolution mitigation, Mild steel, Oxadiazole derivative
National Category
Surface- and Corrosion Engineering Materials Chemistry
Identifiers
URN: urn:nbn:se:kth:diva-367376DOI: 10.1007/s11356-024-32678-3ISI: 001176979100012PubMedID: 38446299Scopus ID: 2-s2.0-85186917806OAI: oai:DiVA.org:kth-367376DiVA, id: diva2:1984694
Note
QC 20260123
2025-07-172025-07-172026-01-23Bibliographically approved