Corrosion inhibition of mild steel in 1M HCl by D-glucose derivatives of dihydropyrido [2,3-d:6,5-d′] dipyrimidine-2, 4, 6, 8(1H,3H, 5H,7H)-tetraone

dc.contributor.authorVerma, Chandrabhan Verma
dc.contributor.authorQuraishi, Mumtaz Ahmad
dc.contributor.authorKluza, Kamil
dc.contributor.authorMakowska-Janusik2, M.
dc.contributor.authorOlasunkanmi3, Lukman O.
dc.contributor.authorEbenso, Eno E.
dc.date.accessioned2023-05-13T17:50:53Z
dc.date.available2023-05-13T17:50:53Z
dc.date.issued2017-02-07
dc.descriptionInternational journal of Scientific Reports, 17p.en_US
dc.description.abstractD-glucose derivatives of dihydropyrido-[2,3-d:6,5-d′]-dipyrimidine-2, 4, 6, 8(1H,3H, 5H,7H)-tetraone (GPHs) have been synthesized and investigated as corrosion inhibitors for mild steel in 1M HCl solution using gravimetric, electrochemical, surface, quantum chemical calculations and Monte Carlo simulations methods. The order of inhibition efficiencies is GPH-3 > GPH-2 > GPH-1. The results further showed that the inhibitor molecules with electron releasing (-OH, -OCH3) substituents exhibit higher efficiency than the parent molecule without any substituents. Polarization study suggests that studied compounds are mixed-type but exhibited predominantly cathodic inhibitive effect. The adsorption of these compounds on mild steel surface obeyed the Langmuir adsorption isotherm. SEM, EDX and AFM analyses were used to confirm the inhibitive actions of the molecules on mild steel surface. Quantum chemical (QC) calculations and Monte Carlo (MC) simulations studies were undertaken to further corroborate the experimental results.en_US
dc.identifier.otherDOI: 10.1038/srep44432
dc.identifier.urihttps://ir.oauife.edu.ng/123456789/5508
dc.language.isoenen_US
dc.publisherNature publishingen_US
dc.subjectCorrosion inhibitionen_US
dc.subjectmild steelen_US
dc.subjectD-glucose derivativesen_US
dc.subjectLangmuir adsorption isothermen_US
dc.subjectdihydropyridoen_US
dc.titleCorrosion inhibition of mild steel in 1M HCl by D-glucose derivatives of dihydropyrido [2,3-d:6,5-d′] dipyrimidine-2, 4, 6, 8(1H,3H, 5H,7H)-tetraoneen_US
dc.typeJournalen_US
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