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Experimental and theoretical studies for mild steel corrosion inhibition in 1.0M HCl by three new quinoxalinone derivatives

dc.contributor.authorTazouti, A.
dc.contributor.authorGalai, M.
dc.contributor.authorTouir, R.
dc.contributor.authorTouhami, M. Ebn
dc.contributor.authorZarrouk, A.
dc.contributor.authorRamli, Y.
dc.contributor.authorSaracoglu, M.
dc.contributor.authorKaya, S.
dc.contributor.authorKandemirli, F.
dc.contributor.authorKaya, C.
dc.date.accessioned2026-01-02T23:46:15Z
dc.date.issued2016-09-01
dc.description.abstractAbstract Three quinoxalinone derivatives, namely (E)-3-styrylquinoxalin-2(1H)-one (SQ), (E)-3-(4-methoxystyryl)quinoxalin-2(1H)-one (MOSQ) and (E)-3-(4-methoxystyryl)-7-methylquinoxalin-2(1H)-one (MOSMQ) were synthesized and characterized. Thus, their inhibition effects on mild steel corrosion in 1.0 M HCl medium were investigated using weight loss method, electrochemical measurements. The effect of temperature on the corrosion behavior of mild steel was studied in the range of 298–328 K. Polarization measurements indicated that, the studied compounds act as a mixed type inhibitors, the inhibition efficiency depends on their concentrations and followed the order MOSQ > MOSMQ > SQ. Electrochemical impedance spectroscopy showed that all compounds act by the formation of a protective film at the metallic surface. The adsorption of three inhibitors on steel surface obeyed Langmuir model, thus the thermodynamic and kinetic parameters were calculated and discussed. In the part based on DFT calculations of this study, some electronic properties of studied molecules were calculated and discussed with the help of B3LYP/6-311G (d,p), B3LYP/6-311 ++G (d,p) and B3LYP/6-311G ++ (2d,2p) methods. The theoretical and experimental results are in good agreement.
dc.description.urihttps://doi.org/10.1016/j.molliq.2016.03.083
dc.description.urihttps://dx.doi.org/10.1016/j.molliq.2016.03.083
dc.description.urihttps://hdl.handle.net/20.500.12418/7205
dc.description.urihttps://avesis.erciyes.edu.tr/publication/details/c9afeb83-8720-42f2-87ec-e2d4684918aa/oai
dc.description.urihttps://doi.org/https://doi.org/20.500.12418/7205
dc.description.urihttps://doi.org/https://doi.org/10.1016/j.molliq.2016.03.083
dc.identifier.doi10.1016/j.molliq.2016.03.083
dc.identifier.endpage832
dc.identifier.issn0167-7322
dc.identifier.openairedoi_dedup___::42199891bad3b9c51e49e67fe775aace
dc.identifier.orcid0009-0003-6383-8230
dc.identifier.orcid0009-0003-2175-7280
dc.identifier.orcid0000-0002-6885-5692
dc.identifier.orcid0000-0003-4027-9643
dc.identifier.scopus2-s2.0-84975789725
dc.identifier.startpage815
dc.identifier.urihttps://hdl.handle.net/20.500.12597/36250
dc.identifier.volume221
dc.identifier.wos000383004100099
dc.language.isoeng
dc.publisherElsevier BV
dc.relation.ispartofJournal of Molecular Liquids
dc.rightsCLOSED
dc.subjectMild steel
dc.subjectComputational chemistry
dc.subjectQuinoxalinone derivatives
dc.subjectCorrosion inhibition
dc.subjectElectrochemical techniques
dc.subject0 M HCl
dc.titleExperimental and theoretical studies for mild steel corrosion inhibition in 1.0M HCl by three new quinoxalinone derivatives
dc.typeArticle
dspace.entity.typePublication
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Thus, their inhibition effects on mild steel corrosion in 1.0 M HCl medium were investigated using weight loss method, electrochemical measurements. The effect of temperature on the corrosion behavior of mild steel was studied in the range of 298–328 K. Polarization measurements indicated that, the studied compounds act as a mixed type inhibitors, the inhibition efficiency depends on their concentrations and followed the order MOSQ > MOSMQ > SQ. Electrochemical impedance spectroscopy showed that all compounds act by the formation of a protective film at the metallic surface. The adsorption of three inhibitors on steel surface obeyed Langmuir model, thus the thermodynamic and kinetic parameters were calculated and discussed. In the part based on DFT calculations of this study, some electronic properties of studied molecules were calculated and discussed with the help of B3LYP/6-311G (d,p), B3LYP/6-311 ++G (d,p) and B3LYP/6-311G ++ (2d,2p) methods. 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