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dc.contributor.authorEl Kacimi, Y.
dc.contributor.authorAzaroual, M. A.
dc.contributor.authorTouir, R.
dc.contributor.authorGalai, M.
dc.contributor.authorAlaoui, K.
dc.contributor.authorSfaira, M.
dc.contributor.authorTouhami, M. Ebn
dc.contributor.authorKaya, S.
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T09:40:14Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T09:40:14Z
dc.date.issued2017
dc.identifier.issn2365-6433
dc.identifier.issn2365-7448
dc.identifier.urihttps://dx.doi.org/10.1007/s41207-016-0011-8
dc.identifier.urihttps://hdl.handle.net/20.500.12418/6648
dc.descriptionWOS: 000459072300001en_US
dc.description.abstractThe inhibition efficiency of three substituted phenyltetrazole compounds, namely 5-(4-chlorophenyl)-1H-tetrazole (Cl-PT), 5-(4-methoxyphenyl)-1H-tetrazole (MO-PT), and 5-phenyl-1H-tetrazole (PT), for mild steel corrosion in 5.0 M HCl solution was investigated using weight loss measurements and electrochemical study. It is showed that these compounds are good inhibitors for mild steel corrosion in 5.0 M HCl solution which act as cathodic type inhibitors. So, the inhibition efficiency was increased with inhibitor concentration in the order of Cl-PT > MO-PT > PT which depended on their molecular structures. It is found also that these compounds toke its performance at different temperatures range from 298 to 328 K. In addition, the thermodynamic adsorption parameters at different concentrations were investigated and discussed. Finally, it is seen that the inhibition efficiency of the studied compounds increased with immersion time to reach a maximum at 12 h.en_US
dc.language.isoengen_US
dc.publisherSPRINGER HEIDELBERGen_US
dc.relation.isversionof10.1007/s41207-016-0011-8en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCorrosion and inhibitionen_US
dc.subjectSubstituted phenyltetrazoleen_US
dc.subjectMild steelen_US
dc.subject5.0 M HClen_US
dc.subjectElectrochemical measurementsen_US
dc.titleCorrosion inhibition studies for mild steel in 5.0 M HCl by substituted phenyltetrazoleen_US
dc.typearticleen_US
dc.relation.journalEURO-MEDITERRANEAN JOURNAL FOR ENVIRONMENTAL INTEGRATIONen_US
dc.contributor.department[El Kacimi, Y. -- Touir, R. -- Galai, M. -- Alaoui, K. -- Touhami, M. Ebn] Univ Ibn Tofail, Fac Sci, Lab Mat Engn & Environm, Modeling & Applicat, BP 133, Kenitra 4000, Morocco -- [Touir, R.] CRMEF, Ave Allal Al Fassi,BP 6210, Rabat, Morocco -- [Azaroual, M. A. -- Sfaira, M.] Fac Sci Dhar El Mahraz, Lab Physicochimitry Anal & Catalyt Mat Environm, BP 1796, Atlas 30000, Fes, Morocco -- [Kaya, S.] Cumhuriyet Univ, Dept Chem, Fac Sci, TR-58140 Sivas, Turkeyen_US
dc.identifier.volume2en_US
dc.identifier.issue1en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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