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Corrosion inhibition capacity of two heterocyclic oximes on copper in nitric acid: Electrochemical, quantum chemical and surface morphological investigations

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dc.contributor.author Varghese, C Sini
dc.contributor.author K, Joby Thomas
dc.contributor.author Raphael, Vinod
dc.contributor.author Shanmughan, Shaju
dc.date.accessioned 2022-03-03T09:26:45Z
dc.date.available 2022-03-03T09:26:45Z
dc.date.issued 2019-03
dc.identifier.citation Varghese,C;K,Joby;Raphael, Vinod;Shanmughan,Shaju.Corrosion inhibition capacity of two heterocyclic oximes on copper in nitric acid: Electrochemical, quantum chemical and surface morphological investigations.Current Chemistry Letters 2019/03/01,VL-8,pages 1-12. en_US
dc.identifier.issn 19277296
dc.identifier.other 10.5267/j.ccl.2018.12.001
dc.identifier.uri http://starc.stthomas.ac.in:8080/xmlui/xmlui/handle/123456789/185
dc.description.abstract Two heterocyclic oximes (E)-N-hydroxy-1-(pyridin-2-yl)methanimine (Hp2ylm) and (E)-N-hydroxy-1-(pyridin-3-yl)methanimine (Hp3ylm) were synthesized from pyridine-2-carbaldehyde and pyridine-3-carbaldehyde, respectively. These oximes were characterized by various spectroscopic tools like UV, IR, MASS and NMR. The inhibition capacity of these oximes against copper corrosion in 0.1 M HNO3 was determined by polarization and impedance spectroscopic studies (EIS). At all concentrations, Hp3ylm exhibited higher inhibition efficiency than Hp2ylm. Attempt was made to illustrate the mechanism of corrosion inhibition by these oximes with the help of adsorption isotherm, scanning electron microscopic (SEM) and quantum chemical studies. en_US
dc.description.sponsorship UGC en_US
dc.language.iso en en_US
dc.publisher Growing Science en_US
dc.subject Corrosion en_US
dc.subject Inhibitor en_US
dc.subject Polarization en_US
dc.subject Impedance en_US
dc.subject Adsorption en_US
dc.title Corrosion inhibition capacity of two heterocyclic oximes on copper in nitric acid: Electrochemical, quantum chemical and surface morphological investigations en_US
dc.type Article en_US


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