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    COMPARISON OF THE INHIBITION PROPERTY OF QUINOXALINE DERIVATIVE ON MILD STEEL IN 1.5M H2SO4, 3M HCL AND 1M H3PO4
    (Journal of materials and Environmental Sciences, 2017) Saranya, J; Sounthari, P; Chitra, S
    Corrosion inhibition of mild steel in 1.5M H2SO4, 3M HCl and 1M H3PO4 was investigated in the absence and presence of different concentrations of quinoxaline derivative namely 2,3-di(furan-2-yl)quinoxaline(FQ). Weight loss, potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) measurements were employed. Impedance measurements showed that the charge transfer resistance increased and double layer capacitance decreased with increase in the inhibitor concentration. Potentiodynamic polarization study showed that the inhibitor acted as mixedtype inhibitors in all the three acids.
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    SYNTHESIS AND CORROSION INHIBITION STUDY OF BENZOTHIAZEPINE DERIVATIVES ON MILD STEEL IN ACID MEDIUM
    (Oriental Journal of Chemistry, 2016-04-12) Sasikala, T; Parameswari, K; Chitra, S
    2-ethoxy-4-(4-phenyl-2, 3-dihydro-1, 5-benzothiazepin-2-yl) phenol (EPBTZ) and 2-(4-methoxyphenyl)-4-phenyl-2, 3-dihydro-1, 5-benzothiazepine (MPPBTZ) were synthesized by the condensation reaction between o-aminothiophenol and chalcone. The synthesized benzothiazepines were characterized by FTIR spectra. Their corrosion inhibition property on mild steel in sulphuric acid medium was investigated by weight loss and electrochemical techniques. Scanning electron microscopic studies were employed to examine the surface morphology of the inhibited and uninhibited metal samples. The compound EPBTZ revealed good corrosion protection property than MPPBTZ at all the temperatures studied. Electrochemical studies showed that the inhibitors behave as mixed type inhibitor retarding both cathodic and anodic corrosion reaction by forming an adsorbed protective layer.
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    SYNTHESIS AND CORROSION INHIBITION STUDY OF BENZOTHIAZEPINE DERIVATIVES ON MILD STEEL IN ACID MEDIUM
    (Oriental Journal of Chemistry, 2016-04-12) Sasikala, T; Parameswari, K; Chitra, S
    2-ethoxy-4-(4-phenyl-2, 3-dihydro-1, 5-benzothiazepin-2-yl) phenol (EPBTZ) and 2-(4-methoxyphenyl)-4-phenyl-2, 3-dihydro-1, 5-benzothiazepine (MPPBTZ) were synthesized by the condensation reaction between o-aminothiophenol and chalcone. The synthesized benzothiazepines were characterized by FTIR spectra. Their corrosion inhibition property on mild steel in sulphuric acid medium was investigated by weight loss and electrochemical techniques. Scanning electron microscopic studies were employed to examine the surface morphology of the inhibited and uninhibited metal samples. The compound EPBTZ revealed good corrosion protection property than MPPBTZ at all the temperatures studied. Electrochemical studies showed that the inhibitors behave as mixed type inhibitor retarding both cathodic and anodic corrosion reaction by forming an adsorbed protective layer.
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    QUANTUM CHEMICAL STUDY ON THE CORROSION INHIBITION PROPERTY OF SOME HETEROCYCLIC AZOLE DERIVATIVES
    (Oriental Journal of Chemistry, 2015-08-20) Anusuya, N; Sounthari, P; Saranya, J; Parameswari, K; Chitra, S
    Quantum chemical calculations based on density functional theory (DFT) method were performed on heterocyclic azole derivatives as corrosion inhibitors for mild steel in acid media to investigate the relationship between molecular structure of the inhibitors and the corresponding inhibition efficiencies (%). Quantum chemical parameters most relevant to their potential action as corrosion inhibitors have been calculated in the non-protonated and protonated forms in aqueous phase for comparison. Results obtained in this study indicate thatin acidic media, both the protonated and non-protonated forms of the azoles represent the better actual experimental situation.
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    ADSORPTION AND INHIBITIVE PROPERTIES OF TRIAZOLOPYRIMIDINE DERIVATIVES IN ACID CORROSION OF MILD STEEL
    (Hindawi, 2011) Parameswari, K; Chitra, S; Kavitha, S; Rajpriya, J; Selvaraj, A
    Inhibitive and adsorption properties of synthesized triazolo- pryimidine derivatives (P1, P2 & P3 ) for the corrosion of mild steel was investigated using weight loss and electrochemical methods. Inhibition efficiency increased as the concentration of the inhibitor increased but decreased with increase in temperature. The triazolopyrimidines were found to act as adsorption inhibitors for the corrosion of mild steel. The adsorption mechanism of the triazolopyrimidine was found to be physisorption, spontaneous and exothermic. Also the adsorption followed Langmuir adsorption isotherm. polarisation studies showed that the inhibitors behave as cathodic type.