Inhibitive effect of ester-quats surfactants in the series of (alcanoyloxy)propyl n-alkyl dimethyl ammonium bromide on the corrosion of iron in acid medium

被引:14
作者
Chami, R. [1 ]
Bensajjay, F. [1 ]
Alehyen, S. [1 ]
El Achouri, M. [1 ]
Bellaouchou, A. [2 ]
Guenbour, A. [2 ]
机构
[1] Univ Mohammed 5, Ecole Normale Super, Lab Physicochim Mat Inorgan & Organ, Rabat, Morocco
[2] Univ Mohammed 5, Fac Sci Rabat, Lab Corros, Rabat, Morocco
关键词
Ester-quats; Surfactants; Iron; Corrosion inhibition; Electrochemical polarization measurement-impedance spectroscopy; MILD-STEEL CORROSION; GEMINI SURFACTANTS; IODIDE-IONS; M H2SO4; ADSORPTION; CHLORIDE; PERFORMANCE; MECHANISM; IMPEDANCE; ALUMINUM;
D O I
10.1016/j.colsurfa.2015.02.044
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ester-quats surfactants in the series of (alcanoyloxy) propyl n-alkyl dimethyl ammonium bromide referred as LC3Cm (where m is the hydrocarbon chain lengths 8, 12 and 14) were synthesized and characterized by the usual spectroscopic methods (RMN, IR, MS). Their critical micellar concentrations were determined by conductimetric measurements. The inhibitory effect of these ester-quats on the corrosion of iron in 1 M HCl was investigated using weight loss, resistance, electrochemical polarization and electrochemical impedance methods. Results obtained show that these compounds are good corrosion inhibitors and the high inhibition efficiencies were observed around their critical micellar concentrations (CMCs). The effect of temperature on the corrosion inhibition of iron has been also studied in the temperature range [20-60 degrees C] and then the activation energies in the absence and presence of different concentrations of surfactants have been evaluated. Kinetic and thermodynamic parameters of adsorption were also determined and discussed. The surface morphology of iron samples immersed in 1 M HCl in the absence and in the presence of inhibitor at various concentrations was studied by scanning electron microscopy (SEM). (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:468 / 476
页数:9
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