Corrosion inhibition of mild steel in 1.0 M hydrochloric acid medium by new photo-cross-linkable polymers

被引:46
作者
Baskar, R. [1 ]
Kesavan, D. [2 ]
Gopiraman, M. [3 ]
Subramanian, K. [1 ]
机构
[1] Anna Univ, Dept Chem, Madras 600025, Tamil Nadu, India
[2] Dhirajlal Gandhi Coll Technol, Dept Chem, Salem 636309, Tamil Nadu, India
[3] Natl Inst Technol, Dept Chem, Tiruchirappalli 620015, Tamil Nadu, India
关键词
Photo-cross-linkable; Corrosion inhibition; Adsorption isotherm; CARBON-STEEL; PROTECTION; CHLORIDE; IRON; ACRYLATE; BEHAVIOR; EXTRACT; LINKING; GLUCOSE; COPPER;
D O I
10.1016/j.porgcoat.2014.01.013
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Photo-cross-linkable polymers namely, poly((E)-(1-(5-(4-(3-(4-chlorophenyl)-3-oxoprop-1-enyl) phenoxy)pentyl)-1H-1,2,3-triazol-4-yl)methyl acrylate) (Cl-5) and poly((E)-(1-(5-(4-(3-(4-chlorophenyl)-3-oxoprop-1-enyl)phenoxy)decyl)-1H-1,2,3-triazol-4-yl)methyl acrylate) (Cl-10) were synthesized by click-chemistry. The polymers were characterized by using various spectroscopic techniques and the rate of cross-linking was evaluated by absorption spectroscopy. The inhibitory action of the photo-cross-linkable polymers was evaluated for mild steel (MS) corrosion in 1.0 M hydrochloric acid solution (HCl) by means of electrochemical impedance spectroscopy, potentiodynamic polarization measurements, adsorption isotherms and surface analysis. To the best of our knowledge, these are the most efficient inhibitors (Cl-5 and C-10) for the corrosion of MS in HCl reported so far. Tafel polarization measurements showed that the polymers act as mixed type inhibitors and the adsorption of the inhibitors onto the MS surface followed the Langmuir adsorption isotherm. The values of the Gibbs free energy of adsorption (Delta G(ads)) strongly supported spontaneous physicochemical adsorption of inhibitor molecules on the MS surface. The SEM-EDX results confirmed that the cross-linked polymers inhibited the corrosion to a greater extent than the intact polymer. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:836 / 844
页数:9
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