This study presents the results on the investigation of the corrosion behavior of carbon steel in model alkaline medium in the presence of very low concentration of polymeric nanoaggregates ͓0.0024 wt % polyethylene oxide ͑PEO͒ 113 -b-PS 70 micelles͔. The steel electrodes were investigated in chloride-free and chloride-containing cement extracts. The electrochemical measurements ͑electrochemical impedance spectroscopy and potentiodynamic polarization͒ indicate that the presence of micelles alters the composition of the surface layers ͑i.e., micelles were indeed absorbed to the steel surface͒ and influences the electrochemical behavior of the steel, i.e., the micelles lead to an initially increased corrosion resistance of the steel whereas no significant improvement was observed within longer immersion periods. Surface analysis, performed by environmental scanning electronic microscopy, energy-dispersive x-ray analysis, and x-ray photoelectron spectroscopy, supports and elucidates the corrosion performance. The product layers in the micelles-containing specimens are more homogenous and compact, presenting protective ␣-Fe 2 O 3 and/or Fe 3 O 4 , whereas the product layers in the micelles-free specimens exhibit mainly FeOOH, FeO, and FeCO 3 , which are prone to chloride attack. Therefore, the increased "barrier effects" along with the layers composition and altered surface morphology denote for the initially increased corrosion resistance of the steel in chloride-containing alkaline medium in the presence of micelles. A well-known fact is that corrosion of steel reinforcement can cause reinforced concrete deterioration and thus affect civil structures durability.1,2 Logically, corrosion-related issues result in a significant economic loss. For example, in the United States, the annual direct cost of bridge infrastructure corrosion was estimated to be $8.3 billion, and the indirect cost was reported to be many times higher.
3In normal conditions, the reinforcing steel embedded in cementbased materials ͑i.e., cement paste, mortar, and concrete͒ is in a passive state because of the high alkalinity ͑pH = 12.6-13.5͒ of the pore solution and the cement paste, respectively. 4,5 However, corrosion can be initiated due to carbonation or chloride contamination. 6 Carbonation can result in a pH drop ͑to about 8-9͒ 7,8 in the pore solution of the bulk cementitious matrix, leading to a general corrosion of the reinforcing steel. In the event of chloride penetration and chloride arrival at the steel/cement paste interface, localized corrosion is initiated; the local pH can drop to even below 6, resulting in fast corrosion propagation. This will cause accelerated damage of the reinforcing steel and possible rapid failure of reinforced concrete.
9To minimize the corrosion processes, various methods and techniques are used. Among them, the polymer-based organic corrosion inhibitors are widely applied because they can provide an easy handling, cost-effective corrosion prevention, delaying corrosion initiation.10-14 The organic inh...