Search

Herein, the corrosion performance of different stainless steel (SS) reinforcing bar grades in alkaline solution is presented, including UNS S32205 duplex stainless steel (DSS), UNS S32304 and UNS S32001 lean DDS (LDSS). The electrochemical dissolution kinetics were studied by potentiodynamic polarization and the Tafel slope method. The environmentally assisted cracking (EAC) mechanisms of the different SS grades in the presence of Cl− were revealed with the slow strain rate test (SSRT). The higher activation of the anodic branch and the loss of toughness were related to the austenite-to-ferrite phase ratio. UNS S32205 DSS presented the slowest anodic dissolution kinetics, mainly due to the higher austenite content compared to the other LDSS; however, it suffered a more severe EAC than the UNS S32304 LDSS. In the case of UNS S32001 LDSS, even while having the lowest Ni content (i.e., large ferrite α-phase ratio), it experienced the least decrease in elongation as well as low anodic dissolution kinetics for Cl− contents up to 8 wt.%, where the Cl− threshold was reached. [ABSTRACT FROM AUTHOR]

In this work, the corrosion performance of a new developed high-entropy alloy (HEA) of the composition Al10Cr30Fe25Mn30Ti5 (at. %) was studied. The corrosion testing of the Al10Cr30Fe25Mn30Ti5 HEA was carried out in 2.5 M NaOH, 0.6 M NaCl, and in 0.5 M H2SO4. The correlation between the microstructure, elemental composition, density, hardness, and corrosion resistance of the new developed Al10Cr30Fe25Mn30Ti5 HEA was investigated. The impedance response showed protective corrosion behavior for the neutral and acidic pH, while the alkaline environment led to a passivity breakdown due to dissolution of Al forming Al(OH)3. The outcome of the presented study suggests that new developed HEA is suitable to be used in industrial environments with a neutral and acidic pH. [ABSTRACT FROM AUTHOR]

The use of nitrite- and nitrate-based inhibitors provides corrosion protection by the development of passive oxide film on the metal surface in reinforced concrete applications. However, the impact of the nitrite and nitrate ratio in the mixture has not been widely studied. In this study, the corrosion protection provided by NaNO2:NaNO3 inhibitor blends with ratios of 0.5:1, 1:1, and 1:0.5 were studied to maximize corrosion inhibition efficiency. The nitrite species imparted higher corrosion protection, as shown by cyclic potentiodynamic polarization, with an icorr of 1.16 × 10–7 A/cm2 for the 1:0.5 mixture, lower than for both the 1:1 and 0.5:1 mixtures. Electrochemical impedance spectroscopy was also performed, with the 1:0.5 mixture consistently displaying high resistance values, showing an Rct of 1.31 × 105 Ω cm2. The effect of temperature was also assessed; the Ea's of the corrosion reaction were calculated to be 12.1, 9.2, and 4.9 kJ/mol for the 0.5:1, 1:1, and 1:0.5 (NO2−:NO3−) mixtures, respectively. Density functional theory was applied to analyze the molecular properties and to determine the relationship between the quantum properties and corrosion inhibition. The ΔE of NO2− was found to be −5.74 eV, lower than that of NO3− (−5.45 eV), corroborating the experimental results. Lastly, commercially available inhibitor mixtures were investigated and nitrite/nitrate concentrations determined to evaluate their corrosion protection performance; amongst the two inhibitor blends tested, Sika was found to outperform Yara due to its greater NO2− concentration. [ABSTRACT FROM AUTHOR]

A review by EFC-WP11 demonstrates that differences exist in this regard between AAMs and Portland cements, and between types of AAMs, mainly caused by differing pore solution compositions. These differences can lead to distinct anodic polarisation curves, low open circuit potentials, and low polarisation resistances for certain AAMs, which might be incorrectly interpreted as indicating active corrosion of the steel reinforcement. However, the present knowledge about how AAMs protect steel reinforcement in concrete elements, and about the significance of the outcomes of electrochemical analytical methods to study this subject, is incomplete. [Extracted from the article]