Action of chelators on solid iron in phosphate-containing aqueous solutions

To study the effect of strong iron-ligands on steel corrosion, mild steel electrodes were immersed in solutions containing 20 mM phosphate buffer (pH=7.2) and between 0.01 mM and 1 M of either the iron(II)-chelators 2,2^′-bipyridine or FerroZine, or the iron(III)-chelators citrate or acetylacetonate. Resulting surface reactions were investigated by quantifying the electrochemical potential (E), the electrochemical polarization resistance (R_p), the corrosion current (I_corr) and the release of iron into solution. The surface was further analyzed by scanning electron microscopy (SEM/SEM-EDAX) and atomic force microscopy. Concentrations of 0.1 mM of any of the chelators led to slight, temporary changes in E, I_corr and R_p. Concentrations of 10 mM resulted in characteristic changes of E, which were the same for all chelators and in the precipitation of FePO₄ in the case of citrate and acetylacetonate, or vivianite [Fe₃(PO₄)₂ · 8H₂O] in the case of bipyridine and FerroZine. Concentrations of 1 mM of both iron(III)-chelators led to a temporary drop of E similar to that found with 0.1 mM chelator. With iron(II)-chelators, E dropped to about −500 mV before oscillating for several days. The amplitudes of the oscillations were up to 200 mV with periods of 30 and 20-25 min for bipyridine and FerroZine, respectively.     

Substitutional adsorption isotherms and corrosion inhibitive properties of some oxadiazol-triazole derivative in acidic solution

A newly synthesized oxadiazol-triazole derivative (TOMP), was investigated as corrosion inhibitor of mild steel in 0.5 M H₂SO₄ solution using weight loss measurements, polarization and electrochemical impedance spectroscopy (EIS) methods. Results obtained revealed that TOMP is effective corrosion inhibitor for mild steel in sulphuric acid and its efficiency attains more than 97.6% at 298 K. The number of water molecules (X) replaced by a molecule of organic adsorbate was determined from the substitutional adsorption isotherms applied to the data obtained from the weight loss experiments performed on mild steel specimen in acidic solution in the 298-333 K range.     

The effects of water pollution on the immersion corrosion of mild and low alloy steels

The short-term immersion corrosion of mild and low alloy steels in seawaters is known to be proportional to the concentration of dissolved oxygen (DO) in the bulk water. Longer-term corrosion is a function of the activity of sulphate-reducing bacteria and is influenced by the concentration of nutrients in the bulk water. These influences are examined in more detail for the corrosion of steels in the brackish waters of the River Thames and for several immersion corrosion sites on the Eastern Australian seaboard and in the North Sea. The published data sources were supplemented with plausible assumptions about environmental conditions. New interpretations of the data are provided based on the previously published model for immersion corrosion. For waters with negligible salinity and sulphate levels early corrosion loss was shown to depend on the dissolved oxygen content of the waters, and later corrosion loss was a direct function of nitrogenous nutrient (pollution) levels. This also applies to longer-term corrosion.     

Quinolin-5-ylmethylene-3-{[8-(trifluoromethyl)quinolin-4-yl]thio}propanohydrazide as an effective inhibitor of mild steel corrosion in HCl solution

Quinolin-5-ylmethylene-3-{[8-(trifluoromethyl)quinolin-4-yl]thio}propanohydrazide (QMQTPH) was synthesized, characterized and tested as a corrosion inhibitor for mild steel in 1 M and 2 M HCl solution using potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). Polarization resistances calculated from the EIS measurements were in good agreement with those obtained from direct current (DC) polarization measurements. The mild steel samples were also analyzed by scanning electron microscopy (SEM). The results showed that QMQTPH is an excellent inhibitor for mild steel in acid medium. The inhibition was assumed to occur via adsorption of the inhibitor molecule on the metal surface. It acts as an anodic inhibitor. In the 30° to 60 °C temperature range, the QMQTPH adsorption follows Langmuir isotherm model. The protection efficiency increased with increasing inhibitor concentration in the range 10⁻⁵ − 10⁻³ M, but slightly decreased with increasing temperature.     

Operational based corrosion analysis in naval ships

Life extension of ageing steel structures such as naval ships requires consideration of plate thickness losses due to corrosion, particularly when protective measures such as paint coatings and sacrificial protection are not entirely effective. Traditionally, corrosion prediction models for ships take no account of the operational profile. Consequently, the corrosion models have an inherently high variability with poor corrosion prediction capability. A new corrosion model for the prediction of corrosion loss in the seawater ballast tanks of naval vessels has been developed. The model incorporates previously available corrosion models for immersion corrosion and atmospheric corrosion and takes account of operational and environmental variables. Experimental validation is presented for a trial on an operational naval vessel.     

Investigation of the effect of disulfiram on corrosion of mild steel in hydrochloric acid solution

The corrosion inhibition properties of disulfiram (DSR) for mild steel in HCl solution were analyzed by electrochemical impedance spectroscopy (EIS), potentiodynamic polarization, atomic force microscopy, scanning electron microscopy and gravimetric methods. Physical adsorption is proposed for the inhibition and the process followed the Langmuir adsorption isotherm and kinetic/thermodynamic model of El-Awady et al. Constant phase elements describing the non-ideal characteristics of the electrochemical interface are introduced. The occurrence of inductive loop is also dealt with, through the introduction of an inductive element L. The use of these elements significantly improved the quality of fit of simulation to the EIS data.     

Corrosion inhibition of mildsteel in sulphuric acid by methanol extract of Luffa aegyptiaca leaves – electrochemical and statistical view

An electrochemical and statistical view of methanol extract of Luffa aegyptiaca leaves (MLA) on the corrosion inhibition of mild steel (MS) in 0.5 M H₂SO₄ medium were investigated by potentiodynamic polarisation and electrochemical impedance spectroscopy. Polarization studies showed that the MLA acts as mixed type inhibitor with predominant cathodic behaviour. The percentage inhibition efficiency was found to increase with MLA concentration and decreased with the temperature. Thermodynamic parameter such as free energy value was negative, that indicates spontaneous adsorption of inhibitor on MS surface. Adsorption of MLA was found to obey Langmuir isotherm. The analysis of variance studies showed that the inhibition efficiencies calculated from the different electrochemical parameters are statistically significant. Surface studies were performed by Fourier transform infrared spectroscopy and atomic force microscopy.     

Electrochemical characterization of polythiophene-coated steel

In situ electropolymerization leading to polythiophene coating has been found to be a new option for providing corrosion protection to mild steel surface. The polythiophene coating thus coated has been diagnosed through polarization and AC impedance analysis, which has demonstrated the passivation role of conducting polythiophene coating. The determination of volume fraction, water uptake and delamination area have been used to further support the corrosion protection of conducting polythiophene coating.     

有限板多孔MSD的应力强度因子计算

首先阐明组合法求解有限板多孔MSD( multiple site damage)应力强度因子的基本原理,然后就组合法运用中比较难以解决的多孔边裂纹间的修正系数问题,提出一种基于复变函数法的有效解决方法.将完善后的组合法应用于有限板多孔MSD应力强度因子的求解,计算某型飞机典型铆接壁板无主裂纹和含主裂纹两种情况的数值算例.通过与有限元结果的比较可知,该方法的计算结果精确、可靠,计算过程简单、易行.提出的近似解析方法能很好地应用于任意分布的有限板多孔MSD裂纹结构,在工程断裂问题中有较好的应用价值.