Influence of the microstructure and alloying element on the polarization behaviour within the crevice of UNS S32304 duplex stainless steel

The influence of microstructure evolution and alloying element redistribution of UNS S32304 duplex stainless steel induced by annealing treatment on the crevice corrosion behaviour was studied. As the annealing temperature was increased from 1030 to 1150 °C, the crevice corrosion resistance was decreased and the active peaks were not only increased in magnitude but also shifted towards the more noble direction. Austenite and ferrite have greatly different polarization behaviour within the crevice. This study provides guidance to the material design and usage in industry field in consideration of different polarization behaviour induced by the evolution of microstructure and alloying elements.     

Corrosion performance of selected stainless steels in brine from reverse osmosis desalination plants

Abstract

The corrosion performances of some commercial stainless steel alloys in the brine reject solution from a reverse osmosis sea water desalination plant was studied in terms of their pitting susceptibilities (investigated under aerated conditions at ambient temperature using a cyclic polarisation technique) and crevice corrosion resistances (evaluated in the plant over a 3 month exposure period using multiple crevice test assemblies). The alloys used were four austenitic steels, UNS S31603, UNSS 31703, UNS N08904, UNS S31254, a ferritic steel UNS S44635, and a duplex steel UNS S32550. Cyclic polarisation studies show that the pitting or breakdown potentials for S31603 and S31703 occurred at more active values than for N08904, S31254, S44635, and S32550 alloys, and indicated a reduced resistance to pitting corrosion. The multiple crevice tests show that the alloys S31603, S31703, and N08904 do suffer crevice corrosion in the brine reject solution at ambient temperature, while the S44635 S32550, and S31254 alloys showed considerably higher crevice corrosion resistance.     

Corrosion fatigue crack growth behavior of oil-grade nickel-base alloy 718. Part 1: Effect of corrosive environment

The effect of corrosive environment on corrosion fatigue crack growth (CFCG) behavior of oil-grade nickel-base alloy 718 is studied. The results demonstrate that there is no obvious effect of 3.5 wt.% NaCl solution at RT, 50 °C and 80 °C on CGCG rates while 21 wt.% NaCl solution at 80 °C produces a deleterious effect on CFCG rates compared to the ones tested in air. Potentiodynamic polarization results show that alloy 718 exhibits passive behavior in 3.5 wt.% NaCl solution, while pitting corrosion resistance decreases with increasing solution temperature. Nevertheless, alloy 718 shows active corrosion behavior in 21 wt.% NaCl solution at 80 °C.     

Orientation dependence of the electrochemical corrosion properties of electrodeposited Cu foils

In this study, the electrochemical corrosion properties of electrodeposited Cu foils in a CuCl₂-containing acidic etching solution were investigated. The main passive product was CuCl and a trace amount of Cu₂O can also be detected. The (2 2 0)-oriented Cu foils exhibited higher corrosion potential and lower corrosion current density than those with (1 1 1) or (2 0 0) texture, suggesting a superior corrosion resistance against the etching solution. It is proposed that the preferred orientation and thus the differences in atomic stacking density on specific planes dominated the corrosion properties of the electrodeposited Cu foils instead of grain size or surface roughness.     

Weld oxide formation on lean duplex stainless steel

Weld oxides have a strong influence on corrosion resistance, but have hitherto only been studied to a limited extent for duplex stainless steels. X-ray photoelectron spectroscopy (XPS) has here been used to study heat tint formed on gas tungsten arc (GTA) welds on the commercial duplex grades LDX 2101 (EN 1.4162/UNS S32101) and 2304 (EN 1.4362/UNS S32304) welded with and without nitrogen additions to the shielding gas. The process of heat tint formation is discussed in terms of transport phenomena to explain the effect of atmosphere, temperature and composition. The oxides formed were found to be enriched in manganese and corrosion testing shows that nitrogen has a strong influence on the weld oxide. A mechanism is proposed including evaporation from the weld pool and subsequent redeposition.     

Effect of small amounts of alloyed tin on the electrochemical behaviour of aluminium in sodium chloride solution

Binary model AlSn alloys containing 30–1000 ppm (by weight) Sn were investigated by electrochemical polarization in 5 wt% chloride solution and subsequent characterization of corrosion morphology. In the homogenized and rolled condition, tin concentration only slightly affected electrochemical behaviour up to 500 ppm, and the pitting potentials were all about −0.8 V_SCE. However, alloy containing 1000 ppm Sn was significantly activated by lowering of the passivity-breakdown potential to −1.38 V_SCE. Annealing at 300 °C caused significant segregation of Sn to the metal surface, and all specimens, independent of bulk Sn concentration, became nearly similarly active with breakdown potentials around −1.2 V_SCE. Corrosion on 300 °C-annealed specimens was uniformly distributed by polarization below the bulk pitting potential of −0.76 V_SCE. Moreover, the activation effect was temporary, and corrosion was significantly reduced as the segregated Sn was etched away from the surface. Thick oxide, formed during water quenching on high Sn concentration samples, containing 500 and 1000 ppm Sn, introduced partial passivation during polarization test. Annealing at 600 °C caused increasing activation with increasing Sn concentration, caused by Sn enrichment at the metal surface by dealloying of aluminium during anodic polarization in chloride solution. Corrosion was localized in the form of grain boundary corrosion for alloyed Sn concentration less than and equal to 500 ppm and pitting following the triple grain boundaries for 1000 ppm.     

Evaluation of the intergranular corrosion susceptibility of UNS S31803 duplex stainless steel with thermoelectric power measurements

In this study, the use of thermoelectric power (TEP) measurements as a nondestructive method for the determination of the degree of sensitization (DOS) in UNS S31803 duplex stainless steel (DSS) is presented. Samples were aged for times up to 240 h and subjected to the double loop electrochemical potentiokinetic reactivation (DL-EPR) test to calculate the DOS induced. The correlation between TEP and the DOS evaluated by the DL-EPR method indicates that the TEP coefficient is sensitive to gradual microstructural changes produced by thermal aging and may be used to monitor the susceptibility to intergranular corrosion in UNS S31803 DSS.     

Influence of the grain orientation spread on the pitting corrosion resistance of duplex stainless steels using electron backscatter diffraction and critical pitting temperature test at the microscale

The corrosion behavior of UNS S32202 duplex stainless steel was studied by combining electron backscatter diffraction (EBSD) measurements and critical pitting temperature tests at the microscale. The grain orientation spread (GOS) value was determined in grains of both phases from EBSD data. It was shown that austenitic sites containing extremely small ferrite grains having a GOS value greater than 1.3° were precursor sites for pitting in 4 M NaCl. The critical pitting temperature range was 45–90 °C. All the other sites of both phases remained passive up to 100 °C.     

Effect of oxygen and biofilms on crevice corrosion of UNS S31803 and UNS N08825 in natural seawater

The effect of oxygen and biofilms on crevice corrosion of UNS S31803 and UNS N08825 in seawater was studied. Passivity breakdown occurred through crevice corrosion in UNS N08825 and through transpassive dissolution in UNS S31803 although both alloys displayed crevice corrosion under potentiodynamic conditions. The most severe crevice corrosion occurred in the absence of oxygen and the presence of a biofilm. Microbial adhesion as investigated by fluorescence microscopy occurred mainly outside the crevice and DNA sequencing revealed a shift in biofilm composition as a function of substratum surface and oxygen pressure.     

Influence of strain-induced martensite in the anodic dissolution of austenitic stainless steels in acid medium

The anodic dissolution of austenitic stainless steel bars in an acid medium (0.5 M HCl + 2 M H₂SO₄) under different polarizations is studied. The material comes from bars formed by hot working (HW) and by cold working (CW). UNS S30403 and S31603 grades are considered. The determining effect of alloying elements and working method are proved. The morphology of the attack at different anodic potentials is analyzed. The important influence of the amount and distribution of strain-induced martensite on corrosion is demonstrated. The effect of the martensite on the anodic polarization curves is quantified using specifically designed software.     

Corrosion of ultra-high-purity Mg in 3.5% NaCl solution saturated with Mg(OH)2

Corrosion was evaluated for ultra-high-purity magnesium (Mg) immersed in 3.5% NaCl solution saturated with Mg(OH)₂. The intrinsic corrosion rate measured with weight loss, P_W = 0.25 ± 0.07 mm y⁻¹, was slightly smaller than that for high-purity Mg. Some specimens had somewhat higher corrosion rates attributed to localised corrosion. The average corrosion rate measured from hydrogen evolution, P_AH, was lower than that measured with weight loss, P_W, attributed to dissolution of some hydrogen in the Mg specimen. The amount of dissolution under electrochemical control was a small amount of the total dissolution. A new hydride dissolution mechanism is suggested.     

Corrosion behaviour of Al–29at%Co alloy in aqueous NaCl

Microstructure and corrosion behaviour of a binary Al–29 at%Co alloy have been studied. The alloy was prepared by arc-melting of Al and Co in high purity Ar and rapidly solidified on a water-cooled Cu mould. The alloy chemical composition and microstructure were characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy and X-ray diffraction. Furthermore, the corrosion behaviour was studied by potentiodynamic polarization in aqueous NaCl (0.6 mol dm⁻³) at room temperature. The alloy was found to consist of three phases: hexagonal Al₅Co₂, Z-phase and AlCo (β). The corrosion resistance of different intermetallic phases is characterized. The results are compared to previously published results of Al–TM (TM = transition metal) alloys.     

2-Mercaptobenzoxazole as a copper corrosion inhibitor in chloride solution: Electrochemistry, 3D-profilometry,and XPS surface analysis

2-Mercaptobenzoxazole (MBOH) was studied as a corrosion inhibitor for Cu in 3 wt.% NaCl solution using EIS, a potentiodynamic curve, 3D-profilometry, and XPS measurements. It was shown that Cu corrosion in solution containing MBOH follows kinetic-controlled and diffusion-controlled processes and that MBOH is a mixed-type inhibitor. The diffusion coefficient of the Cu ions travelling through the solid surface layers was estimated to be on the order of 10⁻¹⁵–10⁻¹⁴ cm² s⁻¹. It was also demonstrated that the Cu(I)–MBOH complex is formed on the Cu surface and that the thickness of this surface layer is 1.4 ± 0.4 nm.     

Adsorption and inhibition effect of Ascorbyl palmitate on corrosion of carbon steel in ethanol blended gasoline containing water as a contaminant

The adsorption and inhibition effect of Ascorbyl palmitate (AP) on carbon steel in ethanol blended gasoline containing water as a contaminant (GE10 + 1%water) was studied by weight loss and electrochemical impedance spectroscopic (EIS) techniques. The results showed that the addition of ethanol and water to gasoline increase the corrosion rate of carbon steel. AP inhibits the corrosion of carbon steel in (GE10 + 1% water) solution to a remarkable extent. The adsorption of AP on the carbon steel surface was found to obey the Langmuir adsorption isotherm model. The values of activation energy (E_a) and various thermodynamic parameters were calculated and discussed.     

Characterization of corrosion products formed on Ni 2.4 wt%–Cu 0.5 wt%–Cr 0.5 wt% weathering steel exposed in marine atmospheres

Weathering steel manufactured with high concentrations of copper (0.5 wt%), chromium (0.5 wt%) and nickel (2.4 wt%) was studied with the aim of furthering knowledge on corrosion product characterization and performance in marine environments. Specimens exposed for two years in a rural atmosphere and two marine environments were characterized by optical microscopy, SEM/EDS, XRD and Raman spectroscopy and corrosion rates measured. The main phases found were ferrihydrite, maghemite and goethite in the inner corrosion layer, and lepidocrocite in the outer layer. Cu and Ni were homogeneously distributed while Cr tended to be concentrated in the inner layer.     

Ultrafine-grained copper produced by machining and its unusual electrochemical corrosion resistance in acidic chloride pickling solutions

Ultrafine-grained (UFG) copper was prepared by facile machining procedure. High resolution transmission electron microscopy images revealed that, in UFG Cu, minimum grain size of 80 nm could be formed when a small machining rake angle was applied. The electrochemical corrosion behavior of UFG Cu in 0.5 M HCl was investigated by potentiodynamic polarization and electrochemical impedance spectroscopy. Comparing with coarse-grained Cu, UFG Cu exhibited notably declined corrosion current density. Particularly, when the size of Cu grains were reduced from 500 μm to 80 nm, the charge transfer resistance of anodic dissolution step dramatically increased from 200 to 621 Ω cm².     

2-Mercaptobenzimidazole as a copper corrosion inhibitor: Part I. Long-term immersion, 3D-profilometry,and electrochemistry

The high corrosion inhibition effectiveness of 2-mercaptobenzimidazole (MBIH) in 3 wt.% aqueous NaCl solution is reported using long term immersion tests, 3D-profilometry, electrochemical impedance spectroscopy, and potentiodynamic curve measurements. The high corrosion inhibition performance was proven after 180 days of immersion. The impedance spectra were characterized by two time constants relating to charge transfer and finite layer thickness or semi-infinite diffusion of copper ions through the surface layer, therefore Cu corrosion in solution containing MBIH follows kinetic-controlled and diffusion-controlled processes. Moreover, it is shown that MBIH is a mixed-type inhibitor.     

Fireside corrosion degradation of ferritic alloys at 600 °C in oxy-fired conditions

This paper reports the results of a study carried out to investigate the effects of simulated coal/biomass combustion conditions on the fireside corrosion. The 1000 h deposit recoat exposure (5 × 200 h cycles) was carried out at 600 °C. In these tests ferritic alloys were used 15Mo3, T22, T23 and T91. Kinetics data were generated for the alloys exposed using both traditional weight change methods and metal loss measurements. The highest rate of corrosion based on EDX results occurred under D1 deposit where provoke mainly by the formation of alkali iron tri-sulphate phase.     

Estimation of residual corrosion rates of steel under cathodic protection in soils via voltammetry

Steel coupons were buried in soil for 2 months under cathodic protection. Their residual corrosion rates were deduced from voltammetry and weight loss measurements. In aerated soils, the current density due to O₂ reduction, j_K,O2, was modelled with a mixed activation–diffusion controlled kinetic. The anodic part j_A of the current density j, computed as j_A = j − j_K,O2, obeyed Tafel law. Its extrapolation to the protection potential gave a corrosion rate (∼7 μm yr⁻¹) consistent with that obtained from weight loss measurements. With a deficient protection, corrosion rates remained at ∼80 μm yr⁻¹, a value given by both methods.     

Hydroxymethyl urea and 1,3-bis(hydroxymethyl) urea as corrosion inhibitors for steel in HCl solution

The inhibition effect of two urea derivatives of hydroxymethyl urea (HMU) and 1,3-bis(hydroxymethyl) urea (BHMU) on the corrosion of cold rolled steel (CRS) in 1.0 M HCl solution was studied by weight loss, potentiodynamic polarization curves and electrochemical impedance spectroscopy (EIS), quantum chemical calculation and molecular dynamics (MD) simulation methods. Inhibition efficiency values of 20.0 mM HMU and BHMU are higher than 80% and 85% at 20–50 °C, respectively. The adsorption of each inhibitor on steel surface obeys Langmuir adsorption isotherm, and is mainly the chemical adsorption. Inhibition efficiency follows the order: BHMU > HMU.