Corrosion behavior and characteristics of the product film of API X100 steel in acidic simulated soil solution

The short-term corrosion behavior of API X100 steel in an acidic simulated soil was investigated by electrochemical measurements and soaking experiments,followed by corrosion morphology observations and X-ray photoelectron spectroscopy analyses.The results show that X100 steel exhibits an obvious pitting susceptibility in an acidic soil environment.Pits nucleate after approximately 10 h of immersion.Along with the nucleation and growth of the pits,the charge-transfer resistance and open-circuit potential first increase sharply,then decrease slowly,and eventually reach a steady state.The maxima of the charge-transfer resistance and open-circuit potential are attained at approximately 10 h.The evolution of the electrochemical process is confirmed by the analysis of the product film.The product film exhibits a porous and loose structure and could not protect the substrate well.The product film is primarily composed of ferrous carbonate and ferrous hydroxide（Fe（OH）2）.The concentration of Fe（OH）2 in the product film increases from the inside to the outside layer.

Effect of hydrogen on the stress corrosion cracking behavior of X80 pipeline steel in Ku'erle soil simulated solution

Hydrogen was a key factor resulting in stress corrosion cracking （SCC） of X80 pipeline steel in Ku＇erle soil simulated solution. In this article, the effect of hydrogen on the SCC susceptibility of X80 steel was investigated further by slow strain rate tensile test, the surface fractures were observed using scanning electron microscopy （SEM）, and the fracture mechanism of SCC was discussed. The results indicate that hydrogen increases the SCC susceptibility. The SEM micrographs of hydrogen precharged samples presents a brittle quasi-cleavage feature, and pits facilitate the transgranular crack initiation. In the electrochemical impedance spectroscopy （EIS） measurement, the decreased polarization resistance and the pitting resistance of samples with hydrogen indicate that hydrogen increases the dissolution rate and deteriorates the pitting corrosion resistance. The potentiodynamic polarization curves present that hydrogen also accelerates the dissolution rate of the crack tip.

Passivation process of X80 pipeline steel in bicarbonate solutions

The passivation process of X80 pipeline steel in bicarbonate solutions was investigated using potentiodynamic, dynamic electro-chemical impedance spectroscopy （DEIS）, and Mott-Schottky measurements. The results show that the shape of polarization curves changes with concentration. The critical ＇passive＇ concentration is 0.009 mol/L for X80 pipeline steel in bicarbonate solutions. No anodic current peak exists in solutions when the concentration is lower than 0.009 mol/L, whereas there are one and two anodic current peaks when the concentration ranges from 0.009 to 0.05 mol/L and is higher than 0.1 mol/L, respectively. DEIS measurements show that there exist active dissolution range, transition range, pre-passive range, passive layer formation range, passive range, and trans-passive range for X80 pipeline steel in the 0.1 mol/L solutions. The results of DEIS measurements are in complete agreement with the potentiodynamic diagram. An equivalent circuit containing three sub-layers is used to explain the Nyquist plots in the passive range. Analyses are well made for explaining the corresponding fitted capacitance and impedance. The Mott-Schottky plots show that the passive film of X80 pipeline steel is an n-type semiconductor, and capacitance measurements are in good accordance with the results of DEIS experiment.

Effects of substrate temperature and deposition time on the morphology and corrosion resistance of FeCoCrNiMo0.3 high-entropy alloy coating fabricated by magnetron sputtering

The effects of substrate temperature and deposition time on the morphology and corrosion resistance of FeCoCrNiMo0.3 coating fabricated by magnetron sputtering were investigated by scanning electron microscopy and electrochemical tests.The FeCoCrNiMo0.3 coating was mainly composed of the face-centered cubic phase.High substrate temperature promoted the densification of the coating,and the pitting resistance and protective ability of the coating in 3.5wt%NaCl solution was thus improved.When the deposition time was prolonged at 500℃,the thickness of the coating remarkably increased.Meanwhile,the pitting resistance improved as the deposition time increased from 1 to 3 h;however,further improvement could not be obtained for the coating sputtered for 5 h.Overall,the pitting resistance of the FeCoCrNiMo0.3 coating sputtered at 500℃for 3 h exceeds those of most of the reported high-entropy alloy coatings.

Stress corrosion cracking of X80 pipeline steel exposed to high pH solutions with different concentrations of bicarbonate

Susceptibilities to stress corrosion cracking （SCC） of X80 pipeline steel in high pH solutions with various concentrations of HC03 at a passive potential of-0.2 V vs. SCE were investigated by slow strain rate tensile （SSRT） test. The SCC mechanism and the effect of HC03 were discussed with the aid of electrochemical techniques. It is indicated that X80 steel shows enhunced susceptibility to SCC with the concentration of HCO3 increasing from 0.15 to 1.00 mol/L, and the susceptibility can be evaluated in terms of current density at -0.2 V vs. SCE. The SCC behavior is controlled by the dissolution-based mechanism in these circumstances. Increasing the concentration of HCO3 not only increases the risk of rupture of passive films but also promotes the anodic dissolution of crack tips. Besides, little susceptibility to SCC is found in dilute solution containing 0.05 mol/L HCO3 for X80 steel. This can be attributed to the inhibited repassivation of passive films, manifesting as a more intensive dissolution in the non-crack tip areas than at the crack tips.

Corrosion behavior and mechanism of the automotive hot-dip galvanized steel with alkaline mud adhesion

The corrosion behavior and mechanism of hot-dip galvanized steel and interstitial-free （IF） substrate with alkaline mud adhesion were investigated by scanning electron microscopy （SEM）, X-ray diffraction （XRD）, electrochemical impedance spectroscopy （EIS）, and linear polarization. The results show that non-uniform corrosion occurs on the galvanized steel and IF substrate during 250 h with the mud adhesion. The corrosion products on the galvanized steel are very loose and porous, which are mainly ZnO, Zn5（OH）8C12·H2O and Zn（OH）2, and Fe-Zn alloy layer with a lower corrosion rate is exposed on the galvanized steel surface; however, the corrosion products on IF substrate are considerably harder and denser, whose compositions of rust are mainly FeOOH and Fe3O4, and several pits appear on their surface. The results of continuous EIS and linear polarization measurements exhibit a corrosion mechanism, that is, under activation control, the charge transfer resistances present different tendencies between the galvanized steel and IF substrate; in addition, the evolution of linear polarization resistances is similar to that of charge transfer resistances. The higher contents of dissolved oxygen and Cl^- ions in the mud play an important role in accelerating the corrosion.

Effects of solution environments under disbonded coatings on the corrosion behaviors of X70 pipeline steel in acidic soils

A rectangle crevice assembly was used to study the effects of cathodic protection （CP） potential, crevice thickness, holiday size, bubbling CO2, and surface condition on the chemical and electrochemical environment of the local solution under disbonded coatings. It is found that the cathodic protection removes dissolved oxygen from the crevice and thus shifts the solution to a more al- kaline state. Furthermore, the potential of the steel reaches the protected potential range. The available protection distance increases with the negative applying potential. The steady potential and pH distribution are easily achieved, but the polarization degree is not satisfied within the thinner crevice. The difference in the solution environment is found to correlate to the holiday size. The smaller the holiday, the smaller the difference is. The presence of CO2 inhibits the formation of an alkaline environment. It is also found that the rust layer dramatically decreases the polarization rate in the crevice.

In-situ Corrosion Characterization of API X80 Steel and Its Corresponding HAZ Microstructures in an Acidic Environment

During heat treatment processing, microstructures of heat affected zone （HAZ） were formed in X80 pipe- line steel. After observation by optical microscopy, scanning electron microscopy and transmission electron microsco- py, microstructure of the as-received X80 steel was confirmed to be acicular ferrite, while the microstructures of quenched, normalized and annealed X80 steels were lath bainite, granular ferrite and quasi-polygonal ferrite, respec- tively. After immersion in the simulated acidic soil solution for 48 h, corrosion rates of these four steels were deter- mined by mass loss measurements and corrosion products were examined by Raman spectroscopy and X-ray photoe lectron spectroscopy. Scanning vibrating electrode technique was used to characterize the micro-galvanic corrosion be- haviors of the synthetic bimetallic electrodes which were formed by coupling each of the simulated HAZ microstruc- tures with the as-received steel in direct physical and electric contact. It is demonstrated that the as-received steel acts as cathode in the as-received/quenched and as-received/normalized couples, while the annealed steel acts as cathode when coupling with the as received steel. The distinction of current density between the galvanic couples reduces with prolonging the immersion time.

A New Understanding of Stress Corrosion Cracking Mechanism of X80 Pipeline Steel at Passive Potential in High-pH Solutions

Susceptibilities to stress corrosion cracking（SCC） of X80 pipeline steel in relatively concentrated carbonate/bicarbonate solutions with different chloride ion concentrations or p H value at a passive potential of-200 m V vs SCE were investigated by slow strain rate tensile test.In order to explore the SCC mechanism and the evaluation criterion for the SCC susceptibility of the steel in passive state,electrochemical measurements were taken.Potentiodynamic polarization curves were obtained at different potential sweep rates,and electrochemical impedance spectroscopy measurements were taken after fast polarization to the passive potential.The effects of chloride ion and p H on SCC behaviors of X80 steel at the passive potential were also discussed.The results showed that the SCC mechanism of X80 pipeline steel was greatly influenced by the passive film formed in these solutions.The SCC behaviors followed the film suppressed anodic dissolution mechanism in these circumstances,because the filming process accounted for a considerable proportion of the overall electrode process.The criteria for evaluating the SCC susceptibility of the steel at passive potential were proposed and validated.Decreasing in the concentration of chloride ion or increasing in p H value resulted in the reduction in SCC susceptibility.The existence of chloride ion greatly lowered the passivation tendency and the film stability,while its concentration determined the dissolution rate of the steel matrix.Higher p H value was responsible for the stable and tenacious passive films and the high repassivation capability.It was also inclined to lower the anodic dissolution rate at crack tips by retarding the cathodic oxygen reduction.

Effects of Lead on the Initial Corrosion Behavior of 316LN Stainless Steel in High-Temperature Alkaline Solution

The effect of lead on the initial corrosion behavior of 316 LN stainless steel has been investigated by U-bend immersion experiments in 4 wt% NaOH solutions at 300 °C. Follow-up studies after soaking were carried out by scanning electron microscope, energy dispersive X-ray spectrometer, X-ray photoelectron spectrometer, Auger electron spectroscopy and Raman spectroscopy. The results show that lead affects the properties of the oxide film by changing the thickness and composition, which leads to an increase in the sensitivity of stress corrosion cracking of 316 LN stainless steel. Pits and cracks appeared on the surface of 316 LN stainless steel under both lead-free and lead-containing conditions. The corrosion products were oxides of Fe, Cr and Ni, and the main spinel structure on the surface of the film was NiCr_2O_4 under both conditions. However, in the presence of lead, the cracks and pits were more obvious, the thickness of the film increased from 50 to 200 nm, and the amount of protective NiCr_2O_4 decreased. Lead was concluded to be involved in the dehydration reactions in the form of Pb(OH)_2, which affected the normal dehydration process of the hydroxides and inhibited the formation of spinel structures. Because of the above characteristics of lead, the stability of the oxide film and its protection of 316 LN stainless steel were reduced.