Bicarbonate, Temperature, and pH Influences on the Passivation of API-X100 Pipeline Steel in Simulated Groundwater Solutions

Author(s):  
Ibrahim M. Gadala ◽  
Akram Alfantazi

The influence of bicarbonate ion (HCO3−) concentration and related environmental parameters such as pH and temperature on the passivation of API-X100 pipeline steel is the focus of this investigation. NS4 solution simulating groundwater trapped under disbonded coatings at regions where near-neutral stress corrosion cracking (SCC) occurs was used as a reference. Bicarbonate content in the solutions was increased steadily and the critical HCO3− concentration at which passivation becomes evident is found using potentiodynamic polarization sweeps. Multi-step dissolution is observed especially in higher pH solutions, owing to the involvement of hydroxide ions (OH−) in the adsorption of hydrous Fe(OH)2. Dynamic electrochemical impedance spectroscopy (DEIS) is used to study and compare interfacial processes in active, pre-passive, passive, and trans-passive regions. The results of the potentiodynamic and DEIS tests achieve good agreement. The protective properties of the passive film formed at three different HCO3− concentrations (critical passivation and two higher concentrations) and temperatures (25, 50, and 75 °C) are studied. The combined effect of HCO3− and temperature resulted in a pH range from ∼6.7 to 9.3 for the nine conditions in the corresponding test matrix. Passive films were formed at a suitable anodic potential and then studied with electrochemical impedance spectroscopy (EIS), Mott-Schottky, and cyclic voltammetry (CV) tests. Evidence of adsorption and diffusion, in addition to significant resistance from the passive film, is observed and accounted for in the equivalent circuit, which achieved good correspondence when fitted with the experimental data. The protective properties of the overall passive film are enhanced with increased bicarbonate and decreased temperature. Positive slopes in the Mott-Schottky plots reveal the n-type semi-conductive behavior of the passive films in all conditions and the CV results highlight the proposed reaction sequences occurring in different potential scan regions. CV measurements also confirm the enhanced protective properties of passive films with increased bicarbonate and lower temperatures observed in the EIS analysis.

2020 ◽  
Vol 1 (1) ◽  
pp. 77-91 ◽  
Author(s):  
Ingmar Bösing ◽  
Georg Marquardt ◽  
Jorg Thöming

Martensitic stainless steels are widely used materials. Their mechanical and corrosion properties are strongly influenced by their microstructure and thereby can be affected by heat treatment. In the present study, the effect of different austenitizing temperatures on the passive film growth kinetics of martensitic stainless steel is studied by electrochemical impedance spectroscopy. The data was further fitted by the point defect model to determine kinetic parameters. We show that an increasing austenitizing temperature leads to a more protective passive film and slows down passive film dissolution in sulfuric acid.


2017 ◽  
Vol 744 ◽  
pp. 380-384
Author(s):  
Hui Tong ◽  
Wen Li Han ◽  
Zhong Ping Xu ◽  
Yan Jun Zhang ◽  
Zhu Lin ◽  
...  

Electrochemical impedance spectroscopy (EIS) is a technology of nondestructive electrochemical testing. In this paper, EIS is applied to study the corrosion processes of Al-Mg coatings. In the initial 24 h of immersion in 3.5% NaCl solution, passive films of Al-Mg coatings dissolve quickly. As time passed, corrosion products increase on surface gradually, which can inhibit corrosion. After 480h of immersion, corrosion products fully cover on Al-Mg coatings’ surface. The EIS of different corrosion processes are fitted by three equivalent circuits corresponding to the three corrosion processes. In the test of open circuit potentials (OCP), OCP is instable in the initial 24 h of immersion. As immersion time goes by, OCP tends to stabilization at about -0.90 V. Measurements of scanning electron microscope (SEM) confirm the conclusions of electrochemical measurements.


2020 ◽  
Vol MA2020-02 (12) ◽  
pp. 1296-1296
Author(s):  
Adrien Barroux ◽  
Nadège Ducommun ◽  
Eric Nivet ◽  
Julien Delgado ◽  
Bernard Tribollet ◽  
...  

CORROSION ◽  
10.5006/2680 ◽  
2018 ◽  
Vol 74 (6) ◽  
pp. 705-714 ◽  
Author(s):  
Yingying Yue ◽  
Chengjun Liu ◽  
Edouard Asselin ◽  
Peiyang Shi ◽  
Maofa Jiang

H2SO4-H2O2 mixtures are a promising and environmentally friendly passivation medium for the stainless-steel pickling process. The corrosion behavior of stainless steel is highly dependent on the kinetics of passive film growth. Long-term electrochemical measurements, including polarization resistance, open circuit potential (OCP), and electrochemical impedance spectroscopy (EIS) measurements were performed to investigate the evolution of the passive state of 304 stainless steel. According to the OCP results, an active-passive transition takes place in 10 ks in 0.5 M H2SO4 solution containing 0.005 M to 0.3 M H2O2. Polarization resistance results indicate that the passive film thickness keeps growing after OCP stabilization in the presence of H2O2. Electrochemical impedance spectroscopy (EIS) results confirmed that the growth of the passive film in H2SO4-H2O2 solutions takes about 9 h. Additionally, according to the Point Defect Model (PDM) and Mott–Schottky analysis, the semiconductor properties of the passive film on 304 stainless steel in H2SO4-H2O2 solution were studied. The results indicate that the passive film is an n-type semiconductor. The donor density is in the range of 1.6 × 10−21 cm−3 to 24 and decreases exponentially with increasing film formation potential (this potential coincides with the final OCP in the corresponding H2SO4-H2O2 solutions). By postulating that most donors are oxygen vacancies, the point defect properties including diffusivity and electrical field strength are obtained.


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