A New Corrosion Mechanism for X100 Pipeline Steel Under Oil-Covered Chloride Droplets

CORROSION ◽  
10.5006/2804 ◽  
2018 ◽  
Vol 74 (9) ◽  
pp. 947-957 ◽  
Author(s):  
Hongxing Liang ◽  
Jing Liu ◽  
Rebecca Filardo Schaller ◽  
Edouard Asselin

A 1.7 mM NaCl droplet on X100 pipeline steel covered by paraffin oil is used to simulate the corrosive environment encountered in heavy oil or bitumen pipelines. The development of corrosion under the droplet was monitored and explored in two stages. In the initial stage (1 h), the distribution of corrosion pits was heterogeneous with one area under the droplet presenting a higher pit density. As the corrosion proceeded (24 h), the localized corrosion in the area under the droplet with the higher pit density switched to general corrosion, while the other region of the droplet continued to pit. The mechanisms driving this new distinctive corrosion form developed beneath an underoil droplet are explained.

2013 ◽  
Vol 743-744 ◽  
pp. 589-596 ◽  
Author(s):  
Meng Liu ◽  
Jian Qiu Wang ◽  
Wei Ke

The corrosion behavior of X52 pipeline steel in H2S solutions was investigated through immersion corrosion test which was carried out in a high temperature and high pressure autoclave at different temperatures and H2S concentrations. General corrosion rates were calculated based on the weight loss of samples. The morphology and the chemical composition of the corrosion products were obtained by Scanning Electron Microscopy (SEM) and Energy Dispersive Spectroscopy (EDS). The crystal structure of corrosion products was analyzed by X-Ray diffraction patterns (XRD). The corrosion products consisted mainly of the sulfide compounds (mackinawite, cubic ferrous sulfide, troilite and pyrrhotite). The corrosion products included two layers: the inner iron-rich layer and the outer sulfur-rich layer. Under H2S concentrations of 27g/L, the corrosion rate increased with the increase of temperature up to 90°C and then decreased at 120°C, finaly increased again. The corrosion rate first increased with H2S concentrations then decreased at 120°C. The structure and stability of the corrosion products due to different corrosion mechanism had a major impact on the corrosion rate. The corrosion resistance of the corrosion products increased as follows: mackinawite < cubic ferrous sulfide < troilite < pyrrhotite.


Metals ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 1975
Author(s):  
Fan Wang ◽  
Jinling Li ◽  
Chengtun Qu ◽  
Tao Yu ◽  
Yan Li ◽  
...  

The corrosion behavior of L360 pipeline steel coated with or without elemental sulfur (S8) in CO2–Cl− medium at different pH was studied. An autoclave was used to simulate the working conditions for forming the corrosion scale, and an electrochemical workstation with a three-electrode cell was used to analyze the electrochemical characterization of the corrosion scale. A wire beam electrode was used to determine the potential and current distribution, and scanning electron microscopy and X-ray diffraction were used to characterize the morphology and composition of the corrosion scale. The results showed that the deposition of S8 on the surface of the electrodes caused serious localized corrosion, especially under acidic conditions. The morphology and localized corrosion intensity index further proved that the deposition of S8 significantly promoted corrosion, especially pitting corrosion. Finally, a novel corrosion mechanism of L360 pipeline steel coated with S8 in a CO2-Cl− environment under acidic conditions was proposed, and we then modeled the theoretical mechanisms that explained the experimental results.


Materials ◽  
2019 ◽  
Vol 12 (3) ◽  
pp. 364 ◽  
Author(s):  
Le Quynh Hoa ◽  
Ralph Baessler ◽  
Dirk Bettge

To study the effects of condensed acid liquid, hereafter referred to as condensate, on the CO2 transport pipeline steels, gas mixtures containing a varying concentration of H2O, O2, NO2, and SO2, were proposed and resulted in the condensate containing H2SO4 and HNO3 with the pH ranging from 0.5 to 2.5. By exposing the pipeline steel to the synthetic condensate with different concentration of acidic components, the corrosion kinetic is significantly changed. Reaction kinetic was studied using electrochemical methods coupled with water analysis and compared with surface analysis (scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and X-ray diffractometry (XRD)) of corroded coupons. The results showed that, although the condensation of NO2 in the form of HNO3 causes faster general corrosion rate, it is the condensation of SO2 in the form of H2SO4 or the combination of SO2 and NO2 that may cause much more severe problems in the form of localized and pitting corrosions. The resulting corrosion forms were depended on the chemical nature of acids and their concentration at the same investigated pH. The effects of changing CO2 flow rate and renewing condensate on pitting corrosion were further studied.


2021 ◽  
Vol 101 (1) ◽  
pp. 251-258
Author(s):  
Clarisa Campechano-Lira ◽  
A. Bedolla ◽  
A. Contreras ◽  
Ricardo Orozco Cruz ◽  
R. Galván Martínez

2013 ◽  
Vol 52 (4) ◽  
pp. 484-487 ◽  
Author(s):  
X Y Peng ◽  
G C Liang ◽  
T Y Jin ◽  
Y Frank Cheng

2017 ◽  
Vol 2017 ◽  
pp. 1-9 ◽  
Author(s):  
Yan-yu Cui ◽  
Jia Li ◽  
Qing-miao Ding

The surface analysis techniques and chemical technical means (polarization curves and AC impedance technique) were applied to research the corrosion characteristics of microorganisms SRB of 2024-T31 aluminum-magnesium alloy in the oil-water system, and the corrosion mechanism was finally analyzed. The results showed that SRB accelerate the corrosion process and cause uneven pitting on the surface of the metal matrix. Passive and biological films control the corrosion of the metal substrate in bacterial oil-water system. In the initial stage of immersion, a loose and uneven biofilm formed on the surface of substrate which accelerated its corrosion. In the midterm, the effect of biofilm gradually weakened while the protective effect of the passive film grew more insistently; the rate of corrosion slowed down. In the later period, localized corrosion cell of large cathode/small anode formed on the surface of the substrate which accelerates the corrosion.


2013 ◽  
Vol 83 (5) ◽  
pp. 864-869 ◽  
Author(s):  
Elisa J. Kassab ◽  
José Ponciano Gomes

ABSTRACT Objective: To assess the influence of fluoride concentration on the corrosion behavior of nickel titanium (NiTi) superelastic wire and to compare the corrosion resistance of NiTi with that of beta titanium alloy in physiological solution with and without addition of fluoride. Materials and Methods: NiTi corrosion resistance was investigated through electrochemical impedance spectroscopy and anodic polarization in sodium chloride (NaCl 0.15 M) with and without addition of 0.02 M sodium fluoride (NaF), and the results were compared with those associated with beta titanium. The influence of fluoride concentration on NiTi corrosion behavior was assessed in NaCl (0.15 M) with and without 0.02, 0.04, 0.05, 0.07, and 0.12 M NaF solution. Galvanic corrosion between NiTi and beta titanium were investigated. All samples were characterized by scanning electron microscopy. Results: Polarization resistance decreased when NaF concentration was increased, and, depending on NaF concentration, NiTi can suffer localized or generalized corrosion. In NaCl solution with 0.02 M NaF, NiTi suffer localized corrosion, while beta titanium alloys remained passive. Current values near zero were observed by galvanic coupling of NiTi and beta titanium. Conclusions: There is a decrease in NiTi corrosion resistance in the presence of fluoride. The corrosion behavior of NiTi alloy depends on fluoride concentration. When 0.02 and 0.04 M of NaF were added to the NaCl solution, NiTi presented localized corrosion. When NaF concentration increased to 0.05, 0.07, and 0.12 M, the alloy presented general corrosion. NiTi corrosion resistance behavior is lower than that of beta titanium. Galvanic coupling of these alloys does not increase corrosion rates.


2011 ◽  
Vol 255-260 ◽  
pp. 514-518
Author(s):  
Zheng Yi Kong ◽  
Shan Hua Xu ◽  
Yu Sheng Chen

Because of the complexity of corrosion, the law of uniform corrosion and localized corrosion is still not clear,so it is difficult to assess their impact on the structure safety. In order to differ them and find their own law, we obtain a lot of corrosion specimens by ways of constant temperature and humidity, and then detect the size of corrosion pits by roughness tester. After that, the method for calculating the thickness of uniform corrosion and localized corrosion is proposed. Then the method is used to analyze the experiment data. The result indicates the thickness of uniform corrosion and localized corrosion all increase with the rate of corrosion, and they all show a power relationship with corrosion rate, so it will provide a basis for distinguishing them in safety assessment.


2020 ◽  
Vol 39 (1) ◽  
pp. 219-227
Author(s):  
Aijun Deng ◽  
Yunjin Xia ◽  
Jie Li ◽  
Dingdong Fan

AbstractThe effect of the addition of 2CaO·SiO2 solid particles on dephosphorization behavior in carbon-saturated hot metal was investigated. The research results showed that the addition of 2CaO·SiO2 particles have little influence on desilication and demanganization, and the removal of [Si] and [Mn] occurred in the first 5 min with different conditions where the contents of 2CaO·SiO2 particles addition for the conditions 1, 2, 3, 4, and 5 are 0, 2.2, 6.4, 8.6, and 13.0 g, respectively. The final dephosphorization ratios for the conditions 1, 2, 3, 4, and 5 are 61.2%, 66.9%, 79.6%, 63.0%, and 78.1%, respectively. The dephosphorization ratio decreases with the increase of 2CaO·SiO2 particles in the first 3 min. The reason for this is that the dephosphorization process between hot metal and slag containing C2S phase consisted of two stages: Stage 1, [P] transfers from hot metal to liquid slag and Stage 2, the dephosphorization production (3CaO·P2O5) in liquid slag reacts with 2CaO·SiO2 to form C2S–C3P solid solution. The increase of 2CaO·SiO2 particles increases the viscosity of slag and weakens the dephosphorization ability of the stage 1. The SEM and XRD analyses show that the phase of dephosphorization slag with the addition of different 2CaO·SiO2 particles is composed of white RO phase, complex liquid silicate phase, and black solid phase (C2S or C2S–C3P). Because the contents of C2S–C3P and 2CaO·SiO2 in slag and the dephosphorization ability of the two stages are different, the dephosphorization ability with different conditions is different.


2018 ◽  
Author(s):  
Lloyd A. Hackel ◽  
Jon E. Rankin

This paper reports substantially enhanced fatigue and corrosion-fatigue lifetimes of propulsion shaft materials, 23284A steel and 23284A steel with In625 weld overlay cladding, as a result of shot or laser peening. Glass reinforced plastic (GRP) coatings and Inconel claddings are used to protect shafts against general corrosion and corrosion pitting. However salt water leakage penetrating under a GRP can actually enhance pitting leading to crack initiation and growth. Fatigue coupons, untreated and with shot or laser peening were tested, including with simultaneous salt water immersion. Controlled corrosion of the surfaces was simulated with electric discharge machining (EDM) of deep pits enabling evaluation of fatigue and corrosion-fatigue lifetimes. Results specifically show high energy laser peening (HELP) to be a superior solution, improving corrosion-fatigue resistance of shaft and cladding metal, reducing the potential for corrosion pits to initiate fatigue cracks and dramatically slowing crack growth rates. At a heavy loading of 110% of the 23284A steel yield stress and with 0.020 inch deep pits, laser peening increased fatigue life of the steel by 1370% and by 350% in the corrosion-fatigue testing.


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