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Journal of Chinese Society for Corrosion and protection  2024, Vol. 44 Issue (5): 1200-1212    DOI: 10.11902/1005.4537.2023.322
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Corrosion Behavior of Casing Steels 13Cr and N80 During Sequestration in an Impure Carbon Dioxide Environment
LIU Guangsheng1,2, WANG Weijun1,2, ZHOU Pei1,2, TAN Jinhao3,4, DING Hongxin3,4, ZHANG Wei3,4, XIANG Yong3,4()
1 Changqing Oilfield Company Oil and Gas Technology Research Institute, Xi'an 710018, China
2 National Engineering Laboratory of Low Permeability Oil and Gas Fields, Xi'an 710018, China
3 School of Mechanical and Storage Engineering, China University of Petroleum (Beijing), Beijing 102249, China
4 Laboratory for Materials Failure and Protection of Low Carbon Energy Equipment, China University of Petroleum (Beijing), Beijing 102249, China
Cite this article: 

LIU Guangsheng, WANG Weijun, ZHOU Pei, TAN Jinhao, DING Hongxin, ZHANG Wei, XIANG Yong. Corrosion Behavior of Casing Steels 13Cr and N80 During Sequestration in an Impure Carbon Dioxide Environment. Journal of Chinese Society for Corrosion and protection, 2024, 44(5): 1200-1212.

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Abstract  

Corrosion of metallic materials, used as wellbore wall is a critical issue that influences the safety of carbon sequestration. This work focuses on understanding the corrosion behavior of casing steels in high-temperature and high-pressure CO2 storage environments. Herein, the corrosion behavior of two steels N80 and 13Cr in supercritical CO2-rich water phases containing impurities (SO2, NO2, and O2) was investigated via a high-temperature and high-pressure reactor by various pressure and stress conditions, aiming to simulate the real service conditions of carbon sequestration. The corrosion rate of steels was determined with mass-loss method, while the films formed on the steel surface were characterized by means of scanning electron microscopy (SEM), X-ray diffractometry (XRD), and X-ray photoelectron spectroscopy (XPS). The results indicated that increasing the pressure led to higher rates of uniform corrosion and pitting corrosion for N80 steel. However, the pressure had inapparent effect on uniform corrosion of 13Cr steel, although severe pitting corrosion was observed by pressure of 20 MPa. Furthermore, the applied tensile stress could induce damage of the corrosion product scales on both N80 and 13Cr steels to certain extent, nevertheless, no cracks were observed on the surface of the steel substrate.

Key words:  supercritical CO2      corrosion process      stress corrosion      CO2 storage     
Received:  12 October 2023      32134.14.1005.4537.2023.322
ZTFLH:  TE980  
Fund: National Natural Science Foundation of China(52271082);Beijing Natural Science Foundation(2222074)
Corresponding Authors:  XIANG Yong, E-mail: xiangy@cup.edu.cn

URL: 

https://www.jcscp.org/EN/10.11902/1005.4537.2023.322     OR     https://www.jcscp.org/EN/Y2024/V44/I5/1200

MaterialCSiMnPSAlCrNiVTiCuMoCo
N800.350.321.550.020.0150.0140.110.130.150.010.030.010.08
13Cr0.220.170.550.0160.008-12.450.250.02-0.20.14-
Table 1  Chemical composition of experimental materials (mass fraction / %)
Fig.1  High temperature and high-pressure reactor
Material

Temperature

oC

Pressure

MPa

Gas compositionEnvironment

Time

h

N80

12010CO2 + 0.1‰ SO2 + 0.1‰ NO2 + 0.1‰ O2Simulation of groundwater phase72
15
20

13Cr

10
15
20
Table 2  Pressure group experiment scheme
Material

Temperature

Pressure

MPa

Gas compositionEnvironment

Loading

stress

Time

h

N8012020CO2 + 0.1‰ SO2 + 0.1‰ NO2 + 0.1‰ O2Simulation of groundwater phase072
25% σs
50% σs
75% σs
13Cr0
25% σs
50% σs
75% σs
Table 3  Stress group experiment scheme
Fig.2  Corrosion rates of N80 and 13Cr steels after 72 h of corrosion in water-rich phase at 120oC under different pressure conditions
Fig.3  SEM images of corrosion products of N80 (a-c) and 13Cr (d-f) steels after 72 h of corrosion in water-rich phase at 120oC under the pressure of 10 MPa (a, d), 15 MPa (b, e) and 20 MPa (c, f)
Fig.4  Cross-sectional morphologies of N80 (a-c) and 13Cr (d-f) steels after 72 h of corrosion in water-rich phase at 120oC under the pressure of 10 MPa (a, d), 15 MPa (b, e) and 20 MPa (c, f)
Fig.5  Pitting rates of N80 and 13Cr steels after 72 h of corrosion in water-rich phase at 120oC under different pressure conditions
Fig.6  3D surface morphologies of N80 (a-c) and 13Cr (d-f) steels after 72 h of corrosion in water-rich phase at 120oC under the pressure of 10 MPa (a, d), 15 MPa (b, e), 20 MPa (c, f)
Fig.7  XRD patterns of N80 steel after 72 h of corrosion in water-rich phase at 120oC under different pressure conditions
Fig.8  XRD patterns of 13Cr steel after 72 h of corrosion in water-rich phase at 120oC under different pressure conditions
Fig.9  XPS of Cr, Fe and O of 13Cr steels after 72 h of corrosion in water-rich phase at 120oC under the pressure of 10 MPa (a), 15 MPa (b) and 20 MPa (c)
Element10 MPa15 MPa20 MPa
Binding energy / eVPeakBinding energy / eVPeakBinding energy / eVPeak
Cr 2p577.1Cr(OH)3577.1Cr(OH)3577.1Cr(OH)3
O 1s531.4FeCO3531.4FeCO3531.4FeCO3
Fe 2p529.7FeOOH--529.7FeOOH
531.7Cr(OH)3531.7Cr(OH)3531.7Cr(OH)3
710.2FeCO3710.2FeCO3710.2FeCO3
711.5FeOOH711.5FeOOH711.5FeOOH
Table 4  Binding energy of corrosion products of 13Cr steel after 72 h of corrosion in water-rich phase at 120oC under different pressure conditions
Fig.10  Surface morphologies of N80 and 13Cr steels after 72 h of corrosion in water-rich phase at 120oC and 20 MPa under the loading stress of 0 (a, e), 25% σs (b, f), 50% σs (c, g) and 75% σs (d, h)
Fig.11  Surface morphologies of N80 (a-d) and 13Cr (e-h) steels after 72 h of corrosion in water-rich phase at 120oC and 20 MPa under the loading stress of 0 (a, e), 25% σs (b, f), 50% σs (c, g) and 75% σs (d, h) after removing the corrosion products
Fig.12  3D surface morphologies of N80 steel after 72 h of corrosion in water-rich phase at 120oC and 20 MPa under the loading stress of 0 (a), 25% σs (b), 50% σs (c) and 75% σs (d)
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