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Chinese Journal of Materials Research  2019, Vol. 33 Issue (10): 749-762    DOI: 10.11901/1005.3093.2019.088
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Corrosion Behavior of Q345q Steel with Oxide Scale in Simulated Typical Atmospheric Environmentin Northwest China
ZHANG Yanwen1,2,GUO Tieming1,2(),SONG Zhitao1,2,NAN Xueli1,2,XU Xiujie1,2,DONG Zhilin1,2
1. State Key Laboratory of Advanced Processing and Recycling of Non-ferrous Metals, Lanzhou University of Technology, Lanzhou 730050, China
2. School of Materials Science and Engineering, Lanzhou University of Technology, Lanzhou 730050, China
Cite this article: 

ZHANG Yanwen,GUO Tieming,SONG Zhitao,NAN Xueli,XU Xiujie,DONG Zhilin. Corrosion Behavior of Q345q Steel with Oxide Scale in Simulated Typical Atmospheric Environmentin Northwest China. Chinese Journal of Materials Research, 2019, 33(10): 749-762.

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Abstract  

The structure of the oxide scale on the as received hot-rolled bridge steel Q345q and the corrosion behavior of the steel Q345q with oxide scale in three simulated atmospheric environments in Northwest China were studied by XRD, scanning electron microscopy, electrochemical technique and wet-dry alternating corrosion test. The results show that the hot-rolled oxide scale composes mainly of Fe3O4 and Fe2O3, which is porous with cracks and other defects. After the dry-wet alternating accelerated corrosion test of the steel Q345q with oxide scale, although the corrosion weight loss is the highest in NaHSO3 solution, the free-corrosion potential increases with the corrosion time, and the free-corrosion current density decreases in the later stage of corrosion. As far as the morphology of the rust layer and the ratio of γ/α* are concerned, the rust layer formed on the steel presents good stability; However, in deicing salt solution, the corrosion rate is the smallest, but the steel suffered mainly from Cl--dominated pitting corrosion with the corrosion characteristics of "large cathode and small anode". Its corrosion products contain such as β-FeOOH and HFeCl4(H2O)6, which results in loose rust layer with poor protectiveness and increased free-corrosive current density; In deicing salt+NaHSO3 solution, both pitting corrosion and general corrosion occur. Due to the synergistic effect of Cl- and HSO3-, the autocatalytic effect of a part of Cl- is reduced, but most α-FeOOH is converted from β-FeOOH, which resulted in the poor protective rust layer.

Key words:  metallic materials      Q345q steel      oxide scale      deicing salt      sodium bisulfite      mixed solution      typical atmosphere in northwest China     
Received:  30 January 2019     
ZTFLH:  TG172.3  
Fund: National Natural Science Foundation of China(51461029);Guangdong Sailing Program to Introduce Innovative Entrepreneurial Team of Special Funding(2015YT02G090);Scientific Research Projects of Gansu Transportation Department(2017-16);Scientific Research Projects of Gansu Transportation Department(2017-19)

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https://www.cjmr.org/EN/10.11901/1005.3093.2019.088     OR     https://www.cjmr.org/EN/Y2019/V33/I10/749

CSiMnPSCEVFe
0.1580.2461.2450.0230.0220.370Bal.
Table1  Chemical composition of Q345q steel (%, mass fraction)
Corrosion solutionCompositionpHGB
Mixed solutionDeicing salt+0.01 mol/L NaHSO34.8±0.2-
Deicing saltNa2SO4 0.500±0.002 g9±0.2GB/T 19746-2005
Na2SO3 0.250±0.002 g
Na2S2O3 0.100±0.002 g
NaCl 52.5±1 g
CaCl2·2H2O 52.5±1 g
NaHSO30.01 mol/LNaHSO34.4±0.2TB/T2375-1993
Table2  Compositions of three corrosion solutions
Fig.1  The corrosion kinetics curves of Q345q with oxide scale in three different solutions (a) weight gain, (b) corrosion rate
Fig.2  Fitting curves of ?W as a function of lgt (a) deicing salt, (b) NaHSO3, (c) mixed solution
Fig.3  XRD spectra of Q345q steel with oxide scale (a) before and after corrosion for different time in (b) deicing salt, (c) NaHSO3 and (d) deicing salt+ NaHSO3 solutions
Sampleβ-FeOOHγ-FeOOHα-FeOOHFe2O3Fe3O4α/γ*
Deicing salt0.220.160.060.250.310.0869
NaHSO3-0.190.240.310.350.4444
Deicing salt+NaHSO30.260.170.120.200.250.1765
Table 3  Relative contents of corrosion products and α/γ* values for Q345q steel with oxide scale after corrosion for 480 h
Fig.4  Macrographs of Q345q steel with oxide scale after corrosion in (a~d) deicing salt, (e~h) NaHSO3 and (i~l) mixed solutions for (a, e, i) 24 h, (b, f, j) 192 h, (c, g, k) 288 h and (d, h, l) 480 h
Fig.5  Surface (a) and Cross-sectional (b) morphologies of original oxide scale of Q345q steel
Fig.6  Surface micromorphologies of Q345q steel with oxide scale after corrosion in (a~c) deicing salt, (d~f) NaHSO3 and (g~i) deicing salt+NaHSO3 solutions for (a, d, g) 24 h, (b, e, h) 192 h and (c, f, i) 288 h
Fig.7  Surface micromorphologies of Q345q steel with oxide scale after corrosion for 480 h in (a) deicing salt, (b) NaHSO3 and (c) deicing salt+NaHSO3 solutions
Fig.8  Cross-sectional morphologies of Q345q steel with oxide scale after corrosion in (a~c) deicing salt, (d~f) NaHSO3 and (g~i) deicing salt+NaHSO3 solutions for (a, d, g) 24 h, (b, e, h) 192 h and (c, f, i) 288 h
Fig.9  Partial cross-sectional morphologies magnified of Q345q steel with oxide scale after corrosion (a, b) in deicing salt and (c, d) mixed solutions for (a, c) 192 h and (b, d) 288 h
Fig.10  Cross-sectional morphologies of Q345q steel with oxide scale after corrosion for 480 h in (a) deicing salt, (b) NaHSO3 and (c) deicing salt+NaHSO3 solutions
Fig.11  Polarization curves of Q345q steel with oxide scale sample after corrosion for different time in (a) deicing salt, (b) NaHSO3 and (c) deicing salt+ NaHSO3
Corrosion solutionParameters24 h72 h144 h288 h480 h
Deicing saltEcorr/V-0.6693-0.6969-0.7279-0.6797-0.6316
Icorr/mA·cm-20.13890.18040.13380.18430.2977
NaHSO3Ecorr/V-0.9795-0.9758-0.8899-0.7693-0.6764
Icorr/mA·cm-20.13050.10480.10920.14750.0558
Deicing salt+NaHSO3Ecorr/V-0.6659-0.7141-0.7798-0.7074-0.6868
Icorr/mA·cm-20.17370.18360.19510.18930.1747
Table 4  Electrochemical parameters of Q345q steel with oxide scale after corrosion for different time in three solutions
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