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Acta Metall Sin  2011, Vol. 47 Issue (7): 809-815    DOI: 10.3724/SP.J.1037.2011.00212
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EFFECTS OF Cl- CONCENTRATION AND TEMPERATURE ON THE CORROSION BEHAVIOR OF ALLOY 690 IN BORATE BUFFER SOLUTION
HUANG Fa, WANG Jianqiu, HAN En-Hou, KE Wei
State Key Laboratory for Corrosion and Protection, Institute of Metal Research, Chinese Academy of Sciences, Shenyang 110016
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HUANG Fa WANG Jianqiu HAN En-Hou KE Wei. EFFECTS OF Cl- CONCENTRATION AND TEMPERATURE ON THE CORROSION BEHAVIOR OF ALLOY 690 IN BORATE BUFFER SOLUTION. Acta Metall Sin, 2011, 47(7): 809-815.

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Abstract  The effects of Cl$^{-}$ concentration (0.5-2 mol/L) and temperature (25-80 ℃) on the corrosion behavior of alloy 690 in borate buffer solution were investigated using potentiodynamic polarization (PD), electrochemical impedence spectroscopy (EIS) and semiconductor capacitance method (Mott-Scottky relation). Atomic force microscope (AFM), X-ray photoelectron spectroscopy (XPS) and potential--pH diagrams were employed to analyze the corrosion products. All of the polarization curves exhibited two passive regions and intergranular corrosion was observed on all samples. With the increase in both Cl- concentration and temperature, the corrosion potential decreased and the corrosion current density became larger. Furthermore, increasing the temperature also resulted in lower pitting potentials and narrower passive regions. After anodic polarization for 45 min, the film formed in the first passive region with lower potential was composed of Cr2O3, Fe2O3 and Ni(OH)2, and behaved like a mixed-type semiconductor, while a thicker but less compact Ni2O3 film was formed in the second passive range with higher potential and behaved like a n-type semiconductor. The influences of Cl- and temperature on the corrosion behavior were discussed.
Key words:  alloy 690      passive film      potentiodynamic polarization      electrochemical impedence spectroscopy (EIS)      Mott-Scottky relation     
Received:  06 April 2011     
Fund: 

Supported by National Basic Research Program of China (No.2011CB610502) and National Natural Science Foundation of China (No.51025104)

URL: 

https://www.ams.org.cn/EN/10.3724/SP.J.1037.2011.00212     OR     https://www.ams.org.cn/EN/Y2011/V47/I7/809

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