Corrosion assessment of nitric acid grade austenitic stainless steels

被引:90
|
作者
Ningshen, S. [1 ]
Mudali, U. Kamachi [1 ]
Amarendra, G. [1 ]
Rai, Baldev [1 ]
机构
[1] Indira Gandhi Ctr Atom Res, Kalpakkam 603102, Tamil Nadu, India
关键词
Stainless steel; Polarization; EIS; AES; Acid corrosion; INTERGRANULAR CORROSION; REPROCESSING PLANTS; ENVIRONMENTS; RESISTANCE; MECHANISM;
D O I
10.1016/j.corsci.2008.09.038
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The corrosion resistance of three indigenous nitric acid grade (NAG) type 304L stainless steel (SS), designated as 304L1, 304L2 and 304L3 and two commercial NAG SS designated as Uranus-16 similar to 304L composition and Uranus-65 similar to type 310L SS were carried out in nitric acid media. Electrochemical measurements and surface film analysis were performed to evaluate the corrosion resistance and passive film property in 6 N and 11.5 N HNO3 media. The results in 6 N HNO3 show that the indigenous NAG 304L SS and Uranus-65 alloy exhibited similar and higher corrosion resistance with lower passive current density compared to Uranus-16 alloy. In higher concentration of 11.5 N HNO3, transpassive potential of all the NAG SS shows a similar range, except for Uranus-16 alloy. Optical micrographs of all the NAG SS revealed changes in microstructure after polarization in 6 N and 11.5 N HNO3 with corrosion attacks at the grain boundaries. Frequency response of the AC impedance of all the NAG SS showed a single semicircle arc. Higher polarization resistance (R-p) and lower capacitance value (CPE-T) revealing higher film stability for indigenous NAG type 304L SS and Uranus-65 alloy. Uranus-16 alloy exhibited the lowest R-p value in both the nitric acid concentration. Auger electron spectroscopy (AES) study in 6 N and 11.5 N HNO3 revealed that the passive films were mainly composed of Cr2O3 and Fe2O3 for all the alloys. The corrosion resistance of different NAG SS to HNO3 corrosion and its relation to compositional variations of the NAG alloys are discussed in this paper. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:322 / 329
页数:8
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