CHEM02200704003 Nilamadhab Pandhy - Homi Bhabha National ...
CHEM02200704003 Nilamadhab Pandhy - Homi Bhabha National ...
CHEM02200704003 Nilamadhab Pandhy - Homi Bhabha National ...
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Chapter 2<br />
is intimately related to the stability of the protective passive film on the material, electrochemical<br />
environment, presence of other oxidizing and reducing species, and rate of cathodic and anodic<br />
process. Austenitic stainless steels, even though are protected by passive film on the surface,<br />
undergo transpassive corrosion when their corrosion potential shifted to the transpassive domain<br />
in some particular nitric acid media especially in presence of hexavalent chromium ion (Cr 6+ ). The<br />
characteristic feature of transpassive dissolution is mainly intergranular corrosion with opening up<br />
of grain boundaries and observed intergranular ditches [1-7]. The schematic of transpasive<br />
corrosion of austenitic stainless steel in nitric acid medium containing hexavalent chromium ion is<br />
shown in Fig. 2.9 [45].<br />
Fig. 2.9: Transpassive dissolution of austenitic stainless steel in nitric acid [45].<br />
If the conditions are sufficiently reducing austenitic stainless steel under goes uniform<br />
dissolution in the active state. If the medium is moderately oxidizing, austenitic stainless steel are<br />
in the passive state. In passive state also austenitic stainless steels are characterized by uniform<br />
passive film but with low surface dissolution. If the medium becomes excessively oxidizing, the<br />
dissolution of passive film initiates specially with oxidation of insoluble Cr 2 O 3 to soluble Cr 2 O - 7 .<br />
The dissolution of passive film results in accelerated transpassive dissolution of oxide covered<br />
material. In the more sever oxidizing medium, grain losses occur, and successive rows of material