CHEM02200704003 Nilamadhab Pandhy - Homi Bhabha National ...
CHEM02200704003 Nilamadhab Pandhy - Homi Bhabha National ...
CHEM02200704003 Nilamadhab Pandhy - Homi Bhabha National ...
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Chapter 4<br />
C H A P T E R 4<br />
<br />
<br />
<br />
Passive film properties of 304L SS in nitric acid medium were investigated in both ex-situ and<br />
in-situ conditions using AFM and EC-AFM techniques. Ex-situ study in 1 M, 4 M, 8 M, and 11.5<br />
M nitric acid revealed that variation in passive film morphology occurs depending upon the<br />
concentration, and time of immersion. In-situ passive film surface morphology investigation<br />
showed formation of chromium hydroxide layer in the form of platelet like structures at lower<br />
concentrations (0.1 M, 0.5 M), and towards higher concentration (0.6 M) the platelets formed<br />
homogenous oxide layer on the surface which started depleting at still higher concentration (1 M)<br />
leading to opening up of oxide boundaries. Compositional analysis of the passive film revealed<br />
duplex nature consisting of hydroxide and oxide layers at lower concentration, and with<br />
increasing concentration oxide layer predominates over the surface.<br />
4.1 Introduction<br />
Electrochemical corrosion initiation at sub-microscopic region involves several<br />
phenomenon starting from breakdown of passive film in stochastic and sporadic way to localized<br />
dissolution of oxide covered material, and mass transport of atoms across the surface to support<br />
the continuing dissolution process [114,115]. The crucial factor controlling all the above<br />
phenomenon is the passive film whose structure, property, and stability is of immense important in<br />
understanding the many details of electrochemical corrosion process as well as central to<br />
controlling corrosion, and use of metallic materials in many technologies. The desirable, and<br />
beneficial property of passivity is directly related with sustainability of material, since corrosion is