Pitting Corrosion of Bare Stainless Steel 304 under Chloride Solution Droplets
Author(s) -
B. Maier,
G. S. Frankel
Publication year - 2010
Publication title -
journal of the electrochemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.258
H-Index - 271
eISSN - 1945-7111
pISSN - 0013-4651
DOI - 10.1149/1.3467850
Subject(s) - cathodic protection , chloride , drop (telecommunication) , corrosion , pitting corrosion , metallurgy , relative humidity , anode , kelvin probe force microscope , current (fluid) , open circuit voltage , materials science , chemistry , humidity , electrode , voltage , atomic force microscopy , nanotechnology , meteorology , telecommunications , physics , electrical engineering , engineering , quantum mechanics , computer science
Pitting corrosion behavior of stainless steel 304 (SS304) under droplets of chloride solution was investigated using a Kelvin probe (KP). Droplets of different volumes of MgCl 2 solution were placed on the steel surface and exposed to a constant low relative humidity (RH). As the concentration increased during the exposure of the drop to low RH, the open-circuit potential (OCP) and the shape change of the drop were monitored by the KP. Pit initiation was detected by a sudden decrease in the OCP. Pits initiated earlier under small droplets than under large drops. The chloride concentration at initiation was between 3.0 and 8.4 M for droplets with a starting concentration of 0.88 M Cl ― . The initiation concentration increased when the initial concentration of the droplet was higher. The anodic current demand of pits growing at the OCP decreased with time as did the available cathodic current. When the current demand exceeded the available cathodic current, the active pit area decreased. A mechanism for pit formation and growth under droplets of MgCl 2 solution was proposed.
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