KCl-Induced Corrosion of a 304-type Austenitic Stainless Steel in O-2 and in O-2 + H2O Environment: The Influence of Temperature
Artikel i vetenskaplig tidskrift, 2009

The oxidation of the 304-type (Fe18Cr10Ni) austenitic stainless steel was investigated in the temperature range 400-600 A degrees C in 5% O-2 and 5% O-2 + 40% H2O. Exposure time was up to 1 week. Prior to exposure, the polished samples were coated with 0.1 mg/cm(2) KCl. Uncoated samples were also exposed and used as references. The oxidized samples were analyzed by gravimetry and by ESEM/EDX, XRD, IC and AES. The results show that KCl is strongly corrosive. Corrosion is initiated by the reaction of KCl with the chromia-containing oxide that normally forms a protective layer on the alloy. This reaction produces potassium chromate particles, leaving a chromium-depleted oxide on the alloy surface. At 500 and 600 A degrees C this results in rapid oxidation, resulting in the formation of a thick scale consisting of a mixture of hematite, spinel oxide ((Fe,Cr,Ni)(3)O-4) and K2CrO4. The thick scale is poorly protective and permeable to e.g. chloride ions. The KCl-induced corrosion of alloy 304L in dry O-2 and in an O-2 + H2O mixture increases strongly with temperature in the range 400-600 A degrees C. The strong temperature dependence is explained partly by the temperature dependence of the chromate-formation reaction and partly by the ability of the chromium-depleted oxide to protect the alloy at low temperature. At 400 A degrees C, the oxide was still protective after 168 h.

304L

Breakaway Corrosion

oxidation

Oxidation

chloride

water-vapor

600-degrees-c

oxide hydroxide evaporation

KCl

Deposit

304l

Författare

Jesper Liske

Chalmers, Kemi- och bioteknik, Oorganisk miljökemi

Jan-Erik Svensson

Chalmers, Kemi- och bioteknik, Oorganisk miljökemi

Lars-Gunnar Johansson

Chalmers, Kemi- och bioteknik, Oorganisk miljökemi

Oxidation of Metals

0030-770X (ISSN) 1573-4889 (eISSN)

Vol. 72 3-4 159-177

Ämneskategorier

Metallurgi och metalliska material

DOI

10.1007/s11085-009-9153-2