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Is KCl(g) corrosive at temperatures above its dew point? - Influence of KCl(g) on initial stages of the high temperature corrosion of 11% Cr steel at 600 degrees C

Karin Segerdahl (Institutionen för oorganisk miljökemi) ; Jesper Pettersson (Institutionen för oorganisk miljökemi) ; Jan-Erik Svensson (Institutionen för oorganisk miljökemi) ; Lars-Gunnar Johansson (Institutionen för oorganisk miljökemi)
High Temperature Corrosion and Protection of Materials 6, Prt 1 and 2, Proceedings Vol. 461-464 (2004), p. 109-116.
[Artikel, refereegranskad vetenskaplig]

The influence of gaseous KCl on the high temperature oxidation of CrMoV11 1 (X20) steel at 600degreesC is reported. The sample temperature was above the dew point of KCl, the partial pressure of KCl being about 5ppm. The samples were investigated by a number of surface analytical techniques including grazing angle XRD, SEM/EDX, and SAM. CrMoV11 1 steel shows protective behaviour in clean dry O-2 and O-2/H2O environment because of the formation of a chromium-rich oxide (alpha-(Fe,Cr)(2)O-3). It is Often considered that alkali salts accelerate the corrosion of steel only when present on the surface in solid or liquid form. In contrast, the present result shows that gaseous KCl is very corrosive, also in the absence of condensation. KCl(g) reacts with chromium in the scale, forming K2CrO4(s). This depletes the protective oxide in chromium and leads to the formation of non-protective hematite, Fe2O3.

Nyckelord: 11%Cr steel; chromia-forming steels; KCl(g); alkali-induced high, temperature corrosion, water-vapor; fe-cr; oxidation; chloride; deposits; alloys

Materials science forum ; 461/464. ISSN: 0255-5476

Denna post skapades 2006-08-29. Senast ändrad 2017-10-03.
CPL Pubid: 6908


Institutioner (Chalmers)

Institutionen för oorganisk miljökemi (1900-2004)



Chalmers infrastruktur