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The Influence of SO2 on the Corrosion of Mg and Mg-Al Alloys

Mohsen Esmaily (Institutionen för kemi och kemiteknik, Oorganisk miljökemi) ; D. B. Blucher ; R. W. Lindstrom ; Jan-Erik Svensson (Institutionen för kemi och kemiteknik, Oorganisk miljökemi) ; Lars-Gunnar Johansson (Institutionen för kemi och kemiteknik, Oorganisk miljökemi)
Journal of the Electrochemical Society (0013-4651). Vol. 162 (2015), 6, p. C260-C269.
[Artikel, refereegranskad vetenskaplig]

The SO2-induced atmospheric corrosion of some magnesium-aluminum (Mg-Al) alloys, including Mg alloy AZ91D, and commercially pure Mg (CP Mg) was investigated using well-controlled laboratory exposures and included real-time measurements of SO2 deposition. The influence of SO2 concentration, alloy composition, humidity, and ppb level additions of O-3 or NO2 on the rate of SO2 deposition was investigated. SO2 accelerates the corrosion of Mg and Mg alloys causing localized corrosion, MgSO(3)6H(2)O being the dominant corrosion product. At 60% RH, traces of O-3 or NO2 strongly increased both the SO2 deposition and the corrosion rate. The rate of SO2 deposition was strongly dependent on humidity; at 70% RH and higher the SO2 deposition rate was very rapid and constant in time while it was transient below 50% RH. At 60% RH, a change from transient to rapid, steady-state, SO2 deposition occurred. The sudden activation is explained by the onset of electrochemical corrosion. The activation behavior was shown to depend on SO2 concentration, the thickness of the surface film and by the presence of ambient O-2.

Denna post skapades 2015-06-04. Senast ändrad 2017-10-03.
CPL Pubid: 218039


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