Discussion: “Radioactive Sulfur Oxide Studies of External Corrosion Reactions on Surfaces” (Krause, H. H., Levy, A., and Reid, William T., 1969, ASME J. Eng. Power, 91, pp. 216–220)

1969 ◽  
Vol 91 (3) ◽  
pp. 222-222
Author(s):  
G. C. Wiedersum
1969 ◽  
Vol 91 (3) ◽  
pp. 216-220 ◽  
Author(s):  
H. H. Krause ◽  
A. Levy ◽  
William T. Reid

Radioactive sulfur-35 has been used as a tracer to determine the roles of SO2 and SO3 in reactions leading to formation of alkali iron trisulfates. The reactivity of 30 ppm SO3 with surfaces containing iron oxides, alone or mixed with alkali sulfates, has been found to be much greater than that of large amounts of SO2 + O2 over the temperature range 900 to 1300 deg F. The SO3 reactivity was found to be a maximum at 1200 deg F, while the SO2 reactivity was at a minimum about 1150 deg F. Complex sulfates were formed most readily with K2SO4-Fe2O3 surfaces, followed by Na2SO4-steel, and Na2SO4-Fe3O3 surfaces.


2018 ◽  
Vol 765 ◽  
pp. 155-159
Author(s):  
Tosapolporn Pornpibunsompop ◽  
Purit Thanakijkasem

High temperature corrosion of 310S austenitic stainless steel in simulated rocket combustion gas at 900 degree Celsius was investigated and discussed in this paper. 310S austenitic stainless steel was chosen because it was used for building some components of a rocket launcher. The corrosive atmosphere was prepared by mixing of hydrochloric acid and distilled water with 5.5 mole per liter then, boiling that solution and feeding into a corrosion testing chamber. The chamber was set up at 900 degree Celsius with duration 210 hrs. After testing, the corroded specimen was microscopically characterized by OM and SEM/EDS techniques. The corrosion layer was classified into three main sublayers: peeling-off scale, external corrosion sublayer, and internal corrosion sublayer. The local chemical information was analyzed by XRD (in case of peeling-off scale) and SEM/EDS (in case of external and internal corrosion sublayers). The peeling off scale mainly comprised Fe2O3and Fe21.3O32ferrous oxides because they needed much oxygen consumption to exist. In case of external and internal sublayers, there were a lot of pore tunnels and corrosion products. Chlorine and/or hydrogen chloride would penetrate through a passive film and, then, metal chlorides was formed on both external and internal corrosion sublayers. Metal chlorides would volatile because of their lower evaporation temperature than the testing temperature. Moreover, they were oxidized by oxygen in wet condition and resulted metal oxides mostly remaining on the external corrosion sublayer.


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