Abstract
The effect of the presence of rust on steel on its further corrosion during outdoor and laboratory exposure to SO2 has been examined. More aggressive initial conditions favour the formation of non-protective, loose rust which-flakes off from the metal surface and increases the subsequent yearly corrosion values. The initial rust present increases the rate of attack during the first 2–3 months, but there is then a general falling off of the corrosion rate with time. SO2-contaminated rust is able to promote corrosion on clean (rust-free) steel, but the amount of corrosion is not dependent on the amount of SO2 adsorbed by the rust. The order of severity of attack on steel by different electrolytes differs from that caused by rust produced by the same electrolytes. Rust contaminated with FeSO4 or FeCl3 enhances the rusting of steel, whereas rust converters (such as phosphates) have beneficial effects. In the further rusting in SO2 of prerusted steel specimens it was found that the duration.of the pre-rusting period determines the subsequent rate of rusting, but the ‘age’ of the rust, rather than its thickness, determines its protective effect. In interrupted SO2 exposure, in which the pre-rusted specimens were first exposed to SO2 and then to humid SO2-free air, it was found that a temperature (18°e) and humidity (50% R.H.) which are too low to initiate the formation of incipient reaction product (FeSO4, 4H2O) on clean metal, allow sufficient formation of these products on rusted specimens to enable rusting to continue in moist SO2-free air.
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