The atmospheric corrosion of zinc and mild steel was investigated in t
he laboratory at relative humidities of 65%, 80% and 90% in unpolluted
atmospheres and at a relative humidity of 80% in atmospheres containi
ng HCl and SO2 pollutant gases. In order to investigate the effect of
atmospheric particulates on corrosion rates, metal samples were contam
inated with three coal and three oil fly-ashes from different industri
al sources. Control specimens were either uncontaminated or contaminat
ed with small glass beads of similar size to the fly-ashes <45 mum. In
unpolluted atmospheres, particulate contamination increased corrosion
in approximate proportion to the quantity of leachable ionic species
present in the fly-ash. Additionally, glass beads slightly increased c
orrosion rates probably due to differential aeration effects and an in
creased local time-of-wetness in the vicinity of the beads. In pollute
d environments, the corrosion rates of the specimens increased and the
additional effect of fly-ash contamination on the corrosion rates was
consequently decreased in proportion to the presentation rate of poll
utant. There was no significant additional increase in corrosion rates
with SO2 pollutant and fly-ash contamination, indicating that effects
due to catalytic oxidation of SO2 to sulphuric acid or sulphates were
not significant. Overall, this study provides strong evidence that th
e atmospheric corrosion rates of metals are dependent on the conductan
ce of the thin-film surface electrolyte and that the first-order effec
t of contaminant particles is to increase solution conductance and hen
ce corrosion rates.