The initial stages of the atmospheric corrosion of statue bronze in th
e presence of sub-ppm concentrations of SO2 and NO2 were studied in th
e laboratory. Trace amounts of NaCl were added, ex situ, to the sample
s prior to exposure to the corrosive atmosphere. Polished and artifici
ally patinated samples were studied. It was concluded from the laborat
ory studies that NO2 is more corrosive towards the bare bronze surface
as compared with SO2. A large increase in the rate of corrosion of po
lished samples was observed upon exposure to an SO2 + NO2-containing a
tmosphere, as compared with exposure to the single gas atmospheres. A
similar synergistic effect was seen on polished samples, pretreated wi
th NaCl, exposed to NO2. Deposition rates of SO2 and NO2 were followed
in real time by continuous monitoring of the inlet and outlet gas con
centrations. HNO2(g) was evolved from the surface of polished samples
exposed to NO2-containing atmospheres.