While N2O3 has been observed previously in the gas phase, in solution and a
s a solid at low temperatures, it has not been reported adsorbed on solids
at room temperature. However, the adsorbed species has been postulated as a
precursor to HONO in the lower atmosphere. We report here the formation of
N2O3 adsorbed on a porous glass surface at room temperature from the precu
rsors NO and NO2 using transmission FTIR spectroscopy. The spectrum of the
porous glass in the presence of NO and NO2 showed broad peaks at approximat
ely 1870 and 1600 cm(-1) attributed to surface adsorbed asym-N2O3 (ONNO2).
These peaks shifted by similar to 30-40 cm(-1) to lower wavenumbers when N-
15-labeled NO was used, consistent with absorption bands previously assigne
d by other researchers to solid asym-N2O3 at low temperature. While the pea
ks assigned to surface-adsorbed asym-N2O3 did not decrease significantly on
exposure to water vapor, measurable concentrations of gas-phase HONO were
formed. The atmospheric implications are discussed.