FTIR studies of the reaction of gaseous NO with HNO3 on porous glass: Implications for conversion of HNO3 to photochemically active NOx in the atmosphere

The heterogeneous reaction of HNO3 adsorbed on porous glass surfaces with g aseous NO was investigated using transmission Fourier transform infrared (F TIR) spectroscopy at room temperature. The amount of adsorbed HNO3 varied f rom (4.2-110) x 10(17) molecules of HNO3 on a 6 cm(2) porous glass plate wh ose BET surface area was measured to be 28.5 +/- 0.6m(2) (2 sigma). The ini tial concentration of gaseous NO varied from (0.2-6) x 10(17) molecules cm( -3). A rapid release of NO2 into the gas phase was observed to occur simult aneously with a decrease in adsorbed HNO3. A trace amount of gaseous HONO w as also formed. The measured yields of NO2 and loss of HNO3 and NO are cons istent with the net reaction 2HNO(3) + NO --> 3NO(2) + H2O which is due to HNO3 + NO --> HONO + NO2, followed by HONO + HNO3 --> 2NO(2) + H2O and/or 2 x (HNO3 + NO --> HONO + NO2) followed by 2HONO --> NO + NO2 + H2O. Both (N O2)-N-15 and (NO2)-N-14 were observed as reaction products when (NO)-N-15 a nd (HNO3)-H-14 were used as the reagent species, indicating that some of th e NO2 produced originates in HNO3. The measured decay rates for adsorbed HN O3 were first order in NO. The rates initially increase with increasing HNO 3 but tend to plateau, consistent with complete surface coverage and the fo rmation of multilayers of HNO3, perhaps in part in the pores. Extrapolation of these results to atmospheric NO levels suggests that this heterogeneous reaction may serve as a mechanism to regenerate photochemically active for ms of NOx and nitrous acid from HNO3 in the atmosphere.