Dry deposition of nitrogen containing species

Nitrogen oxides (NO_x) emissions and the oxidation products formed by photochemical interactions in the atmosphere are responsible for a significant fraction of both dry and wet acid deposition fluxes. In his paper a vertically-resolved, Lagrangian trajectory model is used to predict the diurnal variation of: NO, NO_2, NO_3, HONO, HONO_2, HO_2NO_2, RONO, RONO_2, RO_2NO_2, N_2O_5 and PAN over an urban airshed. Particular attention is given to the fate of nitric acid and its reaction with gaseous ammonia to form, aerosol phase, ammonium nitrate. A simple model for estimating the deposition fluxes of these species is also presented. A study of the fate of nitrogen oxides emissions, in the South Coast Air Basin of southern California, is used to illustrate the procedures

The dynamics of nitric acid production and the fate of nitrogen oxides

A mathematical model is used to study the fate of nitrogen oxides (NO_x) emissions and the reactions responsible for the formation of nitric acid (HNO_3). Model results indicate that the majority of the NO_x inserted into an air parcel in the Los Angeles basin is removed by dry deposition at the ground during the first 24 h of travel, and that HNO_3 is the largest single contributor to this deposition flux. A significant amount of the nitric acid is produced at night by N_2O_5 hydrolysis. Perturbation of the N_2O_5 hydrolysis rate constant within the chemical mechanism results in redistribution of the pathway by which HNO_3 is formed, but does not greatly affect the total amount of HNO_3 produced. Inclusion of NO_3-aerosol and N_2O_5-aerosol reactions does not affect the system greatly at collision efficiencies, α, of 0.001, but at α = 0.1 or α = 1.0, a great deal of nitric acid could be produced by heterogeneous chemical processes. Ability to account for the observed nitrate radical (NO_3) concentrations in the atmosphere provides a key test of the air quality modeling procedure. Predicted NO_3 concentrations compare well with those measured by Platt et al. (Geophys. Res. Lett.7, 89–92, 1980). Analysis shows that transport, deposition and emissions, as well as chemistry, are important in explaining the behavior of NO_3 in the atmosphere

Review of BEIS3 formulation and consequences relative to air quality standards

Issued as final repor

Sensitivity of Air Pollution-Induced Premature Mortality to Precursor Emissions Under the Influence of Climate Change

The relative contributions of PM2.5 and ozone precursor emissions to air pollution-related premature mortality modulated by climate change are estimated for the U.S. using sensitivities of air pollutants to precursor emissions and health outcomes for 2001 and 2050. Result suggests that states with high emission rates and significant premature mortality increases induced by PM2.5 will substantially benefit in the future from SO2, anthropogenic NOX and NH3 emissions reductions while states with premature mortality increases induced by O3 will benefit mainly from anthropogenic NOX emissions reduction. Much of the increase in premature mortality expected from climate changeinduced pollutant increases can be offset by targeting a specific precursor emission in most states based on the modeling approach followed here