The ammonium nitrate particle equivalent of NOx emissions for wintertime conditions in Central California's San Joaquin Valley

被引:62
作者
Stockwell, WR
Watson, JG
Robinson, NF
Steiner, W
Sylte, WW
机构
[1] Energy & Environm Engn Ctr, Desert Res Inst, Reno, NV 89512 USA
[2] Woodward Clyde Consultants, URS Greiner, Portland, OR 97201 USA
关键词
PM2.5; secondary aerosol; nitrate; San Joaquin Valley; emissions trading;
D O I
10.1016/S1352-2310(00)00148-5
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A new method has been developed to assess the aerosol particle formation reactivity of nitrogen oxide (NOx) emissions. The method involves using a photochemical box model with gas-phase photochemistry, aerosol production and deposition to calculate the ammonium nitrate particle equivalent of NOx emissions. The yields of ammonium nitrate particles used in the box model were determined from parametric simulations made with an equilibrium model that calculated the fraction of nitric acid that reacts to produce ammonium nitrate from the temperature, relative humidity and ammonium-to-nitrate ratios. For the wintertime conditions of emissions and meteorology in the San Joaquin Valley of central California, approximately 80% of the moles of nitric acid produced was found to be in the particulate nitrate phase and about 33% of the moles of emitted NOx was converted to particulate nitrate. The particle equivalent of NOx emissions was found to be on the order of 0.6 g of ammonium nitrate for each gram of NOx emitted (the mass of NOx calculated as NO2). This estimate is in reasonable agreement with an analysis of field measurements made in central California. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:4711 / 4717
页数:7
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