Open AccessEffects of aerosols on tropospheric oxidants: A global model study
Author(s) -
Tie Xuexi,
Brasseur Guy,
Emmons Louisa,
Horowitz Larry,
Kinnison Douglas
Publication year - 2001
Publication title -
journal of geophysical research: atmospheres
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.67
H-Index - 298
eISSN - 2156-2202
pISSN - 0148-0227
DOI - 10.1029/2001jd900206
Subject(s) - aerosol , sulfate , chemical transport model , sulfate aerosol , troposphere , ozone , atmospheric sciences , soot , atmosphere (unit) , environmental science , chemistry , meteorology , combustion , geology , physics , organic chemistry
The global distributions of sulfate and soot particles in the atmosphere are calculated, and the effect of aerosol particles on tropospheric oxidants is studied using a global chemical/transport/aerosol model. The model is developed in the framework of the National Center for Atmospheric Research (NCAR) global three‐dimensional chemical/transport model (Model for Ozone and Related Chemical Tracers (MOZART)). In addition to the gas‐phase photochemistry implemented in the MOZART model, the present study also accounts for the formation of sulfate and black carbon aerosols as well as for heterogeneous reactions on particles. The simulated global sulfate aerosol distributions and seasonal variation are compared with observations. The seasonal variation of sulfate aerosols is in agreement with measurements, except in the Arctic region. The calculated vertical profiles of sulfate aerosol agree well with the observations over North America. In the case of black carbon the calculated surface distribution is in fair agreement with observations. The effects of aerosol formation and heterogeneous reactions on the surface of sulfate aerosols are studied. The model calculations show the following: (1) The concentration of H 2 O 2 is reduced when sulfate aerosols are formed due to the reaction of SO 2 + H 2 O 2 in cloud droplets. The gas‐phase reaction SO 2 + OH converts OH to HO 2 , but the reduction of OH and enhancement of HO 2 are insignificant (<3%). (2) The heterogeneous reaction of HO 2 on the surface of sulfate aerosols produces up to 10% reduction of hydroperoxyl radical (HO 2 ) with an uptake coefficient of 0.2. However, this uptake coefficient could be overestimated, and the results should be regard as an upper limit estimation. (3) The N 2 O 5 reaction on the surface of sulfate aerosols leads to an 80% reduction of NO x at middle to high latitudes during winter. Because ozone production efficiency is low in winter, ozone decreases by only 10% as a result of this reaction. However, during summer the N 2 O 5 reaction reduces NO x by 15% and O 3 by 8–10% at middle to high latitudes. (4) The heterogeneous reaction of CH 2 O on sulfate aerosols with an upper limit uptake coefficient (γ = 0.01) leads to an 80 to 90% decrease in CH 2 O and 8 to 10% reduction of HO 2 at middle to high latitudes during winter. Many uncertainties remain in our understanding of heterogeneous chemical processes and in the estimate of kinetic parameters. This model study should therefore be regarded as exploratory and subject to further improvements before final conclusions can be made.