Abstract

Time-resolved chemical ionization mass spectrometry (CIMS) has been used to investigate the variations of the mixing ratios of benzene, toluene and the C 2-benzenes (xylenes and ethyl benzene) in automotive exhaust during transient engine operation. A significant increase of the benzene/toluene ratios from 0.35 to 1.31 (median) was found upon introduction of a catalytic converter system. A preliminary emission model was developed from these test stand measurements to simulate benzene/toluene ratios of passenger car fleets with variable proportions of three-way catalyst vehicles. Although only the emissions of gasoline-driven passenger cars have been considered so far, the predicted increase of the benzene/toluene ratios during the introduction period of the three-way catalyst from 1980 to 2000 is in good agreement with the observed increase of the atmospheric benzene/toluene ratio measured at a suburban monitoring site (Dübendorf, Switzerland) which is strongly influenced by road traffic emissions. At this site, the atmospheric concentrations of benzene and alkyl benzenes have been detected at hourly intervals since 1993. A steady decrease of the yearly mean from 3.54 to 2.00 ppb for toluene and from 2.87 to 1.33 ppb for the sum of C 2-benzenes was found from 1994 to 1998, respectively, when the proportion of three-way catalyst passenger cars increased from 60 to 82%. Nevertheless, the mean benzene concentration was only affected to a small degree (from 1.10 to 0.97 ppb) within the same period of time. Thus, the observed increase of the atmospheric benzene/toluene-mixing ratios from 0.32 to 0.58 (mean) is in good agreement with the predicted values from the presented emission model. Reduced catalyst conversion efficiency for benzene with respect to alkylated benzenes can explain most of the observed increase of the benzene/toluene and benzene/C 2-benzenes mixing rations. In addition, benzene emissions e.g. from the class of light duty vehicles, which are operated more frequently at sub-optimal combustion conditions, may also contribute to the unexpectedly stable atmospheric benzene concentration at the investigated suburban monitoring site.

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