Abstract
Abstract A meteorological and chemical modeling system is used to determine the effect of ethene and propene point source emission rates on the magnitude and distribution of ozone in the vicinity of Houston. The model performance is evaluated using surface and airborne meteorological and chemical measurements made as part of the 2000 Texas Air Quality Study. A simulation that employed the reported mobile, area, biogenic, and point source emissions produced ozone mixing ratios as high as 120 ppb and distributions of nitrogen oxides that were similar to measurements at most locations, but the model underestimated ozone mixing ratios greater than 140 ppb that were located just downwind of petrochemical facilities. When the point source emission rates of ethene and propene were increased by a factor of 10, the simulated peak ozone levels were in better agreement with surface, aircraft, and lidar observations. The magnitude of the simulated ethene and olefin concentrations were in better agreement with canister samples aloft as well; however, there was still a large amount of scatter in the results. While the highest ozone mixing ratios were produced just downwind of large point source emissions of VOCs, sensitivity simulations also showed that reductions in anthropogenic emissions of NO x would be needed to reduce ozone mixing ratios over a larger area.
Published Version
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