Emissions inventories significantly affect photochemical air quality model performance and the development of effective control strategies. However, there have been very few studies to evaluate their accuracy. Here, to evaluate a volatile organic compound (VOC) emissions inventory, we implemented a combined approach: comparing the ratios of carbon bond (CB)-IV VOC groups to nitrogen oxides (NO x ) or carbon monoxide (CO) using an emission preprocessing model, comparing the ratios of VOC source contributions from a source apportionment technique to NO x or CO, and comparing ratios of CB-IV VOC groups to NO x or CO and the absolute concentrations of CB-IV VOC groups using an air quality model, with the corresponding ratios and concentrations observed at three sites (Maryland, Washington, DC, and New Jersey). The comparisons of the ethene/NO x ratio, the xylene group (XYL)/NO x ratio, and ethene and XYL concentrations between estimates and measurements showed some differences, depending on the comparison approach, at the Maryland and Washington, DC sites. On the other hand, consistent results at the New Jersey site were observed, implying a possible overestimation of vehicle exhaust. However, in the case of the toluene group (TOL), which is emitted mainly from surface coating and printing sources in the solvent utilization category, the ratios of TOL/ NO x or CO, as well as the absolute concentrations revealed an overestimate of these solvent sources by a factor of 1.5 to 3 at all three sites. In addition, the overestimate of these solvent sources agreed with the comparisons of surface coating and printing source contributions relative to NO x from a source apportionment technique to the corresponding value of estimates at the Maryland site. Other studies have also suggested an overestimate of solvent sources, implying a possibility of inaccurate emission factors in estimating VOC emissions from surface coating and printing sources. We tested the impact of these overestimates with a chemical transport model and found little change in ozone but substantial changes in calculated secondary organic aerosol concentrations.
INTRODUCTIONAir quality models, composed of meteorology, chemistry, and emissions, have been widely implemented to simulate the chemistry and physics of the atmosphere and to understand the cause-effect relationships between pollutants and their precursors. Potential control measures for target air pollutants have been determined, based on those modeling results. Hence, inaccurate results from air quality modeling can lead to negative impacts that are both economic and environmental in nature. The usefulness of the output of air quality models is largely dependent on the quality of their inputs. Previous studies indicate that the uncertainties in atmospheric model results may originate mainly from the uncertainties in the emission inventories. [1][2][3] There have been very few attempts to evaluate emissions inventories. Previous studies described in detail the limitations and difficulties ass...