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A study was carried out to increase our understanding of the emissions of air toxics from normal and high-emitting vehicles. This study is part of a larger study on fuel effects in high-emitting vehicles, and is part of the Auto/Oil Air Quality Improvement Research Program (AQIRP). Detailed measurements were carried out on the emissions of two vehicles run on industry-average gasoline. The two vehicles, having similar emissions control technologies, represent a high-emitting vehicle and a normal-emitting vehicle. In addition to the regulated emissions (HC, CO, and NOx), a detailed chemical analysis was carried out on the gas - and particle-phase non-regulated emissions. The vehicles were tested over the U.S. EPA UDDS driving schedule. The high emitter was highly variable with regard to emissions, but always operated rich of the stoichiometric point. Up to 46% of fuel carbon was emitted as CO and unburned HC for the high emitter, compared to less than 1.4% for the normal emitter.

Two cooperative programs to measure polycyclic aromatic hydrocarbons (PAH) in extracts from diesel particulate emissions were conducted by project groups of the Coordinating Research Council's Air Pollution Research Advisory Committee. The use of a uniform analysis method by all participating laboratories gave better precision than the use of different methods selected by each participant. Results from eight laboratories gave relative standard deviations for nine PAH which ranged from 15 to 34% using the uniform method. These results show that this method for PAH provides adequate precision for diesel fuel-and-vehicle studies as well as for health effects assessment.

Speciation of sulfurous acid, sulfuric acid and ammonium sulfate collected from the aerosol phase on a Fluoropore filter has been readily accomplished using techniques of chemical ionization mass spectrometry combined with thermal separation. Thermal separation of ammonium hydrogen sulfate from ammonium sulfate was not possible. Spectral separation of these species by selective ionization is proposed. Analysis of sulfate aerosols collected from ambient air and catalyzed vehicle emissions is described. It was found that sulfuric acid aerosol was rapidly converted to ammonium sulfate or ammonium hydrogen sulfate in the presence of ambient concentrations of ammonia. Ambient samples collected in the Detroit metropolitan area have been found to contain only trace quantities of sulfuric aicd. Sulfate samples collected from a dilution tube into which catalyzed vehicle exhaust was injected were found to contain significant quantities of ammonium sulfate in addition to sulfuric acid.