Dominant Mechanisms that Shape the Airborne Particle Size and Composition Distribution in Central California

Herner, JD; Ying, Q; Aw, J; Gao, O; Chang, DPY; Kleeman, MJ

HERO ID

135981

Reference Type

Journal Article

Year

2006

HERO ID 135981
In Press No
Year 2006
Title Dominant Mechanisms that Shape the Airborne Particle Size and Composition Distribution in Central California
Authors Herner, JD; Ying, Q; Aw, J; Gao, O; Chang, DPY; Kleeman, MJ
Journal Aerosol Science and Technology
Volume 40
Issue 10
Page Numbers 827-844
Abstract The size and composition of ambient airborne particulate matter is reported for winter conditions at five locations in (or near) the San Joaquin Valley in central California. Two distinct types of airborne particles were identified based on diurnal patterns and size distribution similarity: hygroscopic sulfate/ammonium/nitrate particles and less hygroscopic particles composed of mostly organic carbon with smaller amounts of elemental carbon. Day-time PM10 concentrations for sulfate/ammonium/nitrate particles were measured to be 10.1 μg m-3, 28.3 μg m-3, and 52.8 μg m-3 at Sacramento, Modesto and Bakersfield, California, respectively. Nighttime concentrations were 10-30% lower, suggesting that these particles are dominated by secondary production. Simulation of the data with a box model suggests that these particles were formed by the condensation of ammonia and nitric acid onto background or primary sulfate particles. These hygroscopic particles had a mass distribution peak in the accumulation mode (0.56-1.0 μm) at all times. Daytime PM10 carbon particle concentrations were measured to be 9.5 μg m-3, 15.1 μg m-3, and 16.2 μg m-3 at Sacramento, Modesto, and Bakersfield, respectively. Corresponding nighttime concentrations were 200-300% higher, suggesting that these particles are dominated by primary emissions. The peak in the carbon particle mass distribution varied between 0.2-1.0 μm. Carbon particles emitted directly from combustion sources typically have a mass distribution peak diameter between 0.1-0.32 μm. Box model calculations suggest that the formation of secondary organic aerosol is negligible under cool winter conditions, and that the observed shift in the carbon particle mass distribution results from coagulation in the heavily polluted concentrations experienced during the current study. The analysis suggests that carbon particles and sulfate/ammonium/nitrate particles exist separately in the atmosphere of the San Joaquin Valley until coagulation mixes them in the accumulation mode.
Doi 10.1080/02786820600728668
Wosid WOS:000239954300010
Url http://www.tandfonline.com/doi/abs/10.1080/02786820600728668
Is Certified Translation No
Dupe Override No
Comments ISSN:
Is Public Yes
Keyword SAN-JOAQUIN VALLEY;FLIGHT MASS-SPECTROMETRY;ON-ROAD VEHICLES;PARTICULATE MATTER;ATMOSPHERIC AEROSOL;FRESNO SUPERSITE;GRAND-CANYON;EMISSIONS;NITRATE;TUNNEL;ENGINEERING, CHEMICAL;ENVIRONMENTAL SCIENCES;METEOROLOGY & ATMOSPHERIC SCIENCES
Is Qa No