Chemistry of new particle growth in mixed urban and biogenic emissions – insights from CARES

Journal Article · Tue Jul 01 04:00:00 EDT 2014 · Atmospheric Chemistry and Physics

DOI:https://doi.org/10.5194/acp-14-6477-2014· OSTI ID:1225172

Setyan, Ari; Song, Chen; Merkel, M.; Knighton, M.; Onasch, Timothy B.; Canagaratna, M. R.; Worsnop, Douglas R.; Wiedensohler, A.; Shilling, John E.; Zhang, Qi

Regional new particle formation and growth events (NPEs) were observed on most days over the Sacramento and western Sierra foothills area of California in June 2010 during the Carbonaceous Aerosols and Radiative Effect Study (CARES). Simultaneous particle measurements at both the T0 (Sacramento, urban site) and the T1 (Cool, rural site located ~40 km northeast of Sacramento) sites of CARES indicate that the NPEs usually occurred in the morning with the appearance of an ultrafine mode at ~15 nm (in mobility diameter, D_m, measured by a mobility particle size spectrometer operating in the range10-858 nm) followed by the growth of this modal diameter to ~50 nm in the afternoon. These events were generally associated with southwesterly winds bringing urban plumes from Sacramento to the T1 site. The growth rate was on average higher at T0 (7.1±2.7 nm h^-1) than at T1 (6.2±2.5 nm h^-1), likely due to stronger anthropogenic influences at T0. Using a high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS), we investigated the evolution of the size-resolved chemical composition of new particles at T1. Our results indicate that the growth of new particles was driven primarily by the condensation of oxygenated organic species and, to a lesser extent, ammonium sulfate. New particles appear to be fully neutralized during growth, consistent with high NH₃ concentration in the region. Nitrogen-containing organic ions (i.e., CHN⁺, CH₄N+,C2H3N⁺, and C₂HN⁺) that are indicative of the presence of alkyl-amine species in submicrometer particles enhanced significantly during the NPE days, suggesting that amines might have played a role in these events. Our results also indicate that the bulk composition of the ultrafine mode organics during NPEs was very similar to that of anthropogenically influenced secondary organic aerosol (SOA) observed in transported urban plumes. In addition, the concentrations of species representative of urban emissions (e.g., black carbon,CO, NO_x, and toluene) were significantly higher whereas thephoto-oxidation products of biogenic VOCs (volatile organic compounds) and the biogenically influenced SOA also increased moderately during the NPE days compared to the non-event days. These results indicate that the frequently occurring NPEs over the Sacramento and Sierra Nevada regions were mainly driven by urban plumes from Sacramento and the San Francisco Bay Area, and that the interaction of regional biogenic emissions with the urban plumes has enhanced the new particle growth. This finding has important implications for quantifying the climate impacts of NPEs on global scale.

• Research Organization: Pacific Northwest National Laboratory (PNNL), Richland, WA (US)
• Sponsoring Organization: USDOE
• DOE Contract Number: AC05-76RL01830
• OSTI ID: 1225172
• Report Number(s): PNNL-SA-105602; KP1701000
• Journal Information: Atmospheric Chemistry and Physics, Journal Name: Atmospheric Chemistry and Physics Journal Issue: 13 Vol. 14; ISSN 1680-7316
• Publisher: European Geosciences Union
• Country of Publication: United States
• Language: English