| Autor: |
Sardar, Satya B.1, Fine, Philip M.1, Mayo, Paul R.1, Sioutas, Constantinos1 sioutas@usc.edu |
| Předmět: |
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| Zdroj: |
Environmental Science & Technology. 2/15/2005, Vol. 39 Issue 4, p932-944. 13p. |
| Abstrakt: |
Ambient ultrafine particles have gained attention with recent evidence showing them to be more toxic than larger ambient particles. Few studies have investigated the distribution of chemical constituents within the ultrafine range. The current study explores the size-fractionated ultratine (10-180 nm) chemical composition at urban source sites (USC and Long Beach) and inland receptor sites (Riverside and Upland) in the Los Angeles basin over three different seasons. Size-fractionated ultrafine particles were collected by a NanoMOUDI over a period of 2 weeks at each site. Measurements of ultrafine mass concentrations varied from 0.86 to 3.5 μ/m³ with the highest concentrations observed in the fall. The chemical composition of ultrafine particles ranged from 32 to 69% for organic carbon (OC), 1-34% for elemental carbon (EC), 0-24% for sulfate, and 0-4% for nitrate. A distinct DC mode was observed between 18 and 56 nm in the summer, possibly indicating photochemical secondary organic aerosol formation. The EC levels are higher in winter at the source sites due to lower inversion heights and are higher in summer at the receptor sites due to increased long-range transport from upwind source areas. Nitrate and sulfate were measurable only in the larger particle size ranges of ultrafine PM. Collocated continuous measurements of particle size distributions and gaseous pollutants helped to differentiate ultrafine particle sources at each site. [ABSTRACT FROM AUTHOR] |
| Databáze: |
GreenFILE |
| Externí odkaz: |
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