TY - JOUR
T1 - Estimated contributions of primary and secondary organic aerosol from fossil fuel combustion during the CalNex and Cal-Mex campaigns
AU - Guzman-Morales, J.
AU - Frossard, A. A.
AU - Corrigan, A. L.
AU - Russell, L. M.
AU - Liu, S.
AU - Takahama, S.
AU - Taylor, J. W.
AU - Allan, J.
AU - Coe, H.
AU - Zhao, Y.
AU - Goldstein, A. H.
N1 - The authors appreciate financial support from the California Air Resources Board (CARB 09-328) and the National Science Foundation (NSF AGS-1009408). Additionally, we would like to thank the UC MEXUS-CONACyT Agreement of Cooperation in Higher Education and Research for the support provided to JGM. The Pasadena SP2 measurements were supported by the UK Natural Environment Research Council through a PhD studentship and the project Multiscale Chemical Composition of Carbonaceous particles and Coatings (MC4) [Grant ref: NE/H008136/1. The authors are also grateful to John Karlik and the Kern County University of California Cooperative Extension staff for support at Bakersfield, to Luisa Molina and the Molina Center for support at Tijuana, to Jason Surratt and Caltech for support at Pasadena, and Patricia Quinn and PMEL for support on the R/V Atlantis. In addition, we would like to thank CARB scientists Nehzat Motallebi, Eileen McCauley, and Scott Scheller for their contributions to this project. The statements and conclusions in this paper are those of the researchers (contractor) and not necessarily those of CARB. The mention of commercial products, their source, or their use in connection with material reported herein is not to be construed as actual or implied endorsement of such products.
PY - 2014
Y1 - 2014
N2 - Observations during CalNex and Cal-Mex field campaigns at Bakersfield, Pasadena, Tijuana, and on board the R/V Atlantis show a substantial contribution of fossil fuel emissions to the ambient particle organic mass (OM). At least two fossil fuel combustion (FFC) factors with a range of contributions of oxidized organic functional groups were identified at each site and accounted for 60-88% of the total OM. Additional marine, vegetative detritus, and biomass burning or biogenic sources contribute up to 40% of the OM. Comparison of the FTIR spectra of four different unburned fossil fuels (gasoline, diesel, motor oil, and ship diesel) with PMF factors from ambient samples shows absorbance peaks from the fuels are retained in organic aerosols, with the spectra of all of the FFC factors containing at least three of the four characteristic alkane peaks observed in fuel standards at 2954, 2923, 2869 and 2855cm-1. Based on this spectral similarity, we estimate the primary OM from FFC sources for each site to be 16-20%, with secondary FFC OM accounting for an additional 42-62%. Two other methods for estimating primary OM that use carbon monoxide (CO) and elemental carbon (EC) as tracers of primary organic mass were investigated, but both approaches were problematic for the CalNex and Cal-Mex urban sites because they were influenced by multiple emission sources that had site-specific and variable initial ratios to OM. For example, using the δPOM/δCO ratio of 0.0094μgppbV-1 proposed by other studies produces unrealistically high estimates of primary FFC OM of 55-100%. © 2013 Elsevier Ltd.
AB - Observations during CalNex and Cal-Mex field campaigns at Bakersfield, Pasadena, Tijuana, and on board the R/V Atlantis show a substantial contribution of fossil fuel emissions to the ambient particle organic mass (OM). At least two fossil fuel combustion (FFC) factors with a range of contributions of oxidized organic functional groups were identified at each site and accounted for 60-88% of the total OM. Additional marine, vegetative detritus, and biomass burning or biogenic sources contribute up to 40% of the OM. Comparison of the FTIR spectra of four different unburned fossil fuels (gasoline, diesel, motor oil, and ship diesel) with PMF factors from ambient samples shows absorbance peaks from the fuels are retained in organic aerosols, with the spectra of all of the FFC factors containing at least three of the four characteristic alkane peaks observed in fuel standards at 2954, 2923, 2869 and 2855cm-1. Based on this spectral similarity, we estimate the primary OM from FFC sources for each site to be 16-20%, with secondary FFC OM accounting for an additional 42-62%. Two other methods for estimating primary OM that use carbon monoxide (CO) and elemental carbon (EC) as tracers of primary organic mass were investigated, but both approaches were problematic for the CalNex and Cal-Mex urban sites because they were influenced by multiple emission sources that had site-specific and variable initial ratios to OM. For example, using the δPOM/δCO ratio of 0.0094μgppbV-1 proposed by other studies produces unrealistically high estimates of primary FFC OM of 55-100%. © 2013 Elsevier Ltd.
KW - Carbonaceous aerosol particles
KW - Fossil fuel combustion sources
KW - FTIR
KW - Primary organic aerosol
KW - Secondary organic aerosol
U2 - 10.1016/j.atmosenv.2013.08.047
DO - 10.1016/j.atmosenv.2013.08.047
M3 - Article
SN - 1352-2310
VL - 88
SP - 330
EP - 340
JO - Atmospheric Environment
JF - Atmospheric Environment
ER -