Source Apportionment of Fine (PM1.8) and Ultrafine (PM0.1) Airborne Particulate Matter during a Severe Winter Pollution Episode

被引:61
作者
Kleeman, Michael J. [1 ]
Riddle, Sarah G. [2 ]
Robert, Michael A. [1 ]
Jakober, Chris A. [3 ]
Fine, Phillip M. [4 ]
Hays, Michael D. [5 ]
Schauer, James J. [6 ]
Hannigan, Michael P. [7 ]
机构
[1] Univ Calif Davis, Dept Civil & Environm Engn, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Chem, Davis, CA 95616 USA
[3] Univ Calif Davis, Agr & Environm Chem Grad Grp, Davis, CA 95616 USA
[4] Univ So Calif, Dept Civil & Environm Engn, Los Angeles, CA USA
[5] US EPA, Natl Risk Management Res Lab, Res Triangle Pk, NC 27711 USA
[6] Univ Wisconsin, Dept Civil & Environm Engn, Madison, WI 53706 USA
[7] Univ Colorado, Dept Mech Engn, Boulder, CO 80309 USA
基金
美国国家环境保护局;
关键词
DUTY DIESEL VEHICLES; SIZE DISTRIBUTION; ORGANIC-COMPOUNDS; PARTICLE MASS; GAS-PHASE; EMISSIONS; CALIFORNIA; GASOLINE; CARBON; COMBUSTION;
D O I
10.1021/es800400m
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Size-resolved samples of airborne particulate matter (PM) collected during a severe winter pollution episode at three sites in the San Joaquin Valley of California were extracted with organic solvents and analyzed for detailed organic compounds using GC-MS. Six particle size fractions were characterized with diameter (Dp) < 1.8 mu m; the smallest size fraction was 0.056 < Dp < 0.1 mu m which accounts for the majority of the mass in the ultrafine (PM0.1) size range. Source profiles for ultrafine particles developed during previous studies were applied to the measurements at each sampling site to calculate source contributions to organic carbon (OC) and elemental carbon (EC) concentrations. Ultrafine EC concentrations ranged from 0.03 mu g m(-3) during the daytime to 0.18 mu g m(-3) during the nighttime. Gasoline fuel, diesel fuel, and lubricating oil combustion products accounted far the majority of the ultrafine EC concentrations, with relatively minor contributions from biomass combustion and meat cooking. Ultrafine OC concentrations ranged from 0.2 mu g m(-3) during the daytime to 0.8 mu g m(-3) during the nighttime. Wood combustion was found to be the largest source of ultrafine OC. Meat cooking was also identified as a significant potential source of PM0.1 mass but further study is required to verify the contributions from this source. Gasoline fuel, diesel fuel, and lubricating oil combustion products made minor contributions to PM0.1 OC mass. Total ultrafine particulate matter concentrations were dominated by contributions from wood combustion and meat cooking during the current study. Future inhalation exposure studies may wish to target these sources as potential causes of adverse health effects.
引用
收藏
页码:272 / 279
页数:8
相关论文
共 24 条
[1]   THE FORMATION OF NITRO-PAH FROM THE GAS-PHASE REACTIONS OF FLUORANTHENE AND PYRENE WITH THE OH RADICAL IN THE PRESENCE OF NOX [J].
AREY, J ;
ZIELINSKA, B ;
ATKINSON, R ;
WINER, AM ;
RAMDAHL, T ;
PITTS, JN .
ATMOSPHERIC ENVIRONMENT, 1986, 20 (12) :2339-2345
[2]   Characterization and source apportionment of atmospheric organic and elemental carbon during fall and winter of 2003 in Xi'an, China [J].
Cao, JJ ;
Wu, F ;
Chow, JC ;
Lee, SC ;
Li, Y ;
Chen, SW ;
An, ZS ;
Fung, KK ;
Watson, JG ;
Zhu, CS ;
Liu, SX .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2005, 5 :3127-3137
[3]  
CHOW JC, 2005, J GEOPHYS RES ATMOS, V111
[4]   Diurnal variations of individual organic compound constituents of ultrafine and accumulation mode particulate matter in the Los Angeles basin [J].
Fine, PM ;
Chakrabarti, B ;
Krudysz, M ;
Schauer, JJ ;
Sioutas, C .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2004, 38 (05) :1296-1304
[5]   Polycyclic aromatic hydrocarbon size distributions in aerosols from appliances of residential wood combustion as determined by direct thermal desorption - GC/MS [J].
Hays, MD ;
Smith, ND ;
Kinsey, J ;
Dong, YJ ;
Kariher, P .
JOURNAL OF AEROSOL SCIENCE, 2003, 34 (08) :1061-1084
[6]   Size and composition distribution of airborne particulate matter in northern California: I-particulate mass, carbon, and water-soluble ions [J].
Herner, JD ;
Aw, J ;
Gao, O ;
Chang, DP ;
Kleeman, MJ .
JOURNAL OF THE AIR & WASTE MANAGEMENT ASSOCIATION, 2005, 55 (01) :30-51
[7]   Dominant mechanisms that shape the airborne particle size and composition distribution in central California [J].
Herner, Jorn D. ;
Ying, Qi ;
Aw, Jeremy ;
Gao, Oliver ;
Chang, Daniel P. Y. ;
Kleeman, Michael J. .
AEROSOL SCIENCE AND TECHNOLOGY, 2006, 40 (10) :827-844
[8]   Size distribution of particle-phase molecular markers during a severe winter pollution episode [J].
Kleeman, Michael J. ;
Riddle, Sarah G. ;
Jakober, Chris A. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2008, 42 (17) :6469-6475
[9]   Size distribution of trace organic species emitted from biomass combustion and meat charbroiling [J].
Kleeman, Michael J. ;
Robert, Michael A. ;
Riddle, Sarah G. ;
Fine, Philip M. ;
Hays, Michael D. ;
Schauer, James J. ;
Hannigan, Michael P. .
ATMOSPHERIC ENVIRONMENT, 2008, 42 (13) :3059-3075
[10]   Lubricating oil and fuel contributions to particulate matter emissions from light-duty gasoline and heavy-duty diesel vehicles [J].
Kleeman, Michael J. ;
Riddle, Sarah G. ;
Robert, Michael A. ;
Jakober, Chris A. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2008, 42 (01) :235-242