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

被引:60
|
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 50 条
  • [21] Fine particulate matter (PM2.5) in Edmonton, Canada: Source apportionment and potential risk for human health
    Bari, Md. Aynul
    Kindzierski, Warren B.
    ENVIRONMENTAL POLLUTION, 2016, 218 : 219 - 229
  • [22] Source apportionment analyses for fine (PM2.5) and coarse (PM2.5-10) mode particulate matter (PM) measured in an urban area in southwestern Nigeria
    Owoade, Kayode O.
    Hopke, Philip K.
    Olise, Felix S.
    Adewole, Olanisun O.
    Ogundele, Lasun T.
    Fawole, Olusegun G.
    ATMOSPHERIC POLLUTION RESEARCH, 2016, 7 (05) : 843 - 857
  • [23] Modeling PM2.5 During Severe Atmospheric Pollution Episode in Lagos, Nigeria: Spatiotemporal Variations, Source Apportionment, and Meteorological Influences
    Sulaymon, Ishaq Dimeji
    Zhang, Yuanxun
    Hopke, Philip K.
    Ye, Fei
    Gong, Kangjia
    Mao, Jianjiong
    Hu, Jianlin
    JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2023, 128 (13)
  • [24] Emission factors of ultrafine particulate matter (PM&lt;0.1 μm) and particle-bound polycyclic aromatic hydrocarbons from biomass combustion for source apportionment
    Samae, Hisam
    Tekasakul, Surajit
    Tekasakul, Perapong
    Furuuchi, Masami
    CHEMOSPHERE, 2021, 262
  • [25] Chemical characterization and source apportionment of atmospheric fine particulate matter (PM2.5) at an urban site in Astana, Kazakhstan
    Ormanova, Gulden
    Hopke, Philip K.
    Dhammapala, Ranil
    Ozturk, Fatma
    Shah, Dhawal
    Torkmahalleh, Mehdi Amouei
    ATMOSPHERIC POLLUTION RESEARCH, 2025, 16 (01)
  • [26] Source apportionment of ambient fine particulate matter in Dearborn, Michigan, using hourly resolved PM chemical composition data
    Pancras, Joseph Patrick
    Landis, Matthew S.
    Norris, Gary A.
    Vedantham, Ram
    Dvonch, J. Timothy
    SCIENCE OF THE TOTAL ENVIRONMENT, 2013, 448 : 2 - 13
  • [27] Water-Soluble Inorganic Anions in Fine Particulate Matter (PM2.5) in Dhaka, Bangladesh: Source Apportionment
    Rumman, Riadul
    Haq, Md Rezaul
    Rahat, Md Masudur Rahman
    Jahan, Farhana
    Moulick, Shyama Prosad
    Nigar, Refayat
    Halder, Chandan
    Liu, Wenbin
    Ferdousi, Farhana Khanam
    Habib, Ahsan
    JOURNAL OF CHEMISTRY, 2024, 2024
  • [28] Chemical Characterization and Source Apportionment of Fine Particulate Matter (PM2.5) at a Rural Site in North Central India
    Satsangi, Aparna
    Agarwal, Awni
    Lakhani, Anita
    Kumari, K. Maharaj
    PROCEEDINGS OF THE INDIAN NATIONAL SCIENCE ACADEMY, 2020, 86 (03): : 1267 - 1277
  • [29] Source apportionment of daily fine particulate matter at Jefferson street, Atlanta, GA, during summer and winter
    Zheng, Mei
    Cass, Glen R.
    Ke, Lin
    Wang, Fu
    Schauer, James J.
    Edgerton, Eric S.
    Russell, Armistead G.
    JOURNAL OF THE AIR & WASTE MANAGEMENT ASSOCIATION, 2007, 57 (02) : 228 - 242
  • [30] Size-Segregated Particulate Matter Down to PM0.1 and Carbon Content during the Rainy and Dry Seasons in Sumatra Island, Indonesia
    Amin, Muhammad
    Putri, Rahmi Mulia
    Handika, Rizki Andre
    Ullah, Aulia
    Goembira, Fadjar
    Phairuang, Worradorn
    Ikemori, Fumikazu
    Hata, Mitsuhiko
    Tekasakul, Perapong
    Furuuchi, Masami
    ATMOSPHERE, 2021, 12 (11)