Mass size distributions and size resolved chemical composition of fine particulate matter at the Pittsburgh supersite

被引:150
作者
Cabada, JC
Rees, S
Takahama, S
Khlystov, A
Pandis, SN [1 ]
Davidson, CI
Robinson, AL
机构
[1] Carnegie Mellon Univ, Dept Chem Engn, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Dept Civil & Environm Engn, Pittsburgh, PA 15213 USA
[3] Carnegie Mellon Univ, Dept Mech Engn, Pittsburgh, PA 15213 USA
[4] Carnegie Mellon Univ, Dept Engn & Publ Policy, Pittsburgh, PA 15213 USA
关键词
MOUDI; PMx; PM size/composition; coridensation mode; droplet mode; ultrafine PM; PAQS;
D O I
10.1016/j.atmosenv.2004.03.004
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 aerosol mass and chemical composition were measured during the Pittsburgh Air Quality Study. Daily samples were collected for 12 months from July 2001 to June 2002. Micro-orifice uniform deposit impactors (MOUDIs) were used to collect aerosol samples of fine particulate matter smaller than 10 mum. Measurements of PM0.056, PM0.10, PM0.18, PM0.32, PM0.56, PM1.0, PM1.8 and PM2.5 with the MOUDI are available for the full study period. Seasonal variations in the concentrations are observed for all size cuts. Higher concentrations are observed during the summer and lower during the winter. Comparison between the PM2.5 measurements by the MOUDI and other integrated PM samplers reveals good agreement. Good correlation is observed for PM10 between the MOUDI and an integrated sampler but the MOUDI underestimates PM10 by 20%. Bouncing of particles from higher stages of the MOUDI ( > PM2.5) is not a major problem because of the low concentrations of coarse particles in the area. The main cause of coarse particle losses appears to be losses to the wall of the MOUDI. Samples were collected on aluminum foils for analysis of carbonaccous material and on Teflon filters for analysis of particle mass and inorganic anions and cations. Daily samples were analyzed during the summer (July 2001) and the winter intensives (January 2002). During the summer around 50% of the organic material is lost from the aluminum foils as compared to a filter-based sampler. These losses are due to volatilization and bounce-off from the MOUDI stages. High nitrate losses from the MOUDI are also observed during the summer (above 70%). Good agreement between the gravimetrically determined mass and the sum of the masses of the individual compounds is obtained, if the lost mass from organics and the aerosol water content are included for the summer. For the winter no significant losses of material are detected and there exists reasonable agreement between the gravimetrical mass and the sum of the concentrations of the individual compounds. Ultrafine particles (below 100 nm) account on average, for < 5 % of the PM2.5 mass, and show different composition for the summer and the winter. During the summer the ultrafine mass is 50% carbonaceous material (organic material and elemental carbon) and 50% inorganic (mainly sulfate and ammonium); during the winter these percentages are 70% and 30%, respectively. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3127 / 3141
页数:15
相关论文
共 43 条
[1]   Sources and composition of PM2.5 at the National Energy Technology Laboratory in Pittsburgh during July and August 2000 [J].
Anderson, RR ;
Martello, DV ;
Rohar, PC ;
Strazisar, BR ;
Tamilia, JP ;
Waldner, K ;
White, CM ;
Modey, WK ;
Mangelson, NF ;
Eatough, DJ .
ENERGY & FUELS, 2002, 16 (02) :261-269
[2]   Sources of atmospheric carbonaceous particulate matter in Pittsburgh, Pennsylvania [J].
Cabada, JC ;
Pandis, SN ;
Robinson, AL .
JOURNAL OF THE AIR & WASTE MANAGEMENT ASSOCIATION, 2002, 52 (06) :732-741
[3]  
CABADA JC, 2002, 21 ANN AAAR C CHARL
[4]  
CABADA JC, 2004, UNPUB AEROSOL SCI TE
[5]   Detection of alkaline ultrafine atmospheric particles at Bakersfield, California [J].
Chung, A ;
Herner, JD ;
Kleeman, MJ .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (11) :2184-2190
[6]   AN ASSOCIATION BETWEEN AIR-POLLUTION AND MORTALITY IN 6 UNITED-STATES CITIES [J].
DOCKERY, DW ;
POPE, CA ;
XU, XP ;
SPENGLER, JD ;
WARE, JH ;
FAY, ME ;
FERRIS, BG ;
SPEIZER, FE .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (24) :1753-1759
[7]   The pulmonary toxicology of ultrafine particles [J].
Donaldson, K ;
Brown, D ;
Clouter, A ;
Duffin, R ;
MacNee, W ;
Renwick, L ;
Tran, L ;
Stone, V .
JOURNAL OF AEROSOL MEDICINE-DEPOSITION CLEARANCE AND EFFECTS IN THE LUNG, 2002, 15 (02) :213-220
[8]   AN AIR MONITORING NETWORK USING CONTINUOUS PARTICLE-SIZE DISTRIBUTION MONITORS - CONNECTING POLLUTANT PROPERTIES TO VISIBILITY VIA MIE SCATTERING CALCULATIONS [J].
ELDERING, A ;
CASS, GR ;
MOON, KC .
ATMOSPHERIC ENVIRONMENT, 1994, 28 (16) :2733-2749
[9]  
*EPA, 1960, EPA600P65001
[10]   PULMONARY RETENTION OF ULTRAFINE AND FINE PARTICLES IN RATS [J].
FERIN, J ;
OBERDORSTER, G ;
PENNEY, DP .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1992, 6 (05) :535-542