Characterization of major chemical components.of fine. particulate matter in North Carolina

被引:51
作者
Aneja, Viney P. [1 ]
Wang, Binyu
Tong, Daniel Q.
Kimball, Hoke
Steger, Joette
机构
[1] N Carolina State Univ, Dept Marine Earth & Atmospher Sci, Raleigh, NC 27695 USA
[2] N Carolina Div Air Qual, Raleigh, NC USA
来源
JOURNAL OF THE AIR & WASTE MANAGEMENT ASSOCIATION | 2006年 / 56卷 / 08期
关键词
D O I
10.1080/10473289.2006.10464529
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This paper presents measurements of daily sampling of fine particulate matter (PM2.5) and its major chemical components at three urban and one rural locations in North Carolina during 2002. At both urban and rural sites, the major insoluble component of PM2.5 is organic matter, and the major soluble components are sulfate (SO42-), ammonium (NH4+), and nitrate (NO3-). NH4+ is neutralized mainly by SO42- rather than by NO3-, except in winter when SO42- concentration is relatively low, whereas NO3- concentration is high. The equivalent ratio of NH4+ to the sum of SO42- and NO3- is < 1, suggesting that SO42- and NO3 are not completely neutralized by NH4+. At both rural and urban sites, SO42- concentration displays a maximum in summer and a minimum in winter, whereas NO3- displays an opposite seasonal trend. Mass ratio of NO3- to SO42- is consistently < 1 at all sites, suggesting that stationary source emissions may play an important role in PM2.5 formation in those areas. Organic carbon and elemental carbon are well correlated at three urban sites although they are poorly correlated at the agriculture site. Other than the daily samples, hourly samples were measured at one urban site. PM2.5 mass concentrations display a peak in early morning, and a second peak in late afternoon. Back trajectory analysis shows that air masses with lower PM2.5 mass content mainly originate from the marine environment or from a continental environment but with a strong subsidence from the upper troposphere. Air masses with high PM2.5 mass concentrations are largely from continental sources. Our study of fine particulate matter and its chemical composition in North Carolina provides crucial information that may used to determine the efficacy of the new National Ambient Air Quality Standard (NAAQS) for PM fine. Moreover, the gas-to-particle conversion processes provide improved prediction of long-range transport of pollutants and air quality.
引用
收藏
页码:1099 / 1107
页数:9
相关论文
共 43 条
[11]  
Draxler R.R., 1992, HYBRID SINGLE PARTIC, P26
[12]  
DRAXLER RR, 1997, ARL224 ERI NOAA
[13]  
DRAXLER RR, 1997, ARL224 NAT OC ATM AD
[14]   CHARACTERISTICS OF ATMOSPHERIC ORGANIC AND ELEMENTAL CARBON PARTICLE CONCENTRATIONS IN LOS-ANGELES [J].
GRAY, HA ;
CASS, GR ;
HUNTZICKER, JJ ;
HEYERDAHL, EK ;
RAU, JA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1986, 20 (06) :580-589
[15]   Sources and processes affecting concentrations of PM10 and PM2.5 particulate matter in Birmingham (UK) [J].
Harrison, RM ;
Deacon, AR ;
Jones, MR ;
Appleby, RS .
ATMOSPHERIC ENVIRONMENT, 1997, 31 (24) :4103-4117
[16]   The characteristics of PM2.5 in Beijing, China [J].
He, KB ;
Yang, FM ;
Ma, YL ;
Zhang, Q ;
Yao, XH ;
Chan, CK ;
Cadle, S ;
Chan, T ;
Mulawa, P .
ATMOSPHERIC ENVIRONMENT, 2001, 35 (29) :4959-4970
[17]  
IEESUCK J, 2002, 12 JOINT C APPL AIR
[18]   SEASONAL-VARIATION IN THE CHEMICAL-COMPOSITION OF ATMOSPHERIC AEROSOLS AND GASEOUS SPECIES IN SAPPORO, JAPAN [J].
KANEYASU, N ;
OHTA, S ;
MURAO, N .
ATMOSPHERIC ENVIRONMENT, 1995, 29 (13) :1559-1568
[19]   Chemical characteristics of principal PM2.5 species in Chongju, South Korea [J].
Lee, HS ;
Kang, BW .
ATMOSPHERIC ENVIRONMENT, 2001, 35 (04) :739-746
[20]   Fine particle measurements at two background sites in Korea between 1996 and 1997 [J].
Lee, JH ;
Kim, YP ;
Moon, KC ;
Kim, HK ;
Lee, CB .
ATMOSPHERIC ENVIRONMENT, 2001, 35 (04) :635-643