Simultaneous measurement of the effective density and chemical composition of ambient aerosol particles

被引:85
作者
Spencer, Matthew T. [1 ]
Shields, Laura G. [1 ]
Prather, Kimberley A. [1 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
关键词
D O I
10.1021/es061425+
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Simultaneous measurements of the effective density and chemical composition of individual ambient particles were made in Riverside, California by coupling a differential mobility analyzer (DMA) with an ultrafine aerosol time-of-flight mass spectrometer (UF-ATOFMS). In the summer, chemically diverse particle types (i.e., aged-OC, vanadium-OC-sulfate-nitrate, biomass) all had similar effective densities when measured during the same time period. This result suggests that during the summer study the majority of particle mass for the different particle types was dominated by secondary species (OC, sulfates, nitrates) of the same density, while only a small fraction of the total particle mass is accounted for by the primary particle cores. Also shown herein, the effective density is a dynamic characteristic of the Riverside, CA ambient aerosol, changing by as much as 40% within 16 h. During the summer measurement period, changes in the ambient atmospheric water content correlated with changes in the measured effective densities which ranged from similar to 1.0 to 1.5 g center dot cm(-3). This correlation is potentially due to evaporation of water from particles in the aerodynamic lens. In contrast, in the fall during a Santa Ana meteorological event, ambient particles with a mobility diameter of 450 nm showed three distinct effective densities, each related to a chemically unique particle class. Particles with effective densities of similar to 0.27 g center dot cm(-3), 0.87 g center dot cm(-3), and 0.93 g center dot cm(-3) were composed mostly of elemental carbon, lubricating oil, and aged organic carbon, respectively. It is interesting to contrast the seasonal differences where in the summer, particle density and mass were determined by high amounts of secondary species, whereas in the fall, relatively clean and dry Santa Ana conditions resulted in freshly emitted particles which retained their distinct source chemistries and densities.
引用
收藏
页码:1303 / 1309
页数:7
相关论文
共 48 条
[11]  
JIMENEZ JL, STUDY ORGANIC AEROSO
[12]  
JMENEZ JL, 2003, J GEOPHYS RES-ATMOS, V108
[13]   Density changes of aerosol particles as a result of chemical reaction [J].
Katrib, Y ;
Martin, ST ;
Rudich, Y ;
Davidovits, P ;
Jayne, JT ;
Worsnop, DR .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2005, 5 :275-291
[14]  
Knutson E. O., 1975, Journal of Aerosol Science, V6, P443, DOI 10.1016/0021-8502(75)90060-9
[15]   Mass spectrometry of individual particles between 50 and 750 nm in diameter at the Baltimore supersite [J].
Lake, DA ;
Tolocka, MP ;
Johnston, MV ;
Wexler, AS .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2003, 37 (15) :3268-3274
[16]   Global impacts of gas-phase chemistry-aerosol interactions on direct radiative forcing by anthropogenic aerosols and ozone [J].
Liao, H ;
Seinfeld, JH .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2005, 110 (D18) :1-22
[17]  
Lide DR., 2004, CRC Handbook of Chemistry and Physics, DOI DOI 10.1080/08893110902764125
[18]   Variations in the size and chemical composition of nitrate-containing particles in Riverside, CA [J].
Liu, DY ;
Prather, KA ;
Hering, SV .
AEROSOL SCIENCE AND TECHNOLOGY, 2000, 33 (1-2) :71-86
[19]   The relationship between mass and mobility for atmospheric particles: A new technique for measuring particle density [J].
McMurry, PH ;
Wang, X ;
Park, K ;
Ehara, K .
AEROSOL SCIENCE AND TECHNOLOGY, 2002, 36 (02) :227-238
[20]   Extending ATOFMS measurements to include refractive index and density [J].
Moffet, RC ;
Prather, KA .
ANALYTICAL CHEMISTRY, 2005, 77 (20) :6535-6541