Aerosol time-of-flight mass spectrometry during the Atlanta Supersite Experiment: 1. Measurements

被引:74
作者
Liu, DY [1 ]
Wenzel, RJ
Prather, KA
机构
[1] Univ Calif Riverside, Dept Chem, Riverside, CA 92521 USA
[2] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
关键词
aerosol; ATOFMS; composition; real time; sources; sulfates;
D O I
10.1029/2001JD001562
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
[1] In August 1999 an intensive field campaign was conducted in Atlanta, Georgia, focusing on the characterization of urban particulate matter. During the study an aerosol time-of-flight mass spectrometer (ATOFMS) was used to measure continuously the aerodynamic size and chemical composition of individual particles in the fine fraction (0.2-2.5 rhom) of the atmospheric aerosol. The inorganic and organic components of the particles were analyzed using laser desorption ionization time-of-flight mass spectrometry, generating positive and/or negative ion mass spectra. Here an overview of the ATOFMS results is presented with respect to the major species detected, including sodium, carbon (EC, OC, EC/OC), dust (Li, Na, Al, K, Ca, Fe), sulfate, nitrate, and ammonium. As described, many of the dust particle types have similar composition to those observed in ATOFMS coal source characterization studies. The ion signals, size distributions, and temporal evolution (30-60 min resolution) of the different particle types are described. The complexity of the Atlanta aerosol is shown here on an individual particle basis, demonstrating how single particle data obtained with ATOFMS can be used to gain unique insights into the mixing state of urban aerosols. The second paper in this two part series focuses on the scaling procedures used for converting the unscaled ATOFMS data presented in this paper into atmospherically representative number concentrations [Wenzel et al., 2002].
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页数:16
相关论文
共 54 条
[1]  
AMANN CA, 1982, AEROSOL SCI TECH, V1, P73
[2]   Ammonia: emission, atmospheric transport and deposition [J].
Asman, WAH ;
Sutton, MA ;
Schjorring, JK .
NEW PHYTOLOGIST, 1998, 139 (01) :27-48
[3]   A field-based approach for determining ATOFMS instrument sensitivities to ammonium and nitrate [J].
Bhave, PV ;
Allen, JO ;
Morrical, BD ;
Fergenson, DP ;
Cass, GR ;
Prather, KA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2002, 36 (22) :4868-4879
[4]   A global high-resolution emission inventory for ammonia [J].
Bouwman, AF ;
Lee, DS ;
Asman, WAH ;
Dentener, FJ ;
VanderHoek, KW ;
Olivier, JGJ .
GLOBAL BIOGEOCHEMICAL CYCLES, 1997, 11 (04) :561-587
[5]   Mathematical model for gas-particle partitioning of secondary organic aerosols [J].
Bowman, FM ;
Odum, JR ;
Seinfeld, JH ;
Pandis, SN .
ATMOSPHERIC ENVIRONMENT, 1997, 31 (23) :3921-3931
[6]   MOLECULAR ION DISTRIBUTIONS IN LASER MICROPROBE MASS-SPECTROMETRY OF CALCIUM-OXIDE AND CALCIUM SALTS [J].
BRUYNSEELS, FJ ;
VANGRIEKEN, RE .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 1983, 38 (5-6) :853-858
[7]  
Finlayson-Pitts B. J., 2000, Chemistry of the Upper and Lower Atmosphere
[8]   Real-time analysis of individual atmospheric aerosol particles: Design and performance of a portable ATOFMS [J].
Gard, E ;
Mayer, JE ;
Morrical, BD ;
Dienes, T ;
Fergenson, DP ;
Prather, KA .
ANALYTICAL CHEMISTRY, 1997, 69 (20) :4083-4091
[9]   Direct observation of heterogeneous chemistry in the atmosphere [J].
Gard, EE ;
Kleeman, MJ ;
Gross, DS ;
Hughes, LS ;
Allen, JO ;
Morrical, BD ;
Fergenson, DP ;
Dienes, T ;
Gälli, ME ;
Johnson, RJ ;
Cass, GR ;
Prather, KA .
SCIENCE, 1998, 279 (5354) :1184-1187
[10]   Characterization of carbonaceous aerosols outflow from India and Arabia:: Biomass/biofuel burning and fossil fuel combustion -: art. no. 4485 [J].
Guazzotti, SA ;
Suess, DT ;
Coffee, KR ;
Quinn, PK ;
Bates, TS ;
Wisthaler, A ;
Hansel, A ;
Ball, WP ;
Dickerson, RR ;
Neusüss, C ;
Crutzen, PJ ;
Prather, KA .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2003, 108 (D15)