Chemical composition of atmospheric nanoparticles during nucleation events in Atlanta

被引:102
作者
Smith, JN
Moore, KF
Eisele, FL
Voisin, D
Ghimire, AK
Sakurai, H
McMurry, PH
机构
[1] Natl Ctr Atmospher Res, Div Atmospher Chem, Boulder, CO 80307 USA
[2] Natl Ctr Atmospher Res, Adv Study Program, Boulder, CO 80307 USA
[3] Georgia Inst Technol, Sch Earth & Atmospher Sci, Atlanta, GA 30332 USA
[4] Univ Aix Marseille 1, Lab Chim & Environm, F-13003 Marseille, France
[5] Univ Minnesota, Dept Mech Engn, Minneapolis, MN 55455 USA
关键词
D O I
10.1029/2005JD005912
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
[1] We report the first direct, in situ measurements of the chemical composition of size-segregated atmospheric nanoparticles in the 6 - 15 nm diameter range. These measurements were made of ambient aerosol directly following nucleation events in Atlanta, Georgia, during the 2002 Aerosol Nucleation and Real-time Characterization Experiment (ANARChE). The recently developed Thermal Desorption Chemical Ionization Mass Spectrometer (TDCIMS) was used to make these measurements and featured a new inlet that delivers mass of charged and size-segregated nanoparticles at sufficiently high rates to enable analysis at a typical time resolution of 10 min. Measurements in both the positive and negative ion spectra revealed that particles formed recently from nucleation events have enhanced concentrations of ammonium and sulfate and that to within the uncertainty of our measurements, ammonium sulfate could account for all of the sampled nanoparticle mass. No other compounds were detected in the particles during these events. Concurrent measurements of particle hygroscopicity and volatility, made using a Nanometer Tandem Differential Mobility Analyzer, support the conclusion that ammonium and sulfate are primary components of these newly formed particles.
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收藏
页码:1 / 13
页数:13
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