Organic particle types by single-particle measurements using a time-of-flight aerosol mass spectrometer coupled with a light scattering module

被引:25
作者
Liu, S. [1 ]
Russell, L. M. [1 ]
Sueper, D. T. [2 ,3 ]
Onasch, T. B. [3 ,4 ]
机构
[1] Univ Calif San Diego, Scripps Inst Oceanog, La Jolla, CA 92093 USA
[2] Univ Colorado, Cooperat Inst Res Environm Studies, Boulder, CO 80309 USA
[3] Aerodyne Res Inc, Ctr Aerosol & Cloud Chem, Billerica, MA USA
[4] Boston Coll, Dept Chem, Chestnut Hill, MA 02167 USA
关键词
HIGH-RESOLUTION; IDENTIFICATION; INSTRUMENT; COOKING; AMBIENT; SIZE; QUANTIFICATION; SPECTROSCOPY; PERFORMANCE; COMPONENTS;
D O I
10.5194/amt-6-187-2013
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Chemical and physical properties of individual ambient aerosol particles can vary greatly, so measuring the chemical composition at the single-particle level is essential for understanding atmospheric sources and transformations. Here we describe 46 days of single-particle measurements of atmospheric particles using a time-of-flight aerosol mass spectrometer coupled with a light scattering module (LS-ToF-AMS). The light scattering module optically detects particles larger than 180 nm vacuum aerodynamic diameter (130 nm geometric diameter) before they arrive at the chemical mass spectrometer and then triggers the saving of single-particle mass spectra. 271 641 particles were detected and sampled during 237 h of sampling in single-particle mode. By comparing timing of the predicted chemical ion signals from the light scattering measurement with the measured chemical ion signals by the mass spectrometer for each particle, particle types were classified and their number fractions determined as follows: prompt vaporization (46 %), delayed vaporization (6 %), and null (48 %), where null was operationally defined as less than 6 ions per particle. Prompt and delayed vaporization particles with sufficient chemical information (i.e., more than 40 ions per particle) were clustered based on similarity of organic mass spectra (using k-means algorithm) to result in three major clusters: highly oxidized particles (dominated by m/z 44), relatively less oxidized particles (dominated by m/z 43), and particles associated with fresh urban emissions. Each of the three organic clusters had limited chemical properties of other clusters, suggesting that all of the sampled organic particle types were internally mixed to some degree; however, the internal mixing was never uniform and distinct particle types existed throughout the study. Furthermore, the single-particle mass spectra and time series of these clusters agreed well with mass-based components identified (using factor analysis) from simultaneous ensemble-averaged measurements, supporting the connection between ensemble-based factors and atmospheric particle sources and processes. Measurements in this study illustrate that LS-ToF-AMS provides unique information about organic particle types by number as well as mass.
引用
收藏
页码:187 / 197
页数:11
相关论文
共 33 条
  • [21] LASER IONIZATION MASS-SPECTROSCOPY OF SINGLE AEROSOL-PARTICLES
    MURPHY, DM
    THOMSON, DS
    [J]. AEROSOL SCIENCE AND TECHNOLOGY, 1995, 22 (03) : 237 - 249
  • [22] Organic aerosol components observed in Northern Hemispheric datasets from Aerosol Mass Spectrometry
    Ng, N. L.
    Canagaratna, M. R.
    Zhang, Q.
    Jimenez, J. L.
    Tian, J.
    Ulbrich, I. M.
    Kroll, J. H.
    Docherty, K. S.
    Chhabra, P. S.
    Bahreini, R.
    Murphy, S. M.
    Seinfeld, J. H.
    Hildebrandt, L.
    Donahue, N. M.
    DeCarlo, P. F.
    Lanz, V. A.
    Prevot, A. S. H.
    Dinar, E.
    Rudich, Y.
    Worsnop, D. R.
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2010, 10 (10) : 4625 - 4641
  • [23] Real-time measurement of correlated size and composition profiles of individual atmospheric aerosol particles
    Noble, CA
    Prather, KA
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (09) : 2667 - 2680
  • [24] Performance of a single ultrafine particle mass spectrometer
    Phares, DJ
    Rhoads, KP
    Wexler, AS
    [J]. AEROSOL SCIENCE AND TECHNOLOGY, 2002, 36 (05) : 583 - 592
  • [25] Single particle analysis of suspended soil dust from Southern California
    Silva, PJ
    Carlin, RA
    Prather, KA
    [J]. ATMOSPHERIC ENVIRONMENT, 2000, 34 (11) : 1811 - 1820
  • [26] OPTIMIZATION AND TESTING OF MASS-SPECTRAL LIBRARY SEARCH ALGORITHMS FOR COMPOUND IDENTIFICATION
    STEIN, SE
    SCOTT, DR
    [J]. JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1994, 5 (09) : 859 - 866
  • [27] Development and characterization of an aerosol time-of-flight mass spectrometer with increased detection efficiency
    Su, YX
    Sipin, MF
    Furutani, H
    Prather, KA
    [J]. ANALYTICAL CHEMISTRY, 2004, 76 (03) : 712 - 719
  • [28] Classification of multiple types of organic carbon composition in atmospheric particles by scanning transmission X-ray microscopy analysis
    Takahama, S.
    Gilardoni, S.
    Russell, L. M.
    Kilcoyne, A. L. D.
    [J]. ATMOSPHERIC ENVIRONMENT, 2007, 41 (40) : 9435 - 9451
  • [29] Particle analysis by laser mass spectrometry WB-57F instrument overview
    Thomson, DS
    Schein, ME
    Murphy, DM
    [J]. AEROSOL SCIENCE AND TECHNOLOGY, 2000, 33 (1-2) : 153 - 169
  • [30] Interpretation of organic components from Positive Matrix Factorization of aerosol mass spectrometric data
    Ulbrich, I. M.
    Canagaratna, M. R.
    Zhang, Q.
    Worsnop, D. R.
    Jimenez, J. L.
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2009, 9 (09) : 2891 - 2918