Comparability of three spectrometers for monitoring urban aerosol

被引:31
作者
Khlystov, A
Kos, GPA
ten Brink, HM
Mirme, A
Tuch, T
Roth, C
Kreyling, WG
机构
[1] Netherlands Energy Res Fdn, ECN, NL-1755 ZG Petten, Netherlands
[2] Univ Tartu, EE-50090 Tartu, Estonia
[3] GSF Natl Res Ctr Environm & Hlth, Inst Inhalat Biol, D-85758 Neuherberg, Germany
[4] Carnegie Mellon Univ, Dept Engn & Publ Policy, Pittsburgh, PA 15213 USA
[5] Univ Maryland, Dept Chem & Biochem, College Pk, MD 20740 USA
关键词
ultrafine aerosol; monitoring; optical size; mobility;
D O I
10.1016/S1352-2310(00)00478-7
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The comparability was tested of three aerosol "spectrometers", used in a program for monitoring the spectra of fine and ultrafine particles in three European cities. Droplets of sebacate, solid ammonium sulfate and agglomerates of elemental carbon were used in the tests, representing the major chemical and structural types of particles encountered in urban aerosol. Particles in the ultrafine range (10-100 nm) are sized by electrical mobility (SMPS, DMPS and EAS) and the "spectrometers" gave very similar size distributions for these aerosols. The integrated number concentrations were on average within 20% of the directly measured total number concentrations. Particles with a size between 0.1 and 2.5 mum, in which most of the volume/mass is concentrated, are being differently classified in the three "spectrometers", respectively, with a low- and a high-flow LAS-X, and field charging in the EAS. The agreement between the three instruments in this size range was less good, which was partly caused by signal overload in the high-flow optical sizer, which was solved using a larger threshold. A complication occurred with the elemental carbon, which was composed of highly agglomerated entities. Particles, sized by the mobility instrumentation as being in the range of 100-400 nm, were not detected by the optical sizers. Volume (spectra) for ammonium sulfate deduced from the number spectra were compared with the mass (spectra) obtained with cascade impacters. The comparison was good for the LAS-Xs; the EAS overestimated volume/mass. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2045 / 2051
页数:7
相关论文
共 13 条
  • [1] BENBRINK HM, 2000, ATMOS ENVIRON, V34, P4230
  • [2] Short-term particulate matter mass and aerosol-size distribution measurements: Transient pollution episodes and bimodal aerosol-mass distributions
    Eldering, A
    Glasgow, RM
    [J]. ATMOSPHERIC ENVIRONMENT, 1998, 32 (11) : 2017 - 2024
  • [3] Statistical characteristics of aerosol in Baltic Sea region
    Kikas, U
    Mirme, A
    Tamm, E
    Raunemaa, T
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1996, 101 (D14) : 19319 - 19327
  • [4] ASSOCIATION OF PARTICULATE AIR-POLLUTION AND ACUTE MORTALITY - INVOLVEMENT OF ULTRAFINE PARTICLES
    OBERDORSTER, G
    GELEIN, RM
    FERIN, J
    WEISS, B
    [J]. INHALATION TOXICOLOGY, 1995, 7 (01) : 111 - 124
  • [5] Respiratory effects are associated with the number of ultrafine particles
    Peters, A
    Wichmann, HE
    Tuch, T
    Heinrich, J
    Heyder, J
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1997, 155 (04) : 1376 - 1383
  • [6] QUANT FR, 1992, J AEROSOL SCI, V23, pS405
  • [7] BIPOLAR DIFFUSION CHARGING OF SPHERES AND AGGLOMERATE AEROSOL-PARTICLES
    ROGAK, SN
    FLAGAN, RC
    [J]. JOURNAL OF AEROSOL SCIENCE, 1992, 23 (07) : 693 - 710
  • [8] RUUSKANEN J, 2001, IN PRESS ATMOSPHERIC
  • [9] Schmidt-Ott A., 1995, J AEROSOL SCI, V26, pS923, DOI DOI 10.1016/0021-8502(95)97369-P
  • [10] Composition/size of the light-scattering aerosol in The Netherlands
    TenBrink, HM
    Kruisz, C
    Kos, GPA
    Berner, A
    [J]. ATMOSPHERIC ENVIRONMENT, 1997, 31 (23) : 3955 - 3962