Comparison of two particle-size spectrometers for ambient aerosol measurements

被引:67
|
作者
Tuch, T [1 ]
Mirme, A
Tamm, E
Heinrich, J
Heyder, J
Brand, P
Roth, C
Wichmann, HE
Pekkanen, J
Kreyling, WG
机构
[1] Univ Munich, Inst Med Data Management Biometr & Epidemiol, Munich, Germany
[2] Tartu State Univ, EE-202400 Tartu, Estonia
[3] Natl Publ Hlth Inst, Environm Epidemiol Unit, Kuopio, Finland
[4] GSF, Natl Res Ctr Environm & Hlth, Inst Epidemiol, Neuherberg, Germany
[5] GSF, Natl Res Ctr Environm & Hlth, Inst Inhalat Biol, Neuherberg, Germany
关键词
aerosol spectrometers; ambient aerosol; particle number distribution;
D O I
10.1016/S1352-2310(99)00248-4
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
There is an ongoing debate on the question which size fraction of particles in ambient air may be responsible for human health effects observed in epidemiological studies. Since there is no single instrument available for the measurement of the particle-size distribution over the full range of the fine fraction (diameter < 2.5 mu m) of the atmospheric aerosol, two instruments, the mobile aerosol spectrometer (MAS) and the electrical aerosol spectrometer (EAS), have been tested in a side-by-side comparison measuring ambient aerosol for a time period of six weeks in spring 1996 in the city of Erfurt, Germany. Furthermore, total particle number concentration measured by a condensation particle counter (CPC) and mass concentrations PM10 and PM2.5 were determined. Both spectrometers, MAS and EAS, are based on electrical mobility measurements for particles < 0.1 mu m and < 0.5 mu m, respectively, while MAS applies optical particle spectrometry and EAS applies again electrical mobility analysis for particles up to 2.5 and 10 mu m, respectively. Both instruments proved to be reliable during this comparison providing data availability of > 94%. To compare the spectral data, particle numbers were integrated within three size ranges: 0.01 - 0.1, 0.1 - 0.5, 0.5 - 25 mu m. Hourly mean number concentrations of each size range observed during the sig week comparison was: 2.6 x 10(4) +/- 19500 (2.48 x 10(4) +/- 1.79 x 10(4)), 3.1 x 10(3) +/- 1.5 x 10(3) (4.1 x 10(3) +/- 2.0 x 10(3)), 50 +/- 45 (1.9 x 10(2) +/- 1.2 x 10(2)) cm(-3) for MAS (EAS), respectively. Both aerosol spectrometers followed the variations of the ambient aerosol in a similar manner and yielded almost identical results for particle number concentrations of particles with diameters smaller than 0.5 mu m Furthermore, the total particle number concentration derived from MAS and EAS measurements (29000 +/- 20000; 29000 +/- 19000 cm(-3)) is well comparable with the number concentration derived from an integral counting CPC (31100 +/- 22000 cm(-3)). The results of this side-by-side comparison suggest that MAS and EAS together with PM2.5 measurements are suitable to reliably characterize size-distribution parameters of number and mass concentration of ambient aerosols. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:139 / 149
页数:11
相关论文
共 50 条
  • [1] A concept of an automated function control for ambient aerosol measurements using mobility particle size spectrometers
    Schladitz, A.
    Merkel, M.
    Bastian, S.
    Birmili, W.
    Weinhold, K.
    Loeschau, G.
    Wiedensohler, A.
    [J]. ATMOSPHERIC MEASUREMENT TECHNIQUES, 2014, 7 (04) : 1065 - 1073
  • [2] INTERCOMPARISON OF PARTICLE-SIZE SPECTROMETERS
    KARG, E
    BRAND, P
    HIETEL, B
    KREYLING, WG
    RUOSS, K
    TSCHIERSCH, J
    TUCH, T
    HEYDER, J
    [J]. JOURNAL OF AEROSOL SCIENCE, 1989, 20 (08) : 1481 - 1484
  • [3] A PARTICLE-SIZE SPECIFIC ELEMENTAL MASS BALANCE FOR THE APPORTIONMENT OF AMBIENT AEROSOL
    PRINGLE, TG
    JERVIS, RE
    [J]. JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY-ARTICLES, 1987, 112 (01): : 243 - 258
  • [4] INTERCOMPARISON OF PARTICLE MEASURING SYSTEMS, INCS PARTICLE-SIZE SPECTROMETERS
    JENSEN, DR
    JECK, R
    TRUSTY, G
    SCHACHER, G
    [J]. OPTICAL ENGINEERING, 1983, 22 (06) : 746 - 752
  • [5] PARTICLE-SIZE ANALYSIS OF AEROSOL SPRAYS
    HIND, G
    [J]. MANUFACTURING CHEMIST, 1990, 61 (08): : 28 - 30
  • [6] PARTICLE-SIZE DISTRIBUTIONS FOR AN OFFICE AEROSOL
    OWEN, MK
    ENSOR, DS
    HOVIS, LS
    TUCKER, WG
    SPARKS, LE
    [J]. AEROSOL SCIENCE AND TECHNOLOGY, 1990, 13 (04) : 486 - 492
  • [7] COMPARISON OF PARTICLE-SIZE ANALYSIS-METHODS BY RHEOLOGICAL MEASUREMENTS
    FUNK, JE
    DINGER, DR
    FUNK, JE
    [J]. AMERICAN CERAMIC SOCIETY BULLETIN, 1984, 63 (08): : 980 - 980
  • [8] PARTICLE-SIZE DISTRIBUTION OF INORGANIC COMPONENTS IN ATMOSPHERIC AEROSOL .2. SEASONAL-VARIATION IN PARTICLE-SIZE DISTRIBUTION OF CHLORIDE AND NITRATE IN THE AMBIENT AIR
    HARA, H
    HONDA, K
    NAGARA, K
    GOTO, A
    [J]. NIPPON KAGAKU KAISHI, 1983, (08) : 1221 - 1225
  • [9] PARTICLE-SIZE DISTRIBUTION OF AN AEROSOL AND ITS SUBFRACTIONS
    VERMA, DK
    SEBESTYEN, A
    JULIAN, JA
    MUIR, DCF
    SHAW, DS
    MACDOUGALL, R
    [J]. ANNALS OF OCCUPATIONAL HYGIENE, 1994, 38 (01): : 45 - 58
  • [10] URBAN AEROSOL TOXICITY - INFLUENCE OF PARTICLE-SIZE
    NATUSCH, DFS
    WALLACE, JR
    [J]. SCIENCE, 1974, 186 (4165) : 695 - 699