Modelling particle number concentrations in a typical street canyon in Germany and analysis of future trends

被引:6
作者
Toenges-Schuller, N. [1 ]
Schneider, Chr. [1 ]
Niederau, A. [1 ]
Vogt, R. [2 ]
Birmili, W. [3 ]
机构
[1] AVISO GmbH, D-52074 Aachen, Germany
[2] Ford Forschungszentrum Aachen GmbH, D-52072 Aachen, Germany
[3] Leibniz Inst Tropospher Res TROPOS, D-04318 Leipzig, Germany
关键词
Particle number; Nucleation; Street canyon; Emission scenarios; Vehicle type; Fuel type; SIZE DISTRIBUTIONS; ULTRAFINE PARTICLES; EXHAUST PLUMES; DYNAMICS; AIR; NUCLEATION; DISPERSION; DIESEL;
D O I
10.1016/j.atmosenv.2015.04.006
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
An aerosol box model and a gas-phase chemistry box model were coupled to simulate particle number (PN) concentrations, both solid and volatile, in a typical street canyon with a high traffic volume in Germany. The simulation accounts for emission, nucleation and aerosol aging processes while dilution is parameterised by a simple two-stage process. Calculations were performed for the years 2010, 2015, 2020 and 2025, and for a vehicle fleet consisting of electric vehicles only ("electric mobility"). Projections including a high fraction of Euro-6 vehicles in the fleet suggest that PN emissions will reduce by 90% in 2025 compared to 2010. Ambient PN concentrations are, however, expected to reduce by merely 29% over the same period. Apart from contributions of urban background air, reductions in primary particles are partially offset by secondary particle formation by nucleating exhaust gases. In the "electric mobility" scenario omitting tailpipe emissions, PN concentrations are expected to reduce by 60% from 2010 to 2025. For an aerosol assumed to be mixed externally only, PN of elemental carbon (EC) was calculated to reduce by 76% from 2010 to 2025, in the "electric mobility" scenario by 87%. Overall, the contribution of solid PN emissions from gasoline vehicles to PN concentration in the street canyon is expected to be approximately 4% in 2025. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:127 / 135
页数:9
相关论文
共 33 条
  • [11] POST-FOG NUCLEATION OF H2SO4-H2O PARTICLES IN SMOG
    KERMINEN, VM
    WEXLER, AS
    [J]. ATMOSPHERIC ENVIRONMENT, 1994, 28 (15) : 2399 - 2406
  • [12] Kessler C., 2010, IMMISSIONSSCHUTZ, V04, P164
  • [13] Modelling the fate of ultrafine particles from exhaust pipe to rural background: an analysis of time scales for dilution, coagulation and deposition
    Ketzel, M
    Berkowicz, R
    [J]. ATMOSPHERIC ENVIRONMENT, 2004, 38 (17) : 2639 - 2652
  • [14] Kluge J., 2007, VDA TECHN C SIND
  • [15] Dynamics and dispersion modelling of nanoparticles from road traffic in the urban atmospheric environment-A review
    Kumar, Prashant
    Ketzel, Matthias
    Vardoulakis, Sotiris
    Pirjola, Liisa
    Britter, Rex
    [J]. JOURNAL OF AEROSOL SCIENCE, 2011, 42 (09) : 580 - 603
  • [16] Correlation of Air Quality Data to Ultrafine Particles (UFP) Concentration and Size Distribution in Ambient Air
    Kwasny, Felicitas
    Madl, Pierre
    Hofmann, Werner
    [J]. ATMOSPHERE, 2010, 1 (01) : 3 - 14
  • [17] Estimating the contribution of photochemical particle formation to ultrafine particle number averages in an urban atmosphere
    Ma, N.
    Birmili, W.
    [J]. SCIENCE OF THE TOTAL ENVIRONMENT, 2015, 512 : 154 - 166
  • [18] Memmesheimer M, 2007, DEV ENVIRONM SCI, V6, P158, DOI 10.1016/S1474-8177(07)06028-7
  • [19] The role of ambient temperature for particle number concentrations in a street canyon
    Olivares, Gustavo
    Johansson, Christer
    Strom, Johan
    Hansson, Hans-Christen
    [J]. ATMOSPHERIC ENVIRONMENT, 2007, 41 (10) : 2145 - 2155
  • [20] Multi-angle absorption photometry -: a new method for the measurement of aerosol light absorption and atmospheric black carbon
    Petzold, A
    Schönlinner, M
    [J]. JOURNAL OF AEROSOL SCIENCE, 2004, 35 (04) : 421 - 441