Characterization of the particulate phase in the exhaust from a diesel car

被引:109
作者
Kerminen, VM
Makela, TE
Ojanen, CH
Hillamo, RE
Vilhunen, JK
Rantanen, L
Havers, N
VonBohlen, A
Klockow, D
机构
[1] NESTE OY,CORP TECHNOL,FIN-06101 PORVOO,FINLAND
[2] NESTE OY,ENGINE LAB,FIN-06101 PORVOO,FINLAND
[3] INST SPEKTROCHEM & ANGEW SPEKTROSKOPIE,D-44013 DORTMUND,GERMANY
关键词
D O I
10.1021/es960520n
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Diesel vehicles are a major source of fine, atmospheric particulate matter in urban environments. The influences diesel particles exert on solar radiation, on atmospheric chemistry, and on humans depend crucially on the size and chemical character of these particles. In this work, size-resolved diesel particle chemistry has been examined by collecting particles directly from a diesel car exhaust with a low-pressure impactor. The impactor samples have been weighed and analyzed chemically to construct continuous size distributions for selected compounds present in the particulate phase. Submicron diesel-particle mass size distributions displayed three log-normal modes that were centered at 0.09, 0.2, and 0.7-1 mu m of particle aerodynamic diameter (EAD) and that had average geometric standard deviations of 1.34, 1.61, and 1.34, respectively. The lowest two modes had approximately the same particulate mass, whereas over 80% of the number of particles were estimated to be found in the mode around 0.1 mu m. The third mode contained about 10% of the total particulate mass but less than 0.1% of the particles. The size distributions of elemental (EC) and organic carbon (OC) were quite different: EC peaked at 0.1 mu m, and OC peaked somewhere between 0.1 and 0.3 mu m of EAD. The mass ratios of OC to EC were between 0.3 and 0.5 in the bulk of the samples but were considerably lower for most of the particles. The presence of a catalytic converter reduced particulate mass by 10-30%, with the removal being more efficient for OC than EC. The principal mechanism producing the mode around 0.1 mu m was shown to be Brownian coagulation between small primary particles formed during the combustion. The two larger size modes in the submicron particle range were hypothesized to be formed by activation and subsequent uptake of condensable organic compounds by some of the mode 1 particles.
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页码:1883 / 1889
页数:7
相关论文
共 44 条
[1]   SEASONALLY DEPENDENT SIZE DISTRIBUTIONS OF ALIPHATIC AND POLYCYCLIC AROMATIC-HYDROCARBONS IN URBAN AEROSOLS FROM DENSELY POPULATED AREAS [J].
ACEVES, M ;
GRIMALT, JO .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1993, 27 (13) :2896-2908
[2]   Measurement of polycyclic aromatic hydrocarbons associated with size-segregated atmospheric aerosols in Massachusetts [J].
Allen, JO ;
Dookeran, KM ;
Smith, KA ;
Sarofim, AF ;
Taghizadeh, K ;
Lafleur, AL .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (03) :1023-1031
[3]  
AMANN CA, 1982, AEROSOL SCI TECH, V1, P73
[4]  
[Anonymous], 1986, ENV POL SUS DEV
[5]   MOBILE SOURCES OF ATMOSPHERIC POLYCYCLIC AROMATIC-HYDROCARBONS - A ROADWAY TUNNEL STUDY [J].
BENNER, BA ;
GORDON, GE ;
WISE, SA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1989, 23 (10) :1269-1278
[6]   MASS SIZE DISTRIBUTIONS OF TRAFFIC AEROSOLS AT VIENNA [J].
BERNER, A ;
LURZER, C .
JOURNAL OF PHYSICAL CHEMISTRY, 1980, 84 (16) :2079-2083
[7]  
BURTSCHER H, 1995, J AEROSOL SCI, V26, pS129
[8]   THE OPTICAL-PROPERTIES AND MORPHOLOGY OF CLOUD-PROCESSED CARBONACEOUS SMOKE [J].
COLBECK, I ;
APPLEBY, L ;
HARDMAN, EJ ;
HARRISON, RM .
JOURNAL OF AEROSOL SCIENCE, 1990, 21 (04) :527-538
[9]   CALCULATIONS OF THE EQUILIBRIUM VAPOR-PRESSURE OF WATER OVER ADHERING 50-200-NM SPHERES [J].
CROUZET, Y ;
MARLOW, WH .
AEROSOL SCIENCE AND TECHNOLOGY, 1995, 22 (01) :43-59
[10]  
DESANTIS F, 1992, ATMOS ENVIRON A-GEN, V26, P3061