Modeling semivolatile organic aerosol mass emissions from combustion systems

被引:119
作者
Shrivastava, MK
Lipsky, EM
Stanier, CO
Robinson, AL [1 ]
机构
[1] Carnegie Mellon Univ, Dept Engn & Publ Policy, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Dept Mech Engn, Pittsburgh, PA 15213 USA
[3] Univ Iowa, Dept Chem & Biochem Engn, Iowa City, IA 52242 USA
关键词
D O I
10.1021/es0522231
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Experimental measurements of gas-particle partitioning and organic aerosol mass in diluted diesel and wood combustion exhaust are interpreted using a two-component absorptive-partitioning model. The model parameters are determined by fitting the experimental data. The changes in partitioning with dilution of both wood smoke and diesel exhaust can be described by two lumped compounds in roughly equal abundance with effective saturation concentrations of similar to 1600 mu g m(-3) and similar to 20 mu g m(-3). The model is used to investigate gas-particle partitioning of emissions across a wide range of atmospheric conditions. Under the highly dilute conditions found in the atmosphere, the partitioning of the emissions is strongly influenced by the ambient temperature and the background organic aerosol concentration. The model predicts large changes in primary organic aerosol mass with varying atmospheric conditions, indicating that it is not possible to specify a single value for the organic aerosol emissions. Since atmospheric conditions vary in both space and time, air quality models need to treat primary organic aerosol emissions as semivolatile. Dilution samplers provide useful information about organic aerosol emissions; however, the measurements can be biased relative to atmospheric conditions and constraining predictions of absorptive-partitioning models requires emissions data across the entire range of atmospherically relevant concentrations.
引用
收藏
页码:2671 / 2677
页数:7
相关论文
共 29 条
[1]  
DONAHUE NM, 2006, IN PRESS ENV SCI TEC
[2]  
*ENVIRON INT CORP, 2005, US GUID CAMX COMPR A
[3]  
GRIESHOP AP, 2005, UNPUB ATMOS ENV
[4]   Organic aerosol formation from the oxidation of biogenic hydrocarbons [J].
Griffin, RJ ;
Cocker, DR ;
Flagan, RC ;
Seinfeld, JH .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1999, 104 (D3) :3555-3567
[5]   QUANTITATIVE CHARACTERIZATION OF URBAN SOURCES OF ORGANIC AEROSOL BY HIGH-RESOLUTION GAS-CHROMATOGRAPHY [J].
HILDEMANN, LM ;
MAZUREK, MA ;
CASS, GR ;
SIMONEIT, BRT .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1991, 25 (07) :1311-1325
[6]   A DILUTION STACK SAMPLER FOR COLLECTION OF ORGANIC AEROSOL EMISSIONS - DESIGN, CHARACTERIZATION AND FIELD-TESTS [J].
HILDEMANN, LM ;
CASS, GR ;
MARKOWSKI, GR .
AEROSOL SCIENCE AND TECHNOLOGY, 1989, 10 (01) :193-204
[7]   CHEMICAL-COMPOSITION OF EMISSIONS FROM URBAN SOURCES OF FINE ORGANIC AEROSOL [J].
HILDEMANN, LM ;
MARKOWSKI, GR ;
CASS, GR .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1991, 25 (04) :744-759
[8]   Physical and chemical characteristics and volatility of PM in the proximity of a light-duty vehicle freeway [J].
Kuhn, T ;
Biswas, S ;
Fine, PM ;
Geller, M ;
Sioutas, C .
AEROSOL SCIENCE AND TECHNOLOGY, 2005, 39 (04) :347-357
[9]   Partitioning of semivolatile organic compounds in the presence of a secondary organic aerosol in a controlled atmosphere [J].
Leach, KB ;
Kamens, RM ;
Strommen, MR ;
Jang, M .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 1999, 33 (03) :241-264
[10]   Gas/particle partitioning of semivolatile organic compounds to model inorganic, organic, and ambient smog aerosols [J].
Liang, CK ;
Pankow, JF ;
Odum, JR ;
Seinfeld, JH .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (11) :3086-3092