Impact of the hydrocarbon to NOx ratio on secondary organic aerosol formation

被引:172
作者
Song, C
Na, KS
Cocker, DR [1 ]
机构
[1] Univ Calif Riverside, CE CERT, Riverside, CA 92521 USA
[2] Univ Calif Riverside, Dept Environm Chem & Engn, Bourns Coll Engn, Riverside, CA 92521 USA
关键词
D O I
10.1021/es0493244
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A series of m-xylene/NOx experiments were conducted in the new Bourns College of Engineering-Center for Environmental Research and Technology dual go m(3) indoor smog chamber to elucidate the role of NOx on the secondary organic aerosol (SOA) formation potential of m-xylene. The results presented herein demonstrate a clear dependence of m-xylene SOA formation potential on NOx, particularly at atmospherically relevant organic aerosol concentration. Experiments with lower NOx levels generated considerably more organic aerosol mass than did experiments with higher NOx levels when reacted m-xylene was held constant. For example, SOA formation from approximately 150 mu g m(-3) reacted m-xylene produced 0.6-9.3 mu g m(-3) aerosol mass for NOx concentrations ranging from 286 to 10 ppb. The increase in SOA formation was not attributable to changes in ozone and nitrate concentration. A general discussion about possible influences of NOx on SOA formation for this system is included.
引用
收藏
页码:3143 / 3149
页数:7
相关论文
共 34 条
[11]   PARAMETERIZATION OF THE FORMATION POTENTIAL OF SECONDARY ORGANIC AEROSOLS [J].
GROSJEAN, D ;
SEINFELD, JH .
ATMOSPHERIC ENVIRONMENT, 1989, 23 (08) :1733-1747
[12]   Organic aerosol formation during the atmospheric degradation of toluene [J].
Hurley, MD ;
Sokolov, O ;
Wallington, TJ ;
Takekawa, H ;
Karasawa, M ;
Klotz, B ;
Barnes, I ;
Becker, KH .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (07) :1358-1366
[13]   PHOTOCHEMICAL AEROSOL FORMATION FROM AROMATIC-HYDROCARBONS IN THE PRESENCE OF NOX [J].
IZUMI, K ;
FUKUYAMA, T .
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1990, 24 (06) :1433-1441
[14]   Heterogeneous atmospheric aerosol production by acid-catalyzed particle-phase reactions [J].
Jang, MS ;
Czoschke, NM ;
Lee, S ;
Kamens, RM .
SCIENCE, 2002, 298 (5594) :814-817
[15]   Characterization of secondary aerosol from the photooxidation of toluene in the presence of NOx and 1-propene [J].
Jang, MS ;
Kamens, RM .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (18) :3626-3639
[16]  
JEFFERIES HE, 1995, COMPOSITION CHEM CLI
[17]   Identification of polymers as major components of atmospheric organic aerosols [J].
Kalberer, M ;
Paulsen, D ;
Sax, M ;
Steinbacher, M ;
Dommen, J ;
Prevot, ASH ;
Fisseha, R ;
Weingartner, E ;
Frankevich, V ;
Zenobi, R ;
Baltensperger, U .
SCIENCE, 2004, 303 (5664) :1659-1662
[18]   OH-initiated oxidation of benzene -: Part II.: Influence of elevated NOx concentrations [J].
Klotz, B ;
Volkamer, R ;
Hurley, MD ;
Andersen, MPS ;
Nielsen, OJ ;
Barnes, I ;
Imamura, T ;
Wirtz, K ;
Becker, KH ;
Platt, U ;
Wallington, TJ ;
Washida, N .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2002, 4 (18) :4399-4411
[19]   CHARACTERISTICS OF SUMMER MIDDAY LOW-VISIBILITY EVENTS IN THE LOS-ANGELES AREA [J].
LARSON, SM ;
CASS, GR .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1989, 23 (03) :281-289
[20]   Primary and secondary carbonaceous species in the atmosphere of Western Riverside County, California [J].
Na, KS ;
Sawant, AA ;
Song, C ;
Cocker, DR .
ATMOSPHERIC ENVIRONMENT, 2004, 38 (09) :1345-1355