Partitioning of semivolatile organic compounds in the presence of a secondary organic aerosol in a controlled atmosphere

被引:28
作者
Leach, KB [1 ]
Kamens, RM [1 ]
Strommen, MR [1 ]
Jang, M [1 ]
机构
[1] Univ N Carolina, Dept Environm Sci & Engn, Chapel Hill, NC 27599 USA
基金
美国国家科学基金会;
关键词
gas-particle partitioning; secondary organic aerosol; alpha-pinene; ozone;
D O I
10.1023/A:1006108430033
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The gas-particle partitioning of select semivolatile organic compounds (SOCs) was studied by injecting the SOCs into a 190 m(3) Teflon film chamber containing a secondary organic aerosol (SOA) generated by volatilizing liquid alpha-pinene into an ozone-concentrated atmosphere. The concentration of total suspended particulates (TSP) and gas and particle-phase SOCs was measured over the course of three experiments spanning a temperature range of 268-297 K and a relative humidity range of 55-100%. An equilibrium partition coefficient, K-p, was calculated for each sampling event. Empirical relationships were then developed to predict the partitioning of the SOCs on the SOA particle source as a function of temperature. Partitioning in this SOA system was compared to that of a SOA generated by the photochemical reaction of NOx with m-xylene. The results indicate that partitioning is similar between the two SOA systems. The effects of multiple particle sources on partitioning was also examined, revealing that a weighted average of predicted K-p values for individual sources can be used to predict partitioning in aerosol mixtures.
引用
收藏
页码:241 / 264
页数:24
相关论文
共 34 条
[2]   VAPOR PARTICLE PARTITIONING OF SEMIVOLATILE ORGANIC-COMPOUNDS - ESTIMATES FROM FIELD COLLECTIONS [J].
BIDLEMAN, TF ;
BILLINGS, WN ;
FOREMAN, WT .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1986, 20 (10) :1038-1043
[3]   cis-pinic acid, a possible precursor for organic aerosol formation from ozonolysis of α-pinene [J].
Christoffersen, TS ;
Hjorth, J ;
Horie, O ;
Jensen, NR ;
Kotzias, D ;
Molander, LL ;
Neeb, P ;
Ruppert, L ;
Winterhalter, R ;
Virkkula, A ;
Wirtz, K ;
Larsen, BR .
ATMOSPHERIC ENVIRONMENT, 1998, 32 (10) :1657-1661
[4]   MODELING OF NITRO-POLYCYCLIC AROMATIC HYDROCARBON FORMATION AND DECAY IN THE ATMOSPHERE [J].
FAN, ZH ;
CHEN, DH ;
BIRLA, P ;
KAMENS, RM .
ATMOSPHERIC ENVIRONMENT, 1995, 29 (10) :1171-1181
[5]   Secondary organic aerosol from the photooxidation of aromatic hydrocarbons: Molecular composition [J].
Forstner, HJL ;
Flagan, RC ;
Seinfeld, JH .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (05) :1345-1358
[6]   Adsorption of VOCs from the gas phase to different minerals and a mineral mixture [J].
Goss, KU ;
Eisenreich, SJ .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (07) :2135-2142
[7]   DIRECT DETERMINATION OF THE PHASE DISTRIBUTIONS OF SEMIVOLATILE POLYCYCLIC AROMATIC-HYDROCARBONS USING ANNULAR DENUDERS [J].
GUNDEL, LA ;
LEE, VC ;
MAHANAMA, KRR ;
STEVENS, RK ;
DAISEY, JM .
ATMOSPHERIC ENVIRONMENT, 1995, 29 (14) :1719-1733
[8]  
Hull L. A., 1981, Atmospheric Biogenic Hydrocarbons, V2, P161
[9]   A thermodynamic approach using group contribution methods to model the partitioning of semivolatile organic compounds on atmospheric particulate matter [J].
Jang, M ;
Kamens, RM ;
Leach, KB ;
Strommen, MR .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (10) :2805-2811
[10]   BENZ[A]ANTHRACENE PHOTODEGRADATION IN THE PRESENCE OF KNOWN ORGANIC-CONSTITUENTS OF ATMOSPHERIC AEROSOLS [J].
JANG, M ;
MCDOW, SR .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1995, 29 (10) :2654-2660