Evaluation of a detailed model of secondary organic aerosol formation from α-pinene against dark ozonolysis experiments

被引:10
作者
Ceulemans, Karl [1 ]
Compernolle, Steven [1 ]
Peeters, Jozef [2 ]
Muller, Jean-Francois [1 ]
机构
[1] BIRA IASB, B-1180 Brussels, Belgium
[2] Catholic Univ Louvain, Dept Chem, B-3001 Louvain, Belgium
关键词
alpha Pinene; Terpenes; Dark ozonolysis; Secondary organic aerosol; Stabilised Criegee intermediates; PURE COMPONENT PROPERTIES; GAS-PHASE OZONOLYSIS; VAPOR-PRESSURES; BIOGENIC HYDROCARBONS; ATMOSPHERIC OXIDATION; PARTICULATE PRODUCTS; NATURAL SUNLIGHT; BETA-PINENE; MCM V3; KINETICS;
D O I
10.1016/j.atmosenv.2010.05.001
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
BOREAM a detailed model for the gas-phase oxidation of alpha-pinene and Its subsequent formation of Secondary Organic Aerosol (SOA) is tested against a large set of SOA yield measurements obtained in dark ozonolysis experiments For the majority of experiments modelled SOA yields are found to agree with measured yields to within a factor 2 However the comparisons point to a general underestimation of modelled SOA yields at high temperatures (above 30 C) reaching an order of magnitude or more in the worst cases whereas modelled SOA yields are often overestimated at lower temperature (by a factor of about 2) Comparisons of results obtained using four different vapour pressure prediction methods indicate a strong sensitivity to the choice of the method although the overestimated temperature dependence of the yields is found in all cases Accounting for non-ideality of the aerosol mixture (based on an adapted UNIFAC method) has significant effects especially at low yields Our simulations show that the formation of oligomers through the gas-phase reactions of Stabilised Criegee Intermediates (SCI) with other molecular organic products could increase the SOA yield significantly only at very low relative humidity (below 1%) Further tests show that the agreement between model and measurements is improved when the ozonolysis mechanism includes additional production of non-volatile compounds (c) 2010 Elsevier Ltd All rights reserved
引用
收藏
页码:5434 / 5442
页数:9
相关论文
共 52 条
[41]   Secondary organic aerosol production from terpene ozonolysis.: 2.: Effect of NOx concentration [J].
Presto, AA ;
Hartz, KEH ;
Donahue, NM .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2005, 39 (18) :7046-7054
[42]   A theoretical study of the reactions of parent and substituted Criegee intermediates with water and the water dimer [J].
Ryzhkov, AB ;
Ariya, PA .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2004, 6 (21) :5042-5050
[43]   Protocol for the development of the Master Chemical Mechanism, MCM v3 (Part A): tropospheric degradation of non-aromatic volatile organic compounds [J].
Saunders, SM ;
Jenkin, ME ;
Derwent, RG ;
Pilling, MJ .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2003, 3 :161-180
[44]   Particle mass yield in secondary organic aerosol formed by the dark ozonolysis of α-pinene [J].
Shilling, J. E. ;
Chen, Q. ;
King, S. M. ;
Rosenoern, T. ;
Kroll, J. H. ;
Worsnop, D. R. ;
McKinney, K. A. ;
Martin, S. T. .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2008, 8 (07) :2073-2088
[45]   Effect of hydrophobic primary organic aerosols on secondary organic aerosol formation from ozonolysis of α-pinene [J].
Song, Chen ;
Zaveri, Rahul A. ;
Alexander, M. Lizabeth ;
Thornton, Joel A. ;
Madronich, Sasha ;
Ortega, John V. ;
Zelenyuk, Alla ;
Yu, Xiao-Ying ;
Laskin, Alexander ;
Maughan, David A. .
GEOPHYSICAL RESEARCH LETTERS, 2007, 34 (20)
[46]   3-methyl-1,2,3-butanetricarboxylic acid:: An atmospheric tracer for terpene secondary organic aerosol [J].
Szmigielski, Rafal ;
Surratt, Jason D. ;
Gomez-Gonzalez, Yadian ;
Van der Veken, Pieter ;
Kourtchev, Ivan ;
Vermeylen, Reinhilde ;
Blockhuys, Frank ;
Jaoui, Mohammed ;
Kleindienst, Tadeusz E. ;
Lewandowski, Michael ;
Offenberg, John H. ;
Edney, Edward O. ;
Seinfeld, John H. ;
Maenhaut, Willy ;
Claeys, Magda .
GEOPHYSICAL RESEARCH LETTERS, 2007, 34 (24)
[47]  
Tillmann R., 2010, Atmospheric Chemistry and Physics Discussions, V10, P3129
[48]   Kinetics of the gas-phase reactions of alcohols, aldehydes, carboxylic acids, and water with the C13 stabilized Criegee intermediate formed from ozonolysis of 1-tetradecene [J].
Tobias, HJ ;
Ziemann, PJ .
JOURNAL OF PHYSICAL CHEMISTRY A, 2001, 105 (25) :6129-6135
[49]   Chemistry of particle inception and growth during α-pinene ozonolysis [J].
Tolocka, MP ;
Heaton, KJ ;
Dreyfus, MA ;
Wang, SY ;
Zordan, CA ;
Saul, TD ;
Johnston, MV .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2006, 40 (06) :1843-1848
[50]   Box model studies of the secondary organic aerosol formation under different HC/NOx conditions using the subset of the Master Chemical Mechanism for α-pinene oxidation [J].
Xia, Adam G. ;
Michelangeli, Diane V. ;
Makar, Paul A. .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2008, 113 (D10)