Laboratory studies on secondary organic aerosol formation from terpenes

被引:54
作者
Iinuma, Y [1 ]
Böge, O [1 ]
Miao, Y [1 ]
Sierau, B [1 ]
Gnauk, T [1 ]
Herrmann, H [1 ]
机构
[1] Leibniz Inst Tropospharenforsch, D-04318 Leipzig, Germany
关键词
D O I
10.1039/b502160j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The formation of secondary organic aerosol (SOA) following the ozonolysis of terpene has been investigated intensively in recent years. The enhancement of SOA yields from the acid catalysed reactions of organics on aerosol surfaces or in the bulk particle phase has been receiving great attention. Recent studies show that the presence of acidic seed particles increases the SOA yield significantly (M. S. Jang and R. M. Kamens, Environ. Sci. Technol., 2001, 35, 4758, ref. 1; M. S. Jang, N. M. Czoschke, S. Lee and R. M. Kamens, Science, 2002, 298, 814, ref. 2; N. M. Czoschke, M. Jang and R. M. Kamens, Atmos. Environ., 2003, 37, 4287, ref. 3; M. S. Jang, B. Carroll, B. Chandramouli and R. M. Kamens, Environ. Sci. Technol., 2003, 37, 3828, ref. 4; Y. Iinuma, O. Boge, T. Gnauk and H. Herrmann, Atmos. Environ., 2004, 38, 76 1, ref. 5; S. Gao, M. Keywood, N. L. Ng, J. Surratt, V. Varutbangkul, R. Bahreini, R. C. Flagan and J. H. Seinfeld, J. Phys. Chem. A, 2004, 108, 10147, ref. 6). More detailed studies report the formation of higher molecular weight products in SOA (refs. 5 and 6; M. P. Tolocka, M. Jang, J. M. Ginter, F. J. Cox, R. M. Kamens and M. V. Johnston, Environ. Sci. Technol., 2004, 38, 1428, ref. 7; S. Gao, N. L. Ng, M. Keywood, V. Varutbangkul, R. Bahreini, A. Nenes, J. He, K. Y. Yoo, J. L. Beauchamp, R. P. Hodyss, R. C. Flagan and J. H. Seinfeld, Environ. Sci. Technol., 2004, 38, 6582, ref. 8) which could result in a non-reversible uptake of organics into the particle phase. Most of the past studies concentrated on the characterisation of the yields of enhanced SOA and its composition from ozonolysis of terpenes in the presence or absence of acidic and neutral seed particles. Recent findings from cyclohexene ozonolysis show that the presence of OH scavengers can also significantly influence the SOA yield.(8) Our new results from the IfT chemistry department aerosol chamber on terpene ozonolysis in the presence of OH scavengers show that the presence of hydroxyl radical scavengers clearly reduces the amount of formed SOA. The OH scavenger strongly depletes the formation of oligomeric compounds in the particle phase in contrast to previous findings (M. D. Keywood, J. H. Kroll, V. Varatbangkul, R. Bahreini, R. C. Flagan and J. H. Seinfeld, Environ. Sci. Technol., 2004, 38, 3343, ref. 9). This result indicates that hydroxyl radicals play an important role in the formation of precursor compounds (e.g., hydroxy pinonaldehyde) for the particle phase heterogeneous acid catalysed reactions leading to the higher molecular weight compounds and thus the enhancement of SOA yields. Better understanding of the role of hydroxyl radicals in the formation of SOA is necessary to distinguish between the contribution of ozonolysis and hydroxyl radicals to the SOA yield. If the recent findings are a ubiquitous phenomenon in the atmosphere, current atmospheric and climate models might underestimate SOA formation yields, particle phase OC contents and its impact on the atmospheric radiation budget.
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页码:279 / 294
页数:16
相关论文
共 43 条
[1]   Atmospheric aerosols: Biogeochemical sources and role in atmospheric chemistry [J].
Andreae, MO ;
Crutzen, PJ .
SCIENCE, 1997, 276 (5315) :1052-1058
[2]   Gas-phase tropospheric chemistry of volatile organic compounds .1. Alkanes and alkenes [J].
Atkinson, R .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1997, 26 (02) :215-290
[3]   Sesquiterpene ozonolysis: Origin of atmospheric new particle formation from biogenic hydrocarbons [J].
Bonn, B ;
Moortgat, GK .
GEOPHYSICAL RESEARCH LETTERS, 2003, 30 (11) :39-1
[4]   Molecular characterization of the water-soluble organic compounds in fogwater by ESIMS/MS [J].
Cappiello, A ;
De Simoni, E ;
Fiorucci, C ;
Mangani, F ;
Palma, P ;
Trufelli, H ;
Decesari, S ;
Facchini, MC ;
Fuzzi, S .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2003, 37 (07) :1229-1240
[5]   A CONVENIENT PROCEDURE FOR PREPARATIVE SCALE OXIDATION OF ENONES [J].
CELLA, JA .
SYNTHETIC COMMUNICATIONS, 1983, 13 (02) :93-98
[6]   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
[7]   Global distribution and climate forcing of carbonaceous aerosols [J].
Chung, SH ;
Seinfeld, JH .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2002, 107 (D19) :AAC14-1
[8]   Effect of acidic seed on biogenic secondary organic aerosol growth [J].
Czoschke, NM ;
Jang, M ;
Kamens, RM .
ATMOSPHERIC ENVIRONMENT, 2003, 37 (30) :4287-4299
[9]   Effects of stabilized Criegee intermediate and OH radical scavengers on aerosol formation from reactions of β-pinene with O3 [J].
Docherty, KS ;
Ziemann, PJ .
AEROSOL SCIENCE AND TECHNOLOGY, 2003, 37 (11) :877-891
[10]   Particle phase acidity and oligomer formation in secondary organic aerosol [J].
Gao, S ;
Ng, NL ;
Keywood, M ;
Varutbangkul, V ;
Bahreini, R ;
Nenes, A ;
He, JW ;
Yoo, KY ;
Beauchamp, JL ;
Hodyss, RP ;
Flagan, RC ;
Seinfeld, JH .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2004, 38 (24) :6582-6589