Formation of oligomers in secondary organic aerosol

被引:423
作者
Tolocka, MP
Jang, M
Ginter, JM
Cox, FJ
Kamens, RM
Johnston, MV [1 ]
机构
[1] Univ Delaware, Dept Chem & Biochem, Newark, DE 19716 USA
[2] Univ N Carolina, Dept Environm Sci & Engn, Chapel Hill, NC 27599 USA
关键词
D O I
10.1021/es035030r
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The formation of oligomeric molecules, an important step in secondary organic aerosol production, is reported. Aerosols were produced by the reaction of alpha-pinene and ozone in the presence of acid seed aerosol and characterized by exact mass measurements and tandem mass spectrometry. Oligomeric products between 200 and 900 u were detected with both electrospray ionization and matrix-assisted laser desorption ionization. The exact masses and dissociation products of these ions were consistent with various combinations of the known primary products of this reaction ("monomers") with and/or without the expected acid-catalyzed decomposition products of the monomers. Oligomers as large as tetramers were detected. Both aldol condensations and gem-diol reactions are suggested as possible pathways for oligomer formation. Exact mass measurements also revealed reaction products that cannot be explained by simple oligomerization of monomers and monomer decomposition products, suggesting the existence of complex reaction channels. Chemical reactions leading to oligomer formation provide a reasonable answer to a difficult problem associated with secondary organic aerosol production in the atmosphere. It is unlikely that monomers alone play an important role in the formation and growth of nuclei in the atmosphere as their Kelvin vapor pressures are too high for them to significantly partition into the particle phase. Polymerization provides a mechanism by which partitioning to the particle phase becomes favored.
引用
收藏
页码:1428 / 1434
页数:7
相关论文
共 60 条
[31]   MUTAGENIC TRANSFORMATIONS OF DILUTE WOOD SMOKE SYSTEMS IN THE PRESENCE OF OZONE AND NITROGEN-DIOXIDE - ANALYSIS OF SELECTED HIGH-PRESSURE LIQUID-CHROMATOGRAPHY FRACTIONS FROM WOOD SMOKE PARTICLE EXTRACTS [J].
KAMENS, R ;
BELL, D ;
DIETRICH, A ;
PERRY, J ;
GOODMAN, R ;
CLAXTON, L ;
TEJADA, S .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1985, 19 (01) :63-69
[32]   Modeling aerosol formation from α-pinene plus NOx in the presence of natural sunlight using gas-phase kinetics and gas-particle partitioning theory [J].
Kamens, RM ;
Jaoui, M .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (07) :1394-1405
[33]   Secondary organic aerosol formation vs primary organic aerosol emission: In situ evidence for the chemical coupling between monoterpene acidic photooxidation products and new particle formation over forests [J].
Kavouras, IG ;
Mihalopoulos, N ;
Stephanou, EG .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1999, 33 (07) :1028-1037
[34]   Secondary organic aerosol formation from the oxidation of aromatic hydrocarbons in the presence of dry submicron ammonium sulfate aerosol [J].
Kleindienst, TE ;
Smith, DF ;
Li, W ;
Edney, EO ;
Driscoll, DJ ;
Speer, RE ;
Weathers, WS .
ATMOSPHERIC ENVIRONMENT, 1999, 33 (22) :3669-3681
[35]   RELATIVE CONTRIBUTION OF OXYGENATED HYDROCARBONS TO THE TOTAL BIOGENIC VOC EMISSIONS OF SELECTED MID-EUROPEAN AGRICULTURAL AND NATURAL PLANT-SPECIES [J].
KONIG, G ;
BRUNDA, M ;
PUXBAUM, H ;
HEWITT, CN ;
DUCKHAM, SC ;
RUDOLPH, J .
ATMOSPHERIC ENVIRONMENT, 1995, 29 (08) :861-874
[36]   Association of fine particulate matter from different sources with daily mortality in six US cities [J].
Laden, F ;
Neas, LM ;
Dockery, DW ;
Schwartz, J .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2000, 108 (10) :941-947
[37]   A BIOGENIC HYDROCARBON EMISSION INVENTORY FOR THE USA USING A SIMPLE FOREST CANOPY MODEL [J].
LAMB, B ;
GAY, D ;
WESTBERG, H ;
PIERCE, T .
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1993, 27 (11) :1673-1690
[38]   CONTRIBUTION OF WOODSMOKE AND MOTOR-VEHICLE EMISSIONS TO AMBIENT AEROSOL MUTAGENICITY [J].
LEWIS, CW ;
BAUMGARDNER, RE ;
STEVENS, RK ;
CLAXTON, LD ;
LEWTAS, J .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1988, 22 (08) :968-971
[39]  
Nielen MWF, 1999, MASS SPECTROM REV, V18, P309, DOI 10.1002/(SICI)1098-2787(1999)18:5<309::AID-MAS2>3.0.CO
[40]  
2-L