Impacts of SO2, Relative Humidity, and Seed Acidity on Secondary Organic Aerosol Formation in the Ozonolysis of Butyl Vinyl Ether

被引:24
作者
Zhang, Peng [1 ,3 ]
Chen, Tianzeng [1 ,3 ]
Liu, Jun [1 ,3 ]
Liu, Changgeng [1 ]
Ma, Jinzhu [1 ,2 ,3 ]
Ma, Qingxin [1 ,2 ,3 ]
Chu, Biwu [1 ,2 ,3 ]
He, Hong [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Res Ctr Ecoenvironm Sci, State Key Joint Lab Environm Simulat & Pollut Con, Beijing 100085, Peoples R China
[2] Chinese Acad Sci, Ctr Excellence Reg Atmospher Environm, Inst Urban Environm, Xiamen 361021, Fujian, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
GAS-PHASE REACTIONS; STATISTICAL OXIDATION MODEL; CRIEGEE INTERMEDIATE; PARTICLE FORMATION; CHEMICAL-COMPOSITION; SULFURIC-ACID; NO3; RADICALS; MONOTERPENE OZONOLYSIS; HIGH-RESOLUTION; AIR-QUALITY;
D O I
10.1021/acs.est.9b02702
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Alkyl vinyl ethers are widely used as fuel additives. Despite this, their atmospheric chemistry and secondary organic aerosol (SOA) formation potentials are still not well-known under complex pollution conditions. In this work, we examined the impact of SO2, relative humidity (RH), and particle acidity on the formation and oxidation state (OSc) of SOA from butyl vinyl ether (BVE) ozonolysis. Increasing SO2 concentration produced a notable promotion of SOA formation and OSc due to the significant increase in H2SO4 particles and formation of more highly oxidized components. Increased RH in the presence of SO2 appeared to promote, suppress, and dominate the formation and OSc of SOA in the dry range (1-10%), low RH range (10-42%), and moderate RH range (42-64%), respectively. This highlights the importance of competition between H2O and SO2 in reacting with the stabilized Criegee intermediate in BVE ozonolysis at ambient RH. Increased particle acidity mainly contributed to the change in chemical composition of BVE-dominated SOA but not to SOA formation. The results presented here extend previous analysis of BVE-derived SOA and further aid our understanding of SOA formation potential of BVE ozonolysis under highly complex pollution conditions.
引用
收藏
页码:8845 / 8853
页数:9
相关论文
共 71 条
[51]   Reactivity of stabilized Criegee intermediates (sCIs) from isoprene and monoterpene ozonolysis toward SO2 and organic acids [J].
Sipila, M. ;
Jokinen, T. ;
Berndt, T. ;
Richters, S. ;
Makkonen, R. ;
Donahue, N. M. ;
Mauldin, R. L., III ;
Kurten, T. ;
Paasonen, P. ;
Sarnela, N. ;
Ehn, M. ;
Junninen, H. ;
Rissanen, M. P. ;
Thornton, J. ;
Stratmann, F. ;
Herrmann, H. ;
Worsnop, D. R. ;
Kulmala, M. ;
Kerminen, V. -M. ;
Petaja, T. .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2014, 14 (22) :12143-12153
[52]   The Role of Sulfuric Acid in Atmospheric Nucleation [J].
Sipila, Mikko ;
Berndt, Torsten ;
Petaja, Tuukka ;
Brus, David ;
Vanhanen, Joonas ;
Stratmann, Frank ;
Patokoski, Johanna ;
Mauldin, Roy L., III ;
Hyvarinen, Antti-Pekka ;
Lihavainen, Heikki ;
Kulmala, Markku .
SCIENCE, 2010, 327 (5970) :1243-1246
[53]   Organosulfate formation in biogenic secondary organic aerosol [J].
Surratt, Jason D. ;
Gomez-Gonzalez, Yadian ;
Chan, Arthur W. H. ;
Vermeylen, Reinhilde ;
Shahgholi, Mona ;
Kleindienst, Tadeusz E. ;
Edney, Edward O. ;
Offenberg, John H. ;
Lewandowski, Michael ;
Jaoui, Mohammed ;
Maenhaut, Willy ;
Claeys, Magda ;
Flagan, Richard C. ;
Seinfeld, John H. .
JOURNAL OF PHYSICAL CHEMISTRY A, 2008, 112 (36) :8345-8378
[54]   Effect of acidity on secondary organic aerosol formation from isoprene [J].
Surratt, Jason D. ;
Lewandowski, Michael ;
Offenberg, John H. ;
Jaoui, Mohammed ;
Kleindienst, Tadeusz E. ;
Edney, Edward O. ;
Seinfeld, John H. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2007, 41 (15) :5363-5369
[55]   Temperature dependence of secondary organic aerosol formation by photo-oxidation of hydrocarbons [J].
Takekawa, H ;
Minoura, H ;
Yamazaki, S .
ATMOSPHERIC ENVIRONMENT, 2003, 37 (24) :3413-3424
[56]   OH and O3-initiated oxidation of ethyl vinyl ether [J].
Thiault, G ;
Thévenet, R ;
Mellouki, A ;
Le Bras, G .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2002, 4 (04) :613-619
[57]   Formation of oligomers in secondary organic aerosol [J].
Tolocka, MP ;
Jang, M ;
Ginter, JM ;
Cox, FJ ;
Kamens, RM ;
Johnston, MV .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2004, 38 (05) :1428-1434
[58]   Complex chemical composition of colored surface films formed from reactions of propanal in sulfuric acid at upper troposphere/lower stratosphere aerosol acidities [J].
Van Wyngarden, A. L. ;
Perez-Montano, S. ;
Bui, J. V. H. ;
Li, E. S. W. ;
Nelson, T. E. ;
Ha, K. T. ;
Leong, L. ;
Iraci, L. T. .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2015, 15 (08) :4225-4239
[59]   Secondary Organic Aerosol Formation from Acetylene (C2H2): seed effect on SOA yields due to organic photochemistry in the aerosol aqueous phase [J].
Volkamer, R. ;
Ziemann, P. J. ;
Molina, M. J. .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2009, 9 (06) :1907-1928
[60]   Secondary organic aerosol formation from anthropogenic air pollution: Rapid and higher than expected [J].
Volkamer, Rainer ;
Jimenez, Jose L. ;
San Martini, Federico ;
Dzepina, Katja ;
Zhang, Qi ;
Salcedo, Dara ;
Molina, Luisa T. ;
Worsnop, Douglas R. ;
Molina, Mario J. .
GEOPHYSICAL RESEARCH LETTERS, 2006, 33 (17)