Secondary organic aerosol formation from anthropogenic air pollution: Rapid and higher than expected

被引:847
作者
Volkamer, Rainer
Jimenez, Jose L.
San Martini, Federico
Dzepina, Katja
Zhang, Qi
Salcedo, Dara
Molina, Luisa T.
Worsnop, Douglas R.
Molina, Mario J.
机构
[1] MIT, Cambridge, MA 02139 USA
[2] Univ Colorado, Dept Chem, Boulder, CO 80309 USA
[3] Univ Colorado, Cooperat Inst Res Environm Sci, Boulder, CO 80309 USA
[4] Univ Autonoma Estado Morelos, Ctr Invest Quim, Cuernavaca 62209, Morelos, Mexico
[5] Aerodyne Res Inc, Billerica, MA 01821 USA
关键词
D O I
10.1029/2006GL026899
中图分类号
P [天文学、地球科学];
学科分类号
07 ;
摘要
The atmospheric chemistry of volatile organic compounds (VOCs) in urban areas results in the formation of 'photochemical smog', including secondary organic aerosol (SOA). State-of-the-art SOA models parameterize the results of simulation chamber experiments that bracket the conditions found in the polluted urban atmosphere. Here we show that in the real urban atmosphere reactive anthropogenic VOCs (AVOCs) produce much larger amounts of SOA than these models predict, even shortly after sunrise. Contrary to current belief, a significant fraction of the excess SOA is formed from first-generation AVOC oxidation products. Global models deem AVOCs a very minor contributor to SOA compared to biogenic VOCs (BVOCs). If our results are extrapolated to other urban areas, AVOCs could be responsible for additional 3 - 25 Tg yr(-1) SOA production globally, and cause up to - 0.1 W m(-2) additional top-of-the-atmosphere radiative cooling.
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