Title of article
Secondary organic aerosol formation from a large number of reactive man-made organic compounds Original Research Article
Author/Authors
Richard G. Derwent، نويسنده , , Michael E. Jenkin، نويسنده , , Steven R. Utembe، نويسنده , , Dudley E. Shallcross، نويسنده , , Tim P. Murrells، نويسنده , , Neil R. Passant، نويسنده ,
Issue Information
دوهفته نامه با شماره پیاپی سال 2010
Pages
8
From page
3374
To page
3381
Abstract
A photochemical trajectory model has been used to examine the relative propensities of a wide variety of volatile organic compounds (VOCs) emitted by human activities to form secondary organic aerosol (SOA) under one set of highly idealised conditions representing northwest Europe. This study applied a detailed speciated VOC emission inventory and the Master Chemical Mechanism version 3.1 (MCM v3.1) gas phase chemistry, coupled with an optimised representation of gas–aerosol absorptive partitioning of 365 oxygenated chemical reaction product species. In all, SOA formation was estimated from the atmospheric oxidation of 113 emitted VOCs. A number of aromatic compounds, together with some alkanes and terpenes, showed significant propensities to form SOA. When these propensities were folded into a detailed speciated emission inventory, 15 organic compounds together accounted for 97% of the SOA formation potential of UK man made VOC emissions and 30 emission source categories accounted for 87% of this potential. After road transport and the chemical industry, SOA formation was dominated by the solvents sector which accounted for 28% of the SOA formation potential.
Keywords
Speciated VOC emissions , VOC oxidation , Degradation mechanisms , Chemical mechanisms , SOA modelling , Tropospheric chemistry
Journal title
Science of the Total Environment
Serial Year
2010
Journal title
Science of the Total Environment
Record number
986790
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