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Journal ArticleDOI

Budget of organic carbon in a polluted atmosphere: Results from the New England Air Quality Study in 2002

TLDR
In this article, an extensive set of volatile organic compounds (VOCs) and particulate organic matter (POM) was measured in polluted air during the New England Air Quality Study in 2002.
Abstract
[1] An extensive set of volatile organic compounds (VOCs) and particulate organic matter (POM) was measured in polluted air during the New England Air Quality Study in 2002. Using VOC ratios, the photochemical age of the sampled air masses was estimated. This approach was validated (1) by comparing the observed rates at which VOCs were removed from the atmosphere with the rates expected from OH oxidation, (2) by comparing the VOC emission ratios inferred from the data with the average composition of urban air, and (3) by the ability to describe the increase of an alkyl nitrate with time in terms of the chemical kinetics. A large part of the variability observed for oxygenated VOCs (OVOCs) and POM could be explained by a description that includes the removal of the primary anthropogenic emissions, the formation and removal of secondary anthropogenic species, and a biogenic contribution parameterized by the emissions of isoprene. The OVOC sources determined from the data are compared with the available literature, and a satisfactory agreement is obtained. The observed sub-μm POM was highly correlated with secondary anthropogenic gas-phase species, strongly suggesting that the POM was from secondary anthropogenic sources. The results are used to describe the speciation and total mass of gas- and particle-phase organic carbon as a function of the photochemical age of an urban air mass. Shortly after emission the organic carbon mass is dominated by primary VOCs, while after two days the dominant contribution is from OVOCs and sub-μm POM. The total measured organic carbon mass decreased by about 40% over the course of two days. The increase in sub-μm POM could not be explained by the removal of aromatic precursors alone, suggesting that other species must have contributed and/or that the mechanism for POM formation is more efficient than previously assumed.

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Citations
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Journal ArticleDOI

Evolution of Organic Aerosols in the Atmosphere

Jose L. Jimenez, +66 more
- 11 Dec 2009 - 
TL;DR: A unifying model framework describing the atmospheric evolution of OA that is constrained by high–time-resolution measurements of its composition, volatility, and oxidation state is presented, which can serve as a basis for improving parameterizations in regional and global models.
Journal ArticleDOI

Rethinking Organic Aerosols: Semivolatile Emissions and Photochemical Aging

TL;DR: Accounting for partitioning and photochemical processing of primary emissions creates a more regionally distributed aerosol and brings model predictions into better agreement with observations, attribute this unexplained secondary organic-aerosol production to the oxidation of low-volatility gas-phase species.
References
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Journal ArticleDOI

A global model of natural volatile organic compound emissions

TL;DR: In this article, the authors developed a global model to estimate emissions of volatile organic compounds from natural sources (NVOC), which has a highly resolved spatial grid and generates hourly average emission estimates.
Journal ArticleDOI

Atmospheric chemistry of VOCs and NOx

TL;DR: The present status of knowledge of the gas phase reactions of inorganic Ox, Hox and NOx species and of selected classes of volatile organic compounds (VOCs) and their degradation products in the troposphere is discussed in this paper.
Journal ArticleDOI

Species contributions to PM2.5 mass concentrations: Revisiting common assumptions for estimating organic mass

TL;DR: The authors revisited common assumptions for estimating PM2.5 mass concentration and found that these assumptions can be used to estimate organic mass in a wide range of scenarios, such as PM1.5.
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Evolution of Organic Aerosols in the Atmosphere

Jose L. Jimenez, +66 more
- 11 Dec 2009 -