Emissions and photochemistry of oxygenated VOCs in urban plumes in the Northeastern United States

R. Sommariva; J. A. de Gouw; M. Trainer; E. Atlas; P. D. Goldan; W. C. Kuster; C. Warneke; F. C. Fehsenfeld

doi:10.5194/acp-11-7081-2011

Emissions and photochemistry of oxygenated VOCs in urban plumes in the Northeastern United States

R. Sommariva, J. A. de Gouw, M. Trainer, E. Atlas, P. D. Goldan, W. C. Kuster, C. Warneke, F. C. Fehsenfeld

School of Environmental Sciences

Research output: Contribution to journal › Article › peer-review

33 Citations (Scopus)

Abstract

Photochemical processes inside urban plumes in the Northeast of the United States have been studied using a highly detailed chemical model, based upon the Master Chemical Mechanism (MCM). The model results have been compared to measurements of oxygenated VOCs (acetone, methyl ethyl ketone, acetaldehyde, acetic acid and methanol) obtained during several flights of the NOAA WP-3D aircraft, which sampled plumes from the New York City area during the ICARTT campaign in 2004. The agreement between the model and the measurements was within 40–60 % for all species, except acetic acid. The model results have been used to study the formation and photochemical evolution of acetone, methyl ethyl ketone and acetaldehyde. Under the conditions encountered during the ICARTT campaign, acetone is produced from the oxidation of propane (24–28 %) and i-propanol (

Original language	English
Pages (from-to)	7081-7096
Number of pages	16
Journal	Atmospheric Chemistry and Physics
Volume	11
Issue number	14
DOIs	https://doi.org/10.5194/acp-11-7081-2011
Publication status	Published - 21 Jul 2011

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10.5194/acp-11-7081-2011Licence: CC BY

Cite this

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title = "Emissions and photochemistry of oxygenated VOCs in urban plumes in the Northeastern United States",

abstract = "Photochemical processes inside urban plumes in the Northeast of the United States have been studied using a highly detailed chemical model, based upon the Master Chemical Mechanism (MCM). The model results have been compared to measurements of oxygenated VOCs (acetone, methyl ethyl ketone, acetaldehyde, acetic acid and methanol) obtained during several flights of the NOAA WP-3D aircraft, which sampled plumes from the New York City area during the ICARTT campaign in 2004. The agreement between the model and the measurements was within 40–60 % for all species, except acetic acid. The model results have been used to study the formation and photochemical evolution of acetone, methyl ethyl ketone and acetaldehyde. Under the conditions encountered during the ICARTT campaign, acetone is produced from the oxidation of propane (24–28 %) and i-propanol (",

author = "R. Sommariva and {de Gouw}, {J. A.} and M. Trainer and E. Atlas and Goldan, {P. D.} and Kuster, {W. C.} and C. Warneke and Fehsenfeld, {F. C.}",

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T1 - Emissions and photochemistry of oxygenated VOCs in urban plumes in the Northeastern United States

AU - Sommariva, R.

AU - de Gouw, J. A.

AU - Trainer, M.

AU - Atlas, E.

AU - Goldan, P. D.

AU - Kuster, W. C.

AU - Warneke, C.

AU - Fehsenfeld, F. C.

PY - 2011/7/21

Y1 - 2011/7/21

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AB - Photochemical processes inside urban plumes in the Northeast of the United States have been studied using a highly detailed chemical model, based upon the Master Chemical Mechanism (MCM). The model results have been compared to measurements of oxygenated VOCs (acetone, methyl ethyl ketone, acetaldehyde, acetic acid and methanol) obtained during several flights of the NOAA WP-3D aircraft, which sampled plumes from the New York City area during the ICARTT campaign in 2004. The agreement between the model and the measurements was within 40–60 % for all species, except acetic acid. The model results have been used to study the formation and photochemical evolution of acetone, methyl ethyl ketone and acetaldehyde. Under the conditions encountered during the ICARTT campaign, acetone is produced from the oxidation of propane (24–28 %) and i-propanol (

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