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The reactions of ozone with alkenes: An important source of HOx in the boundary layer

Paulson, Suzanne E., Orlando, John J.·1996·Geophysical Research Letters

Abstract

The reactions of ozone with alkenes have been shown recently to lead to the direct production of OH radicals. Organic peroxy radicals (RO 2) probably accompany the production of OH. In this paper, we draw attention to the potential importance of these reactions in the primary production of HO x (HO x = OH, HO 2 and RO 2) radicals in various regions of the boundary layer. The reactions of ozone with anthropogenic alkenes are shown to be the most important source of HO x in many urban settings during the day and evening, and a significant source at night. The majority of HO x comes from trace quantities of alkenes with internal double bonds. Reaction of O 3 with isoprene and terpenes can be an important source of HO x in forested regions; we show that these reactions are the dominant radical source in the late afternoon and into the night. This additional HO x source is expected to increase predicted OH concentrations compared to those calculated by models that do not include the O 3‐alkene source.

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Metadata

Authors
Paulson, S. E., & Orlando, J. J.
Venue
Geophysical Research Letters
Published
1996-12-15
Volume
23
Issue
25
Pages
3727-3730
ISSN
  • 0094-8276 (ISSN-L)
  • 1944-8007
OpenAlex
W2046901677
Cited by
314
References
0
FWCI
7.77
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: The reactions of ozone with alkenes: An important source of HOx in the boundary layer. https://app.cochat.ai/papers/10.1029/96gl03477
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Paulson, S. E., & Orlando, J. J. (1996). The reactions of ozone with alkenes: An important source of HOx in the boundary layer. Geophysical Research Letters. https://doi.org/10.1029/96gl03477

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.