Articles | Volume 23, issue 5
https://doi.org/10.5194/acp-23-3147-2023
© Author(s) 2023. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-23-3147-2023
© Author(s) 2023. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Comparison of isoprene chemical mechanisms under atmospheric night-time conditions in chamber experiments: evidence of hydroperoxy aldehydes and epoxy products from NO3 oxidation
Philip T. M. Carlsson
CORRESPONDING AUTHOR
Institute of Energy and Climate Research, IEK-8: Troposphere, Forschungszentrum Jülich GmbH, 52428 Jülich, Germany
Luc Vereecken
Institute of Energy and Climate Research, IEK-8: Troposphere, Forschungszentrum Jülich GmbH, 52428 Jülich, Germany
Anna Novelli
Institute of Energy and Climate Research, IEK-8: Troposphere, Forschungszentrum Jülich GmbH, 52428 Jülich, Germany
François Bernard
Institut de Combustion, Aérothermique, Réactivité et Environnement (ICARE), UPR CNRS, 45071 Orléans, France
Steven S. Brown
NOAA Chemical Sciences Laboratory, Boulder, Colorado 80309, USA
Department of Chemistry, University of Colorado Boulder, Boulder, Colorado 80309, USA
Bellamy Brownwood
Department of Chemistry, Reed College, Portland, Oregon 97202, USA
Changmin Cho
Institute of Energy and Climate Research, IEK-8: Troposphere, Forschungszentrum Jülich GmbH, 52428 Jülich, Germany
now at: School of Earth Sciences and Environmental Engineering, Gwangju Institute of Science and Technology, Gwangju, South Korea
John N. Crowley
Atmospheric Chemistry Department, Max-Planck-Institut für Chemie, 55128 Mainz, Germany
Patrick Dewald
Atmospheric Chemistry Department, Max-Planck-Institut für Chemie, 55128 Mainz, Germany
Peter M. Edwards
Wolfson Atmospheric Chemistry Laboratories, Department of Chemistry, University of York, Heslington, York, UK
Nils Friedrich
Atmospheric Chemistry Department, Max-Planck-Institut für Chemie, 55128 Mainz, Germany
Juliane L. Fry
Department of Chemistry, Reed College, Portland, Oregon 97202, USA
now at: Environmental Sciences Group, Wageningen University & Research, 6708 HB Wageningen, the Netherlands
Mattias Hallquist
Department of Chemistry and Molecular Biology, University of Gothenburg, 41296 Gothenburg, Sweden
Luisa Hantschke
Institute of Energy and Climate Research, IEK-8: Troposphere, Forschungszentrum Jülich GmbH, 52428 Jülich, Germany
Thorsten Hohaus
Institute of Energy and Climate Research, IEK-8: Troposphere, Forschungszentrum Jülich GmbH, 52428 Jülich, Germany
Sungah Kang
Institute of Energy and Climate Research, IEK-8: Troposphere, Forschungszentrum Jülich GmbH, 52428 Jülich, Germany
Jonathan Liebmann
Atmospheric Chemistry Department, Max-Planck-Institut für Chemie, 55128 Mainz, Germany
Alfred W. Mayhew
Wolfson Atmospheric Chemistry Laboratories, Department of Chemistry, University of York, Heslington, York, UK
Thomas Mentel
Institute of Energy and Climate Research, IEK-8: Troposphere, Forschungszentrum Jülich GmbH, 52428 Jülich, Germany
David Reimer
Institute of Energy and Climate Research, IEK-8: Troposphere, Forschungszentrum Jülich GmbH, 52428 Jülich, Germany
Franz Rohrer
Institute of Energy and Climate Research, IEK-8: Troposphere, Forschungszentrum Jülich GmbH, 52428 Jülich, Germany
Justin Shenolikar
Atmospheric Chemistry Department, Max-Planck-Institut für Chemie, 55128 Mainz, Germany
Ralf Tillmann
Institute of Energy and Climate Research, IEK-8: Troposphere, Forschungszentrum Jülich GmbH, 52428 Jülich, Germany
Epameinondas Tsiligiannis
Department of Chemistry and Molecular Biology, University of Gothenburg, 41296 Gothenburg, Sweden
Rongrong Wu
Institute of Energy and Climate Research, IEK-8: Troposphere, Forschungszentrum Jülich GmbH, 52428 Jülich, Germany
Andreas Wahner
Institute of Energy and Climate Research, IEK-8: Troposphere, Forschungszentrum Jülich GmbH, 52428 Jülich, Germany
Astrid Kiendler-Scharr
Institute of Energy and Climate Research, IEK-8: Troposphere, Forschungszentrum Jülich GmbH, 52428 Jülich, Germany
Fachgruppe Physik, Universität zu Köln, 50932 Cologne, Germany
deceased
Institute of Energy and Climate Research, IEK-8: Troposphere, Forschungszentrum Jülich GmbH, 52428 Jülich, Germany
Fachgruppe Physik, Universität zu Köln, 50932 Cologne, Germany
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Cited
7 citations as recorded by crossref.
- Application of fuzzy c-means clustering for analysis of chemical ionization mass spectra: insights into the gas phase chemistry of NO3-initiated oxidation of isoprene R. Wu et al. 10.5194/amt-17-1811-2024
- Measuring Biogenic Volatile Organic Compounds from Leaves Exposed to Submicron Black Carbon Using Portable Sensor Q. Liu & Y. Liu 10.3390/pollutants4020012
- Daytime isoprene nitrates under changing NOx and O3 A. Mayhew et al. 10.5194/acp-23-8473-2023
- Development of a multiphase chemical mechanism to improve secondary organic aerosol formation in CAABA/MECCA (version 4.7.0) F. Wieser et al. 10.5194/gmd-17-4311-2024
- Observation-constrained kinetic modeling of isoprene SOA formation in the atmosphere C. Shen et al. 10.5194/acp-24-6153-2024
- Gas-Phase Photolysis and Photo-Oxidation of Isoprene-Derived Atmospherically Relevant Hydroxy Nitrates R. Verma et al. 10.1021/acsestair.4c00010
- Online Calibration of a Chemical Ionization Mass Spectrometer for Multifunctional Biogenic Organic Nitrates M. Robinson et al. 10.1021/acsestair.4c00056
7 citations as recorded by crossref.
- Application of fuzzy c-means clustering for analysis of chemical ionization mass spectra: insights into the gas phase chemistry of NO3-initiated oxidation of isoprene R. Wu et al. 10.5194/amt-17-1811-2024
- Measuring Biogenic Volatile Organic Compounds from Leaves Exposed to Submicron Black Carbon Using Portable Sensor Q. Liu & Y. Liu 10.3390/pollutants4020012
- Daytime isoprene nitrates under changing NOx and O3 A. Mayhew et al. 10.5194/acp-23-8473-2023
- Development of a multiphase chemical mechanism to improve secondary organic aerosol formation in CAABA/MECCA (version 4.7.0) F. Wieser et al. 10.5194/gmd-17-4311-2024
- Observation-constrained kinetic modeling of isoprene SOA formation in the atmosphere C. Shen et al. 10.5194/acp-24-6153-2024
- Gas-Phase Photolysis and Photo-Oxidation of Isoprene-Derived Atmospherically Relevant Hydroxy Nitrates R. Verma et al. 10.1021/acsestair.4c00010
- Online Calibration of a Chemical Ionization Mass Spectrometer for Multifunctional Biogenic Organic Nitrates M. Robinson et al. 10.1021/acsestair.4c00056
Latest update: 13 Dec 2024
Short summary
The investigation of the night-time oxidation of the most abundant hydrocarbon, isoprene, in chamber experiments shows the importance of reaction pathways leading to epoxy products, which could enhance particle formation, that have so far not been accounted for. The chemical lifetime of organic nitrates from isoprene is long enough for the majority to be further oxidized the next day by daytime oxidants.
The investigation of the night-time oxidation of the most abundant hydrocarbon, isoprene, in...
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