Published February 12, 2025 | Version Published
Journal Article Open

Quantifying primary oxidation products in the OH-initiated reaction of benzyl alcohol

  • 1. ROR icon California Institute of Technology

Abstract

Benzyl alcohol is found in many volatile chemical products (VCPs) including a number of personal care products and industrial solvents. We report here on the products of the gas-phase oxidation of benzyl alcohol by OH and its dependence on nitric oxide (NO) levels. Using a gas chromatography in tandem with a chemical ionization mass spectrometer (CIMS) and gas chromatographer with a flame ionization detector (GC-FID), we measure the branching fractions to the major gas-phase oxidation products: hydroxybenzyl alcohol (HBA) and benzaldehyde. Later-generation oxidation products from both HBA and benzaldehyde pathways are also observed. In particular, catechol is a major gas-phase product of HBA. The fraction of H abstraction from benzyl alcohol leading to benzaldehyde formation is unaffected by [NO], with an average branching fraction of (21±10) %. The fraction of OH addition leading to HBA formation (36±18) % also does not appear to vary with [NO]. Consistent with the known high SOA yields of catechol, we find that HBA has a very high secondary organic aerosol (SOA) yield. Thus, benzyl alcohol and its oxidation products efficiently produce secondary organic aerosol – under some conditions approaching unity. Insights from the present study can help elucidate the chemistry of other atmospherically relevant aromatic compounds, especially those found in VCPs.

Copyright and License

© Author(s) 2025. This work is distributed under the Creative Commons Attribution 4.0 License.

Published by Copernicus Publications on behalf of the European Geosciences Union.

Acknowledgement

The authors thank Yuanlong Huang for help in troubleshooting instrumentation in the lab, Nathan Dalleska for his insights into the GC-FID, and Katherine Ball for calibrations. We thank Henrik Kjaaragard, Copenhagen University, for providing the dipole moments and polarizabilities listed in Table B1.

Funding

This research has been supported by the National Science Foundation (grant no. CHE-2305204 and 1745301) and the Alfred P. Sloan Foundation (grant no. G-2019-12281).

Data Availability

Data from this study can be made available upon request. Data for experiments P1 and P2 can be found through the Integrated Chamber Atmospheric Data Repository for Unified Science (ICARUS) and upon request.

Additional Information

This paper was edited by Frank Keutsch and reviewed by two anonymous referees.

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Additional details

Related works

Is new version of
Discussion Paper: 10.5194/egusphere-2023-2483 (DOI)

Funding

National Science Foundation
CHE-2305204
National Science Foundation
DGE-1745301
Alfred P. Sloan Foundation
G-2019-12281

Dates

Accepted
2024-09-16

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Caltech groups
Division of Chemistry and Chemical Engineering (CCE), Division of Engineering and Applied Science (EAS), Division of Geological and Planetary Sciences (GPS)
Publication Status
Published