Accretion product formation in the self- and cross-reactions of small β-hydroxy peroxy radicals
Open Access
- 27 October 2025
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Environmental Science: Atmospheres
- Vol. 5 (12) , 1312-1325
Abstract
The formation of a peroxide accretion product (ROOR) has recently been shown to be a significant channel in self- and cross-reactions of peroxy radicals (RO2) in the gas-phase. Here, we examine the formation of this accretion product in the self- and cross-reactions of RO2 derived from the OH-initiated oxidation of propene, cis-2-butene, and methylpropene in the presence of ethene. We measure the formation rate coefficient of the various accretion products in each system relative to the formation rate coefficient of the ethene-derived ROOR, which was measured in our previous work. We find that the accretion product forms in all of the studied self- and cross-reactions. The measured ROOR formation rate coefficient for the self-reaction decreases by approximately an order of magnitude with increasing substitution, with average rate coefficients of 4.7 × 10−13 cm3 molec−1 s−1 for primary hydroxy peroxy radicals, 2.7 × 10−14 cm3 molec−1 s−1 for secondary hydroxy peroxy radicals, and 8.0 × 10−16 cm3 molec−1 s−1 for the tertiary hydroxy peroxy radical. The cross-reaction rate coefficients of secondary and tertiary peroxy radicals with primary peroxy radicals are both higher than the corresponsing self-reactions, and also decrease with increasing radical substitution. We estimate the branching fraction to the formation of the ROOR for these peroxy radical self- and cross-reactions and find that branching fractions range from 0.03–0.33, with self- and cross-reactions of primary peroxy radicals having the highest branching fractions. Finally, we compare the reaction and ROOR formation rate coefficients of self- and cross-reactions of small RO2, and determine that the arithmetic mean of self-reaction rate coefficients provides a suitable method for estimating cross-reaction rate coefficients.Keywords
Funding Information
- Division of Chemistry (CHE-1905340, CHE-2305204)
- Villum Fonden (VIL50443)
- National Science Foundation
This publication has 42 references indexed in Scilit:
- Effects of a Carboxyl Group on the Products, Mechanism, and Kinetics of the OH Radical-Initiated Oxidation of 3-Butenoic Acid Under Low NOx ConditionsThe Journal of Physical Chemistry A, 2025
- Dimeric product formation in the self-reaction of small peroxy radicals using synchrotron radiation vacuum ultraviolet photoionization mass spectrometryChemosphere, 2024
- Comparing Reaction Routes for 3(RO···OR′) Intermediates Formed in Peroxy Radical Self- and Cross-ReactionsThe Journal of Physical Chemistry A, 2020
- Accretion Product Formation from Ozonolysis and OH Radical Reaction of α-Pinene: Mechanistic Insight and the Influence of Isoprene and EthyleneEnvironmental Science & Technology, 2018
- Gas-Phase Reactions of Isoprene and Its Major Oxidation ProductsChemical Reviews, 2018
- Calculation of conformationally weighted dipole moments useful in ion–molecule collision rate estimatesChemical Physics Letters, 2009
- Measurement of Gas-Phase Hydroperoxides by Chemical Ionization Mass SpectrometryAnalytical Chemistry, 2006
- Self- and cross-reactions of β-hydroxyperoxy radicals of relevance to tropospheric monoterpene oxidation: structure–activity relationships for rate coefficientsAtmospheric Environment, 2003
- Ozone and other secondary photochemical pollutants: chemical processes governing their formation in the planetary boundary layerAtmospheric Environment, 2000
- Organic peroxy radicals: Kinetics, spectroscopy and tropospheric chemistryAtmospheric Environment. Part A. General Topics, 1992