| Title: | Comprehensive Analysis of Products and the Development of a Quantitative Mechanism for the OH Radical-Initiated Oxidation of 1-Alkenes in the Presence of NO(x) |
| Author(s): | Bakker-Arkema JG; Ziemann PJ; |
| Address: | "Department of Chemistry, University of Colorado, Boulder, Colorado 80309, United States. Cooperative Institute for Research in Environmental Sciences (CIRES), Boulder, Colorado 80309, United States" |
| ISSN/ISBN: | 1520-5215 (Electronic) 1089-5639 (Linking) |
| Abstract: | "The reactions of 1-tetradecene and 1-pentadecene, the C(14) and C(15) linear 1-alkenes, with OH radicals in the presence of NO(x) were investigated in a series of environmental chamber experiments. Particle-phase beta-hydroxynitrates, dihydroxynitrates, dihydroxycarbonyls, and 1,4-hydroxynitrates and gas-phase aldehydes were sampled and then identified and quantified using a suite of offline analytical techniques that included derivatization, gas and liquid chromatography, and multiple types of mass spectrometry. Measured molar yields of products formed by OH radical addition to the C horizontal lineC double bond, including beta-hydroxynitrates, dihydroxynitrates, dihydroxycarbonyls (which have not been previously directly quantified with high accuracy), and aldehydes were 0.125 +/- 0.01, 0.048 +/- 0.005, 0.240 +/- 0.04, and 0.268 +/- 0.03 (0.264 +/- 0.02 and 0.271 +/- 0.04 for the formaldehyde and tridecanal/tetradecanal co-products of beta-hydroxyalkoxy radical decomposition), respectively. These values give a total molar yield of 0.681 +/- 0.05, which agrees very well with the results of kinetics measurements that indicate that the fraction of reaction that occurs by OH radical addition is 0.70. The yields were used to calculate branching ratios for all OH radical addition pathways, including a value of 0.18 for the formation of dihydroxynitrates from the reaction of dihydroxyperoxy radicals with NO and values of 0.47 and 0.53 for beta-hydroxyalkoxy radical decomposition and isomerization. The results were used with literature data on the yields of aldehydes measured for similar reactions of smaller alkenes, a model for the effect of carbon number on branching ratios for organic nitrate formation, and a mechanism for H atom abstraction derived from studies of linear alkanes to achieve a complete, quantitative gas-phase reaction mechanism for 1-alkenes. The results should also be useful for constructing mechanisms for more complex reactions of volatile organic compounds" |
| Notes: | "PubMed-not-MEDLINEBakker-Arkema, Julia G Ziemann, Paul J eng 2021/06/26 J Phys Chem A. 2021 Jul 8; 125(26):5829-5840. doi: 10.1021/acs.jpca.1c03688. Epub 2021 Jun 25" |
