Unraveling The Structure And Chemical Mechanisms Of Highly Oxygenated Intermediates In Oxidation Of Organic Compounds
Keywords
Autooxidation; Ignition; Mass spectrometry; Peroxides; Secondary organic aerosol
Abstract
Decades of research on the autooxidation of organic compounds have provided fundamental and practical insights into these processes; however, the structure of many key autooxidation intermediates and the reactions leading to their formation still remain unclear. This work provides additional experimental evidence that highly oxygenated intermediates with one or more hydroperoxy groups are prevalent in the autooxidation of various oxygenated (e.g., alcohol, aldehyde, keto compounds, ether, and ester) and nonoxygenated (e.g., normal alkane, branched alkane, and cycloalkane) organic compounds. These findings improve our understanding of autooxidation reaction mechanisms that are routinely used to predict fuel ignition and oxidative stability of liquid hydrocarbons, while also providing insights relevant to the formation mechanisms of tropospheric aerosol building blocks. The direct observation of highly oxygenated intermediates for the autooxidation of alkanes at 500–600 K builds upon prior observations made in atmospheric conditions for the autooxidation of terpenes and other unsaturated hydrocarbons; it shows that highly oxygenated intermediates are stable at conditions above room temperature. These results further reveal that highly oxygenated intermediates are not only accessible by chemical activation but also by thermal activation. Theoretical calculations on H-atom migration reactions are presented to rationalize the relationship between the organic compound’s molecular structure (n-alkane, branched alkane, and cycloalkane) and its propensity to produce highly oxygenated intermediates via extensive autooxidation of hydroperoxyalkylperoxy radicals. Finally, detailed chemical kinetic simulations demonstrate the influence of these additional reaction pathways on the ignition of practical fuels.
Publication Date
12-12-2017
Publication Title
Proceedings of the National Academy of Sciences of the United States of America
Volume
114
Issue
50
Number of Pages
13102-13107
Document Type
Article
Personal Identifier
scopus
DOI Link
https://doi.org/10.1073/pnas.1707564114
Copyright Status
Unknown
Socpus ID
85030324274 (Scopus)
Source API URL
https://api.elsevier.com/content/abstract/scopus_id/85030324274
STARS Citation
Wang, Zhandong; Popolan-Vaida, Denisia M.; Chen, Bingjie; Moshammer, Kai; and Mohamed, Samah Y., "Unraveling The Structure And Chemical Mechanisms Of Highly Oxygenated Intermediates In Oxidation Of Organic Compounds" (2017). Scopus Export 2015-2019. 5200.
https://stars.library.ucf.edu/scopus2015/5200