Low Temperature (550-700 K) Oxidation Pathways Of Cyclic Ketones: Dominance Of Ho≪Inf≫2≪/Inf≫-Elimination Channels Yielding Conjugated Cyclic Coproducts
Abstract
The low-temperature oxidation of three cyclic ketones, cyclopentanone (CPO; C5H8O), cyclohexanone (CHO; C6H10O), and 2-methyl-cyclopentanone (2-Me-CPO; CH3-C5H7O), is studied between 550 and 700 K and at 4 or 8 Torr total pressure. Initial fuel radicals R are formed via fast H-abstraction from the ketones by laser-photolytically generated chlorine atoms. Intermediates and products from the subsequent reactions of these radicals in the presence of excess O2 are probed with time and isomeric resolution using multiplexed photoionization mass spectrometry with tunable synchrotron ionizing radiation. For CPO and CHO the dominant product channel in the R + O2 reactions is chain-terminating HO2-elimination yielding the conjugated cyclic coproducts 2-cyclopentenone and 2-cyclohexenone, respectively. Results on oxidation of 2-Me-CPO also show a dominant contribution from HO2-elimination. The photoionization spectrum of the co-product suggests formation of 2-methyl-2-cyclopentenone and/or 2-cyclohexenone, resulting from a rapid Dowd-Beckwith rearrangement, preceding addition to O2, of the initial (2-oxocyclopentyl)methyl radical to 3-oxocyclohexyl. Cyclic ethers, markers for hydroperoxyalkyl radicals (QOOH), key intermediates in chain-propagating and chain-branching low-temperature combustion pathways, are only minor products. The interpretation of the experimental results is supported by stationary point calculations on the potential energy surfaces of the associated R + O2 reactions at the CBS-QB3 level. The calculations indicate that HO2-elimination channels are energetically favored and product formation via QOOH is disfavored. The prominence of chain-terminating pathways linked with HO2 formation in low-temperature oxidation of cyclic ketones suggests little low-temperature reactivity of these species as fuels in internal combustion engines.
Publication Date
5-14-2015
Publication Title
Physical Chemistry Chemical Physics
Volume
17
Issue
18
Number of Pages
12124-12134
Document Type
Article
Personal Identifier
scopus
DOI Link
https://doi.org/10.1039/c4cp06097k
Copyright Status
Unknown
Socpus ID
84928902391 (Scopus)
Source API URL
https://api.elsevier.com/content/abstract/scopus_id/84928902391
STARS Citation
Scheer, Adam M.; Welz, Oliver; Vasu, Subith S.; Osborn, David L.; and Taatjes, Craig A., "Low Temperature (550-700 K) Oxidation Pathways Of Cyclic Ketones: Dominance Of Ho≪Inf≫2≪/Inf≫-Elimination Channels Yielding Conjugated Cyclic Coproducts" (2015). Scopus Export 2015-2019. 263.
https://stars.library.ucf.edu/scopus2015/263