New insights into the low-temperature oxidation of 2-methylhexane
Popolan-Vaida, Denisia M.
KAUST DepartmentChemical Engineering Program
Clean Combustion Research Center
Combustion and Pyrolysis Chemistry (CPC) Group
Mechanical Engineering Program
Physical Science and Engineering (PSE) Division
Online Publication Date2016-09-24
Print Publication Date2017
Permanent link to this recordhttp://hdl.handle.net/10754/622317
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AbstractIn this work, we studied the low-temperature oxidation of a stoichiometric 2-methylhexane/O2/Ar mixture in a jet-stirred reactor coupled with synchrotron vacuum ultraviolet photoionization molecular-beam mass spectrometry. The initial gas mixture was composed of 2% 2-methyhexane, 22% O2 and 76% Ar and the pressure of the reactor was kept at 780Torr. Low-temperature oxidation intermediates with two to five oxygen atoms were observed. The detection of C7H14O5 and C7H12O4 species suggests that a third O2 addition process occurs in 2-methylhexane low-temperature oxidation. A detailed kinetic model was developed that describes the third O2 addition and subsequent reactions leading to C7H14O5 (keto-dihydroperoxide and dihydroperoxy cyclic ether) and C7H12O4 (diketo-hydroperoxide and keto-hydroperoxy cyclic ether) species. The kinetics of the third O2 addition reactions are discussed and model calculations were performed that reveal that third O2 addition reactions promote 2-methylhexane auto-ignition at low temperatures. © 2016 The Combustion Institute.
CitationWang Z, Mohamed SY, Zhang L, Moshammer K, Popolan-Vaida DM, et al. (2016) New insights into the low-temperature oxidation of 2-methylhexane. Proceedings of the Combustion Institute. Available: http://dx.doi.org/10.1016/j.proci.2016.06.085.
SponsorsThis work was supported by: King Abdullah University of Science and Technology (KAUST) and Saudi Aramco under the FUELCOM program; National Key Scientific Instruments and Equipment Development Program of China2012YQ22011305; Department of Energy Gas Phase Chemical Physics Program at Lawrence Berkeley National LaboratoryDEAC02-05CH11231; German DFG ProjectKo1363/31-1; European Research Council under FP7/2007-2013/ERC Grant 291049-2G-CSafe; Sandia Corporation, a Lockheed Martin Company, and under National Nuclear Security Administration Contract DE-AC04-94-AL85000. The Advanced Light Source is supported by the Director, Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy under Contract no. DEAC02-05CH11231.