| Autor: |
Scheer AM; Combustion Research Facility, Sandia National Laboratories , MS 9055, Livermore, California 94551, United States., Eskola AJ; Combustion Research Facility, Sandia National Laboratories , MS 9055, Livermore, California 94551, United States., Osborn DL; Combustion Research Facility, Sandia National Laboratories , MS 9055, Livermore, California 94551, United States., Sheps L; Combustion Research Facility, Sandia National Laboratories , MS 9055, Livermore, California 94551, United States., Taatjes CA; Combustion Research Facility, Sandia National Laboratories , MS 9055, Livermore, California 94551, United States. |
| Jazyk: |
angličtina |
| Zdroj: |
The journal of physical chemistry. A [J Phys Chem A] 2016 Nov 03; Vol. 120 (43), pp. 8625-8636. Date of Electronic Publication: 2016 Oct 25. |
| DOI: |
10.1021/acs.jpca.6b07370 |
| Abstrakt: |
The pulsed photolytic chlorine-initiated oxidation of diethyl ketone [DEK; (CH 3 CH 2 ) 2 C═O], 2,2,4,4-d 4 -DEK [d 4 -DEK; (CH 3 CD 2 ) 2 C═O], and 1,1,1,5,5,5-d 6 -DEK [d 6 -DEK; (CD 3 CH 2 ) 2 C═O] is studied at 8 torr and 1-2 atm and from 400-625 K. Cl atoms produced by laser photolysis react with diethyl ketone to form either primary (3-pentan-on-1-yl, R P ) or secondary (3-pentan-on-2-yl, R S ) radicals, which in turn react with O 2 . Multiplexed time-of-flight mass spectrometry, coupled to either a hydrogen discharge lamp or tunable synchrotron photoionizing radiation, is used to detect products as a function of mass, time, and photon energy. At 8 torr, the nature of the chain propagating cyclic ether + OH channel changes as a function of temperature. At 450 K, the production of OH is mainly in conjunction with formation of 2,4-dimethyloxetan-3-one, resulting from reaction of the resonance-stabilized secondary R S with O 2 . In contrast, at 550 K and 8 torr, 2-methyl-tetrahydrofuran-3-one, originating from oxidation of the primary radical (R P ), is observed as the dominant cyclic ether product. Formation of both of these cyclic ether production channels proceeds via a resonance-stabilized hydroperoxy alkyl (QOOH) intermediate. Little or no ketohydroperoxide (KHP) is observed under the low-pressure conditions. At higher O 2 concentrations and higher pressures (1-2 atm), a strong KHP signal appears as the temperature is increased above 450 K. Definitive isomeric identification from measurements on the deuterated DEK isotopologues indicates the favored pathway produces a γ-KHP via resonance-stabilized alkyl, QOOH, and HOOPOOH radicals. Time-resolved measurements reveal the KHP formation becomes faster and signal more intense upon increasing temperature from 450 to 575 K before intensity drops significantly at 625 K. The KHP time profile also shows a peak followed by a gradual depletion for the extent of experiment. Several tertiary products exhibit a slow accumulation in coincidence with the observed KHP decay. These products can be associated with decomposition of KHP by β-scission pathways or via isomerization of a γ-KHP into a cyclic peroxide intermediate (Korcek mechanism). The oxidation of d 4 -DEK, where kinetic isotope effects disfavor γ-KHP formation, shows greatly reduced KHP formation and associated signatures from KHP decomposition products. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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