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Pyrolysis of Methyl Formate and the Reaction of Methyl Formate with H Atoms: Shock Tube Experiments and Statistical Rate Theory.
Wenz, Johannes; Pazdera, Tobias M; Golka, Leonie; Olzmann, Matthias.
Afiliação
  • Wenz J; Institut für Physikalische Chemie, Karlsruher Institut für Technologie (KIT), Kaiserstr. 12, 76131 Karlsruhe, Germany.
  • Pazdera TM; Institut für Physikalische Chemie, Karlsruher Institut für Technologie (KIT), Kaiserstr. 12, 76131 Karlsruhe, Germany.
  • Golka L; Institut für Physikalische Chemie, Karlsruher Institut für Technologie (KIT), Kaiserstr. 12, 76131 Karlsruhe, Germany.
  • Olzmann M; Institut für Physikalische Chemie, Karlsruher Institut für Technologie (KIT), Kaiserstr. 12, 76131 Karlsruhe, Germany.
J Phys Chem A ; 127(4): 1036-1045, 2023 Feb 02.
Article em En | MEDLINE | ID: mdl-36683280
Methyl formate (MF) is the smallest carboxylic ester and currently considered a promising alternative fuel. It can also serve as a model compound to study the combustion chemistry of the ester group, which is a typical structural feature in many biodiesel components. In the present work, the pyrolysis of MF was investigated behind reflected shock waves at temperatures between 1430 and 2070 K at a nominal pressure of 1.1 bar. Both time-resolved hydrogen atom resonance absorption spectroscopy (H-ARAS) and time-resolved time-of-flight mass spectrometry (TOF-MS) were used for species detection. Additionally, the reaction of MF and perdeuterated MF-d4 with H atoms was investigated at temperatures between 1000 and 1300 K at nominal pressures of 0.4 and 1.1 bar with H-ARAS. In the latter experiments, ethyl iodide served as precursor for H atoms. Rate coefficients of seven parallel unimolecular decomposition channels of MF and five parallel reaction channels of the MF + H reaction were calculated from statistical rate theory on the basis of molecular and transition state data from quantum chemical calculations. These calculated rate coefficients were implemented into an MF pyrolysis/oxidation mechanism from the literature, and the experimental concentration-time profiles of H (from ARAS) as well as MF, CH3OH, HCHO, and CO (from TOF-MS) were modeled. It turned out that the literature mechanism, which was originally validated against flow-reactor experiments, ignition delay times, and laminar burning velocities, was generally able to fit also the concentration-time profiles from the shock tube experiments reasonably well. The agreement could still be improved by substituting the original rate coefficients, which were estimated from structure-reactivity relationships, by the values calculated from statistical rate theory in the present work. Details of the channel branching are discussed, and the updated mechanism is given, also in machine-readable form.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article