Abstract
This work reports the mid-IR spectroscopy and reaction kinetics of 2-methyl-1,3-dioxolane (2M13DO). We carried out spectroscopic measurements to deduce temperature-dependent absorption cross-sections of 2M13DO over a broad wavelength range of 8.4–10.5 μm (950–1190 cm−1). For these measurements, we employed a rapidly tuning MIRcat-QT™ laser that can be operated either at a fixed wavelength or scanned mode over wide wavelength regions. By operating the laser at a fixed wavelength, we monitored the decay of 2M13DO behind reflected shock waves over T5 = 1050–1400 K and P5 = 0.7 and 2.6 bar. Our measured concentration time-histories of 2M13DO allowed us to directly extract the overall rate coefficients for the unimolecular decomposition of 2M13DO using the first-order rate law. We did not observe any pressure dependence in the measured rate coefficients, indicating that the reaction is close to the high-pressure limit. By employing the W1U composite method, we explored the important pyrolysis reaction pathways of 2M13DO in the reactive potential energy surface. Three important reaction channels, namely, 2M13DO → CH2[dbnd]CHOCH2CH2OH (IM1), 2M13DO → 2CH3CHO (P3), 2M13DO → CH3 + 1,3-dioxolan-2-yl (P4) were identified. Below 700 K, IM1 forming channel is dominant, whereas CH3CHO formation is dominant under our experimental conditions. Above 1500 K, the radical forming channel (CH3+P4) takes over other channels. At higher temperatures, the contribution of the radical forming channel continually increases, accounting for ∼ 99% at 2000 K. We used the stochastic RRKM-ME model to predict the pressure and temperature dependence of the rate coefficients, k(T, P), and time-resolved species profiles. Our theory showed excellent agreement with the measured rate coefficients. These are the first direct determination of the rate coefficients of the unimolecular decomposition of 2M13DO.
Original language | English (US) |
---|---|
Pages (from-to) | 100165 |
Journal | Journal of Photochemistry and Photobiology |
Volume | 13 |
DOIs | |
State | Published - Jan 31 2023 |
Bibliographical note
KAUST Repository Item: Exported on 2023-02-22Acknowledgements: The research work reported in this publication was supported by King Abdullah University of Science and Technology (KAUST). This work also received financial support from Vietnam National Foundation for Science and Technology Development (NAFOSTED) under grant number 104.06-2020.45. Further financial support has been provided by the National Research, Development, and Innovation Fund (Hungary) within the TKP2021-NVA-14 project.