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- 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, CHOH, 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.
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Sci Rep
January 2025
Department of Physical Chemistry, Gdańsk University of Technology, Narutowicza 11/12, Gdańsk, 80-233, Poland.
The study investigated the degradation of 3-methoxy-1-propanol (3M1P) by OH using the M06-2X/6-311++G(d, p) level, with CCSD(T) single-point corrections. We focused on hydrogen atom abstraction from various alkyl groups within the molecule. The rate coefficient for 3M1P degradation was calculated from the sum of the rate coefficients corresponding to the removal of H-atoms from primary (-CH), secondary (-CH-), tertiary (-CH< ), and alcohol (-ΟH) groups.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Beijing National Laboratory for Molecular Sciences, N, ew Corner-Stone Science Laboratory, College of Chemistry and Molecular Engineering, Peking University, Beijing, 100871, China.
Metal carbides with earth-abundant elements are widely regarded as promising alternatives to noble metal catalysts. Although comparable catalytic performances have been observed for metal carbides in several types of reactions, precise control of reaction pathways on them remains a formidable challenge, partially due to strong adsorption of reactants or intermediates. In this study, we show that bimolecular dehydrogenation of methanol to methyl formate and H is kinetically favored on bare α-MoC catalysts, while monomolecular dehydrogenation to CO and H becomes the dominant pathway when α-MoC is decorated with crowding atomic Ni species.
View Article and Find Full Text PDFJ Phys Chem A
January 2025
Division of Electron Collisions Physics, Institute of Physics and Applied Computer Science, Faculty of Applied Physics and Mathematics, Gdańsk University of Technology, ul. Gabriela Narutowicza 11/12, 80-233 Gdańsk, Poland.
The absolute total cross section for electron collisions with acetic acid has been measured using an electrostatic electron spectrometer and linear transmission method for collision energies ranging from 0.4 to 300 eV. Elastic electron scattering from acetic acid within a low-energy range has also been studied theoretically using the Schwinger multichannel and R-matrix methods, in the static-exchange and static-exchange plus polarization levels of approximation for energies up to 15 eV.
View Article and Find Full Text PDFACS Appl Mater Interfaces
October 2024
Department of Chemical Sciences, Ariel University, Ariel 40700, Israel.
The shift toward renewable energy sources plays a central role in the quest for a circular economy. In this context, methyl formate (MF) has garnered attention as a compelling hydrogen carrier and alternative fuel, because of its remarkable characteristics (energy density, ease of storage and transport, and low boiling point). In this study, DFT calculations supported by online electrochemical mass spectroscopy (OE-MS) were performed to investigate the MF electro-oxidation (MFEO) on PtPdSn (111).
View Article and Find Full Text PDFDalton Trans
October 2024
School of Physical Science and Technology, ShanghaiTech University, 393 Middle Huaxia Road, Shanghai 201210, China.
The development of hydrogen energy is widely recognized as a key approach to addressing the energy and carbon emission challenges. Methanol steam reforming is a promising hydrogen production scheme that can provide high-purity hydrogen. In this work, we studied the primary reaction mechanisms of methanol steam reforming over the Cu(111) and Cu(211) surfaces using density functional theory (DFT) calculations and microkinetic simulations.
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