EXPERIMENTAL AND KINETIC MODELLING STUDY OF THE OXIDATION OF CYCLOPENTANE AND METHYLCYCLOPENTANE AT ATMOSPHERIC PRESSURE

International audienceCyclopentane and methylcyclopentane oxidation was investigated in a jet-stirred reactor at 1 atm, over temperatures ranging from 900 K to 1250 K, for fuel-lean, stoichiometric, and fuel-rich mixtures at a constant residence time of 70 ms. The initial mole fraction of both fuels was kept constant at 1000 ppm. The reactants were highly diluted by a flow of nitrogen to ensure thermal homogeneity. Samples of the reacting mixture were analyzed on-line or off-line by Fourier transform infrared spectroscopy and gas chromatography. A detailed kinetic mechanism consisting of 590 species involved in 3469 reversible reactions was developed and validated against these new experimental results and previously reported ignition delays. Reaction pathways analysis as well as sensitivity analyses were performed to get insights into the differences observed during the oxidation process of cyclopentane and methylcyclopentane

Ketohydroperoxides and Korcek mechanism identified during the oxidation of dipropyl ether in a JSR by high-resolution mass spectrometry

International audienceWith the growing interest for biomass-derived fuels the understanding of the combustion chemistry of ethers becomes of major scientific importance. Ethers usually develop strong cool flames at relatively low temperatures. Very complex processes occur there, with the formation of peroxidized intermediates such as ketohydroperoxides and highly oxidized molecules. Such chemicals are relatively unstable and difficult to analyze.We studied the low-temperature oxidation of dipropyl ether in a jet-stirred reactor. The experimental conditions were selected to maximize the production of ketohydroperoxides, based on the kinetic model of Serinyel et al. (2019). We oxidized 5000 ppm of dipropyl ether at 1 bar, T = 520–530 K, an equivalence ratio of 0.5, and at a residence time of 1 s. Analyses were performed on solubilized products of dipropyl ether oxidation in cooled acetonitrile. The samples were analyzed using soft HESI electrospray ionization (+/-) and an Orbitrap mass spectrometer (resolution: 140,000, mass accuracy RO2 QOOH; QOOH + O2 OOQOOH HOOQ’OOH followed by HOOQ’OOH + O2 (HOO)2Q’OO (i) (HOO)2POOH → OH + (HOO)2P=O (i.e., C6H12O6) and (ii) (HOO)2POOH + O2 → (HOO)3POO (HOO)3P’OOH → OH + (HOO)3P=O (i.e., C6H12O8).The so-called Korcek mechanism through which ketohydroperoxides are transformed into stable products, namely propanoic acid here, was also observed. Hydrogen–Deuterium exchange reactions using D2O served to confirm the presence of –OH groups in the products

Highly oxygenates molecules formed by oxidation of terpenes in a jet-stirred reactor

International audienceWith the growing interest for biomass-derived fuels the understanding of the combustion chemistry of terpenes becomes of major scientific importance. Terpenes have been proposed as biofuels for aviation because of their high energy density. They usually develop cool flames below 800 K. Very complex processes occur there, with the formation of peroxides intermediates such as ketohydroperoxides and highly oxidized molecules (HOMs) containing both hydroperoxy and carbonyl groups. Such chemicals are relatively unstable and difficult to analyze.We studied the low-temperature oxidation of alpha-pinene, beta-pinene, and limonene (C10H16) in a jet-stirred reactor. The experimental conditions were selected to maximize the production of ketohydroperoxides. We oxidized 5000 ppm of these three terpenes at 1 bar, T = 590 K, an equivalence ratio of 0.5, and at a residence time of 1 s. High-resolution mass spectrometry analyses were performed on solubilized products of terpenes oxidation in cooled acetonitrile. The samples were analyzed using soft HESI electrospray ionization (+/-) and an Orbitrap® mass spectrometer (resolution: 140,000, mass accuracy RO2 QOOH; QOOH + O2 OOQOOH HOOQ’OOH followed by HOOQ’OOH + O2 (HOO)2Q’OO (i) (HOO)2POOH → OH + (HOO)2P=O (i.e., C10H14O5) and (ii) (HOO)2POOH + O2 → (HOO)3POO (HOO)3P’OOH → OH + (HOO)3P=O (i.e., C10H14O7). Fourth oxygen addition yielding C10H14O9 was also observed in the present work. Hydrogen–Deuterium exchange reactions using D2O were used to confirm the presence of –OH groups in the products