4.7 Article

Oxidation of diethyl ether: Extensive characterization of products formed at low temperature using high resolution mass spectrometry

Journal

COMBUSTION AND FLAME
Volume 228, Issue -, Pages 340-350

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.combustflame.2021.02.007

Keywords

Jet-stirred reactor; High resolution mass spectrometry; Cool-flame; Diethyl ether; carbonyl hydroperoxides; Ketohydroperoxides; Highly oxygenated molecules

Funding

  1. Labex Caprysses [ANR-11-LABX-0006-01]
  2. Region Centre Val de Loire
  3. EFRD
  4. CPER (project PROMESTOCK)
  5. CPER (project APROPORE)

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The oxidation of a stoichiometric diethyl ether-oxygen-nitrogen mixture containing 500 ppm of fuel was studied in a jet-stirred reactor at 10 atm and a residence time of 1 s. Various techniques were used to analyze the products, including gas chromatography, mass spectrometry, and FTIR. Multiple fuel-specific products were detected, including hydroperoxides, diols, carbonyl hydroperoxides, acetic acid, di-keto ethers, cyclic ethers, and highly oxygenated molecules.
The oxidation of a stoichiometric diethyl ether-oxygen-nitrogen mixture containing 50 0 0 ppm of fuel was studied in a jet-stirred reactor at 10 atm and a residence times of 1 s. Experimental temperatures varied stepwise for 440 to 740 K and products were quantified by gas chromatography with TCD and FID, gas chromatography-mass spectrometry, and FTIR. Other experiments in the temperature range 480 to 570 K were performed for characterizing elusive cool flame products. To this end, gas samples were trapped in acetonitrile for flow injection analyses and liquid chromatography-mass spectrometry (Orbitrap Q-Exactive (R)). For ionization, we used positive and negative atmospheric pressure chemical ionization (APCI). Among fuel-specific products, hydroperoxides and diols (C4H10O3), carbonyl hydroperoxides (C4H8O4), acetic acid, di-keto ethers (C4H6O3), cyclic ethers (C4H8O2) and highly oxygenated molecules, i.e., keto-dihydroperoxides (C4H8O6), keto-trihydroperoxides (C4H8O8), di-keto-hydroperoxides (C4H6O5), and diketo-dihydroperoxides (C4H6O7), were detected. To confirm the presence of -OH or -OOH groups in oxidation products, H/D exchange with D2O was used. DNPH derivatization was used to identify carbonyls present in samples, especially those with a molecular weight below 50 amu which cannot be detected directly by the mass spectrometer. Chemical kinetic modeling using a mechanism taken from the literature was performed. Although reasonable agreement between the data and the simulations was observed for several species, some discrepancies between experimental and computed mole fractions were observed. (C) 2021 The Combustion Institute. Published by Elsevier Inc. All rights reserved.

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