Combustion chemistry and flame structure of furan group biofuels using molecular-beam mass spectrometry and gas chromatography - Part III : 2,5-Dimethylfuran

This work is the third part of a study focusing on the combustion chemistry and flame structure of furan and selected alkylated derivatives, i.e. furan in Part I, 2-methylfuran (MF) in Part II, and 2,5-dimethylfuran (DMF) in the present work. Two premixed low-pressure (20 and 40 mbar) flat argon-dil...

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Veröffentlicht in:Combustion and flame. - 1999. - 161(2014), 3 vom: 01. März, Seite 780-797
1. Verfasser: Togbé, Casimir (VerfasserIn)
Weitere Verfasser: Tran, Luc-Sy, Liu, Dong, Felsmann, Daniel, Oßwald, Patrick, Glaude, Pierre-Alexandre, Sirjean, Baptiste, Fournet, René, Battin-Leclerc, Frédérique, Kohse-Höinghaus, Katharina
Format: Aufsatz
Sprache:English
Veröffentlicht: 2014
Zugriff auf das übergeordnete Werk:Combustion and flame
Schlagworte:Journal Article 2,5-dimethylfuran gas chromatography low-pressure flame model molecular-beam mass spectrometry reaction flow analysis reaction mechanism
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520 |a This work is the third part of a study focusing on the combustion chemistry and flame structure of furan and selected alkylated derivatives, i.e. furan in Part I, 2-methylfuran (MF) in Part II, and 2,5-dimethylfuran (DMF) in the present work. Two premixed low-pressure (20 and 40 mbar) flat argon-diluted (50%) flames of DMF were studied with electron-ionization molecular-beam mass spectrometry (EI-MBMS) and gas chromatography (GC) under two equivalence ratios (φ=1.0 and 1.7). Mole fractions of reactants, products, and stable and radical intermediates were measured as a function of the distance to the burner. Kinetic modeling was performed using a reaction mechanism that was further developed in the present series, including Part I and Part II. A reasonable agreement between the present experimental results and the simulation is observed. The main reaction pathways of DMF consumption were derived from a reaction flow analysis. Also, a comparison of the key features for the three flames is presented, as well as a comparison between these flames of furanic compounds and those of other fuels. An a priori surprising ability of DMF to form soot precursors (e.g. 1,3-cyclopentadiene or benzene) compared to less substituted furans and to other fuels has been experimentally observed and is well explained in the model 
650 4 |a Journal Article 
650 4 |a 2,5-dimethylfuran 
650 4 |a gas chromatography 
650 4 |a low-pressure flame 
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650 4 |a molecular-beam mass spectrometry 
650 4 |a reaction flow analysis 
650 4 |a reaction mechanism 
700 1 |a Tran, Luc-Sy  |e verfasserin  |4 aut 
700 1 |a Liu, Dong  |e verfasserin  |4 aut 
700 1 |a Felsmann, Daniel  |e verfasserin  |4 aut 
700 1 |a Oßwald, Patrick  |e verfasserin  |4 aut 
700 1 |a Glaude, Pierre-Alexandre  |e verfasserin  |4 aut 
700 1 |a Sirjean, Baptiste  |e verfasserin  |4 aut 
700 1 |a Fournet, René  |e verfasserin  |4 aut 
700 1 |a Battin-Leclerc, Frédérique  |e verfasserin  |4 aut 
700 1 |a Kohse-Höinghaus, Katharina  |e verfasserin  |4 aut 
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