Abstract

Blending petroleum-based fuels with biofuel components is deemed attractive to reduce soot and CO2 emissions, but fundamental studies of the combustion behavior of such fuel blends suited for model development and validation remain rather scarce. To contribute to the understanding of the combustion chemistry effects of such blending strategies, we have investigated laminar premixed low-pressure flames of three hydrocarbon base fuels, namely 1-butene (1-C4H8), isobutene (i-C4H8), and ethene (C2H4), blended each with two different ester fuels, namely methyl crotonate (C5H8O2, MC) and methyl butanoate (C5H10O2, MB). A series of 13 flames with different argon dilution was investigated to study effects of the specific fuel structure on the combustion chemistry. Full speciation analyses were performed for fuel-rich (ϕ = 1.6) conditions by electron ionization molecular-beam mass spectrometry (EI-MBMS). More than 35 species in the range of C0–C7 were identified and quantified in these flames, resulting in ∼450 mol fraction profiles. The experimental data were compared to simulations by the kinetic model reported by Yang et al. [Proc. Combust. Inst. 2011, Phys. Chem. Chem. Phys. 2013] that was chosen because it includes basic mechanisms of all studied fuels. Overall, the agreement of experiment and this model seems satisfactory but calls for further improvements regarding ester as well as hydrocarbon sub-mechanisms. It was noted that the unsaturation degree in the methyl esters affects the formation of hydrocarbons, that depend mainly on the structure of the respective base fuel, and of oxygenated intermediates. The methyl esters have different decomposition pathways leading to some specific oxygenated species. Both methyl esters promote the formation of formaldehyde and methanol, while acetic acid is significantly increased by the presence of MB. The effect of the ester addition is also influenced by the species pool of the respective hydrocarbon base fuel.

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