Abstract
The effects of methanol, dimethoxymethane (DMM), and dimethylcarbonate (DMC) on laminar premixed low pressure (30Torr) n-heptane flames were investigated by using synchrotron photoionization and molecular-beam mass spectrometry (PI–MBMS) techniques. The overall C/O ratio was maintained constant (0.507) and the equivalence ratio was kept around 1.6 for all the tested flames. The composition of unburned mixtures was adjusted such that the post-flame temperatures were nearly equivalent for all the test conditions. Mole fraction profiles of major and intermediate species were derived and compared among the flames. Parallel computations were performed based on a modified model, and the predicted concentrations of flame species agree reasonably well with the measured results. Early production of CO2 was observed in the DMC-doped flame. Reaction flux analysis suggested that it was caused by the decomposition of CH3OCO radical, DMC molecule and CH3OCOO radical. As oxygenated fuels were added, the concentrations of most C1C5 hydrocarbon intermediates were reduced while that of benzene (C6H6) also decreased apparently, and the extent of benzene reduction showed little difference among the oxygenate-doped flames. Reaction flux analysis indicated that, in all the tested flames, the primary pathway leading from small aliphatics to C6H6 was through C3+C3 reactions, including the self-recombination reaction of propargyl radical (C3H3) and the cross reaction between C3H3 and allyl radical (a-C3H5). Considering that the temperatures of the tested flames were almost equivalent, the reduction of C6H6 concentration when doped with oxygenated fuels should be resulted from the reduced concentrations of its precursors. Furthermore, concentrations of certain oxygenated intermediates were also examined. The concentration of formaldehyde (CH2O) was found to increase when flames were doped with oxygenated fuels, while those of acetaldehyde (CH3CHO) and vinyl alcohol (C2H3OH) were nearly equivalent for all the flames. Methyl formate (CH3OCHO) was detected only in the DMM-doped flame, which was attributed to the efficient CH3OCHO formation pathway through the decomposition of CH3OCHOCH3 radical in the flame.