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Plasma-Assisted Combustion

2:00 pm – 4:15 pm, Wednesday October 15 Session IW4 COEX, Room E6
Chair:
Joseph Lefkowitz, Technion - Israel Institute of Technology
Topics:

Kinetic study of CH3OCH3/CO2 reforming in a nanosecond pulsed discharge

3:30 pm – 3:45 pm
Presenter: Haodong Chen (Tsinghua University)
Authors: Zhaoying Li (Tsinghua University), Bin Yang (Tsinghua University)

The chemical kinetics of CO2 reforming of dimethyl ether (DME) is explored experimentally and numerically. Experiments are conducted in a flow reactor (DME/CO2/Ar, 340K, 30 Torr) with a nanosecond pulsed dielectric barrier discharge (DBD). Synchrotron vacuum ultraviolet photoionization mass spectrometry (SVUV-PIMS) is employed to achieve the species measurement in this system. Nine ions are observed, including CH3+, O+, Ar2+, CO+, CHO+, Ar+, CO2+, CH3OCH2+, and CH3OCH3+. Several intermediate species and products are identified based on the mass spectra and photoionization efficiency (PIE) spectra, such as methane (CH4), water (H2O),carbon dioxide (CO), formaldehyde (CH2O), methanol (CH3OH), ketene (CH2CO), ethyl methyl ether (C2H5OCH3), methyl formate (CH3OCHO), and dimethoxymethane (CH3OCH2OCH3). Species mole fraction profiles as a function of inlet CO2 concentrations are obtained with the inlet CO2 varying from 3% to 18% in the DME/CO2/Ar mixture (nDME=3%). The consumption of DME is promoted with the addition of CO2, and the mole fractions of some products such as H2O, CO, CH3OH, MF, and DMM increase firstly and then decrease. A kinetic mechanism incorporating plasma reactions and combustion reactions is developed for this system, and its prediction performance is tested against the experimental data. Rate of production (ROP) analysis indicates that DME is consumed through two channels, the H-atom abstractions with O/H/OH radicals and dissociations with plasma activated species such as electrons, Ar+, and Ar*. With the increase of the inlet CO2 mole fractions, the former pathways are enhanced and the latter channels are weakened. The dissociation reactions with electrons and Ar* and ionic reactions account for most of the CO formation, and H-atom abstraction reaction of DME and CHO radical by H radical are responsible for the H2 formation. The oxygnated species like CH3OCHO is generated from reactions of peroxides, while C2H5OCH3 and CH3OCH2OCH3 are formed through radical recombination. 

PRESENTATIONS (9)