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In this study, the ignition delay times of DME/n-C4H10 fuel blends (neat DME, 50/50 and neat n-C4H10) diluted with argon were measured behind reflected shock waves. The experiments were performed in the temperature range of 1250 - 1600 K, at pressure of 2.0 MPa and equivalence ratios from 0.5 to 2.0. A latest kinetic mechanism NUIG Aramco Mech 1.3 was validated against the present ignition data and used to conducted chemical kinetic analysis. Different equivalence-ratio-dependent was exhibited at different temperature regimes for DME, n-C4H10, and their blend. Fuel flux analysis, sensitive analysis and mole fraction analysis were carried out for understanding the interaction between the ignition chemistries of DME and n-C4H10.

Ignition delay times of stoichiometric dimethyl ether (DME) and n-butane blends were measured in a shock tube at varied DME blending ratios, temperatures and pressures. Simulation work extended the pressure to 20 atm by using Chemkin and NUI C4_47 mechanism. The experimental ignition delay times of DME/n-butane were obtained at different DME blending ratios. Measured ignition delay times were compared to simulations based on NUI C4_47 mechanisms by Curran et al. The mechanism predicts the magnitude of ignition delay times well and a slightly higher activation energy. The ignition delay times increase linearly with the increase of 1000/T and the overall activation energy keeps almost the same value at the conditions in this study. Increasing pressure decreases exponentially the ignition delay time. Ignition delay time decreases linearly with the increase of DME blending ratio.