Search Results

Ignition delay, using a rapid compression machine (RCM), is defined as the time period between the end of compression and the maximum rate of pressure rise due to combustion, at a given compressed condition of temperature and pressure. The same compressed conditions can be reached by a variety of combinations of compression ratio, initial temperature, initial pressure, diluent gas composition, etc. It has been assumed that the value of ignition delay, for a given fuel and at a given set of compressed conditions, would be the same, irrespective of the variety of the above-mentioned combinations that were used to achieve the compressed conditions. In this study, a range of initial conditions and compression ratios are studied to determine their effect on ignition delay time and to show how ignition delay time can differ even at the same compressed conditions.

Iso-Octane (2,2,4-trimethlypentane) is an important gasoline primary reference fuel (PRF) surrogate. Auto ignition of iso-octane was examined using a rapid compression machine (RCM) with iso-octane, air and carbon dioxide (CO2) mixtures. Experiments were conducted over a temperature range of 650K-900K at 20bar and 10 bar compressed conditions for equivalence ratios (Φ =) 0.6, 0.8, 1.0 and 1.3. CO2 dilution by mass was introduced at 0%, 15% and 30% levels with the O2:N2 mole ratio fixed at 1:3.76 emulating the exhaust gas recirculation (EGR) substitution in spark ignition (SI) engines. In this study the direct test chamber (DTC) approach is used for introducing iso-octane directly into the RCM test chamber via a direct injector. The results using this approach are compared with other RCM data available in the literature at undiluted Φ = 1.0 and 20 bar compressed pressure and show good agreement.

In this work autoignition delay times of two multi-component surrogates (high and low RON) were experimentally compared with their target full blend gasoline fuels. The study was conducted in a rapid compression machine (RCM) test facility and a direct test chamber (DTC) charge preparation approach was used for mixture preparation. Experiments were carried over the temperature range of 650K-900K and at 10 bar and 20 bar compressed pressure conditions for equivalence ratios of (Φ =) 0.6-1.3. Dilution in the reactant mixture was varied from 0% to 30% CO2 (by mass), with the O2:N2 mole ratio fixed at 1:3.76. This dilution strategy emulates exhaust gas recirculation (EGR) substitution in spark ignition (SI) engines. The multicomponent surrogate captured the reactivity trends of the gasoline-air mixtures reasonably well in comparison to the single component (iso-octane) surrogate.