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Reductions in combustion noise are necessary in high load diesel engine operation and multiple fuel injections can achieve this with the resulting reductions in the maximum rate of pressure rise. In 2014, Dr. Fuyuto reported the phenomenon that the combustion noise produced in the first combustion can be reduced by the combustion noise of the second fuel injection, and this has been named “Noise Cancelling Spike Combustion (NCS combustion)”. To investigate more details of NCS combustion, the effects of timings and heating values of the first and second heat releases on the reduction of overall combustion noise are investigated in this paper. The engine employed in the research here is a supercharged, single cylinder DI diesel engine with a high pressure common rail fuel injection system.

Silent, clean, and efficient combustion was realized with emulsified blends of aqueous ethanol and diesel fuel in a DI diesel with pilot injection and cooled EGR. The pilot injection sufficiently suppressed the rapid combustion to acceptable levels. The thermal efficiency with the emulsified fuel improved as the heat release with the pilot injection was retarded to near top dead center, due to poor ignitability and also due to a reduction in afterburning. With the emulsified fuel containing 40 vol% ethanol and 10 vol% water (E40W10), the smokeless operation range can be considerably extended even under low fuel injection pressure or low intake oxygen content conditions.

To execute the computational fluid dynamics coupling with fuel chemistry in internal combustion engines, simplified chemical kinetic models which capture the low-temperature oxidation kinetics would be required. A steady-state analysis was applied to see the complicated reaction mechanism of alkylperoxy radicals by assuming the steady state for hydroperoxyalkyl (QOOH) and hydroperoxyalkylperoxy (OOQOOH) radicals. This analysis clearly shows the systematic trend of the reaction rate for the chain-branching and non-branching process of alkylperoxy (ROO) radicals as a function of the chain length and the carbon class. These trends make it possible to classify alkylperoxy radicals by their chemical structures, and suggest a reduced low-temperature oxidation chemistry.