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Time resolved changes in unburned hydrocarbon emissions and their components were investigated in a DI diesel engine with a specially developed gas sampling system and gas chromatography. The tested transient operations include starting and increasing loads. At start-up with high equivalence ratios the total hydrocarbon (THC) at first increased, and after a maximum gradually decreased to reach a steady state value. Reducing the equivalence ratio of the high fueling at start-up and shortening the high fueling duration are effective to reduce THC emissions as long as sufficient startability is maintained. Lower hydrocarbons, mainly C1-C8, were the dominant components of the THC and mainly determined the THC behavior in the transient operations while the proportion of hydrocarbon (HC) components did not significantly change. The unregulated toxic substances, 1,3 butadiene and benzene were detected in small quantities.

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.

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.