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In a natural gas fueled engine ignited by diesel fuel, the addition of hydrogen to the engine could be a possible way to improve thermal efficiency and reduce unburned methane which has a warming potential many times that of carbon dioxide as it promotes a more rapid and complete combustion. This study carried out engine experiments using a single cylinder engine with natural gas and hydrogen delivered separately into the intake pipe, and with pilot-injection of diesel fuel. The percentages of hydrogen in the natural gas-hydrogen mixtures were varied from 0% to 50% of the heat value. The results showed that the hydrogen addition has an insignificant effect on the ignition delay of the diesel fuel and that it shortens the combustion duration. The increase in the hydrogen ratio decreased the unburned hydrocarbon emissions more than the reduction of the amount of natural gas that was replaced by the hydrogen.

A spark assist system was installed in a gasoline direct-injection single-cylinder test engine with the aim of controlling the ignition timing and accomplishing combustion of gasoline fuel by auto/compression ignition. A primary reference fuel having an octane number of 90 (PRF 90) was used to evaluate experimentally the spark assist function for gasoline auto/compression ignition and to examine the feasibility of combustion with a short ignition delay equivalent to conventional diesel combustion using the engine system. An optically accessible single-cylinder test engine was also used to evaluate and investigate spark-assisted auto/compression ignition. Ignition timing controllability with combinations of spark and injection timings for gasoline auto/compression ignition was also investigated under different operating load conditions.

The Dual-Fuel (DF) combustion is a promising technology for efficient, low NOx and low exhaust particulate matter (PM) engine operation. To achieve equivalent performance to a DF engine with only the use of conventional liquid fuel, this study proposes the implementation of an on-board fuel reformation process by piston compression. For concept verification, DF combustion tests with representative reformed gas components were conducted. Based on the results, the controllability of the reformed gas composition by variations in the operating conditions of the reformer cylinder were discussed.

Ammonia-selective catalytic reduction (SCR) systems have been introduced commercially in diesel vehicles, however catalyst systems with higher conversion efficiency and better control characteristics are required to know the actual emissions during operation and the emissions in random test cycles. Computational fluid dynamics (CFD) is an effective approach when applied to SCR catalyst development, and many models have been proposed, but these models need experimental verification and are limited in the situations they apply to. Further, taking account of redox cycle is important to have better accuracy in transient operation, however there are few models considering the cycle. Model development considering the redox reactions in a zeolite catalyst, Cu-ZSM-5, is the object of the research here, and the effects of exhaust gas composition on the SCR reaction and NH3 oxidation at high temperatures are investigated.

To extend the operational range of premixed diesel combustion, fuel reformation by piston induced compression of rich homogeneous air-fuel mixtures was conducted in this study. Reformed gas compositions and chemical processes were first simulated with the chemistry dynamics simulation, CHEMKIN Pro, by changing the intake oxygen content, intake air temperature, and compression ratio. A single cylinder diesel engine was utilized to verify the simulation results. With the simulation and experiments, the characteristics of the reformed gas with respect to the reformer cylinder operating condition were obtained. Further, the thermal decomposition and partial oxidation reaction mechanisms of the fuel in extremely low oxygen concentrations were obtained with the characteristics of the gas production at the various reaction temperatures.