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Ultra-low NOx and smokeless operation at higher loads up to half of the rated torque is attempted with large ratios of cold EGR. NOx decreases below 6 ppm (0.05 g/(kW·h)) and soot significantly increases when first decreasing the oxygen concentration to 16% with cold EGR, but after peaking at 12-14% oxygen, soot then deceases sharply to essentially zero at 9-10% oxygen while maintaining ultra low NOx and regardless of fuel injection quantity. However, at higher loads, with the oxygen concentration below 9-10%, the air/fuel ratio has to be over-rich to exceed half of rated torque, and thermal efficiency, CO, and THC deteriorate significantly. As EGR rate increases, exhaust gas emissions and thermal efficiency vary with the intake oxygen content rather than with the excess air ratio.

The thermal cracking and polyaromatic hydrocarbon (PAH) formation processes of dimethyl ether (DME), ethanol, and ethane were investigated with chemical kinetics to determine the soot formation mechanism of oxygenated fuels. The modeling analyzed three processes, an isothermal constant pressure condition, a temperature rising condition under a constant pressure, and an unsteady condition approximating diesel combustion. With the same mole number of oxygen atoms, the DME rich mixtures form much carbon monoxide and methane and very little non-methane HC and PAH, in comparison with ethanol or ethane mixtures. This suggests that the existence of the C-C bond promotes the formation of PAH and soot.

Most countries consider it is harmful for humans to inhale SPM of fine organic particles and elemental carbon less than 2.5 μ in diameter1,2). It is generally believed that organic matters in SPM are mainly composed of diesel exhaust particulate and soot from residential chimneys or industrial smokestacks3,4). To determine the contribution ratios of several organic substances to SPM, we characterized SPM, diesel exhaust particulate (DEP), powdered summer radial tire, and bitumen, using high performance liquid chromatography, field desorption mass spectrometry and linear theory.

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.

Diesel combustion and emissions with four kinds of oxygenated agents as main fuels were investigated. Significant improvements in smoke, particulate matter, NOx, THC, and thermal efficiency were simultaneously realized with the oxygenates, and engine noise was also remarkably reduced for the oxygenates with higher ignitability. The improvements in the exhaust emissions and the thermal efficiency depended almost entirely on the oxygen content in the fuels regardless of the oxygenate to diesel fuel blend ratios and type of oxygenate. The unburned THC emission and odor intensity under starting condition with an oxygenate were also much lower than with conventional diesel fuel.

A new method to simultaneously measure temperature and concentration distributions in unsteady gas jets was established with an adaptation of the laser-induced fluorescence of iodine molecules seeded into ambient gas. Using the temperature dependence of iodine fluorescence spectra, the local temperature inside jets was determined with the ratio between the fluorescence intensities of two visualized images with different wavelengths. Jet concentrations were also determined with the images for the temperature measurements. The method was applied to an unsteady argon jet injected into hot argon-iodine ambient gases. The experimental results showed that the local temperature distribution in an unsteady gas jet were quite similar to the local concentration distributions.

The effect of eight kinds of oxygenated agents added to diesel fuels on the combustion and emissions was investigated in a DI diesel engine. The results showed significant smoke and particulate suppression without increases in NOx with every oxygenated agent. The emissions decreased linearly with increasing oxygen content in the fuels, almost regardless of the kind of oxygenated agent. The improvement in smoke and particulate emissions with the oxygenated agent addition was more significant for lower volatility fuels. Combustion analysis with the two-dimensional two color method showed that soot concentration in the flame during the combustion process decreased with the addition of the oxygenated agent while the flame temperature distribution was almost unchanged.

The effect of several aqueous metal-salt solutions on NOx and smoke lowering in an IDI diesel engine were examined. The solutions were directly injected into a divided chamber independent of the fuel injection. The results showed that significant lowering in NOx and smoke over a wide operation range could be achieved simultaneously with alkali metal solutions which were injected just prior to the fuel injection. With sodium-salt solutions, for instance, NOx decreased by more than 60 % and smoke decreased 50 % below conventional operation. The sodium-salt solution reduced dry soot significantly, while total particulate matter increased with increases in the water soluble fractions.

Diesel combustion and exhaust gas emissions under transient operation (when fuel amounts abruptly increased) were investigated under a wide range of operating conditions with a newly developed gas sampling system. The relation between gas emissions and piston wall temperatures was also investigated. The results indicated that after the start of acceleration NOx, THC and smoke showed transient behaviors before reaching the steady state condition. Of the three gases, THC was most affected by piston wall temperature; its concentration decreased as the wall temperature increased throughout the acceleration except immediately after the start of acceleration. The number of cycles, at which gas concentrations reach the steady-state value after the start of acceleration, were about 1.2 times the cycle constant of the piston wall temperature for THC, and 2.3 times for smoke.

Time-resolved and local ambient gas entrainment processes in intermittent gas jets with a range of injection conditions were evaluated by a LIFA (Laser-Induced Fluorescence of Ambient gas) technique. The gas injection conditions tested were: mean discharge velocity, um; mean discharge turbulence intensity, u′m; kinematic viscosity of the gas jet, ν; specific gravity of the gas jet, ρj; and of the ambient gas, ρa. Experimental results showed that the entrainment of jets are enhanced with higher eddy kinematic viscosity, νt, measured by a hot wire anemometer. In conclusion, the mean jet concentration was approximated with only one parameter, (ρj/ρa)D2/[(ν+νt)Δt].

The influence of the molecular structure of hydrocarbon fuels on soot, SOF, and NOx emissions from a diesel engine was analyzed while ignition delay and other physical fuel properties were kept constant. Mixtures of normal paraffin (n-tetradecane) and iso-paraffin (heptamethylnonane) were used as a base fuel and one of 5 kinds of hydrocarbons including mono-aromatic, di-aromatic, and non-aromatic was added. The aromatic content varied in the range of 0-60 vol % for the mono-aromatic fuels and 0-40 vol % for the di-aromatic fuels. The experimental results showed that regardless of the molecular structure of the fuel, both particulate and NOx emissions increased linearly with the C/H atomic ratio of the fuels under constant ignition lag. The increase in particulate emissions with C/H atomic ratio was caused by increases in dry soot. The SOF, THC, and BSEC were little affected by the C/H atomic ratio and molecular structure of the fuels.

Mixture formation processes of intermittent gas jets were visualized and quantified with high accuracy by a uniquely developed LIF technique (LIFA). Mixture strength inside gas jets was quantified by the fluorescence of iodine in the ambient gas excited by the sheet light of a Nd:YAG laser Two dimensional images of intermittent gas jets of various velocities were continuously recorded with VTR and quantified with high accuracy. The optimum conditions for measurements and accuracy with the LIFA technique were investigated. At the optimum setting of the initial iodine concentration in the ambient gas, accuracies better than 95% were obtained for the ambient gas entrainment ratio or jet concentration. The experimental results show that considerable amounts of ambient gas entrain just under the umbrella-like profile at the top of the jet. The mean jet concentration decreased with decreased nozzle diameter (D), and time elapsed after injection (Δt).

The effects of several fuel property variables on the emissions from a D.I. diesel engine were individually analyzed. The results showed that the smoke and dry soot increased with increased kinematic viscosity, shorter ignition lag, and higher aromatic content, especially at high equivalence ratios. Over the whole range of equivalence ratios, SOF depended on and increased with only ignition lag. The NOx improved slightly with increased kinematic viscosity, higher ignitability, and decreased aromatic content. The unburnt HC also improved with decreased kinematic viscosity and higher ignitability. The distribution shape of distillation curves had little influence on the emissions.

The influence of aromatic content in fuels on the soot and NOx emissions from a diesel engine was analyzed under controlled ignition lags with spark-assisted operation. Monocyclic aromatic hydrocarbons and n-hexane mixtures were used as fuels, and the aromatic content was varied from 0 to 75 v-%. The experiments showed that, at the same equivalence ratio and regardless of the molecular structure of the fuel, the soot concentration in the exhaust gas could be described by a linear-combination function with two variables representing the ignition lag and C/H atom-ratio of the fuels. For unchanged ignition lags, the soot emissions increased linearly with increased C/H atom-ratios, which are controlled by the aromatic content. The degree of increase in soot emissions with increasing C/H atom-ratio decreased with decreasing equivalence ratios. The NOx emission increased slightly with increases in the C/H atom-ratio and ignition lag.

Diesel soot suppression effects of catalytic fuel additives for a range of fuels with different properties were investigated with calcium naphthenate. A single cylinder DI diesel engine and a thermobalance were used to determine the soot reduction and its mechanism for seven kinds of fuels. Experimental results showed that the catalytic effect of the fuel additive was different for the different fuels, and could be described by a parameter considering cetane number and kinematic viscosity. The fuel additives reduced soot more effectively for fuels with higher cetane number and lower kinematic viscosity. This result was explained by soot oxidation characteristics for the different fuels. Oxidation of soot with the metallic additive proceeds in two stages: stage I, a very rapid oxidation stage; and stage II, a following slow or ordinary oxidation stage.

Soot emission from diesel engines generally increases with shorter ignition lags. However, the detailed process and mechanism of this phenomenon has not been well understood. This investigation attempts to observe and analyze the in-chamber soot formation process at various ignition lags by high-speed photography of the direct flame images and laser shadowgraphs as well as the laser light extinction. In the experiment, the separation of soot concentration from the soot-fuel mixture concentration was established by subtracting the laser light extinction intensity through a non-firing chamber from that through a firing chamber. It was found that the soot concentration in the swirl chamber reached a maximum value immediately after the start of combustion, and then decreased rapidly. With shorter ignition lags, the maximum and final soot concentrations in the chamber increased.

The oxidations of Crapped diesel soots containing catalytic metals such as Ca, Ba, Fe, or Ni were characterized through thermogravimetric analysis with a thermobalance. Soot particles were generated by a single cylinder IDI diesel engine with metallic fuel additives. A two-stage oxidation process was observed with the metalcontalning soots. It was found that the first stage of oxidation is catalytically promoted by metal additives resulting in an enhanced reaction rate and a reduced activation energy. Soot reduction in the rapid first stage increases with increases in metal content. Soots containing Ba and Ca are oxidized most rapidly due to the larger reduction during the first stage. The second stage of oxidation is also slightly promoted by metal addition. The ignition temperature of the collected soot is substantially reduced by the metal additives.

This paper provides information on measurements and measurement techniques for particulate and unburnt hydrocarbon emissions from diesel engines. A dilution mini-tunnel was used to characterize the effects of the dilution ratio and sample temperature on the total particulate mass and soluble organic fraction(SOF) constituents. Increasing the sample temperature resulted in changes in the polynuclear aromatic hydrocarbon(PAH) constituents in SOF. The SOF was isolated by column chromatography, and the PAH fraction was determined by high performance liquid chromatography(HPLC). Column chromatography with silicagel, an octadecylsilan-bonded column, and keeping at high temperatures improved the analytical efficiency of HPLC. The gaseous hydrocarbon in raw exhaust was analysed by GC with FID. The temperature of the sample glass syringe affected measurements of high boiling point hydrocarbon constituents.

Experiments on a large number of soluble fuel additives were systematically conducted for diesel soot reduction. It was found that Ca and Ba were the most effective soot suppressors. The main determinants of soot reduction were: the metal mol-content of the fuel, the excess air factor, and the gas turbulence in the combustion chamber. The soot reduction ratio was expressed by an exponential function of the metal mol-content in the fuel, depending on the metal but independent of the metal compound. A rise in excess air factor or gas turbulence increased the value of a coefficient in the function, resulting in larger reductions in soot with the fuel additives. High-speed soot sampling from the cylinder showed that with the metal additive, the soot concentration in the combustion chamber was substantially reduced during the whole period of combustion. It is thought that the additive acts as a catalyst not only to improve soot oxidation but also to suppress soot formation.

This paper is a systematic investigation of the effects of combustion and injection systems on hydrocarbon(HC) and particulate emissions from a DI diesel engine. Piston cavity diameter, swirl ratio, number of injection nozzle openings, and injection direction are varied as the experimental parameters, and the constituents in the soluble organic fraction (SOF) of the particulate were analyzed. The results show that the emission characteristics of deep dish chambers greatly differ from those of shallow dish chambers varying with the number of nozzle openings, the injection direction, and swirl intensity. The HC analysis shows mainly low carbon number gaseous HC constituents, and there is a tendency towards increasing polynucleation of polynuclear aromatic hydrocarbon(PAH) in SOF with increasing soot formation.