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A novel engine management strategy for achieving fast catalyst light-off without the use of an exhaust air pump in a port-fuel-injected, spark ignition engine was developed. A conventional 4-cylinder engine was operated with three cylinders running rich and the fourth one as an air pump to supply air to the exhaust manifold. Under steady-state cold coolant conditions, this strategy achieved near total oxidation of CO and HC with sufficiently retarded spark timing, resulting in a 400% increase in feedgas enthalpy flow and a 90% reduction in feedgas HC emissions compared to conventional operation. The strategy was also evaluated for crank starts. Using the existing engine hardware, implementing the strategy resulted in a reduction in catalyst light-off time from 28.0 seconds under conventional operation to 9.1 seconds.

The interaction of intake port gas flow with the fuel spray in a port-fuel-injection engine is studied to see whether there are opportunities to facilitate the mixture preparation process and to improve the HC emissions through this interaction. The operating regime of interest is the fast idle period in a cold start. For single pulse injection, the HC emissions were not sensitive to injection details for closed-valve injection; emissions increased with open-valve injection. Then a split injection strategy was used in which the fuel was divided into two pulses. The first pulse was delivered during valve-closed; the second pulse was injected in the back flow period. Under cold-valve conditions, a small benefit (compared to close valve injection) was obtained with a second pulse fuel of 25%: 6% decrease in Specific HC emissions and 4.5% increase in the fuel delivery fraction.

A strategy to facilitate the mixture preparation process in PFI engines is to delay the Intake Valve Opening (IVO) by shifting the cam phasing so that the cylinder pressure is sub-atmospheric when the valve opens. The physics of the effect are discussed in terms of the pressure differential between the manifold and the cylinder, and the resulting flow and charge temperature history. The effect was evaluated by measuring the equivalence ratio of the trapped charge and the exhaust HC emissions in the first cycle of cranking in a 2.4L engine. When the IVO timing was changed from 18° BTDC to 21° ATDC, the in-cylinder fuel equivalence ratio increased by approximately 10%. This increase was attributed mainly to the enrichment of the charge by displacing the leaner mixture at the top of the cylinder in the period between BDC and IVC. The exhaust HC, however, increased by 40%. No conclusive explanation was established for this increase in HC emissions.

The catalyst oxygen storage capacities were measured over a test matrix consisted of fuels with 7, 33, 266 and 500 ppm sulfur, and of dynamometer-aged catalysts simulating 4K, 50K and 150K vehicle miles. A methodology was developed to relate the post-catalyst λ sensor response following an engine lean-step-transient to the total oxygen storage sites available. The time resolved NOx concentration profiles (which were most sensitive to the oxygen storage) in the catalyst were measured with the engine operating at λ modulations of various amplitudes and frequencies. The oxygen storage capacity deterioration comprised two multiplicative factors - an age factor which decreased quickly initially (by a factor of 2 from 4K to 50K miles), and then more modestly (by 30% from 50 to 150K miles), and a fuel sulfur factor which decreased by 10% for every 150 ppm increase in sulfur level.

Engine Hydrocarbon (HC) emissions behaviors in the shut down and re-start processes were examined in a production 4-cylinder 2.4 L engine. Depending on when the power to the ECU was cut off relative to the engine events, there could be two or three mis-fired cylinders (i.e. cylinders with fuel injected but no ignition). The total HC pumped out by the engine into the catalyst in the stopping process was ∼ 4 mg (approximately equaled to the amount of one injection at idle condition). Because the size of the catalyst was larger than the total exhaust volume in the stopping process, this HC was not observed at the catalyst exit. The catalyst temperature was also not affected. When the engine was purged after shut down (by cranking the engine with the injectors and ignition disconnected), the total exit HC was 33 mg. In a restart 90 minutes after shut down, the integrated amount of HC emissions due to residual fuel from the stopping process was 16 mg.

The mixture preparation and hydrocarbon (HC) emissions behaviors for a single-cylinder port-fuel-injection SI engine were examined in an engine/dynamometer set up that simulated the first cycle of cranking. The engine was motored continuously at a fixed low speed with the ignition on, and fuel was injected every 8 cycles. Unlike the real engine cranking process, the set up provided a well controlled and repeatable environment to study the cranking process. The parameters were the Engine Coolant Temperature (ECT), speed, and the fuel injection pulse width. The in-cylinder and exhaust HC were measured simultaneously with two Fast-response Flame Ionization Detectors. A large amount of injected fuel (an order of magnitude larger than the normal amount that would produce a stoichiometric mixture in a warm-up engine) was required to form a combustible mixture at low temperatures.

The purpose of this work was to develop an understanding of how liquid fuel transported into the cylinder of a port-fuel-injected gasoline-fueled SI engine contributes to hydrocarbon (HC) emissions. To simulate the liquid fuel flow from the valve seat region into the cylinder, a specially designed fuel probe was developed and used to inject controlled amounts of liquid fuel onto the port wall close to the valve seat. By operating the engine on pre-vaporized Indolene, and injecting a small amount of liquid fuel close to the valve seat while the intake valve was open, we examined the effects of liquid fuel entering the cylinder at different circumferential locations around the valve seat. Similar experiments were also carried out with closed valve injection of liquid fuel at the valve seat to assess the effects of residual blowback, and of evaporation from the intake valve and port surfaces.

A cycle by cycle analysis of engine behavior during the first few cycles of cranking and start-up was performed on a production four-cylinder engine. Experiments were performed to elucidate the effects of initial engine position (rest position after last engine shut-down), first and second cycle fueling, engine temperature, and spark timing on fuel delivery to the cylinder, engine-out Hydrocarbon (EOHC) emissions, and Gross Indicated Mean Effective Pressure (IMEPg). The most important effect of the piston starting position is on the first firing cycle engine rpm, which influences the IMEPg through combustion phasing. Because of the low rpm values for the first cycle, combustion is usually too advanced with typical production engine ignition timing. For both the hot start and the ambient start, the threshold for firing is at an in-cylinder air equivalence ratio (λ) of 1.1.

This paper describes the development of a spark ignition engine operating in a stratified-EGR mode at part load. The concept is to reduce the pumping loss with high levels of EGR while maintaining stable combustion via charge stratification. Since the engine operates stoichiometrically, the ability to control NOx emissions by the three-way catalyst is retained. The configuration of introducing the stoichiometric fresh mixture to the center portion of the combustion chamber with the EGR gas on the two sides is visualized in a transparent engine using planar laser-induced fluorescence (PLIF) and Mie scattering. Visualization results showed that the stratification between air/fuel mixture and EGR gas was relatively well established during the intake stroke. There was, however, significant mixing in the late part of the compression stroke.

A research program designed to measure the contribution from fuel absorption in the thin layer of oil, lubricating the cylinder liner, to the total and speciated HC emissions from a spark ignition engine has been performed. The logic of the experiment design was to test the oil layer mechanism via variations in the oil layer thickness (through the lubricant formulations), solubility of the fuel components in the lubricants, and variations in the crankcase gas phase HC concentration (through crankcase purging). A set of preliminary experiments were carried out to determine the solubility and diffusivity of the fuel components in the individual lubricants. Engine tests showed similar HC emissions among the tested lubricants. No consistent increase was observed with oil viscosity (oil film thickness), contrary to what would be expected if fuel-oil absorption was contributing significantly to engine-out HC. Similarly, no effect of crankcase purging could be observed.

A sampling system was developed to measure the evolution of the speciated hydrocarbon emissions from a single-cylinder SI engine in a simulated starting and warm-up procedure. A sequence of exhaust samples was drawn and stored for gas chromatograph analysis. The individual sampling aperture was set at 0.13 s which corresponds to ∼ 1 cycle at 900 rpm. The positions of the apertures (in time) were controlled by a computer and were spaced appropriately to capture the warm-up process. The time resolution was of the order of 1 to 2 cycles (at 900 rpm). Results for four different fuels are reported: n-pentane/iso-octane mixture at volume ratio of 20/80 to study the effect of a light fuel component in the mixture; n-decane/iso-octane mixture at 10/90 to study the effect of a heavy fuel component in the mixture; m-xylene and iso-octane at 25/75 to study the effect of an aromatics in the mixture; and a calibration gasoline.

The effect of engine operating parameters (speed, spark timing, and fuel-air equivalence ratio [Φ]) on hydrocarbon (HC) oxidation within the cylinder and exhaust system is examined using propane or isooctane fuel. Quench gas (CO2) is introduced at two locations in the exhaust system (exhaust valve or port exit) to stop the oxidation process. Increasing the speed from 1500 to 2500 RPM at MBT spark timing decreases the total, cylinder-exit HC emissions by ∼50% while oxidation in the exhaust system remains at 40% for both fuels. For propane fuel at 1500 rpm, increasing Φ from 0.9 (fuel lean) to 1.1 (fuel rich) reduces oxidation in the exhaust system from 42% to 26%; at 2500 RPM, exhaust system oxidation decreases from 40% to approximately 0% for Φ = 0.9 and 1.1, respectively. Retarded spark increases oxidation in the cylinder and exhaust system for both fuels. Decreases in total HC emissions are accompanied by increased olefinic content and atmospheric reactivity.

The oxidation chemistry of paraffins, aromatics, olefins and MTBE were examined. Detailed chemical kinetics calculations were carried out for oxidation of these compounds in the engine cycle. The oxidation rates are very sensitive to temperature. At temperatures of over 1400 K (depending on the fuel), all the hydrocarbons are essentially oxidized for typical residence time in the engine. Based on the kinetics calculations, a threshold temperature is defined for the conversion of the fuel species to CO, CO2, H2O and partially oxidized products. The difference in the survival fraction between aromatics and non-aromatics is attributed to the higher threshold temperature of the aromatics.

The engine-out (EO) total and speciated hydrocarbon emissions data from the Auto-Oil Program Phase II Heavy Hydrocarbon Study had been analyzed. The methodology was to first investigate the stabilized EO emissions (Bag 2) of a specific vehicle (Vehicle 04B, a 1989 Model Year Ford Taurus); then the vehicle-to-vehicle differences in Bag2 emissions were considered. Finally, the differences in the Bag2 and the starting/warm-up EO emissions (Bag1) were examined. The speciated emissions may be interpreted as a “feed-through” part due to the unreacted fuel species, and an “offset” part due to the decomposition products. The significant non-fuel emitted species were methane and the olefins. The HC emissions for vehicles with different total emissions were similar in species composition. For both the total and speciated emissions, there was no substantial difference between the Bag1 and Bag2 values for Vehicle 04B.

A fuel volatility model based on the major species present in the fuel has been formulated. The model accurately predicts the ASTM distillation curves and Reid Vapor Pressure for hydrocarbon fuels. The model may be used to assess the fuel effects on the extent of evaporation and the vapor composition in the mixture preparation process.

To understand the effects of crevices on the engine-out hydrocarbon emissions, a series of engine experiments was carried out with different piston crevice volumes and with simulated head gasket crevices. The engine-out HC level was found to be modestly sensitive to the piston crevice size in both the warmed-up and the cold engines, but more sensitive to the crevice volume in the head gasket region. A substantial decrease in HC in the cold-to-warm-up engine transition was observed and is attributed mostly to the change in port oxidation.

This paper provides an overview of spark-ignition engine unburned hydrocarbon emissions mechanisms, and then uses this framework to relate measured engine-out hydrocarbon emission levels to the processes within the engine from which they result. Typically, spark-ignition engine-out HC levels are 1.5 to 2 percent of the gasoline fuel flow into the engine; about half this amount is unburned fuel and half is partially reacted fuel components. The different mechanisms by which hydrocarbons in the gasoline escape burning during the normal engine combustion process are described and approximately quantified. The in-cylinder oxidation of these HC during the expansion and exhaust processes, the fraction which exit the cylinder, and the fraction oxidized in the exhaust port and manifold are also estimated.

When gas sample is continuously drawn from the cylinder of an internal combustion engine, the sample that appears at the end of the sampling system corresponds to the in-cylinder content sometime ago because of the finite transit time which is a function of the cylinder pressure history. This variable delay causes a dispersion of the sample signal and makes the interpretation of the signal difficult An unsteady flow analysis of a typical sampling system was carried out for selected engine loads and speeds. For typical engine operation, a window in which the delay is approximately constant may be found. This window gets smaller with increase in engine speed, with decrease in load, and with the increase in exit pressure of the sampling system.