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Engine-out HC emissions from a PFI spark ignition engine were measured using a gas chromatograph and a flame ionization detector (FID). Two port fuel injectors were used respectively for ethanol and gasoline so that the delivered fuel was comprised of 0, 25, 50, 75 and 100% (by volume) of ethanol. Tests were run at 1.5, 3.8 and 7.5 bar NIMEP and two speeds (1500 and 2500 rpm). The main species identified with pure gasoline were partial reaction products (e.g. methane and ethyne) and aromatics, whereas with ethanol/gasoline mixtures, substantial amounts of ethanol and acetaldehyde were detected. Indeed, using pure ethanol, 74% of total HC moles were oxygenates. In addition, the molar ratio of ethanol to acetaldehyde was determined to be 5.5 to 1. The amount (as mole fraction of total HC moles) of exhaust aromatics decreased linearly with increasing ethanol in the fuel, while oxygenate species correspondingly increased.

Global ethanol trade is forecast to increase 25-fold by 2020. Most of it will be blended with gasoline to make biofuel. However, blending ethanol with gasoline has a profound effect on the evaporation characteristics of the mixture. In particular, the thermodynamic properties of the blends can be significantly different than the constituents. A clear understanding of the blend's properties is essential for optimizing engine design, e.g. utilizing charge cooling effect. Data available in the literature is very limited, considering ethanol-gasoline blends will be used as a fuel in large scale worldwide. In this work, comprehensive measurements of vapor pressures were carried out. The enthalpies of vaporization were derived from vapor pressure data using the Clausius-Clapeyron equation. Maximum vapor pressure occurs with 20% ethanol-gasoline blend at which a positive azeotrope is formed. The trend is different in enthalpy of vaporization.

The engine out particular matter number (PN) distributions at engine coolant temperature (ECT) of 0° C to 40° C for ethanol/ gasoline blends (E0 to E85) have been measured for a direct-injection spark ignition engine under cold fast idle condition. For E10 to E85, PN increases modestly when the ECT is lowered. The distributions, however, are insensitive to the ethanol content of the fuel. The PN for E0 is substantially higher than the gasohol fuels at ECT below 20° C. The total PN values (obtained from integrating the PN distribution from 15 to 350 run) are approximately the same for all fuels (E0 to E85) when ECT is above 20° C. When ECT is decreased below 20° C, the total PN values for E10 to E85 increase modestly, and they are insensitive to the ethanol content. For E0, however, the total PN increases substantially. This sharp change in PN from E0 to E10 is confirmed by running the tests with E2.5 and E5. The midpoint of the transition occurs at approximately E5.

The blending of oxygenated compounds with gasoline is projected to increase because oxygenate fuels can be produced renewably, and because their high octane rating allows them to be used in substitution of the aromatic fraction in gasoline. Blending oxygenates with gasoline changes the fuels' properties and can have a profound affect on the distillation curve, both of which are known to affect engine-out emissions. In this work, the effect of blending methanol and ethanol with gasoline on unburned hydrocarbon and particulate emissions is experimentally determined in a spray guided direct injection engine. Particulate number concentration and size distribution were measured using a Cambustion DMS500. These data are presented for different air fuel ratios, loads, ignition timings and injection timings. In addition, the ASTM D86 distillation curve was modeled using the binary activity coefficients method for the fuel blends used in the experiments.

Ethanol and acetaldehyde emissions from a direct ignition spark ignition were measured using mass spectrometry. Previous methods focused on eliminating or minimizing interference from exhaust species with identical atomic mass and fragment ions created in ionization process. This paper describes a new technique which exploits the fragment ions from ethanol and acetaldehyde. A survey of mass spectra of all major species of exhaust gas was conducted. It was found that ethanol contributes most ions in mass number 31 and that no other gas species produces ions at this mass number. Acetaldehyde detection suffers more interference. Nevertheless, it was estimated that detection at mass number 43 is possible with 10% error from 2-methylbutane. This new technique was validated in an engine experiment. By running the engine with pure gasoline and E85, the validity of the technique can be checked.

Exhaust gas temperatures in a 1.4 L, sparked ignition engine have been measured using fine wire thermocouples at different loads and speeds. However the thermocouples are not fast enough to resolve the rapid change in exhaust temperature. This paper discusses a new thermocouple compensation technique to resolve the cycle-by-cycle variations in exhaust temperature by segmentation. Simulation results show that the technique can find the lower time constants during blowdown, reducing the bias from 28 to 4%. Several estimators and model structures have been compared. The best one is the difference equation-least squares technique, which has the combined error between -4.4 to 7.6% at 60 dB signal-to-noise ratio. The compensated temperatures have been compared against combustion parameters on a cycle-by-cycle basis. The results show that the cycle-by-cycle variations of the exhaust temperatures and combustion are correlated.

Factors affecting the pressure rise rate, and consequently the high-load limit, in the sequential ignition of a homogeneous charge in a temperature gradient have been identified. The pressure rise rate decreases with an increase in the magnitude of the temperature gradient and an increase in the sensitivity of the constant volume ignition delay time to temperature. It increases with an increase in the intrinsic reaction rate (i.e., the reaction rate for a charge of uniform composition and temperature). Since the ignition delay time and the intrinsic reaction rate are directly related to fuel properties, the high-load limit is sensitive to fuel selection. The above three factors are used to explain the high-load limit obtained from a knock limited Controlled Auto-Ignition (CAI) engine with a homogeneous charge operating with three different fuels. The fuel comparisons are made with the engine operating at the same combustion phasing.

The NOx emission and knock characteristics of a PFI engine operating on ethanol/gasoline mixtures were assessed at 1500 and 2000 rpm with λ =1 under Wide-Open-Throttle condition. There was no significant charge cooling due to fuel evaporation. The decrease in NOx emission and exhaust temperature could be explained by the change in adiabatic flame temperature of the mixture. The fuel knock resistance improved significantly with the gasohol so that ignition could be timed at a value much closer or at MBT timing. Changing from 0% to 100% ethanol in the fuel, this combustion phasing improvement led to a 20% increase in NIMEP and 8 percentage points in fuel conversion efficiency at 1500 rpm. At 2000 rpm, where knocking was less severe, the improvement was about half (10% increase in NIMEP and 4 percentage points in fuel conversion efficiency).