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Ethanol, used widely as a spark-ignition (SI) engine fuel, has seen minimal success as a compression ignition (CI) engine fuel. The lack of success of ethanol in CI engines is mainly due to ethanol's very low cetane number and its poor lubricity properties. Past researchers have utilized nearly pure ethanol in a CI engine by either increasing the compression ratio which requires extensive engine modification and/or using an expensive ignition improver. The objective of this work was to demonstrate the ability of a hydrogen port fuel injection (PFI) system to facilitate the combustion of ethanol in a CI engine. Non-denatured anhydrous ethanol, mixed with a lubricity additive, was used in a variable compression ratio CI engine. Testing was conducted by varying the amount of bottled hydrogen gas injected into the intake manifold via a PFI system. The hydrogen flowrates were varied from 0 - 10 slpm.

A 1.9 liter Volkswagen TDI engine has been modified to accomodate the addition of hydrogen into the intake manifold via timed port fuel injection. Engine out particulate matter and the emissions of oxides of nitrogen were investigated. Two fuels,low sulfur diesel fuel (BP50) and soy methyl ester (SME) biodiesel (B99), were tested with supplemental hydrogen fueling. Three test conditions were selected to represent a range of engine operating modes. The tests were executed at 20, 40, and 60 % rated load with a constant engine speed o 1700 RPM. At each test condition the percentage of power from hydrogen energy was varied from 0 to 40 %. This corresponds to hydrogen flow rates ranging from 7 to 85 liters per minute. Particulate matter (PM) emissions were measured using a scaning mobility particle sizer (SMPS) and a two stage micro dilution system. Oxides of nitrogen were also monitored.

Earlier work [1] shows that kinetics of Diesel soot oxidation is different from that of ethylene diffusion flame soot oxidation [2], possibly due to metals from lube oil. This study investigates the influence of metals on soot oxidation and the exhaust particle emissions using lube oil dosed fuel (2 % by volume). This method does not simulate normal lube oil consumption, but is used as a means of adding metals to particles for oxidation studies. This study also provides insight into the effect of systems that mix lube oil with fuel to minimize oil change service. The HTO-TDMA (High Temperature Oxidation-Tandem Differential Mobility Analyzer) technique [1] was used to measure the surface specific oxidation rate of Diesel particles over the temperature range 500-750 °C. Diesel particles sampled from the exhaust stream of a Diesel engine were size segregated by differential mobility and oxidized in situ in air in a heated flow tube of known residence time and temperature profile.

Diesel exhaust particle number concentrations and size distributions, as well as gaseous and particulate mass emissions, were measured during steady-state tests on a US heavy-duty engine and a European passenger car engine. Two fuels were compared, namely a Fischer-Tropsch diesel fuel manufactured from natural gas, and a US D2 on-highway diesel fuel. With both engines, the Fischer-Tropsch fuel showed a considerable reduction in the number of particles formed by nucleation, when compared with the D2 fuel. At most test modes, particle number emissions were dominated by nucleation mode particles. Consequently, there were generally large reductions (up to 93%) in the total particle number emissions with the Fischer-Tropsch fuel. It is thought that the most probable cause for the reduction in nucleation mode particles is the negligible sulphur content of the Fischer-Tropsch fuel. In general, there were also reductions in all the regulated emissions with the Fischer-Tropsch fuel.

Experiments were performed to measure the number-weighted particle size distributions emitted from a gasoline direct injection (GDI) engine. Measurements were made on a late model vehicle equipped with a direct injection spark ignition engine. The vehicle was placed on a chassis dynamometer, which was used to load the engine to road load at five different vehicle speeds ranging from 15 - 100 km/hr. Dilution of the exhaust aerosol was carried out using a two-stage dilution system in which the first stage dilution occurs as a free jet. Particle size distributions were measured using a TSI 3934 scanning mobility particle sizer. Generally speaking, the presence of the additives did not have a strong, consistent influence on the particle emissions from this engine. The polyether amine demonstrated a reduction in particle number concentration as compared to unadditized base fuel.

Two types of in-cylinder optical probes were applied to a single cylinder CFR engine to detect knocking combustion. The first probe was integrated directly into the engine spark plug to monitor the radiation from burned gas in the combustion process. The second was built into a steel body and installed near the end gas region of the combustion chamber. It measured the radiant emission from the end gas in which knock originates. The measurements were centered in the near infrared region because thermal radiation from the combustion products was believed to be the main source of radiation from a spark ignition engine. As a result, ordinary photo detectors can be applied to the system to reduce its cost and complexity. It was found that the measured luminous intensity was strongly dependent upon the location of the optical sensor.

This report describes tests of a fuel additive in a medium-duty, high-swirl, direct-injection diesel engine. The additive was found to have little influence on general combustion performance or on NOx emissions. On the other hand, it had a profound effect on particulate emissions. This was most clear under high load where particle emissions are highest. Here, when the engine was switched from running on the base fuel to the additive treated fuel, particle emissions at first increased and then fell to levels about 40% lower (by particle volume) than those initially produced by the base fuel. The additive had a long lasting effect. After running with the additive for about 25 hours, emission levels with the base fuel were only slightly higher than those with the additive treated fuel. We believe that the additive action is associated with a combination of cleaning and surface conditioning. More work should be done to understand the relative importance of these two mechanisms.

Carbon black particles, which morphologically and chemically simulate a diesel exhaust soot, were mixed with the intake air of a single-cylinder direct injection diesel engine to investigate the efficiency of their removal by oxidation in the combustion chamber. An aerosol generation system, which is capable of generating carbon black aerosol of a size distribution and mass flow rate comparable to those of the soot agglomerates, was developed first. The aerosol was then introduced into the engine which was operating on conventional fuel. Four methods were used to characterize the exhaust particles: an electrical aerosol analyzer, a condensation nuclei counter, a low volume filter, and a micro-orifice cascade impactor. The size distribution and concentration of the diesel soot particles in the lubricants were investigated by methods of photosedimentation and quantitative spectrophotometry, respectively.

Soot is the largest component of contaminants found in the diesel engine lubricating oil. The soot enters lubricating oil mainly through thermophoretic deposition on the cylinder wall. Although the mechanism is still not fully understood, it is generally accepted that soot particles promote engine wear, reducing engine component service life, fuel efficiency and performance. This problem will be further exacerbated when more and more diesel engines use EGR to reduce NOx emissions and when lubricating oil consumption is drastically reduced to control particulate emissions. In this study, lubricating oil samples were taken from 7 different operating diesel engines. The size distribution and concentration of the diesel soot particles in the lubricants were investigated by methods of photosedimentation and quantitative spectrophotometry. The size distributions were compared to those of soot particles in the exhaust.

An adaptive control system which determines the optimum system parameters based on the engine response to changes in those parameters, has been tested as an ignition timing control system on several gaseous fueled engines. The changes in the MBT timing for speed, load, air-fuel ratio, and fuel type were explored. The ability of the control system to correct the timing for these parameters was demonstrated. An air-fuel ratio control based on the same technique is also discussed.

This study examines the effect of a ceramic particle trap and a manganese fuel additive on the mutagenic activity and chemical composition of diesel exhaust particulate matter from a heavy-duty mining engine. Particles were collected by dilution tunnel sampling from a 4-cylinder, Caterpillar 3304, naturally-aspirated, indirect-injection engine operated at six steady-state conditions. Depending on engine load and speed the ceramic particle trap reduced the following emissions: particulate matter, 80 – 94%; soluble organic fraction (SOF), 83 – 95%; 1-nitropyrene, 94 – 96%; and SOF mutagencity, 72% (cycle-weighted average). When the Mn fuel additive was used without a ceramic particle trap the total cycle mutagenic activity emitted increased 7-fold, in part, due to elevated emissions of 1-nitropyrene.

Particle mass and size distribution measurements have been made on the exhaust of an Onan prechamber diesel engine. Seven fuels were examined: no. 1 and no. 2 diesel fuel, 40 and 50 cetane number secondary reference fuels, and no. 2 diesel fuel doped with three different concentrations of Lubrizol 565, a barium-based smoke suppressant. The no. 1 and no. 2 diesel fuels and the 50 cetane number reference fuels produced very similar emissions with emission indices in the range 0.3-1.3 mg (gm-fuel)-1 and volume mean diameters between .09 and 0.15 μm. The 40 cetane number reference fuel produced both smaller emission indices, 0.2 to 0.8 mg (gm-fuel)-1, and particle diameters, 0.03 to 0.09 μm. These reductions were apparently related to the longer ignition delay period of the 40 cetane number fuel, which allowed better mixing of the fuel and air prior to combustion.

This paper describes the performance and emissions of a hydrogen-fueled, spark-ignited engine. An electronic control device, designed to provide the engine with a timed injection of the fuel, is shown to give high mean effective pressures and high efficiencies. The oxides of nitrogen from the exhaust gases have been analyzed and the mechanism for their formation is reviewed. The paper further describes an experiment with traces of hydrocarbons added to the hydrogen in an attempt to explain any additional phenomena that may be taking place during the combustion, such as “prompt NO” which is known to occur in hydrocarbon flames only. As it turns out, such additions have a negligible effect on the NOx formation in the region investigated.