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An investigation of cyclic variability in a spark ignition engine is reported. Specifically, the predictions of an engine code have been compared with experimental data obtained using a well-characterized SI engine. The engine used for the experimental work and modeled in the code is the single cylinder research engine developed at Sandia National Laboratories and now operating at Drexel University. The data used for comparison were cylinder pressure histories for 110 engine cycles gathered during operation at a single engine operating condition. The code allows the various factors that could influence cyclic variability to be examined independently. Specifically, a model has been used to independently examine the effects of variations in equivalence ratio and of the turbulence intensity on cycle-to-cycle variations in the peak cylinder pressure, the crankangle of occurrence of peak pressure, the flame development angle, and the rapid burning angle.

It is commonly believed that running-in behavior is related to engine reliability and fuel economy. This paper uses a methodology to find the influence of running-in, based on telematics data. In this paper, the key related telematics parameters are identified to assess running-in behaviors through feature analytics with telematics vehicle real-road data. By analyzing these parameters, truck groups subjected to different running-in behaviors are classified to evaluate the relationship between running-in behaviors and fuel economy.

The effect of Di-tertiary Butyl Peroxide (DTBP) on Primary Reference Fuels (PRFs) in Homogeneous Charge Compression Ignition (HCCI) engines was investigated numerically and was compared with trends from previous experimental observations. A detailed kinetic mechanism for PRF combustion containing more than a thousand species and four thousand reactions was combined with a twenty one species, sixty-nine reaction mechanism for DTBP decomposition. This mechanism predicted the observed experimental trends reasonably well and was used to examine how DTBP addition acts to advance combustion timing and to induce hot ignition for lean and high octane number mixtures. The study suggests that DTBP's predominant mode of action for low Octane Number (ON) fuels is thermal, while for high ON fuels it is chemical. The extended kinetic model compiled for this study and the results obtained can be used to aid in the understanding and development of tailored additives for HCCI engines.

Inevitably a fraction of the hydrocarbon fuel in spark ignition engines escapes in-cylinder combustion and flows out with the burned products. Post combustion oxidation in the cylinder and exhaust port may consume a part of this fuel and plays an important role in determining exhaust emission levels. This paper presents results from experiments designed to identify the factors that control post-combustion oxidation. Regulated exhaust components and detailed hydrocarbon species were measured using seven neat hydrocarbons and four blends as fuel. The fuels were selected to compare the relative rates of mixing and chemical kinetics. The results indicate that exhaust temperature, diffusion rates and fuel kinetics each play a complicated role in determining emission levels.

This paper presents a model for the lubrication and friction between a twin land oil control ring and the liner within an engine cycle. This model is based on the deterministic method, which considers micro geometry of the liner finish and its effects on both hydrodynamic lubrication and asperity contact. In this particular application, the liner surface micro features are solely responsible for hydrodynamic pressure generation due to the flat face profile of a typical twin land oil control ring, contrasting to the traditional average model where ring surface macro geometry is most important in generating hydrodynamic pressure.

A general deterministic hydrodynamic lubrication model [1] was modified to study the interaction between a Twin Land Oil Control Ring (TLOCR) and a liner with cross-hatch liner finish. Efforts were made to customize the general model to simulate the particular sliding condition of TLOCR/liner interaction with proper boundary conditions. The results show that model is consistent, robust, and efficient. The lubricant mass conservation was justified and discussed. Then analysis was conducted on the lubricant transport between the deep grooves/valleys and plateau part of the surface to illustrate the importance of deep grooves in oil supply to the plateau part and hydrodynamic pressure generation. Furthermore, since the TLOCR land running surface is completely flat and parallel to the nominal liner axis, the liner finish micro geometry is fully responsible for the hydrodynamic pressure rise, which was found to be sufficient to support significant portion of the total ring radial load.

The role of post-combustion oxidation in influencing exhaust hydrocarbon emissions from spark ignition engines has been identified as one of the major uncertainties in hydrocarbon emissions research [l]*. While we know that post-combustion oxidation plays a significant role, the factors that control the oxidation are not well known. In order to address some of these issues a research program has been initiated at Drexel University. In preliminary studies, seven gaseous fuels: methane, ethane,ethene,propane,propene, n-butane, 1-butene and their blends were used to examine the effect of fuel structure on exhaust emissions. The results of the studies presented in an earlier paper [2] showed that the effect of fuel structure is manifested through its effect on the post-combustion environment and the associated oxidation process. A combination of factors like temperatures, fuel diffusion and reaction rates were used to examine and explain the exhaust hydrocarbon emission levels.

Time resolved exhaust port sampling results show that the gas mixture in the port at exhaust valve closing contains high concentrations of hydrocarbons. These hydrocarbons are mixed with hot in-cylinder gases during blowdown and can react either via gas phase kinetics in the exhaust port/runner system or subsequently on the exhaust catalyst before they are emitted. Studies were conducted on a single cylinder, four stroke engine in our laboratory to determine the interaction between the hot blowdown gases and the hydrocarbons which remain in the exhaust port. A preselected concentration and volume of hydrocarbon tracers (propane, propene, n-butane, and 1-butene) in either oxygen/nitrogen mixtures or pure nitrogen were injected into the exhaust port just behind the exhaust valve to control the initial conditions for any potential oxidation in the port.

Homogeneous Charge Compression Ignition (HCCI) engines have the possibility of low NOx and particulate emissions and high fuel efficiencies. In HCCI the oxidation chemistry determines the auto-ignition timing, the heat release rate, the reaction intermediates, and the ultimate products of combustion. This paper reports an initial effort to apply our reduced chemical kinetic model to HCCI processes. The model was developed to study the pre-ignition characteristics (pre-ignition heat release and start of ignition) of primary reference fuels (PRF) and includes 29 reactions and 20 active species. The only modifications to the model were to make the proscribed adjustments to the fuel specific rate constants, and to enhance the H2O2 decomposition rate to agree with published data.

In Homogeneous Charge Compression Ignition (HCCI) engines, fuel oxidation chemistry determines the auto-ignition timing, the heat release, the reaction intermediates, and the ultimate products of combustion. Therefore a model that correctly simulates fuel oxidation at these conditions would be a useful design tool. Detailed models of hydrocarbon fuel oxidation, consisting of hundreds of chemical species and thousands of reactions, when coupled with engine transport process models, require tremendous computational resources. A way to lessen the burden is to use a “skeletal” reaction model, containing only tens of species and reactions. This paper reports an initial effort to extend our skeletal chemical kinetic model of pre-ignition through the entire HCCI combustion process. The model was developed from our existing preignition model, which has 29 reactions and 20 active species, to yield a new model with 69 reactions and 45 active species.

As the intake noise is a major contributing factor to automotive passenger compartment noise levels, it has received much more attention than before. Because the plastic manifolds could induce and transmit more noise owing to their lighter weight, aerodynamic noise has become a more serious problem in plastic manifolds than in conventional aluminum-made manifolds. Due to the complexity of aerodynamic noise of the intake system, it is difficult to predict the noise precisely, especially for the part whose frequency is higher than 1000 Hz. This paper introduces a new co-simulation method to simulate the aerodynamic noise at the engine inlet. With the coupled simulation between two programs, GT-Power and Fluent, it could simulate the gas flow inside the engine intake system, under the actual running condition of engine.

The detailed chemical reactions leading to autoignition of n-pentane are investigated in this study. A single-cylinder engine operating in a nonfired mode was used. The engine is supercharged and the temperature of the inlet fuel/air mixture is varied. By increasing the inlet manifold temperature, at a given inlet manifold pressure, the fuel/air mixture can be made to undergo autoignition. In-cylinder pressure and temperature profiles were measured. Gas samples from the combustion chamber were extracted and analyzed using gas chromatography techniques. The detailed chemical reaction mechanisms explaining the products from the different stages of the fuel oxidation process are presented. It is speculated that the generation of OH radicals from the peroxide (QOOH) decomposition is responsible for the autoignition of the n-pentane fuel/air mixture.

An inhibitor package which is silicate-, nitrate-, borate- and phosphate-free has been developed as the basis for a world-wide automotive coolant formulation. The formulation contains aliphatic mono- and dicarboxylic acids and tolyltriazole as the sole inhibitors. Formulations containing carboxylic acid inhibitors have been studied in ASTM bench tests and found to sufficiently protect all prevalent cooling system metals. In addition, fleet tests have shown that carboxylic acid inhibitors deplete much more slowly than conventional inhibitors, making possible a much longer life coolant. Results from laboratory tests which simulate extended usage indicated that carboxylic acid-containing coolants have a significantly longer life span for the protection of all cooling system metals. Finally, the carboxylic acid/tolyltriazole inhibitor package is completely adaptable to a propylene glycol base.

This paper presents results of studies investigating the effect of octane enhancing ethers on the reactivity of an 87 octane mixture of primary reference fuels, 87 PRF, in a motored engine. 87 PRF was blended with small percentages of MTBE, ETBE, TAME and DIPE based on a constant gravimetric oxygen percentage in the fuel. The experiments were conducted in a modified single-cylinder Wisconsin AENL engine at compression ratios of 5.2 and 8.2. Supercharging and heating of the intake charge were used to control reactivity. The inlet gas temperature was increased from 320 K, where no reactivity occurred, until either autoignition occurred or the maximum temperature of the facility was reached. Exhaust carbon monoxide levels and in-cylinder pressure histories were monitored in order to determine and quantify reactivity.

High lead solder coupons are frequently tested in ASTM D 1384-87 and D 2570-91 tests to determine the corrosion protection provided by engine coolants. In contrast to 70/30 solder, high lead solder is often observed to show relatively high corrosion rates in D 1384-87 testing. Surprisingly, the high lead solder corrosion rates tend to be lower in the D 2570-91 test, despite the longer duration of this test. The basis of this effect has been investigated in different coolant formulations and in both ethylene glycol and propylene glycol. The corrosion of high lead solder was found to be directly related to the presence of oxygen in the D 1384-87 test. Replacement of the air purge with a nitrogen purge significantly reduced the corrosion rate of high lead solder in inhibited coolants. These results are interpreted in terms of the solder composition.

The effect of small amounts of silicate on coolant performance has been studied. The corrosion protection provided by different coolant technologies was evaluated for different silicate contents. This work includes results from electrochemical tests and static and dynamic heat-rejecting tests on aluminum surfaces. The results indicate that small amounts of silicate have a negative effect on the corrosion protection of aluminum. Depletion of silicates can therefor be expected to affect aluminum heat-rejecting surfaces. The use of carboxylic acid corrosion inhibitors can overcome this problem.

Automobile coolant pump failure rates have been observed to be influenced by the coolant inhibitor package. A fleet test consisting of 196 1991 Ford Crown Victoria taxi cabs was utilized to test six coolant formulations. Four of the test formulations were monobasic/dibasic organic acid technology coolants and two were traditional technology coolants containing nitrate, phosphate, and silicate. Coolant pump failure rates were monitored as a function of mileage. Results indicate that the service life of coolant pumps for those systems employing organic acid technology coolants was significantly greater than those systems utilizing traditional inhibitor technology coolants.

Mixtures of a novel corrosion inhibitor, based on the synergistic combination of aliphatic mono- and dibasic acids with a traditional coolant have been evaluated in: a stability test an electrochemical test the ASTM D 1384 Glassware Corrosion Test the ASTM D 4340 Aluminum Heat-Rejection Test a Dynamic Heat-Transfer Test. This paper discusses the results of these tests and the relevance of the tests in assessing the performance of the coolant mixtures. Recommendations are made to the selection of methods that provide significant information on coolant compatibility.

Autoignition chemistry of n-heptane, iso-octane and an 87 octane blend, 87 PRF, was studied in a single-cylinder modified Wisconsin model AENL engine under motored conditions. Use of a fast-acting sampling valve and gas chromatographic analysis allowed measurement of in-cylinder gas composition during the ignition process. Crank angle resolved species evolution profiles were generated for all three fuels at a fixed inlet temperature of 376 K. For n-heptane, the measurements were made during a cyclically repeatable two stage ignition process up to the point of hot ignition (the second stage ignition). These n-heptane experiments were run at ø = 0.3 to avoid excessive pressure rise at hot ignition which might damage our engine. iso-Octane and 87 PRF were run at stoichiometric equivalence ratio which did not have a second stage ignition, and species were measured only during the first stage of ignition.

Coolant formulations based on organic acid corrosion inhibitor technology have been tested in over 180 heavy duty engines for a total of more than 50 million kilometers. This testing has been used to document long life coolant performance in various engine types from four major engine manufacturers. Inspections of engines using organic acid based coolant (with no supplemental coolant additive) for up to 610,000 kilometers showed excellent protection of metal engine components. Improved protection was observed against cylinder liner, water pump, and aluminum spacer deck corrosion. In addition, data accumulated from this testing were used to develop depletion rate curves for long life coolant corrosion inhibitors, including tolyltriazole and nitrite. Nitrite was observed to deplete less rapidly in long life coolants than in conventional formulations.