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The generally accepted explanation of autoignition in engines is that the reactivity is driven by temperature, where autoignition occurs after the mixture has reached some critical temperature (approx. 1000 K) by a combination of self-heating due to preignition reactions and compression heating due to piston motion and flame propagation. During the course of our investigations into autoignition processes and homogeneous charge compression ignition we have observed some ignitions that begin at much lower temperature (< 550 K). In this paper we describe these observations, our attempts to investigate their origins, and an alternative explanation that proposes that traditional models may be missing the chemistry that explains this behavior. Finally, applications of lower temperature chemical reactions are discussed.

The interaction of turbocharger characteristics with engine design and performance parameters is presented. Turbocharger matching requires a compromise among the following variables: combustion air-fuel ratio, turbocharger characteristics, peak cylinder pressures, engine speed range capability, transient response, and overall package efficiency. The mechanisms of interactions of the above variables are reviewed to highlight the turbocharged engine designers problems. The impact of turbocharger performance limits on overall engine characteristics is reviewed with special attention focused on what limitations point out as the turbomachinery designers' job for the future.

Recently, studies were conducted on a single cylinder, four stroke engine to investigate the effect of temperature and local mixedness on exhaust port hydrocarbon oxidation. To examine the effect of temperature, hydrocarbon tracers (propane, propene, 1-butene, n-butane, and n-pentane) were individually injected into the exhaust port just behind the exhaust valve for operating conditions that provided different exhaust port temperatures. For the local mixedness experiments, tracer mixtures (propane + n-butane, 1-butene + n-butane, propene + n-butane) were injected into the exhaust port just behind either a normal exhaust valve or a shrouded exhaust valve. The concentration of tracers and their reaction products were measured using gas chromatography of samples withdrawn from the exhaust stream. The tracer consumption behavior with changing port temperature confirmed that there is a minimum port temperature for hydrocarbon oxidation.

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.

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.

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.

This experimental study was conducted in a motored research engine to investigate the effect of blending methanol and ethanol on hydrocarbon oxidation and autoignition. An 87 octane mixture of primary reference fuels, 87 PRF, was blended with small percentages of the alcohols to yield a constant gravimetric oxygen percentage in the fuel. The stoichiometric fuel mixtures and neat methanol and ethanol were tested in a modified single-cylinder engine at a compression ratio of 8.2. Supercharging and heating of the intake charge were used to control reactivity. The inlet gas temperature was increased from 325 K to the point of autoignition or the maximum achievable temperature of 500 K. Exhaust carbon monoxide levels and in-cylinder pressure histories were monitored in order to determine and quantify reactivity.

The potential for catalytically enhanced ignition in low-heat rejection Diesel engines has been experimentally studied under engine simulated conditions in a high pressure chemical flow reactor. Results are presented for propane oxidation on platinum at 6 and 10 atmospheres, at temperatures from 800K to 1050K, and at equivalence ratios from 0.5 to 4.0. For turbulent transport rates which are typical of those in an engine, as much as 20% of the fuel was found to react on the catalyst before the onset of the gas-phase ignition reactions. Depending on the adiabaticity of the combustion chamber walls, this could lead to significant thermal enhancement of the gas-phase ignition process. Evidence of chemical enhancement was also observed, at 10 atm under very fuel rich conditions, in terms of a change in the concentration and distribution of the hydrocarbon intermediate species. Possible mechanisms for the observed chemical enhancement due to surface generated species are discussed.

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.

NOx and soot emissions remain critical issues in diesel engines. One method to address these problems is to achieve homogeneous combustion at lower peak temperatures - the goal of research on controlled autoignition. In this paper n-heptane is used to represent a large hydrocarbon fuel and some of the effects of internal and external EGR, oxygen concentration, and engine speed on its combustion have been examined through simulation and experiment. Simulations were conducted using our existing skeletal chemical kinetic model, which combines the chemistry of the low, intermediate, and high temperature regimes. Experiments were carried out in a single cylinder, four-stroke, air cooled engine and a single cylinder, two stroke, water cooled engine. In the four-stroke engine experiments the effects of EGR were examined using heated N2 addition as a surrogate for external EGR and engine modifications to increase internal EGR.

The application of planar laser-induced Rayleigh scattering for quantitative 2-D measurements of vapor-phase fuel concentration in the main combustion zone of a direct-injection Diesel engine has been explored, developed and demonstrated. All studies were conducted in an optically accessible direct-injection Diesel engine of the “heavy-duty” size class at 1200 rpm and motored TDC conditions which were typical of the production version of this engine. First, this study verifies that beyond 27 mm from the injector all the fuel is vapor phase. This was done by investigating the Diesel jet under high magnification using 2-D elastic scatter imaging and subsequently evaluating the signal intensities from the droplets and other interfering particles (Mie scattering) and the vapor (Rayleigh scattering).

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.

Recently, we reported the development of a new reduced chemical kinetic model for predicting reactivity and autoignition behavior of primary reference fuels in a motored research engine. The predicted oxidation behavior (ignition delay, preignition heat release, and evolution of key chemical species) is in fairly good agreement with experiments. In addition, the model reproduced the experimentally observed dependence of overall reactivity on charge density and manifold inlet conditions. This paper reports our initial effort to apply this new reduced chemical kinetic model to other fuels. Specifically, the model was tested using neat n-butane and n-butane/iso-butane blends (10, 20, and 48 percent by volume iso-butane) under skip fired conditions. The only adjustments made in the model were to the fuel specific rate parameters of the RO2· isomerization reaction, the reaction of aldehydes with OH·, and the reaction forming cyclic ethers.

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.

This work investigates the potential of in-cylinder thermal stratification for reducing the pressure-rise rate in HCCI engines, and the coupling between thermal stratification and combustion-phasing retard. A combination of computational and experimental results is employed. The computations were conducted using both a custom multi-zone version and the standard single-zone version of the Senkin application of the CHEMKIN III kinetics-rate code, and kinetic mechanisms for iso-octane. This study shows that the potential for extending the high-load operating limit by adjusting the thermal stratification is very large. With appropriate stratification, even a stoichiometric charge can be combusted with low pressure-rise rates, giving an output of 16 bar IMEPg for naturally aspirated operation. For more typical HCCI fueling rates (ϕ = 0.38 - 0.45), the optimal charge-temperature distribution is found to depend on both the amount of fuel and the combustion phasing.

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.

Enhancement of methanol combustion in a direct injected Diesel engine using catalytically coated glow plugs was examined for platinum and palladium catalysts and compared to a non-catalytic baseline case. Experiments were performed for 6 and 10 brake Kilowatts (bKW) at 2500 rpm. Comparisons were made based on combustion, performance, and emissions including carbon monoxide (CO), oxides of nitrogen (NOx), unburned hydrocarbons (UHC), unburned methanol (UBM), and aldehydes. Results show a decrease in glow plug temperature of 100 K is achievable using platinum catalysts, and 150 K for palladium. Furthermore, the palladium catalyst was found to provide better combustion characteristics than the platinum catalyst. Also, the use of both catalysts produced lower aldehyde emissions, and the palladium reduced NOx emissions as well. However, unburned methanol increased for both catalytic glow plugs with respect to the non-catalytic case.

Empirical and analytical data on the minimum possible flame temperatures for combustion processes rapid enough to be effective for engine operation are presented. The fundamental basis for these minimum temperatures is explored with chemical kinetic analysis. The combination of these minimum temperatures and the time scales associated with engine processes yield minimum possible levels of in-cylinder NOx production for both diesel and spark-ignition engines. These minimum NOx levels are identified and validated empirically. Legislated NOx levels lower than those indicated will require exhaust aftertreatment in addition to in-cylinder combustion control.

As a group of diesel engine exhaust products, oxygenated hydrocarbons have been found to be responsible for the characteristic diesel odor. Contadictory effects of fuel properties on the emission levels of these species in both diesel engines and spray burner experiments have been reported. In the present study, a prevaporized premixed flat flame was used to investigate the fuel and diluent effects on these species. The results suggest a definite fuel effect on formation rates of oxygenates. In general, aromatic fuels produced higher concentration levels of oxygenates than paraffins, and the oxygenate concentration increases as the carbon number increases for the straight chain compounds. GC/MS analysis of the oxygenate fraction of the samples indicated a similar oxidation mechanism for all alkanes. Branching of alkanes was found to lead to more cyclization, but not always higher oxygenate levels.

The objective of this research was to characterize the effects of fuel component volatility on gasoline direct injection (GDI) engine cold start. Three different fuel components, representing gasoline light end, mid-point and heavy end components, were used to form three fuel blends of different volatility. Performance tests and in-cylinder fuel distribution imaging tests using these fuel blends were carried out in a firing single-cylinder optically-accessible engine following a simulated cold start test schedule. Performance results, based on in-cylinder pressure and engine-out hydrocarbon measurements, during the initial transient phase of GDI cold start showed significantly degraded performance with the low volatility fuel blend, while the high volatility blend showed slightly improved performance. Neither the low nor high volatility fuel, however, showed a discernable effect on the quasi-steady state cold start performance.