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EGR coolers are effective to reduce NOx emissions from diesel engines due to lower intake charge temperature. EGR cooler fouling reduces heat transfer capacity of the cooler significantly and increases pressure drop across the cooler. Engine coolant provided at 40–90 C is used to cool EGR coolers. The presence of a cold surface in the cooler causes particulate soot deposition and hydrocarbon condensation. The experimental data also indicates that the fouling is mainly caused by soot and hydrocarbons. In this study, a 1-D model is extended to simulate particulate soot and hydrocarbon deposition on a concentric tube EGR cooler with a constant wall temperature. The soot deposition caused by thermophoresis phenomena is taken into account the model. Condensation of a wide range of hydrocarbon molecules are also modeled but the results show condensation of only heavy molecules at coolant temperature.

The effects of combining premixed, low temperature combustion (LTC) with biodiesel are relatively unknown to this point. This mode allows simultaneously low soot and NOx emissions by using high rates of EGR and increasing ignition delay. This paper compares engine performance and emissions of neat, soy-based methyl ester biodiesel (B100), B20, B50, pure ultra low sulfur diesel (ULSD) and a Swedish, low aromatic diesel in a multi-cylinder diesel engine operating in a late-injection premixed LTC mode. Using heat release analysis, the progression of LTC combustion was explored by comparing fuel mass fraction burned. B100 had a comparatively long ignition delay compared with Swedish diesel when measured by start of ignition (SOI) to 10% fuel mass fraction burned (CA10). Differences were not as apparent when measured by SOI to start of combustion (SOC) even though their cetane numbers are comparable.

Low-sulfur “clean” diesel fuel has been mandated in the US and Europe. However, quality of diesel fuel, particularly the sulfur content, varies significantly in other parts of the world. Due to logistical issues in various theaters of operation, the Army is often forced to rely on local fuel supplies, which exposes vehicles to diesel fuel or jet fuel (JP-8) with elevated levels of sulfur. Modern engines typically use cooled Exhaust Gas Recirculation (EGR) to meet emissions regulations. Using high-sulfur fuels and cooled EGR elevates problems associated with cooler fouling and corrosion of engine components. Hence, an experimental study has been carried out in a heavy-duty diesel engine running on standard JP-8 fuel and fuel doped with 2870 ppm of sulfur. Gas was sampled from the EGR cooler and analyzed using a condensate collection device developed according to a modified ASTM 3226-73T standard. Engine-out emissions were analyzed in parallel.

Premixed low temperature combustion (LTC) in diesel engines simultaneously reduces soot and NOx at the expense of increased hydrocarbon (HC) and CO emissions. The use of biodiesel in the LTC regime has been shown to produce lower HC emissions than petroleum diesel; however, unburned methyl esters from biodiesel are more susceptible to particulate matter (PM) formation following atmospheric dilution due to their low volatility. In this study, the efficacy of a production-type diesel oxidation catalyst (DOC) for the conversion of light hydrocarbons species and heavier, semi-volatile species like those in unburned fuel is examined. Experimental data were taken from a high speed direct-injection diesel engine operating in a mid-load, late injection partially premixed LTC mode on ultra-low sulfur diesel (ULSD) and neat soy-based biodiesel (B100). Gaseous emissions were recorded using a conventional suite of analyzers and individual light HCs were measured using an FT-IR analyzer.

Post-injection strategies aimed at reducing engine-out emissions of unburned hydrocarbons (UHC) were investigated in an optical heavy-duty diesel engine operating at a low-load, low-temperature combustion (LTC) condition with high dilution (12.7% intake oxygen) where UHC emissions are problematic. Exhaust gas measurements showed that a carefully selected post injection reduced engine-out load-specific UHC emissions by 20% compared to operation with a single injection in the same load range. High-speed in-cylinder chemiluminescence imaging revealed that without a post injection, most of the chemiluminescence emission occurs close to the bowl wall, with no significant chemiluminescence signal within 27 mm of the injector. Previous studies have shown that over-leaning in this near-injector region after the end of injection causes the local equivalence ratio to fall below the ignitability limit.

The combustion process in a diesel engine was simulated using KIVA-II, a multi-dimensional computer code. The original combustion model in KIVA-II is based on chemical kinetics, and thus fails to capture the effects of turbulence on combustion. A mixing-controlled, eddy break-up combustion model was implemented into the code. Realistic diesel fuel data were also compiled. Subsequently, the sensitivity of the code to a number of parameters related to fuel injection, mixing, and combustion was studied. Spray injection parameters were found to have a strong influence on the model's predictions. Higher injection velocity and shorter injection duration result in a higher combustion rate and peak pressure and temperature. The droplet size specified at injection significantly affects the rate of spray penetration and evaporation, and thus the combustion rate. Contrary to expectation, the level of turbulence at the beginning of the calculation did not affect fuel burning rate.

Previous work has shown that it may be advantageous to use gasoline type fuels with long ignition delays compared to today's diesel fuels in compression ignition engines. In the present work we investigate if high volatility is also needed along with low cetane (high octane) to get more premixed combustion leading to low NO and smoke. A single-cylinder light-duty compression ignition engine is run on four fuels in the diesel boiling range and three fuels in the gasoline boiling range. The lowest cetane diesel boiling range fuel (DCN = 22) also has very high aromatic content (75%vol) but the engine can be run on this to give very low NO (≺ 0.4 g/kWh) and smoke (FSN ≺ 0.1), e.g,. at 4 bar and 10 bar IMEP at 2000 RPM like the gasoline fuels but unlike the diesel fuels with DCNs of 40 and 56. If the combustion phasing and delay are matched for any two fuels at a given operating condition, their emissions behavior is also matched regardless of the differences in volatility and composition.

The first stage of ignition in saturated hydrocarbon fuels is characterized as low temperature heat release (LTHR) or cool flame combustion. LTHR takes place as a series of isomerization reactions at temperatures from 600K to 900K, and is often detectable in HCCI, rapid compression machines, and early injection low temperature combustion (LTC). The experimental investigation presented attempts to determine the behavior of LTHR in late injection low temperature combustion in a medium duty diesel as fuel varies and the influence of such behavior on LTC torque and emissions.

Stringent emission regulations and the anticipated climate change call for a paradigm shift in the design of the conventional internal combustion engines. One way to combat this problem is oxy-fuel combustion in which the combustion products are mainly water vapor and carbon dioxide. Water vapor can be easily separated by condensation and carbon dioxide is then easily captured and stored. However, many technical challenges are associated with this mode of combustion. There are many challenges facing oxy-fuel combustion before it find its way to commercial production especially for internal combustion engines. One such challenge is the relatively high temperature of the oxy-fuel combustion. A solution to this problem is the recirculation of the generated CO2 to moderate the in-cylinder temperature. Therefore, careful study of the effect of recirculating the CO2 back to combustion chamber is needed before the implementation of such a concept.

This paper analyzes and compares reactor and engine behavior of a diesel oxidation catalyst (DOC) in the presence of conventional diesel exhaust and low temperature premixed compression ignition (PCI) diesel exhaust. Surrogate exhaust mixtures of n-undecane (C11H24), ethene (C2H4), CO, O2, H2O, NO and N2 are defined for conventional and PCI combustion and used in the gas flow reactor tests. Both engine and reactor tests use a DOC containing platinum, palladium and a hydrocarbon storage component (zeolite). On both the engine and reactor, the composition of PCI exhaust increases light-off temperature relative to conventional combustion. However, while nominal conditions are similar, the catalyst behaves differently on the two experimental setups. The engine DOC shows higher initial apparent HC conversion efficiencies because the engine exhaust contains a higher fraction of trappable (i.e., high boiling point) HC.

Experiments on a modern DI Diesel engine were carried out: The engine was fuelled with standard Diesel fuel, RME and a mixture of 85% standard Diesel fuel, 5% RME and 10% higher alcohols under low load conditions (4 bar IMEP). During these experiments, different external EGR levels were applied while the injection timing was chosen in a way to keep the location of 50% heat release constant. Emission analysis results were in accordance with widely known correlations: Increasing EGR rates lowered NOx emissions. This is explained by a decrease of global air-fuel ratio entailing longer ignition delay. Local gas-fuel ratio increases during ignition delay and local combustion temperature is lowered. Exhaust gas analysis indicated further a strong increase of CO, PM and unburned HC emissions at high EGR levels. This resulted in lower combustion efficiency. PM emissions however, decreased above 50% EGR which was also in accordance with previously reported results.

Biodiesel remains an alternative fuel of interest for use in diesel engines. A common characteristic of biodiesel, relative to petroleum diesel, is a lowered heating value (or energy content of the fuel). A lower heating value of the fuel would, presuming all other parameters are equal, result in decreased engine torque. Since engine torque is often user-demanded, the lower heating value of the fuel generally translates into increased brake specific fuel consumption. Several literature report this characteristic of biodiesel. In spite of the wealth of fuel consumption characteristic data available for biodiesel, it is not clear how other engine performance parameters may change with the use of biodiesel. Characterizing these parameters becomes complicated when considering the interactions of the various engine systems, such as a variable geometry turbocharger with exhaust gas recirculation.

An HSDI Diesel engine was fuelled with standard Swedish environmental class 1 Diesel fuel (MK1), Soy methyl ester (B100) and n-heptane (PRF0) to study the effects of both operating conditions and fuel properties on engine performance, resulting emissions and spray characteristics. All experiments were based on single injection diesel combustion. A load sweep was carried out between 2 and 10 bar IMEPg. For B100, a loss in combustion efficiency as well as ITE was observed at low load conditions. Observed differences in exhaust emissions were related to differences in mixing properties and spray characteristics. For B100, the emission results differed strongest at low load conditions but converged to MK1-like results with increasing load and increasing intake pressures. For these cases, spray geometry calculations indicated a longer spray tip penetration length. For low-density fuels (PRF0) the spray spreading angle was higher.

A diesel engine developed for an international market must be able to run on different fuels considering the diesel fuel qualities and the increasing selection of biofuels in the world. This leads to the question of how different fuels perform relative to a standard diesel fuel when not changing the hardware settings. In this study five fuels (Japanese diesel, MK3, EN590 with 10% RME, EN590 with 30% RME and pure RME) have been compared to a reference diesel fuel (Swedish MK1) when run on three different speeds and three different loads at each speed. The experiments are run on a Scania 13l Euro5 engine with standard settings for Swedish MK1 diesel. In general the differences were not large between the fuels. NO x usually increased compared to MK1 and then soot decreased as would be expected. The combustion efficiency increased with increased RME contents of the fuel but the indicated efficiency was not influenced by RME except for at higher loads.

Premixed diesel combustion is intended to supplant conventional combustion in the light to mid load range. This paper demonstrates the operating load limits, limiting criteria, and load-based emissions behavior of a direct-injection, diesel-fueled, premixed combustion mode across a range of test fuels. Testing was conducted on a modern single-cylinder engine fueled with a range of ultra-low sulfur fuels with cetane number ranging from 42 to 53. Operating limits were defined on the basis of emissions, noise, and combustion stability. The emissions behavior and operating limits of the tested premixed combustion mode are independent of fuel cetane number. Combustion stability, along with CO and HC emissions levels, dictate the light load limit. The high load limit is solely dictated by equivalence ratio: high PM, CO, and HC emissions result as overall equivalence ratio approaches stoichiometric.

Previous work has showed that it may be advantageous to use fuels of lower cetane numbers compared to today's diesel fuels in compression ignition engines. The benefits come from the longer ignition delays that these fuels have. There is more time available for the fuel and air to mix before combustion starts which is favourable for achieving low emissions of NOx and smoke though premixing usually leads to higher emissions of CO and unburned hydrocarbons. In the present work, operation of a single-cylinder light-duty compression ignition engine on four different fuels of different octane numbers, in the gasoline boiling range, is compared to running on a diesel fuel. The gasoline fuels have research octane numbers (RON) of 91, 84, 78, and 72. These are compared at a low load/low speed condition (4 bar IMEP / 1200 rpm) in SOI sweeps as well as at a higher load and speeds (10 bar IMEP / 2000 and 3000 rpm) in EGR sweeps.

The Homogeneous Charge Compression Ignition (HCCI) combustion concept is currently under widespread investigation due to its potential to increase thermal efficiency while greatly decreasing harmful exhaust pollutants. Simulation tools have been developed to explore the implications of initial mixture thermodynamic state on engine performance and emissions. In most cases these modeling efforts have coupled a detailed fuel chemistry mechanism with empirical descriptions of the in-cylinder heat transfer processes. The primary objective of this paper is to present a fundamentally based boundary layer heat transfer model. The two-zone combustion model couples an adiabatic core zone with a boundary layer heat transfer model. The model predicts film coefficient, with approximately the same universal shape and magnitudes as an existing global model.

The effect of crevice volumes on the emissions of unburned hydrocarbons from a Homogeneous Charge Compression Ignition (HCCI) engine has been experimentally investigated. By varying the size and the geometry of the largest crevice, the piston topland, it was possible to ascertain whether or not crevices are the largest source of HC. Additionally, information on quenching distances for ultra lean mixtures was obtained. The tests were performed on a single cylinder engine fuelled with iso-octane. The results showed that most of the unburned hydrocarbons descend from the crevices. Increasing the topland width to some degree lead to an increase in HC. A further increase in topland width (>1.3 mm) resulted in a reduction of HC when using mixtures richer than λ ≈ 2.8, indicating that some of the mixture trapped in the topland participates in the combustion. In conditions when combustion occurred in the topland, the HC was rather insensitive to the height of the topland.

Natural gas quality, in terms of the volume fraction of higher hydrocarbons, strongly affects the auto-ignition characteristics of the air-fuel mixture, the engine performance and its controllability. The influence of natural gas composition on engine operation has been investigated both experimentally and through chemical kinetic based cycle simulation. A range of two component gas mixtures has been tested with methane as the base fuel. The equivalence ratio (0.3), the compression ratio (19.8), and the engine speed (1000 rpm) were held constant in order to isolate the impact of fuel autoignition chemistry. For each fuel mixture, the start of combustion was phased near top dead center (TDC) and then the inlet mixture temperature was reduced. These experimental results have been utilized as a source of data for the validation of a chemical kinetic based full-cycle simulation.

When automobile hydrocarbons are exhausted into the atmosphere in the presence of NOx and sunlight, ground-level ozone is formed. While researchers have used Maximum Incremental Reactivity (MIR) factors to estimate ozone production, this procedure often overestimates Local Ozone Production (LOP) because it does not consider local atmospheric conditions. In this paper, an enhanced MIR methodology for estimating actual LOP attributable to a vehicle in a particular ozone problem area is presented. In addition to using tabulated MIR factors, the procedure also uses local hydrocarbon reaction terms and a relative mechanistic reactivity term that account for local atmospheric conditions. Through this approach, the effects of hydrocarbon reaction rates, hydrocarbon residence times, and prevailing HC/NOx ratio are accounted for. The procedure is intended to enable automotive engineers to more realistically estimate actual local ozone production resulting from hydrocarbon emissions.