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COMPARISON of work capacity per unit mass and volume of different energy carriers shows that liquid hydrocarbons are superior to other energy sources. Solar and nuclear powerplants as well as their use in conjunction with a steam engine are examined in this paper. Suitability of an electric drive is discussed. Using a production 2-stroke diesel engine and its development forecast, a comparison is made of spark ignition, diesel, and gas turbine engines. The status of the free-piston engine turbine combination is reviewed.

This study evaluated multi-layer steel and composite head gaskets of various thicknesses (0.43 to 1.5 mm) and fire-ring diameters to determine the influence of head gasket crevices on engine-out hydrocarbon (HC) emissions. The upper limit in the percent reduction in HC emissions from gasket-design modifications is estimated to be about 15%. At part-load conditions, the lowest HC emissions were measured for head-gasket thickness of about 1 mm. Significantly smaller thicknesses of the order of 0.4 mm result in an increase in HC emissions. Substantial hydrocarbon-emissions advantage may be realized by minimizing the gasket-to-cylinder bore offset.

Diesel exhaust gas dilution and odor intensity were measured in the immediate vicinity of a transit bus equipped with a rear-mounted horizontal exhaust pipe, a rear-mounted vertical exhaust pipe, and a roof-top diffusion system. Exhaust dilution ratios were measured indoors during vehicle idle operation, using propane added to the exhaust gas as a tracer. Exhaust odor intensities were measured also indoors during vehicle idle operation by a human panel, using a threshold odor measurement technique. On the average, the dilution of the exhaust gas around the bus with the vertical exhaust pipe was about eight times greater than it was with the horizontal pipe. Odor intensity, as measured by the threshold response distance, was about 35% less with the vertical pipe than with the horizontal pipe. The roof-top diffuser was not as effective as the vertical exhaust pipe in increasing exhaust gas dilution or in reducing exhaust odor intensity.

A NOx trap catalyst was evaluated in a light-duty diesel engine bench under steady-state speed/load conditions with alternating lean and rich exhaust streams. The NOx conversion was correlated with several engine operating and control parameters, such as speed, lean / rich timing and catalyst temperature. The NOx conversion is a result of balance between stored NOx in a lean stream and the quantity of reductant applied in a rich transient pulse. The conversion is inversely proportional to the lean / rich ratio, R, (at R< 17) and engine speed. At a given speed and lean/rich ratio, the conversion is proportional to the catalyst inlet temperature. If the temperature is too high, thermal NOx release may decrease the overall NOx conversion. With a fully regenerated NOx trap catalyst, its cumulative NOx storage, at a given trapping period (or an instantaneous NOx trapping efficiency), is proportional to engine speed.

In order to meet progressively stringent regulations on particulate emission from diesel engines, GM has developed and tested a variety of trap oxidizer systems over the years. A particulate trap system for a light duty diesel engine has been selected and developed based on this experience, with particular emphasis on production feasibility. The system components have been designed and developed in collaboration with potential suppliers, to the extent possible. The technical performance of this system has been demonstrated by successful system durability testing in the test cell and vehicle experience in computer controlled automatic operation mode. Although the system shows promise, its production readiness will require more development and extensive vehicle validation under all operating conditions.

Strategic Materials at Reaction Temperatures (SMART) is an approach used to design washcoat systems for passive 4-way emission control catalysts. Light duty diesel vehicles need to meet the European Motor Vehicle Emissions Group (MVEG) cycle or U. S. Federal test procedure (FTP 75). Emissions that are monitored include hydrocarbon (HC), nitrogen oxides (NOx), carbon monoxide (CO) and total particulate matter (TPM). Low engine-exhaust temperatures (< 200°C during city driving) and high temperatures (> 500-800°C under full load and wide-open throttle) make emission control a formidable task for the catalyst designer Gas phase HC, CO and NOx reactions must be balanced with the removal of the soluble organic fraction for the vehicle to be in compliance with regulations. The SMART approach uses model gases under typical operating conditions in the laboratory to better understand the function of individual washcoat components.

A running loss test procedure has been developed which integrates a point-source collection method to measure fuel evaporative running loss from vehicles during their operation on the chassis dynamometer. The point-source method is part of a complete running loss test procedure which employs the combination of site-specific collection devices on the vehicle, and a sampling pump with sampling lines. Fugitive fuel vapor is drawn into these collectors which have been matched to characteristics of the vehicle and the test cell. The composite vapor sample is routed to a collection bag through an adaptation of the ordinary constant volume dilution system typically used for vehicle exhaust gas sampling. Analysis of the contents of such bags provides an accurate measure of the mass and species of running loss collected during each of three LA-4* driving cycles. Other running loss sampling methods were considered by the Auto-Oil Air Quality Improvement Research Program (AQIRP or Program).

The ozone forming potential (OFP) and specific reactivity (SR) of tailpipe exhaust are among the regulated factors that determine the environmental impact of a motor vehicle. OFP and SR measurements require a lengthy determination of about 160 non-methane hydrocarbon species. A rapid gas chromatography (GC) instrument has been constructed to separate both the light (C2 - C4) and the midrange (C5 - C12) hydrocarbons in less than 10 minutes. The limit of detection was about 0.002 parts per million carbon (ppmC). Twelve exhaust samples from two vehicles were analyzed to compare the rapid GC method with the standard GC method, which required 40-minute analyses on two different instruments. Speciation and reactivity data from the two methods were comparable. The increased sample throughput of rapid GC promises to improve OFP and SR measurements, particularly when good statistical data are necessary to insure accurate, precise results for low emission vehicles

The development of a plasma jet ignition system is described on a 4-cyl, 140 in3 engine. Performance was evaluated on the basis of combustion flame photographs in a single-cylinder engine at 20/1 A/F dynamometer tests on a modified 4-cyl engine, and cold start emissions, fuel economy, and drivability in a vehicle at 19/1 air fuel ratio. In addition to adjustable engine variables such as air-fuel ratio and spark advance, system electrical and mechanical parameters were varied to improve combustion of lean mixtures. As examples, the air-fuel ratio range was 16-22/1, secondary ignition current was varied from 40 to 6000 mA, and plasma jet cavity and electrode geometry were optimized. It is shown that the plasma jet produces on ignition source which penetrates the mixture ahead of the initial flame front and reduces oxides of nitrogen emission, in comparison to a conventional production combustion chamber.

Base metal oxide diesel oxidation catalyst technology having low sulfate making tendencies was evaluated using the ECE R-49 Test procedure on medium and heavy duty diesel engines and found to achieve substantial reduction of particulate, gas phase HC and CO emissions. Although the engines met the current European standards, further reduction in these emissions for vehicles operated in congested urban areas, such as buses, would have a positive impact on general air quality. A study of varying fuel sulfur levels (110-770 ppm S) showed that the catalyst was effective for control of sulfate-make such that overall particulate removal in the test was not compromised. However, it was found that lower fuel sulfur levels (< 550 ppm S) gave the best results for the ECE R-49 test which places emphasis on test modes yielding the highest exhaust temperatures.

Catalytic reduction of NOx from heavy duty diesel engines via addition of reductant to the exhaust is accompanied by a substantial exotherm in the catalyst bed which does not occur, for example, in a diesel oxidation catalyst. Engine tests show that thermal management in the aftertreatment system is required for optimum reductant use and maximum NOx conversion by the low-temperature (200-300°C) catalyst NSP-5, but of less importance with the high temperature (> 350°C) Catalyst A. Understanding thermal effects is also important for reconciling test results in the near-adiabatic environment of a full-sized catalyst on an engine with the near-isothermal one of a test piece in a laboratory reactor. The effects of reductant type and concentration on NOx conversion on NSP-5 were shown to result in part from non-steady state behavior of the catalyst during steady state engine operation.

Because of their relatively low particulate make, lean burn natural gas vehicles (NGV's) are a viable approach to meeting the ULEV particulate standards in urban environments where NGV's are substituted for diesel powered buses and other fleet vehicles. Our experience with oxidation catalyst technology for natural gas vehicle emissions abatement has been consistent: that palladium based catalysts maintain excellent NMHC activity and particulate reduction, but methane activity, while initially very high, decreases within the first 50 hours of operation. This paper will show that sulfur oxides at sub-ppm concentrations diminish catalyst methane activity, and that inorganic ash components from the lubricating oil (P, Zn, Ca) do not significantly contribute to the initial catalyst deactivation. Using laboratory simulations, we explore systems approaches to increasing catalyst life.

A novel process for coating and assembling metal converters utilizing precoated foil as building blocks has been developed which yields a converter capable of withstanding typical industry specified hot vibration protocols. The precoating process used here results in uniform catalyst coating distributions with coating adhesion to the foil on a par with the coatings' adhesion to ceramic substrates. FTP and MVEG vehicle emission performance of this unique precoated metal converter design versus a more conventional dip-coated metal monolith (parts with the same volume, cell density, and tri-metal catalyst coating), exhibited improved catalyst emission breakthrough efficiencies with respect to HC, CO, and NOx after two different engine-aging protocols. These advantages were observed on three different test vehicles across most phases of these driving cycles.

The goal of this study is to assess the total Life Cycle Global Warming Impact of the current HFC-134a (R134a) refrigeration system and compare it with the effect of proposed alternatives, HFC-134a Enhanced, HFC-152 (R152a), R744, R744 Enhanced and R290, based on life cycle analysis (LCA). The enhanced systems include control strategies to elevate the compressor suction pressure as the evaporator load is reduced. The hydrofluorocarbons HFC-134a and HFC-152a are greenhouse gases (GHGs) and are subject to the Kyoto Protocol timetables, which when the treaty takes effect will require participating developed countries to reduce their overall CO2 equivalent emissions of six GHGs by at least 5% by 2012 from 1990 levels.

Analytical procedures for the speciation of hydrocarbons and oxygenates (ethers, aldehydes, ketones and alcohols) in vehicle evaporative and tailpipe exhaust emissions have been improved for Phase II studies of the Auto/Oil Air Quality Improvement Research Program (AQIRP). One gas chromatograph (GC) was used for measurement of C1-C4 species and a second GC for C4-C12 species. Detection limits for this technique are 0.005 ppm C or 0.1 mg/mile exhaust emission level at a chromatographic signal-to-noise ratio of 3/1, a ten-fold improvement over the Phase I technique. The Phase I library was modified to include additional species for a total of 154 species. A 23-component gas standard was used to establish a calibration scale for automated computer identification of species. This method identifies 95±3% of the total hydrocarbon mass measured by GC for a typical exhaust sample. Solid adsorbent cartridges or impingers were used to collect aldehydes and ketones.

The Federal Test Procedure (FTP) test contains an initial period, prior to the catalyst becoming fully activated, during which hydrocarbons escape the vehicle. These hydrocarbons constitute 60-80% of the total emitted over the entire FTP test. To meet future emission levels mandated by the California Air Resources Board, alternate technologies must be created that deal effectively with these cold start hydrocarbons. This paper describes an adsorbent bed/catalyst system that can trap approximately 70% of the available nonmethane hydrocarbons over the first two minutes of the FTP test. Importantly, the trap does not require bypass valves because of a unique heat exchange approach to catalytically consuming the trapped hydrocarbons, and because the trapping materials are unaffected by engine exhaust temperatures below 800°C. Experiments with a prototype system demonstrate that LEV emissions are possible.

FIGURE 1 The 200 HP high performance 4.3L Vortec V6 engine has been developed to satisfy the need for a fuel efficient performance powerplant in the General Motors small truck platforms. Marketing requirements included strong low and mid range torque, relatively high specific power, smoothness and noise comparable to the best competitive six cylinder engines, excellent driveability, and a new technology image. Maintaining the 4.3L engine record of high reliability and customer satisfaction was an absolute requirement. Fuel economy and exhaust emission performance had to meet expected customer and legislated requirements in the mid 1990's.

In 1968, a major oil company cancelled its annual automobile economy run after sponsoring it for 18 consecutive years -presumably due to lack of interest from the public and the press. Almost coincident with that cancellation was the beginning of production automobile exhaust emission control on a national basis and a downward inflection in the historic trend of automobile fuel economy. In contrast, the past year has seen a major revival of interest, by both the public and the press, in fuel economy. In the next few weeks, the nation will be introduced to a new direction in automotive exhaust emission control which will profoundly affect the fuel economy trend. Perhaps equally, or even more important, the next few months are expected to see major national decisions on future automobile emission control which will likely have a significant influence on the direction taken by automobile fuel economy a few years hence.

The ozone forming potential (OFP) and specific reactivity (SR) of tailpipe exhaust are among the factors that determine the environmental impact of a motor vehicle. OFP and SR measurements require a lengthy determination of about 190 non-methane hydrocarbon species. A rapid gas chromatography (GC) instrument has been constructed to separate both the light (C2 - C4) and the midrange (C5 - C12) hydrocarbons in less than 10 minutes. The limit of detection is about 0.002 parts per million carbon (ppmC). Thirty exhaust samples from natural gas vehicles (NGV's) were analyzed to compare the rapid GC method with the standard GC method, which required 40-minute analyses on two different instruments. In general, evaluation of the commercial prototype from Separation Systems, Inc., indicates that a high speed, high resolution gas chromatograph can meet the need for fast, efficient exhaust hydrocarbon speciation.

A previous paper reported (SAE Paper 2002-01-2884) that it was possible to decrease mode-weighted NOx emissions compared to the OEM calibration with corresponding increases in particulate matter (PM) emissions. These PM emission increases were partially overcome with the use of oxygenated diesel fuel additives. We wanted to know if compounds of toxicological concern were emitted more or less using oxygenated diesel fuel additives that were used in conjunction with a modified engine operating strategy to lower engine-out NOx emissions. Emissions of toxicologically relevant compounds from fuels containing triproplyene glycol monomethyl ether and dibutyl maleate were the same or lower compared to a low sulfur fuel (15 ppm sulfur) even under engine operating conditions designed to lower engine-out NOx emissions.