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Experimental tests were conducted on a Cummins B5.9 direct-injected diesel engine fueled with biodiesel blends. 20% and 50% blend levels were tested, as was 100% (neat) biodiesel. Emissions of particulate matter (PM), nitrogen oxides (NOx), hydrocarbons (HC) and CO were measured under steady-state operating conditions. The effect of biodiesel on total PM emissions was mixed; however, the contribution of the volatile organic fraction to total PM was greater for higher biodiesel blend levels. When only non-volatile PM mass was considered, reductions were observed for the biodiesel blends as well as for neat biodiesel. The biodiesel test fuels increased NOx, while HC and CO emissions were reduced. PM collected on quartz filters during the experimental runs were analyzed for carbon-14 content using accelerator mass spectrometry (AMS).

This research investigates how the handling of mixing and heat transfer in a multi-zone kinetic solver affects the prediction of carbon monoxide and hydrocarbon emissions for simulations of HCCI engine combustion. A detailed kinetics multi-zone model is now more closely coordinated with the KIVA3V computational fluid dynamics code for simulation of the compression and expansion processes. The fluid mechanics is solved with high spatial and temporal resolution (40,000 cells). The chemistry is simulated with high temporal resolution, but low spatial resolution (20 computational zones). This paper presents comparison of simulation results using this enhanced multi-zone model to experimental data from an isooctane HCCI engine.

A summary is presented of experimental results obtained from a Cummins B5.9 175 hp, direct-injected diesel engine fueled with oxygenated diesel blends. The oxygenates tested were dimethoxy methane (DMM), diethyl ether, a blend of monoglyme and diglyme, and ethanol. The experimental results show that particulate matter (PM) reduction is controlled largely by the oxygen content of the blend fuel. For the fuels tested, the effect of chemical structure was observed to be small. Isotopic tracer tests with ethanol blends reveal that carbon from ethanol does contribute to soot formation, but is about 50% less likely to form soot when compared to carbon from the diesel portion of the fuel. Numerical modeling was carried out to investigate the effect of oxygenate addition on soot formation. This effort was conducted using a chemical kinetic mechanism incorporating n-heptane, DMM and ethanol chemistry, along with reactions describing soot formation.

The dynamic stage of combustion - the intrinsic process for pushing the compression polytrope away from the expansion polytrope to generate the indicator work output of a piston engine - was studied to reveal the influence of the air/fuel ratio on the effectiveness with which the fuel was utilized. The results of tests carried out for this purpose, using a 12 liter diesel engine, were reported last year [SAE 1999-01-0517]. Presented here is an analytic interpretation of the data obtained for part-load operation at 1200 and 1800 rpm. A solution is thus provided for an inverse problem: deduction of information on the dynamic features of the exothermic process of combustion from measured pressure record. Provided thereby, in particular, is information on the effectiveness with which fuel was utilized in the course of this process - a parameter reflecting the effect of energy lost by heat transfer to the walls.

The refinement of heat release analysis stems from the recognition that a combustion system is intrinsically non-linear. Thus, as appropriate for such an entity, its properties are expressed in terms of a thermochemical phase (or state) space, of which the thermodynamic aspects are exposed on a so-called Le Chatelier diagram, providing the fundamental background for the development of micro-electronic control to attain the most effective utilization of fuel. Implementation of this method of approach is illustrated by the analysis of the exothermic process taking place in two typical internal combustion engines, spark-ignition and diesel.

A single cylinder investigation was conducted to determine concentration of oxides of nitrogen resulting from combustion of ammonia and air in a spark ignition engine over a range of fuel-air ratios typical of normal engine operation with ammonia. Nitric oxide concentrations exceeded that with hydrocarbons. Spectroscopic observations during the expansion process gave concentrations in some instances an order of magnitude greater than exhaust gas determinations. The results imply a different mechanism for nitric oxide formation with ammonia fuel than with hydrocarbons and that some equilibrating process may take place between combustion and exhaust to reduce otherwise even greater than measured exhaust gas concentrations.

This is a continuation of the presentation of thermodynamic properties of selected fuel-air mixtures in chart form, suitable for utilization in engine performance calculations. Methane and propane, representative of natural gas and LPG are the two fuels considered. Using these charts, comparisons are made between the performance to be expected with these gaseous fuels compared to octane, as representative of gasoline. Reduced engine power is predicted and this is confirmed by experience of other investigators.

A theoretical and experimental study was undertaken to establish whether or not parametric correlations could be satisfactorily applied to combustion of ammonia in gas turbine combustors. It was found that a usual parameter of the form I (Re)0.7 was satisfactory for establishing blowout limits in modeling. However, the attainable values of chemical loading I were at least an order of magnitude less than those attainable with hydrocarbon fuels.

Anhydrous ammonia has been demonstrated to operate successfully as a fuel for spark ignition engines. Principal requirements are that it be introduced in the vapor phase and partly decomposed to hydrogen and nitrogen. Spark timing for maximum performance must be advanced slightly for ammonia but sensitivity to spark timing is little greater than with hydrocarbons. Increasing the cylinder wall temperature aids in effecting successful and reliable operation. The maximum theoretically possible indicated output using ammonia vapor is about 77% of that with hydrocarbon. Specific fuel consumption increase twofold at maximum power and 2-1/2 fold at maximum economy when using ammonia as a replacement for hydrocarbon.

Three factors are of consequence when considering the comparative performance of alcohols and hydrocarbons as spark ignition engine fuels. These are: relative amounts of products of combustion produced per unit of inducted charge, energy inducted per unit of charge, and latent heat differences among the fuels. Simple analysis showed significant increases in output can be expected from the use of methyl alcohol as compared to hydrocarbon and somewhat lesser improvement can be expected from ethyl alcohol. Attendant increases in fuel consumption, disproportionate to the power increase, can also be predicted. More sophisticated analysis, based upon thermodynamic charts of combustion products, do not necessarily improve correspondence between prediction and engine results.

A digital computer and special program were used, along with new thermodynamic data, to recalculate and extend the scope and range of the classic combustion gas charts of Hottel and co-workers. A series of hydrocarbon and nonhydrocarbon fuels was treated over a range of fuel-air ratios, with temperatures extended up to 7200 R and pressures up to 15,000 psia. This, the first paper of a series, incorporates the resulting charts for isooctane at four mixture ratios ranging from 20% lean to 40% rich. Auxiliary charts for inducted mixture properties determination and a set of sample calculations are also included.