IC Engine Exhaust Emissions

Section 7

Pollutant Formation and Control All IC engines produce undesirable emissions as a result of combustion.

The emissions of concern are unburned hydrocarbons (UHC), carbon monoxide (CO), oxides of nitrogen such as nitric oxide and nitrogen dioxide (NOx), sulfur dioxide, and solid carbon particulates.

These emissions pollute the environment and contribute to acid rain, smogodors, and respiratory and other health problems.

HC emissions from gasoline-powered vehicles include a number of toxic substances such as benzene, polycyclic aromatic hydrocarbons (PAHs), 1,3-butadiene and three aldehydes (formaldehyde, acetaldehyde, acrolein).

Carbon dioxide is an emission that is not regulated but is the primary greenhouse gas responsible for global warming.

During the 1940s air pollution as a problem was first recognized in the Los Angeles basin.

Two causes of this were the large population density and the natural weatherconditions. Smoke and other pollutants combined with fog to form smog.

In 1966 HC and CO emission limits were introduced in California.

All of North America usually follows Californias lead (all US in 1968).

By making more fuel efficient engines and with the use of exhaust after treatment, emissions per vehicle of HC, CO, and NOx were reduced by about 95% during the 1970s and 1980s.

Automobiles are more fuel efficient now (2x compared to 1970) but there aremore of them and the trend is to larger SUVs, as a result fuel usage is unchanged over this period.Historical Perspective

Ontario Drive Clean ProgramIn Ontario every vehicle must undergo a tail pipe emission test every other year to check compliance with regulation:

Nitrogen Oxide 984 ppm @ 3000 rpm

Carbon Monoxide 0.48% @ 3000 rpm and 1.0% @ 800 rpm

Unburned hydrocarbons 86 ppm @ 3000 rpm and 200 ppm @ 800 rpm

Particulates (diesels only at present) 30% opacity

Evaporative Emissions (SI only at present)

Test results between 1999 and March 2004

Light-Duty Program*: 14.6% failed test

Heavy-Duty Diesel**: 4% failed test

Heavy-Duty Non-Diesel**: 27.3% failed test

* 6 million vehicles (automobiles, vans, SUVs, pick-ups) in program** 200,000 vehicles in programOntario Drive Clean Program Stats

Nitrogen Oxides NOx includes nitric oxide (NO) and nitrogen dioxide (NO2)

In SI engines the dominant component of NOx is NO

Forms as a result of dissociation of molecular nitrogen and oxygen.

Since the activation energy of the critical elementary reaction O+N2NO+Nis high the reaction rate is very temperature dependent, w'' ~ exp (-E/RT)

Therefore NO is only formed at high temperatures and the reaction rate is relatively slow.

At temperatures below 2000K the reaction rate is extremely slow, so NO formation not important.

Since the cylinder temperature changes throughout the cycle the NO reaction rate also changes.

Each fluid element burns to its AFT based on its initial temperature, elements that burn first near the spark plug achieve a higher temperature.

Since the chemistry is not fast enough the actual NO concentration tends toward but never achieves the equilibrium value. If NO concentration is lower than equilibrium value NO forms If NO concentration is higher than equilibrium value NO decomposes

Once the element temperature reaches 2000K the reaction rate becomes so slow that the NO concentration effectively freezes at a value greater than the equilibrium value.

The total amount of NO that appears in the exhaust is calculated by summing the frozen mass fractions for all the fluid elements: SI Engine In-cylinder NO Formation

x = 0-15o (x = 0)x = 125o (x = 1)x = 0x = 1 Equilibrium concentration:based on the local temperature, pressure, equivalence ratio, residual fraction

Actual NO concentration:based on kinetics(assuming no mixing of fluid elements)

One would expect the peak NO concentrations to coincide with highest AFT.

Typically peak NO concentrations occur for slightly lean mixtures that corresponds to lower AFT but higher oxygen concentration.Effect of Equivalence Ratio on NO Concentration

Effect of Various Parameters on NO ConcentrationIncreased spark advance and intake manifold pressure both result in higher cylinder temperatures and thus higher NO concentrations in the exhaust gas

= 0.97= 1.31= 1.27= 0.96Pi= 354 mm HgPi= 658 mm Hg

Exhaust NO Concentration ReductionSince the formation of NO is highly dependent on cylinder gas temperature anymeasures taken to reduce the AFT are effective:

increased residual gas exhaust gas recirculation (EGR) moisture in the inlet air

In CI engines the cylinder gas temperature is governed by the load and injection timingIDI/NA indirect injection naturally aspirated

DI/NA direct injection naturally aspirated

HydrocarbonsHydrocarbon emissions result from the presence of unburned fuel in the engine exhaust.

However, some of the exhaust hydrocarbons are not found in the fuel, but are hydrocarbons derived from the fuel whose structure was altered do to chemical reaction that did not go to completion. For example: acetaldehyde, formaldehyde, 1,3 butadiene, and benzene all classified as toxic emissions.

About 9% of the fuel supplied to the engine is not burned during the normal combustion phase of the expansion stroke.

Only 2% ends up in the exhaust the rest is consumed during the other three strokes.

As a consequence hydrocarbon emissions cause a decrease in the thermal efficiency, as well as being an air pollutant.

Hydrocarbon Emission Sources for SI EnginesThere are six principal mechanisms believed to be responsible for hydrocarbon emissions: % fuel escaping Sourcenormal combustion% HC emissions

Crevices5.238Oil layers1.016Deposits1.016Liquid fuel1.220Flame quench0.5 5Exhaust valve leakage0.1 5

Total9.0100

Hydrocarbon Emission SourcesCrevices these are narrow regions in the combustion chamber into whichthe flame cannot propagate because it is smaller than the quenching distance.

Crevices are located around the piston, head gasket, spark plug and valve seats and represent about 1 to 2% of the clearance volume.

The crevice around the piston is by far the largest, during compression the fuelair mixture is forced into the crevice (density higher than cylinder gas since gas is cooler near walls) and released during expansion.CrevicePiston ring

Oil layers - Since the piston ring is not 100% effective in preventing oil migration into the cylinder above the piston, oil layers exist within the combustion chamber. This oil layer traps fuel and releases it later during expansion.

Deposits With continued use carbon deposits build up on the valves, cylinder and piston head. These deposits are porous with pore sizes smaller than thequenching distance so trapped fuel cannot burn. The fuel is released later during expansion.

Liquid fuel For some fuel injection systems there is a possibility that liquid fuel is introduced into the cylinder past an open intake valve. The less volatilefuel constituents may not vaporize (especially during engine warm-up) and be absorbed by the crevices or carbon deposits.

Flame quenching It has been shown that the flame does not burn completelyto the internal surfaces, the flame extinguishes at a small but finite distance from the wall. Most of this gas eventually diffuses into the burned gas duringexpansion stroke.Hydrocarbon Emission Sources

Hydrocarbon Exhaust ProcessWhen the exhaust valve opens the large rush of gas escaping the cylinder drags with it some of the hydrocarbons released from the crevices, oil layer and deposits.

During the exhaust stroke the piston rolls the hydrocarbons distributed along the walls into a large vortex that ultimately becomes large enough that a portion of it is exhausted.BlowdownExhaustStroke

Hydrocarbon Exhaust ProcessExhaust valve opensExhaust valve closesThe first peak is due to blowdown and the second peak is due to vortex roll upand exhaust (vortex reaches exhaust valve at roughly 290o)TCBC

Hydrocarbon Emission Sources for CI EnginesCrevices - Fuel trapped along the wall by crevices, deposits, or oil due to impingement by the fuel spray (not as important as in SI engines).

Undermixing of fuel and air - Fuel leaving the injector nozzle at low velocity, at the end of the injection process cannot completely mix with air and burn.

Overmixing of fuel and air - During the ignition delay period evaporated fuel mixes with the air, regions of fuel-air mixture are produced that are too lean to burn. Some of this fuel makes its way out the exhaust.Longer ignition delay more fuel becomes overmixed.Exhaust HC, ppm C

Note for the direct injection diesel the hydrocarbon emission are the worst at light load (long ignition delay)

ParticulatesA high concentration of particulate matter (PM) is manifested as visible smoke in the exhaust gases.

Particulates are any substance other than water that can be collected by filtering the exhaust, classified as:1) solid carbon material or soot2) condensed hydrocarbons and their partial oxidation products

Diesel particulates consist of solid carbon (soot) at exhaust gas temperatures below 500oC HC compounds become absorbed on the surface.

In a properly adjusted SI engines soot is not usually a problem

Particulate can arise if leaded fuel or overly rich fuel-air mixture are used.burning crankcase oil will also produce smoke especially during engine warm up where the HC condense in the exhaust gas.

Most particulate material results from incomplete combustion of fuel HC which occurs in fuel rich mixtures.

Based on equilibrium the composition of the fuel-oxidizer mixture at the onsetof soot formation occurs when x 2a (or x/2a 1) in the following reaction:

Particulates (soot)i.e. when the (C/O) ratio exceeds 1. Experimentally it is found that the criticalC/O ratio for onset of soot formation is between 0.5 and 0.8

The CO, H2, and C(s) are subsequently oxidized in the diffusion flame to CO2 and H2O via the following second stageAny carbon not oxidized in the cylinder ends up as soot in the exhaust!

Particulates are a major emissions problem for CI engines.

Exhaust smoke limits the full load overall equivalence ratio to about 0.7Particulates and CI EnginesAn outstanding problem for diesel engine designers is that in order to reduce NOx one wants to reduce the AFT but this has the adverse effect of decreasingthe amount of soot oxidized, or increases the amount of soot in the exhaust.f = 0.7f = 0.5f = 0.3One technique for measuring particulate involves diluting the exhaust gas with cool air to freeze the chemistry before measurements

An example of this dilemma is changing the start of injection, e.g., increasing the advance increases the AFT Crank angle bTC for start of injectionParticulates and CI Engines

Carbon Monoxide Carbon monoxide appears in the exhaust of fuel rich running engines.

For fuel rich mixtures there is insufficient oxygen to convert all the carbon in the fuel to carbon dioxide.C8H18-air

Carbon MonoxideThe C-O-H system is more or less at equilibrium during combustion and expansion.

Late in the expansion stroke when the cylinder temperature gets down to around 1700K the chemistry in the C-O-H system becomes rate limited and starts to deviate from equilibrium.

In practice it is often assumed that the C-O-H system is in equilibrium until the exhaust valve opens at which time it freezes instantaneously.

The highest CO emission occurs during engine start up (warm up) when the engine is run fuel rich to compensate for poor fuel evaporation.

Since CI engines run lean overall, emission of CO is generally low and notconsidered a problem.

Emission ControlThe current emission limits for HC, CO and NOx have been reduced to 4%, 4% and 10% of the uncontrolled pre-1968 values, respectively.

Three basic methods used to control engine emissions:

Engineering of combustion process - advances in fuel injectors, oxygen sensors, and on-board computers.

2) Optimizing the choice of operating parameters - two NOx control measures that have been used in automobile engines since 1970s are spark retard and EGR.

3) After treatment devices in the exhaust system - catalytic converter

Catalytic ConverterAll catalytic converters are built in a honeycomb or pellet geometry to exposethe exhaust gases to a large surface made of one or more noble metals: platinum, palladium and rhodium.

Rhodium used to remove NO and platinum used to remove HC and CO.Lead and sulfur in the exhaust gas severely inhibit the operation of a catalytic converter (poison).

Three-way Catalytic ConverterA catalyst forces a reaction at a temperature lower than normally occurs.

As the exhaust gases flow through the catalyst, the NO reacts with the CO,HC and H2 via a reduction reaction on the catalyst surface.e.g., NO+CON2+CO2 , NO+H2 N2+H2O, and others

The remaining CO and HC are removed through an oxidation reaction formingCO2 and H2O products (air added to exhaust after exhaust valve).

A three-way catalysts will function correctly only if the exhaust gas compositioncorresponds to nearly (1%) stoichiometric combustion.

If the exhaust is too lean NO are not destroyedIf the exhaust is too rich CO and HC are not destroyed

A closed-loop control system with an oxygen sensor in the exhaust is used to determine the actual A/F ratio and used to adjust the fuel injector so that theA/F ratio is near stoichiometric.

Since thermal efficiency is highest for slightly lean conditions it may seem that the use of a catalytic converter is a rather severe constraint.

The same high efficiency can be achieved using a near stoichiometric mixtureand diluting by EGREffect of Mixture Composition

Effect of TemperatureThe temperature at which the converter becomes 50% efficient is referred to as the light-off temperature.

The converter is not very effective during the warm up period of the engine

Catalytic Converter for DieselsFor Diesel engines catalytic converters are used to control HC and CO, butreduction of NO emissions is poor because the engine runs lean in order to avoid excess smoke.

The NO is controlled by retarding the fuel injection from 20o to 5o before TC in order to reduce the peak combustion temperature.

This has a slight negative impact, increases the fuel consumption by about 15%.

IC Engine FuelsCrude oil contains a large number of hydrocarbon compounds (25,000).

The purpose of refining is to separate crude oil into various fractions via adistillation process, and then chemically process the fractions into fuels and other products.

A still is used to heat a sample, preferentially boiling off lighter componentswhich are then condensed and recovered.

The group of compounds that boil off between two temperatures are referred to as fractions.

The order of the fractions as they leave the still are naptha, distillate, gas oil, and residual oil. These are further subdivided using adjectives light, middle, and heavy.

The adjectives virgin or straight run are often used to signify that no chemical processing has been done to a fraction.

Distillation ProcessRefining Process

GasolineLight virgin (or straight run) naptha can be used as gasoline.

Gasoline fuel is a blend of hydrocarbon distillates with a range of boiling pointsbetween 25 and 225oC (for diesel fuel between 180 and 360oC)

Chemical processing is used to:

Produce gasoline from a fraction other than light virgin, or

Upgrade a given fraction (e.g., Alkylation increases the MW and octane number of fuel: produce isooctane by reacting butene with isobutane in the presence of a catalyst.

Reformulated GasolineIn order to reduce CO and HC the oxygen content of gasoline is increased to about 3% by weight (U.S. oxygenated fuels program, winter only).

The U.S. reformulated gasoline program is a year-round program used to reduce ozone by requiring a minimum oxygen content of 2% by weight and maximum benzene content of 1%.

The primary oxygenates are MTBE (CH3)OC(CH3)3 and ethanol (C2H5OH)

Also as part of the reformulated gasoline program sulfur is restricted to 31 ppm

Note: gasoline with 10% ethanol by volume also marketed as gasohol