Combustion Fundamentals

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Combustion Fundamentals

Dr. Mike Klassen, P.E.

Combustion Science &

Engineering, Inc.MKlassen@csefire.com

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What is NOx?

• NOx stands for Nitrogen Oxides

 – NO, N2O, NO2, etc.

• Some NOx will always be formed when fuel is

burned in air • There are several ways that NOx is formed

 – Most important path is the reaction of the N2 and

O2 to form NO – the Zeldovich reaction

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NOx formation pathways

• Zeldovich reaction (thermal NOx)

• N2O reaction

• Prompt NOx

• Fuel NOx

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Zeldovich Reaction

• Reaction 1: O + N2 => NO + N

• Reaction 2: N + O2 => NO + O

• Net reaction: N2 + O2 => 2NO

• Reaction rate increases exponentially

with flame temperature

• Often called “thermal” NOx

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Impact of GT Conditions on

Thermal NOx formation

• The Zeldovich reaction also increaseswith the square root of pressure, so gasturbine designers are faced with a truedilemma

• Higher pressure ratios and higher firingtemperatures yield higher efficienciesbut also produce more thermal NOx

• Which would you choose?

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Impact of GT Compressor Discharge

Conditions on NO Formation

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N2O Pathway

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Prompt NOx

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Impact of Fuel Nitrogen

Content

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NO2 Formation

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How is CO formed?

• In a flame the carbon atoms in a fuel will

react with O2 in the air to form CO2

• But this occurs in a “two step” process

 – Step 1: one oxygen atom reacts with acarbon atom to form CO

 – Step 2: another oxygen atom reacts with

CO to form CO2

• Without “step 2” you get CO emissions

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“Quenching” causes CO

• Step 2 will not happen if the combustionproducts are “quenched” or cooled

prematurely

 – Typically this happens in regions where cooling air

is mixed into the flow

• Step will also not happen if there is a

shortage of O atoms – fuel-rich combustion

 – Typically not encountered in gas turbines

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Regions of High CO in a GT

combustor 

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NO & CO

• In general, hotter firing temperatures

produce more NOx and less CO

• Conversely, lower firing temperatures

produce more CO and less NOx• Also, longer residence time in the flame

zone gives more time for NOx form and

for CO to be consumed

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Optimal Combustor Design

• Now we will examine how to design a

combustor to minimize both NOx and

CO

• But first, we need to go over somecombustion fundamentals

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Important Concepts

• Air/Fuel Ratio (A/F)

• Stoichiometric A/F Ratio (A/F)ST

• Equivalence Ratio (ø)

• Adiabatic Flame Temperature

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 Air/Fuel Ratio

• Ratio of air flow to fuel flow in a flame

• Can be a volume (or mole) ratio or a

mass ratio (lbs-air/lbs-fuel)

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Stoichiometric A/F

• The air/fuel ratio that results in all of the

fuel and oxygen being consumed

• In air, for every mole (or molecule or

cubic foot) of O2 there are 3.77 moles

(or molecules or cubic feet) of N2

• So after all the O2 has been consumed

you still have a lot of N2 in the exhaust

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Stoichiometric Combustion of

Methane• CH4 + 2x(O2 + 3.77N2) => CO2 + 2H2O +

7.54N2

• (A/F)ST = 2x(1+3.77)/1 =

9.54 ft

3

-air/ft

3

-CH4

• (A/F)ST = (2x32+2x3.77x28)/16 =

17.2 lbs-air/lb-CH4

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Equivalence Ratio (Ø)

• Ø = (A/F)ST /(A/F)actual

• Ø = 1, stoichiometric combustion

• Ø < 1, fuel-lean combustion (excess air)

• Ø > 1, fuel-rich combustion (excess

fuel)

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 Adiabatic Flame Temperature

• The temperature the products ofcombustion will reach if there is no heatloss from the flame zone

• Function of (A/F), fuel type, and thetemperature of the reactants

• For CH4, with Ø = 1 & 59°F reactants, AFT = 3565°F (note: titanium melts at3036°F!!!)

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Combustion Properties of

some Gaseous Fuels

38322.5CarbonMonoxide, CO

382434.2Hydrogen, H2

359015.6Propane, C3H8

357916.1Ethane, C2H6

356517.2Methane, CH4

Adia. Flame

Temp., °F

(A/F)ST

(lb/lb)

Fuel

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How will Adiabatic Flame T

change as Ø changes?

AFT

Ø10 2

(no fuel) (stoich.) (excess fuel)

CDT

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 Adiabatic Flame T is

maximized around Ø = 1

Thermal NOx formation is also

maximized around Ø = 1

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Ø vs NOx and AFT

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Optimal Conditions

• To minimize NOx, must operate in fuel-

lean conditions (Ø < 1)

• Cannot be too lean or CO emissions will

become too high

• Cannot operate fuel-rich because

unburned hydrocarbons and CO will be

too high

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AIRFLOW

60%

FUEL

2900°F

1870 K

40%AIRFLOW

30%4100°F

2530 K

70%

FUEL

Conventional

Lean-Premixed

Same

Turbine

Inlet

Temp

Diffusion vs Pre-Mixed

©Solar Turbines Incorporated

©Solar Turbines Incorporated

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Diffusion vs Pre-Mixed Flames

• Fuel & air are separatebefore flame zone

• Fuel burns over rangeof fuel/air mixtures

• Burn rate depends on

rate of fuel & air supply

and degree of mixing

• “Over-ventilated” flame

temps near max• No flammability limits

• Fuel and air are well-mixed before flamezone

• Fuel burns at specificair/fuel ratio, Ø

• Flame temperaturevaries as function of Øand fuel type

• Flammability limits are a

function of Ø and fueltype

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Special Considerations for

Pre-mixed Flames

• Good Mixing

• Flammability limits

• Blow-off & Flashback

• Dynamic Instabilities or “Humming”

• Auto-Ignition

• Part-Load Operation

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Ø = 1.68

Ø = 1.0

Ø = 0.50

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Flammability Limits &

Materials Limits• The maximum adiabatic flame temperature a

turbine blade can withstand corresponds to Ø

< 0.5 (typically 0.4 for modern designs)

• The lower flammability limit of CH4 is at Ø =0.5 (and CO emissions would be too high at

that condition also)

• Conclusion: some air must by-pass the flame

zone even in a pre-mixed combustor 

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Blow-off and Flashback

• If the “flame speed” does not match theflow speed of the reactants, the flamefront will move

• If flame speed is too high, you can getflashback (flame moving upstream intofuel nozzle)

• If flame speed is too low, you can getblow-off (flame pushed downstream)

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What determines flame

speed?

• Flame speed is determined by the

combustion reaction rates and those

rates depend on:

 – Equivalence Ratio, Ø (there is it again!) – Fuel type

 – Flow regime (laminar or turbulent)

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Flame speed vs fuel type

42.9Carbon Monoxide, CO

291.2Hydrogen, H2

42.7Propane, C3H8

44.2Ethane, C2H6

37.3Methane, CH4

Max. flame speed

(cm/s)

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Pre-mixed Combustor with Diffusion Pilot Flame

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Dynamic Instabilities or

“Humming”

• Combustion instabilities occur when a

forcing mechanism drives pressure

fluctuations at the resonant frequencies

of the the combustion chamber.

• Combustion instabilities can lead to:

 – Excessive wear and eventually component

failure – Increased emissions of NOx and UHC

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What Can Cause Humming?

• Combustion instabilities can be caused bynumerous mechanisms, but are generallyrelated to the coupling of heat release withpressure (or acoustic) waves. Amplitudes

and frequencies of the instabilities candepend on: – Inlet air and fuel temperatures

 – Fuel Type

 – Fuel Injector geometry

 – Combustor geometry

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 Auto-Ignition

• When fuel and air are pre-mixed, one

always has to worry about the mixture

igniting before it reaches a spark (or

flame)• The temperature above which a fuel-air

mixture can spontaneously ignite is

called the auto-ignition temperature.

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Part-Load Operation

• As gas turbines reduce load, the turbine

rotor inlet temperature decreases, which

means that the overall fuel-air ratio must

decrease• This poses problems for pre-mixed flames

 because of the lower flammability limit

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Part-Load Strategies

• Some manufacturers only operate in pre-

mixed mode over a limited load range

 – At low loads the combustion switches to a

diffusion flame (with higher emissions)

• Some manufacturers extend the load range

of pre-mixed operation by air-staging or

fuel-staging

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Fuel-Staging Example

Source: GE Report 3568E

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Annular Combustor

Fuel Staging

Source: GE Report 3568E

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Gas

Turbines

with Air-

Staging

(combustor by-pass

valve)