4310 Combustion Introduction Lecture 14

download 4310 Combustion Introduction Lecture 14

of 15

Transcript of 4310 Combustion Introduction Lecture 14

  • 8/8/2019 4310 Combustion Introduction Lecture 14

    1/15

    1

    MAE 5310: COMBUSTION FUNDAMENTALS

    Coupled Thermodynamic and Chemical Systems:

    Well-Stirred Reactor (WSR) Theory

    October 8, 2009

    Mechanical and Aerospace Engineering Department

    Florida Institute of Technology

    D. R. Kirk

  • 8/8/2019 4310 Combustion Introduction Lecture 14

    2/15

    2

    WELL-STIRRED REACTOR THEORY OVERVIEW

    Well-Stirred Reactor (WSR) or Perfectly-Stirred Reactor (PSR) is an ideal reactor

    in which perfect mixing is achieved inside the control volume

    Extremely useful construct to study flame stabilization, NOx formation, etc.

  • 8/8/2019 4310 Combustion Introduction Lecture 14

    3/15

    3

    APPLICATION OF CONSERVATION LAWS

    ( ) 0,,

    ,,

    ,

    =+

    =

    =

    +=

    outiiniiii

    ii

    iii

    outiinii

    cvi

    YYmVMW

    Ymm

    MWm

    mmmVdt

    dm

    Rate at which mass of i accumulates

    within control volume

    Rate at which mass of i is

    generated within control volume

    Mass flow of i into control volume

    Mass flow of i out of control volume

    Relationship between mass generation rate of a

    species related to the net production rate

  • 8/8/2019 4310 Combustion Introduction Lecture 14

    4/15

    4

    APPLICATION OF CONSERVATION LAWS

    [ ]( ) [ ]( )

    [ ]

    [ ]

    ( )

    ( ) ( )

    =

    =

    =

    ==

    ==

    =

    N

    i

    iniini

    N

    i

    iouti

    inout

    N

    j

    jj

    iii

    outicvii

    ThYThYmQ

    hhmQ

    MWX

    MWXY

    TXfTXf

    1

    ,

    1

    ,

    1

    ,,

    Outlet mass fraction, Yi,out is equalto the mass fraction within the reactor

    Conversion of molar concentration into mass fraction

    (see slide 2)

    So far, N equations with N+1 unknowns, need to close set

    Application of steady-flow energy equation

    Energy equation in terms

    of individual species

  • 8/8/2019 4310 Combustion Introduction Lecture 14

    5/15

    5

    WSR SUMMARY

    Solving for temperature and species mass fraction is similar to calculation of adiabatic flame

    temperature (Glassman, Chapter 1)

    The difference is that now the product composition is constrained by chemical kinetics

    rather than by chemical equilibrium

    WSR (or PSR) is assumed to be operating at steady-state, so there is no time dependence

    Compared with the constant pressure and constant volume reactor models considered

    previously

    The equations describing the WSR are a set of coupled (T and species concentration)nonlinear algebraic equations

    Compared with constant pressure and constant volume reactor models which were

    governed by a set of coupled linear, 1st order ODEs

    Net production rate term, although it appears to have a time derivative above it, depends

    only on the mass fraction (or concentration) and temperature, not time Solve this system of equations using Newton method for solution of nonlinear equations

    Common to define a mean residence time, res, for gases in WSR

    RT

    PMW

    m

    V

    mix

    res

    =

    =

  • 8/8/2019 4310 Combustion Introduction Lecture 14

    6/15

    6

    EXAMPLE 1: WSR MODELING

    Develop a WSR model using same simplified chemistry and thermodynamic used in previous example

    Equal constant cps, MWs, one-step global kinetics for C2H

    6

    Use model to develop blowout characteristics of a spherical reactor with premixed reactants (C2H

    6and

    Air) entering at 298 K. Diameter of reactor is 80 mm. Plot at blowout as a function of mass flow rate for 1.0 and assume that reactor is adiabatic

    ( ) ( )

    ( ) ( )

    ( ) ( ) 0

    01

    023.0

    023.0

    ,,

    Pr

    65.11.0

    75.1

    ,

    65.11.0

    75.1

    ,

    =+

    =

    =

    =

    inPinFFFf

    OxF

    OxFGOxinOx

    OxFGFinF

    TTcYYh

    YYY

    YYRT

    PMWVk

    F

    AYYm

    YY

    RT

    PMWVkYYm

    Set of 4 coupled nonlinear algebraic equations with unknowns, YF, Y

    Ox, Y

    Pr, and T

    Treat mass flow rate and volume as known parameters

    To determine reactor blowout characteristic, solve nonlinear algebraic equations on previous slide for a

    sufficiently small value of mass flow rate that allows combustion at given equivalence ratio Increase mass flow rate until failure to achieve a solution or until solution yields input values

  • 8/8/2019 4310 Combustion Introduction Lecture 14

    7/15

    7

    EXAMPLE 1: RESULTS AND COMMENTS

    Decreasing conversion of fuel to products as mass flow rate is increased to blowout condition

    Decreased temperature as flow rate is increased to blowout condition

    Mass flow rate for blowout is about 0.193 kg/s

    Ratio of blowout temperature to adiabatic flame temperature is 1738 / 2381 = 0.73

    Repeat calculations at various equivalence ratios generates the blowout characteristic curve

    Reactor is more easily blown out as the fuel-air mixture becomes leaner Shape of blowout curve is similar to experimental for gas turbine engine combustors

  • 8/8/2019 4310 Combustion Introduction Lecture 14

    8/15

    8

    EXAMPLE 2: GAS TURBINE COMBUSTOR CHALLENGES

    Based on material limits of turbine (Tt4), combustors must operate below

    stoichiometric values

    For most relevant hydrocarbon fuels, s ~ 0.06 (based on mass)

    Comparison of actual fuel-to-air and stoichiometric ratio is called equivalence

    ratio

    Equivalence ratio = = /stoich

    For most modern aircraft ~ 0.3

    Summary

    If = 1: Stoichiometric

    If > 1: Fuel Rich

    If < 1: Fuel Lean

  • 8/8/2019 4310 Combustion Introduction Lecture 14

    9/15

    9

    EXAMPLE 2: WHY IS THIS RELEVANT?

    Most mixtures will NOT burn so far away fromstoichiometric

    Often called Flammability Limit

    Highly pressure dependent

    Increased pressure, increased flammabilitylimit

    Requirements for combustion, roughly > 0.8

    Gas turbine can NOT operate at (or even near)stoichiometric levels

    Temperatures (adiabatic flame temperatures)associated with stoichiometric combustion areway too hot for turbine

    Fixed Tt4 implies roughly < 0.5

    What do we do?

    Burn (keep combustion going) near =1 withsome of ingested air

    Then mix very hot gases with remaining air tolower temperature for turbine

  • 8/8/2019 4310 Combustion Introduction Lecture 14

    10/15

    10

    SOLUTION: BURNING REGIONS

    Air

    Comp

    ressor

    Turb

    ine

    ~ 1.0

    T>2000 K

    ~0.3

    Primary

    Zone

  • 8/8/2019 4310 Combustion Introduction Lecture 14

    11/15

    11

    COMBUSTOR ZONES: MORE DETAILS

    1. Primary Zone

    Anchors Flame

    Provides sufficient time, mixing, temperature for complete oxidation of fuel Equivalence ratio near =1

    1. Intermediate (Secondary Zone)

    Low altitude operation (higher pressures in combustor)

    Recover dissociation losses (primarily CO CO2) and Soot Oxidation

    Complete burning of anything left over from primary due to poor mixing High altitude operation (lower pressures in combustor)

    Low pressure implies slower rate of reaction in primary zone

    Serves basically as an extension of primary zone (increased res)

    L/D ~ 0.7

    1. Dilution Zone (critical to durability of turbine)

    Mix in air to lower temperature to acceptable value for turbine

    Tailor temperature profile (low at root and tip, high in middle)

    Uses about 20-40% of total ingested core mass flow

    L/D ~ 1.5-1.8

  • 8/8/2019 4310 Combustion Introduction Lecture 14

    12/15

    12

    EXAMPLE 2: GAS TURBINE ENGINE COMBUSTOR

    Consider the primary combustion zone of a gas turbine as a well-stirred reactor with

    volume of 900 cm3. Kerosene (C12H

    24) and stoichiometric air at 298 K flow into the reactor,

    which is operating at 10 atm and 2,000 K

    The following assumptions may be employed to simplify the problem

    Neglect dissociation and assume that the system is operating adiabatically

    LHV of fuel is 42,500 KJ/kg

    Use one-step global kinetics, which is of the following form

    Eais 30,000 cal/mol = 125,600 J/mol

    Concentrations in units of mol/cm3

    Find fractional amount of fuel burned,

    Find fuel flow rate

    Find residence time inside reactor, res

    [ ] [ ]5.125.011 exp105 oxfuel

    afuel XX

    RTEx =

  • 8/8/2019 4310 Combustion Introduction Lecture 14

    13/15

    13

    EXAMPLE 2: FURTHER COMMENTS

    Consider again the WSR model for the gas turbine combustor primary zone, however now

    treat temperature T as a variable.

    At low T, fuel mass flow rate and are low

    At high T, is close to unity but fuel mass flow rate is low because the concentration

    [F] is low ([F]=FP/RT), which reduces reaction rate

    In the limit of =1, T=Tflame

    and the fuel mass flow rate approaches zero

    For a given fuel flow rate two temperature solutions are possible with two different heat

    outputs are possible

    =1, kerosene-air mixture

    V=900 cm3

    P=10 atm

    LHVmQ f =

  • 8/8/2019 4310 Combustion Introduction Lecture 14

    14/15

    14

    EXAMPLE #3: HOW CHEMKIN WORKS Detailed mechanism for H2 combustion

    Reactor is adiabatic, operates at 1 atm, =1.0, and V=67.4 cm3

    For residence time, res , between equilibrium and blow-out limits, plot T, H2O, H2, OH,

    O2, O, and NO vs res .

  • 8/8/2019 4310 Combustion Introduction Lecture 14

    15/15

    15

    EXAMPLE #3: HOW CHEMKIN WORKS

    Input quantities in CHEMKIN:

    Chemical mechanismReactant stream constituents

    Equivalence ratio

    Inlet temperature and pressure

    Reactor volume

    res (1 ms ~ essentially equilibrated conditions)

    Tflame and H2O

    concentration drop as res

    becomes shorter

    H2 and O2 concentrations rise

    Behavior of OH and O

    radicals is more complicated

    NO concentration falls rapidly

    as res falls below 10-2 s