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    CHAPTER 2 FUNDAMENTALS OF BOILING HEAT

    TRANSFER AND TWO-PHASE FLOW

    2.1 Nucleation Theory

    2.1.1 Homogeneous Nucleation

    Thermodynamic Limit of Superheat

    T = TC

    T=T2>T1

    T=T1

    Critical point

    Vapor spinodal

    Vapor saturation

    Mechanical

    unstable region

    Specific volume ()

    Pressure

    ( p )

    Liquid

    saturation

    Subcooledliquid

    A

    B C

    E

    F

    G

    "

    "

    "

    "

    ""

    "

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    #$%&'()*+,-./0123/0456

    78/09:;?

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    Mechanical Stability Limit :

    0

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    2.The minimum in the P-v isotherms , i.e., the minimum

    pressure corresponding to a given T , is given by thefollowing two criteria :

    Thus,

    cc

    n

    c vbvRTa 3

    1

    8

    9 1==

    +

    The state equation can be non-dimensionalized as

    3

    8

    3

    132

    =

    +

    n

    Where B=P/PC C=T/TC and D=v/vC

    002

    2

    >

    =

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    ( )3

    1

    413

    =+n

    Applying these criteria one obtains the following equation along

    the spinodal

    Procedure to determine the thermodynamic limit

    1.GiveCand solve for D2.Using the state equation to determine B

    Eberhart & Schnyders J. physical Chemistry vol. 77 No.23, pp.2730-2736, 1973

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    Kinetic limit of superheat

    At a given temperature liquid molecules have an energy distribution

    such that there is a small but finite fraction having energies

    considerably greater than the average, therefore is a small but finite

    probability of a cluster of molecules with vapor like energies coming

    together to form a vapor embryo of the size of the equilibrium nucleus.

    Vapor phase is created and grown based on the surrounding

    liquid superheat .Given a liquid superheat, an equilibrium radius of

    embryo can be evaluated as follows

    Refs. a. Collier & Tome, 1994, convective boiling and condensation, ch1.b. Hsu & Graham, 1989, Transport process in boiling and

    two-phase system, ch1.

    c. Van Stralen & Cole, 1979, Boiling phenomena, ch2.

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    Superheat needed to sustain a vapor nucleus of radius of r

    Tsat = The saturation temperature corresponding to the liquid pressure, Pf

    Tl

    = The liquid temperature > Tsat (the liquid is superheated)

    Question: Tl Tsat =? in order to sustain a vapor nucleus of radius of r ?

    "

    lPlT

    r

    vP

    Tsat = The saturation temperature corresponding to the liquid pressure, Pf

    Tl

    = The liquid temperature > Tsat (the liquid is superheated)

    Question: Tl Tsat =? in order to sustain a vapor nucleus of radius of r ?

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    The Clausius Clapeyron equation (for a flat vapor liquid interface)

    The Clausius Clapeyron equation defines the slope of

    saturation pressure vs. temperature.

    P

    Tsat

    T

    lvlv

    lvlv

    lvsat

    lv

    T

    vvv

    iii

    T

    i

    dT

    dP

    sat

    ==

    =

    "

    Vapor pressure curve

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    Laplace equation (mechanical force balance )

    rPP lv 2= E : surface tension

    C1

    C2r1

    r2

    r2

    r1C1r2C2

    Vapor liquid interface

    Pv

    lP

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    Force balance requires that

    ( )

    [ ]212121

    1222111211

    2

    1sin2

    2

    1sin2

    rr

    rrrrPP lv

    +

    +

    =

    +=

    21

    11

    rrPP lv

    For a spherical bulle rPPrrr

    lv

    2

    21 ===Form the Clausius-Clapeyron relation,

    lv

    lvsat

    i

    vTPT =

    Neglecting the possible bubble curvature effect on the vapor pressure

    ( )

    lv

    lvsat

    lv

    lvsatvlsatl

    i

    vT

    r

    ivTPPTT

    =

    2

    This is the superheat needed to sustain a vapor nucleus of radius r

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    Conversely the equilibrium radius for a nucleus in the liquid with a

    superheat of Tl

    -Tsat

    is:

    lv

    lvsat

    satl

    ei

    vT

    TTr

    =

    2

    Carey (1992) derived the following equation for rebased on the equilibrium of chemical potential:

    ( ) ( )[ ]{ } lllsatlllsate

    PRTTPPvTPr

    =

    /exp

    2

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    Now, the remaining question is that how many nuclei are

    formed and grown per unit time per unit volume?

    See the boiling process, the nucleation rate must be >109 to1013 m-3s-1.

    The free energy to form a nucleus of radius r , FG(r) , is given by :

    ( )lv PPrrrG =32

    3

    44)(

    Free energy Additional

    surface energy

    Work done by the vapor

    to the surrounding liquid

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    At a given temperature (liquid superheat)

    elv rPP

    2

    =

    =

    =

    e

    e

    r

    rr

    rrrrG

    3

    214

    2

    3

    44)(

    2

    32

    1

    FGmax

    r/re

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    It can be shown that

    [ ] erratdr

    rGd == 0)(( )2

    32

    316

    34)(

    lv

    eePP

    rrG

    ==

    Since the free energy is less, a nucleus smaller than re will collapse

    and a nucleus larger than re will grow spontaneously.

    If one more molecules collides with the equilibrium nucleus ,than the nucleus will grow and vice versa.

    Rate of nucleation: J

    J = the number of critical size nuclei per unit volume per unit timewhich grow to macroscopic size .

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    Boiling occurs if J > 109 to 1013 m-3s-1

    )( erNJ=N(re) = number of equilibrium nuclei per unit volumeG = collision frequency

    l

    e

    kT

    rG

    le NrN

    )(

    exp)(

    =

    N(re) is given by the Boltzmann equation

    k = Boltzmann constant

    Nl= Number density of liquid molecules

    =Bernath

    m

    Westwaterh

    kTl

    2

    1

    2

    h is Planks constant

    m is the mass of a single liquid molecule

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    For water at 100H , G=1012 ~ 1013 s-1

    Solution produce to determine the limit of superheat

    1. At a give a superheat , evaluate re from the following eq.

    lv

    lvsat

    satl

    ei

    vT

    TTr

    =

    2

    2. Evaluate 2

    3

    4)(

    ee

    rrG =

    3. Evaluate le

    kT

    rG

    le NrN

    )(

    exp)(

    =

    4. Evaluate le

    kT

    rG

    lNJ

    )(

    exp

    =

    5. J > 109 to 1013 m-3s-1 , if yes, then Tl- Tsat is the superheat of

    homogeneous nucleation , if not, repeat the procedure form 1 to 5

    lT

    J

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    Lienhards correlation:8

    ,,,, 095.0905.0 satrsatrsatrlr TTTT +=

    Water Superheat for Homogeneous Nucleation

    1 70 155

    Van der Waals 175(174)* 11.2(14) * -5.75(-7.1) *

    Berthelot 223(223) * 47.2(49.2) * 10.3(10.2) *

    Kinetic 206 49.3 10.4

    Lienhard 214 46.0 10.6

    P(bar)T

    l-Tsat

    *IJKLMN)OP%.N

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    2.2 Heterogeneous Nucleation

    Vapor formation with the presence of foreignbodies or container surface .

    With the presence of non-condensible gases

    a

    e

    lv

    e

    lav

    Pr

    PP

    r

    PPP

    =

    =+

    2

    2

    The presence of dissolved gas reduces the

    superheat requirement to maintain a nucleus of radius re

    With the presence of a flat solid surface surface

    wettability effect

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    Contact Angle

    VaporLiquid

    C

    C: contact angle , measuring from liquid sideC= 0 Q perfect wetting ; eq. Freon on metal surface.

    C= 180Qpoor wetting.Typically , C = 60Q~ 90 Q

    Soild

    "

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    Static advancing / receding contact angle

    Cs,A

    Cs,R

    Liquid Supply Liquid Withdrawal

    Static advancing Static receding

    Cd,A

    Cd,R

    Vapor/air

    Vapor/air

    Dynamic advancing

    Dynamic receding

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    Flat surface

    B-C

    C

    re

    vs ls

    vV

    lvA

    vsA

    Vapor

    Force balance at the triple point

    cos

    )cos(

    lvlsvs

    lslvvs

    ==+

    =lv

    lP

    vP

    "

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    Free energy to form a vapor nucleous on a flat surface

    )()(lvvlsvsvsvslvlve

    PPVAAArG +=

    [ ]

    +=

    +=

    e

    vvslv

    e

    lvvlsvsvslvlv

    r

    VAA

    rVAA

    2cos

    2

    lvlvA vsvsA +

    lsvsA

    )( lvv PPV

    : Addition surface energy

    : Liquid-solid interface replaced by vapor-solid interface

    : Work done by the vapor on the liquid system

    ( )

    ( )

    233

    222

    sincos3

    cos13

    2

    sin;cos12

    eev

    evselv

    rrV

    rArA

    ++=

    =+=

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    )(3

    4

    4

    sincoscos22

    3

    4)(

    2

    22

    e

    ee

    r

    rrG

    =

    ++=

    2

    3

    4er

    )(

    )(

    : free energy for forming an equilibrium nucleous in the

    homogeneous liquid .

    C= 0Q , i.e. in perfect wetting liquid.

    C=180Q, i.e. poor wetting liquid.

    0.0

    0.5

    1.0

    0o

    90o 180o

    )(

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    ))(

    exp()( 32

    g

    ee

    kT

    rGNrN

    =

    At low contact angles, the superheat required for homogeneous

    nucleation is lower than for heterogeneous nucleation with the

    presence of a flat surface. At a contact angle of approximately 68Q

    , the two modes are equally probable .For C= 90Q, the superheatis reduced by approximately 35%.

    The reduction in superheat is insufficient to explain the very much

    lower superheat found in practical situations, particularly with water,compared with those required for homogeneous nucleation.

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    Initiation heat-transfer and nucleation-site data(Form Van Stralen R Cole)Site q , kW /m 2 T w - T s, K R ,T m Type of s i te

    1 27.9 6.8 5

    2 28.1 7.2

    4 29 .0 8 .0 6

    8 29 .0 8 .3 4

    18 29 .6 9 .0 5 .5

    19 29 .6 9 .0 2 .5

    20 29 .6 9 .0 1 .5

    33 33 .9 9 .3 3

    34 34 .3 9 .5 2

    41 35 .1 9 .5 1 .5

    42 35 .1 9 .5 1 .5

    44 44 .6 10 .2 2 .5

    45 44 .6 10 .5 1 .5

    50 44 .6 10 .6 1

    Pit , deep in par t

    Largest cavi ty in c ra ter of 80T mdiameter

    End o f g roove ,12 T m w ide

    Pit , deep centra l par t of 4T m

    diameter

    Pit , e longated and d eep, 6 18 T m

    Pit , deep in par ts

    Si te a t end of groove, 20 T m

    wide

    Pit , deep in par ts

    Pi t , deep in par ts

    Elong ated pi t , deep a t one end

    Pit, largest in crater of 90 T mdiameter

    Pit , deep par t of 2 T m diamete r

    Pit , deep par t of scra tch, 1T m w i d e

    Pit , shal low cra ter 25T m w ide

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    Scanning-electron-mircoscope photographs of selected natural nucleation site.

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    Vapor Trapping Mechanisms Proposed by Bankoff

    U

    C

    Liquid

    For C>U, the flood of liquidwould tend to leave a vapor or

    embryp in the cavity

    U

    C

    BVC

    LiquidGas(or vapor)

    Gas(or vapor)

    For C>BVU, gas or vapor woulddisplace the liquid in the cavity.

    Advance of a liquid sheet

    Retreating of a liquid sheat

    (advancing of a gas-liquid interface)

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    Limiting cavity conditions

    Case Type of cavity Condition Trapping Ability

    1 steep (U small)

    2 steep (U small)

    3 shallow(U big)

    4 shallow (U big)

    Poorly wetted (C big,

    C >U , C >B VU )

    Well wetted(C smallC

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    C> 90

    Surface tension tends to resist

    further penetration of the liquid

    Effective Nucleation Site

    C< 90Surface tension at the interface

    tends to lead liquid to penetrate

    and cause the cavity to be ineffective

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    Re-entrant Cavity

    C< 90 Natural re-enterant cavity

    C

    Artficially fabricated re-entrantcauity

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    Cavity Nucleation Process

    ra

    r2

    r3

    r1

    Curvature of a liquid-vapor interface emerging form a conical cavity.

    Form Van Stralen R Cole

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    U

    C

    rc

    U

    C

    rc

    Advancing liquid front

    Vapor trapping model of Lorentz, Mikic, and Rohsenow

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    Form Tong et al. 1990 (Int. J. Heat Mass Transfer, vol.33, pp.91-103)

    ( )

    3

    1

    2

    3

    2

    3

    3

    2tan

    2tan

    1

    1

    2tan

    2tan

    2sin2sin32

    2tan

    2cos

    2sin2sin

    sin

    +

    +

    =

    cr

    r CXU,in rad

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    2.3 Boiling Incipience and Size Range of Nucleation

    Ref. Y.Y.Hsu, On the size range of active nucleation cavity on

    a heating surface, J. Heat Transfer, pp.207-216 1962

    Engineering surface is characterized by a distribution of cavities

    with various size and geometries.

    Experimental observations have indicated that for a given superheat

    , there exists a size range of active cavities.

    At higher heat fluxes or superheat, the range of active cavities isextended in both directions to both larger and smaller cavities.

    Griffith and Wallis experiment:

    For 25Tm diameter of artificial cavities, the wall superheat ofboiling incipience is 11k rather than 1.3k predicted by :

    =

    =

    clv

    lvsat

    T

    c

    satri

    vT

    dT

    dprTT

    sat

    212

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    Transient Heat Conduction in Thermal Boundary Layer

    G.E.

    t

    T

    y

    T l

    l

    l

    =

    12

    2

    I.C. t =0, = TTl

    B.C.

    ==

    ==

    =

    TTy

    caseqq

    caseTTy

    o

    wl

    2

    10

    Zyb

    y

    rb

    0qqorTT w ==

    T[

    Case 1

    ( )

    +

    =

    =

    =

    2

    22

    1

    expsincos2

    tnyn

    ny

    TT

    TT l

    nw

    l

    yt

    = ,

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    Bubble interior Temperature

    lv

    lvsat

    b

    satv

    i

    vT

    rTT 2

    =

    Criterion for the bubble embryo to grow is the condition that the liquid

    temperature at the bubble cap (y=yb)is equal to or greater than the

    bubble interior temperature.

    lv

    lvsat

    b

    satbli

    vTr

    TyyT 2)( +=

    2111

    ===== forrrycrcr cbbcb Rwhere

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    rc,maxrc,min

    Tl-T

    [

    Tsat

    -T[

    t

    Steady state temperature distribution

    y or rc

    lv

    lvsat

    b

    satvi

    vT

    rTT 2

    =

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    Size range of nucleation

    max,min, cc rrr

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    Boiling incipience

    No cavity will be effective if the discrininant in the above two

    equation is negative

    04

    1

    2

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    2.4 Bubble Dynamics

    In homogeneous medium

    In heterogeneous medium

    More relevant to experimental boiling heat transferbut is more difficult to tackle

    Extended Rayleigh Equation

    "

    R0

    Rb

    P

    vP

    l

    Mechanical energy balance

    drrtPdrrv b

    b

    R

    RR l

    222 4)(42

    1

    0

    =

    FP(t) = Excess pressure of bubble

    Continuity equation

    dt

    dRRwhere

    Rr

    RrRRvr

    b

    b

    b

    b

    bb

    =

    ==

    &

    &&2

    2

    22)(44

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    Substituting the continuity equation into mechanical energy balance

    equation results in

    =

    =

    b

    b

    ob

    R

    Rbbl

    R

    RR

    bbl

    drrtPRR

    drrtPdrrrRR

    0

    223

    22

    2

    2

    2

    )()(2

    1

    4)(2

    4

    &

    &

    Operating on the above equation by

    ( )[ ]2223

    )()(2

    1

    0 bb

    R

    Rb

    b

    bbl

    b

    b

    RtPRdrrtPRdt

    dR

    RRdt

    d

    Rdt

    dR

    dt

    d

    b

    =

    =

    =

    &&

    l

    bbb

    tPRRR

    )()(

    2

    3 2 =+ &&&

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    ( )Rrr

    b

    lvR

    PPtP

    +=2

    )(

    = Vapor pressure inside the bubble.vP Vapor pressure corresponding to the instantaneous liquidtemperature at the interface.

    lP =Imposed static pressure well away form the bubble.

    bR

    2

    =Capillary pressure due to the bubble interface.

    = V

    dr

    dvrlRrr b

    r

    3

    22)( =Normal stress due to the liquid motion

    ( ) bbRr Rdt

    dRv &==

    ( )R

    bb

    b

    rrr

    r

    RR

    Rr

    vv

    Rvr

    dr

    d

    rv

    +=

    +== &

    &r 221 222

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    ( )

    = b

    bR

    blRrr

    RRr

    Rb

    && 1

    3

    4

    3

    4

    ( )

    r

    RrRR

    r

    R bbbr

    R

    b

    b

    +

    =

    &&&

    0lim

    b

    b

    R

    b

    b

    bb

    b

    b

    b

    b

    bbb

    R

    R

    r

    R

    RR

    rR

    R

    rR

    R

    rR

    rR

    RrRR

    b

    &&

    &&&&&

    )2(

    211

    1

    1

    )()(

    2

    22

    2

    =

    =

    +

    =+

    =+

    b

    bl

    b

    b

    b

    blrr

    R

    R

    R

    R

    R

    R &&& 4

    3

    4)2(

    3

    4=

    =

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    Extended Rayleigh Equation

    =+

    b

    b

    l

    b

    lv

    l

    bbb

    R

    R

    R

    PPRRR&

    &&&

    421

    )(

    2

    3 2

    Pv and E are function of liquid temperature at the bubble interface.Therefore, the energy equation for the liquid region must be solved

    simultaneously.

    Liquid energy equation

    r

    Tr

    rrT

    t

    Tv

    t

    Tlr

    ==

    + 2

    2

    2 1b

    br R

    r

    Rv &

    2

    2

    =

    Initial conditions

    l

    b

    b

    TrT

    R

    RR

    ==

    =

    ),0(

    0)0(

    )0(0

    &

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    Boundary conditions

    )(3

    )3

    4(

    4

    1

    ),(

    3

    2

    3

    2 vb

    b

    lv

    bv

    b

    lv

    R

    l

    l

    Rdt

    d

    R

    iR

    dt

    d

    Ri

    r

    Tk

    TtT

    b

    ==

    =

    Inertial controlled bubble growth, valid for initial growth stage

    Neglect the capillary pressure and viscous stress andPv-Pl = constant = FP Thus,

    ( )[ ]

    ( ) cRPRR

    dRRP

    dtdt

    dRR

    PdtRR

    PRRd

    PRR

    dt

    d

    RR

    PRRR

    b

    l

    bb

    bb

    l

    bb

    l

    bb

    l

    bb

    l

    bb

    bb

    l

    bbb

    +

    =

    =

    =

    =

    =

    =+

    232

    22232

    32

    2

    2

    3

    12

    222

    )(2

    1

    )(2

    3

    &

    &&

    &

    &

    &&&

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    0)0(

    0)0(

    =2Uas Bankoff suggested and

    rc,min

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    -Poisson distribution

    n = local nucleation site density

    nb= mean nucleation site density

    a = the area of an area element

    3.5 Boil ing Chaos

    Nucleate boiling heat transfer is influenced by many variables such as

    surface material, geometry orientation, working fluid and its

    wettability, etc.Nucleate boiling heat transfer is highly nonlinear and boiling chaos is

    thus of no surprise

    )!(

    )()( na

    eannaP

    anna

    b

    b

    =

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    ]^_3`ab;cCz{s+def

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    Ma & Pan, 1999

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    Ma & Pan, 1999a

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    Ma & Pan, 1990a

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    Ma & Pan, 1999b

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    Ma & Pan, 1999b

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    Kacamustafaogullari & Ishii, 1983

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    Point et al., 1996

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    Kenning and Yan, 1996

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    Kenning and Yan, 1996

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    Shoji, 1998

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    Nelson et al., 1996

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    Nelson et al., 1996

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    Sadasivan et al., 1995

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    Sadasivan et al., 1995

    CHAPTER4 Nucleate Boil ing Heat Transfer

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    and Forced Convective Evaporation

    Topics to be presented in this chapter

    Onset of Nucleate Boiling

    Subcooled Nucleate Boiling

    Saturated Nucleate Boiling and Two-Phase Convective Heat Transfer

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    From: Collier, 1981

    4.1 Onset of Nucleate Boil ing

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    Review of single-phase heat transfer

    Energy balance

    +=

    =

    =

    =

    =

    =

    z

    l

    lil

    z

    lilll

    zdzqGDCp

    TzT

    w

    smkgfluxmassG

    skgGD

    flowliguidofratemassm

    TzTCpmDdzzq

    0

    2

    2

    0

    )(4

    )(

    )/(

    )/(41

    ))(()(

    &

    &dz

    D

    Z

    Wf(kg/s)

    Length of subcooled region, zscb h l h h b

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    Let zscbe the entrance length where , zsc can be

    determined by the following equation.

    subcoolinglocalzTTzTsubcoolinginletTTT

    Tq

    GDCpz

    qzqge

    zdzqGDCp

    TTzT

    lsatsat

    ilsatisat

    isub

    l

    sc

    z

    l

    lisatscl

    sc

    ====

    =

    =

    +==

    )()(

    4

    )(..

    )(4

    )(

    ,,

    ,

    0

    0

    0

    satl TT

    Wall temperature distribution in single-phase region

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    tcoefficientransferheath

    hzqzTzT

    zTzThzq

    lw

    lw

    =+=

    =

    /)()()(

    )]()([)(

    For turbulent flow in a pipe

    Dittus-Boeiter correlation

    10000Reand50z/DFor

    023.0

    PrRe023.0Nu

    33.08.0

    33.08.0

    >>

    =

    =

    lll

    k

    CpGD

    k

    hD

    However, it is commonly used in entrance region.

    Boiling incipience (Onset of subcooled nucleate boiling)

    For boiling to occur T must be at least gT

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    For boiling to occur Tw must be at least gTsat

    isublisat

    l

    sat

    l

    li

    l

    lil

    z

    l

    lil

    satlw

    TTThGDCp

    zqor

    ThGDCp

    zqT

    zqGDCp

    T(z)T

    qzqif

    dzzqGDCp

    TzT

    Th

    zq

    zTT

    ,

    0

    ]14

    [

    ]14

    [

    4

    constand)(

    )(4

    )(

    thatRecall

    )(

    )(

    =+

    ++

    +=

    ==

    +=

    +=

    q

    isubT ,

    isub

    l

    ThGDCp

    zq ,14 =

    +

    Non-boiling region

    Recall that, assuming that a wide range of cavity size available,

    ik1

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    for the onset of nucleate boiling.

    For water, the correlation of Bergles and Rohsenows correlation

    maybe used:

    For a tube with a constant heat flux, , a mass flux, G, the location

    of boiling incipience may be evaluated in the following way:

    lvsat

    lvl

    ONBsatONBvT

    ikTq

    )2(4

    1,

    =

    0234.0463.0

    156.1, ]1082[556.0

    PONB

    ONBsat

    q

    T

    =

    q

    hqzTzT lw /)()( +=

    For the criterion for the onset of nucleate boiling,

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    Thus,

    4)(

    thatRecall

    )(8

    )()(

    Thus,

    )(8

    ,

    5.0

    5.0

    5.0

    5.0

    l

    ill

    lvl

    lvsatsatONBl

    lvl

    lvsatsatw

    GDCp

    zqTzT

    qik

    vTT

    h

    qzT

    q

    ik

    vTTT

    +=

    =

    +

    =

    5.0

    5.0

    )(84

    qik

    vTT

    h

    q

    GDCp

    zqT

    lvl

    lvsatsat

    l

    ONBli

    =

    +

    +

    +

    = 5.0

    5.0

    )(8

    4q

    k

    vT

    h

    qT

    GDCpz lvsatisat

    lONB

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    , )(4

    qikhq lvl

    isatONB

    +

    =

    0234.0463.0

    156.1,]

    1082[556.0

    4

    PONBisat

    lONB

    P

    q

    h

    qT

    q

    GDCpz

    If water is used as the working fluid.

    q Relation between heat flux and wall

    h t t th iti i i i t

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    atw TTT =

    ONBq superheat at the position incipientboiling (Form Hino & Ueda, 1985

    Int. J. Multiphase Flow vol.11,No.3, pp.269-281 )

    figuretheinEq

    ri

    TkTT

    r

    kq

    figuretheinEq

    vT

    ikTTq

    vlv

    satlONBsatw

    lONB

    lvsat

    lvlONBsatwONB

    )4.(...........

    ..)(

    2)(

    )3.(...............

    .)2(

    )(4

    1

    2

    maxmax

    2

    =

    =

    Boiling hysteresis

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    wT

    q

    ONBTsatT

    Partial subcooled nucleate boiling

    Fully developed subcooled nucleate boiling

    Single-phase liquid

    Non-boiling region

    q KT

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    q KTw

    satws TTT = mzDistanceBoiling curve hysteresis Wall temperature profiles

    Form: Hino and Ueda, 1985, Studies on Heat Transfer and Flow

    Characteristics in Subcooled Flow Boiling Part1, Boling

    Characteristics, Int. J. Multiphase Flow, vol.11, pp.269-281

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    satEXP

    lONB

    ONBsat

    TofvaluereportedfromX

    q

    T

    X

    = Pr)()(

    5.0

    05.0X

    XEXP

    Experimental data for the onset of boiling compared with eq.

    (Forost and Dzakowic34) Form Collier, 1981

    4.2 Heat Transfer in Subcooled Nucleate Boil ing

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    I. Partial subcooled boiling

    i. Few nucleation sites

    ii. Heat transferred by normal single-phase process

    between patches of bubble + boiling

    II. Fully developed subcooled boiling

    i. Whole surface is covered by bubbles and their influence regions.

    ii. Velocity and subcooling has little or no effect on

    the surface temperature.

    Partial subcooled boiling

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    Single-phase heat transferSubcooled boiling

    heat transfer

    Rohsenow correlation

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    =

    =

    +=

    fluidsotherfor

    waterfor

    l

    ll

    vllvl

    scBsf

    lv

    satl

    scB

    lwspL

    scBspL

    k

    Cp

    gi

    qC

    i

    TCp

    q

    ncorrelatioBoelterDittush

    TThq

    qqq

    7.1

    0.133.0

    )(

    :

    :

    ][

    boilingnucleatesubcooled:scBliquidphasesingle:spL

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    Values of Csfin eq. Obtained in the reduction of the forced

    (and natural) convection subcooled boiling data of various investigators

    (Form Collier, 1981)

    q Full developed

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    "

    "

    "

    "

    satT ONBwT )(

    Cq

    ONBq

    wT Wall temp

    Full developed

    Partial

    B

    C

    E

    "

    C

    D

    scBq

    Bergles and Rohsenow correlation

    50

    [ ] 5.02)( ++= qqqq

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    Calculation procedure

    1. Pick Tw

    2. Evaluate and

    3. Determine C, ie

    form the incipience boiling model

    4. Evaluate from fully-developed

    equation but setting

    5.02

    11

    +=

    scB

    C

    spL

    scB

    spL

    q

    q

    q

    qqq

    scBq )]([ satwspL TThq =

    ))(..( ONBWONB Tsvq

    Cq ONBww TT )(=

    [ ]5.0

    2

    11

    )(

    +=

    ++=

    scB

    c

    spL

    scBspL

    CscBspL

    qq

    qqq

    qqqq

    Fully developed subcooled boiling

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    -Surface is covered by bubbles and their influence region

    -Velocity and subcooling has little or no effect on the surface temperature

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    )ln( lw TT

    )ln(q

    )ln( lw TT

    )ln(q

    Fullydeveloped

    boiling

    H

    L

    H

    L

    Low subcooling

    High subcooling

    H Low G

    L High G

    Correlations for fully developed subcooled boiling

    -Jens and Lottes correlation(1951)

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    -Ranges of data for water only

    i.d = 3.63 to 5.74 mm , P = 7 to 172 bar , Tl = 115 to 340H

    G = 11 to 1.0510-4

    kg/m2

    s , up to 12.5 MW/m2

    -Thom et al (1965)

    for water only

    barin,Mw/mink,in

    )(25

    2

    6225.0

    PqT

    eqT

    sat

    P

    sat

    =

    q

    barin,MW/mink,in

    )(65.22

    2

    875.0

    PqT

    eqT

    sat

    P

    sat

    =

    -Jens and Lottes correlation in terms of heat transfer coefficients

    62250)(25

    P

    T

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    6225.0)(25sat eqT =

    superheat.wallinincreasewithincreasesh

    )(

    25

    1)(

    25

    1

    flux.heatinincreasewithincreasesh

    )](25

    1[

    )(25

    3

    4

    62

    4

    4

    62

    75.062

    6225.0

    sat

    P

    sat

    sat

    P

    sat

    P

    P

    sat

    Te

    T

    Te

    T

    qh

    or

    qe

    eq

    q

    T

    qh

    =

    =

    =

    =

    =

    =

    ??

    15570,/10 26

    ==

    hT

    barandbarPmWq

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    ?? == hTsat

    At P=70bar

    At P=150bar

    kmWkmMWeh

    keTsat

    25275.062

    70

    62

    70

    25.0

    /1024.1/124.01]25

    1

    [

    1.8)1(25

    ===

    ==

    kmWkmMWeh

    keTsat

    25275.062

    155

    62

    155

    25.0

    /1087.4/487.01]25

    1[

    1.2)1(25

    ===

    ==

    It is summarizes the present data

    of heat transfer of subcooled flow

    boiling of water in the swirl tube

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    boiling of water in the swirl tube

    and hypervapotron under one side

    heating conditions. The data areobtained by experiments in

    regions fro non-boiling to highly

    subcooled partial flow boiling

    under conditions that surface heat

    fluxes, flow velocities, and local

    pressure range form 2 to 3

    MW/m2, 4 to 16 m/s and 0.5, 1.9

    and 1.5 MPa respectively. In the

    figure, a new heat transfer

    correlation for such subcooled

    partial flow boiling under one

    sides heating conditions on which

    no literature exists is proposed.

    Heat transfer of subcooled water flowingin a swirl tube(Form: S.Toda, Advanced

    Researches of Thermal-Hydraulics under

    High Heat Load in Fusion Reactor, Proc.

    NURETH-8. pp.942-957,1997)

    -Shah(1977), ASHRAE Trans. Vol.83, Part1, pp.202-217

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    satw

    lsat

    l

    TP

    satw

    lsat

    l

    TP

    satw

    lsat

    TT

    TT

    h

    hthen

    TT

    TTif

    h

    hthen

    TT

    TTif

    +=>

    =10000

    -Correlation of Bjorge, Hall and Rohsenow, 1982

    Int. J. Heat Mass Transfer, vol.25, No.6 pp.753-757

    For subcooled and low quality region

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    For subcooled and low quality region

    f

    fw

    bl

    blfl

    flbl

    FC

    FC

    lwFCsubsatFCFC

    sat

    ONBsatscbFC

    Tbulkb

    TTfilmf

    k

    CpGD

    k

    Dh

    eqColburnbyecaluatedish

    TThTThq

    TTqqq

    ,

    2023.0

    .

    )()(

    )(1)()(

    3/1

    ,

    ,,

    8.0

    ,,

    5.02

    3

    22

    =

    ==

    =

    ==

    +=

    .eqRohsenowbyevaluatedisqscB

    3

    8/18/58/98/7

    8/18/198/172/15.0

    )()( sat

    satvllvl

    vlllM

    vllvl

    scB TTi

    CpkBgi

    q

    =

    BM Depends upon boiling surface cavity size distribution

    and fluids properties For water only, BM=1.8910-4 in SI units.

    For rc,min>rmax (the radius of largest cavity, rmax)

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    [ ]

    ONBsatlv

    lvsatcritc

    l

    FC

    FClvsat

    lvl

    subONBsat

    critc

    subONBsat

    Ti

    vTr

    k

    rhN

    hvT

    ik

    TT

    rrfor

    TN

    NN

    T

    )(

    4

    8

    )41(12

    1)(

    )

    4

    1(

    1

    1)(

    ,

    max

    2/1

    max,

    =

    =

    =

    ++

    =

    =

    =

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    CyT

    dy

    dT

    +==

    ++

    +

    +

    Pr

    Pr

    1

    1

    Applying the B.C. at y+ = Z+

    ++++

    ++++

    ++

    +===

    +==

    Pr0Pr*0)0(

    PrPr

    Pr

    sat

    sat

    sat

    TyT

    TyT

    TC

    5,Pr)( =

    = ++

    +

    satw

    w

    sat TTq

    CpuT

    satT

    +y

    +

    5

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    ++

    ++

    +

    +++

    ++

    +

    ++

    +++==

    ++==

    ++=

    +=

    sat

    sat

    TyT

    CTT

    Cy

    T

    dydTy

    )]1Pr

    1

    (5ln[5)]1Pr

    1

    (5

    5

    ln[5)5(

    )]1Pr

    1(5ln[5)(

    )]1Pr

    1(

    5ln[5

    ]5

    )1Pr1[(1

    )(

    1

    1

    +++

    + +++= satTy

    T )]1Pr

    1(

    5ln[5)]1

    Pr

    1(

    5ln[5

    ++y

    sa

    5 30

    At y+=5, temperature evaluated from the buffer zone must be equal to

    that from the viscous sublayer.

    R ll th t f th i bl

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    Recall that for the viscous sublayer

    Pr5)]1Pr

    1(

    5ln[5Prln50)0(

    Pr5)]1Pr

    1(

    5ln[5Prln5

    )]1Pr

    1(

    5ln[5)]1

    Pr

    1(1ln[55Pr)5(

    Pr

    2

    2

    2

    2

    ++====

    ++=

    +++=+=

    +=

    ++

    ++

    ++

    ++

    +

    ++

    sat

    sat

    sat

    TCyT

    TC

    TCT

    CyT

    Pr5)]1Pr

    1(

    5ln[5Prln5 +++=

    ++

    satT

    ++=

    +++=

    +

    +

    )]15

    Pr(1ln[Pr5

    Pr5)]1Pr1(

    5ln[5Prln5)(

    satw

    w

    TTq

    Cpu

    or

    30),3( >+Case

    For the turbulent core region++ dTy

    ])11

    [(1

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    Recall that

    for the viscous sublayer,

    for the butter zone

    so, the continuity of temperature at y+ = 5 results in

    +++

    +

    +

    +++=

    +=

    satTy

    T

    dy

    y

    )]1Pr

    1(

    5.2ln[5.2)]1

    Pr

    1(

    5.2ln[5.2

    ]5.2

    )1Pr

    [(1

    ++

    = yT Pr

    Cy

    T ++=+

    + )]1Pr

    1(

    5ln[5

    Pr5ln(Pr)5

    ln(Pr)5)]1Pr

    1(1ln[5Pr5

    +=

    +=++=

    C

    CC

    So, for the buffer zone

    Pr5ln(Pr)5)]1Pr

    1(

    5ln[5 +++=

    ++ yT

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    The continuity of temperature at y+ = 30 results in

    Pr5ln(Pr)5]Pr

    15ln[5

    )]1Pr

    1(

    5.2

    30ln[5.2)]1

    Pr

    1(

    5.2ln[5.2

    Pr5Prln5)]1Pr

    1(6ln[5

    )]1Pr

    1(

    5.2ln[5.2)]1

    Pr

    1(

    5.2

    30ln[5.2

    ++++

    ++=

    +++=

    +++

    ++

    ++

    sat

    sat

    T

    T

    +

    ++++=

    +

    + ]

    )1Pr

    1

    5.2

    30(

    )1Pr

    1

    5.2(

    ln[2

    1)1Pr5ln(Pr5

    satT

    1Pr

    )30

    ln(2

    1)1Pr5ln(Pr5

    ++++

    +

    if

    Tsat

    +

    ++

    5Pr

    )(

    TTC

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    >

    +++

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    U = average liquid flow rate assuming full pipe flow

    +

    +

    +

    +

    +

    +

    =

    ====

    =

    =

    =

    sat

    satsatsat

    sat

    sat

    satw

    TU

    u

    TU

    u

    v

    DUv

    T

    Du

    kT

    CpDu

    k

    hDNu

    T

    Cpuh

    h

    CpuT

    hq

    TT

    1RePr

    1))()((

    1

    +

    5Re

    u

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    >

    +++

    +

    =

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    TP

    TP

    TP

    TP

    TP

    tttt

    S

    XX

    eR70

    0.70eR5.32

    5.32eR

    1.0

    ])e(R42.01[

    ])e(R12.01[

    10.0)213.0(35.2

    178.0

    114.1

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    From: Collier, 1981

    2

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    2

    kWmq

    CTsat Comparison of Chens correlation with Thoms and Jens-Lottess correlations.

    P=10MPa, G=5.4Mgm-2s-1, De =0.3cm.

    From: Hewitt, Delhaye & Zuber, 1986. Vol.2 ch3.

    Modification Chens correlation

    -Hahne, et al.s correlation, 1989.

    Hahne Shen & Spindles 1989 Int J Heat Mass Transfer

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    Hahne, Shen & Spindles, 1989 Int. J. Heat Mass Transfer

    , vol.32, No.10 1799-1808, 1989

    [ ]

    133.0

    0

    27.0

    0

    736.0

    4.0

    8.0

    )())()1(

    8.1

    4.4()(1.2)(

    1.0/1213.0)/1(35.2

    1.0/11

    Pr)1(

    023.0

    p

    p

    c

    c

    c

    m

    o

    NCB

    tttt

    tt

    ll

    l

    c

    NCBcTPW

    R

    R

    P

    P

    P

    PP

    P

    q

    q

    hh

    XXF

    XF

    D

    kDxGh

    ShFhh

    ++

    =

    >+=

    =

    =

    +=

    k

    gh

    kS

    l

    vl

    c

    l

    5.0

    5.0

    ])(

    [041.0

    )1(exp1

    =

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    KmWh

    Rfor

    P

    Pm

    fluidsorganicfor

    DINbydefinedroughnesssurfacetheisR

    mRmWq

    gh

    c

    p

    p

    l

    vlc

    23

    0

    3.0

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    6

    0

    24

    0

    /103.2

    12

    3.09.0

    )4262(

    101,/102

    )(041.0

    =

    =

    ==

    --Effect of flow direction is also studied in this paper. There is no clear

    effect of flow direction

    --Upwards or downwards with a minimum liquid velocity of 0.25 m/s

    -Gungor-Winterton Correlation

    Ref: Gungor. K.E and Winterton, R.H.S(1986),A general correlation

    for flow Boiling in tubes and annuli, Int. J. Heat Mass Transfer.

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    Vol.29 pp.351-358

    crrrNCB

    lvtt

    ll

    l

    c

    NCBcTP

    P

    PPqMPPh

    Gi

    qBo

    XBoF

    D

    kDxGh

    ShFhh

    ==

    =++=

    =

    +=

    67.05.055.012.0

    86.016.1

    4.0

    8.0

    )())ln(4343.0(55

    ,)1

    (37.1240001

    Pr)1(

    023.0

    DxG

    ES

    weightMolecularM

    l

    117.126

    )1(Re

    ]Re1015.11[

    ,

    =

    +=

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    KmWinhmWinqwhere

    l

    l

    22 /;/

    Re

    =

    )()(

    &

    05.0

    )(.

    )21.0(

    2

    2

    satwNCBlwl

    Fr

    l

    TTShTThqboilingflowsubcooledFor

    FrSSEFrE

    FrIf

    gD

    G

    NoFroudeFr

    boilingflowhorizontalFor

    +=

    ==

    00030,01)461(

    0003.0,0.12305.0

    5.0

    BoifhBo

    BoifhBo

    l

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    =

    >

    +

    =

    0011.043.15

    0011.070.14

    1.0)74.2exp(

    1.00.1)74.2exp(

    0003.0,0.1)461(

    15.05.0

    1.05.0

    Boif

    BoifF

    ifhFBo

    ifhFBo

    BoifhBo

    h

    l

    l

    l

    NCB

    lvGi

    q

    Bo

    =

    CHAPTER5 Critical Heat F luxIndividual

    bubble

    region

    Vapor

    mushroom

    regionq

    q

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    Topics to be discussed

    Critical Heat Flux for Pool Boiling

    Critical Heat Flux for Flow Boiling-Dryout: Dryout of the liquid film, theoretical modeling

    -DNB: Departure from nucleate boiling, theoretical modeling

    Empirical Correlation for Flow Boiling CHF

    regionCHFq

    trq

    satw TT

    5.1 Critical Heat Flux for Pool Boiling

    Kutateladze (1951) used dimensional analysis to obtain that

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    Zubers modelRef.: N. Zuber, 1958, On the Stability of Boiling Heat Transfer,

    Trans. ASME, vol.80, 711

    Recall that for the Helmhotz instability to take place,

    =

    =

    Lienhard

    CollierC

    gCiq vlvlvCHF

    131.0

    16.0

    )]([ 4/12/1

    2/12/1

    2

    2

    )(

    )(

    2

    )()(

    =

    ==

    ++

    vl

    vl

    lv

    lv

    lv

    lv

    g

    gk

    UU

    k

    From the Taylor instability and assume that the bubble is sphere,

    Liquid

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    [ ]

    [ ]

    ),)4

    (3

    4(

    24)

    2(

    1)

    4(

    3

    4

    )()(

    )()(

    )()(

    3

    2

    3

    2/12

    22

    2/12

    periodwavetheisvolumebubbletheis

    iiq

    gU

    UUU

    gUU

    vlvvlvCHF

    vl

    vlvlv

    vlv

    vl

    vl

    vllv

    ==

    +=

    +=

    Q

    Vapor Vapor

    At the critical heat flux point

    vU

    =

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    Haramura and Kattos model

    Ref.: Haramura & Katto, 1983, Int. J. Heat and Mass Transfer,

    vol.26, No.3, pp.389-399

    4/12/12/1

    4/12/12/1

    4/12/1

    )]([][131.0

    )]([][24

    )]([][24

    vl

    l

    vlvlv

    vl

    l

    vlvlv

    vl

    vl

    vlvlvCHF

    gi

    gi

    giq

    +

    =

    +

    =

    +

    =

    Vapor bubble

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    22

    2/1

    2/1

    )()(2

    4

    1

    )(23

    q

    i

    A

    A

    thicknessmacrolayer

    g

    yinstabilitTaylortheforlengthwavewavelengthdangerousmostThe

    lvv

    w

    v

    vl

    vl

    Hc

    vl

    D

    +

    =

    =

    =

    D D D

    c

    At CHF

    Hovering period for a bubble of volumetric growth ratevl

    lvvwclwd iAAAq )( =

    )11

    (4 vl +

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    Haramura and Katto postulated that CHF appears when the liquid

    film evaporates away at the end of the hovering period.

    )()(),/(

    ])(

    )

    16

    (

    [)43(

    23

    2

    5/15/35/1

    DlvvDl

    l

    vl

    vl

    d

    withinbubbleones

    miqv

    vg

    =

    =

    modelsZubertheassame

    theispredictedqAssume

    A

    A

    A

    A

    A

    A

    g

    i

    q

    CHF

    v

    l

    v

    l

    w

    v

    v

    l

    v

    l

    w

    v

    w

    v

    v

    vl

    lvv

    CHF

    ')1(

    )116

    11(

    0654.0

    )116

    11(

    )1(

    132)(

    2/1

    5/3

    16/5

    5/3

    16/58/516/1

    211

    4

    4/1

    2

    +

    +=

    +

    +

    =

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    High heat flux boiling of water on

    a horizontal 35-mm diameter

    copper disk (Katto et al., 1970)

    Behavior of vapor mass above a10-mm diameter disk observed by

    Katto and Yokoya(1976) (Interval

    between each frame: 11.3 ms for

    No. 1-5 and 8.8 ms for No.5-10)

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    Void fraction at midplane of a

    vertical rectangular plate of contact

    angle of 27 deg measured by Liaw

    and Dhir (1989)

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    Existing data and predictions for

    initial macrolayer thickness in

    water boiling at atm. Pressure.

    Comparison of initial macrolayerthickness measured by Okuyama

    et al. (1989) for R-113 boiling with

    the prediction of Haramura and

    Kattoss equation.

    Parameter effect on pool boiling CHF

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    From El-Wakil, Nuclear Heat Transport, 1978 .

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    )/10( 26 mW

    qCHF

    Pressure (kPa)

    Effect of system pressure on CHF (From Pan & Lin, 1990)

    CHFT)(

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    From: J. H. Lienhard, Burnout on Cylinders, J. Heat Transport,

    vol.110, pp.1271-1286,1988.

    26

    qCHF

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    )/10(26

    mW

    Tsub (K)

    (From Pan & Lin, 1990)

    ]102.01[

    1

    )()(1.0

    ]1[

    75.0

    +

    +=

    =

    +=

    Ja

    Jak

    i

    CpB

    TBqq

    sub

    lv

    l

    v

    l

    subZuberCHF

    lv

    subl

    v

    l

    vl

    i

    TCpJa

    JaJa

    k

    =

    =

    =

    75.0

    75.0

    )(

    )/(

    10

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    Horizontal ribbons oriented

    vertically

    horizontal ribbons, one side insulated

    (From: Lienhard, 1981, A Heat Transfer Textbook)

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    The peak pool boiling heat flux on several heaters

    (From: Lienhard, 1981, A Heat Transfer Textbook)

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    From: Lienhard, A Heat Transfer Textbook Prentice-Hall 1981

    2/15/3

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    CHF

    (MW/m2)

    Contact Angle

    Effect of surface wettability on the critical heat flux:

    comparison between model prediction and experimental data

    (From Pan & Lin, 1990)

    2;00179.0

    1

    11611

    5/3

    ==

    +

    +

    =

    nC

    CA

    A

    v

    l

    v

    l

    n

    w

    v

    5.2 Dryout Modeling (Dryout heat flux)

    Following (1)Isbin and his co-workers (2)Whalley

    Ref.: J.Weisman, 1985 Theoretically Based Predictions of Critical

    Heat Flux in Rod Bundles

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    The liquid film flow (in a round tube) is determined by a balance

    between entrainment,evaporation and deposition.

    )(

    )/(

    ][

    mdiametertubeD

    skgrateflowfilmliquidW

    Ddzi

    qDdzE

    dzdz

    dWW

    dzDDW

    l

    lv

    l

    l

    dl

    =

    =

    +

    ++

    =+

    dz

    Wf

    D

    Deposition

    Entrainment

    evaporation

    DrateinflowW

    smkgfilmthefromdropletsofratetentrainmenE

    smkgfilmtheontodropletsofratedepositionD

    l

    d

    =

    =

    =

    )/(

    )/(

    2

    2

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    ][lv

    d

    l

    i

    qEDD

    dz

    dW =

    dz

    Wf

    Deposition

    Entrainment

    evaporation

    Similarly, the entrained liquid flow

    rate satisfy the following eq.][ d

    E DEDdz

    dW=

    ratenevaporatioDdzi

    q

    rateentraimentDdzE

    rateoutflowdzdz

    dWW

    ratedepositiondzDD

    lv

    ll

    d

    =

    =

    =+

    =

    ][

    Deposition rate

    =

    =dsmtcoefficientransfermassordepositionThe

    CD

    )/(K

    "

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    =

    ==

    +=

    =

    ==

    z

    zlv

    v

    vvlEE

    vi

    k

    l

    s

    dzzqGDi

    zx

    Wzx

    vaporofrateflowMassWmkgWWW

    ionconcentratDroplet

    HewittbyproposedequationempiricaluD

    u

    )(4

    )(

    )(

    )/())/()//[(

    C

    )(/;][87

    3

    2/12

    Entrainment rate

    -Based on the observation that, under equilibrium conditions during

    adiabatic operation, the entrainment and deposition rates equal.

    Dd=mCE=E

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    Where CE is droplet concentration under equilibrium conditions

    It is assumed that the same relationship holds away from equilibrium.

    CE can be correlated as a function of iiZ/E

    )/( 3mkgCE

    /iCorrelation of equilibrium entrained droplet concentration

    (Hutchinson and Whalley) Form Collier, 1981

    To determine ii and Z, the triangular relationship may be used.[Relations between Wl, dP/dz, & Z]

    Initial condition:

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    Given Wl , WE & WvSo that the above set of ODE can now be solved.

    E.g. using an explicit scheme.

    (1) Evaluate (Dp/dz) & _ at z = 0(2) Evaluate Z & ii(3) Evaluate C & CE(4) Evaluate Dd & DE

    (5) Evaluate Wl , WE and Wv at z =z+dz(6) Repeat the process

    CHF occurs while Wl=0

    Summary

    " Conservation of liquid film mass

    ][ dl qEDD

    dW =

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    "Conservation of entrainment mass

    "Deposition mass flux

    C is droplet concentration

    lvidz

    ][ dE DED

    dz

    dW=

    v

    v

    l

    E

    E

    l

    l

    v

    i

    d WW

    W

    DCD

    +==

    2

    87k

    "Entrainment flux

    li

    EEED

    CCD

    287k ==

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    "Equilibrium entrainment droplet concentrationlv

    lv

    G

    GEln

    vEln

    vi

    inE

    i

    Dq

    dz

    dW

    D

    WWWf

    WWWfdz

    dP

    gdz

    dPR

    fC

    =

    =+=

    +=

    =

    =

    )1(2),,(

    ),(

    ][2

    )(

    )/(

    , see, e.g., Martinelli correlation

    , see, e.g., Martinelli

    correlation

    Ishii & Mishima model of Droplet Entrainment Correlation in

    Annular Two-Phase Flow

    Ref.: Ishii & Mishima, Int. J. Heat Mass Transfer, vol.32, No.10,

    pp.1835-1846, 1989

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    -Inception criterion

    (For Rel>2 for vertical downflow and Rel>160 for vertical up

    or horizontal flow for Nuk1/15 )

    l

    lll

    Dj

    =Re

    [ ]

    2/12/1

    8.0

    3/18.02/1

    ))(/(/

    1635Re

    1635ReRe78.11)(

    vlll

    l

    ll

    l

    vvl

    gnumberViscosityN

    forN

    forNj

    ==

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    3/12

    )(

    )Re1025.7tanh(

    v

    vlvv

    l

    DjWe

    We

    =

    =

    Govan et al. (1988) model for droplet deposition and entrainment inannular two-phase flow (From: Collier & Thom, 1994)

    2/1)(

    Dk v

    kC=D

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    65.02/1

    2/1

    )/(083.0)(

    3.0

    18.0)(

    3.0

    =

    >

    =

    >>>+

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    >>>>>

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    >>>>

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    The characteristics of the set of equations can be evaluated by the

    homogeneous part, i.e.,

    0)()( =

    +

    z

    uuB

    t

    uuA

    vv )()(

    tzieouuLet

    =

    0)()()()( =

    tzieouuBuAi vvvThus,

    The characteristic equation is hence given by:

    0)()( = uBuA vv

    The eigenvalue can then be determined. If is a complex number,

    the system is unstable and the problem is ill-posed.

    7.6 One-Dimensional Homogeneous F low Model

    The homogeneous flow model assumes that both phase have same

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    velocity and temperature.

    -Quality vs. void fraction

    >>>>>>>

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    ( ) zmvwvwwwmmmm

    gD

    Pz

    wz

    wt

    ++

    =

    +

    ll

    42

    or

    zmmm

    e

    mmmm gw

    DfP

    zw

    zw

    t

    +

    =

    + 2

    2

    2

    2

    11

    Similarly the mixture energy equation can be obtained by combining

    the phasic energy equation as:

    mmw

    H

    mmmmm P

    zwP

    tq

    Piw

    zi

    t+

    +

    +=

    + "

    where

    =mi mixture enthalpy[ ]>>

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    [ ] vvm

    llll

    ( ) >>

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    Ref.: Zuber, N. and Findlay, J.A. , 1965, Average Volumetric

    Concentration in Two-Phase Flow System, J. of Heat Transfer, pp.453-468.

    -Define the vapor drift velocity as the difference between vapor velocity(in the axial direction) and mixture superficial velocity.

    jww vvj =-Gas phase velocity:

    >>=>=>>

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    The drift velocity is also a function of flow pattern:For bubbly and churn flow,

    For slug flow

    l /2.02.1 voC =

    41

    2

    )(53.1

    >>=>=

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    >>>=>>>=>=>>>=< vjom

    vv

    v wjCz

    )1(

    l

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    m

    Similarly, the mixture momentum equation can be expressed as

    zmmm

    e

    mmmm gwD

    fz

    Pw

    zw

    t +

    =+

    2

    2

    2

    2

    11

    [ ]

    >>

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    Based on the homogenous assumption, , thus,>>=>>>>>=

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    (2) Interactions between each phase and wall

    (3) Turbulent model in two-phase flow

    8.1 I nter facial Area Density

    Recall that the time-averaged 3-D phasic equation includes the

    following interfacial term

    i

    T kis

    adensityarealInterfacia

    volumemixture

    arealInterfacia

    LnVTs

    ====

    11

    vv

    Ishii proposed that volumetric interfacial transfer rate=aidriving forceIshii and Mishima correlation

    -For bubbly or dispersed droplet flow

    sm

    d

    id

    di

    d

    di

    rAV

    A

    V

    a 3

    /3

    3===

    where Vd is the volume of a bubble or droplet,

    Ai is the surface area of a bubble or droplet

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    i p

    rsm is the Sauter mean radius . For a spherical bubble or droplet, rsm=r

    Cross sectionally area averaged ai of bubbly, slug or churn-turbulent flow:

    gs

    gssm

    gs

    gs

    gs

    i forrD

    a

    >>==

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    --For subcooled boiling

    Lahey and Moodys model

    for water, H0=0.075H /s

    -Local mass transfer rate

    { }])([

    ])([))((

    )( 0lsatl

    llvlsatlllvvldsatl

    ldlvHv iTi

    Cpv

    H

    iTiiiTi

    ii

    A

    Pq

    >=<

    viv ma &=

    for bubbly flow regime

    where hli is the heat transfer coefficient between liquid and bubble.

    Wolfert et al.s model

    lv

    illiv

    i

    TThm

    )( =&

    2/1]2

    [t

    llr

    lllik

    Cp

    R

    vCph =

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    For dispersed flow, i.e., liquid droplet flowing in superheated vapor

    ]1[l

    ll

    b

    k

    kk

    R+

    v

    drv

    dvd

    d

    vvd

    lv

    satvvd

    Dv

    D

    kh

    i

    TThm

    =+=

    =

    Re],PrRe74.02[

    )(

    3/12/1

    &

    8.3 Interfacial M omentum Transfer RateRecall that

    w

    k

    L

    k

    v

    k

    D

    k

    d

    k

    d

    kkkikikk

    MMMMM

    MPVM

    +++=

    ++=v

    =DkM=vkM

    Interfacial drag force due to relative velocity

    Virtual mass force due to relative acceleration

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    k

    =LkM=wkM

    Interfacial lift force due to velocity gradient

    Wall force near the wall (still subject to discussion)-Interfacial drag force

    Ishii shows that the interfacial drag force may be expressed as:

    ]

    2

    )4

    (

    4

    [ rrc

    i

    dDi

    D

    k

    VV

    A

    ACaM

    =

    CD is the drag coefficient.

    Ad is the projected area in the moving direction of the particle.

    A is the surface area of the article..

    Table Local drag coefficients in multiparticle system(From: Ishii and mishima)

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    CdCdCL

    D

    k VVVCM = )( CL=lift coefficientThe theoretical value for CL from ideal fluid flow analysis is 0.25,

    Wang et al. show that CL=0.02 for bubbly flow.

    -Interfacial lift force

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    The present mixture viscosity model compared to existing models for solid particle system.(From: Zuber&Ishii)

    -Virtual mass forceTheoretical result from ideal fluid flow analysis,

    Ishii and Mishimas model gives:--For bubbly flow

    dt

    VdF rc

    dv

    d

    v

    2

    =

    ][211

    Cdrd

    d

    v

    d VVVVV

    Mvvvv

    ++

    =

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    --For standard slug flow

    ][12

    Crrdc

    d

    dd VVVVt

    M +

    ][)](27.066.0[5 Crrdr

    cbb

    d

    v

    d VVVVt

    V

    L

    DLM

    vvvv+

    +=

    8.4 Interactions Energy Transfer RateRecall that

    and have been discussed previously in the

    models for mass transfer.

    8.5 I nter facial between Each Phase and Wall

    Heat transfer bet een all and each phase

    )( kikikikiikikik qimaqai +=+ &

    k kiq

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    -Heat transfer between wall and each phase

    For single-phase liquid flow or for nucleate boiling region, i.e.,

    the surface is all or mostly covered by liquid.Thus,

    Conversely, for film boiling region the surface is mostly covered by

    vapor. Thus,

    CHFwCHF TTqq ,

    0= lwH

    lw qA

    P

    qPH

    vwlw = ;0

    For transition boiling, TCHF<

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    f

    lv

    v

    vw

    f

    lv

    l

    lw

    z

    P

    zM

    z

    P

    z

    zM

    ,22

    ,22

    )(

    )(

    >==>>

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    where is the turbulent diffusivity. For two-phase bubbly flow,

    it may be evaluated by a modified k-j model as following:

    t

    kv

    tb

    k

    k

    kt

    k vk

    Cv +=

    2

    where is the turbulent diffusivity due to bubble agitation,

    and may be evaluated by the model of Sato et al.(1981)

    tb

    kv

    rb

    tb

    l VRv 2.1=

    kkand jkare the turbulent kinetic energy and dissipation rateand may be evaluated by a modified two-equation model for

    two-phase flow with dilute concentration of dispersed phase.

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    Chapter 9 TWO-PHASE FLOW PRESSURE DROP9.1 Two-Phase Flow Pressure Drop Based on Homogeneous Flow Model

    From the steady state momentum equation

    zm

    mm

    gG

    D

    fG

    dz

    d

    dz

    dP

    ++

    =

    2

    2

    2

    2

    11

    gradientpressureFrictionaldz

    dP

    F

    =

    ( )vxvGfGf ll +==2

    2

    2

    2

    1111

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    ( )vm

    vxvGD

    fD

    f ll +2222

    nture gradieonal pressAcceleratidz

    dP

    A =

    ( )

    +=+=

    =

    dz

    dP

    dP

    dvx

    dz

    dxvGvxv

    dz

    dG

    G

    dz

    d v

    vv

    m

    lll

    22

    2

    Where the liquid phase is assumed to be incompressible.

    tre gradiennal pressuGravitatiodz

    dP

    G =

    v

    zzm

    vxv

    gg

    ll +==

    The frictional pressure gradient can also be expressed as( ):

    +

    =

    +=

    l

    l

    ll

    l

    llv

    vx

    dz

    dP

    v

    vxvG

    Df

    dz

    dP v

    oF

    v

    o 112

    11

    ,

    2

    Let be the two-phase frictional multiplier defined as:

    lv

    xdz

    dP

    vF +=

    12

    + 11v

    x v

    02 lff =

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    l

    l

    lv

    x

    dz

    dP

    oF

    o +=

    1

    ,

    += 11

    lvx v

    At low pressures vv >> vl , can be as high as several hundreds.

    For example, for saturated water at 1 atm, vv/vl=1603, =17.0 for

    x=0.01,for =61.2, for x=0.1 =802,for x=0.5, =802, for x=0.5

    2

    0l

    2

    0l

    2

    0l

    2

    0l 2

    0l

    Combining the three pressure gradients together yields,

    dPdvxG

    v

    vxv

    g

    dz

    dxvG

    v

    vxvG

    D

    f

    dz

    dP

    v

    v

    zv

    v

    2

    222

    1

    1

    12

    1

    +

    +

    ++

    +

    = ll

    l

    l

    l

    l

    l

    In general, 12

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    Considering a boiling channel with a uniform heat flux distribution.

    Thus, the vapor quality is increased linearly from x1, to x2 . The qualitygradient in the channel can then be evaluated by the following equatio

    12

    12

    zz

    xx

    dz

    dx

    = dxxx

    zzdz

    12

    12

    =or

    Further assuming that , ,integration of

    the pressure gradient equation gives:

    12

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    9.2 Two-Phase F low Pressure Drop Based on Two-F luid Model

    Recall the steady-state momentum equations for liquid and vapor

    phase, respectively:

    Liquid-phase momentum equation

    zww gPdz

    dw

    dz

    dlllllllll =

    42

    Vapor-phase momentum equation

    Assume and combing above two equations yields.

    zvvvwvwvvvvv gPdz

    dw

    dz

    d =

    42

    PPPv==l

    [ ] ( )vwvwwwvvvD

    wwdz

    d

    dz

    dP +++= lllll

    422

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    ( ) zvv g ++ llusing the following fundamental relationships with _v = _

    =

    1

    )1( xvGw

    l

    l

    xvGw

    v

    v=

    The above equation can be expressed as:

    2222

    2

    2

    1

    1

    )1(o

    ov vGD

    fvxvx

    dz

    dG

    dz

    dPll

    ll

    +

    +

    =

    [ ] zv g ++ l)1(

    : Acceleratial pressure gradient F i i l di

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    : Frictional pressure gradient

    : Gravitational pressure gradientThe accelerational pressure gradient can also be expressed as:

    +

    =

    2

    2

    2

    2

    2

    )1(

    )1(

    1

    )1(22

    v

    pA

    vx

    x

    vx

    x

    vxxv

    dz

    dxG

    dz

    dP lll

    dz

    dPvxvx

    PdP

    dvxG v

    x

    v

    ++2

    2

    2

    222

    )1(

    )1(

    l

    +

    +

    +

    +

    =

    2

    2

    2

    222

    2

    2

    2

    2222

    )1(

    )1(1

    )1()1(

    1)1(22

    211

    v

    x

    v

    v

    p

    voo

    vxv

    x

    PdP

    dvxG

    vxvxx

    vxxvdzdxGG

    Df

    dz

    dP

    l

    l

    lll

    +

    +

    ++

    2

    2

    2

    22

    2

    )1(

    )1(1

    ])1[(

    v

    x

    v

    zv

    vxv

    x

    PdP

    dvxG

    g

    l

    l

    In general

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    In general,

    Again, for a boiling channel with a constant heat flux distribution,

    the pressure drop can be obtained by integrating above equation as:

    1)1(

    )1(2

    2

    2

    222

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    Lockhart & Martinelli (1949) found that can be correlated as a

    function of the Martinelli parameter, defined as:0l

    vF

    F

    dz

    dP

    dz

    dP

    X

    ,

    ,2

    = l

    If both phases are flowing as turbulent flow

    , it can be shown that:

    channelsametheinalonephasevaporofdroppressurefrictional

    channelsametheinalonephaseliquidofdroppressurefrictional=

    2.08.1

    2 1

    =

    v

    vtt

    x

    xX

    l

    l

    2

    ,

    2 11

    )(

    )(

    XX

    c

    zP

    z

    P

    lF

    F

    ++=

    =l 2

    ,

    2

    1)(

    )(

    XcX

    z

    P

    z

    P

    vF

    F

    v ++=

    =

    Liquid Vapor c

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    211

    XcX

    X

    ++=

    where c is given by the following table

    Turbulent Turbulent 20

    Laminar Turbulent 12

    Turbulent Laminar 10

    Laminar Laminar 5

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    Lockhart & Martinelli, 1949

    If both phase are turbulent, and is related by the following equation:20l

    2l

    8.122 )1( xo = ll 2.08.1

    1.05.0

    9.09.08.1 )1(20)1(

    +

    +=

    l

    l

    l

    l

    v

    v

    v

    v

    xxxx

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    Martinelli & Nelson, 1949 Martinelli & Nelson, 1948

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    Martinelli & Nelson, 1948

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    Martinelli & Nelson, 1948

    B is given in the following table

    -Chisholms (1973) correlation for two-phase frictional multiplier

    { }nnno xxBxIx ++= 22/)2()2(22 )1()1(1)(l

    =

    =tuberough

    ntubesmooth

    I

    v

    n

    v

    v

    ,

    2.0,

    5.0

    2/5.0

    l

    l

    l

    Where

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    I )/( 2smkgG

    B

    < 9 . 5

    1900

    1900500

    500

    I

    IG

    /21

    )/(520 5.0

    > 2 8 )/(1500 5.02 GI

    -Friedels (1979) model for two-phase frictional multiplier

    +=

    vo

    vo

    f

    fxxA

    l

    l22

    1 )1(

    2240780 )1(A

    035.0

    2

    045.0

    2

    32

    1

    2 24.3

    WeFr

    AAAo +=l

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    224.078.0

    2 )1( xxA =7.019.091.0

    3

    =l

    l

    l

    l

    vv

    v

    A

    ( )22

    2 v

    xvvgD

    GFr

    ll +=( )vxvv

    DGWe ll +=

    2

    2

    9.3 Secondary Two-Phase Pressure Drop-Pressure change through a sudden expansion

    Considering force balance in the control volume shown in fig.:

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    Using the following basic equations:

    )()( 12122221 lll wwWwwWAPAP vvv +=

    1

    1

    11

    111 vv

    v

    xG

    A

    xAGw ==

    == 11112AxGxAG

    wv

    )1()1(

    )1()1(

    1

    1

    11

    11

    1

    ==

    ll

    lxG

    AxAGw

    =

    =2

    1

    2

    1

    22

    11

    2)1(

    )1(

    )1(

    )1(

    A

    AxG

    A

    xAGw

    ll

    l

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    2222

    2AA

    wvv

    v

    The pressure change through the sudden expansion can be expressed as:

    +

    +

    =

    2

    2

    2

    2

    2

    1

    1

    2

    1

    2

    2

    12

    112)1(

    )1(

    1

    )1(

    x

    v

    vx

    A

    Ax

    v

    vx

    A

    AvGPP vv

    ll

    l

    If the void fraction is unchanged through the expansion,

    +

    =

    22

    2

    1

    2

    12

    1121

    )1(1

    x

    v

    vx

    A

    A

    A

    AvGPP v

    l

    l

    -Pressure change through a sudden contraction

    Considering force balance for the control volume shown in Fig.

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    21212222212

    1

    2

    1

    2

    1

    2

    1vvvv wwwwPP += llll

    2

    11

    22

    2

    11

    22

    2

    2

    2

    2

    2

    2

    2

    1

    )1(

    )1(

    2

    1

    2

    1

    )1(

    )1(

    2

    1

    +

    =

    v

    v

    v

    vA

    xGA

    A

    xGAxGxG

    l

    l

    l

    l

    ( ) ( )

    +

    =

    2

    1

    2

    12

    2

    112

    2

    2

    2

    2

    2

    22

    2)1(

    )1(

    )1(

    )1(

    2

    1

    A

    x

    v

    v

    A

    xx

    v

    vxvG vv

    ll

    l

    If the void fraction is unchanged, the above equation can be simplied as:

    ( )

    +

    =

    2

    2

    2

    2

    2

    12

    2

    221)1(

    )1(11

    2

    1

    x

    v

    vx

    AvGPP v

    l

    l

    2112 /AAAwhere =

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    CHAPTER 10 Steady-State Two-Phase Pipe F lows

    Topics to be discussed

    l Two-phase flow characteristics in a boiling channel basedon the 1-D drift flux model

    l Two-phase flow characteristics in a boiling channel basedon the 1-D two-fluid model

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    on the 1-D two-fluid model

    l Two-phase flow characteristics in a boiling channel basedon the multi-dimensional two-fluid modell Adiabatic two-phase bubbly pipe flow

    10.1 Two-phase flow characteristics in a boiling channel basedon the 1-D drift flux model

    Zsc)( satlTii=

    Saha & Zubers model for bubble departure point

    l

    l

    k

    DCpq"0022.0 000,70

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    ZONB

    Zd

    ldii=

    G

    Where X and is the liquidsubcooling at the bubble departure point. From the

    energy balance the bubble departure point can

    be determined as:

    ll kGDCpPe /= dsubi ,

    )("4"

    )(,,

    ,,

    dsubinsub

    H

    dsubinsub

    d iiq

    GD

    Pq

    iiGAz =

    =

    Conservation of mass for vapor phase

    Conservation of mass for liquid phase

    Assume both liquid and vapor densities are constant, the above

    two equations can be expressed as:

    vvvwdz

    d=)(

    [ ] vwdzd

    = ll )1(

    vwd

    )( ( )d )1(

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    Combined the above two equations yields,

    Thus,

    vvv vwdz

    =)( ( ) ll vwdz

    v= )1(

    [ ] vvvvv vvvwwdz

    dlll ==+ )()1(

    vvvjdz

    dl=

    For the saturated boiling region,

    For the subcooled boiling region, the vapor generation rate maybe approximated by the following equation:

    Di

    q

    v

    satv

    l

    "4==

    ,satdsc

    dv

    zz

    zz

    = scd zzz

    iGD

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    where

    "4

    ,

    q

    iGDz

    insub

    sc

    =

    vsat

    dsc

    d vzz

    zzl

    scd zzz

    =dz

    dj

    vsatvl sczz

    Integration of the above equation gives:

    The vapor velocity can then be determined based on the drift flux model:

    Th h h l i b d

    )(

    )(

    2

    2

    dsc

    dvsatin

    zz

    zzvw

    + l scd zzz

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    Thus, the vapor phase velocity can be expressed as:

    vj

    dsc

    dvsatino w

    zz

    zzvwC +

    +

    )(

    )(

    2

    12

    l scd zzz

    Integration of mass conservation equation for the vapor phase gives,

    )(

    )(

    2

    12

    dsc

    d

    vsatzz

    zzv

    scd zzz

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    distribution in the channel:

    vjzz

    zz

    vsatino

    zz

    zz

    vsat

    wvwC

    v

    dsc

    d

    dsc

    d

    ++

    ][)(

    )(

    21

    )(

    )(

    21

    2

    2

    l

    scd zzz

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    +++

    ++

    + + vj

    dsc

    dpcho w

    zzzzNC

    )()(

    211

    2

    +++

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    ++

    zzsc1

    =+ )(zwl

    ++

    ++

    + )(

    )(

    12

    11

    )(1

    12

    dsc

    d

    v

    pch

    zz

    zz

    R

    N

    z l

    +++

    + dscv

    pch

    zzzR

    N

    z 2

    1

    2

    1

    12

    11

    )(1

    1

    l

    [ ]dsubsubpch

    d NNN

    z ,1 =+ subpch

    sc NN

    z 1=+

    hspchRPeN0022.0 000,70Pe

    numberchangephasevLPq

    N vH

    pch ==l

    "

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    gpviGA v

    pch

    ll

    numbersubcoolingv

    v

    i

    iN v

    v

    insub

    sub =

    =l

    l

    l

    ,

    numberPeclet

    k

    GDCpPe ==

    l

    l

    LP

    AR

    H

    hs =l

    lv

    vR vv =

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    NPCH=5.2 Nsub=2.3 Rvl=20 Pe=95600 Rhs=2.510-2

    10.2 Two-phase flow characteristics in a boiling channel based on 1-D

    two-fluid model

    Ref.: Hu & Pan, 1995

    Mass conservation equation for vapor phase:

    Mass conservation equation for liquid phase:

    vvv

    wdz

    d

    =)(

    [ ]wd

    = )1(

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    Mixture momentum equation:

    [ ] vwdz

    = ll )1(

    dz

    dww

    dz

    dww vvv

    l

    ll )1( +

    [ ] lll wvvv MgdzdPww += )1()(

    Equation by eliminating pressure gradient in two momentum equations

    [ ] Divivv

    v Mwwwdz

    dwA

    dz

    dwA =+ )1( l

    ll

    ll wv Mg ++ )()1(

    [ ] vvv wA )1( = [ ] lll wA )1( =

    Liquid phase energy equation

    "Pd

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    [ ] vvh

    i

    "qP

    iw)1(dz

    d

    = lll

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    10.3 Two-phase flow characteristics in a boiling channel based on

    multidimensional two-phase flow model

    Ref.: Kurul & Podowski, 1990, 1991; Lai & Farouk, 1993

    Conservation of mass

    Conservation of momentum

    ( ) ( ) kkkkkk Vt

    =+

    vk ,l=

    ( ) ( ) ( ) ( )[ ] gVPVVVt

    kkk

    t

    kkkkkkkkkkk

    v +++=+

    +++ vD MMM vk l

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    Conservation of energy

    +++ kv

    k

    D

    k MMM vk ,l=

    ( ) ( )

    ( )[ ] vlkPVtP

    AqiCpkk

    Viit

    kk

    kk

    kkwkwkikk

    t

    kkk

    kkkkkkk

    ,/ =+

    ++++=

    +

    v

    Some closure equations

    ( ) LvLviD

    D

    v

    D VVVVaCMM ll == 8

    1

    ( )

    +

    ==

    ll

    l

    ll

    vvvvvvVVVV

    t

    V

    t

    VMM

    vv

    v

    v

    V

    v

    V 2

    1

    vki VVM lll ==

    vblvvdbvw NfiDq 3

    ,6

    1=

    vwlw qqq =

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    10.4 Adiabatic two-phase bubbly two-phase flow

    Ref.: Lahey and his coworkers

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    (b)

    Steady-state mass conservation equation

    0= kkk V vk ,l=

    Steady-state momentum equation

    ( ) kkkT

    kkkkkkkkk MgPVVvvvv ++

    ++= vk ,l=

    Where

    VVVstressyonldsRe tl'k

    'kk

    T

    k === pWLVD MMMMMMllllll

    ++++=2

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    lMMv =

    w

    b

    r

    v

    bW nRV

    yRM 147.01.0

    ll

    +=

    lll = ip PM

    2

    rvpi VCPP

    lll =

    lvb

    l

    lt

    l VVD.kC vv +=

    60

    jland klare given by the k-j model:

    ( ) ( )llllllll += GkvkV t

    +

    =

    l

    l

    l

    ll

    ll

    l

    llll

    v

    kC

    k

    GC

    vV

    t 2

    21

    Where Gl is the turbulence generation rate defined as:

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    Where Glis the turbulence generation rate defined as:

    ( lllll VVVvG Tt += :

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    CHAPTER 11 TWO-PHASE FLOW INSTABI LI TY

    Ref.1 Lahey & Moody, 1977, The Thermal Hydraulics of a Boiling

    Water Nuclear Reactor, ANS.

    2. Lahey & Podowski, On the Analysis of Various Instability inTwo-Phase Flow, in Hewitt, Delhaye, Zuber, Multiphase

    Science and Technology, Vol.4 Hemisphse publishing.

    Two-phase flow instability

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    Two-phase flow instability

    -Interfacial instability: 1.Taylor instability2. Helmhotz instability

    -Channel or system instability :1.Ledinegg instability

    2.Density-wave oscillation

    3.Nuclear-coupled Density wave

    oscillation4.etc

    11.1 Classification of instability

    Static instabilities - can be explained in terms of steady-state laws.

    Dynamic instabilities - require a consideration of the transient

    conservation equations.

    Examples of static instabilities:

    1.Excursive (Ledinegg) instabilities

    2.Flow regime relaxation instabilities

    3.Nucleation instabilities

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    Examples of Dynamic instabilities

    1.Density-wave oscillations

    2.Pressure-drop oscillations

    3.Nuclear-coupled density wave instability.

    11.2 Excursive