Plug Flow Reactor Equilibrium Conversion

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    The highest conversion that can be achieved inreversible reactions is the equilibrium conversion.

    For endothermic reactions, the equilibrium conversion

    increases with increasing temperature up to amaximum of 1.0.

    For exothermic reactions the equilibrium conversion

    decreases with increasing temperature.

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    EXOTHERMIC REACTIONS

    To determine the maximum conversion that can be achieved inan exothermic reaction carried out adiabatically, we find the

    intersection of the equilibrium conversion as a function of

    temperature:

    T

    TpR

    0

    Rx

    n

    1i

    T

    Tpii

    R

    0

    dTCTH

    dTC

    X (1.57)

    with temperature-conversion relationships from the energy

    balance (eq. 1.46). For Ti0 = T0,

    C

    C

    eK1

    KX

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    Graphical solution of equilibrium and energy balance equations

    to obtain the adiabatic temperature and the adiabatic equilibrium

    conversion Xe

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    EXAMPLE 1.5

    For the elementary solid-catalyzed liquid-phase reaction:

    A Bmake a plot of equilibrium conversion as a function of

    temperature. Determine the adiabatic equilibrium

    temperature and conversion when pure A is fed to the

    reactor at a temperature of 300 K.

    Additional information:

    molcal000,40K298H0

    A

    molcal000,60K298H0

    B

    K.molcal50CAp K.molcal50C

    Bp

    K298at000,100Ke

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    SOLUTION

    e

    B

    AA

    K

    CCkrRate law:

    Equilibrium, rA = 0, so:

    C

    Be

    AeK

    CC

    Stoichiometry (v = v0) yields

    C

    e0A

    e0AKXCX1C

    TK1

    TKX

    e

    e

    e

    (a)

    (b)

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    Equilibrium constant:

    T

    1

    T

    1

    R

    HexpTKTK

    1

    0

    Rx

    1ee

    molcal000,20HHH 0

    A

    0

    B

    0

    Rx

    T

    1

    298

    1

    987.1

    000,20exp000,100TK

    e

    T

    298T78.33exp000,100TK

    e

    T298T78.33exp000,1001

    T298T78.33exp000,100X

    e

    Substituting eq. (c) into (b)

    (c)

    (d)

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    T (K) Ke Xe

    298 100000.00 1.0000

    300 79835.65 1.0000

    325 6042.58 0.9998

    350 661.28 0.9985

    375 97.20 0.9898

    400 18.16 0.9478

    425 4.13 0.8051

    450 1.11 0.5257

    475 0.34 0.2545

    500 0.12 0.1058

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    For a reaction carried out adiabatically, the energy balance

    reduces to

    THTTC

    THTTC

    X

    Rx

    0p

    Rx

    0pii A

    300T105.2000,20

    300T50X

    3

    T Xe

    300 0.0000

    350 0.1250

    400 0.2500

    450 0.3750

    500 0.5000

    (e)

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    0.00

    0.20

    0.40

    0.60

    0.80

    1.00

    1.20

    300 350 400 450 500 550 600

    X

    T (K)

    TK1

    TKX

    e

    e

    e

    TH

    TTCX

    Rx

    0p

    e

    A

    0.40

    460

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    For a feed temperature of 300 K, the adiabatic equilibrium

    temperature is 460 K, and the corresponding adiabatic

    conversion is 0.40.

    Higher conversions than those shown in the previous figure

    can be achieved for adiabatic operations by connecting

    reactors in series with inter-stage cooling:

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    Increasing conversion by inter-stage cooling

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    What conversion could be achieved in Example 1.5 if two

    interstage coolers were available that had the capacity to coolthe exit stream to 350 K? Also determine the heat duty of

    each exchanger for a molar feed rate of A of 40 moles. Assume

    that 95% of equilibrium conversion is achieved in each reactor.

    The feed temperature to the first reactor is 300 K.

    EXAMPLE 1.6

    SOLUTION

    In Example 1.5, for an entering temperature of 300 K the

    adiabatic equilibrium conversion was 0.40.

    For 95% of equilibrium conversion, the conversion exiting

    the first reactor is 0.38.

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    The exit temperature from the first reactor is found from a

    rearrangement of Equation (e):

    300T105.2X 3

    45230038.0400300X400T

    We now cool the gas stream exiting the reactor at 460 K

    down to 350 K in a heat exchanger.

    The gas stream is then sent to the second reactor.

    The first reactor

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    T02 = 350 and X1 = 0.38

    The energy balance leads to

    The second reactor

    (f)

    Intersecting eq. (f) with eq. (d) yields in the maximum/

    equilibrium conversion in the second reactor:

    61.0X2

    e

    95% of Xe2 = X2 = 0.58

    The corresponding exit temperature is

    20122 TXX400T

    35038.0X400T22

    43035038.058.0400T2

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    T03 = 350 and X2 = 0.58

    The energy balance leads to

    The third reactor

    (g)

    Intersecting eq. (g) with eq. (d) yields in the maximum/

    equilibrium conversion in the second reactor:

    78.0X3e

    95% of Xe3 = X3 = 0.75

    The corresponding exit temperature is

    30233 TXX400T

    35058.0X400T33

    41835058.075.0400T3

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    0.00

    0.20

    0.40

    0.60

    0.80

    1.00

    1.20

    300 350 400 450 500 550 600

    X

    T (K)

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    ENDOTHERMIC REACTIONS

    Another example of the need for inter-stage heat transfer in a

    series of reactors can be found when upgrading the octanenumber of gasoline. The more compact the hydrocarbon

    molecule for a given number of carbon atoms, the higher the

    octane rating. Consequently, it is desirable to convert straight-

    chain hydrocarbons to branched isomers, naphthenes, andaromatics.

    The reaction sequence is

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    The first reaction step (k1) is slow compared to the second

    step, and each step is highly endothermic. The allowable

    temperature range for which this reaction can be carried outis quite narrow: Above 530C undesirable side reactions occur

    and below 430C the reaction virtually does not take place. A

    typical feed stock might consist of 75% straight chains, 15%

    naphthas, and 10% aromatics.

    One arrangement currently used to carry out these reactions

    is shown in the figure below. Typical sizes of the reactors are

    on the order of 10 to 20 m high and 2 to 5 m in diameter. A

    typical feed rate of gasoline is approximately 200 m3/h at 2

    atm. Hydrogen is usually separated from the product stream

    and recycled.

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    V or W

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