chapter 8_steadystate non-isothermal reactor

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  • 7/25/2019 Chapter 8_Steadystate Non-isothermal Reactor

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    Chemical Engineering

    Department

    CDB 2043 KINETICS AND REACTOR DESIGN

    CHAPTER 8. STEADY STATE NONISOTHERMAL REACTOR

    1

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    At the end of this chapter, student should be able to:

    1. Explain the importance of energy balance in designing

    reactors

    2. Apply the concept of energy balance to reactor design

    for both adiabatic reaction and reaction involving heat

    exchange

    3. Evaluate the optimum conversion in reactors where

    chemical equilibrium is the limitations.

    2

    LEARNING OUTCOME OF CHAPTER 8

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    LECTURE 1WHY WE NEED THE ENERGY BALANCE EQUATION?

    HOW TO DEVELOP THE ENERGY BALANCE EQUATION

    3

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    Why we need energy balance equation?

    What do we have so far?

    Mole balance

    (design) equation

    0dV

    dX

    PFor

    :

    A

    A

    F

    r

    FRExample

    Rate law &

    Arrhenius

    equation

    21

    1

    11exp

    TTR

    Ekk

    kCrAA

    Stoichiometry

    )1(0

    00

    0

    0

    XCC

    vCF

    vCFvv

    AA

    AA

    AA

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    Why energy balance?

    Mole balance(design) equation

    0dV

    dX

    PFor

    :

    A

    A

    F

    r

    FR

    Example

    Rate law &

    Arrhenius

    equation

    TTR

    Ekk

    kCrAA

    11exp1

    1

    Stoichiometry

    )1(0

    00

    0

    0

    XCCvCF

    vCF

    vv

    AA

    AA

    AA

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    Why energy balance?

    1st order, exothermic, adiabatic reaction

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    Combining these three equations gives:

    Why energy balance?

    XCF

    TTR

    Ek

    dV

    dXA

    A

    1

    11exp

    0

    0

    1

    1

    For non-isothermal operation: k depends on T (affects final

    conversion, X)

    T varies with V (reactor length)

    Need either

    X=f(T) or

    T=f(V)

    0dV

    dX

    A

    A

    F

    r

    AA C

    TTR

    Ekr

    11exp

    1

    1

    )1(0 XCC AA

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    Set valuefor X

    CalculateT

    Calculatek

    CalculaterA

    Calculate(FA0/-rA)

    8

    General approach in solving non-isothermal

    reactor problem

    Use energy

    balance to

    relate X

    and T

    Use Levenspiel

    plot techniqueto solve

    problem

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    The energy balance

    General energy balance for open system

    outou tinin

    ..

    ^

    sysEFEFWQ

    dt

    Ed

    Zero for closed system

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    The energy balance

    For n species, the equation becomes:

    outi

    n

    1i

    iini

    n

    1i

    i

    ..

    ^

    sysEFEFWQ

    dt

    Ed

    Qs is how can we

    make this equationUSEABLE @ USER

    FRIENDLY?

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    Steps to a more user-friendly equation

    Evaluate the work term to get the equation in terms of enthalpies

    ou ti

    n

    1i

    iini

    n

    1i

    i

    ..

    ^

    sysEFEFWQ

    dt

    Ed

    isys

    Hfdt

    Ed

    ^

    Dissect the steady state molar flow rate terms to get the equation in terms of heats of

    reaction

    Rxsys

    Hfdt

    Ed

    ^

    Dissect the enthalpies terms to get the equation in terms of heat capacity.

    pisys

    Cfdt

    Ed

    ^

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    Resulting equation based on energy balance* for steady stateflow system:

    where:

    The energy balance

    *Full derivation: pg 474 - 486, Fogler

    0)( 01

    0

    ..

    THXFTTCFWQ RXAA

    n

    i

    iopiiAs

    RpRRXRX TTCTHTH 0

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    How do we apply the equation in designing

    reactors?

    0)( 01

    0

    ..

    THXFTTCFWQ RXAA

    n

    i

    iopiiAs

    dtr

    dXN

    V

    r

    XFV

    F

    r

    A

    A

    A

    A

    A

    A

    0

    0

    0dV

    dX

    Solve using

    Numerical technique

    ODE solver

    Graphical method

    e.g: Levenspiel plot

    method

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    8.3 Adiabatic energy balance

    General Energy Balance Equation

    Consider an adiabatic system with no work done.

    )1(

    )(

    RpR

    o

    Rx

    iopii

    TTCTH

    TTCX

    0W,0Q s..

    0)( 01

    0

    ..

    THXFTTCFWQ RXAA

    n

    i

    iopiiAs

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    Adiabatic tubular reactor

    Rearrangement of equation 1 gives:

    Couple with mole balance equation:

    we can develop the temperature, conversion and

    concentration profiles along the reactor.

    )2(

    0

    PPii

    RPPiiRRX

    CXC

    TCXTCTHX

    T

    ),(0 TXrdV

    dXF

    AA

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    Since the second term in the denominator is usually zero, aplot of XEB vs T gives:

    X

    T

    Use together with mole balanceequation in solving reactionengineering problem

    XEB XMB

    Adiabatic energy balance

    )( RoRxiopii

    EBTH

    TTCX

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    CHECKPOINT!

    For non-isothermal system, we need 2

    equations to describe the conversion, X

    XMB, which is based on Material

    Balance

    XEB, which is based on Energy

    Balance

    The final conversion is the value that satisfy

    both these equations

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    Example 8-2: Heat of reaction

    Calculate the heat of reaction for the synthesis of ammonia from hydrogen

    and nitrogen at 150oC in kcal/mol of N2 reacted and also in H2 reacted. The

    reaction is given below:

    N2 + 3H2 2NH3

    Info:Heat of formation of NH3 at 25

    oC = -11,020 cal/mol.N2 reacted

    Heat of formation of elements at 25oC = 0

    Heat capacities at 25oC

    CP,NH3 = 8.92 cal/mol.K

    CP,N2 = 6.984 cal/mol.K

    CP,H2 = 6.992 cal/mol.K

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    Heat of formation at reference temperature (25o

    C):

    Heat of reaction at any temperature:

    19

    Solution to Example 8.2

    )()()()()( 00000RARBRcRDRRx

    THTHa

    bTH

    a

    cTH

    a

    dTH

    RPRRxRx

    TTCTHTH )()( 0

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    Using these equations, we will get:

    20

    Solution to Example 8.2

    reactedNmol

    kcalKH

    Rx

    2

    004.22298

    KreactedNmol

    calCp

    2

    12.10

    2

    3.23Nmol

    kcalH

    Rx

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    Example 8-3: Liquid phase isomerisation of normal

    butane

    Additional Information:

    HRx = -6900 J/mol butane

    Activation Energy = 65.7 kJ/molKc = 3.03 at 60

    oC

    CA0 = 9.3 kmol/dm3

    CPn-B = 141 J/mol.KCPi-B = 141 J/mol.K

    CPi-P = 161 J/mol.K

    Handout

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    END OF LECTURE

    22

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    LECTURE 2STEADY STATE TUBULAR REACTOR WITH HEAT EXCHANGE

    CASE 1: CONSTANT TEMPERATURE HEAT EXCHANGE

    CASE 2: VARIABLE TEMPERATURE HEAT EXCHANGE

    23

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    Steady state tubular reactor with heat

    exchange (Case 1)

    d b l h h

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    From:

    Deriving the energy balance equation General energy balance equation, with no work done:

    Steady state tubular reactor with heat

    exchange (Case 1)

    TTVUaQ

    where

    HFHFQ

    a

    vviivii

    .

    .

    :

    0

    0

    ..

    vviiviiS HFHFWQ

    S d b l h h

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    Deriving the energy balance equation After further substitution of the terms, the energy balance

    equation for tubular reactor with heat exchange is:

    Steady state tubular reactor with heat

    exchange (Case 1)

    Pii

    aRxA

    CF

    TTUaHr

    dV

    dT

    Heat generated Heat removed

    Full derivation: Fogler, pg 496

    VALID FOR CONSTANT

    TEMPERATURE HEAT EXCHANGE

    MEDIUM ONLY!!

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    From Example 8.3, the vapour pressure at the exit to theadiabatic reactor at 360K is 1.5MPa for isobutene, which is

    greater than the rupture pressure of the glass vessel used. Given

    the information below, will the reactor temperature rise above

    325K?

    Reactor volume (10 banks): 6 m3 (volume of each reactor)

    Ua: 5000 kJ/h.m3.K

    Ta = 37oC

    All other information : refer to Example 8.3

    27

    Example 8.4: Butane Isomerisation

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    WHAT IF THETEMPERATURE OF THE

    COOLING / HEATINGMEDIUM IS NOT A

    CONSTANT?

    28

    S d b l i h h

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    Energy balance on coolant fluid

    Steady state tubular reactor with heat

    exchange (Case 2)

    St d t t t b l t ith h t

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    Energy balance on coolant fluid For co-current case:

    For counter-current case:

    Steady state tubular reactor with heat

    exchange (Case 2)

    Pcc

    aa

    Cm

    TTUa

    dV

    dT

    .

    Pcc

    aa

    Cm

    TTUa

    dV

    dT

    .

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    One of the steps in the production of acetic anhydride is the vapourphase cracking of acetone to ketene and methane. The reaction is first

    order with respect to acetone and the reaction rate is given below (T in

    K).

    The feed to the reactor consist og 7850 kg/hr acetone. The reactor

    consist of a bank of 1000 tubes of 1 inch diameter. The inlet

    temperature and pressure are the same of both cases at 1035 K and 162

    kPa. Plot the conversion and temperature profile along the length of thereactor for the following cases:

    Example 8-5: Production of acetic anhydride

    Tk

    CHCOCHCOCHCH

    222,3434.34ln

    4233

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    1. The reactor is operated adiabatically

    2. The reactor is surrounded by a heat exchanger where the heat

    transfer coefficient is 110 J/m2.s.K and the temperature of the

    heating medium is constant at 1150 K.

    3. Same as part (2) but reactor is subjected to heating medium with

    changing temperature

    Example 8-5: Production of acetic anhydride

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    END OF LECTURE 2

    33

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    LECTURE 3EQUILIBRIUM CONVERSION

    34

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    Equilibrium conversion

    Will consider the following:A. How adiabatic temperature is related to equilibrium

    conversion for the following cases:

    1. Exothermic reaction

    2. Endothermic reaction

    B. How to find optimum feed temperature

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    A. Adiabatic temperature vs Xe

    Exothermic reaction

    Equilibrium

    TO TO1

    TO1>TO

    T

    X

    Xe

    Adiabatic

    temperature

    RX

    opiiEB

    H

    TTCX

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    How do we increase Xe for exothermic reaction?

    A. Adiabatic temperature vs Xe

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    Endothermic reaction

    A. Adiabatic temperature vs Xe

    X

    T

    Xe

    Adiabatic

    temperature

    TO

    RX

    opiiEB

    H

    TTCX

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    How do we increase Xe for endothermic reaction?

    A. Adiabatic temperature vs Xe

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    Consider reversible & exothermic reaction under adiabaticoperation

    B. Optimum feed temperature

    Analysis on Xe vs. T(from energybalance) gives thefollowing profile:

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    Analysis on conversion vs. reactor length gives the following profile:

    B. Optimum feed temperature

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    B. Optimum feed temperature

    Therefore, if we analyse the achievable conversion in a reactor for a

    given entering temperature, we will find:

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    END OF LECTURE

    43

    STEP 1 Evaluate the work term to get the equation in terms

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    44

    STEP 1: Evaluate the work term to get the equation in terms

    of enthalpies

    STEP 2: Dissect the steady state molar flow rate terms to

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    45

    STEP 2: Dissect the steady state molar flow rate terms to

    get the equation in terms of heats of reaction

    STEP 2: Dissect the steady state molar flow rate terms to

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    46

    STEP 2: Dissect the steady state molar flow rate terms to

    get the equation in terms of heats of reaction

    STEP 3: Dissect the enthalpies terms to get the equation in

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    47

    STEP 3: Dissect the enthalpies terms to get the equation in

    terms of heat capacity.

    STEP 3: Dissect the enthalpies terms to get the equation in

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    48

    STEP 3: Dissect the enthalpies terms to get the equation in

    terms of heat capacity.

    STEP 3: Dissect the enthalpies terms to get the equation in

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    STEP 3: Dissect the enthalpies terms to get the equation in

    terms of heat capacity.