abstrip-nonisothermal2

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    Nonisothermal case: adiabatic approach

    Prof. Dr. Marco Mazzotti - Institut fr Verfahrenstechnik

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    1. Approach

    Therefore two new concepts become important:

    1. Energy balances

    2. Changes of L and G within the column

    In the adiabatic approach energy balances are calculated under following assumptions:

    There is no heat exchange through the walls of the column

    The gas and liquid stream leaving a stage are at the same temperature

    Calculating changes of L and G within the column are important when dealing with large solute

    fractions. This is often the case when calculating non-isothermal columns.

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    Once, pressure and initial composition and temperature of the solvent are set we can consider them as data. This

    is a list of known variables:

    Specifications

    y1Gas final composition, y1

    Gn+1

    TG

    n+1

    Data and set values

    yn+1

    x0Pressure,p

    Gas flow rate, Gin

    Gas initial composition, yn+1

    Solvent initial composition,x0

    Equilibrium data, y=f(x,T)

    p

    y = f(x,T)

    TL0

    Gas Temp. at inlet TG1

    Liquid Temp. at inlet, TL2

    Ln

    TLn

    Unknowns

    xn

    Solvent flow rate at inlet, L2

    Number of stages, n

    Solvent final composition,xn

    G1 L0

    n

    Solvent flow rate outlet, L1

    TG1

    Gas Temp. at outlet TG2

    Gas Temp. at outlet TL1

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    2. Balances

    Material Balance of column:

    T)f(x,y

    yGxLyGxL

    GLGL

    11nn1n1n00

    1n1n0

    The amount of liquid increases from the bottom to the top of the column. It is calculated by adding up the

    amount of solvent and the amount of absorbed solute. The same way the amount of gas is calculated. It

    deacreases from the top to the bottom of the column as the solute absorbs to the liquid.

    Energy Balance of column

    )T(TcpHH

    H)T(TcpHH

    HGHLHGHL

    0

    G

    0

    GG

    S

    0

    L

    0

    LL

    G11Lnn1Gn1nL00

    HS represents the molar enthalpy of mixing or the integral heat of solution, at the prevailing concentrationand at the base temperature T0

    J/(mol K)Heat capacitycp

    J/molChange of solute enthalpy

    between liquid and gas

    phase

    Hs

    J/molEnthalpy at reference stateH0

    J/molEnthalpyH

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    To solve the problem the gas outlet temperature and the amount of liquid solvent have to be estimated or

    calculated by a nother method, e.g. the isothermal approach

    3. Solution of the system

    Now all necessary values of the bottom of the column can be calculated by the energy and mass

    balances.

    From the bottom of the column a new set of mass and material balances can be made including the first

    stage. (green canvas) From these balances all unknowns of the first stage can be calculated. This is

    repeated including one more stage every time until the required specification is reached.