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Chapter 4 Lecture 5 (1)
Chapter 4 Lecture 5 (1)
Chapter 4 Lecture 5 (1)
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4.2 GAS–LIQUID OPERATIONS: LIQUID DISPERSED
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4.2 GAS–LIQUID OPERATIONS: LIQUID DISPERSED
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This wall factor Kw can be important for columns with an inadequate ratio of effective particle
diameter to inside column diameter, and is given by
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4.2 GAS–LIQUID OPERATIONS: LIQUID DISPERSED
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where “a” must be in units of m2/m3, hL,S is the liquid holdup at loading.
For operation in the preloading region, as usual, the liquid holdup can
be estimated from equations
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4.2 GAS–LIQUID OPERATIONS: LIQUID DISPERSED
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4.2 GAS–LIQUID OPERATIONS: LIQUID DISPERSED
Further since the interfacial area between gas and liquid is not directly measured,
the flux of mass transfer cannot be determined but instead only the rate as the
product of the flux and the total interfacial area.
By dividing these rated by the volume of the packing the results appear as volumetric
overall coefficients Kxa, Kya, KGa, etc.
The individual fluid mass transfer coefficients (kx, ky, FL, FG)
and interfacial area “a” which make ups these overall
volumetric coefficient are differently dependent upon fluid
properties, flow rates and type of packing.
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The overall volumetric coefficients are therefore useful only in the design of towers
filled with the same packing and handling the same chemical system at the same
flowrates and concentration as existed during measurement.
For general design purposes the individual coefficient and the interfacial area are
necessary.
To obtain individual coefficients, the general approach has been to choose
experimental conditions such that the resistance to mass transfer in the gas phase is
negligible in compassion with that in the liquid.
This is the case fore for the absorption or desorption of very insoluble gases such
as oxygen or hydrogen in water.
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4.2 GAS–LIQUID OPERATIONS: LIQUID DISPERSED
Measurement in such systems then leads to values of kxa, kLa, and FLa which can be
correlated in terms of system variables
There are evidently no systems involving absorption or desorption where the solute
is so soluble in the liquid that liquid phase resistance is entirely negligible.
But by subtracting the known liquid resistance from the overall resistance it is
possible to arrive at the gas‐phase coefficients kya, kGa, FGa and to correlate
them in terms of system variables.
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4.2 GAS–LIQUID OPERATIONS: LIQUID DISPERSED
where CL is an empirical
constant characteristic of the
packing, as shown in Table
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where CV is an empirical
constant included in Table
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4.2 GAS–LIQUID OPERATIONS: LIQUID DISPERSED
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