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Catalytic reactions are generally carried out in fixed bed reactors, because of
simplicity of technology and operation. This simplicity is evident for adiabatic
reactors, but when important heat of reaction is involved, heat exchange may be
preferable, for optimum operation, to avoid runway and catalyst deactivation.
Thus heat transfer is very often the major problem encountered in design of
fixed bed reactors.
Three important classes of non adiabatic reactors are as follows:
Multiband adiabatic reactors with intermediate heat exchange leading to
non-sinusoidal waveform temperature profiles.
Reactors with internal multitublar heat exchangers.
Multitublar reactors.
The last two are generally preferred to the multibed adiabatic reactor when
highly exothermic or endothermic reactions take place, or when an optimum
temperature profile is desirable.
Another aspect is the pressure drop through the bed. In order to limit it, larger
catalyst particle may be used, but diffusion limitations will also increase.
Classification of models:
Fixed bed reactors are essentially described by continuum type model, but cell
models have been developed to account for the two phase structure of the
reactor. Most catalytic reactions are classic axial flow reactions, the most
reliable model are classic continuum model.
According to Froment & Bischoff, these continuum model may be classified in
two general categories depending on the direction is made between the fluid and
solid phases.
Pseudo-homogeneous model(PH)
[Temperature and concentrations are supported to be identical in both
phases at a given position in the reactor].
Heterogeneous model(HT)
[Account for temperature and concentrations gradients inside and around
the catalyst particle].
Each category is classified in different types of model based on more and more
sophistication involved in description of flow & transfer phenomenon.
Pseudo-Homogeneous Models:
The basic one dimensional model
In the one dimensional model, uniformly is assumed in a cross section of the
reactors.
u + r =0 ...38.1
( )
u C +4 r (H) = 0 ...38.2
= u f/gd ...38.3
This relation derived with spherical particles, is still valid for other shapes
provided that void fraction does not exceed 0.5 and using the equivalent
diameter.
d =6 ...38.7
d 2t dT
u C u (T T ) / d r (H ) 0 ...38.9
ea dz 2 G p dz t w t ma
The pressure drop equation of Eq. (38.1) is not modified.
Boundary conditions for a closed diffusion reactor are
Atz 0,
u(c c) = D ...38.10
u C (T T) = ...38.11
Atz L ;
R
=0 ...38.12
=0 ...38.13
The solution of equation (38.1) to (38.6) can predict possible multiple steady
states in very shallow beds when very exothermic reactions with high activation
energy are carried out.
According to Young and Finlayson, axial dispersion may be neglected when
( ) Pe
...38.14
And
[(H)r d /u C (T T )] Pe
These conditions are valid only when the reaction rate is maximum at the inlet.
If not they are changed to:
Pe dx d(z/d ) ...38.15a
d(TT )
Pe d(z/d ) ...38.15b
Pe = Peclet number.
Heat transfer is even more complex, because of the solid phase and various
radiation effects
= + ...38.16
The dynamic contribution has been correlated by De Wasch and Froment
(1972) as
The static contribution has been described by a complex model due to Kunii &
Smith on the basis of electrical energy.
Transfer through the fluid in the voids
a) Conduction
b) Radiation from void to void
Transfer involving the solid phase:
a) Conduction through the particles
b) Conduction through the contact surface between the particles
c) Conduction through the film near the contact surface
d) Radiation from particle to particle
Another complication in the use of 2D model is the supposed decrease of
near the wall owing to fixed bed structure. Thus a supplementary wall interface
heat transfer is introduced, by a wall coefficient so that
= (T T) ...38.18
At = 2
= + ...38.19
In the case where volume change, pressure drop and axial dispersion may be
neglected, the steady state model equations are:
+ =0 ...38.20
+ ( ) = 0 ...38.21
Atz 0; c c ,T T r 0;
o o
r 0; = =0