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INTRODUCTION TO
FLUIDIZED BEDS

CHEMICAL REACTION ENGINEERING LABORATORY
Outline/Contents









Introduction.
Fluidization Flow Regimes.
Overall Gas (Voidage) and solids Hold-up.
Radial and Axial Solids Hold-Up Profiles.
Radial and Axial voidage distribution.
Gas and Solid Mixing.
Scale-Up.
Reactor Modeling.

CHEMICAL REACTION ENGINEERING LABORATORY
Fluidized Bed Reactor Components
Inlet to cyclone

The material fluidized is a solid (catalyst).
The fluidizing medium is either
a gas or a liquid.

Gas distributor

CHEMICAL REACTION ENGINEERING LABORATORY
Advantages
 It has the ability to
process large volumes
of fluid.
 Excellent gas-solid
contacting.
 Heat and mass transfer
rates between gas and
particles are high when
compared with other
modes of contacting.
 No hot spot even with
highly exothermic
reaction.
 Ease of solids handling.

Disadvantages
 Broad or even bimodal
residence time
distribution of the gas
due to dispersion and
bypass in the form of
bubbles.
 Broad residence time
distribution of solids due
to intense solids mixing.
 Erosion of internals.
 Attrition
of
catalyst
particles.
 Difficult Scale-up due to
complex hydrodynamics.

CHEMICAL REACTION ENGINEERING LABORATORY
Industrial Applications of Fluidized Bed Reactor
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













Acrylonitrile by the Sohio Process.
Yang 2003
Fischer-Tropsch Synthesis.
Phthalic anhydride synthesis.
Methanol to gasoline and olefin processes.
Cracking of Hydrocarbons (Fluid Catalytic Cracking, etc).
Coal combustion.
Coal gasification
Cement clinker production.
Titanium dioxide production.
Calcination of AL(OH)3.
Granulation drying of yeast.
Heat exchange
Absorption
Nuclear energy (Uranium processing, nuclear fuel fabrication,
reprocessing of fuel and waste disposal).

CHEMICAL REACTION ENGINEERING LABORATORY
Fluidization Flow Regimes

CHEMICAL REACTION ENGINEERING LABORATORY
Geldart's Classification of Powders
 Group A (Aeratable)
:- (e.g.,
Ammoxidation of propylene) small
mean particle size and/or low particle
density (<~1.4 g/cm3), gas bubbles
appear at minimum bubbling velocity
(Umb).
 Group B (Sand-Like) :- (e.g.,Starch)
particle size 40 μm to 500 μm and
density 1.4 to 4 g/cm3, gas bubbles
appear at the minimum fluidization
velocity (Umb).

Kunii and Levenspiel (1991)

kg^ 3

 Group C (Cohesive)
:- very fine
particle, particle size < 30 μm, difficult
to fluidize because inter-particle
forces are relatively large, compared
to those resulting from the action of
gas.
 Group D (Spoutable) :- (e.g., Roasting
coffee beans) large particle, stable
spouted beds can be easily formed in
this group of powders.

Diagram of the Geldart classification of
particles, Geldart (1973 ).
Flow Regimes in Fluidized Beds
J. Ruud van Ommen, 2003

CHEMICAL REACTION ENGINEERING LABORATORY
Minimum Fluidization Velocity
This equation can be used to calculate the minimum fluidization velocity
U if the void fraction εmf at incipient fluidization is known.
mf

2
 f umf
 p   f g 
3
 s D p mf

150   mf 

1
 1.75

  s D p umf  f




Experimentally, the most common method of measurement requires that pressure drop
across the bed be recorded as the superficial velocity is increased stepwise through Umf
and beyond, Umf is then taken at the intersection of the straight lines corresponding to
the fixed bed and fluidized bed portions of the graph obtained when Pbed is plotted
against U on log-log coordinates.

Kunii and Levenspiel (1991)
Bubbling Fluidization
 This type of fluidization has
been called ‘aggregative
fluidization’, and under
these conditions, the bed
appears to be divided into
two phases, the bubble
phase and the emulsion
phase.

 The bubbles appear to
be very similar to gas
bubbles formed in a
liquid and they behave
in a similar manner. The
bubbles coalesce as
they rise through the
bed.

CHEMICAL REACTION ENGINEERING LABORATORY
Turbulent Fluidization

Turbulent regime has the following features: High solid hold-ups (typically 25-35 %
by volume).
 Limited axial mixing of gas.
 Suitable for exothermic and fast
reactions.
 Good gas-solid contact and hence,
favors reactant conversion.
 high gas flow-rates operation and good
for isothermal operation.
 Favorable bed to surface heat transfer.
Canada et al. 1978

CHEMICAL REACTION ENGINEERING LABORATORY
Some commercial processes in turbulent
fluidization
Process

Particle classification

Typical gas velocity
(m/s)

FCC regenerators

Group A

0.5-1.5

Acrylonitrile

Group A

~0.5

Maleic anhydride

Group A

~0.5

Phthalic anhydride

Group A

~0.5

Ethylene dichloride

Group A

~0.5

Roasting of zinc sulfide

Group A

~1.5

Bi et al. 2000

CHEMICAL REACTION ENGINEERING LABORATORY
Fast Fluidized Bed
 The fast fluidization occurs as a result of
continuing increasing in operating velocity
beyond that required at turbulent
fluidization, a critical velocity, commonly
called the transport velocity (Utr), will be
reached where a significant particle
entrainment occurs.
 The CFB has significant industrial
applications because of its efficiency,
operational
flexibility,
and
overall
profitability (Berruti et al., 1995).

CHEMICAL REACTION ENGINEERING LABORATORY
Transition between Fluidization Regimes.


Grace (1986a) summarized the effects of particles properties and operating conditions
on fluidization behavior and prepared a flow regime diagram. The flow regime diagram
was further modified by Kunii and Levenspiel (1997).



For given particles and operating velocity, the gas-solid contact pattern can be
determined using this diagram. Likewise, for a given flow regime, this diagram could
provide available combinations of particle properties and gas velocity.

Yang 2003
Fluidization diagram

Us 

U





Gs

Solid hold-up

 av
Yerushalmi and Cankurt, 1970
Methods for Regime Transition Identification
Several measurement methods have been utilized to
determine the transition from bubbling or slugging to
turbulent fluidization which can be classified into three
groups:-






Visual Observation,.
Pressure Drop-versus Velocity diagram.
local and overall bed expansion.
Based on signals from pressure transducers, capacitance
probes, optical fiber probes, X-ray facilities.

Bi et al. 2000

CHEMICAL REACTION ENGINEERING LABORATORY
Generalized effect of operating and design parameters on
flow regime transition
Parameter

Effect on flow regime transition

Pressure

In general, pressure accelerates the flow regime transition, thereby decrease
transition velocity (Lanneau , 1960, Cai et al. 1989, Yates 1996).

Temperature

Transition velocity increases as the temperature is increased, (Peeler et al.,
1999, Cai et al., 1989 and Foka et al., 1996).

Static Bed Height

The transition velocity was almost independent of the static bed height, which
varied from 0.4 to 1.0 m (Grace and Sun 1990). Similar results were reported by
Cai (1989) and Satija and Fan (1985) with (Hmf/Dt) > 2. On the other hand, for
a shallow fluidized bed of (Hmf/Dt) < 2 with Group B and D particles, Canada et
al. (1978) and Dunham et al. (1993) found that Uc increased with static bed
height. This could be related to the undeveloped bubble flow in shallow beds
before transition to turbulent fluidization can occur (Bi et al. 2000).

Particle Size and
Density

Uc increases with increasing mean particle size and density (Cai et al. 1989, Bi
et al. 2000).

Column Diameter

Transition velocity decreases with increasing column diameter for small column,
becoming insensitive to column diameter for Dt > 0.2 m, (Cai, 1989). Similar
trends were observed by (Zhao and Yang, 1991) with internals.

Internals

Transition to turbulent fluidization tends to occur at lower gas velocities in the
presence of internals which usually restrict bubble growth and promote bubble
breakup.
Effect of column diameter

Cai (1989)

 Uc decreases with increasing column diameter for small columns
(less than 2 m), becoming insensitive to column diameter for Dt >
0.2 m.
 Similar trends were observed by Zhao and Yang (1991) in
columns with internals.

CHEMICAL REACTION ENGINEERING LABORATORY
Some Selected References
 Cai et al., 1989, “Effect of operating temperature and pressure on
the transition from bubbling to turbulent fluidization”, AICHE
Symposium series, 85, 37-43.
 Chehbouni et al., (1994), “Characterization of the flow transition
between bubbling and turbulent fluidization”, Ind. Eng. Chem. Res.,
33, 1889-1896.
 Bi et al., (2000), “A state-of-art review of gas-solid turbulent
fluidization”, Chemical engineering science, 55, 4789-4825.
 Andreux et al. (2005), “New description of fluidization regimes”,
AICHE Journal, 51, No.4, 1125-1130.

CHEMICAL REACTION ENGINEERING LABORATORY

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Fluidized bed introduction by mohabat ali malik(MUET,jamshoro)

  • 1. INTRODUCTION TO FLUIDIZED BEDS CHEMICAL REACTION ENGINEERING LABORATORY
  • 2. Outline/Contents         Introduction. Fluidization Flow Regimes. Overall Gas (Voidage) and solids Hold-up. Radial and Axial Solids Hold-Up Profiles. Radial and Axial voidage distribution. Gas and Solid Mixing. Scale-Up. Reactor Modeling. CHEMICAL REACTION ENGINEERING LABORATORY
  • 3. Fluidized Bed Reactor Components Inlet to cyclone The material fluidized is a solid (catalyst). The fluidizing medium is either a gas or a liquid. Gas distributor CHEMICAL REACTION ENGINEERING LABORATORY
  • 4. Advantages  It has the ability to process large volumes of fluid.  Excellent gas-solid contacting.  Heat and mass transfer rates between gas and particles are high when compared with other modes of contacting.  No hot spot even with highly exothermic reaction.  Ease of solids handling. Disadvantages  Broad or even bimodal residence time distribution of the gas due to dispersion and bypass in the form of bubbles.  Broad residence time distribution of solids due to intense solids mixing.  Erosion of internals.  Attrition of catalyst particles.  Difficult Scale-up due to complex hydrodynamics. CHEMICAL REACTION ENGINEERING LABORATORY
  • 5. Industrial Applications of Fluidized Bed Reactor               Acrylonitrile by the Sohio Process. Yang 2003 Fischer-Tropsch Synthesis. Phthalic anhydride synthesis. Methanol to gasoline and olefin processes. Cracking of Hydrocarbons (Fluid Catalytic Cracking, etc). Coal combustion. Coal gasification Cement clinker production. Titanium dioxide production. Calcination of AL(OH)3. Granulation drying of yeast. Heat exchange Absorption Nuclear energy (Uranium processing, nuclear fuel fabrication, reprocessing of fuel and waste disposal). CHEMICAL REACTION ENGINEERING LABORATORY
  • 6. Fluidization Flow Regimes CHEMICAL REACTION ENGINEERING LABORATORY
  • 7. Geldart's Classification of Powders  Group A (Aeratable) :- (e.g., Ammoxidation of propylene) small mean particle size and/or low particle density (<~1.4 g/cm3), gas bubbles appear at minimum bubbling velocity (Umb).  Group B (Sand-Like) :- (e.g.,Starch) particle size 40 μm to 500 μm and density 1.4 to 4 g/cm3, gas bubbles appear at the minimum fluidization velocity (Umb). Kunii and Levenspiel (1991) kg^ 3  Group C (Cohesive) :- very fine particle, particle size < 30 μm, difficult to fluidize because inter-particle forces are relatively large, compared to those resulting from the action of gas.  Group D (Spoutable) :- (e.g., Roasting coffee beans) large particle, stable spouted beds can be easily formed in this group of powders. Diagram of the Geldart classification of particles, Geldart (1973 ).
  • 8. Flow Regimes in Fluidized Beds J. Ruud van Ommen, 2003 CHEMICAL REACTION ENGINEERING LABORATORY
  • 9. Minimum Fluidization Velocity This equation can be used to calculate the minimum fluidization velocity U if the void fraction εmf at incipient fluidization is known. mf 2  f umf  p   f g  3  s D p mf 150   mf   1  1.75    s D p umf  f    Experimentally, the most common method of measurement requires that pressure drop across the bed be recorded as the superficial velocity is increased stepwise through Umf and beyond, Umf is then taken at the intersection of the straight lines corresponding to the fixed bed and fluidized bed portions of the graph obtained when Pbed is plotted against U on log-log coordinates. Kunii and Levenspiel (1991)
  • 10. Bubbling Fluidization  This type of fluidization has been called ‘aggregative fluidization’, and under these conditions, the bed appears to be divided into two phases, the bubble phase and the emulsion phase.  The bubbles appear to be very similar to gas bubbles formed in a liquid and they behave in a similar manner. The bubbles coalesce as they rise through the bed. CHEMICAL REACTION ENGINEERING LABORATORY
  • 11. Turbulent Fluidization Turbulent regime has the following features: High solid hold-ups (typically 25-35 % by volume).  Limited axial mixing of gas.  Suitable for exothermic and fast reactions.  Good gas-solid contact and hence, favors reactant conversion.  high gas flow-rates operation and good for isothermal operation.  Favorable bed to surface heat transfer. Canada et al. 1978 CHEMICAL REACTION ENGINEERING LABORATORY
  • 12. Some commercial processes in turbulent fluidization Process Particle classification Typical gas velocity (m/s) FCC regenerators Group A 0.5-1.5 Acrylonitrile Group A ~0.5 Maleic anhydride Group A ~0.5 Phthalic anhydride Group A ~0.5 Ethylene dichloride Group A ~0.5 Roasting of zinc sulfide Group A ~1.5 Bi et al. 2000 CHEMICAL REACTION ENGINEERING LABORATORY
  • 13. Fast Fluidized Bed  The fast fluidization occurs as a result of continuing increasing in operating velocity beyond that required at turbulent fluidization, a critical velocity, commonly called the transport velocity (Utr), will be reached where a significant particle entrainment occurs.  The CFB has significant industrial applications because of its efficiency, operational flexibility, and overall profitability (Berruti et al., 1995). CHEMICAL REACTION ENGINEERING LABORATORY
  • 14. Transition between Fluidization Regimes.  Grace (1986a) summarized the effects of particles properties and operating conditions on fluidization behavior and prepared a flow regime diagram. The flow regime diagram was further modified by Kunii and Levenspiel (1997).  For given particles and operating velocity, the gas-solid contact pattern can be determined using this diagram. Likewise, for a given flow regime, this diagram could provide available combinations of particle properties and gas velocity. Yang 2003
  • 15. Fluidization diagram Us  U   Gs Solid hold-up  av Yerushalmi and Cankurt, 1970
  • 16. Methods for Regime Transition Identification Several measurement methods have been utilized to determine the transition from bubbling or slugging to turbulent fluidization which can be classified into three groups:-     Visual Observation,. Pressure Drop-versus Velocity diagram. local and overall bed expansion. Based on signals from pressure transducers, capacitance probes, optical fiber probes, X-ray facilities. Bi et al. 2000 CHEMICAL REACTION ENGINEERING LABORATORY
  • 17. Generalized effect of operating and design parameters on flow regime transition Parameter Effect on flow regime transition Pressure In general, pressure accelerates the flow regime transition, thereby decrease transition velocity (Lanneau , 1960, Cai et al. 1989, Yates 1996). Temperature Transition velocity increases as the temperature is increased, (Peeler et al., 1999, Cai et al., 1989 and Foka et al., 1996). Static Bed Height The transition velocity was almost independent of the static bed height, which varied from 0.4 to 1.0 m (Grace and Sun 1990). Similar results were reported by Cai (1989) and Satija and Fan (1985) with (Hmf/Dt) > 2. On the other hand, for a shallow fluidized bed of (Hmf/Dt) < 2 with Group B and D particles, Canada et al. (1978) and Dunham et al. (1993) found that Uc increased with static bed height. This could be related to the undeveloped bubble flow in shallow beds before transition to turbulent fluidization can occur (Bi et al. 2000). Particle Size and Density Uc increases with increasing mean particle size and density (Cai et al. 1989, Bi et al. 2000). Column Diameter Transition velocity decreases with increasing column diameter for small column, becoming insensitive to column diameter for Dt > 0.2 m, (Cai, 1989). Similar trends were observed by (Zhao and Yang, 1991) with internals. Internals Transition to turbulent fluidization tends to occur at lower gas velocities in the presence of internals which usually restrict bubble growth and promote bubble breakup.
  • 18. Effect of column diameter Cai (1989)  Uc decreases with increasing column diameter for small columns (less than 2 m), becoming insensitive to column diameter for Dt > 0.2 m.  Similar trends were observed by Zhao and Yang (1991) in columns with internals. CHEMICAL REACTION ENGINEERING LABORATORY
  • 19. Some Selected References  Cai et al., 1989, “Effect of operating temperature and pressure on the transition from bubbling to turbulent fluidization”, AICHE Symposium series, 85, 37-43.  Chehbouni et al., (1994), “Characterization of the flow transition between bubbling and turbulent fluidization”, Ind. Eng. Chem. Res., 33, 1889-1896.  Bi et al., (2000), “A state-of-art review of gas-solid turbulent fluidization”, Chemical engineering science, 55, 4789-4825.  Andreux et al. (2005), “New description of fluidization regimes”, AICHE Journal, 51, No.4, 1125-1130. CHEMICAL REACTION ENGINEERING LABORATORY