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Presented by :
Umama Noor
Kainat Zahra
Warda Rai
Definition of bioreactors
 Bioreactor may refer to any manufactured and engineered device or
system that support a biological active environment.
 A bioreactor is a vessels which has provision of cell cultivation
under sterile condition and control of environmental condition e.g.,
ph , temperature , concentration of product and substrate and liquid
flow rate and some gasses like dissolved oxygen , nitrogen & carbon
dioxide etc.
 This process can be either aerobic or anaerobic.
 Bioreactor are commonly cylindrical in shape ,ranges in size
from liters to cubic meters and often made up of stainless
steel.
A typical bioreactor consists of following parts:
 Agitator-it is used for the mixing of the reactors which
keeps the cell in the perfect homogenous condition for better
transport of nutrients and oxygen to the desired product .
 Buffles-to avoid vortex formation
to avoid vibration
to hold tubes in place
 Sparger-to pass air into the vessel e.g. Porous sparger,
Nozzle sparger.
 jacket-the jacket provide the annular area for the circulation
of constant temperature of water which keeps the
temperature of bioreactor at a constant value.
 Antiform- Forming produced either by
agitation or by components used in the
medium like proteins. Foaming cause the
adhesion of cells to inner surface of vessel.
To avoid foaming antifoams are used like
pluronic f68, liquid paraffin and oil in some
cultures.
 Stirred tank
 Air lift reactors
 Bubble column
 Packed bed reactors
 Fluidized bed reactor
 Photobioreactor
 Mixing medium: Mechanical Agitation
 Large input required
 Application: Waste water treatment
 Continuous operation
 Good temperature control
 Good control
 Simplicity of construction
 Low operating (labor) cost
 Easy to clean
 Shear forces may kill cells
 The need for shaft seals and bearings.
 Size limitation by motor size, shaft length
and weight.
 Mixing method: Air lift
 Central Draught-tube
 Up flowing stream and
down flowing stream
 Homogenization of all
components
 Simple design :with no moving parts or agitator for less
maintenance, less risk of defects.
 No agitator shaft parts
 Low Energy requirement VS stirred tank : Obviously
doesn’t need the energy for the moving parts (agitator
shaft).
 Greater heat-removal VS stirred tank: At the Airlift
bioreactor it doesn’t need the heat plate to control the
temperature, because the Draught-Tube which is inside
the bioreactor can be designed to serve as internal heat
exchanger. It is difference to the Stirred tank bioreactor
that needs the heat coat or plate surrounding the tank to
make warm bioreactor. It is clear enough that the Airlift
bioreactor has greater heat-removal compare to Stirred
tank.
 Very low cost
 Greater air throughput and higher pressures
needed .
 Extra foaming occur.
 NO bubbles breaker .
 These bioreactors do not have
any mechanical or otherwise
moving parts.
 The upper section of the BC is
often widened to encourage gas
separation.
 BCs require very little
maintenance or floor space and
have low operating costs
compared to other reactor
types.
 Used in production of Baker’s yeast, beer &
vinegar.
 Also used in aeration and treatment of waste
water.
 In bubble column, the hydrodynamics and
mass transfer depend on the size of bubble
and how they are released from the sparger.
 Simple design.
 Required low energy.
 Greater heat removal.
 Very low cost.
 Require high pressure through sparger.
 Occur extra foaming.
 No bubble breaker.
 Column with attached
biocatalyst
 Pump is required to move
the fluid through packed
bed
 Application: Waste water
treatment
 Continuous operation
 Low operation cost
 No moving parts to wear out
 Catalyst stays in reactor
 Catalyst separation is easy
 Effective at high temperature and pressure
 Difficult to control pH by adding acids or
alkalis
 Difficult to clean
 Difficult to replace catalyst
 Undesirable side reactions
 When the packed beds are
operated in up flow mode
the bed expands at high
liquid flow rates due to
upward motion of particles
 Energy is required
 Suitable for a reaction
which carries enzymes
 Waste water treatment
 Uniform particle mixing
 Uniform temperature gradient
 Ability to operate reactor in continuous state
 Increased reactor vessel size
 Pumping requirements and pressure drop
 Particle entrainment
 Erosion of internal components
 Pressure loss scenarios
 Bioreactors specialized for fermentation that can
be carried out either by exposing to sunlight
 Certain important compounds are produced by
employing photo-bioreactors e.g. astaxanthin
 They are made up of glass or more commonly
transparent plastic
 Photo-bioreactors are usually operated in a
continuous mode at a temperature in the range
of 25-40°C.
 The organisms grow during day light while the
products are produced during night.
 Microalgae and cyanobacteria
Bioreactors

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Bioreactors

  • 1. Presented by : Umama Noor Kainat Zahra Warda Rai
  • 2. Definition of bioreactors  Bioreactor may refer to any manufactured and engineered device or system that support a biological active environment.  A bioreactor is a vessels which has provision of cell cultivation under sterile condition and control of environmental condition e.g., ph , temperature , concentration of product and substrate and liquid flow rate and some gasses like dissolved oxygen , nitrogen & carbon dioxide etc.  This process can be either aerobic or anaerobic.
  • 3.  Bioreactor are commonly cylindrical in shape ,ranges in size from liters to cubic meters and often made up of stainless steel.
  • 4.
  • 5. A typical bioreactor consists of following parts:  Agitator-it is used for the mixing of the reactors which keeps the cell in the perfect homogenous condition for better transport of nutrients and oxygen to the desired product .  Buffles-to avoid vortex formation to avoid vibration to hold tubes in place  Sparger-to pass air into the vessel e.g. Porous sparger, Nozzle sparger.  jacket-the jacket provide the annular area for the circulation of constant temperature of water which keeps the temperature of bioreactor at a constant value.
  • 6.  Antiform- Forming produced either by agitation or by components used in the medium like proteins. Foaming cause the adhesion of cells to inner surface of vessel. To avoid foaming antifoams are used like pluronic f68, liquid paraffin and oil in some cultures.
  • 7.  Stirred tank  Air lift reactors  Bubble column  Packed bed reactors  Fluidized bed reactor  Photobioreactor
  • 8.  Mixing medium: Mechanical Agitation  Large input required  Application: Waste water treatment
  • 9.  Continuous operation  Good temperature control  Good control  Simplicity of construction  Low operating (labor) cost  Easy to clean
  • 10.  Shear forces may kill cells  The need for shaft seals and bearings.  Size limitation by motor size, shaft length and weight.
  • 11.  Mixing method: Air lift  Central Draught-tube  Up flowing stream and down flowing stream  Homogenization of all components
  • 12.  Simple design :with no moving parts or agitator for less maintenance, less risk of defects.  No agitator shaft parts  Low Energy requirement VS stirred tank : Obviously doesn’t need the energy for the moving parts (agitator shaft).  Greater heat-removal VS stirred tank: At the Airlift bioreactor it doesn’t need the heat plate to control the temperature, because the Draught-Tube which is inside the bioreactor can be designed to serve as internal heat exchanger. It is difference to the Stirred tank bioreactor that needs the heat coat or plate surrounding the tank to make warm bioreactor. It is clear enough that the Airlift bioreactor has greater heat-removal compare to Stirred tank.  Very low cost
  • 13.  Greater air throughput and higher pressures needed .  Extra foaming occur.  NO bubbles breaker .
  • 14.  These bioreactors do not have any mechanical or otherwise moving parts.  The upper section of the BC is often widened to encourage gas separation.  BCs require very little maintenance or floor space and have low operating costs compared to other reactor types.
  • 15.  Used in production of Baker’s yeast, beer & vinegar.  Also used in aeration and treatment of waste water.  In bubble column, the hydrodynamics and mass transfer depend on the size of bubble and how they are released from the sparger.
  • 16.  Simple design.  Required low energy.  Greater heat removal.  Very low cost.
  • 17.  Require high pressure through sparger.  Occur extra foaming.  No bubble breaker.
  • 18.  Column with attached biocatalyst  Pump is required to move the fluid through packed bed  Application: Waste water treatment
  • 19.  Continuous operation  Low operation cost  No moving parts to wear out  Catalyst stays in reactor  Catalyst separation is easy  Effective at high temperature and pressure
  • 20.  Difficult to control pH by adding acids or alkalis  Difficult to clean  Difficult to replace catalyst  Undesirable side reactions
  • 21.  When the packed beds are operated in up flow mode the bed expands at high liquid flow rates due to upward motion of particles  Energy is required  Suitable for a reaction which carries enzymes  Waste water treatment
  • 22.  Uniform particle mixing  Uniform temperature gradient  Ability to operate reactor in continuous state
  • 23.  Increased reactor vessel size  Pumping requirements and pressure drop  Particle entrainment  Erosion of internal components  Pressure loss scenarios
  • 24.  Bioreactors specialized for fermentation that can be carried out either by exposing to sunlight  Certain important compounds are produced by employing photo-bioreactors e.g. astaxanthin  They are made up of glass or more commonly transparent plastic  Photo-bioreactors are usually operated in a continuous mode at a temperature in the range of 25-40°C.  The organisms grow during day light while the products are produced during night.  Microalgae and cyanobacteria