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Unit 3 Catalytic Cracking

Catalytic cracking is a process that breaks down complex hydrocarbons into simpler molecules to produce lighter, more desirable products like gasoline and LPG while reducing residuals. The process involves reactions with catalysts, regeneration of catalysts, and fractionation of products, typically operating under low pressure and high temperatures. Various types of catalytic cracking processes include Fluid Catalytic Cracking (FCC), Moving-bed catalytic cracking, and Thermofor catalytic cracking, each with specific operational characteristics and conditions.

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0% found this document useful (0 votes)
11 views41 pages

Unit 3 Catalytic Cracking

Catalytic cracking is a process that breaks down complex hydrocarbons into simpler molecules to produce lighter, more desirable products like gasoline and LPG while reducing residuals. The process involves reactions with catalysts, regeneration of catalysts, and fractionation of products, typically operating under low pressure and high temperatures. Various types of catalytic cracking processes include Fluid Catalytic Cracking (FCC), Moving-bed catalytic cracking, and Thermofor catalytic cracking, each with specific operational characteristics and conditions.

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CATALYTIC CRACKING

Catalytic Cracking
Feedstock From Process Typical products . . . . To

Gas oils . . . . Towers, Decomposition, Gasoline . . . . . . . . . Treater or blend


coker alteration Gases . . . . . . . . . . Gas plant
visbreaker

Deasphalted Middle distillates . . .Hydrotreat,


oils . . . . . . . Deasphalter blend, recycle
Petrochem feedstock . . Petrochem or
other
Residue . . . . . . . . . . . Residual fuel
blend
Catalytic cracking
 What it does?
 Catalyticcracking breaks complex hydrocarbons into
simpler molecules
 Why?
 Inorder to increase the quality and quantity of lighter,
more desirable products
 decrease the amount of residuals.
Catalytic cracking
 This process rearranges the molecular structure of
hydrocarbon compounds to convert heavy
hydrocarbon feedstock into lighter fractions such
as kerosene, gasoline, LPG, heating oil, and
petrochemical feedstock.
Conditions
 FCC is a low pressure, intermediate to high
temperature process.

Reactor Temperature, 0C 470-540

Regenerator Temperature, 0C 590-610

Reactor Pressure, kPa 232

Regenerator Pressure, kPa 274

Fractionator Pressure, kPa 225


Basic functions in the catalytic cracking
process

 Reaction: Feedstock reacts with catalyst and


cracks into different hydrocarbons

 Regeneration: Catalyst is reactivated by burning


off coke

 Fractionation: Cracked hydrocarbon stream is


separated into various products.
Types of catalytic cracking processes

 Fluid catalytic cracking (FCC)

 Moving-bed catalytic cracking

 Thermofor catalytic cracking (TCC)


Fluid Catalytic Cracking
Working of FCC
Fluid cracker consists of
 Catalyst section
 Reactor

 catalyst circulation unit


 regenerator,standpipe and riser

 Fractionating section
FCC Process
 The fluid catalyst is continuously circulated
between the reactor and the regenerator using air,
oil vapors, and steam as the conveying media
FCC Process
 mixing a preheated hydrocarbon charge with hot,
regenerated catalyst as it enters the riser leading
to the reactor
 The charge is combined with a recycle stream
within the riser, vaporized, and raised to reactor
temperature (900°-1,000° F) by the hot catalyst
FCC Process
 As the mixture travels up the riser, the charge is
cracked at 10-30 psi
 This cracking continues until the oil vapors are
separated from the catalyst in the reactor cyclones.
 The resultant product stream (cracked product) is
then charged to a fractionating column where it is
separated into fractions, and some of the heavy oil is
recycled to the riser.
FCC Process
 Spent catalyst flows through the catalyst stripper
to the regenerator, where most of the coke
deposits burn off at the bottom where preheated
air and spent catalyst are mixed.
Catalysts
 A catalyst consists of an active substance applied
on a carrier substance having large extended
surface area
 Particles have enormous porosity and very large
internal surface area
 Promotors: Added to improve the performance of
the catalysts
Catalysts
 Activity: Estimated in terms of yield of the end
product relative to the use of the starting material
 Selectivity: The capability of the catalyst to
accelerate a desirable reaction and retain the rate
of the undesirable one

 Activity and selectivity is gradually lost due to


ageing
Regeneration
 By burning off coke deposited on the catalyst
particles
 By raising the temperature within the reactor
 By adding fresh circulating catalysts to compensate for
the loss of the original one
Catalyst
Catalysts used Form
 zeolite  powders

 aluminum  beads
hydrosilicate  pellets or

 treated bentonite clay  shaped materials

 fuller's earth called extrudites


 bauxite

 silica-alumina
Process Variables: Reactor Section

 Fresh feed rate  Catalyst to oil ratio


 Fresh feed  Recycle rate
temperature  Recycle temperature
 Reactor Temperature  Catalyst activity
 Reactor level
 Reactor pressure
 Stripping steam rate
Fresh Feed rate
 Increasing the feed rate will increase the space
velocity and lower the conversion

 Space velocity (Weight Hourly Space Velocity-


WHSV) = kg/h of feed divided by kg of catalyst hold
up in the reaction zone
Fresh Feed temperature
 Combined feed temperature increases. This leads
to
 Decrease in conversion
 Increase in regenerator temperature

 Reduction in coke yield

 Reduction in oil/catalyst ratio


Reactor temperature
 Increase in reactor temperature leads to
 Increase in C1, C2, C3 and C4 yield
 Decrease in gasoline yield

 Increase in olefin content

 Increase in RON
Reactor level
 Increasing the reactor level (Weight of catalyst)
leads to
 Increase in conversion
 Decrease gasoline yield

 Increase regenerator temperature

 Increase coke yield

 Decrease in olefin content


Reactor Pressure
 Increase in pressure will lead to
 Increase in conversion
 Increase in regeneration temperature

 Decrease in reactor velocity and cyclone inlet velocity


Stripping steam rate
 Determined by catalyst circulation rate
 Generally 1-2.5 kg per ton of catalyst circulated
 Conditions that demand for increase in the rate
 Increase in feed rate and recycle rate
 Increase in reactor pressure

 Decrease in combined feed temperature and reactor


temperature
 A deterioration in catalyst particle size distribution
Catalyst/Oil ratio
 Increase in this ratio leads to increase in
conversion
 It increases with increase in reactor temperature
and decrease in regenerator and combined feed
temperatures.
Recycle rate
 Cycle oils recycled to increase gasoline yield
Recycle temperature
 Increases combined feed temperature
Catalyst activity
 Results in higher conversion
 Average specific surface of about 80-100 m2/g is
desirable for maximizing middle distillate
production
Process Variables: Regeneration Section

 Dense Phase temperature


 Regenerator pressure
 Catalyst circulation rate
 Regeneration air rate
 Air distribution
 Torch oil
 Spray water
 Catalyst condition
Dense phase temperature
 Regenerator temperature increases with increase
in:
 Sp.gravity or Avg. B.P of the feed
 Carbon residue

 combined feed temperature

 reactor level

 Reactor temperature

 Reactor pressure
Regenerator pressure
 Lowering of pressure will
 Decrease blower power consumption
 Improve air distribution

 Increase catalyst entrainment to cyclones

 Increase cyclone efficiency


Catalyst circulation rate
 Increase in catalyst circulation rate reduces catalyst
residence time and has an adverse effect on
regeneration
Regeneration air rate
 Most important variable.. Can be controlled by the
operator
 Insufficient air leads to coke build up
 Too much air leads to excess oxygen in flue gas and
after burning occurs
Regeneration air rate
 Most important variable.. Can be controlled by the
operator
 Insufficient air leads to coke build up
 Too much air leads to excess oxygen in flue gas and
after burning occurs

Oxidation of CO to CO2
Increases temperature
Air Distribution
 Unconsumed oxygen passing through the section
of the bed will cause abnormal afterburning
Torch oil
 Distillate sprayed through nozzles to give
additional coke to satisfy heating requirements of
the unit
Spray water
 At the inlet of first stage cyclone
 To protect the cyclone from excessive temperature
 During upset conditions
Catalyst condition
 A substantial loss of fines will result in poor
fluidization and will increase the carbon content.
 This will lead to after burning
Moving-bed catalytic cracking process

 It is similar to the FCC process.


 The catalyst is in the form of pellets that are
moved continuously to the top of the unit by
conveyor or pneumatic lift tubes to a storage
hopper, then flow downward by gravity through
the reactor, and finally to a regenerator.
 The cracked product is separated into recycle gas,
oil, clarified oil, distillate, naphtha, and wet gas.
Thermofor Catalytic Cracking
 The preheated feedstock flows by gravity
through the catalytic reactor bed.
 The vapors are separated from the catalyst and
sent to a fractionating tower.
 The spent catalyst is regenerated, cooled, and
recycled.
 The flue gas from regeneration is sent to a
carbon-monoxide boiler for heat recovery.

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