Course: Chemical Technology (Organic) Module VI

Lecture 5
Catalytic Cracking: Fluid
Catalytic Cracking And
Hydrocracking
 LECTURE 5
CATALYTIC CRACKING
Catalytic cracking process was developed in1920 by Eugene Houdry for upgradation of residue
was commercialized latter in 1930. Houdry process was based on cyclic fixed bed configuration.
There has been continuous upgradation in catalytic in catalytic cracking process from its incept
of fixed bed technology to latter fluidized bed catalytic cracking (FCC).The feed stock for
catalytic cracking is normally light gas oil from vacuum distillation column. Catalytic cracking
cracks low value high molecular weight hydrocarbons to more value added products (low
molecular weight) like gasoline, LPG Diesel along with very important petrochemical feedstock
like propylene, C4 gases like isobutylene, Isobutane, butane and butane. Main Catalytic Cracking
Reaction is given in Table M-VI 5.1.

Main reactions involved in catalytic cracking are

 Cracking
 Isomerisation
 Dehydrogenenation
 Hydrogen transfer
 Cyclization
 Condensation
 Alkylation and dealkylation
Major primary reactions taking place in catalytic cracking is given in Table
Paraffins Smaller paraffins + olefins
Alkyl naphthene naphthene + olefin
Alkyl aromatic aromatic + olefin
Multiring naphthene alkylated naphthene with fewer rings

Table M-VI 5.1 Main Catalytic Cracking Reaction

Paraffins Cracking Paraffins + Olefins
Olefins

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 Cyclization Coke

Naphthenes

Aromatics

Trans alkylation Different alkyl aromatics

FLUID CATALYTIC CRACKING

Fluid catalytic cracking is now major secondary conversion process in Petroleum refinery since
1942. there are more than 400 FCC units in world. The process provides around 50 percent of all
transportation fuel and 35percent of total gasoline pool. Major land marks in the history of FCC
has been:[Ghosh,2002]

 Introduction of zeolite catalyst during 1960 which has resulted in lower residence time
 Introduction of ultra stable Y-zeolite in mid 60’s
 Switch over from bed cracking to riser cracking
 Introduction of large number of additives for boosting of gasoline octane/yield of light
naphtha
 SOx control
 Nickel and vanadium passivation

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FCC is a multi-comp
ponent cataly
yst system with
w circulatiing fluid bedd reactor sysstem with reeactor
Regeneraator system configuratio
on. Figure M-VI
M 5.1 shhows details of FCC pprocess and FCC
reactor.
Flue Gas
G Re
eactor vapors
Over head gasess
Process Air

Treated gas

Power
P
Re
ecovery
Steam

Boiler Feed
Water
LPG

Unsaturatted Gas
Concenntrator

Sppent
Cattalysis Main
Fractionating
Catalyst Fluid Cattalytic Column Heavy
generator
Reg Cracking n
naphtha Gasoline
Reacttor
Process Air Regenerrated
Cataly
yst

Light
Cycle Oil

Steam Raw oil


Fuel Oil

Fig
gure M-VII 5.1: Fluiid Catalytiic Crackin
ng Processs and FCC
C Reactor
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FEED STOCK
Vacuum gas oil (VGO), Hydro-treated VGO, Hydro-cracker bottom, Coker gas oil (CGO), De-
asphalted oil (DAO), Reduced crude oil (RCO), Vacuum residue (VR)
 Typical feedstock consists of Vacuum and Atmosphere gas oil but may include other
heavy stream.
 Major contaminant in the feed includes carbon residue and metals.
 While FCC process feed containing up to 4% Conradson carbon MSCC can process all
kinds of feed.
Process Steps
Three basic functions in the catalytic cracking process are:
Reaction - Feedstock reacts with catalyst and cracks into different hydrocarbons;
Regeneration - Catalyst is reactivated by burning off coke; and recerculated to reactor
Fractionation - Cracked hydrocarbon stream is separated into various products like LPG and
gasoline, like light cycle oil and heavy cycle oil are withdrawn as side stream

Reactor and Regenerator Section: Catalyst section consists mainly of the reactor and
regenerator
 The feed to unit along with recycle streams is preheated to temperature of 365oC-370Oc
and enters the riser where it comes in contact with hot regenerated catalyst ( at a
temperature of about 640-660oC. Finely divided catalyst is maintained in an aerated or
fluidized state by the oil vapors.
 The catalyst section contains the reactor and regenerator & catalyst re circulates between
the two.
 Spent catalyst is regenerated to get rid of coke that collects on the catalyst during the
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. Fresh catalyst is added and worn-out catalyst removed to optimize the cracking
process
Fractionation - Cracked hydrocarbon stream is separated into various products. LPG and gasile
are removed overhead as vpour. Unconverted product like light cycle oil and heavy cycle oil are

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withdrawn as side stream. Overhead product is sent to stabilsation section where stablised
gasoline is separated from light products from which LPG is recovered.

Typical operating parameter of FCC

Raw oil feed at heater inlet : 114 cubic meter /h
Furnace outlet temperature : 291oC
Reactor feed temperature : 371oC
Reactor Vapour temperature : 549oC

Product Obtained
 Light gas -H2, C1, and C2s
 LPG C3s and C4s – includes light olefins
 Gasoline C5+ high octane component for gasoline pool or light fuel
 Light cycle oil (LCO) blend component for diesel pool or light fuel
 Heavy cycle oil (HCO) Optional heavy cycle oil product for fuel oil or cutter stock
 Clarified oil (CLO) or decant oil: slurry for fuel oil
 Coke by-product consumed in the regenerator to provide the reactor heat demand

FCC Catalysts
Major breakthrough in the catalytic racking process was development zeolite catalysts which
demonstrated vastly superior activity, gasoline selectivity, and stability characteristics compared
to original amorphous silica alumina catalyst [Hemler & Smith, 2004].

Year 1950 1970 1990

Zeolite content, wt% 0 10 Upto 40
Particle density, g/cc 0.9 1 1.4
Relative Attrition Index 20 5 1

Today’s FCC catalysts Porous spray dried micro-spherical powder

 Particle size distribution of 20 -120 micron & particle density ~ 1400 kg/m3

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  Comprising Y zeolite in many derivatives of varying properties
 Supplied under various grades of particle sizes & attrition resistance
 Continuing improvement metal tolerance, coke selectivity
New bread of catalyst are high metal tolerance with high matrix catalyst having better
accessibility, regenerability and strippability [Ghosh, 2006]

Options for Clean Fuel:

For upgrading FCC products into acceptable blending components following three steps are
being used [Letzsch, 2005];
 Severe hydro processing of feed to FCC
 Treating each of the products in hydrotreater
 Combination of both upstream and downstream processing

MODIFIED CATALYTIC CRACKING PROCESSES

Resid FCC (RFCC) Process:
The RFCC process uses similar reactor technology as the FCC process and is targeted for
residual feeds greater than 4 wt-% Conradson carbon. A two stage regenerator with catalyst
cooling is typically used to control the higher coke production and resulting heat.

Deep Catalytic Cracking (DCC):

Milli Second Catalytic cracking (MSCC) Process:
Improvements in riser termination devices have led to significant decreases in post-riser
residence time and post-riser cracking. The benefits of shorter catalyst-and oil contact time have
been lower dry gas yields, lower delta coke on catalyst and more selective cracking to gasoline
and light olefins.
• Due to improvement in reactor design there is lower regenerator temperature and higher
catalyst recovery.

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Petro FCC Process
The Petro FCC process targets the production of petrochemical feedstock rather than fuel
products. This new process, which utilizes a uniquely designed FCC unit, can produce very high
yields of light olefins and aromatics when coupled with aromatics complex. The catalyst section
of the Petro FCC process uses a high-conversion, short-contact time reaction zone that operates
at elevated reactor riser outlet temperatures

Indmax Technology- Residue to Olefin was developed by IOC R&D center and has
been successfully commissioned in IOC Guwahati Unit [Bhatacharya, 2001]
Some of the special features of the technology are:
Operational features of Indmax technology
 Very high cat/oil ratio(15-25)
 Higher riser temperature (>5500 C)
 Higher riser steam rate
 Relatively lower regeneration temperature.
Benefits
 LPG 35-65 wt%
 Propylene 17-25 wt% feed
 High octane gasoline (95+)
Multifunctional proprietary catalyst
 Higher propylene selectivity
 Superior metal tolerance
 Lower coke mate

Maximizing Propylene Output in FCC

New FCC processes are being operated to maximize the yield of propylene due to growing
demand of propylene. Significant scope exists in the refinery in Asia region to enhance the
production of propylene in Asia region [Ghosh, 2006]. Maximizing propylene yield from FCC is
typically accomplished by combining a low rare earth catalyst system with severe reaction
condition [Amano,T.,Wilcox,J. and Pouwels,C. “ Process and catalysis factors to maximize
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propylene output” Petroleum Technology Quarterly 3, 2012,p.17]. some of the olefin
maximizing technology are deep catalytic cracking (DCC) based on riser bed catalytic cracking,
Propylene –Max technology by ABBS Lummus global, Maxofin Process by Mobil-M.W. Kellog

HYDROCRACKING
The development of upgrading technology for heavier stocks having high sulfur, nitrogen and
heavy metal (Ni, V) are becoming important. Hydrocracking is one of the most versatile
processes for the conversion of low quality feed stocks into high quality products like gasoline,
naphtha, kerosene, diesel, and hydrowax which can be used as petrochemical feed stock. Its
importance is growing more as a refiners search for low investment option for producing clean
fuel. New environmental legislations require increasing and expensive efforts to meet stringent
product quality demands.
Hydrocracking processes uses a wide variety of feed stocks like naphtha, atmospheric gas oil,
vacuum gas oils, coke oils, catalytically cracked light and heavy cycle oil, cracked residue,
deasphalted oils and produces high quality product with excellent product quality with low sulfur
contents. Comparison of catalytic cracking and hydrocracking is given in Table M-VI 5.1.
The history of the hydrocracking process goes back to late 1920 when hydrocracking technology
for coal conversion was developed in Germany. During World War II, two stage hydrocracking
were applied in Germany, USA and Britain. However, real breakthrough in hydrocracking
process was with the development of improved catalyst due to which processing at lower
pressure. Hydrocracking can process wide variety of feedstocks producing wide range of
products.
Feed: Straight run gas oil, Vacuum gas oils, Cycle oils, Coker Gas oils, thermally cracked
stocks, Solvent deasphalted residual oils, straight run naphtha, cracked naphtha.
Product: Liquefied petroleum gas (LPG), Motor gasoline, Reformer feeds, Aviation turbine
fuel, Diesel fuels, heating oils, Solvent and thinners, Lube oil, FCC feed

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Table M-VI 5.1: Comparison of Catalytic Cracking and Hydrocracking
Catalytic Cracking Hydro-cracking
Carbon rejection Hydrogen addition
Riser-regenerator-configuration Downflow packed bed
LPG/gasoline Kerosene/diesel
Product rich in unsaturated components Few aromatics, low S- and N-content in
product

Recent Development Hydrocracking:

There has been continuous development in the hydrocracking technology both in process and
catalyst. Some of the important development in hydrocracking has been mild hydrocracking and
resid hydrocracking. Mild hydrcracking (MHC) is characterized by relatively low conversion
(20-40%) as compared to convention hydrocracking which give 70-100% conversion of heavy
distillate at high pressure. MHC route produces low sulphur (10 ppm sulphur as desired by future
diesel specification) diesel. New mild hydrocracking route produces 10 ppm sulphur diesel
which is produced by hydro-cracking under mild pressure. MHC allows increasing diesel
production through VGO hydro-conversion.
The yield of middle distillates obtained from hydro cracker is much more than that obtained from
other processes also, hydro cracker does not yield coke or pitches as by product. The increased
demand for environmentally acceptable products forced the refiners to accept stringent
specifications for gasoline & diesel necessitating the use of hydrocracking technology to limit
sulphur & aromatic in petroleum products. No post treatment is required for the hydro cracker
products.

Hydro-treatment & Hydrocracking Catalyst

Hydrocracking processes involved two types of catalyst:
 Hydro pretreatment catalyst
 Hydrocracking catalyst

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Hydrotreating (Pretreat) Catalyst
The main objective of pretreat catalyst is to remove organic nitrogen from the hydro cracker feed
allowing
(i) Better performance of second stage hydrocracking catalyst, and
(ii) The initiation of the sequence of hydrocracking reactions by saturation of aromatic
compounds
Pretreat catalyst must have adequate activity to achieve above objectives within the operating
limits of the hydrogen partial pressure, temperature and LHSV.

Hydrocracking Catalyst
Hydrocracking catalyst is a bi-functional catalyst and has a cracking function and hydrogenation-
dehydrogenation function. The former is provided by an acidic support whereas the latter is
imparted by metals. Acid sites (Crystalline zeolite, amorphous silica alumina, mixture of
crystalline zeolite and amorphous oxides) provide cracking activity. Metals [Noble metal (Pd, Pt)
or non noble metal sulphides (Mo, Wo or Co, Ni)] provide hydrogenation dehydrogenation
activity. These metals catalyze the hydrogenation of feedstocks making them more reactive for
cracking and hetero-atom removal as well reducing the coke rate
Zeolite based hydrocracking catalysts have following advantages of greater acidity resulting in
greater cracking activity; better thermal/hydrothermal stability; better naphtha selectivity; better
resistance to nitrogen and sulphur compounds; low coke forming tendency, and easy
regenerability.

Once though Hydrocracking Process

The unit consists of the following sections:
 Furnace
 First stage Reactor section
 Second stage Reactor section
 High pressure separator
 Fractionation Section
 Light Ends Recovery section

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In single stage process both treating and cracking steps are combined in a single reactor. Single
stage hydrocracking flow diagram is show in Figure M-VI 5.3[ Mall,2007].
In this process the feed along with recycle unconverted residue from the fractionator is first
hydro-treated in a reactor and then the combined stream gases are fed to second reactor where
cracking takes place in the presence of hydro-cracking catalyst.
In the single stage process the catalysts work under high H2S and NH3 partial pressure.

Gas to
Make up
amine LPG
Hydrogen Recycle treatment
Gasoline
I II

D istilla tion
Kerosene

S tripp er
1st R e acto r

2 nd R ea ctor

S e pa ra tor
Furnace Diesel

Preheater

Residue

Hydrogen
Feed

Figure M-VI 5.3: Once Through Hydrocracking

Two Stage Hydrocracking Process

The unit consists of the following sections:
 Furnace
 First stage Reactor section.
 Second stage Reactor section
 Third stage reactor
 Fractionation Section

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  Light Ends Recovery section
Preheated feed is first hydro treated in a reactor for desulphurization and denitrogenation in
presence of pretreat catalyst followed by hydrocracking in second reactor in presence of strongly
acidic catalyst with a relatively low hydrogenation activity. In the first stage reactor the sulphur
and nitrogen compounds are converted to hydrogen sulphide and ammonia with limited
hydrocarcking. The two stages process employs interstage product separation that removes H2S
and NH3. In case of two stage process, hydrocracking catalyst works under low H2S and NH3.
Process flow diagram for two stage hydrocracking process is shown in Figure M-VI 5.4 [ mall
2007].
Gas to amine
treatment
Reactor1 LPG

Reactor2
Reactor3 Gasoline
Heater

Distillation
Stripper
Kerosene

Diesel

Heater

Feed
Residue
Separator

Hydrogen

Figure M-VI 5.4: Two Stage Hydrocracking Process

HYDROCRACKING CHEMISTRY
Hydrocracking process is a catalytic cracking process which takes place in the presence of an
elevated partial pressure of hydrogen and is facilitated by bio-functional catalyst having acidic
sites and metallic sites. During hydrocracking process hydrotreating reactions and hydrocracking
reactions are two major reactions which take place.
A typical hydrocracking reaction is as follows.

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 C22 H46 + H2 C16H34 + C6H14
Various hydrotreating reactions are hydrodesulphurization, denitrogenation, hydro
deoxygenation, hydro metallization, olefin hydrogenation partial aromatics saturation.
Various hydrocracking reactions are splitting of C-C bond and or C-C rearrangement reaction
(hydrisomerisation process) Hydrogenation and dehydrogenation catalyst.

Effect of Operating Parameters

Various operating parameters affecting hydrocracking are
 Reaction temperature
 Hydrogen partial pressure
 Hourly feed velocity of the feed
 Hydrogen recycle ratio
Temperature increase in temperature accelerates cracking reaction on acid sites and displaces the
equilibrium of hydrogenation reactions towards dehydrogenation. Too high temperature limits
the hydrocracking of aromatic structure [Raseev, 2003].
The pressure influences significantly the equilibrium of dehydrogenation-hydrogenation
reactions that takes place on the metallic sites. The increase in pressure for a given molar ratio
H2/feed corresponds to increase in the partial pressure of hydrogen, will produce an increase the
conversion of the aromatic structures to saturated products which will improve the quality of jet
fuel, diesel fuel and oil with very high viscosity index.

Effect of Feedstock: a higher content of aromatic hydrocarbons requires higher pressure and
higher hydrogen/feed ratio, the lowest possible temperature and a higher hydrogen consumption
of hydrogen and the severity of the process
Effects of Feed Impurities: Hydrogen sulphide, nitrogen compounds and aromatic molecules
present in the feed affect the hydrocracking reactions. Increase in nitrogen result in lower
conversion.
Ammonia inhibits the hydrocracking catalyst activity, requiring higher operating temperatures.
Polymeric compounds have substantial inhibiting and poisoning effects. Polynuclear aromatics
present in small amount in the residue deactivate the catalyst.

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Effect of various parameters on catalyst life:
Variable Change Effect on catalyst life
Feed rate Increase-Decrease
Conversion Increase-Decrease
Hydrogen partial pressure Increase-Increase
Reactor pressure Increase-Increase
Recycle gas rate Increase -Increase
Recycle gas purity Increase -Increase

HYDRO-CRACKING TECHNOLOGY PROVIDER

 Chevron: Isocracking
 UOP: Uni-cracking
 IFP: Hydrocarcking
 B.P. U.K: Hydrocracking
 Shell: Hydrocracking
 Standard Oil: Ultracracking
 Linde: Hydrocarking
 Union Oil Co.: Uni-cracking

CATALYST DEACTIVATION
Catalyst activation may occur due to coke deposition and metal accumulation.
Coke Depositions may be due to condensation of poly-nuclear and olefinic compounds into high
molecular weight which cover active sites. Metal Accumulation occurs at the pore entrances or
near the outer surface of the catalyst

CATALYST REGENERATION

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Catalyst regeneration is done by burning off the carbon, and sulphur and circulation of circulate
nitrogen with the recycle compressor, injecting a small quantity of air and maintaining catalyst
temperature above the coke ignition temperature.

REFERENCES
1. Amano, T., Wilcox, J., Pouwels, C., “Process and catalysis factors to maximize propylene
output”, Petroleum Technology Quarterly, 3, 2012, p.17
2. Debasis Bhattacharyya, “Fluid Catalytic Cracking: Process Fundamentals”, 6th Summer
School on Petroleum Refining & Petrochemicals 6th–10th June, 2011
3. Ghosh, S “Fluid catalytic cracking: An overview & future scenario”, Indian Chemical
Engineer special Issue, Vol 1,2002, p.27
4. Ghosh, S. “Recent advances in fluid catalytic cracking”, Petrotech society’s summer school
program on advances in Petroleum Refining industry, 3-8 July 2006 held at IIPM, Gurgaon
5. Hemler, C.L. and Smith, L.F., “UOP fluid catalytic cracking Process” in Hand book of
Petroleum refining Processes edited by Meyers, R.A. Third edition The McGraw-Hill
Publication data 2004.
6. Letzsch, W., “Improve catalytic cracking to produce clean fuels”, Hydrocarbon processing
Feb, 2005,p.77
7. Mall,I.D. “Petrochemical processes technology” First Edi., New Delhi, Macmillan India,
2007
8. Raseev, S. “Hydrocracking in Thermal and Catalytic Processes in Petroleum refining”
Marcel Dekker, Inc2003, p.681.
9. Verma, RP. “Hydroprocessing:Indian scenario” Indian Chemical Engineer Special issue,
Vol 1, 2002.

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